Prof Peter Hoffmann
Professor and Lloyd Sansom Chair of Biomaterials Engineering and Nanomedicine
School of Pharmacy and Biomedical Science
College of Health
Professor Peter Hoffmann is President of the Australasian Proteomics Society, Conference Chair for the National Meeting of the Australasian Proteomics Society, and is Treasurer of the international Human Proteome Organisation (HUPO). For ten years, Peter’s research has delved into the identification of low abundant proteins and the mapping of their posttranslational modifications and their use as potential biomarkers for early detection of diseases, one of the biggest challenges in proteomics. He is leader in the field of Mass Spectrometry Imaging and his research group was the first to use this technology in Australia. He is Director of the NCRIS Bioplatforms Astralia Node for Tissue Imaging Mass Spectrometry. He has experience transforming research into industry-relevant outcomes, forming Onco DX to commercialise patented biomarkers for the early detection of ovarian and gastric cancer.
| Date | Position | Institution name |
|---|---|---|
| 2015 - ongoing | Professor | University of Adelaide |
| 2012 - ongoing | Director, National NCRIS facility for Tissue Imaging Mass Spectrometry | University of Adelaide |
| 2012 - ongoing | Deputy Director, Institute for Photonics and Advanced Sensing (IPAS) | University of Adelaide |
| 2012 - 2014 | Associate Professor | University of Adelaide |
| 2005 - ongoing | Director, Adelaide Proteomics Centre | University of Adelaide |
| 2005 - 2012 | Senior Lecturer | University of Adelaide |
| 2003 - 2005 | Postdoctoral Fellow | University of Leipzig |
| 2001 - 2003 | Head, Proteomics Unit | St Vincent’s Institute of Medical Research |
| 1999 - 2001 | Postdoctoral Fellow | Ludwig Institute For Cancer Research & The Walter and Eliza Hall Institute of Medical Research |
| Date | Institution name | Country | Title |
|---|---|---|---|
| 1999 | Saarland University | Germany | PhD in Analytical Chemistry |
| 1995 | Saarland University | Germany | Master’s degree, Diploma in Chemistry |
| Year | Citation |
|---|---|
| 2025 | Redden, L. D., Grubauer, B., Hoffmann, P., Langenbucher, A., Riaz, K. M., Gatinel, D., . . . Wendelstein, J. A. (2025). Response to Comment on: Intraocular Lens Power Calculation-Comparing Big Data Approaches to Established Formulas. AMERICAN JOURNAL OF OPHTHALMOLOGY, 276, 397-399. |
| 2025 | Langenbucher, A., Szentmary, N., Cayless, A., Hoffmann, P., & Wendelstein, J. (2025). Deciphering the performance of different surface models for corneal topography. OPHTHALMIC AND PHYSIOLOGICAL OPTICS, 45(6), 1270-1281. |
| 2025 | Langenbucher, A., Szentmary, N., Wendelstein, J., Cayless, A., Hoffmann, P., & Cooke, D. (2025). Repeatability of biometric measures from the LenStar LS900 in a cataractous population. PLOS ONE, 20(5), 13 pages. |
| 2025 | Langenbucher, A., Wendelstein, J., Cayless, A., Olsen, T., Hoffmann, P., & Szentmary, N. (2025). Jackknife and bootstrapping resampling techniques to evaluate the precision of lens formula constants. ACTA OPHTHALMOLOGICA, 103(6), e422-e433. |
| 2025 | Hoffmann, P., Potvin, R., Anello, R. D., Hengerer, F., Auffarth, G., Guldenfels, Y., . . . Relucio, A. S. (2025). Comparing Rotational Stability Over Time Between Four Monofocal Toric Intraocular Lenses. CLINICAL OPHTHALMOLOGY, 19, 1345-1355. WoS1 |
| 2025 | Ang, R. E. T., Khoramnia, R., Uy, H. S., Hoffmann, P., Anello, R. D., Zalewski, D., . . . Relucio, A. S. (2025). Comparison of Visual Acuity Outcomes of Enhanced Monofocal Versus Standard Monofocal Intraocular Lenses from a Randomized, Multicenter, Active-Controlled Trial. JOURNAL OF REFRACTIVE SURGERY, 41(4), 13 pages. WoS1 |
| 2025 | Langenbucher, A., Szentmary, N., Wendelstein, J., Cayless, A., Fassbind, B., & Hoffmann, P. (2025). Considerations on the Haigis formula: Are better outcomes possible with tuning?. ACTA OPHTHALMOLOGICA, 103(5), e298-e309. |
| 2025 | Westhofen, R., Weidinger, G., Hoffmann, P., Daxecker, A., & Antonitsch, L. (2025). Vitamin D: Harmless Nutritional Supplement or Serious Medication?. CLINICAL CASE REPORTS, 13(4), 4 pages. |
| 2025 | Langenbucher, A., Szentmary, N., Cayless, A., Cooke, D., Hoffmann, P., & Wendelstein, J. (2025). Prediction of refraction error after toric lens implantation with biometric input data uncertainties and power labelling tolerance (vol 53, pg 26, 2025). CLINICAL AND EXPERIMENTAL OPHTHALMOLOGY, 53(6), 735. |
| 2025 | Redden, L. D., Grubauer, B., Hoffmann, P., Langenbucher, A., Riaz, K. M., Gatinel, D., . . . Wendelstein, J. A. (2025). Intraocular Lens Power Calculation-Comparing Big Data Approaches to Established Formulas. AMERICAN JOURNAL OF OPHTHALMOLOGY, 273, 141-150. WoS2 |
| 2025 | Langenbucher, A., Szentmary, N., Cayless, A., Al Karam, M., Hoffmann, P., Seiler, T. G., & Wendelstein, J. (2025). Repeatability of Corneal Astigmatism and Equivalent Power with the MS-39 Tomographer Derived from Model Surface Fitting in a Cataractous Population. SENSORS, 25(19), 20 pages. |
| 2025 | Langenbucher, A., Hoffmann, P., Cayless, A., Wendelstein, J., & Szentmary, N. (2025). Conversion of disclosed lens power formula constants. JOURNAL OF CATARACT AND REFRACTIVE SURGERY, 51(8), 679-686. |
| 2025 | Bracher-Smith, M., Melograna, F., Ulm, B., Bellenguez, C., Grenier-Boley, B., Duroux, D., . . . Hiltunen, M. (2025). Machine learning in Alzheimer’s disease genetics. Nature Communications, 16(1). Europe PMC2 |
| 2025 | Nicolai, J., Miller, A. J., Hahn, N., Fazaal, J., Bunte, A., Silvery, J., . . . Dilthey, A. T. (2025). Large-scale SARS-CoV-2 sequencing indicates prior community circulation of the viral strain associated with Germany’s largest meat processing plant. Scientific Reports, 15(1). |
| 2025 | David, F. S., Frank, J., Stein, F., Meinert, S., Zillich, L., Sirignano, L., . . . Forstner, A. J. (2025). Blood-based DNA methylation profiles in major depressive disorder, bipolar disorder, and schizophrenia spectrum disorders. COMPREHENSIVE PSYCHIATRY, 143, 12 pages. |
| 2025 | Glässner, A., Steffens, M., Fatangare, A., Wurpts, G., Hoffmann, P., Deck, P. N., . . . Sachs, B. (2025). Analysis of differential gene expression of PBMC for the in vitro detection of drug sensitization. Allergology International, 74(3), 414-423. Scopus1 WoS1 Europe PMC1 |
| 2025 | Ose, S. O., Lestander, H. A., Hoffmann, P. L., Bokseth, Y., Sundnes, L., Skjelbred, N. O., . . . Thaulow, K. (2025). Exploring VR in municipal mental health services: A pilot study. JOURNAL OF REHABILITATION AND ASSISTIVE TECHNOLOGIES ENGINEERING, 12, 9 pages. |
| 2025 | Desire, C. T., Dilmetz, B. A., Degenhardt, J., Donnellan, L., Condina, M. R., Young, C., & Hoffmann, P. (2025). The Importance of Denaturing Conditions for Protein and Peptide Quantification by Tryptophan Fluorescence. ACS Omega, 10(46), 56795-56805. |
| 2025 | Donnellan, L., Fenech, M., Dhillon, V. S., Young, C., Hoffmann, P., & Deo, P. (2025). Role of methylglyoxal protein modifications in DNA damage and chromosomal instability: Emerging molecular mechanisms. Mutation Research Reviews in Mutation Research, 796(108558), 10 pages. Scopus3 WoS3 Europe PMC2 |
| 2025 | Jasni, N., Khairul, K. B., Kin, W. W., Lau, D., Young, C., Hoffmann, P., & Othman, N. (2025). In-silico, in-vitro, and proteomics analyses on repurposed drugs in targeting the small GTPase, Rho subfamily protein (Rho GTPase), and putative Rho GTPase-activating protein (RhoGAP) of Giardia lamblia. Journal of Genetic Engineering and Biotechnology, 23(4), 13 pages. |
| 2025 | Ngai, Y. T., Lau, D., Mittal, P., & Hoffmann, P. (2025). Mini Review: Highlight of Recent Advances and Applications of MALDI Mass Spectrometry Imaging in 2024. Analytical Science Advances, 6(1), 11 pages. Scopus5 WoS4 Europe PMC4 |
| 2025 | Juhasz, A. L., Kastury, F., Jones, R., Seeborun, M., Caceres, T., Herde, C., . . . Hoffmann, P. (2025). PFOA, PFOS and PFHxS toxicokinetic considerations for the development of an in vivo approach for assessing PFAS relative bioavailability in soil. Environment International, 195(109232), 11 pages. Scopus3 WoS3 Europe PMC2 |
| 2025 | Schwendinger, S., Jaschke, W., Walder, T., Hench, J., Vogi, V., Frank, S., . . . Jukic, E. (2025). DNA Methylation Array Analysis Identifies Biological Subgroups of Cutaneous Melanoma and Reveals Extensive Differences with Benign Melanocytic Nevi. Diagnostics, 15(5). Scopus1 WoS1 Europe PMC1 |
| 2025 | Dand, N., Stuart, P. E., Bowes, J., Ellinghaus, D., Nititham, J., Saklatvala, J. R., . . . Elder, J. T. (2025). GWAS meta-analysis of psoriasis identifies new susceptibility alleles impacting disease mechanisms and therapeutic targets. Nature Communications, 16(1). Scopus16 WoS16 Europe PMC20 |
| 2025 | Meller, T., Lundberg, C., Maj, C., Hoffmann, P., Forstner, A. J., Nöthen, M. M., & Nenadić, I. (2025). Schizotypy, Psychosis Proneness, and the Polygenic Risk for Schizophrenia and Resilience. Schizophrenia Bulletin, 51, S85-S94. Scopus4 WoS4 Europe PMC4 |
| 2025 | Hoffmann, J., Meller, T., Maj, C., Hoffmann, P., Forstner, A. J., Nöthen, M. M., & Nenadić, I. (2025). Differential Association of Schizotypy Dimensions With Brain Structural Connectivity and Moderation by Schizophrenia Polygenic Risk. Schizophrenia Bulletin, 51, S149-S159. WoS1 |
| 2025 | Schulz, H., Abdelfattah, F., Heinrich, A., Melnik, D., Sandt, V., Krüger, M., . . . Grimm, D. (2025). Omics Investigations of Prostate Cancer Cells Exposed to Simulated Microgravity Conditions. Biomolecules, 15(2). Scopus1 |
| 2025 | Lau, D., Donnellan, L., Briggs, M., Klingler Hoffmann, M., & Hoffmann, P. (2025). MALDI Mass spectrometry imaging of metabolites in cereal grains and legumes: repurposing for industrial applications. Food Reviews International, 41(4), 1200-1221. Scopus4 WoS4 |
| 2025 | Adams, M. J., Streit, F., Meng, X., Awasthi, S., Adey, B. N., Choi, K. W., . . . Einarsson, G. (2025). Trans-ancestry genome-wide study of depression identifies 697 associations implicating cell types and pharmacotherapies. Cell, 188(3), 640-652.e9. Scopus45 WoS48 Europe PMC73 |
| 2025 | Lau, D., Donnellan, L., Harris, J. C., Hayes, J. E., Croser, J., & Hoffmann, P. (2025). Proteomic and lipidomic analyses reveal novel molecular insights into oat (Avena sativa L.) lipid regulation and crosstalk with starch synthesis during grain development.. International Journal of Biological Macromolecules, 306(Part 1), 141305-1-141305-11. |
| 2025 | Lau, W. C. D., Donnellan, L., Harris, J. C., Seidel, J., Hayes, J. E., Croser, J., & Hoffmann, P. (2025). Coupling proteomics and lipidomics for insights into regulation of oat (Avena sativa) grain lipid synthesis. Food Chemistry, 478(143644), 143644-1-143644-12. Scopus3 WoS2 |
| 2025 | Aralappanavar, V. K., Sarkar, B., Doolette, C. L., Rose, M., Donnellan, L., Smith, E., . . . Lombi, E. (2025). A diffusive gradients in thin-films (DGT) methodology for in situ measurement of imazamox and imazapyr herbicide residues. Talanta, 295(128350), 1-11. Scopus1 WoS1 |
| 2025 | Noye, T. M., Mittal, P., Price, Z. K., Fewster, A., Williams, G., Pukala, T. L., . . . Ricciardelli, C. (2025). Identification of Proteins Associated with Ovarian Cancer Chemotherapy Resistance Using MALDI-MSI. International Journal of Molecular Sciences, 26(12), 5893. |
| 2025 | Langenbucher, A., Wendelstein, J., Cayless, A., Szentmáry, N., Hoffmann, P., Cooke, D., . . . Olsen, T. (2025). Deciphering corneal astigmatism - Calculation pitfalls and how to avoid them. Journal of Cataract and Refractive Surgery, 51(10), 933-935. Scopus1 WoS1 |
| 2025 | Aralappanavar, V. K., Sarkar, B., Doolette, C. L., Donnellan, L., Mason, S., Rose, M., . . . Lombi, E. (2025). Diffusive gradients in thin films (DGT) for measuring potentially bioavailable pesticide residues in soil systems: current challenges and perspectives. Critical Reviews In Environmental Science And Technology, online(17), 1-22. |
| 2025 | Pires, M. C., Jungbauer, A., Lau, D., Young, C., Hoffmann, P., de Pádua, T. F., & Gerstweiler, L. (2025). Column ageing of agarose-based chromatography in industrial lactoferrin purification. Journal of Chromatography A, 1760(466274), 466274. |
| 2025 | Lee, J. H., Sumer Bayraktar, Z., Mittal, P., Donnellan, L., Young, C., Rushworth, R. L., . . . Meyer, E. J. (2025). Mass spectrometric detection of neutrophil elastase cleaved corticosteroid binding globulin and its association with Asn347 site glycosylation, in septic shock patients. Clinica Chimica Acta, 567(120108), 1-8. Scopus1 WoS1 Europe PMC1 |
| 2025 | Seidel, J. D., Young, C., Klingler Hoffmann, M., Condina, M. R., Shah, A., Ramarathinam, S., . . . Hoffmann, P. (2025). Analytical methods for in-depth characterisation of cell culture bioreactors: A case study. Journal of Chromatography Open, 8(100248), 1-13. |
| 2025 | Ngai, Y. T., Young, C., Parkinson-Lawrence, E. J., Wimmer-Kleikamp, S., Mittal, P., Beard, H., . . . Hoffmann, P. (2025). Defining lung pathogenesis in a murine model of mucopolysaccharidosis Type I by proteomic analysis. Molecular Genetics and Metabolism, 146(1-2), 109231. |
| 2025 | Subramaniam, S., Donnellan, L., Wignall, A., Woodcock, J., Coolen, C., Pitson, S., . . . Joyce, P. (2025). Polymeric-lipid nanoparticles that leverage cationic helper lipids and the protein corona for lung-targeted delivery of a novel anti-cancer drug. Journal of Controlled Release, 388(Pt 1), 15 pages. |
| 2025 | Lokman, N. A., Macpherson, A. M., Thompson, A. R., Price, Z. K., Goonetilleke, L., Condina, M. R., . . . Ricciardelli, C. (2025). Proteomics analysis of serum extracellular vesicle identifies UCHL1 as a potential therapeutic target for high grade serous ovarian cancer. British Journal of Cancer, 13 pages. |
| 2024 | Seidel, J. D., Condina, M. R., Klingler Hoffmann, M., Young, C., Donnellan, L., Kyngdon, C., & Hoffmann, P. (2024). Development of an optimized LC-MS workflow for host cell protein characterization to support upstream process development. Journal of Proteome Research, 24(1), 234-243. Scopus1 WoS1 |
| 2024 | Dilmetz, B. A., Desire, C. T., Meneses, J., Klingler-Hoffmann, M., Young, C., & Hoffmann, P. (2024). Impact of propagation time on yeast physiology during bottle conditioning of beer on an industrial scale. Food Chemistry, 435, 1-9. Scopus2 WoS1 Europe PMC1 |
| 2024 | Sukjoi, W., Young, C., Acland, M., Siritutsoontorn, S., Roytrakul, S., Klingler Hoffmann, M., . . . Jitrapakdee, S. (2024). Proteomic analysis of holocarboxylase synthetase deficient-MDA-MB-231 breast cancer cells revealed the biochemical changes associated with cell death, impaired growth signaling, and metabolism. Frontiers in Molecular Biosciences, 10, 1-16. Scopus1 WoS1 Europe PMC1 |
| 2024 | Ou, A. H., Rosenthal, S. B., Adli, M., Akiyama, K., Akula, N., Alda, M., . . . Kelsoe, J. R. (2024). Lithium response in bipolar disorder is associated with focal adhesion and PI3K-Akt networks: a multi-omics replication study. Translational Psychiatry, 14(1), 109-1-109-9. Scopus16 WoS13 Europe PMC12 |
| 2024 | Li, C. M. Y., Briggs, M. T., Lee, Y. -R., Tin, T., Young, C., Pierides, J., . . . Fenix, K. (2024). Use of tryptic peptide MALDI mass spectrometry imaging to identify the spatial proteomic landscape of colorectal cancer liver metastases.. Clin Exp Med, 24(1), 53. Scopus6 WoS6 Europe PMC3 |
| 2024 | Ngai, Y. T., Briggs, M. T., Mittal, P., Young, C., Parkinson-Lawrence, E., Klingler-Hoffmann, M., . . . Hoffmann, P. (2024). Mass spectrometry imaging protocol for spatial mapping of lipids, N-glycans and peptides in murine lung tissue. Rapid Communications in Mass Spectrometry, 38(9), e9721. Scopus6 WoS4 Europe PMC3 |
| 2024 | Moxon, J. V., Pretorius, C., Trollope, A. F., Mittal, P., Klingler-Hoffmann, M., Hoffmann, P., & Golledge, J. (2024). A systematic review and in silico analysis of studies investigating the ischaemic penumbra proteome in animal models of experimental stroke. Journal of Cerebral Blood Flow and Metabolism, 44(10), 1709-1722. Scopus2 WoS3 Europe PMC2 |
| 2024 | Herrera-Rivero, M., Adli, M., Akiyama, K., Akula, N., Amare, A. T., Ardau, R., . . . Baune, B. T. (2024). Exploring the genetics of lithium response in bipolar disorders. International Journal of Bipolar Disorders, 12(1), 20-1-20-11. Scopus7 WoS6 Europe PMC7 |
| 2024 | Dilmetz, B. A., Brar, G., Desire, C. T., Meneses, J., Klingler Hoffmann, M., Young, C., & Hoffmann, P. (2024). Performance of different Saccharomyces strains on secondary fermentation during the production of beer. Foods, 13(16, article no. 2593), 1-17. |
| 2024 | Lau, W. C. D., Donnellan, L., Briggs, M., Rupasinghe, T., Harris, J. C., Hayes, J. E., & Hoffmann, P. (2024). Sodium doping and trapped ion mobility spectrometry improve lipid detection for novel MALDI-MSI analysis of oats. Food Chemistry, 433(137275), 1-10. Scopus10 WoS10 Europe PMC8 |
| 2024 | Schmidt, A., Casadei, N., Brand, F., Demidov, G., Vojgani, E., Abolhassani, A., . . . Ludwig, K. U. (2024). Systematic assessment of COVID-19 host genetics using whole genome sequencing data. Plos Pathogens, 20(12 December). |
| 2024 | Desrivières, S., Miller, A., Mathey, C. M., Yu, X., Chen, D., Agunbiade, K., . . . Walter, H. (2024). Multi-omics analyses of the environMENTAL project provide insights into mental health and disease. Nature Mental Health, 2(10), 1131-1133. Scopus1 |
| 2024 | Goldblatt, R., Holz, N., Tate, G. W., Sherman, K., Ghebremicael, S., Bhuyan, S. S., . . . Calhoun, V. D. (2024). Linking neuroimaging and mental health data from the ABCD Study to UrbanSat measurements of macro environmental factors. Nature Mental Health, 2(11), 1285-1297. Scopus4 WoS2 |
| 2024 | Neidhart, M., Kjelkenes, R., Jansone, K., Rehák Bučková, B., Holz, N., Nees, F., . . . Heinz, A. (2024). A protocol for data harmonization in large cohorts. Nature Mental Health, 2(10), 1134-1137. Scopus1 WoS1 |
| 2024 | Cheaib, M., Hornung, N., Dragano, N., Frank, M., Hoffmann, P., Nöthen, M. M., . . . Schmidt, B. (2024). Socioeconomic position interacts with the genetic effect of a CRP gene common variant to influence C-reactive protein values. Scientific Reports, 14(1). Scopus1 WoS1 Europe PMC1 |
| 2024 | Choe, K., Ali, M., Lardenoije, R., Riemens, R. J. M., Pishva, E., Bickel, H., . . . van den Hove, D. L. A. (2024). Alzheimer’s disease-specific transcriptomic and epigenomic changes in the tryptophan catabolic pathway. Alzheimer S Research and Therapy, 16(1). Scopus6 WoS5 Europe PMC4 |
| 2024 | Yde Ohki, C. M., Walter, N. M., Rickli, M., Iseli, C., Werling, A. M., Döring, C., . . . Grünblatt, E. (2024). Generation of induced pluripotent stem cells from ADHD patients who do or do not respond to Methylphenidate treatment. Stem Cell Research, 81. Scopus2 WoS2 Europe PMC2 |
| 2024 | Thomsen, H., Chattopadhyay, S., Weinhold, N., Vodicka, P., Vodickova, L., Hoffmann, P., . . . Försti, A. (2024). Haplotype analysis identifies functional elements in monoclonal gammopathy of unknown significance. Blood Cancer Journal, 14(1). Scopus2 WoS2 Europe PMC1 |
| 2024 | Mathey, C. M., Maj, C., Eriksson, N., Krebs, K., Westmeier, J., David, F. S., . . . Forstner, A. J. (2024). Meta-analysis of ACE inhibitor–induced angioedema identifies novel risk locus. Journal of Allergy and Clinical Immunology, 153(4), 1073-1082. Scopus9 WoS8 Europe PMC10 |
| 2024 | Hench, J., Hultschig, C., Brugger, J., Mariani, L., Guzman, R., Soleman, J., . . . Frank, S. (2024). EpiDiP/NanoDiP: a versatile unsupervised machine learning edge computing platform for epigenomic tumour diagnostics. Acta Neuropathologica Communications, 12(1), 16 pages. Scopus20 WoS18 Europe PMC16 |
| 2024 | Tremmel, R., Martínez Pereyra, V., Broders, I., Schaeffeler, E., Hoffmann, P., Nöthen, M. M., . . . Ong, P. (2024). Genetic associations of cardiovascular risk genes in European patients with coronary artery spasm. Clinical Research in Cardiology, 113(12), 1733-1744. Scopus1 WoS2 Europe PMC1 |
| 2024 | Pelgrim, T. A. D., Philipsen, A., Young, A. H., Juruena, M., Jimenez, E., Vieta, E., . . . van Westrhenen, R. (2024). A New Intervention for Implementation of Pharmacogenetics in Psychiatry: A Description of the PSY-PGx Clinical Study. Pharmaceuticals, 17(2), 15 pages. Scopus11 WoS8 Europe PMC7 |
| 2024 | Sebben, D. A., Semple, S. J., Condina, M. R., Dilmetz, B. A., Hoffmann, P., Claudie, D. J., . . . Beattie, D. A. (2024). Extraction and surface activity of Australian native plant extracts: Alphitonia excelsa. Colloids and Interfaces, 8(4), 1-14. |
| 2024 | Hutchings, J. L., Grebneva, Y., Dilmetz, S. J., Pincher, D. W. M., & Hoffmann, P. (2024). Analytical methods for the analysis of bromoform in red seaweed Asparagopsis armata and Asparagopsis taxiformis – A review. Algal Research, 79(103478), 19 pages. Scopus13 WoS11 |
| 2024 | Langenbucher, A., Hoffmann, P., Cayless, A., Wendelstein, J., & Szentmary, N. (2024). Limitations of constant optimization with disclosed intraocular lens power formulae. JOURNAL OF CATARACT AND REFRACTIVE SURGERY, 50(3), 201-208. WoS13 |
| 2024 | Gatinel, D., Hoffmann, P. C., Cooke, D. L., Chingan, A., Debellemaniere, G., Langenbucher, A., & Wendelstein, J. A. (2024). Leaving trusted paths: Estimating corneal keratometric index in cataract surgery eyes with zero-power implants. GRAEFES ARCHIVE FOR CLINICAL AND EXPERIMENTAL OPHTHALMOLOGY, 262(8), 2533-2539. WoS3 |
| 2024 | Wendelstein, J. A., Hoffmann, P. C., Hoffer, K. J., Langenbucher, A., Findl, O., Ruiss, M., . . . Savini, G. (2024). Differences Between Keratometry and Total Keratometry Measurements in a Large Dataset Obtained With a Modern Swept Source Optical Coherence Tomography Biometer. AMERICAN JOURNAL OF OPHTHALMOLOGY, 260, 102-114. WoS11 |
| 2024 | Strom, N. I., Verhulst, B., Bacanu, S. -A., Cheesman, R., Purves, K. L., Gedik, H., . . . Hettema, J. M. (2024). Genome-wide association study of major anxiety disorders in 122,341 European-ancestry cases identifies 58 loci and highlights GABAergic signaling.. medRxiv. |
| 2023 | Gehlen, J., Stundl, A., Debiec, R., Fontana, F., Krane, M., Sharipova, D., . . . Schumacher, J. (2023). Elucidation of the genetic causes of bicuspid aortic valve disease. Cardiovascular Research, 119(3), 857-866. Scopus29 WoS27 Europe PMC32 |
| 2023 | Yde Ohki, C. M., Walter, N. M., Rickli, M., Van Puyenbroeck, P., Döring, C., Hoffmann, P., . . . Grünblatt, E. (2023). Generation of induced pluripotent stem cells from two ADHD patients and two healthy controls. Stem Cell Research, 69, 5 pages. Scopus5 WoS5 Europe PMC6 |
| 2023 | David, F. S., Stein, F., Andlauer, T. F. M., Streit, F., Witt, S. H., Herms, S., . . . Forstner, A. J. (2023). Genetic contributions to transdiagnostic symptom dimensions in patients with major depressive disorder, bipolar disorder, and schizophrenia spectrum disorders. Schizophrenia Research, 252, 161-171. Scopus17 WoS19 Europe PMC17 |
| 2023 | Lechner, L., Opitz, R., Silver, M. J., Krabusch, P. M., Prentice, A. M., Field, M. S., . . . Kühnen, P. (2023). Early-set POMC methylation variability is accompanied by increased risk for obesity and is addressable by MC4R agonist treatment. Science Translational Medicine, 15(705), 15 pages. Scopus14 WoS11 Europe PMC10 |
| 2023 | Ose, S. O., Thaulow, K., Faerevik, H., Hoffmann, P. L., Lestander, H., Stiles, T., & Lindgren, M. (2023). Development of a social skills training programme to target social isolation using virtual reality technology in primary mental health care. JOURNAL OF REHABILITATION AND ASSISTIVE TECHNOLOGIES ENGINEERING, 10, 10 pages. WoS1 |
| 2023 | Hess, T., Maj, C., Gehlen, J., Borisov, O., Haas, S. L., Gockel, I., . . . Adolfsson, R. (2023). Dissecting the genetic heterogeneity of gastric cancer. Ebiomedicine, 92, 13 pages. Scopus20 WoS21 Europe PMC20 |
| 2023 | Wendelstein, J. A., Hinterberger, S., Hoffmann, P. C., Hirnschall, N., Koss, M. J., Langenbucher, A., . . . Bolz, M. (2023). Evaluation of phakic intraocular lens power calculation using the new Linz-Homburg-Castrop formula and comparison with four conventional methods. JOURNAL OF CATARACT AND REFRACTIVE SURGERY, 49(2), 119-125. WoS4 |
| 2023 | Wendelstein, J. A., Rothbaecher, J., Heath, M., Mcdonald, M. C., Hoffmann, P. C., Cooke, D. L., . . . Riaz, K. M. (2023). Influence and predictive value of optional parameters in new-generation intraocular lens formulas. JOURNAL OF CATARACT AND REFRACTIVE SURGERY, 49(8), 795-803. WoS12 |
| 2023 | Wendelstein, J. A., Reifeltshammer, S. A., Cooke, D. L., Hirnschall, N., Hoffmann, P. C., Langenbucher, A., . . . Riaz, K. M. (2023). The 10,000 Eyes Study: Analysis of Keratometry, Abulafia-Koch regression transformation, and Biometric Eye Parameters Obtained With Swept-Source Optical Coherence Tomography. AMERICAN JOURNAL OF OPHTHALMOLOGY, 245, 44-60. WoS8 |
| 2023 | Grey, A. C., Lin, Q., Low, T. Y., Wu, W., Haynes, P. A., Chung, M. C. M., . . . Poon, T. C. W. (2023). 11th Asia Oceania Human Proteome Organization Congress Report. Molecular and Cellular Proteomics, 22(9), 8 pages. |
| 2023 | Subramaniam, S., Joyce, P., Donnellan, L., Young, C., Wignall, A., Hoffmann, P., & Prestidge, C. A. (2023). Protein adsorption determines pulmonary cell uptake of lipid-based nanoparticles. Journal of Colloid and Interface Science, 641, 36-47. Scopus32 WoS31 Europe PMC23 |
| 2023 | Kumarasamy, G., Ismail, M. N., Tuan Sharif, S. E., Desire, C., Mittal, P., Hoffmann, P., & Kaur, G. (2023). Protein profiling in human papillomavirus-associated cervical carcinogenesis: cornulin as a biomarker for disease progression. Current Issues in Molecular Biology, 45(4), 3603-3627. Scopus4 WoS3 Europe PMC3 |
| 2023 | Zhao, L., Mühleisen, T. W., Pelzer, D. I., Burger, B., Beins, E. C., Forstner, A. J., . . . Cichon, S. (2023). Relationships between neurotransmitter receptor densities and expression levels of their corresponding genes in the human hippocampus. Neuroimage, 273, 13 pages. Scopus5 WoS5 Europe PMC5 |
| 2023 | Schumann, G., Andreassen, O. A., Banaschewski, T., Calhoun, V. D., Clinton, N., Desrivieres, S., . . . Westlye, L. (2023). Addressing Global Environmental Challenges to Mental Health Using Population Neuroscience: A Review. JAMA Psychiatry, 80(10), 1066-1074. Scopus21 WoS15 Europe PMC16 |
| 2023 | Glässner, A., Wurpts, G., Röseler, S., Yazdi, A. S., Krämer, C., Fatangare, A., . . . Sachs, B. (2023). IFN-γ secretion of PBMC from non-drug-allergic control persons: Considerations for the validity of a positive lymphocyte transformation test. Journal of Immunological Methods, 519, 5 pages. Scopus2 WoS2 Europe PMC2 |
| 2023 | de Rojas, I., Moreno-Grau, S., Tesi, N., Grenier-Boley, B., Andrade, V., Jansen, I. E., . . . Rodriguez-Rodriguez, E. (2023). Author Correction: Common variants in Alzheimer’s disease and risk stratification by polygenic risk scores (Nature Communications, (2021), 12, 1, (3417), 10.1038/s41467-021-22491-8). Nature Communications, 14(1), 2 pages. |
| 2023 | Sebastian, S., Hoffmann, M. K., Howard, D., Young, C., Washington, J., Unterweger, H., . . . Kempson, I. (2023). Kinetic effects of transferrin-conjugated gold nanoparticles on the antioxidant glutathione-thioredoxin pathway. Antioxidants, 12(8, article no. 1617), 1-21. Scopus8 WoS8 Europe PMC7 |
| 2023 | Docherty, A. R., Mullins, N., Ashley-Koch, A. E., Qin, X., Coleman, J. R. I., Shabalin, A., . . . Adolfsson, R. (2023). GWAS Meta-Analysis of Suicide Attempt: Identification of 12 Genome-Wide Significant Loci and Implication of Genetic Risks for Specific Health Factors. American Journal of Psychiatry, 180(10), 723-738. Scopus83 WoS81 Europe PMC99 |
| 2023 | Arentz, G., Mittal, P., Klingler-Hoffmann, M., Condina, M. R., Ricciardelli, C., Lokman, N. A., . . . Hoffmann, P. (2023). Label-Free Quantification Mass Spectrometry Identifies Protein Markers of Chemotherapy Response in High-Grade Serous Ovarian Cancer. Cancers, 15(7), 14 pages. Scopus4 WoS5 Europe PMC4 |
| 2023 | Dilmetz, B. A., Desire, C. T., Donnellan, L., Meneses, J., Klingler Hoffmann, M., & Young, C. (2023). Assessment of yeast physiology during industrial-scale brewing practices using the redox-sensitive dye resazurin. Yeast, 40(5-6), 171-181. Scopus2 WoS2 Europe PMC1 |
| 2023 | Amare, A. T., Thalamuthu, A., Schubert, K. O., Fullerton, J. M., Ahmed, M., Hartmann, S., . . . Baune, B. T. (2023). Association of polygenic score and the involvement of cholinergic and glutamatergic pathways with lithium treatment response in patients with bipolar disorder. Molecular Psychiatry, 28(12), 5251-5261. Scopus22 WoS21 Europe PMC26 |
| 2023 | Hua, Q. Q. H., Young, C., Pukala, T. L., Martino, J. C., Hoffmann, P., Gillanders, B. M., & Doubleday, Z. A. (2023). Better late than never: Optimising the proteomic analysis of field-collected octopus.. PloS one, 18(7), e0288084. Scopus1 WoS1 Europe PMC1 |
| 2023 | Lee, Y. -R., Briggs, M. T., Kuliwaba, J. S., Jagiello, J., Anderson, P. H., & Hoffmann, P. (2023). Complex-Type <i>N</i>-Glycans Are Associated with Cartilage Degeneration within Different Loading Sites of the Tibial Plateau for Knee Osteoarthritis Patients. Journal of Proteome Research, 22(8), 2694-2702. Scopus4 WoS4 Europe PMC3 |
| 2023 | Lee, Y. -R., Briggs, M. T., Kuliwaba, J. S., Jagiello, J., Anderson, P. H., & Hoffmann, P. (2023). High-Resolution <i>N</i>-Glycan MALDI Mass Spectrometry Imaging of Subchondral Bone Tissue Microarrays in Patients with Knee Osteoarthritis. Analytical Chemistry, 95(34), 12575-12992. Scopus3 WoS3 Europe PMC5 |
| 2023 | Niemi, M. E. K., Karjalainen, J., Liao, R. G., Neale, B. M., Daly, M., Ganna, A., . . . Sedaghati-Khayat, B. (2023). Erratum to: Mapping the human genetic architecture of COVID-19 (Nature, (2021), 600, 7889, (472-477), 10.1038/s41586-021-03767-x). Nature, 621(7977), E7-E26. Scopus63 WoS76 Europe PMC71 |
| 2022 | McNab, J. M., Briggs, M. T., Williamson, J. E., Hoffmann, P., Rodriguez, J., & Karuso, P. (2022). Structural Characterization and Spatial Mapping of Tetrodotoxins in Australian Polyclads. Marine Drugs, 20(12), 15 pages. Scopus6 WoS6 Europe PMC2 |
| 2022 | Jäger, S., Cabral, M., Kopp, J. F., Hoffmann, P., Ng, E., Whitfield, J. B., . . . Schulze, M. B. (2022). Blood copper and risk of cardiometabolic diseases: A Mendelian randomization study. Human Molecular Genetics, 31(5), 783-791. Scopus23 WoS22 Europe PMC19 |
| 2022 | Thalamuthu, A., Mills, N. T., Berger, K., Minnerup, H., Grotegerd, D., Dannlowski, U., . . . Baune, B. T. (2022). Genome-wide interaction study with major depression identifies novel variants associated with cognitive function.. Mol Psychiatry, 27(2), 1111-1119. Scopus37 WoS35 Europe PMC32 |
| 2022 | Mullins, N., Kang, J. E., Campos, A. I., Coleman, J. R. I., Edwards, A. C., Galfalvy, H., . . . Braff, D. L. (2022). Dissecting the Shared Genetic Architecture of Suicide Attempt, Psychiatric Disorders, and Known Risk Factors. Biological Psychiatry, 91(3), 313-327. Scopus174 WoS160 Europe PMC173 |
| 2022 | Cearns, M., Amare, A. T., Schubert, K. O., Thalamuthu, A., Frank, J., Streit, F., . . . Baune, B. T. (2022). Using polygenic scores and clinical data for bipolar disorder patient stratification and lithium response prediction: machine learning approach. The British Journal of Psychiatry, 220(4), 219-228. Scopus21 WoS22 Europe PMC23 |
| 2022 | Lin, V. J. T., Hu, J., Zolekar, A., Salick, M. R., Mittal, P., Bird, J. T., . . . Wang, Y. C. (2022). Deficiency of N-glycanase 1 perturbs neurogenesis and cerebral development modeled by human organoids. Cell Death & Disease, 13(3, article no. 262), 1-13. Scopus13 WoS11 Europe PMC9 |
| 2022 | Donnellan, L., Young, C., Simpson, B. S., Acland, M., Dhillon, V. S., Costabile, M., . . . Deo, P. (2022). Proteomic analysis of methylglyoxal modifications reveals susceptibility of glycolytic enzymes to dicarbonyl stress. International Journal of Molecular Sciences, 23(7, article no. 3689), 1-15. Scopus26 WoS25 Europe PMC25 |
| 2022 | Trubetskoy, V., Pardiñas, A. F., Qi, T., Panagiotaropoulou, G., Benyamin, B., & O'Donovan, M. C. (2022). Mapping genomic loci implicates genes and synaptic biology in schizophrenia. Nature, 604(7906), 502-508. Scopus1583 WoS1545 Europe PMC1973 |
| 2022 | Donnellan, L., Young, C., Simpson, B. S., Dhillon, V. S., Costabile, M., Hoffmann, P., . . . Deo, P. (2022). Methylglyoxal impairs sister chromatid separation in lymphocytes. International Journal of Molecular Sciences, 23(8, article no. 4139), 1-11. Scopus4 WoS4 Europe PMC3 |
| 2022 | Acland, M., Lokman, N. A., Young, C., Anderson, D., Condina, M., Desire, C., . . . Klingler-Hoffmann, M. (2022). Chemoresistant Cancer Cell Lines Are Characterized by Migratory, Amino Acid Metabolism, Protein Catabolism and IFN1 Signalling Perturbations. Cancers, 14(11), 1-24. Scopus6 WoS6 Europe PMC7 |
| 2022 | Cearns, M., Amare, A. T., Schubert, K. O., Thalamuthu, A., Frank, J., Streit, F., . . . Stamm, T. (2022). Erratum: Using polygenic scores and clinical data for bipolar disorder patient stratification and lithium response prediction: Machine learning approach (The British Journal of Psychiatry (2022) (1–10) DOI: 10.1192/bjp.2022.28). British Journal of Psychiatry, 221(2), 494. Scopus5 WoS3 Europe PMC4 |
| 2022 | Schubert, K. O., Thalamuthu, A., Amare, A. T., Frank, J., Streit, F., Adl, M., . . . Baune, B. T. (2022). Correction: Combining schizophrenia and depression polygenic risk scores improves the genetic prediction of lithium response in bipolar disorder patients.. Translational psychiatry, 12(1), 278. WoS3 |
| 2022 | Acland, M., Mittal, P., Arentz, G., Whitehead, F., Hoffmann, P., Klingler Hoffmann, M., & Oehler, M. K. (2022). A protocol for the acquisition of comprehensive proteomics data from single cases using formalin-fixed paraffin embedded sections. Methods and Protocols, 5(4, article no. 57), 1-17. Scopus3 WoS3 Europe PMC3 |
| 2022 | Cathro, P., McCarthy, P., Hoffmann, P., Kidd, S., & Zilm, P. (2022). Enterococcus faecalis V583 cell membrane protein expression to alkaline stress.. FEMS Microbiology Letters, 369(1), fnac082-1-fnac082-5. Scopus6 WoS6 Europe PMC4 |
| 2022 | Lee, Y. -R., Briggs, M. T., Young, C., Condina, M. R., Kuliwaba, J. S., Anderson, P. H., & Hoffmann, P. (2022). Mass spectrometry imaging spatially identifies complex-type N-glycans as putative cartilage degradation markers in human knee osteoarthritis tissue. Analytical and Bioanalytical Chemistry, 414(26), 7597-7607. Scopus9 WoS9 Europe PMC7 |
| 2022 | Kumar, R., Kamath, K. S., Carroll, L., Hoffmann, P., Gecz, J., & Jolly, L. A. (2022). Endogenous protein interactomes resolved through immunoprecipitation-coupled quantitative proteomics in cell lines. STAR protocols, 3(4), 1-31. Scopus4 WoS4 Europe PMC4 |
| 2022 | Pham, Q. N., Winter, M., Milanova, V., Young, C., Condina, M. R., Hoffmann, P., . . . Thierry, B. (2022). Magnetic enrichment of immuno-specific extracellular vesicles for mass spectrometry using biofilm-derived iron oxide nanowires. Nanoscale, 15(3), 1236-1247. Scopus8 WoS7 Europe PMC6 |
| 2022 | Fritz, N., Berens, S., Dong, Y., Martinez, C., Schmitteckert, S., Houghton, L. A., . . . Niesler, B. (2022). The serotonin receptor 3E variant is a risk factor for female IBS-D. JOURNAL OF MOLECULAR MEDICINE-JMM, 100(11), 1617-1627. WoS4 |
| 2022 | Mathey, C. M., Maj, C., Scheer, A. B., Fazaal, J., Wedi, B., Wieczorek, D., . . . Forstner, A. J. (2022). Molecular Genetic Screening in Patients With ACE Inhibitor/Angiotensin Receptor Blocker-Induced Angioedema to Explore the Role of Hereditary Angioedema Genes. Frontiers in Genetics, 13, 11 pages. Scopus12 WoS10 |
| 2022 | Ludwig, K. U., Schmithausen, R. M., Li, D., Jacobs, M. L., Hollstein, R., Blumenstock, K., . . . Schmid-Burgk, J. L. (2022). Author Correction: LAMP-Seq enables sensitive, multiplexed COVID-19 diagnostics using molecular barcoding (Nature Biotechnology, (2021), 39, 12, (1556-1562), 10.1038/s41587-021-00966-9). Nature Biotechnology, 40(8), 1295. |
| 2022 | Zillich, L., Poisel, E., Frank, J., Foo, J. C., Friske, M. M., Streit, F., . . . Witt, S. H. (2022). Multi-omics signatures of alcohol use disorder in the dorsal and ventral striatum. Translational Psychiatry, 12(1), 9 pages. Scopus22 WoS21 Europe PMC21 |
| 2022 | Tielke, A., Martins, H., Pelzl, M. A., Maaser-Hecker, A., David, F. S., Reinbold, C. S., . . . Forstner, A. J. (2022). Genetic and functional analyses implicate microRNA 499A in bipolar disorder development. Translational Psychiatry, 12(1), 10 pages. Scopus11 WoS8 Europe PMC8 |
| 2022 | Wendelstein, J. A., Reifeltshammer, S. A., Hoffmann, P. C., Fischinger, I., Mariacher, S., Bolz, M., . . . Hirnschall, N. (2022). Project Hyperopic Power Prediction II: The Effects of Second Eye Refinement Methods on Prediction Error in Hyperopic Eyes. CURRENT EYE RESEARCH, 47(8), 1121-1130. WoS4 |
| 2022 | Wendelstein, J. A., Hoffmann, P. C., Schwarzenbacher, L., Fischinger, I. R., Hirnschall, N., Menapace, R., . . . Bolz, M. (2022). Lasting Effects: Seven Year Results of the Castrop Nomogram for Femtosecond Laser-Assisted Paired Corneal Arcuate Incisions. CURRENT EYE RESEARCH, 47(2), 225-232. WoS11 |
| 2022 | Degenhardt, F., Ellinghaus, D., Juzenas, S., Lerga-Jaso, J., Wendorff, M., Maya-Miles, D., . . . Casalone, E. (2022). Detailed stratified GWAS analysis for severe COVID-19 in four European populations. Human Molecular Genetics, 31(23), 3945-3966. Scopus59 WoS58 Europe PMC71 |
| 2022 | Kumar, V., Pouw, R. B., Autio, M., Sagmeister, M. G., Phua, Z. Y., Borghini, L., . . . Davila, S. (2022). Variation in <i>CFHR3</i> determines susceptibility to meningococcal disease by controlling factor H concentrations. AMERICAN JOURNAL OF HUMAN GENETICS, 109(9), 1680-1691. WoS7 |
| 2022 | Tremmel, R., Nies, A. T., van Eijck, B. A. C., Handin, N., Haag, M., Winter, S., . . . Schaeffeler, E. (2022). Hepatic Expression of the Na+ -Taurocholate Cotransporting Polypeptide Is Independent from Genetic Variation. International Journal of Molecular Sciences, 23(13), 30 pages. Scopus9 WoS9 |
| 2022 | Kaut, O., Schmitt, I., Stahl, F., Fröhlich, H., Hoffmann, P., Gonzalez, F. J., & Wüllner, U. (2022). Epigenome-Wide Analysis of DNA Methylation in Parkinson’s Disease Cortex. Life, 12(4), 11 pages. Scopus27 WoS23 |
| 2022 | Clay-Gilmour, A., Chattopadhyay, S., Hildebrandt, M. A. T., Thomsen, H., Weinhold, N., Vodicka, P., . . . Hemminki, K. (2022). Genome-wide meta-analysis of monoclonal gammopathy of undetermined significance (MGUS) identifies risk loci impacting IRF-6. Blood Cancer Journal, 12(4), 5 pages. Scopus2 WoS2 Europe PMC2 |
| 2022 | Bellenguez, C., Küçükali, F., Jansen, I. E., Kleineidam, L., Moreno-Grau, S., Amin, N., . . . del Ser, T. (2022). New insights into the genetic etiology of Alzheimer’s disease and related dementias. Nature Genetics, 54(4), 412-436. Scopus1392 WoS1371 Europe PMC1823 |
| 2022 | Baak, L., Frank, M., Duerig, J., Duehrsen, U., Hoffmann, P., Noethen, M. M., . . . Schmidt, B. (2022). A genetic risk score of alleles related to MGUS interacts with socioeconomic position in a population-based cohort. SCIENTIFIC REPORTS, 12(1), 9 pages. |
| 2022 | Rickenbacher, M., Reinbold, C. S., Herms, S., Hoffmann, P., Cichon, S., Wueest, A. S., . . . Goettel, N. (2022). Genome-wide Association Study of Postoperative Cognitive Dysfunction in Older Surgical Patients. Journal of Neurosurgical Anesthesiology, 34(2), 248-250. Scopus6 WoS6 Europe PMC5 |
| 2022 | Uellendahl-Werth, F., Maj, C., Borisov, O., Juzenas, S., Wacker, E. M., Jørgensen, I. F., . . . Ellinghaus, D. (2022). Cross-tissue transcriptome-wide association studies identify susceptibility genes shared between schizophrenia and inflammatory bowel disease. Communications Biology, 5(1), 15 pages. Scopus26 WoS27 Europe PMC26 |
| 2022 | Zillich, L., Frank, J., Streit, F., Friske, M. M., Foo, J. C., Sirignano, L., . . . Witt, S. H. (2022). Epigenome-wide association study of alcohol use disorder in five brain regions. Neuropsychopharmacology, 47(4), 832-839. Scopus26 WoS24 Europe PMC34 |
| 2021 | Heinrich, M., Sieg, M., Kruppa, J., Nürnberg, P., Schreier, P. H., Heilmann-Heimbach, S., . . . Spies, C. D. (2021). Association between genetic variants of the cholinergic system and postoperative delirium and cognitive dysfunction in elderly patients. BMC Medical Genomics, 14(1), 10 pages. Scopus16 WoS16 Europe PMC14 |
| 2021 | Forstner, A. J., Awasthi, S., Wolf, C., Maron, E., Erhardt, A., Czamara, D., . . . Schumacher, J. (2021). Genome-wide association study of panic disorder reveals genetic overlap with neuroticism and depression. Molecular Psychiatry, 26(8), 4179-4190. Scopus85 WoS77 Europe PMC87 |
| 2021 | Kim, H., Momen-Heravi, F., Chen, S., Hoffmann, P., Kebschull, M., & Papapanou, P. N. (2021). Differential DNA methylation and mRNA transcription in gingival tissues in periodontal health and disease. Journal of Clinical Periodontology, 48(9), 1152-1164. Scopus35 WoS36 Europe PMC34 |
| 2021 | Niazi, Y., Thomsen, H., Smolkova, B., Vodickova, L., Vodenkova, S., Kroupa, M., . . . Försti, A. (2021). DNA Repair Gene Polymorphisms and Chromosomal Aberrations in Exposed Populations. Frontiers in Genetics, 12, 9 pages. Scopus9 WoS9 |
| 2021 | Yde Ohki, C. M., Grossmann, L., Döring, C., Hoffmann, P., Herms, S., Werling, A. M., . . . Grünblatt, E. (2021). Generation of integration-free induced pluripotent stem cells from healthy individuals. Stem Cell Research, 53, 4 pages. Scopus10 WoS10 Europe PMC11 |
| 2021 | Ludwig, K. U., Schmithausen, R. M., Li, D., Jacobs, M. L., Hollstein, R., Blumenstock, K., . . . Schmid-Burgk, J. L. (2021). LAMP-Seq enables sensitive, multiplexed COVID-19 diagnostics using molecular barcoding. Nature Biotechnology, 39(12), 1556-1562. Scopus58 WoS59 Europe PMC51 |
| 2021 | Sønderby, I. E., van der Meer, D., Moreau, C., Kaufmann, T., Walters, G. B., Ellegaard, M., . . . Ophoff, R. A. (2021). 1q21.1 distal copy number variants are associated with cerebral and cognitive alterations in humans. Translational Psychiatry, 11(1), 16 pages. Scopus31 WoS29 Europe PMC33 |
| 2021 | Gialluisi, A., Andlauer, T. F. M., Mirza-Schreiber, N., Moll, K., Becker, J., Hoffmann, P., . . . Schulte-Körne, G. (2021). Genome-wide association study reveals new insights into the heritability and genetic correlates of developmental dyslexia. Molecular Psychiatry, 26(7), 3004-3017. Scopus84 WoS83 Europe PMC60 |
| 2021 | Frank, M., Hensel, J., Baak, L., Schramm, S., Dragano, N., Weimar, C., . . . Schmidt, B. (2021). Interaction of alzheimer's disease-associated genetic risk with indicators of socioeconomic position on mild cognitive impairment in the heinz nixdorf recall study. Journal of Alzheimer S Disease, 82(4), 1715-1725. Scopus10 WoS9 Europe PMC10 |
| 2021 | Polushina, T., Banerjee, N., Giddaluru, S., Bettella, F., Espeseth, T., Lundervold, A. J., . . . Le Hellard, S. (2021). Identification of pleiotropy at the gene level between psychiatric disorders and related traits. Translational Psychiatry, 11(1), 9 pages. Scopus13 WoS13 Europe PMC14 |
| 2021 | Saunders, C. N., Chattopadhyay, S., Huhn, S., Weinhold, N., Hoffmann, P., Nöthen, M. M., . . . Hemminki, K. (2021). Search for AL amyloidosis risk factors using Mendelian randomization. Blood Advances, 5(13), 2725-2731. Scopus7 WoS8 |
| 2021 | Torres, G. G., Nygaard, M., Caliebe, A., Blanché, H., Chantalat, S., Galan, P., . . . Nebel, A. (2021). Exome-Wide Association Study Identifies FN3KRP and PGP as New Candidate Longevity Genes. Journals of Gerontology Series A Biological Sciences and Medical Sciences, 76(5), 786-795. Scopus16 WoS16 Europe PMC15 |
| 2021 | de Rojas, I., Moreno-Grau, S., Tesi, N., Grenier-Boley, B., Andrade, V., Jansen, I. E., . . . Rodriguez-Rodriguez, E. (2021). Common variants in Alzheimer’s disease and risk stratification by polygenic risk scores. Nature Communications, 12(1). Scopus207 WoS201 Europe PMC234 |
| 2021 | Pechlivanis, S., Jung, D., Moebus, S., Lehmann, N., Mahabadi, A. A., Hoffmann, P., . . . Bachmann, H. S. (2021). Pharmacogenetic association of diabetes-associated genetic risk score with rapid progression of coronary artery calcification following treatment with HMG-CoA-reductase inhibitors —results of the Heinz Nixdorf Recall Study. Naunyn Schmiedeberg S Archives of Pharmacology, 394(8), 1713-1725. Scopus6 WoS6 Europe PMC5 |
| 2021 | Khanam, T., Sandmann, S., Seggewiss, J., Ruether, C., Zimmermann, M., Norvil, A. B., . . . Burkhardt, B. (2021). Integrative genomic analysis of pediatric T-cell lymphoblastic lymphoma reveals candidates of clinical significance. Blood, 137(17), 2347-2359. Scopus42 WoS42 Europe PMC36 |
| 2021 | Niazi, Y., Thomsen, H., Smolkova, B., Vodickova, L., Vodenkova, S., Kroupa, M., . . . Hemminki, K. (2021). DNA repair gene polymorphisms and chromosomal aberrations in healthy, nonsmoking population. DNA Repair, 101. Scopus6 WoS6 Europe PMC6 |
| 2021 | Andlauer, T. F. M., Mühleisen, T. W., Hoffstaedter, F., Teumer, A., Wittfeld, K., Teuber, A., . . . Cichon, S. (2021). Genetic factors influencing a neurobiological substrate for psychiatric disorders. Translational Psychiatry, 11(1). Scopus8 WoS8 Europe PMC10 |
| 2021 | Herrera-Rivero, M., Stoll, M., Hegenbarth, J. -C., Ruehle, F., Limperger, V., Junker, R., . . . Nowak-Goettl, U. (2021). Single- and Multimarker Genome-Wide Scans Evidence Novel Genetic Risk Modifiers for Venous Thromboembolism. THROMBOSIS AND HAEMOSTASIS, 121(09), 1169-1180. WoS10 |
| 2021 | Shadrin, A. A., Mucha, S., Ellinghaus, D., Makarious, M. B., Blauwendraat, C., Sreelatha, A. A. K., . . . Sharma, M. (2021). Shared Genetics of Multiple System Atrophy and Inflammatory Bowel Disease. Movement Disorders, 36(2), 449-459. Scopus17 WoS15 Europe PMC16 |
| 2021 | Guzman-Parra, J., Streit, F., Forstner, A. J., Strohmaier, J., González, M. J., Gil Flores, S., . . . Rietschel, M. (2021). Clinical and genetic differences between bipolar disorder type 1 and 2 in multiplex families. Translational Psychiatry, 11(1). Scopus31 WoS32 Europe PMC31 |
| 2021 | Wendelstein, J. A., Hoffmann, P. C., Mariacher, S., Wingert, T., Hirnschall, N., Findl, O., & Bolz, M. (2021). Precision and refractive predictability of a new nomogram for femtosecond laser-assisted corneal arcuate incisions. ACTA OPHTHALMOLOGICA, 99(8), E1297-E1306. WoS17 |
| 2021 | Grossmann, L., Yde Ohki, C. M., Döring, C., Hoffmann, P., Herms, S., Werling, A. M., . . . Grünblatt, E. (2021). Generation of integration-free induced pluripotent stem cell lines from four pediatric ADHD patients. Stem Cell Research, 53, 4 pages. Scopus10 WoS10 Europe PMC11 |
| 2021 | Niemi, M. E. K., Karjalainen, J., Liao, R. G., Neale, B. M., Daly, M., Ganna, A., . . . Donohue, C. (2021). Mapping the human genetic architecture of COVID-19. Nature, 600(7889), 472-477. Scopus654 WoS573 Europe PMC710 |
| 2021 | Schubert, K. O., Thalamuthu, A., Amare, A. T., Frank, J., Streit, F., Adl, M., . . . Baune, B. T. (2021). Combining schizophrenia and depression polygenic risk scores improves the genetic prediction of lithium response in bipolar disorder patients. Translational Psychiatry, 11(1), 100-108. Scopus44 WoS42 Europe PMC45 |
| 2021 | Smigielski, L., Papiol, S., Theodoridou, A., Heekeren, K., Gerstenberg, M., Wotruba, D., . . . Grünblatt, E. (2021). Polygenic risk scores across the extended psychosis spectrum. Translational Psychiatry, 11(1), 11 pages. Scopus22 WoS20 Europe PMC19 |
| 2021 | Mittal, P., Condina, M. R., Klingler-Hoffmann, M., Kaur, G., Oehler, M. K., Sieber, O. M., . . . Hoffmann, P. (2021). Cancer tissue classification using supervised machine learning applied to maldi mass spectrometry imaging. Cancers, 13(21), 16 pages. Scopus29 WoS23 Europe PMC15 |
| 2021 | Mullins, N., Forstner, A. J., O’Connell, K. S., Coombes, B., Coleman, J. R. I., Qiao, Z., . . . Kalman, J. L. (2021). Genome-wide association study of more than 40,000 bipolar disorder cases provides new insights into the underlying biology. Nature Genetics, 53(6), 817-829. Scopus935 WoS902 Europe PMC1122 |
| 2021 | Young, C., Condina, M. R., Briggs, M. T., Moh, E. S. X., Kaur, G., Oehler, M. K., & Hoffmann, P. (2021). In-House Packed Porous Graphitic Carbon Columns for Liquid Chromatography-Mass Spectrometry Analysis of <i>N-</i>Glycans.. Frontiers in chemistry, 9(article no. 653959), 653959. Scopus18 WoS16 Europe PMC12 |
| 2021 | Lokman, N. A., Ricciardelli, C., Stephens, A. N., Jobling, T. W., Hoffmann, P., & Oehler, M. K. (2021). Diagnostic Value of Plasma Annexin A2 in Early-Stage High-Grade Serous Ovarian Cancer. Diagnostics, 11(1), 1-10. Scopus10 WoS9 Europe PMC8 |
| 2021 | Thorn, D. C., Bahraminejad, E., Grosas, A. B., Koudelka, T., Hoffmann, P., Mata, J. P., . . . Carver, J. A. (2021). Native disulphide-linked dimers facilitate amyloid fibril formation by bovine milk α(S2)-casein. Biophysical Chemistry, 270(106530), 106530-1-106530-12. Scopus16 Europe PMC9 |
| 2021 | Bastow, C. R., Bunting, M. D., Kara, E. E., McKenzie, D. R., Caon, A., Devi, S., . . . Comerford, I. (2021). Scavenging of soluble and immobilized CCL21 by ACKR4 regulates peripheral dendritic cell emigration. Proceedings of the National Academy of Sciences of USA, 118(17), e2025763118-1-e2025763118-9. Scopus31 WoS29 Europe PMC28 |
| 2021 | Munn-Chernoff, M. A., Johnson, E. C., Chou, Y. L., Coleman, J. R. I., Thornton, L. M., Walters, R. K., . . . La Via, M. C. (2021). Shared genetic risk between eating disorder- and substance-use-related phenotypes: Evidence from genome-wide association studies. Addiction Biology, 26(1), 20 pages. Scopus45 WoS38 Europe PMC36 |
| 2021 | Amare, A. T., Schubert, K. O., Hou, L., Clark, S. R., Papiol, S., Cearns, M., . . . Binder, E. B. (2021). Association of polygenic score for major depression with response to lithium in patients with bipolar disorder. Molecular Psychiatry, 26(6), 2457-2470. Scopus59 WoS64 Europe PMC66 |
| 2021 | Lee, Y. R., Briggs, M. T., Kuliwaba, J. S., Anderson, P. H., Condina, M. R., & Hoffmann, P. (2021). Gelatin-coated indium tin oxide slides improve human cartilage-bone tissue adherence and N-glycan signal intensity for mass spectrometry imaging. Analytical and Bioanalytical Chemistry, 413(10), 2675-2682. Scopus14 WoS14 Europe PMC11 |
| 2021 | Mittal, P., Briggs, M., Klingler-Hoffmann, M., Kaur, G., Packer, N. H., Oehler, M. K., & Hoffmann, P. (2021). Altered N-linked glycosylation in endometrial cancer. Analytical and Bioanalytical Chemistry, 413(10), 2721-2733. Scopus20 WoS20 Europe PMC20 |
| 2021 | Enot, M. M., Weiland, F., Mittal, P., Hoffmann, P., Sillero-Mahinay, M., & Pukala, T. (2021). Differential proteome analysis of the leaves of lead hyperaccumulator, Rhoeo discolor (L. Her.) Hance. Journal of Mass Spectrometry, 56(4), e4689-1-e4689-11. Scopus10 WoS6 Europe PMC3 |
| 2021 | Dilmetz, B. A., Lee, Y. R., Condina, M. R., Briggs, M., Young, C., Desire, C. T., . . . Hoffmann, P. (2021). Novel technical developments in mass spectrometry imaging in 2020: A mini review. Analytical Science Advances, 2(3-4), 225-237. Scopus27 WoS25 Europe PMC26 |
| 2020 | Acland, M., Arentz, G., Mussared, M., Whitehead, F., Hoffmann, P., Klingler Hoffmann, M., & Oehler, M. K. (2020). Proteomic analysis of pre-invasive serous lesions of the endometrium and fallopian tube reveals their metastatic potential. Frontiers in Oncology, 10(article no. 523989), 1-12. Scopus5 WoS5 Europe PMC5 |
| 2020 | Grasby, K. L., Jahanshad, N., Painter, J. N., Colodro-Conde, L., Bralten, J., Hibar, D. P., . . . Milaneschi, Y. (2020). The genetic architecture of the human cerebral cortex. Science, 367(6484), 1-14. Scopus587 WoS547 Europe PMC566 |
| 2020 | Goltermann, J., Opel, N., Redlich, R., Repple, J., Kaehler, C., Grotegerd, D., . . . Dannlowski, U. (2020). Replication of a hippocampus specific effect of the tescalcin regulating variant rs7294919 on gray matter structure. European Neuropsychopharmacology, 36, 10-17. Scopus1 WoS1 Europe PMC1 |
| 2020 | Lee, Y. R., Briggs, M. T., Condina, M. R., Puddy, H., Anderson, P. H., Hoffmann, P., & Kuliwaba, J. S. (2020). Mass spectrometry imaging as a potential tool to investigate human osteoarthritis at the tissue level. International Journal of Molecular Sciences, 21(17), 6414-1-6414-13. Scopus14 WoS12 Europe PMC11 |
| 2020 | Boyle, S. T., Mittal, P., Kaur, G., Hoffmann, P., Samuel, M. S., & Klingler-Hoffmann, M. (2020). Uncovering tumor−stroma inter-relationships using MALDI Mass spectrometry imaging. Journal of Proteome Research, 19(10), 4093-4103. Scopus16 WoS15 Europe PMC13 |
| 2020 | Weiland, F., Lokman, N. A., Klingler-Hoffmann, M., Jobling, T., Stephens, A. N., Sundfeldt, K., . . . Oehler, M. K. (2020). Ovarian Blood Sampling Identifies Junction Plakoglobin as a Novel Biomarker of Early Ovarian Cancer. Frontiers in Oncology, 10(1767), 1-10. Scopus10 WoS10 Europe PMC13 |
| 2020 | Coleman, J. R. I., Peyrot, W. J., Purves, K. L., Davis, K. A. S., Rayner, C., Choi, S. W., . . . Mullins, N. (2020). Genome-wide gene-environment analyses of major depressive disorder and reported lifetime traumatic experiences in UK Biobank. Molecular Psychiatry, Onlinepubl(7), 1-17. Scopus126 WoS123 Europe PMC152 |
| 2020 | Imahorn, E., Aushev, M., Herms, S., Hoffmann, P., Cichon, S., Reichelt, J., . . . Burger, B. (2020). Gene expression is stable in a complete CIB1 knockout keratinocyte model. Scientific Reports, 10(1), 9 pages. Scopus3 WoS3 Europe PMC3 |
| 2020 | Streeck, H., Schulte, B., Kümmerer, B. M., Richter, E., Höller, T., Fuhrmann, C., . . . Hartmann, G. (2020). Infection fatality rate of SARS-CoV2 in a super-spreading event in Germany. Nature Communications, 11(1), 12 pages. Scopus143 WoS158 Europe PMC236 |
| 2020 | Jäger, S., Cuadrat, R., Hoffmann, P., Wittenbecher, C., & Schulze, M. B. (2020). Desaturase activity and the risk of type 2 diabetes and coronary artery disease: A mendelian randomization study. Nutrients, 12(8), 1-18. Scopus17 WoS18 Europe PMC19 |
| 2020 | Nashef, A., Matthias, M., Weiss, E., Loos, B. G., Jepsen, S., van der Velde, N., . . . Iraqi, F. A. (2020). Translation of mouse model to human gives insights into periodontitis etiology. Scientific Reports, 10(1), 10 pages. Scopus15 WoS16 Europe PMC11 |
| 2020 | Glanville, K. P., Coleman, J. R. I., Hanscombe, K. B., Euesden, J., Choi, S. W., Purves, K. L., . . . Jansen, R. (2020). Classical human leukocyte antigen alleles and C4 haplotypes are not significantly associated with depression. Biological Psychiatry, 87(5), 419-430. Scopus26 WoS28 Europe PMC27 |
| 2020 | Jäger, S., Cuadrat, R., Wittenbecher, C., Floegel, A., Hoffmann, P., Prehn, C., . . . Schulze, M. B. (2020). Mendelian randomization study on amino acid metabolism suggests tyrosine as causal trait for type 2 diabetes. Nutrients, 12(12), 1-18. Scopus11 WoS9 Europe PMC10 |
| 2020 | Palladino, V. S., Chiocchetti, A. G., Frank, L., Haslinger, D., McNeill, R., Radtke, F., . . . Kittel-Schneider, S. (2020). Energy metabolism disturbances in cell models of PARK2 CNV carriers with ADHD. Journal of Clinical Medicine, 9(12), 20 pages. Scopus12 WoS12 |
| 2020 | Niazi, Y., Thomsen, H., Smolkova, B., Vodickova, L., Vodenkova, S., Kroupa, M., . . . Försti, A. (2020). Impact of genetic polymorphisms in kinetochore and spindle assembly genes on chromosomal aberration frequency in healthy humans. Mutation Research Genetic Toxicology and Environmental Mutagenesis, 858-860. Scopus4 WoS4 Europe PMC2 |
| 2020 | Pechlivanis, S., Lehmann, N., Hoffmann, P., Nöthen, M. M., Jöckel, K. H., Erbel, R., & Moebus, S. (2020). Risk prediction for coronary heart disease by a genetic risk score - Results from the Heinz Nixdorf Recall study. BMC Medical Genetics, 21(1). Scopus17 WoS15 Europe PMC16 |
| 2020 | Corominas, J., Klein, M., Zayats, T., Rivero, O., Ziegler, G. C., Pauper, M., . . . Lesch, K. P. (2020). Identification of ADHD risk genes in extended pedigrees by combining linkage analysis and whole-exome sequencing. Molecular Psychiatry, 25(9), 2047-2057. Scopus18 WoS18 Europe PMC13 |
| 2020 | Krug, A., Wöhr, M., Seffer, D., Rippberger, H., Sungur, A. Ö., Dietsche, B., . . . Kircher, T. (2020). Advanced paternal age as a risk factor for neurodevelopmental disorders: A translational study. Molecular Autism, 11(1). Scopus23 WoS23 Europe PMC16 |
| 2020 | Pechlivanis, S., Moebus, S., Lehmann, N., Erbel, R., Mahabadi, A. A., Hoffmann, P., . . . Bachmann, H. S. (2020). Genetic risk scores for coronary artery disease and its traditional risk factors: Their role in the progression of coronary artery calcification—Results of the Heinz Nixdorf Recall study. Plos One, 15(5). Scopus11 WoS12 Europe PMC10 |
| 2020 | Sønderby, I. E., Gústafsson, Ó., Doan, N. T., Hibar, D. P., Martin-Brevet, S., Abdellaoui, A., . . . Prieto, C. (2020). Dose response of the 16p11.2 distal copy number variant on intracranial volume and basal ganglia. Molecular Psychiatry, 25(3), 584-602. Scopus49 WoS49 Europe PMC57 |
| 2020 | Adorjan, K., Mekonnen, Z., Tessema, F., Ayana, M., Degenhardt, F., Hoffmann, P., . . . Mattheisen, M. (2020). Genotype-phenotype feasibility studies on khat abuse, traumatic experiences and psychosis in Ethiopia. Psychiatric Genetics, 30(1), 34-38. Scopus1 WoS1 |
| 2020 | Van Der Meer, D., Sønderby, I. E., Kaufmann, T., Walters, G. B., Abdellaoui, A., Ames, D., . . . Sachdev, P. S. (2020). Association of Copy Number Variation of the 15q11.2 BP1-BP2 Region with Cortical and Subcortical Morphology and Cognition. JAMA Psychiatry, 77(4), 420-430. Scopus63 WoS61 Europe PMC65 |
| 2020 | Mucha, S., Baurecht, H., Novak, N., Rodríguez, E., Bej, S., Mayr, G., . . . Ellinghaus, D. (2020). Protein-coding variants contribute to the risk of atopic dermatitis and skin-specific gene expression. Journal of Allergy and Clinical Immunology, 145(4), 1208-1218. Scopus39 WoS34 Europe PMC34 |
| 2020 | Chattopadhyay, S., Thomsen, H., Weinhold, N., Meziane, I., Huhn, S., da Silva Filho, M. I., . . . Försti, A. (2020). Eight novel loci implicate shared genetic etiology in multiple myeloma, AL amyloidosis, and monoclonal gammopathy of unknown significance. Leukemia, 34(4), 1187-1191. Scopus14 WoS13 Europe PMC12 |
| 2020 | Thomsen, H., Chattopadhyay, S., Hoffmann, P., Nöthen, M. M., Kalirai, H., Coupland, S. E., . . . Försti, A. (2020). Genome-wide study on uveal melanoma patients finds association to DNA repair gene TDP1. Melanoma Research, 30(2), 166-172. Scopus11 WoS9 Europe PMC10 |
| 2020 | Pechlivanis, S., Mahabadi, A. A., Hoffmann, P., Nöthen, M. M., Broecker-Preuss, M., Erbel, R., . . . Jöckel, K. H. (2020). Association between lipoprotein(a) (Lp(a)) levels and Lp(a) genetic variants with coronary artery calcification. BMC Medical Genetics, 21(1). Scopus33 WoS34 Europe PMC27 |
| 2020 | Sønderby, I. E., Gústafsson, Ó., Doan, N. T., Hibar, D. P., Martin-Brevet, S., Abdellaoui, A., . . . Prieto, C. (2020). Correction: Dose response of the 16p11.2 distal copy number variant on intracranial volume and basal ganglia (Molecular Psychiatry, (2020), 25, 3, (584-602), 10.1038/s41380-018-0118-1). Molecular Psychiatry, 25(3), 692-695. Scopus1 WoS2 Europe PMC2 |
| 2020 | Forstner, A. J., Fischer, S. B., Schenk, L. M., Strohmaier, J., Maaser-Hecker, A., Reinbold, C. S., . . . Cichon, S. (2020). Whole-exome sequencing of 81 individuals from 27 multiply affected bipolar disorder families. Translational Psychiatry, 10(1). Scopus28 WoS27 Europe PMC28 |
| 2020 | Caspers, S., Röckner, M. E., Jockwitz, C., Bittner, N., Teumer, A., Herms, S., . . . Mühleisen, T. W. (2020). Pathway-Specific Genetic Risk for Alzheimer's Disease Differentiates Regional Patterns of Cortical Atrophy in Older Adults. Cerebral Cortex, 30(2), 801-811. Scopus19 WoS18 Europe PMC18 |
| 2020 | Ludwig, K. U., Schmidt, A., Hoffmann, P., & Noethen, M. M. (2020). Combating the SARS-CoV-2 pandemic: How can the field of Human Genetics contribute?. MEDIZINISCHE GENETIK, 32(2), 163-167. |
| 2020 | Forstner, A. J., Hoffmann, P., Markus, M. N., & Cichon, S. (2020). Insights into the genomics of affective disorders. Medizinische Genetik, 32(1), 9-18. Scopus2 WoS2 |
| 2020 | Mühleisen, T. W., Forstner, A. J., Hoffmann, P., & Cichon, S. (2020). Brain imaging genomics: Influences of genomic variability on the structure and function of the human brain. Medizinische Genetik, 32(1), 47-56. Scopus3 WoS2 |
| 2019 | Dalmasso, M. C., Brusco, L. I., Olivar, N., Muchnik, C., Hanses, C., Milz, E., . . . Ramirez, A. (2019). Transethnic meta-analysis of rare coding variants in PLCG2, ABI3, and TREM2 supports their general contribution to Alzheimer’s disease. Translational Psychiatry, 9(1), 6 pages. Scopus35 WoS33 Europe PMC36 |
| 2019 | Lardenoije, R., Roubroeks, J. A. Y., Pishva, E., Leber, M., Wagner, H., Iatrou, A., . . . van den Hove, D. L. A. (2019). Alzheimer's disease-associated (hydroxy)methylomic changes in the brain and blood. CLINICAL EPIGENETICS, 11(1), 15 pages. WoS90 |
| 2019 | Takahashi, H., Cornish, A. J., Sud, A., Law, P. J., Kinnersley, B., Ostrom, Q. T., . . . Houlston, R. S. (2019). Publisher Correction: Mendelian randomisation study of the relationship between vitamin D and risk of glioma (Scientific Reports, (2018), 8, 1, (2339), 10.1038/s41598-018-20844-w). Scientific Reports, 9(1). WoS1 |
| 2019 | Palladino, V. S., Subrata, N. O. C., Geburtig-Chiocchetti, A., McNeill, R., Hoffmann, P., Reif, A., & Kittel-Schneider, S. (2019). Generation of human induced pluripotent stem cell lines (hiPSC) from one bipolar disorder patient carrier of a DGKH risk haplotype and one non-risk-variant-carrier bipolar disorder patient (vol 32, pg 104, 2018). STEM CELL RESEARCH, 36, 1 page. |
| 2019 | Schulz, H., Ruppert, A. K., Zara, F., Madia, F., Iacomino, M., S. Vari, M., . . . Sander, T. (2019). No evidence for a BRD2 promoter hypermethylation in blood leukocytes of Europeans with juvenile myoclonic epilepsy. Epilepsia, 60(5), e31-e36. Scopus6 WoS6 Europe PMC4 |
| 2019 | Went, M., Kinnersley, B., Sud, A., Johnson, D. C., Weinhold, N., Försti, A., . . . Houlston, R. S. (2019). Transcriptome-wide association study of multiple myeloma identifies candidate susceptibility genes. Human Genomics, 13(1), 37. Scopus16 WoS15 Europe PMC11 |
| 2019 | Kunkle, B. W., Grenier-Boley, B., Sims, R., Bis, J. C., Damotte, V., Naj, A. C., . . . Benito, Y. A. (2019). Author Correction: Genetic meta-analysis of diagnosed Alzheimer’s disease identifies new risk loci and implicates Aβ, tau, immunity and lipid processing (Nature Genetics, (2019), 51, 3, (414-430), 10.1038/s41588-019-0358-2). Nature Genetics, 51(9), 1423-1424. Scopus59 WoS47 Europe PMC51 |
| 2019 | Niazi, Y., Thomsen, H., Smolkova, B., Vodickova, L., Vodenkova, S., Kroupa, M., . . . Försti, A. (2019). Distinct pathways associated with chromosomal aberration frequency in a cohort exposed to genotoxic compounds compared to general population. Mutagenesis, 34(4), 1-8. Scopus7 WoS5 Europe PMC5 |
| 2019 | Haertle, L., Müller, T., Lardenoije, R., Maierhofer, A., Dittrich, M., Riemens, R. J. M., . . . Mégarbané, A. (2019). Methylomic profiling in trisomy 21 identifies cognition-and Alzheimer's disease-related dysregulation. Clinical Epigenetics, 11(1). Scopus12 WoS12 Europe PMC12 |
| 2019 | Went, M., Sud, A., Speedy, H., Sunter, N. J., Försti, A., Law, P. J., . . . Houlston, R. S. (2019). Genetic correlation between multiple myeloma and chronic lymphocytic leukaemia provides evidence for shared aetiology. Blood Cancer Journal, 9(1). Scopus16 WoS14 Europe PMC17 |
| 2019 | Munz, M., Richter, G. M., Loos, B. G., Jepsen, S., Divaris, K., Offenbacher, S., . . . Schaefer, A. S. (2019). Meta-analysis of genome-wide association studies of aggressive and chronic periodontitis identifies two novel risk loci. European Journal of Human Genetics, 27(1), 102-113. Scopus68 WoS65 Europe PMC64 |
| 2019 | Huckins, L. M., Dobbyn, A., Ruderfer, D. M., Hoffman, G., Lee, S. H., & Im, H. K. (2019). Gene expression imputation across multiple brain regions provides insights into schizophrenia risk. Nature Genetics, 51(4), 659-674. Scopus142 WoS139 Europe PMC151 |
| 2019 | Harold, D., Connolly, S., Riley, B. P., Kendler, K. S., McCarthy, S. E., McCombie, W. R., . . . Lee, S. H. (2019). Population-based identity-by-descent mapping combined with exome sequencing to detect rare risk variants for schizophrenia. American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics, 180(3), 223-231. WoS4 |
| 2019 | Leonenko, G., Sims, R., Shoai, M., Frizzati, A., Bossu, P., Spalletta, G., . . . Munger, R. (2019). Polygenic risk and hazard scores for Alzheimer's disease prediction. ANNALS OF CLINICAL AND TRANSLATIONAL NEUROLOGY, 6(3), 456-465. WoS65 |
| 2019 | Kunkle, B. W., Grenier-Boley, B., Sims, R., Bis, J. C., Damotte, V., Naj, A. C., . . . Benito, Y. A. (2019). Genetic meta-analysis of diagnosed Alzheimer’s disease identifies new risk loci and implicates Aβ, tau, immunity and lipid processing. Nature Genetics, 51(3), 414-430. Scopus2085 WoS2046 Europe PMC2357 |
| 2019 | Takahashi, H., Cornish, A. J., Sud, A., Law, P. J., Disney-Hogg, L., Calvocoressi, L., . . . Houlston, R. S. (2019). Mendelian randomization provides support for obesity as a risk factor for meningioma. Scientific Reports, 9(1). Scopus23 WoS18 Europe PMC19 |
| 2019 | Niazi, Y., Thomsen, H., Smolkova, B., Vodickova, L., Vodenkova, S., Kroupa, M., . . . Försti, A. (2019). Genetic variation associated with chromosomal aberration frequency: A genome-wide association study. Environmental and Molecular Mutagenesis, 60(1), 17-28. Scopus11 WoS9 Europe PMC6 |
| 2019 | Schwarz, E., Doan, N. T., Pergola, G., Westlye, L. T., Kaufmann, T., Wolfers, T., . . . Orhan, F. (2019). Reproducible grey matter patterns index a multivariate, global alteration of brain structure in schizophrenia and bipolar disorder. Translational Psychiatry, 9(1). Scopus44 WoS40 Europe PMC35 |
| 2019 | Condina, M. R., Mittal, P., Briggs, M. T., Oehler, M. K., Klingler-Hoffmann, M., & Hoffmann, P. (2019). Egg white as a quality control in matrix assisted laser desorption/ionization mass spectrometry imaging (MALDI-MSI).. Analytical chemistry, 91(23), 14846-14853. Scopus13 WoS14 Europe PMC10 |
| 2019 | Andlauer, T. F. M., Guzman-Parra, J., Streit, F., Strohmaier, J., González, M. J., Gil Flores, S., . . . Giambartolomei, C. (2019). Bipolar multiplex families have an increased burden of common risk variants for psychiatric disorders. Molecular Psychiatry, 26(4), 1286-1298. Scopus35 WoS34 Europe PMC35 |
| 2019 | Lee, P. H., Anttila, V., Won, H., Feng, Y. C. A., Rosenthal, J., Zhu, Z., . . . Buxbaum, J. D. (2019). Genomic Relationships, Novel Loci, and Pleiotropic Mechanisms across Eight Psychiatric Disorders. Cell, 179(7), 1469-1482.e11. Scopus905 WoS877 Europe PMC1013 |
| 2019 | Polimanti, R., Peterson, R. E., Ong, J. -S., MacGregor, S., Edwards, A. C., Clarke, T. -K., . . . Neale, B. M. (2019). Evidence of causal effect of major depression on alcohol dependence: findings from the psychiatric genomics consortium. PSYCHOLOGICAL MEDICINE, 49(7), 1218-1226. WoS27 Europe PMC81 |
| 2019 | Briggs, M. T., Condina, M. R., Ho, Y. Y., Everest-Dass, A. V., Mittal, P., Kaur, G., . . . Hoffmann, P. (2019). MALDI mass spectrometry imaging of early- and late-stage serous ovarian cancer tissue reveals stage-specific N-glycans. Proteomics, 19(21-22), 1800482-1-1800482-11. Scopus52 WoS46 Europe PMC41 |
| 2019 | Horan, M. P., Hoffmann, P., Briggs, M. T., Condina, M., Herbert, S., Ito, J., . . . Badrick, T. (2019). An external quality assurance trial to assess mass spectrometry protein testing facilities for identifying multiple human peptides. Analytical and bioanalytical chemistry, 411(25), 6575-6581. Scopus2 WoS1 |
| 2019 | Chatterjee, S., Lee, L. Y., Kawahara, R., Abrahams, J. L., Briggs, M. T., Hoffman, P., & Thaysen Andersen, M. (2019). Protein paucimannosylation is an enriched N-Glycosylation signature of human cancers. Proteomics, 19(21-22, article no. 1900010), 1-13. Scopus57 WoS64 Europe PMC55 |
| 2019 | Briggs, M. T., Condina, M. R., Klingler-Hoffmann, M., Arentz, G., Everest-Dass, A. V., Kaur, G., . . . Hoffmann, P. (2019). Translating N-Glycan Analytical Applications into Clinical Strategies for Ovarian Cancer. Proteomics - Clinical Applications, 13(3), 1-5. Scopus23 WoS18 Europe PMC12 |
| 2019 | Choi, K. W., Chen, C. Y., Stein, M. B., Klimentidis, Y. C., Wang, M. J., Koenen, K. C., . . . Painter, J. N. (2019). Assessment of bidirectional relationships between physical activity and depression among adults a 2-sample Mendelian randomization study. JAMA Psychiatry, 76(4), 399-408. Scopus576 WoS545 Europe PMC493 |
| 2019 | Law, P. J., Timofeeva, M., Fernandez-Rozadilla, C., Broderick, P., Studd, J., Fernandez-Tajes, J., . . . Koutros, S. (2019). Association analyses identify 31 new risk loci for colorectal cancer susceptibility. Nature Communications, 10(1). Scopus175 WoS176 Europe PMC184 |
| 2019 | Condina, M. R., Dilmetz, B. A., Razavi Bazaz, S., Meneses, J., Ebrahimi Warkiani, M., & Hoffmann, P. (2019). Rapid separation and identification of beer spoilage bacteria by inertial microfluidics and MALDI-TOF mass spectrometry. Lab on a Chip, 19(11), 1961-1970. Scopus61 WoS56 Europe PMC32 |
| 2019 | Musliner, K. L., Mortensen, P. B., McGrath, J. J., Suppli, N. P., Hougaard, D. M., Bybjerg-Grauholm, J., . . . Sklar, P. (2019). Association of Polygenic Liabilities for Major Depression, Bipolar Disorder, and Schizophrenia With Risk for Depression in the Danish Population. JAMA PSYCHIATRY, 76(5), 516-525. WoS82 Europe PMC85 |
| 2019 | Mullins, N., Bigdeli, T. B., Børglum, A. D., Coleman, J. R. I., Demontis, D., Mehta, D., . . . Air, T. (2019). GWAS of suicide attempt in psychiatric disorders and association with major depression polygenic risk scores. American Journal of Psychiatry, 176(8), 651-660. Scopus195 WoS184 Europe PMC184 |
| 2019 | Czamara, D., Eraslan, G., Page, C. M., Lahti, J., Lahti-Pulkkinen, M., Hämäläinen, E., . . . Baune, B. T. (2019). Integrated analysis of environmental and genetic influences on cord blood DNA methylation in new-borns. Nature Communications, 10(1), 18 pages. Scopus104 WoS99 Europe PMC91 |
| 2019 | Janos, K., Serg, P., Clark, S. R., Schubert, K. O., Baune, B. T., & Schulze, T. (2019). Investigating polygenic burden in age at disease onset in bipolar disorder: findings from an international multicentric study.. Bipolar Disorders, 21(1), 68-75. Scopus23 WoS23 Europe PMC24 |
| 2019 | Foo, J. C., Streit, F., Frank, J., Witt, S. H., Treutlein, J., Baune, B. T., . . . Air, T. (2019). Evidence for increased genetic risk load for major depression in patients assigned to electroconvulsive therapy. American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics, 180(1), 35-45. Scopus17 WoS18 Europe PMC19 |
| 2019 | Marshall, A. C., Kidd, S. E., Lamont-Friedrich, S. J., Arentz, G., Hoffmann, P., Coad, B. R., & Bruning, J. B. (2019). Structure, mechanism, and inhibition of aspergillus fumigatus thioredoxin reductase. Antimicrobial Agents and Chemotherapy, 63(3), 1-15. Scopus32 WoS30 Europe PMC25 |
| 2019 | Li, Y. Q., Ngo, A., Hoffmann, P., Ferrante, A., & Hii, C. S. (2019). Regulation of endothelial cell survival and death by the MAP kinase/ERK kinase kinase 3 - glyceraldehyde-3-phosphate dehydrogenase signaling axis. Cellular Signalling, 58, 20-33. Scopus10 WoS10 Europe PMC8 |
| 2019 | Grove, J., Ripke, S., Als, T. D., Mattheisen, M., Walters, R. K., Won, H., . . . Baune, B. (2019). Identification of common genetic risk variants for autism spectrum disorder. Nature Genetics, 51(3), 431-+. Scopus1603 WoS1511 Europe PMC1762 |
| 2019 | Arnau-Soler, A., Macdonald-Dunlop, E., Adams, M. J., Clarke, T. -K., MacIntyre, D. J., Milburn, K., . . . Sullivan, P. F. (2019). Genome-wide by environment interaction studies of depressive symptoms and psychosocial stress in UK Biobank and Generation Scotland. TRANSLATIONAL PSYCHIATRY, 9(1), 13 pages. WoS91 Europe PMC83 |
| 2019 | Vijayakrishnan, J., Studd, J., Broderick, P., Kinnersley, B., Holroyd, A., Law, P., . . . Kim, J. (2019). Erratum to: Genome-wide association study identifies susceptibility loci for B-cell childhood acute lymphoblastic leukemia (Nature Communications, (2018), 9, 1, (1340), 10.1038/s41467-018-03178-z). Nature Communications, 10(1), 419. |
| 2019 | Went, M., Sud, A., Försti, A., Halvarsson, B., Weinhold, N., Kimber, S., . . . Giles, G. (2019). Erratum to: Identification of multiple risk loci and regulatory mechanisms influencing susceptibility to multiple myeloma (Nature Communications, (2018), 9, 1, (3707), 10.1038/s41467-018-04989-w). Nature Communications, 10(1), 213. Scopus4 WoS3 Europe PMC2 |
| 2019 | Sud, A., Thomsen, H., Law, P., Försti, A., da Silva Filho, M., Holroyd, A., . . . Usmani, N. (2019). Erratum to: Genome-wide association study of classical Hodgkin lymphoma identifies key regulators of disease susceptibility (Nature Communications, (2017), 8, 1, (1892), 10.1038/s41467-017-00320-1). Nature Communications, 10(1), 157. WoS2 |
| 2019 | Domingues, F. S., König, E., Schwienbacher, C., Volpato, C. B., Picard, A., Cantaloni, C., . . . Pramstaller, P. P. (2019). Compound heterozygous SZT2 mutations in two siblings with early-onset epilepsy, intellectual disability and macrocephaly. Seizure, 66, 81-85. Scopus14 WoS13 Europe PMC12 |
| 2019 | Thomsen, H., Chattopadhyay, S., Weinhold, N., Vodicka, P., Vodickova, L., Hoffmann, P., . . . Försti, A. (2019). Genome-wide association study of monoclonal gammopathy of unknown significance (MGUS): comparison with multiple myeloma. Leukemia, 33(7), 1817-1821. Scopus16 WoS15 Europe PMC10 |
| 2019 | Gialluisi, A., Andlauer, T. F. M., Mirza-Schreiber, N., Moll, K., Becker, J., Hoffmann, P., . . . Schulte-Körne, G. (2019). Genome-wide association scan identifies new variants associated with a cognitive predictor of dyslexia. Translational Psychiatry, 9(1). Scopus79 WoS73 Europe PMC63 |
| 2019 | Mittal, P., Price, Z. K., Lokman, N. A., Ricciardelli, C., Oehler, M. K., Klingler-Hoffmann, M., & Hoffmann, P. (2019). Matrix Assisted Laser Desorption/Ionization Mass Spectrometry Imaging (MALDI MSI) for monitoring of drug response in primary cancer spheroids. Proteomics, 19(21 - 22), e1900146-1-e1900146-4. Scopus22 WoS20 Europe PMC16 |
| 2019 | Klingler-Hoffmann, M., Mittal, P., & Hoffmann, P. (2019). The Emerging Role of Cytoskeletal Proteins as Reliable Biomarkers.. Proteomics, 19(21-22), e1800483. Scopus16 WoS12 Europe PMC9 |
| 2018 | Hughes, T., Sønderby, I. E., Polushina, T., Hansson, L., Holmgren, A., Athanasiu, L., . . . Djurovic, S. (2018). Elevated expression of a minor isoform of ANK3 is a risk factor for bipolar disorder. Translational Psychiatry, 8(1), 12 pages. Scopus23 WoS18 Europe PMC23 |
| 2018 | Kröger, A., Hülsmann, C., Fickl, S., Spinell, T., Hüttig, F., Kaufmann, F., . . . Kebschull, M. (2018). The severity of human peri-implantitis lesions correlates with the level of submucosal microbial dysbiosis. Journal of Clinical Periodontology, 45(12), 1498-1509. Scopus78 WoS65 Europe PMC57 |
| 2018 | Vijayakrishnan, J., Studd, J., Broderick, P., Kinnersley, B., Holroyd, A., Law, P. J., . . . Menegaux, F. (2018). Genome-wide association study identifies susceptibility loci for B-cell childhood acute lymphoblastic leukemia. Nature Communications, 9(1), 9 pages. Scopus57 WoS56 Europe PMC56 |
| 2018 | Anttila, V., Bulik-Sullivan, B., Finucane, H. K., Walters, R. K., Bras, J., Duncan, L., . . . Smith, A. G. (2018). Analysis of shared heritability in common disorders of the brain. Science, 360(6395), 1313-+. Scopus1479 WoS1296 Europe PMC1173 |
| 2018 | Gustafsson, O. J. R., Briggs, M. T., Condina, M. R., Winderbaum, L. J., Pelzing, M., McColl, S. R., . . . Hoffmann, P. (2018). Raw N-glycan mass spectrometry imaging data on formalin-fixed mouse kidney. Data in Brief, 21, 185-188. Scopus4 WoS3 Europe PMC3 |
| 2018 | Ruderfer, D. M., Ripke, S., McQuillin, A., Boocock, J., Stahl, E. A., Pavlides, J. M. W., . . . Kendler, K. S. (2018). Genomic dissection of bipolar disorder and schizophrenia, including 28 subphenotypes. Cell, 173(7), 1705-1715.e16. Scopus497 WoS538 Europe PMC545 |
| 2018 | Acland, M., Mittal, P., Lokman, N., Klingler-Hoffmann, M., Oehler, M., & Hoffmann, P. (2018). Mass spectrometry analyses of multicellular tumor spheroids. Proteomics Clinical Applications, 12(3), 1700124-1-1700124-13. Scopus23 WoS21 Europe PMC19 |
| 2018 | Alanazi, I., Ebrahimie, E., Hoffmann, P., & Adelson, D. (2018). Correction to: Combined gene expression and proteomic analysis of EGF induced apoptosis in A431 cells suggests multiple pathways trigger apoptosis (Apoptosis, (2013), 18, 11, (1291-1305), 10.1007/s10495-013-0887-6). Apoptosis, 23(1), 92. Scopus1 WoS1 Europe PMC1 |
| 2018 | Schubert, K., Stacey, D., Arentz, G., Clark, S., Air, T., Hoffmann, P., & Baune, B. (2018). Targeted proteomic analysis of cognitive dysfunction in remitted major depressive disorder: Opportunities of multi-omics approaches towards predictive, preventive, and personalized psychiatry. Journal of Proteomics, 188, 63-70. Scopus22 WoS20 Europe PMC18 |
| 2018 | Wray, N., Ripke, S., Mattheisen, M., Trzaskowski, M., Byrne, E., Abdellaoui, A., . . . Ng, B. (2018). Genome-wide association analyses identify 44 risk variants and refine the genetic architecture of major depression. Nature Genetics, 50(5), 668-681. Scopus2161 WoS1763 Europe PMC2207 |
| 2018 | Reinbold, C. S., Clark, S. R., Schubert, K. O., Baune, B. T., & Cichon, S. (2018). Analysis of the influence of microRNAs in Lithium Response in Bipolar Disorder. Frontiers in Psychiatry, 9(MAY), 207-1-207-9. Scopus33 WoS28 Europe PMC21 |
| 2018 | Zolekar, A., Lin, V. J. T., Mishra, N. M., Ho, Y. Y., Hayatshahi, H. S., Parab, A., . . . Wang, Y. C. (2018). Stress and interferon signalling-mediated apoptosis contributes to pleiotropic anticancer responses induced by targeting NGLY1. British journal of cancer, 119(12), 1538-1551. Scopus22 WoS20 Europe PMC18 |
| 2018 | Gustafsson, O. J. R., Winderbaum, L. J., Condina, M. R., Boughton, B. A., Hamilton, B. R., Undheim, E. A. B., . . . Hoffmann, P. (2018). Balancing sufficiency and impact in reporting standards for mass spectrometry imaging experiments. GigaScience, 7(10), 1-13. Scopus17 Europe PMC9 |
| 2018 | Walters, R. K., Polimanti, R., Johnson, E. C., McClintick, J. N., Adams, M. J., Adkins, A. E., . . . Frye, M. A. (2018). Transancestral GWAS of alcohol dependence reveals common genetic underpinnings with psychiatric disorders. Nature Neuroscience, 21(12), 1656-1669. Scopus456 WoS431 Europe PMC532 |
| 2018 | de Jong, S., Diniz, M. J. A., Saloma, A., Gadelha, A., Santoro, M. L., Ota, V. K., . . . Baune, B. T. (2018). Applying polygenic risk scoring for psychiatric disorders to a large family with bipolar disorder and major depressive disorder. Communications Biology, 1(163), 10 pages. Scopus14 WoS16 Europe PMC16 |
| 2018 | Amare, A., Schubert, K., Hou, L., Clark, S., Papiol, S., Heilbronner, U., . . . Baune, B. (2018). Association of polygenic score for schizophrenia and HLA antigen and inflammation genes with response to lithium in bipolar affective disorder: a genome-wide association study. JAMA psychiatry, 75(1), 65-74. Scopus165 WoS141 Europe PMC151 |
| 2018 | Maaser, A., Forstner, A. J., Strohmaier, J., Hecker, J., Ludwig, K. U., Sivalingam, S., . . . Nöthen, M. M. (2018). Exome sequencing in large, multiplex bipolar disorder families from Cuba. Plos One, 13(10). Scopus17 WoS16 Europe PMC14 |
| 2018 | Fernandez-Rebollo, E., Eipel, M., Seefried, L., Hoffmann, P., Strathmann, K., Jakob, F., & Wagner, W. (2018). Primary Osteoporosis Is Not Reflected by Disease-Specific DNA Methylation or Accelerated Epigenetic Age in Blood. Journal of Bone and Mineral Research, 33(2), 356-361. Scopus42 WoS38 Europe PMC35 |
| 2018 | Hench, J., Bihl, M., Bratic Hench, I., Hoffmann, P., Tolnay, M., Bösch Al Jadooa, N., . . . Frank, S. (2018). Satisfying your neuro-oncologist: A fast approach to routine molecular glioma diagnostics. Neuro Oncology, 20(12), 1682-1683. Scopus5 WoS8 Europe PMC7 |
| 2018 | Kayser, K., Degenhardt, F., Holzapfel, S., Horpaopan, S., Peters, S., Spier, I., . . . Steinke-Lange, V. (2018). Copy number variation analysis and targeted NGS in 77 families with suspected Lynch syndrome reveals novel potential causative genes. International Journal of Cancer, 143(11), 2800-2813. Scopus10 WoS9 Europe PMC12 |
| 2018 | Claus, E. B., Cornish, A. J., Broderick, P., Schildkraut, J. M., Dobbins, S. E., Holroyd, A., . . . Wiemels, J. L. (2018). Genome-wide association analysis identifies a meningioma risk locus at 11p15.5. Neuro Oncology, 20(11), 1485-1493. Scopus24 WoS20 Europe PMC19 |
| 2018 | Palladino, V. S., Subrata, N. O. C., Geburtig-Chiocchetti, A., McNeill, R., Hoffmann, P., Reif, A., & Kittel-Schneider, S. (2018). Generation of human induced pluripotent stem cell lines (hiPSC) from one bipolar disorder patient carrier of a <i>DGKH</i> risk haplotype and one non-riskvariant-carrier bipolar disorder patient. STEM CELL RESEARCH, 32, 104-109. WoS9 |
| 2018 | Foo, J. C., Streit, F., Treutlein, J., Ripke, S., Witt, S. H., Strohmaier, J., . . . Frank, J. (2018). Shared genetic etiology between alcohol dependence and major depressive disorder. Psychiatric Genetics, 28(4), 66-70. Scopus23 WoS18 Europe PMC15 |
| 2018 | Chattopadhyay, S., Thomsen, H., Da Silva Filho, M. I., Weinhold, N., Hoffmann, P., Nöthen, M. M., . . . Försti, A. (2018). Enrichment of B cell receptor signaling and epidermal growth factor receptor pathways in monoclonal gammopathy of undetermined significance: A genome-wide genetic interaction study. Molecular Medicine, 24(1). Scopus10 WoS10 Europe PMC9 |
| 2018 | Nashef, A., Qabaja, R., Salaymeh, Y., Botzman, M., Munz, M., Dommisch, H., . . . Haddad, Y. H. (2018). Integration of Murine and Human Studies for Mapping Periodontitis Susceptibility. JOURNAL OF DENTAL RESEARCH, 97(5), 537-546. WoS23 |
| 2018 | Disney-Hogg, L., Sud, A., Law, P. J., Cornish, A. J., Kinnersley, B., Ostrom, Q. T., . . . Houlston, R. S. (2018). Influence of obesity-related risk factors in the aetiology of glioma /631/67/68 /631/67/2324 article. British Journal of Cancer, 118(7), 1020-1027. Scopus27 WoS29 Europe PMC29 |
| 2018 | Disney-Hogg, L., Cornish, A. J., Sud, A., Law, P. J., Kinnersley, B., Jacobs, D. I., . . . Houlston, R. S. (2018). Impact of atopy on risk of glioma: A Mendelian randomisation study. BMC Medicine, 16(1). Scopus40 WoS40 Europe PMC41 |
| 2018 | Munz, M., Willenborg, C., Richter, G. M., Jockel-Schneider, Y., Graetz, C., Staufenbiel, I., . . . Schaefer, A. S. (2018). Corrigendum: A genome-wide association study identifies nucleotide variants at SIGLEC5 and DEFA1A3 as risk loci for periodontitis [Human Molecular Genetics., 26, 13, (2017) (2577-2588)] DOI: 10.1093/hmg/ddx151. Human Molecular Genetics, 27(5), 941-942. Scopus18 WoS17 Europe PMC14 |
| 2018 | Mühleisen, T. W., Reinbold, C. S., Forstner, A. J., Abramova, L. I., Alda, M., Babadjanova, G., . . . Cichon, S. (2018). Gene set enrichment analysis and expression pattern exploration implicate an involvement of neurodevelopmental processes in bipolar disorder. Journal of Affective Disorders, 228, 20-25. Scopus13 WoS8 Europe PMC7 |
| 2018 | Takahashi, H., Cornish, A. J., Sud, A., Law, P. J., Kinnersley, B., Ostrom, Q. T., . . . Houlston, R. S. (2018). Mendelian randomisation study of the relationship between Vitamin D and risk of glioma. Scientific Reports, 8(1). Scopus21 WoS20 Europe PMC19 |
| 2018 | Munz, M., Richter, G. M., Loos, B. G., Jepsen, S., Divaris, K., Offenbacher, S., . . . Schaefer, A. S. (2018). Genome-wide association meta-analysis of coronary artery disease and periodontitis reveals a novel shared risk locus. Scientific Reports, 8(1), 10 pages. Scopus43 WoS43 Europe PMC36 |
| 2018 | Sud, A., Thomsen, H., Orlando, G., Asta Försti., Law, P. J., Broderick, P., . . . Houlston, R. S. (2018). Genome-wide association study implicates immune dysfunction in the development of Hodgkin lymphoma. Blood, 132(19), 2040-2052. Scopus22 WoS19 Europe PMC18 |
| 2017 | Jäger, S., Wahl, S., Kröger, J., Sharma, S., Hoffmann, P., Floegel, A., . . . Meidtner, K. (2017). Genetic variants including markers from the exome chip and metabolite traits of type 2 diabetes. Scientific Reports, 7(1), 12 pages. Scopus13 WoS12 Europe PMC10 |
| 2017 | Treutlein, J., Frank, J., Streit, F., Reinbold, C. S., Juraeva, D., Degenhardt, F., . . . Rietschel, M. (2017). Genetic contribution to alcohol dependence: investigation of a heterogeneous German sample of individuals with alcohol dependence, chronic alcoholic pancreatitis, and alcohol-related cirrhosis. Genes, 8(7). Scopus9 WoS8 Europe PMC7 |
| 2017 | Horpaopan, S., Kirfel, J., Peters, S., Kloth, M., Hüneburg, R., Altmüller, J., . . . Aretz, S. (2017). Exome sequencing characterizes the somatic mutation spectrum of early serrated lesions in a patient with serrated polyposis syndrome (SPS). Hereditary Cancer in Clinical Practice, 15(1). Scopus7 WoS7 |
| 2017 | Meziane, I., Huhn, S., Da Silva Filho, M. I., Weinhold, N., Campo, C., Nickel, J., . . . Hemminki, K. (2017). Genome-wide association study of clinical parameters in immunoglobulin light chain amyloidosis in three patient cohorts. Haematologica, 102(10), e411-e414. Scopus7 WoS7 Europe PMC5 |
| 2017 | Schulz, H., Ruppert, A. K., Herms, S., Wolf, C., Mirza-Schreiber, N., Stegle, O., . . . Cichon, S. (2017). Genome-wide mapping of genetic determinants influencing DNA methylation and gene expression in human hippocampus. Nature Communications, 8(1). Scopus57 WoS55 Europe PMC62 |
| 2017 | Treutlein, J., Strohmaier, J., Frank, J., Witt, S. H., Rietschel, L., Forstner, A. J., . . . Rietschel, M. (2017). Association between neuropeptide y receptor Y2 promoter variant rs6857715 and major depressive disorder. Psychiatric Genetics, 27(1), 34-37. Scopus15 WoS13 Europe PMC12 |
| 2017 | Forstner, A. J., Hecker, J., Hofmann, A., Maaser, A., Reinbold, C. S., Muehleisen, T. W., . . . Noethen, M. M. (2017). Identification of shared risk loci and pathways for bipolar disorder and schizophrenia. PLOS ONE, 12(2), 14 pages. WoS70 |
| 2017 | Law, P. J., Sud, A., Mitchell, J. S., Henrion, M., Orlando, G., Lenive, O., . . . Houlston, R. S. (2017). Genome-wide association analysis of chronic lymphocytic leukaemia, Hodgkin lymphoma and multiple myeloma identifies pleiotropic risk loci. Scientific Reports, 7. Scopus35 WoS34 Europe PMC39 |
| 2017 | Went, M., Sud, A., Law, P. J., Johnson, D. C., Weinhold, N., Försti, A., . . . Houlston, R. S. (2017). Assessing the effect of obesity-related traits on multiple myeloma using a Mendelian randomisation approach. Blood Cancer Journal, 7(6). Scopus11 WoS11 Europe PMC11 |
| 2017 | Thomsen, H., Campo, C., Weinhold, N., da Silva Filho, M. I., Pour, L., Gregora, E., . . . Försti, A. (2017). Genomewide association study on monoclonal gammopathy of unknown significance (MGUS). European Journal of Haematology, 99(1), 70-79. Scopus18 WoS17 Europe PMC13 |
| 2017 | Munz, M., Willenborg, C., Richter, G. M., Jockel-Schneider, Y., Graetz, C., Staufenbiel, I., . . . Schaefer, A. S. (2017). A genome-wide association study identifies nucleotide variants at SIGLEC5 and DEFA1A3 as risk loci for periodontitis. Human Molecular Genetics, 26(13), 2577-2588. Scopus90 WoS93 Europe PMC86 |
| 2017 | Tsoi, L. C., Stuart, P. E., Tian, C., Gudjonsson, J. E., Das, S., Zawistowski, M., . . . Elder, J. T. (2017). Large scale meta-analysis characterizes genetic architecture for common psoriasis associated variants. Nature Communications, 8. Scopus293 WoS288 Europe PMC258 |
| 2017 | Da Silva Filho, M. I., Försti, A., Weinhold, N., Meziane, I., Campo, C., Huhn, S., . . . Hemminki, K. (2017). Genome-wide association study of immunoglobulin light chain amyloidosis in three patient cohorts: Comparison with myeloma. Leukemia, 31(8), 1735-1742. Scopus37 WoS30 Europe PMC29 |
| 2017 | Schröder, C., Leitão, E., Wallner, S., Schmitz, G., Klein-Hitpass, L., Sinha, A., . . . Horsthemke, B. (2017). Regions of common inter-individual DNA methylation differences in human monocytes: Genetic basis and potential function. Epigenetics and Chromatin, 10(1). Scopus19 WoS18 Europe PMC18 |
| 2017 | Sims, R., Van Der Lee, S. J., Naj, A. C., Bellenguez, C., Badarinarayan, N., Jakobsdottir, J., . . . Boccardi, V. (2017). Rare coding variants in PLCG2, ABI3, and TREM2 implicate microglial-mediated innate immunity in Alzheimer's disease. Nature Genetics, 49(9), 1373-1384. Scopus739 WoS701 Europe PMC772 |
| 2017 | Briggs, M., Ho, Y., Kaur, G., Oehler, M., Everest-Dass, A., Packer, N., & Hoffmann, P. (2017). N-Glycan matrix-assisted laser desorption/ionization mass spectrometry imaging protocol for formalin-fixed paraffin-embedded tissues. Rapid Communications in Mass Spectrometry, 31(10), 825-841. Scopus25 WoS23 Europe PMC20 |
| 2017 | Ng, Y., Sorvina, A., Bader, C., Weiland, F., Lopez, A., Hoffmann, P., . . . Brooks, D. (2017). Proteome analysis of Drosophila mutants identifies a regulatory role for 14-3-3ε in metabolic pathways. Journal of Proteome Research, 16(5), 1976-1987. Scopus1 WoS1 Europe PMC1 |
| 2017 | Chai, M., Weiland, F., Harvey, R., Hoffmann, P., Ogunniyi, A., & Paton, J. (2017). Proteomic comparisons of opaque and transparent variants of Streptococcus pneumoniae by two dimensional-differential gel electrophoresis. Scientific Reports, 7(1), 2453-1-2453-11. Scopus3 WoS3 Europe PMC2 |
| 2017 | Turvey, M. E., Weiland, F., Keller, E. J., & Hoffmann, P. (2017). The changing face of microbial quality control practices in the brewing industry: Introducing mass spectrometry proteomic fingerprinting for microbial identification. Journal of the Institute of Brewing, 123(3), 373-387. Scopus12 WoS9 |
| 2017 | Witt, S., Streit, F., Jungkunz, M., Frank, J., Awasthi, S., Reinbold, C., . . . McQuillin, A. (2017). Genome-wide association study of borderline personality disorder reveals genetic overlap with bipolar disorder, major depression and schizophrenia. Translational psychiatry, 7(6), e1155. Scopus140 WoS125 Europe PMC113 |
| 2017 | Ricciardelli, C., Lokman, N., Pyragius, C., Ween, M., Macpherson, A., Ruszkiewicz, A., . . . Oehler, M. (2017). Keratin 5 overexpression is associated with serous ovarian cancer recurrence and chemotherapy resistance. Oncotarget, 8(11), 17819-17832. Scopus51 WoS47 Europe PMC50 |
| 2017 | Mittal, P., Klingler-Hoffmann, M., Arentz, G., Winderbaum, L., Kaur, G., Anderson, L., . . . Oehler, M. (2017). Annexin A2 and alpha actinin 4 expression correlates with metastatic potential of primary endometrial cancer.. Biochim Biophys Acta, 1865(7), 846-857. Scopus25 WoS25 Europe PMC22 |
| 2017 | Bigdeli, T. B., Ripke, S., Peterson, R. E., Trzaskowski, M., Bacanu, S. A., Abdellaoui, A., . . . Kendler, K. S. (2017). Genetic effects influencing risk for major depressive disorder in China and Europe. Translational Psychiatry, 7(3), 7 pages. Scopus58 WoS57 Europe PMC56 |
| 2017 | Sud, A., Thomsen, H., Law, P., Försti, A., Filho, M., Holroyd, A., . . . Usmani, N. (2017). Genome-wide association study of classical Hodgkin lymphoma identifies key regulators of disease susceptibility. Nature Communications, 8(1), 1892. Scopus43 WoS39 Europe PMC35 |
| 2017 | Webb, T. R., Erdmann, J., Stirrups, K. E., Stitziel, N. O., Masca, N. G. D., Jansen, H., . . . Kathiresan, S. (2017). Systematic Evaluation of Pleiotropy Identifies 6 Further Loci Associated With Coronary Artery Disease. JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, 69(7), 823-836. WoS192 Europe PMC192 |
| 2017 | Polushina, T., Giddaluru, S., Bettella, F., Espeseth, T., Lundervold, A. J., Djurovic, S., . . . Le Hellard, S. (2017). Analysis of the joint effect of SNPs to identify independent loci and allelic heterogeneity in schizophrenia GWAS data. Translational Psychiatry, 7(12), 9 pages. Scopus7 WoS6 Europe PMC6 |
| 2017 | Fernandez-Rebollo, E., Mentrup, B., Ebert, R., Franzen, J., Abagnale, G., Sieben, T., . . . Wagner, W. (2017). Human Platelet Lysate versus Fetal Calf Serum: These Supplements Do Not Select for Different Mesenchymal Stromal Cells. Scientific Reports, 7(1), 8 pages. Scopus60 WoS54 Europe PMC48 |
| 2016 | Brosens, E., Marsch, F., De Jong, E. M., Zaveri, H. P., Hilger, A. C., Choinitzki, V. G., . . . De Klein, A. (2016). Copy number variations in 375 patients with oesophageal atresia and/or tracheoesophageal fistula. European Journal of Human Genetics, 24(12), 1715-1723. Scopus25 WoS27 Europe PMC24 |
| 2016 | Stitziel, N. O., Stirrups, K. E., Masca, N. G. D., Erdmann, J., Ferrario, P. G., Koenig, I. R., . . . Schunkert, H. (2016). Coding Variation in <i>ANGPTL4</i>, <i>LPL</i>, and <i>SVEP1</i> and the Risk of Coronary Disease. NEW ENGLAND JOURNAL OF MEDICINE, 374(12), 1134-1144. WoS288 Europe PMC391 |
| 2016 | Zammit, C., Weiland, F., Brugger, J., Wade, B., Winderbaum, L., Nies, D., . . . Reith, F. (2016). Proteomic responses to gold(III)-toxicity in the bacterium Cupriavidus metallidurans CH34. Metallomics, 8(11), 1204-1216. Scopus34 WoS31 Europe PMC17 |
| 2016 | Weiland, F., Arentz, G., Klingler-Hoffmann, M., McCarthy, P., Lokman, N., Kaur, G., . . . Hoffmann, P. (2016). A novel IEF peptide fractionation method reveals a detailed profile of N-terminal Acetylation in chemotherapy-responsive and -resistant ovarian cancer cells. Journal of Proteome Research, 15(11), 4073-4081. Scopus8 WoS7 Europe PMC4 |
| 2016 | Mittal, P., Klingler-Hoffmann, M., Arentz, G., Zhang, C., Kaur, G., Oehler, M., & Hoffmann, P. (2016). Proteomics of endometrial cancer diagnosis, treatment, and prognosis. Proteomics - Clinical Applications, 10(3), 217-229. Scopus24 WoS22 Europe PMC18 |
| 2016 | Turvey, M., Weiland, F., Meneses, J., Sterenberg, N., & Hoffmann, P. (2016). Identification of beer spoilage microorganisms using the MALDI Biotyper platform. Applied Microbiology and Biotechnology, 100(6), 2761-2773. Scopus29 WoS28 Europe PMC12 |
| 2016 | Eyre, N., Hampton-Smith, R., Aloia, A., Eddes, J., Simpson, K., Hoffmann, P., & Beard, M. (2016). Phosphorylation of NS5A Serine-235 is essential to hepatitis C virus RNA replication and normal replication compartment formation. Virology, 491, 27-44. Scopus30 WoS30 Europe PMC30 |
| 2016 | Reynolds, T., François, A., Riesen, N., Turvey, M., Nicholls, S., Hoffmann, P., & Monro, T. (2016). Dynamic self-referencing approach to whispering gallery mode biosensing and its application to measurement within undiluted serum. Analytical Chemistry, 88(7), 4036-4040. Scopus45 WoS43 Europe PMC10 |
| 2016 | Briggs, M., Kuliwaba, J., Muratovic, D., Everest-Dass, A., Packer, N., Findlay, D., & Hoffmann, P. (2016). MALDI mass spectrometry imaging of N-glycans on tibial cartilage and subchondral bone proteins in knee osteoarthritis. Proteomics, 16(11-12), 1736-1741. Scopus44 WoS42 Europe PMC39 |
| 2016 | Winderbaum, L., Koch, I., Mittal, P., & Hoffmann, P. (2016). Classification of MALDI-MS imaging data of tissue microarrays using canonical correlation analysis based variable selection. Proteomics, 16(11-12), 1731-1735. Scopus9 WoS9 Europe PMC7 |
| 2016 | Mittal, P., Klingler-Hoffmann, M., Arentz, G., Winderbaum, L., Lokman, N., Zhang, C., . . . Hoffmann, P. (2016). Lymph node metastasis of primary endometrial cancers: associated proteins revealed by MALDI imaging. Proteomics, 16(11-12), 1793-1801. Scopus27 WoS27 Europe PMC24 |
| 2016 | Schubert, K., Weiland, F., Baune, B., & Hoffmann, P. (2016). The use of MALDI-MSI in the investigation of psychiatric and neurodegenerative disorders: a review. Proteomics, 16(11-12), 1747-1758. Scopus42 WoS40 Europe PMC37 |
| 2016 | Cathro, P., Mccarthy, P., Hoffmann, P., & Zilm, P. (2016). Isolation and identification of Enterococcus faecalis membrane proteins using membrane shaving, 1D SDS/PAGE, and mass spectrometry. FEBS Open Bio, 6(6), 586-593. Scopus11 WoS12 Europe PMC7 |
| 2016 | Zhang, C., Arentz, G., Winderbaum, L., Lokman, N., Klingler-Hoffmann, M., Mittal, P., . . . Hoffmann, P. (2016). MALDI mass spectrometry imaging reveals decreased CK5 levels in vulvar squamous cell carcinomas compared to the precursor lesion differentiated vulvar intraepithelial neoplasia. International Journal of Molecular Sciences, 17(7), 1088-1-1088-12. Scopus12 WoS9 Europe PMC11 |
| 2016 | Everest-Dass, A., Briggs, M., Kaur, G., Oehler, M., Hoffmann, P., & Packer, N. (2016). N-glycan MALDI imaging mass spectrometry on formalin-fixed paraffin-embedded tissue enables the delineation of ovarian cancer tissues. Molecular and Cellular Proteomics, 15(9), 3003-3016. Scopus108 WoS104 Europe PMC93 |
| 2016 | Hoffer, K. J., Hoffmann, P. C., & Savini, G. (2016). Comparison of a new optical biometer using swept-source optical coherence tomography and a biometer using optical low-coherence reflectometry. JOURNAL OF CATARACT AND REFRACTIVE SURGERY, 42(8), 1165-1172. WoS74 |
| 2016 | Stitziel, N. O., Stirrups, K. E., Masca, N. G. D., Erdmann, J., Ferrario, P. G., Koenig, I. R., . . . Schunkert, H. (2016). Coding Variation in <i>ANGPTL4</i>, <i>LPL</i>, and <i>SVEP1</i> and the Risk of Coronary Disease (vol 374, pg 1134, 2016). NEW ENGLAND JOURNAL OF MEDICINE, 374(19), 1898. |
| 2016 | Spier, I., Kerick, M., Drichel, D., Horpaopan, S., Altmüller, J., Laner, A., . . . Aretz, S. (2016). Exome sequencing identifies potential novel candidate genes in patients with unexplained colorectal adenomatous polyposis. Familial Cancer, 15(2), 281-288. Scopus46 WoS42 Europe PMC39 |
| 2016 | Mitchell, J. S., Li, N., Weinhold, N., Försti, A., Ali, M., Van Duin, M., . . . Houlston, R. S. (2016). Genome-wide association study identifies multiple susceptibility loci for multiple myeloma. Nature Communications, 7. Scopus146 WoS141 Europe PMC133 |
| 2016 | Flachsbart, F., Ellinghaus, D., Gentschew, L., Heinsen, F. A., Caliebe, A., Christiansen, L., . . . Nebel, A. (2016). Immunochip analysis identifies association of the RAD50/IL13 region with human longevity. Aging Cell, 15(3), 585-588. Scopus20 WoS21 Europe PMC20 |
| 2016 | Thomsen, H., da Silva Filho, M. I., Fuchs, M., Ponader, S., von Strandmann, E. P., Eisele, L., . . . Försti, A. (2016). Evidence of inbreeding in Hodgkin lymphoma. Plos One, 11(4), 15 pages. Scopus8 WoS7 Europe PMC9 |
| 2016 | Thomsen, H., Chen, B., Figlioli, G., Elisei, R., Romei, C., Cipollini, M., . . . Försti, A. (2016). Runs of homozygosity and inbreeding in thyroid cancer. BMC Cancer, 16(1), 11 pages. Scopus17 WoS16 Europe PMC17 |
| 2016 | Johnson, D. C., Weinhold, N., Mitchell, J., Chen, B., Stephens, O. W., Försti, A., . . . Morgan, G. J. (2016). Genetic factors influencing the risk of multiple myeloma bone disease. Leukemia, 30(4), 883-888. Scopus12 WoS9 Europe PMC10 |
| 2016 | Spier, I., Drichel, D., Kerick, M., Kirfel, J., Horpaopan, S., Laner, A., . . . Aretz, S. (2016). Low-level APC mutational mosaicism is the underlying cause in a substantial fraction of unexplained colorectal adenomatous polyposis cases. Journal of Medical Genetics, 53(3), 172-179. Scopus54 WoS50 Europe PMC43 |
| 2016 | Degenhardt, F., Heinemann, B., Strohmaier, J., Pfohl, M. A., Giegling, I., Hofmann, A., . . . Nöthen, M. M. (2016). Identification of rare variants in KCTD13 at the schizophrenia risk locus 16p11.2. Psychiatric Genetics, 26(6), 293-296. Scopus7 WoS7 Europe PMC8 |
| 2016 | Schwantes-An, T. H., Zhang, J., Chen, L. S., Hartz, S. M., Culverhouse, R. C., Chen, X., . . . Philibert, R. A. (2016). Association of the OPRM1 Variant rs1799971 (A118G) with Non-Specific Liability to Substance Dependence in a Collaborative de novo Meta-Analysis of European-Ancestry Cohorts. Behavior Genetics, 46(2), 151-169. Scopus95 WoS80 Europe PMC75 |
| 2016 | Ibrahim-Verbaas, C. A., Bressler, J., Debette, S., Schuur, M., Smith, A. V., Bis, J. C., . . . Mosley, T. H. (2016). GWAS for executive function and processing speed suggests involvement of the <i>CADM2</i> gene. MOLECULAR PSYCHIATRY, 21(2), 189-197. WoS107 |
| 2016 | Johnson, D. C., Weinhold, N., Mitchell, J. S., Chen, B., Kaiser, M., Begum, D. B., . . . Morgan, G. J. (2016). Genome-wide association study identifies variation at 6q25.1 associated with survival in multiple myeloma. Nature Communications, 7, 7 pages. Scopus30 WoS26 Europe PMC26 |
| 2016 | Weinhold, L., Wahl, S., Pechlivanis, S., Hoffmann, P., & Schmid, M. (2016). A statistical model for the analysis of beta values in DNA methylation studies. BMC Bioinformatics, 17(1). Scopus39 WoS38 Europe PMC33 |
| 2015 | Kaut, O., Schmitt, I., Hofmann, A., Hoffmann, P., Schlaepfer, T. E., Wüllner, U., & Hurlemann, R. (2015). Aberrant NMDA receptor DNA methylation detected by epigenome-wide analysis of hippocampus and prefrontal cortex in major depression. European Archives of Psychiatry and Clinical Neuroscience, 265(4), 331-341. Scopus60 WoS53 Europe PMC49 |
| 2015 | Weber, S., Hofmann, A., Herms, S., Hoffmann, P., & Doerfler, W. (2015). Destabilization of the human epigenome: Consequences of foreign DNA insertions. Epigenomics, 7(5), 745-755. Scopus16 WoS15 Europe PMC12 |
| 2015 | Stieber, C., Grumach, A. S., Cordeiro, E., Constantino-Silva, R. N., Barth, S., Hoffmann, P., . . . Cichon, S. (2015). First report of a FXII gene mutation in a Brazilian family with hereditary angio-oedema with normal C1 inhibitor. British Journal of Dermatology, 173(4), 1102-1104. Scopus5 WoS5 Europe PMC5 |
| 2015 | Thomsen, H., Filho, M. I. D. S., Woltmann, A., Johansson, R., Eyfjörd, J. E., Hamann, U., . . . Försti, A. (2015). Inbreeding and homozygosity in breast cancer survival. Scientific Reports, 5, 12 pages. Scopus5 WoS4 Europe PMC4 |
| 2015 | Stuart, P. E., Nair, R. P., Tsoi, L. C., Tejasvi, T., Das, S., Kang, H. M., . . . Elder, J. T. (2015). Genome-wide Association Analysis of Psoriatic Arthritis and Cutaneous Psoriasis Reveals Differences in Their Genetic Architecture. American Journal of Human Genetics, 97(6), 816-836. Scopus266 WoS246 Europe PMC231 |
| 2015 | Forstner, A. J., Hofmann, A., Maaser, A., Sumer, S., Khudayberdiev, S., Mühleisen, T. W., . . . Nöthen, M. M. (2015). Genome-wide analysis implicates microRNAs and their target genes in the development of bipolar disorder. Translational Psychiatry, 5(11), 8 pages. Scopus68 WoS60 Europe PMC51 |
| 2015 | Vijayakrishnan, J., Henrion, M., Moorman, A. V., Fiege, B., Kumar, R., Inacio Da Silva Filho, M., . . . Houlston, R. S. (2015). The 9p21.3 risk of childhood acute lymphoblastic leukaemia is explained by a rare high-impact variant in CDKN2A. Scientific Reports, 5, 8 pages. Scopus29 WoS28 Europe PMC31 |
| 2015 | Lal, D., Pernhorst, K., Klein, K. M., Reif, P., Tozzi, R., Toliat, M. R., . . . Weber, Y. G. (2015). Extending the phenotypic spectrum of RBFOX1 deletions: Sporadic focal epilepsy. Epilepsia, 56(9), e129-e133. Scopus33 WoS31 Europe PMC32 |
| 2015 | Basmanav, F. B., Forstner, A. J., Fier, H., Herms, S., Meier, S., Degenhardt, F., . . . Cichon, S. (2015). Investigation of the role of TCF4 rare sequence variants in schizophrenia. American Journal of Medical Genetics Part B Neuropsychiatric Genetics, 168(5), 354-362. Scopus11 WoS12 Europe PMC12 |
| 2015 | Spier, I., Holzapfel, S., Altmüller, J., Zhao, B., Horpaopan, S., Vogt, S., . . . Aretz, S. (2015). Frequency and phenotypic spectrum of germline mutations in POLE and seven other polymerase genes in 266 patients with colorectal adenomas and carcinomas. International Journal of Cancer, 137(2), 320-331. Scopus133 WoS121 Europe PMC105 |
| 2015 | Van Setten, J., Išgum, I., Pechlivanis, S., Tragante, V., De Jong, P. A., Smolonska, J., . . . De Bakker, P. I. W. (2015). Serum Lipid Levels, Body Mass Index, and Their Role in Coronary Artery Calcification: A Polygenic Analysis. Circulation Cardiovascular Genetics, 8(2), 327-333. Scopus14 WoS14 Europe PMC11 |
| 2015 | Weinhold, N., Meissner, T., Johnson, D. C., Seckinger, A., Moreaux, J., Försti, A., . . . Hemminki, K. (2015). The 7p15.3 (rs4487645) association for multiple myeloma shows strong allele-specific regulation of the myc-interacting gene cdca7l in malignant plasma cells. Haematologica, 100(3), e110-e113. Scopus29 WoS29 Europe PMC25 |
| 2015 | Nettersheim, D., Jostes, S., Sharma, R., Schneider, S., Hofmann, A., Ferreira, H. J., . . . Schorle, H. (2015). BMP Inhibition in Seminomas Initiates Acquisition of Pluripotency via NODAL Signaling Resulting in Reprogramming to an Embryonal Carcinoma. Plos Genetics, 11(7). Scopus60 WoS57 Europe PMC54 |
| 2015 | Sharma, A., Jamil, M. A., Nuesgen, N., Schreiner, F., Priebe, L., Hoffmann, P., . . . El-Maarri, O. (2015). DNA methylation signature in peripheral blood reveals distinct characteristics of human X chromosome numerical aberrations. Clinical Epigenetics, 7(1). Scopus68 WoS61 |
| 2015 | Briggs, M., Everest Dass, A., Oehler, M., Packer, N., & Hoffman, P. (2015). The glycomic quest for the holy grail: an early stage biomarker for ovarian cancer. Australian biochemist, 46(3), 20-23. |
| 2015 | Horpaopan, S., Spier, I., Zink, A. M., Altmüller, J., Holzapfel, S., Laner, A., . . . Aretz, S. (2015). Genome-wide CNV analysis in 221 unrelated patients and targeted high-throughput sequencing reveal novel causative candidate genes for colorectal adenomatous polyposis. International Journal of Cancer, 136(6), E578-E589. Scopus54 WoS53 Europe PMC51 |
| 2015 | Figlioli, G., Chen, B., Elisei, R., Romei, C., Campo, C., Cipollini, M., . . . Försti, A. (2015). Novel genetic variants in differentiated thyroid cancer and assessment of the cumulative risk. Scientific Reports, 5, 7 pages. Scopus23 WoS23 Europe PMC22 |
| 2015 | Johnson, M. R., Behmoaras, J., Bottolo, L., Krishnan, M. L., Pernhorst, K., Santoscoy, P. L. M., . . . Petretto, E. (2015). Systems genetics identifies Sestrin 3 as a regulator of a proconvulsant gene network in human epileptic hippocampus. NATURE COMMUNICATIONS, 6, 11 pages. WoS123 |
| 2015 | Juraeva, D., Treutlein, J., Scholz, H., Frank, J., Degenhardt, F., Cichon, S., . . . Rietschel, M. (2015). XRCC5 as a risk gene for alcohol dependence: Evidence from a genome-wide gene-set-based analysis and follow-up studies in drosophila and humans. Neuropsychopharmacology, 40(2), 361-371. Scopus13 WoS8 Europe PMC10 |
| 2015 | Klantsataya, E., François, A., Ebendorff-Heidepriem, H., Hoffmann, P., & Monro, T. (2015). Surface plasmon scattering in exposed core optical fiber for enhanced resolution refractive index sensing. Sensors, 15(10), 25090-25102. Scopus96 WoS92 Europe PMC17 |
| 2015 | Ricciardelli, C., Lokman, N., Cheruvu, S., Tan, I., Ween, M., Pyragius, C., . . . Oehler, M. (2015). Transketolase is upregulated in metastatic peritoneal implants and promotes ovarian cancer cell proliferation. Clinical & Experimental Metastasis, 32(5), 441-455. Scopus64 WoS64 Europe PMC57 |
| 2015 | Turvey, M., Klingler-Hoffmann, M., Hoffmann, P., & McColl, S. (2015). p84 forms a negative regulatory complex with p110γ to control PI3Kγ signalling during cell migration. Immunology and Cell Biology, 93(8), 735-743. Scopus7 WoS7 Europe PMC7 |
| 2015 | Alanazi, I., Hoffmann, P., & Adelson, D. (2015). MicroRNAs are part of the regulatory network that controls EGF induced apoptosis, including elements of the JAK/STAT pathway, in A431 cells. PLoS One, 10(3), e0120337-1-e0120337-20. Scopus22 WoS21 Europe PMC21 |
| 2015 | Wessel, J., Chu, A. Y., Willems, S. M., Wang, S., Yaghootkar, H., Brody, J. A., . . . Malerba, G. (2015). Low-frequency and rare exome chip variants associate with fasting glucose and type 2 diabetes susceptibility. Nature Communications, 6(1), 16 pages. Scopus164 WoS155 Europe PMC154 |
| 2015 | Gustafsson, O., Arentz, G., & Hoffmann, P. (2015). Proteomic developments in the analysis of formalin-fixed tissue. Biochimica et Biophysica Acta, 1854(6), 559-580. Scopus102 WoS96 Europe PMC88 |
| 2015 | Bui, L., Hoffmann, P., Turnidge, J., Zilm, P., & Kidd, S. (2015). Prolonged growth of a clinical Staphylococcus aureus strain selects for a stable small-colony-variant cell type. Infection and Immunity, 83(2), 470-481. Scopus41 WoS37 Europe PMC34 |
| 2015 | Arentz, G., Weiland, F., Oehler, M., & Hoffmann, P. (2015). State of the art of 2D DIGE. Proteomics - Clinical Applications, 9(3-4), 277-288. Scopus95 WoS72 Europe PMC67 |
| 2015 | Winderbaum, L., Koch, I., Gustafsson, O., Meding, S., & Hoffmann, P. (2015). Feature extraction for proteomics imaging mass spectrometry data. Annals of Applied Statistics, 9(4), 1973-1996. Scopus12 WoS10 |
| 2015 | Gustafsson, O., Briggs, M., Condina, M., Winderbaum, L., Pelzing, M., McColl, S., . . . Hoffmann, P. (2015). MALDI imaging mass spectrometry of N-linked glycans on formalin-fixed paraffin-embedded murine kidney. Analytical and Bioanalytical Chemistry, 407(8), 2127-2139. Scopus76 WoS75 Europe PMC68 |
| 2014 | Koch, I., Hoffmann, P., & Marron, J. (2014). Proteomics profiles from mass spectrometry. Electronic Journal of Statistics, 8(2), 1703-1713. Scopus12 WoS12 |
| 2014 | Turvey, M., Koudelka, T., Comerford, I., Greer, J., Carroll, W., Bernard, C., . . . McColl, S. (2014). Quantitative proteome profiling of CNS-infiltrating autoreactive CD4⁺ cells reveals selective changes during experimental autoimmune encephalomyelitis. Journal of Proteome Research, 13(8), 3655-3670. Scopus15 WoS13 Europe PMC13 |
| 2014 | Hughes, P., Moretta, M., Lim, A., Grasby, D., Bird, D., Brierley, S., . . . Krumbiegel, D. (2014). Immune derived opioidergic inhibition of viscerosensory afferents is decreased in Irritable Bowel Syndrome patients. Brain, Behavior, and Immunity, 42, 191-203. Scopus48 WoS44 Europe PMC40 |
| 2014 | Weiland, F., Zammit, C., Reith, F., & Hoffmann, P. (2014). High resolution two-dimensional electrophoresis of native proteins. Electrophoresis, 35(12-13), 1893-1902. Scopus15 WoS13 Europe PMC8 |
| 2014 | Humphries, J., Penno, M., Weiland, F., Klingler-Hoffmann, M., Zuber, A., Boussioutas, A., . . . Hoffmann, P. (2014). Identification and validation of novel candidate protein biomarkers for the detection of human gastric cancer. Biochimica et Biophysica Acta - Proteins and Proteomics, 1844(5), 1051-1058. Scopus52 WoS51 Europe PMC38 |
| 2014 | Marron, J. S., Koch, I., & Hoffmann, P. (2014). Rejoinder: analysis of proteomics data. Electronic journal of statistics, 8(1), 1756-1758. Scopus1 |
| 2014 | Jarick, I., Volckmar, A. L., Pütter, C., Pechlivanis, S., Nguyen, T. T., Dauvermann, M. R., . . . Hinney, A. (2014). Genome-wide analysis of rare copy number variations reveals PARK2 as a candidate gene for attention-deficit/hyperactivity disorder. Molecular Psychiatry, 19(1), 115-121. Scopus73 WoS59 Europe PMC58 |
| 2014 | Schackert, H. K., Agha-Hosseini, F., Görgens, H., Jatzwauk, M., von Kannen, S., Noack, B., . . . Mehdipour, P. (2014). Complete homozygous deletion of CTSC in an Iranian family with Papillon-Lefèvre syndrome. International Journal of Dermatology, 53(7), 885-887. Scopus10 WoS4 Europe PMC7 |
| 2014 | Weinhold, N., Foersti, A., da Silva Filho, M. I., Nickel, J., Campo, C., Hoffmann, P., . . . Hemminki, K. (2014). Immunoglobulin light-chain amyloidosis shares genetic susceptibility with multiple myeloma. LEUKEMIA, 28(11), 2254-2256. WoS9 |
| 2014 | Ramirez, A., van der Flier, W. M., Herold, C., Ramonet, D., Heilmann, S., Lewczuk, P., . . . Noethen, M. M. (2014). <i>SUCLG2</i> identified as both a determinator of CSF Aβ<sub>1-42</sub> levels and an attenuator of cognitive decline in Alzheimer's disease. HUMAN MOLECULAR GENETICS, 23(24), 6644-6658. WoS40 |
| 2014 | Reinthaler, E. M., Lal, D., Lebon, S., Hildebrand, M. S., Dahl, H. H. M., Regan, B. M., . . . Neubauer, B. A. (2014). 16p11.2 600 kb duplications confer risk for typical and atypical rolandic epilepsy. Human Molecular Genetics, 23(22), 6069-6080. Scopus57 WoS53 Europe PMC52 |
| 2014 | Figlioli, G., Köhler, A., Chen, B., Elisei, R., Romei, C., Cipollini, M., . . . Gemignani, F. (2014). Novel genome-wide association study-based candidate loci for differentiated thyroid cancer risk. Journal of Clinical Endocrinology and Metabolism, 99(10), E2084-E2092. Scopus43 WoS43 Europe PMC39 |
| 2014 | Forstner, A. J., Buket Basmanav, F., Mattheisen, M., Böhmer, A. C., Hollegaard, M. V., Janson, E., . . . Cichon, S. (2014). Investigation of the involvement of MIR185 and its target genes in the development of schizophrenia. Journal of Psychiatry and Neuroscience, 39(6), 386-396. Scopus25 WoS22 Europe PMC20 |
| 2014 | Arking, D. E., Pulit, S. L., Crotti, L., Van Der Harst, P., Munroe, P. B., Koopmann, T. T., . . . Jula, A. (2014). Genetic association study of QT interval highlights role for calcium signaling pathways in myocardial repolarization. Nature Genetics, 46(8), 826-836. Scopus260 WoS238 Europe PMC237 |
| 2014 | Ripke, S., Neale, B. M., Corvin, A., Walters, J. T. R., Farh, K. H., Holmans, P. A., . . . Joa, I. (2014). Biological insights from 108 schizophrenia-associated genetic loci. Nature, 511(7510), 421-427. Scopus6169 WoS5888 Europe PMC5721 |
| 2014 | Al Chawa, T., Ludwig, K. U., Fier, H., Pötzsch, B., Reich, R. H., Schmidt, G., . . . Mangold, E. (2014). Nonsyndromic cleft lip with or without cleft palate: Increased burden of rare variants within Gremlin-1, a component of the bone morphogenetic protein 4 pathway. Birth Defects Research Part A Clinical and Molecular Teratology, 100(6), 493-498. Scopus18 WoS17 Europe PMC16 |
| 2014 | Ludwig, K. U., Boehmer, A. C., Rubini, M., Mossey, P. A., Herms, S., Nowak, S., . . . Mangold, E. (2014). Strong Association of Variants around <i>FOXE1</i> and Orofacial Clefting. JOURNAL OF DENTAL RESEARCH, 93(4), 376-381. WoS46 |
| 2014 | Weinhold, N., Johnson, D. C., Rawstron, A. C., Försti, A., Doughty, C., Vijayakrishnan, J., . . . Houlston, R. S. (2014). Inherited genetic susceptibility to monoclonal gammopathy of unknown significance. Blood, 123(16), 2513-2517. Scopus37 WoS32 Europe PMC28 |
| 2014 | Mühleisen, T. W., Leber, M., Schulze, T. G., Strohmaier, J., Degenhardt, F., Treutlein, J., . . . Cichon, S. (2014). Genome-wide association study reveals two new risk loci for bipolar disorder. Nature Communications, 5, 8 pages. Scopus272 WoS261 Europe PMC244 |
| 2014 | Schütte, U., Bisht, S., Heukamp, L. C., Kebschull, M., Florin, A., Haarmann, J., . . . Feldmann, G. (2014). Hippo signaling mediates proliferation, invasiveness, and metastatic potential of clear cell renal cell carcinoma. Translational Oncology, 7(2), 309-321. Scopus66 WoS68 |
| 2014 | Hoffmann, P. C., Abraham, M., Hirnschall, N., & Findl, O. (2014). Prediction of Residual Astigmatism After Cataract Surgery Using Swept Source Fourier Domain Optical Coherence Tomography. CURRENT EYE RESEARCH, 39(12), 1178-1186. WoS52 |
| 2014 | Hirnschall, N., Hoffmann, P. C., Draschl, P., Maedel, S., & Findl, O. (2014). Evaluation of Factors Influencing the Remaining Astigmatism After Toric Intraocular Lens Implantation. JOURNAL OF REFRACTIVE SURGERY, 30(6), 394-+. WoS50 |
| 2014 | Pernhorst, K., Van Loo, K. M. J., Von Lehe, M., Priebe, L., Cichon, S., Herms, S., . . . Becker, A. J. (2014). Erratum: Rs6295 promoter variants of the serotonin type 1A receptor are differentially activated by c-Jun in vitro and correlate to transcript levels in human epileptic brain tissue (Brain Research 1499 (2013) (136-144)). Brain Research, 1555, 97-98. |
| 2014 | Woltmann, A., Chen, B., Lascorz, J., Johansson, R., Eyfjörd, J. E., Hamann, U., . . . Försti, A. (2014). Systematic pathway enrichment analysis of a genome-wide association study on breast cancer survival reveals an influence of genes involved in cell adhesion and calcium signaling on the patients' clinical outcome. Plos One, 9(6), 14 pages. Scopus15 WoS15 Europe PMC15 |
| 2014 | Hammer, C., Degenhardt, F., Priebe, L., Stütz, A. M., Heilmann, S., Waszak, S. M., . . . Niesler, B. (2014). A common microdeletion affecting a hippocampus- and amygdala-specific isoform of tryptophan hydroxylase 2 is not associated with affective disorders. Bipolar Disorders, 16(7), 764-768. Scopus2 WoS2 Europe PMC2 |
| 2014 | Schmidt, B., Dragano, N., Scherag, A., Pechlivanis, S., Hoffmann, P., Nöthen, M. M., . . . Moebus, S. (2014). Exploring genetic variants predisposing to diabetes mellitus and their association with indicators of socioeconomic status. BMC Public Health, 14(1). Scopus1 WoS1 Europe PMC1 |
| 2014 | Gockel, I., Becker, J., Wouters, M. M., Niebisch, S., Gockel, H. R., Hess, T., . . . Schumacher, J. (2014). Common variants in the HLA-DQ region confer susceptibility to idiopathic achalasia. Nature Genetics, 46(8), 901-904. Scopus95 WoS84 Europe PMC67 |
| 2014 | Becker, J., Czamara, D., Scerri, T. S., Ramus, F., Csépe, V., Talcott, J. B., . . . Schumacher, J. (2014). Genetic analysis of dyslexia candidate genes in the European cross-linguistic NeuroDys cohort. European Journal of Human Genetics, 22(5), 675-680. Scopus54 WoS55 Europe PMC41 |
| 2013 | Weinhold, N., Johnson, D. C., Chubb, D., Chen, B., Försti, A., Hosking, F. J., . . . Hemminki, K. (2013). The CCND1 c.870G>A polymorphism is a risk factor for t(11;14)(q13;q32) multiple myeloma. Nature Genetics, 45(5), 522-525. Scopus100 WoS94 Europe PMC87 |
| 2013 | Ludwig, K. U., Sämann, P., Alexander, M., Becker, J., Bruder, J., Moll, K., . . . Czamara, D. (2013). A common variant in Myosin-18B contributes to mathematical abilities in children with dyslexia and intraparietal sulcus variability in adults. Translational Psychiatry, 3. Scopus31 WoS24 Europe PMC21 |
| 2013 | Pechlivanis, S., Mühleisen, T. W., Möhlenkamp, S., Schadendorf, D., Erbel, R., Jöckel, K. H., . . . Moebus, S. (2013). Risk loci for coronary artery calcification replicated at 9p21 and 6q24 in the Heinz Nixdorf Recall Study. BMC Medical Genetics, 14(1). Scopus38 WoS38 Europe PMC35 |
| 2013 | Draaken, M., Mughal, S. S., Pennimpede, T., Wolter, S., Wittler, L., Ebert, A. K., . . . Ludwig, M. (2013). Isolated bladder exstrophy associated with a de novo 0.9 Mb microduplication on chromosome 19p13.12. Birth Defects Research Part A Clinical and Molecular Teratology, 97(3), 133-139. Scopus20 WoS18 Europe PMC14 |
| 2013 | Pernhorst, K., Van Loo, K. M. J., Von Lehe, M., Priebe, L., Cichon, S., Herms, S., . . . Becker, A. J. (2013). Rs6295 promoter variants of the serotonin type 1A receptor are differentially activated by c-Jun in vitro and correlate to transcript levels in human epileptic brain tissue. Brain Research, 1499, 136-144. Scopus15 WoS14 Europe PMC11 |
| 2013 | Pernhorst, K., Herms, S., Hoffmann, P., Cichon, S., Schulz, H., Sander, T., . . . Grote, A. (2013). TLR4, ATF-3 and IL8 inflammation mediator expression correlates with seizure frequency in human epileptic brain tissue. Seizure, 22(8), 675-678. Scopus82 WoS75 Europe PMC67 |
| 2013 | Hoffmann, P. C., & Lindemann, C. R. (2013). Intraocular lens calculation for aspheric intraocular lenses. JOURNAL OF CATARACT AND REFRACTIVE SURGERY, 39(6), 867-872. WoS17 |
| 2013 | Hoffmann, P. C., Wahl, J., Huetz, W. W., & Preussner, P. -R. (2013). A Ray Tracing Approach to Calculate Toric Intraocular Lenses. JOURNAL OF REFRACTIVE SURGERY, 29(6), 402-+. WoS38 |
| 2013 | Stich, B., Urbany, C., Hoffmann, P., & Gebhardt, C. (2013). Population structure and linkage disequilibrium in diploid and tetraploid potato revealed by genome-wide high-density genotyping using the SolCAP SNP array. PLANT BREEDING, 132(6), 718-724. WoS45 |
| 2013 | Easton, A. C., Lucchesi, W., Lourdusamy, A., Lenz, B., Solati, J., Golub, Y., . . . Mueller, C. P. (2013). aCaMKII Autophosphorylation Controls the Establishment of Alcohol Drinking Behavior (vol 38, pg 1636, 2013). NEUROPSYCHOPHARMACOLOGY, 38(13), 2735. WoS1 |
| 2013 | Grimminger, T., Pernhorst, K., Surges, R., Niehusmann, P., Priebe, L., von Lehe, M., . . . Becker, A. J. (2013). Levetiracetam resistance: Synaptic signatures & corresponding promoter SNPs in epileptic hippocampi. NEUROBIOLOGY OF DISEASE, 60, 115-125. WoS19 |
| 2013 | Migliorini, G., Fiege, B., Hosking, F. J., Ma, Y., Kumar, R., Sherborne, A. L., . . . Houlston, R. S. (2013). Variation at 10p12.2 and 10p14 influences risk of childhood B-cell acute lymphoblastic leukemia and phenotype. Blood, 122(19), 3298-3307. Scopus140 WoS128 Europe PMC122 |
| 2013 | Frampton, M., Da Silva Filho, M. I., Broderick, P., Thomsen, H., Försti, A., Vijayakrishnan, J., . . . Houlston, R. S. (2013). Variation at 3p24.1 and 6q23.3 influences the risk of Hodgkin's lymphoma. Nature Communications, 4, 7 pages. Scopus60 WoS51 Europe PMC51 |
| 2013 | Köhler, A., Chen, B., Gemignani, F., Elisei, R., Romei, C., Figlioli, G., . . . Försti, A. (2013). Genome-wide association study on differentiated thyroid cancer. Journal of Clinical Endocrinology and Metabolism, 98(10), E1674-E1681. Scopus100 WoS98 Europe PMC91 |
| 2013 | Chubb, D., Weinhold, N., Broderick, P., Chen, B., Johnson, D. C., Försti, A., . . . Goldschmidt, H. (2013). Common variation at 3q26.2, 6p21.33, 17p11.2 and 22q13.1 influences multiple myeloma risk. Nature Genetics, 45(10), 1221-1225. Scopus147 WoS140 Europe PMC129 |
| 2013 | Yildiz, Y., Hoffmann, P., Vom Dahl, S., Breiden, B., Sandhoff, R., Niederau, C., . . . Mattheisen, M. (2013). Functional and genetic characterization of the non-lysosomal glucosylceramidase 2 as a modifier for Gaucher disease. Orphanet Journal of Rare Diseases, 8(1), 8 pages. Scopus25 WoS24 Europe PMC22 |
| 2013 | Lemke, J. R., Lal, D., Reinthaler, E. M., Steiner, I., Nothnagel, M., Alber, M., . . . Von Spiczak, S. (2013). Mutations in GRIN2A cause idiopathic focal epilepsy with rolandic spikes. Nature Genetics, 45(9), 1067-1072. Scopus379 WoS344 Europe PMC300 |
| 2013 | Easton, A. C., Lucchesi, W., Lourdusamy, A., Lenz, B., Solati, J., Golub, Y., . . . Mueller, C. P. (2013). αCaMKII Autophosphorylation Controls the Establishment of Alcohol Drinking Behavior. NEUROPSYCHOPHARMACOLOGY, 38(9), 1636-1647. WoS58 |
| 2013 | Priebe, L., Degenhardt, F., Strohmaier, J., Breuer, R., Herms, S., Witt, S. H., . . . Cichon, S. (2013). Copy Number Variants in German Patients with Schizophrenia. Plos One, 8(7), 5 pages. Scopus19 WoS19 Europe PMC20 |
| 2013 | Ellinghaus, D., Baurecht, H., Esparza-Gordillo, J., Rodríguez, E., Matanovic, A., Marenholz, I., . . . Weidinger, S. (2013). High-density genotyping study identifies four new susceptibility loci for atopic dermatitis. Nature Genetics, 45(7), 808-812. Scopus175 WoS159 Europe PMC136 |
| 2013 | Albayrak, O., Pütter, C., Volckmar, A. L., Cichon, S., Hoffmann, P., Nöthen, M. M., . . . Hinney, A. (2013). Common obesity risk alleles in childhood attention-deficit/hyperactivity disorder. American Journal of Medical Genetics Part B Neuropsychiatric Genetics, 162(4), 295-305. Scopus80 WoS76 Europe PMC62 |
| 2013 | González-Carmona, M. A., Quasdorff, M., Vogt, A., Tamke, A., Yildiz, Y., Hoffmann, P., . . . Caselmann, W. H. (2013). Inhibition of hepatitis C virus RNA translation by antisense bile acid conjugated phosphorothioate modified oligodeoxynucleotides (ODN). Antiviral Research, 97(1), 49-59. Scopus11 WoS9 Europe PMC7 |
| 2013 | Nokhbehsaim, M., Eick, S., Nogueira, A. V. B., Hoffmann, P., Herms, S., Fröhlich, H., . . . Deschner, J. (2013). Stimulation of MMP-1 and CCL2 by NAMPT in PDL cells. Mediators of Inflammation, 2013, 12 pages. Scopus46 WoS16 Europe PMC37 |
| 2013 | Degenhardt, F., Priebe, L., Strohmaier, J., Herms, S., Hoffmann, P., Mattheisen, M., . . . Cichon, S. (2013). No evidence for an involvement of copy number variation in ABCA13 in schizophrenia, bipolar disorder, or major depressive disorder. Psychiatric Genetics, 23(1), 45-46. Scopus6 WoS6 Europe PMC6 |
| 2013 | Nowak, M., Krämer, B., Haupt, M., Papapanou, P. N., Kebschull, J., Hoffmann, P., . . . Kebschull, M. (2013). Activation of invariant NK T cells in periodontitis lesions. Journal of Immunology, 190(5), 2282-2291. Scopus27 WoS23 Europe PMC21 |
| 2013 | Alanazi, I., Ebrahimie, E., Hoffmann, P., & Adelson, D. (2013). Combined gene expression and proteomic analysis of EGF induced apoptosis in A431 cells suggests multiple pathways trigger apoptosis. Apoptosis, 18(11), 1291-1305. Scopus23 WoS19 Europe PMC20 |
| 2013 | Lokman, N., Elder, A., Ween, M., Pyragius, C., Hoffmann, P., Oehler, M., & Ricciardelli, C. (2013). Annexin A2 is regulated by ovarian cancer-peritoneal cell interactions and promotes metastasis. Oncotarget, 4(8), 1199-1211. Scopus64 WoS57 Europe PMC56 |
| 2013 | Rowland, K., François, A., Hoffmann, P., & Monro, T. (2013). Fluorescent polymer coated capillaries as optofluidic refractometric sensors. Optics Express, 21(9), 11492-11505. Scopus43 WoS40 Europe PMC12 |
| 2013 | Sciacca, B., François, A., Hoffmann, P., & Monro, T. (2013). Multiplexing of radiative-surface plasmon resonance for the detection of gastric cancer biomarkers in a single optical fiber. Sensors and Actuators B-Chemical, 183, 454-458. Scopus55 WoS41 |
| 2013 | Sciacca, B., François, A., Klingler-Hoffmann, M., Brazzatti, J., Penno, M., Hoffmann, P., & Monro, T. (2013). Radiative-surface plasmon resonance for the detection of apolipoprotein E in medical diagnostics applications. Nanomedicine: Nanotechnology, Biology & Medicine, 9(4), 550-557. Scopus52 WoS38 Europe PMC13 |
| 2013 | Meding, S., Martin, K., Gustafsson, O., Eddes, J., Hack, S., Oehler, M., & Hoffmann, P. (2013). Tryptic peptide reference data sets for MALDI imaging mass spectrometry on formalin-fixed ovarian cancer tissues. Journal of Proteome Research, 12(1), 308-315. Scopus51 Europe PMC37 |
| 2013 | Gustafsson, O., Eddes, J., Meding, S., McColl, S., Oehler, M., & Hoffmann, P. (2013). Matrix-assisted laser desorption/ionization imaging protocol for in situ characterization of tryptic peptide identity and distribution in formalin-fixed tissue. Rapid Communications in Mass Spectrometry, 27(6), 655-670. Scopus61 WoS56 Europe PMC48 |
| 2013 | Niu, M., Klingler-Hoffmann, M., Brazzatti, J., Forbes, B., Akekawatchai, C., Hoffmann, P., & McColl, S. (2013). Comparative proteomic analysis implicates eEF2 as a novel target of PI3Kγ in the MDA-MB-231 metastatic breast cancer cell line. Proteome Science, 11(1), 1-12. Scopus7 WoS3 Europe PMC4 |
| 2012 | Penno, M., Klingler-Hoffmann, M., Brazzatti, J., Boussioutas, A., Putoczki, T., Ernst, M., & Hoffmann, P. (2012). 2D-DIGE analysis of sera from transgenic mouse models reveals novel candidate protein biomarkers for human gastric cancer. Journal of Proteomics, 77, 40-58. Scopus26 WoS25 Europe PMC21 |
| 2012 | Weiland, F., Martin, K., Oehler, M., & Hoffmann, P. (2012). Deciphering the molecular nature of ovarian cancer biomarker CA125. International Journal of Molecular Sciences, 13(8), 10568-10582. Scopus31 WoS31 Europe PMC28 |
| 2012 | Stone, G., Clifford, D., Gustafsson, O., McColl, S., & Hoffmann, P. (2012). Visualisation in imaging mass spectrometry using the minimum noise fraction transform. BMC Research Notes, 5(1), 1-6. Scopus8 Europe PMC4 |
| 2012 | Evans, J., Hollis, C., Hack, S., Gentleman, A., Hoffmann, P., Buntine, M., & Sumby, C. (2012). Anion-π interactions of hexaaryl[3]radialenes. Journal of Physical Chemistry A, 116(30), 8001-8007. Scopus14 WoS13 Europe PMC9 |
| 2012 | Gustafsson, O., Eddes, J., Meding, S., Koudelka, T., Oehler, M., McColl, S., & Hoffmann, P. (2012). Internal calibrants allow high accuracy peptide matching between MALDI imaging MS and LC-MS/MS. Journal of Proteomics, 75(16), 5093-5105. Scopus49 WoS47 Europe PMC36 |
| 2012 | Weiland, F., Fritz, K., Oehler, M., & Hoffmann, P. (2012). Methods for identification of CA125 from ovarian cancer ascites by high resolution mass spectrometry. International Journal of Molecular Sciences, 13(8), 9942-9958. Scopus27 WoS28 Europe PMC24 |
| 2012 | Penno, M., Colegate, S., Michalski, W., & Hoffmann, P. (2012). Detection and measurement of carbohydrate deficient transferrin in serum using immuno-capture mass spectrometry: Diagnostic applications for annual ryegrass toxicity and corynetoxin exposure. Research in Veterinary Science, 93(2), 611-617. Scopus4 WoS3 Europe PMC2 |
| 2012 | Brazzatti, J., Klingler-Hoffmann, M., Haylock-Jacobs, S., Harata-Lee, Y., Niu, M., Higgins, M., . . . McColl, S. (2012). Differential roles for the p101 and p84 regulatory subunits of PI3Kγ in tumor growth and metastasis. Oncogene, 31(18), 2350-2361. Scopus48 WoS46 Europe PMC45 |
| 2012 | Koudelka, T., Dehle, F., Musgrave, I., Hoffmann, P., & Carver, J. (2012). Methionine oxidation enhances κ-casein amyloid fibril formation. Journal of Agricultural and Food Chemistry, 60(16), 4144-4155. Scopus31 WoS30 Europe PMC21 |
| 2012 | Ho, Y., Penno, M., Perugini, M., Lewis, I., & Hoffmann, P. (2012). Evaluating the efficacy of subcellular fractionation of blast cells using live cell labeling and 2D DIGE. Methods in molecular biology, 854, 319-332. |
| 2012 | Sandow, J., Jabbour, A., Condina, M., Daunt, C., Stomski, F., Green, B., . . . Ekert, P. (2012). Cytokine receptor signaling activates an IKK-dependent phosphorylation of PUMA to prevent cell death. Cell Death and Differentiation, 19(4), 633-641. Scopus28 WoS24 Europe PMC24 |
| 2012 | Penno, M., Ernst, M., & Hoffmann, P. (2012). Comparative 2D DIGE analysis of the depleted serum proteome for biomarker discovery. Methods in molecular biology, 854, 207-220. Scopus3 Europe PMC4 |
| 2012 | Kopetz, V., Penno, M., Hoffmann, P., Wilson, D., & Beltrame, J. (2012). Potential mechanisms of the acute coronary syndrome presentation in patients with the coronary slow flow phenomenon - Insight from a plasma proteomic approach. International Journal of Cardiology, 156(1), 84-91. Scopus39 WoS33 Europe PMC28 |
| 2012 | Arentz, G., Chataway, T., Condina, M., Price, T., Hoffmann, P., & Hardingham, J. (2012). Increased phospho-keratin 8 isoforms in colorectal tumors associated with EGFR pathway activation and reduced apoptosis. ISRN Molecular Biology, 2012(706545), 1-8. Europe PMC3 |
| 2012 | Fung, K. Y. C., Cursaro, C., Lewanowitsch, T., Cosgrove, L., & Hoffmann, P. (2012). A combined free flow electrophoresis and DIGE approach to compare proteins in complex biological samples. Methods in Molecular Biology, 869, 135-146. |
| 2012 | Tsoi, L. C., Spain, S. L., Knight, J., Ellinghaus, E., Stuart, P. E., Capon, F., . . . Badorf, P. (2012). Identification of 15 new psoriasis susceptibility loci highlights the role of innate immunity. Nature Genetics, 44(12), 1341-1348. Scopus856 WoS802 Europe PMC778 |
| 2012 | Hilger, A., Schramm, C., Draaken, M., Mughal, S. S., Dworschak, G., Bartels, E., . . . Ludwig, M. (2012). Familial occurrence of the VATER/VACTERL association. Pediatric Surgery International, 28(7), 725-729. Scopus37 WoS37 Europe PMC33 |
| 2012 | Spier, I., Horpaopan, S., Vogt, S., Uhlhaas, S., Morak, M., Stienen, D., . . . Aretz, S. (2012). Deep intronic APC mutations explain a substantial proportion of patients with familial or early-onset adenomatous polyposis. Human Mutation, 33(7), 1045-1050. Scopus66 WoS61 Europe PMC55 |
| 2012 | Nasser, E., Mangold, E., Tradowsky, D. C., Fier, H., Becker, J., Boehmer, A. C., . . . Ludwig, K. U. (2012). Resequencing of VAX1 in patients with nonsyndromic cleft lip with or without cleft palate. BIRTH DEFECTS RESEARCH PART A-CLINICAL AND MOLECULAR TERATOLOGY, 94(11), 925-933. WoS12 Europe PMC11 |
| 2012 | Frank, J., Cichon, S., Treutlein, J., Ridinger, M., Mattheisen, M., Hoffmann, P., . . . Rietschel, M. (2012). Genome-wide significant association between alcohol dependence and a variant in the ADH gene cluster. Addiction Biology, 17(1), 171-180. Scopus144 WoS124 Europe PMC125 |
| 2012 | Wilcke, A., Jana Burkhardt, C. L., Alexander, M., Wolf, C., Quente, E., Ahnert, P., . . . Kirsten, H. (2012). Erratum: Imaging genetics of FOXP2 in dyslexia (European Journal of Human Genetics (2012) 20 (224-229) DOI: 10.1038/ejhg.2011.160). European Journal of Human Genetics, 20(6), 714. |
| 2012 | Becker, J., Czamara, D., Hoffmann, P., Landerl, K., Blomert, L., Brandeis, D., . . . Schumacher, J. (2012). Evidence for the involvement of ZNF804A in cognitive processes of relevance to reading and spelling. Translational Psychiatry, 2(7), e136. Scopus16 WoS15 Europe PMC14 |
| 2012 | Bartels, E., Schulz, A. C., Mora, N. W., Pineda-Alvarez, D. E., Wijers, C. H. W., Marcelis, C. M., . . . Reutter, H. M. (2012). VATER/VACTERL association: Identification of seven new twin pairs, a systematic review of the literature, and a classical twin analysis. Clinical Dysmorphology, 21(4), 191-195. Scopus22 WoS18 Europe PMC14 |
| 2012 | Degenhardt, F., Priebe, L., Herms, S., Mattheisen, M., Mühleisen, T. W., Meier, S., . . . Cichon, S. (2012). Association between copy number variants in 16p11.2 and major depressive disorder in a German case-control sample. American Journal of Medical Genetics Part B Neuropsychiatric Genetics, 159 B(3), 263-273. Scopus32 WoS30 Europe PMC28 |
| 2012 | Mattheisen, M., Mühleisen, T. W., Strohmaier, J., Treutlein, J., Nenadic, I., Alblas, M., . . . Cichon, S. (2012). Genetic variation at the synaptic vesicle gene SV2A is associated with schizophrenia. Schizophrenia Research, 141(2-3), 262-265. Scopus14 WoS13 Europe PMC13 |
| 2012 | Wilcke, A., Ligges, C., Burkhardt, J., Alexander, M., Wolf, C., Quente, E., . . . Kirsten, H. (2012). Imaging genetics of FOXP2 in dyslexia. European Journal of Human Genetics, 20(2), 224-229. Scopus46 WoS38 Europe PMC38 |
| 2012 | Thier, M., Wörsdörfer, P., Lakes, Y. B., Gorris, R., Herms, S., Opitz, T., . . . Edenhofer, F. (2012). Direct conversion of fibroblasts into stably expandable neural stem cells. Cell Stem Cell, 10(4), 473-479. Scopus458 WoS414 Europe PMC384 |
| 2012 | Ludwig, K. U., Mangold, E., Herms, S., Nowak, S., Reutter, H., Paul, A., . . . Nöthen, M. M. (2012). Genome-wide meta-analyses of nonsyndromic cleft lip with or without cleft palate identify six new risk loci. Nature Genetics, 44(9), 968-971. Scopus286 WoS277 Europe PMC277 |
| 2012 | Mühleisen, T. W., Mattheisen, M., Strohmaier, J., Degenhardt, F., Priebe, L., Schultz, C. C., . . . Cichon, S. (2012). Association between schizophrenia and common variation in neurocan (NCAN), a genetic risk factor for bipolar disorder. Schizophrenia Research, 138(1), 69-73. Scopus69 WoS62 Europe PMC65 |
| 2012 | Anthoni, H., Sucheston, L. E., Lewis, B. A., Tapia-Páez, I., Fan, X., Zucchelli, M., . . . Kere, J. (2012). The aromatase gene CYP19A1: Several genetic and functional lines of evidence supporting a role in reading, speech and language. Behavior Genetics, 42(4), 509-527. Scopus63 WoS58 Europe PMC51 |
| 2012 | Broderick, P., Chubb, D., Johnson, D. C., Weinhold, N., Försti, A., Lloyd, A., . . . Houlston, R. S. (2012). Common variation at 3p22.1 and 7p15.3 influences multiple myeloma risk. Nature Genetics, 44(1), 58-61. Scopus139 WoS127 Europe PMC118 |
| 2012 | Rietschel, M., Mattheisen, M., Degenhardt, F., Mühleisen, T. W., Kirsch, P., Esslinger, C., . . . Cichon, S. (2012). Association between genetic variation in a region on chromosome 11 and schizophrenia in large samples from Europe. Molecular Psychiatry, 17(9), 906-917. Scopus96 WoS97 Europe PMC89 |
| 2011 | Dobbins, S. E., Broderick, P., Melin, B., Feychting, M., Johansen, C., Andersson, U., . . . Houlston, R. S. (2011). Common variation at 10p12.31 near MLLT10 influences meningioma risk. Nature Genetics, 43(9), 825-827. Scopus46 WoS42 Europe PMC42 |
| 2011 | König, I. R., Schumacher, J., Hoffmann, P., Kleensang, A., Ludwig, K. U., Grimm, T., . . . Schulte-Körne, G. (2011). Mapping for dyslexia and related cognitive trait loci provides strong evidence for further risk genes on chromosome 6p21. American Journal of Medical Genetics Part B Neuropsychiatric Genetics, 156(1), 36-43. Scopus31 WoS23 Europe PMC23 |
| 2011 | Shi, H., Bevier, M., Johansson, R., Grzybowska, E., Chen, B., Eyfjörd, J. E., . . . Försti, A. (2011). Single nucleotide polymorphisms in the 20q13 amplicon genes in relation to breast cancer risk and clinical outcome. Breast Cancer Research and Treatment, 130(3), 905-916. Scopus29 WoS30 Europe PMC30 |
| 2011 | Koch, P., Breuer, P., Peitz, M., Jungverdorben, J., Kesavan, J., Poppe, D., . . . Brüstle, O. (2011). Excitation-induced ataxin-3 aggregation in neurons from patients with Machado-Joseph disease. Nature, 480(7378), 543-546. Scopus278 WoS256 Europe PMC238 |
| 2011 | Pernhorst, K., Raabe, A., Niehusmann, P., Van Loo, K. M. J., Grote, A., Hoffmann, P., . . . Becker, A. J. (2011). Promoter variants determine γ-aminobutyric acid homeostasis-related gene transcription in human epileptic hippocampi. Journal of Neuropathology and Experimental Neurology, 70(12), 1080-1088. Scopus16 WoS17 Europe PMC13 |
| 2011 | Schramm, C., Draaken, M., Bartels, E., Boemers, T. M., Schmiedeke, E., Grasshoff-Derr, S., . . . Reutter, H. (2011). De novo duplication of 18p11.21-18q12.1 in a female with anorectal malformation. American Journal of Medical Genetics Part A, 155(2), 445-449. Scopus21 WoS20 Europe PMC15 |
| 2011 | Schramm, C., Draaken, M., Tewes, G., Bartels, E., Schmiedeke, E., Märzheuser, S., . . . Ludwig, M. (2011). Autosomal-dominant non-syndromic anal atresia: Sequencing of candidate genes, array-based molecular karyotyping, and review of the literature. European Journal of Pediatrics, 170(6), 741-746. Scopus16 WoS17 Europe PMC14 |
| 2011 | de Assis, N. A., Nowak, S., Ludwig, K. U., Reutter, H., Vollmer, J., Heilmann, S., . . . Mangold, E. (2011). SUMO1 as a candidate gene for non-syndromic cleft lip with or without cleft palate: No evidence for the involvement of common or rare variants in Central European patients. International Journal of Pediatric Otorhinolaryngology, 75(1), 49-52. Scopus10 WoS9 Europe PMC8 |
| 2011 | Roeske, D., Ludwig, K. U., Neuhoff, N., Becker, J., Bartling, J., Bruder, J., . . . Schulte-Körne, G. (2011). First genome-wide association scan on neurophysiological endophenotypes points to trans-regulation effects on SLC2A3 in dyslexic children. Molecular Psychiatry, 16(1), 97-107. Scopus81 WoS70 Europe PMC66 |
| 2011 | Hoffmann, P. (2011). Correction, Stabilisation and Presentation: the fourth phase of the Bremen Cog project. INTERNATIONAL JOURNAL OF NAUTICAL ARCHAEOLOGY, 40(1), 151-161. WoS2 |
| 2011 | Hoffmann, P. C., Auel, S., & Huetz, W. W. (2011). Results of higher power toric intraocular lens implantation. JOURNAL OF CATARACT AND REFRACTIVE SURGERY, 37(8), 1411-1418. WoS62 |
| 2011 | González-Carmona, M. A., Vogt, A., Heinicke, T., Quasdorff, M., Hoffmann, P., Yildiz, Y., . . . Caselmann, W. H. (2011). Inhibition of hepatitis C virus gene expression by adenoviral vectors encoding antisense RNA in vitro and in vivo. Journal of Hepatology, 55(1), 19-28. Scopus10 WoS9 Europe PMC8 |
| 2011 | Czamara, D., Bruder, J., Becker, J., Bartling, J., Hoffmann, P., Ludwig, K. U., . . . Schulte-Körne, G. (2011). Association of a rare variant with mismatch negativity in a region between KIAA0319 and DCDC2 in dyslexia. Behavior Genetics, 41(1), 110-119. Scopus45 WoS39 Europe PMC38 |
| 2011 | Tran, T., Wang, T., Hack, S., Hoffmann, P., & Bowie, J. (2011). Can collision-induced negative-ion fragmentations of [M-H]- anions be used to identify phosphorylation sites in peptides?. Rapid Communications in Mass Spectrometry, 25(23), 3537-3548. Scopus9 WoS9 Europe PMC9 |
| 2011 | Fung, K., Cursaro, V., Lewanowitsch, T., Brierley, G., McColl, S., Lockett, T., . . . Cosgrove, L. (2011). A combined free-flow electrophoresis and DIGE approach to identify proteins regulated by butyrate in HT29 cells. Proteomics, 11(5), 964-971. Scopus11 WoS9 Europe PMC7 |
| 2011 | Ween, M., Lokman, N., Hoffmann, P., Rodgers, R., Ricciardelli, C., & Oehler, M. (2011). Transforming growth factor-beta-induced protein secreted by peritoneal cells increases the metastatic potential of ovarian cancer cells. International Journal of Cancer, 128(7), 1-15. Scopus62 WoS60 Europe PMC62 |
| 2011 | Fung, K., Brierley, G., Henderson, S., Hoffmann, P., McColl, S., Lockett, T., . . . Cosgrove, L. (2011). Butyrate-induced apoptosis in HCT116 colorectal cancer cells includes induction of a cell stress response. Journal of Proteome Research, 10(4), 1860-1869. Scopus71 WoS67 Europe PMC55 |
| 2011 | Scholz, R., Gustafsson, O., Hoffmann, P., Jaiswal, M., Ahmadian, M., Eisler, S., . . . Olayioye, M. (2011). The tumor suppressor protein DLC1 is regulated by PKD-mediated GAP domain phosphorylation. Experimental Cell Research, 317(4), 496-503. Scopus17 WoS17 Europe PMC15 |
| 2011 | Gustafsson, O., Oehler, M., Ruszkiewicz, A., McColl, S., & Hoffmann, P. (2011). MALDI Imaging Mass Spectrometry (MALDI-IMS): application of spatial proteomics for ovarian cancer classification and diagnosis. International Journal of Molecular Sciences (Online), 12(1), 773-794. Scopus89 WoS85 Europe PMC70 |
| 2011 | Martin, K., Ricciardelli, C., Hoffmann, P., & Oehler, M. (2011). Exploring the immunoproteome for ovarian cancer biomarker discovery. International Journal of Molecular Sciences (Online), 12(1), 410-428. Scopus7 WoS5 Europe PMC4 |
| 2011 | Hinney, A., Scherag, A., Jarick, I., Albayrak, O., Pütter, C., Pechlivanis, S., . . . Nelson, S. (2011). Genome-wide association study in German patients with attention deficit/hyperactivity disorder. American Journal of Medical Genetics Part B Neuropsychiatric Genetics, 156(8), 888-897. Scopus78 WoS76 Europe PMC69 |
| 2010 | Mrozik, K., Zilm, P., Bagley, C., Hack, S., Hoffmann, P., Gronthos, S., & Bartold, P. (2010). Proteomic characterization of mesenchymal stem cell-like populations derived from ovine periodontal ligament, dental pulp, and bone marrow: Analysis of differentially expressed proteins. Stem Cells and Development, 19(10), 1485-1499. Scopus64 WoS54 Europe PMC46 |
| 2010 | Gustafsson, O., Oehler, M., McColl, S., & Hoffmann, P. (2010). Citric Acid Antigen Retrieval (CAAR) for tryptic peptide imaging directly on archived formalin-fixed paraffin-embedded tissue. Journal of Proteome Research, 9(9), 4315-4328. Scopus93 WoS90 Europe PMC79 |
| 2010 | Ogunniyi, A., Mahdi, L., Jennings, M., McEwan, A., McDevitt, C., Van der Hoek, M., . . . Paton, J. (2010). Central role of manganese in regulation of stress responses, physiology, and metabolism in Streptococcus pneumoniae. Journal of Bacteriology, 192(17), 4489-4497. Scopus89 WoS84 Europe PMC79 |
| 2010 | Condina, M., Gustafsson, O., Klingler-Hoffmann, M., Bagley, C., McColl, S., & Hoffmann, P. (2010). EZYprep LC-coupled MALDI-TOF/TOF MS: an improved matrix spray application for phosphopeptide characterisation. Proteomics, 10(13), 2516-2530. Scopus7 WoS7 Europe PMC6 |
| 2010 | Condina, M., Klingler-Hoffmann, M., & Hoffmann, P. (2010). Tyrosine phosphorylation enrichment and subsequent analysis by MALDI-TOF/TOF MS/MS and LC-ESI-IT-MS/MS. Current Protocols in Protein Science, Suppl 2(13.11), 1-26. Scopus6 Europe PMC2 |
| 2010 | Hoffmann, P. C., & Huetz, W. W. (2010). Analysis of biometry and prevalence data for corneal astigmatism in 23 239 eyes. JOURNAL OF CATARACT AND REFRACTIVE SURGERY, 36(9), 1479-1485. WoS354 |
| 2010 | Hoffmann, P. (2010). On the long-term visco-elastic behaviour of polyethylene glycol (PEG) impregnated archaeological oak wood. HOLZFORSCHUNG, 64(6), 725-728. WoS29 |
| 2010 | Draaken, M., Reutter, H., Schramm, C., Bartels, E., Boemers, T. M., Ebert, A. K., . . . Ludwig, M. (2010). Microduplications at 22q11.21 are associated with non-syndromic classic bladder exstrophy. European Journal of Medical Genetics, 53(2), 55-60. Scopus41 WoS41 Europe PMC39 |
| 2010 | Ludwig, K. U., Roeske, D., Herms, S., Schumacher, J., Warnke, A., Plume, E., . . . Hoffmann, P. (2010). Variation in GRIN2B contributes to weak performance in verbal short-term memory in children with dyslexia. American Journal of Medical Genetics Part B Neuropsychiatric Genetics, 153(2), 503-511. Scopus36 WoS32 Europe PMC29 |
| 2010 | Pagnamenta, A. T., Bacchelli, E., De Jonge, M. V., Mirza, G., Scerri, T. S., Minopoli, F., . . . Monaco, A. P. (2010). Characterization of a family with rare deletions in CNTNAP5 and DOCK4 suggests novel risk loci for autism and dyslexia. Biological Psychiatry, 68(4), 320-328. Scopus128 WoS119 Europe PMC118 |
| 2010 | Mangold, E., Ludwig, K. U., Birnbaum, S., Baluardo, C., Ferrian, M., Herms, S., . . . Nöthen, M. M. (2010). Genome-wide association study identifies two susceptibility loci for nonsyndromic cleft lip with or without cleft palate. Nature Genetics, 42(1), 24-26. Scopus359 WoS344 Europe PMC329 |
| 2010 | Nikopensius, T., Birnbaum, S., Ludwig, K. U., Jagomägi, T., Saag, M., Herms, S., . . . Mangold, E. (2010). Susceptibility locus for non-syndromic cleft lip with or without cleft palate on chromosome 10q25 confers risk in Estonian patients. European Journal of Oral Sciences, 118(3), 317-319. Scopus19 WoS19 Europe PMC21 |
| 2010 | Rojas-Martinez, A., Reutter, H., Chacon-Camacho, O., Leon-Cachon, R. B. R., Munoz-Jimenez, S. G., Nowak, S., . . . Mangold, E. (2010). Genetic risk factors for nonsyndromic cleft lip with or without cleft palate in a mesoamerican population: Evidence for IRF6 and variants at 8q24 and 10q25. Birth Defects Research Part A Clinical and Molecular Teratology, 88(7), 535-537. Scopus54 WoS51 Europe PMC50 |
| 2010 | Reutter, H., Rüschendorf, F., Mattheisen, M., Draaken, M., Bartels, E., Hübner, N., . . . Ludwig, M. (2010). Evidence for linkage of the bladder exstrophy-epispadias complex on chromosome 4q31.21-22 and 19q13.31-41 from a consanguineous Iranian family. Birth Defects Research Part A Clinical and Molecular Teratology, 88(9), 757-761. Scopus8 WoS8 Europe PMC6 |
| 2009 | Reutter, H., Birnbaum, S., Mende, M., Almeida de Assis, N., Hoffmann, P., Lacava, A. D., . . . Mangold, E. (2009). Transforming growth factor-beta receptor type 1 (TGFBR1) is not associated with non-syndromic cleft lip with or without cleft palate in patients of Central European descent. International Journal of Pediatric Otorhinolaryngology, 73(10), 1334-1338. Scopus3 WoS1 Europe PMC3 |
| 2009 | Ludwig, K. U., Mattheisen, M., Mühleisen, T. W., Roeske, D., Schmäl, C., Breuer, R., . . . Cichon, S. (2009). Supporting evidence for LRRTM1 imprinting effects in schizophrenia. Molecular Psychiatry, 14(8), 743-745. Scopus49 WoS48 Europe PMC45 |
| 2009 | Nikopensius, T., Ambrozaityte, L., Ludwig, K. U., Birnbaum, S., Jagomägi, T., Saag, M., . . . Mangold, E. (2009). Replication of novel susceptibility locus for nonsyndromic cleft lip with or without cleft palate on chromosome 8q24 in Estonian and Lithuanian patients. American Journal of Medical Genetics Part A, 149(11), 2551-2553. Scopus30 WoS27 Europe PMC30 |
| 2009 | Schumacher, J., Laje, G., Jamra, R. A., Becker, T., Mühleisen, T. W., Vasilescu, C., . . . Cichon, S. (2009). The DISC locus and schizophrenia: Evidence from an association study in a central European sample and from a meta-analysis across different European populations. Human Molecular Genetics, 18(14), 2719-2727. Scopus75 WoS66 Europe PMC57 |
| 2009 | Birnbaum, S., Ludwig, K. U., Reutter, H., Herms, S., Steffens, M., Rubini, M., . . . Mangold, E. (2009). Key susceptibility locus for nonsyndromic cleft lip with or without cleft palate on chromosome 8q24. Nature Genetics, 41(4), 473-477. Scopus386 WoS368 Europe PMC365 |
| 2009 | Rujescu, D., Ingason, A., Cichon, S., Pietiläinen, O. P. H., Barnes, M. R., Toulopoulou, T., . . . Myin-Germeys, I. (2009). Disruption of the neurexin 1 gene is associated with schizophrenia. Human Molecular Genetics, 18(5), 988-996. Scopus399 WoS362 Europe PMC347 |
| 2009 | O'Donovan, M. C., Norton, N., Williams, H., Peirce, T., Moskvina, V., Nikolov, I., . . . Cloninger, C. R. (2009). Analysis of 10 independent samples provides evidence for association between schizophrenia and a SNP flanking fibroblast growth factor receptor 2. Molecular Psychiatry, 14(1), 30-36. Scopus60 WoS59 Europe PMC52 |
| 2009 | Birnbaum, S., Ludwig, K. U., Reutter, H., Herms, S., De Assis, N. A., Diaz-Lacava, A., . . . Mangold, E. (2009). IRF6 gene variants in Central European patients with non-syndromic cleft lip with or without cleft palate. European Journal of Oral Sciences, 117(6), 766-769. Scopus43 WoS43 Europe PMC37 |
| 2009 | Hoffmann, G., & Hoffmann, P. (2009). Sailing the Bremen Cog. INTERNATIONAL JOURNAL OF NAUTICAL ARCHAEOLOGY, 38(2), 281-296. WoS4 |
| 2009 | Lowe, R., Guild, G., Harpas, P., Kirkbride, P., Hoffmann, P., Voelcker, N., & Kobus, H. (2009). Rapid drug detection in oral samples by porous silicon assisted laser desorption/ionization mass spectrometry. Rapid Communications in Mass Spectrometry, 23(22), 3543-3548. Scopus29 WoS26 Europe PMC20 |
| 2009 | Penno, M., Ernst, M., & Hoffmann, P. (2009). Optimal preparation methods for automated matrix-assisted laser desorption/ionization time-of-flight mass spectrometry profiling of low molecular weight proteins and peptides. Rapid Communications in Mass Spectrometry, 23(17), 2656-2662. Scopus23 WoS23 Europe PMC23 |
| 2009 | Koudelka, T., Hoffmann, P., & Carver, J. (2009). Dephosphorylation of αs- and β-Caseins and Its Effect on Chaperone Activity: A Structural and Functional Investigation. Journal of Agricultural and Food Chemistry, 57(13), 5956-5964. Scopus40 WoS38 Europe PMC25 |
| 2009 | Andreazza, H., Wang, T., Bagley, C., Hoffmann, P., & Bowie, J. (2009). Negative ion fragmentations of deprotonated peptides. The unusual case of isoAsp: a joint experimental and theoretical study. Comparison with positive ion cleavages. Rapid Communications in Mass Spectrometry, 23(13), 1993-2002. Scopus12 WoS12 Europe PMC10 |
| 2009 | Condina, M., Guthridge, M., McColl, S., & Hoffmann, P. (2009). A sensitive magnetic bead method for the detection and identification of tyrosine phosphorylation in proteins by MALDI-TOF/TOF MS. Proteomics, 9(11), 3047-3057. Scopus18 WoS17 Europe PMC16 |
| 2009 | Andreazza, H., Wang, T., Bilusich, D., Hoffmann, P., & Bowie, J. (2009). Negative ion fragmentations of deprotonated peptides containing post-translational modifications: diphosphorylated systems containing Ser, Thr and Tyr. A characteristic phosphate/phosphate cyclisation. A joint experimental and theoretical study. Rapid Communications in Mass Spectrometry, 23(12), 1825-1833. Scopus8 WoS8 Europe PMC5 |
| 2009 | Penno, M., Bacic, A., Colegate, S., Hoffmann, P., & Michalski, W. (2009). Identifying candidate serum biomarkers of exposure to tunicamycins in rats using two-dimensional electrophoresis. Journal of Proteome Research, 8(6), 2812-2826. Scopus4 WoS4 Europe PMC4 |
| 2009 | Barry, E., Felquer, F., Powell, J., Biggs, L., Stomski, F., Urbani, A., . . . Guthridge, M. (2009). 14-3-3:Shc scaffolds integrate phosphoserine and phosphotyrosine signaling to regulate phosphatidylinositol 3-kinase activation and cell survival. Journal of Biological Chemistry, 284(18), 12080-12090. Scopus35 WoS32 Europe PMC29 |
| 2009 | Fung, K., Lewanowitsch, T., Henderson, S., Priebe, I., Hoffmann, P., McColl, S., . . . Cosgrove, L. (2009). Proteomic analysis of butyrate effects and loss of butyrate sensitivity in HT29 colorectal cancer cells. Journal of Proteome Research, 8(3), 1220-1227. Scopus26 WoS24 Europe PMC20 |
| 2008 | Gustafsson, O., McColl, S., & Hoffmann, P. (2008). Imaging mass spectrometry and its methodological application to murine tissue. Journal of Proteomics and Bioinformatics, 1(9), 458-463. |
| 2008 | Hoffmann, P., Woon, J., Rowley, K., Karschimkus, C., Nelson, C., Dragicevic, G., . . . Jenkins, A. (2008). Glutathionyl haemoglobin is not increased in diabetes nor related to glycaemia, complications, dyslipidaemia, inflammation or other measures of oxidative stress. Diabetes Research and Clinical Practice, 80(2), e1-e3. Scopus9 Europe PMC3 |
| 2008 | Andreazza, H., Fitzgerald, M., Bilusich, D., Hoffmann, R., Hoffmann, P., Eichinger, P., & Bowie, J. (2008). Characteristic negative ion fragmentations of deprotonated peptides containing post-translational modifications: mono-phosphorylated Ser, Thr and Tyr. A joint experimental and theoretical study. Rapid Communications in Mass Spectrometry, 22(20), 3305-3312. Scopus8 WoS10 Europe PMC9 |
| 2008 | Ruan, Y., Foo, H., Warren-Smith, S., Hoffmann, P., Moore, R., Ebendorff-Heidepriem, H., & Monro, T. (2008). Antibody immobilization within glass microstructured fibers: A route to sensitive and selective biosensors. Optics Express, 16(22), 18514-18523. Scopus72 WoS60 Europe PMC24 |
| 2008 | Ecroyd, H., Koudelka, T., Thorn, D., Williams, D., Devlin, G., Hoffmann, P., & Carver, J. (2008). Dissociation from the oligomeric state is the rate-limiting step in fibril formation by kappa-casein. Journal of Biological Chemistry, 283(14), 9012-9022. Scopus81 WoS71 Europe PMC54 |
| 2008 | Head, R. J., Fung, K. Y. C., Ooi, C., Zucker, M., Lewanowitsch, T., Henderson, S., . . . Lockett, T. (2008). Integrating biological acitvity in food with genomic and proteomic characteristics. Journal of Nutrigenetics and Nutrigenomics, 1(4), 185. |
| 2008 | O'Donovan, M. C., Craddock, N., Norton, N., Williams, H., Peirce, T., Moskvina, V., . . . Owen, M. J. (2008). Identification of loci associated with schizophrenia by genome-wide association and follow-up. Nature Genetics, 40(9), 1053-1055. Scopus962 WoS858 Europe PMC794 |
| 2008 | Schirmbeck, F., Georgi, A., Strohmaier, J., Schmael, C., Boesshenz, K. V., Mühleisen, T. W., . . . Schulze, T. G. (2008). Brief report: No association between premorbid adjustment in adult-onset schizophrenia and genetic variation in dysbindin. Journal of Autism and Developmental Disorders, 38(10), 1977-1981. |
| 2008 | Ludwig, K. U., Schumacher, J., Schulte-Körne, G., König, I. R., Warnke, A., Plume, E., . . . Hoffmann, P. (2008). Investigation of the DCDC2 intron 2 deletion/compound short tandem repeat polymorphism in a large German dyslexia sample. Psychiatric Genetics, 18(6), 310-312. Scopus48 WoS47 Europe PMC42 |
| 2008 | Ludwig, K. U., Roeske, D., Schumacher, J., Schulte-Körne, G., König, I. R., Warnke, A., . . . Hoffmann, P. (2008). Investigation of interaction between DCDC2 and KIAA0319 in a large German dyslexia sample. Journal of Neural Transmission, 115(11), 1587-1589. Scopus42 WoS39 Europe PMC33 |
| 2007 | Anthoni, H., Zucchelli, M., Matsson, H., Müller-Myhsok, B., Fransson, I., Schumacher, J., . . . Peyrard-Janvid, M. (2007). A locus on 2p12 containing the co-regulated MRPL19 and C2ORF3 genes is associated to dyslexia. Human Molecular Genetics, 16(6), 667-677. Scopus101 WoS93 Europe PMC79 |
| 2007 | Schumacher, J., Hoffmann, P., Schmäl, C., Schulte-Körne, G., & Nöthen, M. M. (2007). Genetics of dyslexia: The evolving landscape. Journal of Medical Genetics, 44(5), 289-297. Scopus126 WoS94 Europe PMC73 |
| 2007 | Schulte-Koerne, G., Ludwig, K. U., el Sharkawy, J., Noethen, M. M., Mueller-Myhsok, B., & Hoffmann, P. (2007). Genetics and Neuroscience in Dyslexia: Perspectives for Education and Remediation. MIND BRAIN AND EDUCATION, 1(4), 162-172. WoS15 |
| 2007 | Sykora, C., Hoffmann, R., & Hoffmann, P. (2007). Enrichment of multiphosphorylated peptides by immobilized metal affinity chromatography using Ga(III)- and Fe(III)-complexes. Protein and Peptide Letters, 14(5), 489-496. Scopus27 WoS26 Europe PMC20 |
| 2007 | Ruan, Y., Schartner, E., Ebendorff-Heidepriem, H., Hoffmann, P., & Monro, T. (2007). Detection of quantum-dot labeled proteins using soft glass microstructured optical fibers. Optics Express, 15(26), 17819-17826. Scopus90 WoS77 Europe PMC21 |
| 2007 | Olayioye, M., Buchholz, M., Schmid, S., Schoffler, P., Hoffmann, P., & Pomorski, T. (2007). Phosphorylation of StarD10 on serine 284 by casein kinase II modulates its lipid transfer activity. Journal of Biological Chemistry, 282(31), 22492-22498. Scopus14 WoS13 Europe PMC9 |
| 2006 | Frolov, A., Hoffmann, P., & Hoffmann, R. (2006). Fragmentation behavior of glycated peptides derived from D-glucose, D-fructose and D-ribose in tandem mass spectrometry. Journal of Mass Spectrometry, 41(11), 1459-1469. Scopus99 WoS98 Europe PMC87 |
| 2006 | González-Carmona, M. A., Märten, A., Hoffmann, P., Schneider, C., Sievers, E., Schmidt-Wolf, I. G. H., . . . Caselmann, W. H. (2006). Patient-derived dendritic cells transduced with an α-fetoprotein-encoding adenovirus and co-cultured with autologous cytokine-induced lymphocytes induce a specific and strong immune response against hepatocellular carcinoma cells. Liver International, 26(3), 369-379. Scopus53 WoS43 Europe PMC31 |
| 2006 | Gonzalez-Carmona, M. A., Schüssler, S., Serwe, M., Alt, M., Ludwig, J., Sproat, B. S., . . . Caselmann, W. H. (2006). Hammerhead ribozymes with cleavage site specificity for NUH and NCH display significant anti-hepatitis C viral effect in vitro and in recombinant HepG2 and CCL13 cells. Journal of Hepatology, 44(6), 1017-1025. Scopus14 WoS10 Europe PMC10 |
| 2005 | Musch, A., Rabe, C., Paik, M. D., Berna, M. J., Schmitz, V., Hoffmann, P., . . . Caselmann, W. H. (2005). Altered expression of TGF-β receptors in hepatocellular carcinoma - Effects of a constitutively active TGF-β type I receptor mutant. Digestion, 71(2), 78-91. Scopus23 Europe PMC16 |
| 2005 | Hoffmann, P., Olayioye, M., Moritz, R., Lindeman, G., Visvader, J., Simpson, R., & Kemp, B. (2005). Breast cancer protein StarD10 identified by three-dimensional separation using free-flow electrophoresis, reversed-phase high-performance liquid chromatography, and sodium dodecyl sulfate-polyacrylamide gel electrophoresis. Electrophoresis, 26(6), 1029-1037. Scopus8 Europe PMC5 |
| 2005 | Ahmed, N., Olivia, K., Barker, G., Hoffmann, P., Reeve, S., Smith, A., . . . Rice, G. (2005). Proteomic tracking of serum protein isoforms as screening biomarkers of ovarian cancer. Proteomics, 5(17), 4625-4636. Scopus107 Europe PMC79 |
| 2004 | Ahmed, N., Barker, G., Olivia, K., Hoffmann, P., Riley, C., Reeve, S., . . . Rice, G. (2004). Proteomic-based identification of haptoglobin-1 precursor as a novel circulating biomarker of ovarian cancer.. British Journal of Cancer, 91(1), 129-140. Scopus113 Europe PMC90 |
| 2004 | Olayioye, M., Hoffmann, P., Pomorski, T., Armes, J., Simpson, R., Kemp, B., . . . Visvader, J. (2004). The Phosphoprotein StarD10 Is Overexpressed in Breast Cancer and Cooperates with ErbB Receptors in Cellular Transformation. Cancer Research, 64(10), 3538-3544. Scopus36 Europe PMC33 |
| 2003 | Danks, J., Ho, P., Notini, A., Katsis, F., Hoffmann, P., Kemp, B., . . . Zajac, J. (2003). Identification of a parathyroid hormone in the fish Fugu rubripes. Journal of Bone and Mineral Research, 18(7), 1326-1331. Scopus63 Europe PMC34 |
| 2003 | Hoffmann, P., Quasdorff, M., González-Carmona, M. A., & Caselmann, W. H. (2003). Recent patents on experimental therapy for hepatitis C virus infection (1999 - 2002). Expert Opinion on Therapeutic Patents, 13(11), 1707-1723. Scopus2 WoS3 |
| 2001 | Hoffmann, P., Ji, H., Moritz, R., Connolly, L., Frecklington, D., Layton, J., . . . Simpson, R. (2001). Continuous free-flow electrophoresis separation of cytosolic proteins from the human colon carcinoma cell line LIM 1215: A non two-dimensional gel electrophoresis-based proteome analysis strategy. Proteomics, 1(7), 807-818. Scopus128 Europe PMC75 |
| 2000 | Wind, M., Hoffmann, P., Wagner, H., & Thormann, W. (2000). Chiral capillary electrophoresis as predictor for separation of drug enantiomers in continuous flow zone electrophoresis. Journal of Chromatography A, 895(1-2), 51-65. Scopus17 Europe PMC13 |
| 2000 | Huetz, W. W., Hoffmann, P. C., Eckhardt, H. B., & Heuring, A. (2000). Paracentral photoablations to correct higher grades of naturally occurring astigmatism. JOURNAL OF CATARACT AND REFRACTIVE SURGERY, 26(4), 547-552. WoS1 |
| 1999 | Hoffmann, P., Wagner, H., Weber, G., Lanz, M., Caslavska, J., & Thormann, W. (1999). Separation and purification of methadone enantiomers by continuous- and interval-flow electrophoresis. Analytical Chemistry, 71(9), 1840-1850. Scopus46 Europe PMC33 |
| 1998 | Hoffmann, P. C., Hutz, W. W., Eckhardt, H. B., & Heuring, A. H. (1998). IOL calculation and ultrasound biometry: immersion vs. contact technique. KLINISCHE MONATSBLATTER FUR AUGENHEILKUNDE, 213(3), 161-165. WoS16 |
| 1997 | Hoffmann, P. C., Hutz, W. W., & Eckhardt, H. B. (1997). Importance of IOL calculation formula for postoperative refraction after cataract surgery. KLINISCHE MONATSBLATTER FUR AUGENHEILKUNDE, 211(3), 168-177. WoS33 |
| 1993 | O'Toole, K. M., Brown, M., & Hoffmann, P. (1993). Pathology of benign and malignant kidney tumors. Urologic Clinics of North America, 20(2), 193-205. Scopus36 Europe PMC21 |
| - | Langenbucher, A., Szentmary, N., Wendelstein, J., Cayless, A., Hoffmann, P., & Gatinel, D. (2025). A two-step formula constant optimization strategy for minimal standard deviation and zero mean prediction error in IOL power calculation. ACTA OPHTHALMOLOGICA, 12 pages. |
| - | Langenbucher, A., Hoffmann, P., Cayless, A., Szentmary, N., Riaz, K., Gatinel, D., . . . Wendelstein, J. (2025). Predictive Correction Model for Corneal Back Surface Astigmatism With IOLMaster700 Keratometry Data in a Cataractous Population. CLINICAL AND EXPERIMENTAL OPHTHALMOLOGY, 12 pages. |
| Year | Citation |
|---|---|
| 2025 | Scheer, K., Yeo, E., Shard, C., Lenin, S., Ormsby, R., Skarne, N., . . . Gomez, G. (2025). Growth rates of patient-derived tumor organoids reflect glioblastoma patients' heterogeneity in survival. In NEURO-ONCOLOGY Vol. 27 (pp. v479). OXFORD UNIV PRESS INC. DOI |
| 2025 | Beins, E., Bajaj, T., Ebert, T., David, F., Stein, F., Meinert, S., . . . Forstner, A. J. (2025). THE INFLUENCE OF GENETIC RISK FOR DEPRESSION AND GLUCOCORTICOID STRESS ON TRANSCRIPTOME AND SECRETOME PROFILES OF INDUCED PLURIPOTENT STEM CELL-DERIVED MICROGLIA. In EUROPEAN NEUROPSYCHOPHARMACOLOGY Vol. 99 (pp. 1 page). ELSEVIER. DOI |
| 2025 | Wiesmann, L., Hameister, J. F., Herms, S., Schultz, S., Steinberger, J., Lindell, A., . . . Mathey, C. (2025). ENHANCING PSYCHIATRIC PHARMACOGENETICS TESTING VIA ADAPTIVE SAMPLING AND LONG-READ SE-QUENCING. In EUROPEAN NEUROPSYCHOPHARMACOLOGY Vol. 99 (pp. 241-242). ELSEVIER. DOI |
| 2024 | Beins, E., Bajaj, T., Hollstein, R., David, F., Meinert, S., Streit, F., . . . Forstner, A. (2024). Does genetic risk for depression influence microglial function? Analyses in human induced pluripotent stem cell-derived microglia. In EUROPEAN JOURNAL OF HUMAN GENETICS Vol. 32 (pp. 1491). GERMANY, Berlin: SPRINGERNATURE. |
| 2024 | Spier, I., Klinkhammer, H., Perne, C., Hoffmann, P., Buettner, R., David, F., . . . Aretz, S. (2024). Effect of a Polygenic Risk Score for colorectal cancer incidence in patients with early-onset, familial, or hereditary colorectal cancer. In EUROPEAN JOURNAL OF HUMAN GENETICS Vol. 32 (pp. 815). GERMANY, Berlin: SPRINGERNATURE. |
| 2024 | Glaessner, A., Steffens, M., Fatangare, A., Wurpts, G., Hoffmann, P., Deck, P. N., . . . Sachs, B. (2024). Analyse differenzieller Genexpression peripherer mononukleärer Blutzellen (PBMC) zum In-vitro-Nachweis einer Arzneimittelallergie. In ALLERGOLOGIE Vol. 47 (pp. 55 pages). DUSTRI-VERLAG DR KARL FEISTLE. |
| 2023 | Beins, E., Hollstein, R., David, F. S., Meinert, S., Stein, F., Streit, F., . . . Forstner, A. J. (2023). DOES GENETIC RISK FOR DEPRESSION INFLUENCE MICROGLIAL FUNCTION? ANALYSES IN HUMAN INDUCED PLURIPOTENT STEM CELL-DERIVED MICROGLIA. In EUROPEAN NEUROPSYCHOPHARMACOLOGY Vol. 75 (pp. S177-S178). CANADA, Montreal: ELSEVIER. DOI |
| 2023 | David, F. S., Streit, F., Frank, J., Stein, F., Winter, A., Meinert, S., . . . Forstner, A. J. (2023). LONGITUDINAL ANALYSIS OF BLOOD-BASED DNA METHYLATION PROFILES IN MAJOR DEPRESSIVE DISORDER. In EUROPEAN NEUROPSYCHOPHARMACOLOGY Vol. 75 (pp. S242). CANADA, Montreal: ELSEVIER. DOI |
| 2023 | Schwerbrock, P., Schmidt, A., Aldisi, R., Zieger, H., Cesarato, N., Herms, S., . . . Basmanav, F. B. (2023). Association of rare genetic variants at the ULBP3 locus with alopecia areata. In EUROPEAN JOURNAL OF HUMAN GENETICS Vol. 31 (pp. 165-166). AUSTRIA, Vienna: SPRINGERNATURE. |
| 2023 | Vogelsang, A., Chung, M. L., Sindermann, L., David, F., Elling, C., Seib-Pfeifer, L. -E., . . . Forstner, A. (2023). Investigation of polygenic scores in patients with social anxiety disorder. In EUROPEAN JOURNAL OF HUMAN GENETICS Vol. 31 (pp. 484-485). AUSTRIA, Vienna: SPRINGERNATURE. |
| 2023 | Jung, D., Pechlivanis, S., Moebus, S., Lehmann, N., Mahabdi, A. A., Hoffmann, P., . . . Bachmann, H. S. (2023). Pharmacogenetic association of diabetes associated genetic risk score with rapid progression of coronary artery calcification following treatment with HMGCoA-reductase inhibitors - results of the Heinz Nixdorf Recall Study. In EUROPEAN JOURNAL OF HUMAN GENETICS Vol. 31 (pp. 621-622). AUSTRIA, Vienna: SPRINGERNATURE. |
| 2023 | David, F., Streit, F., Frank, J., Sirignano, L., Zillich, L., Herms, S., . . . Forstner, A. (2023). Methylome-wide association studies of major depressive disorder, bipolar disorder and schizophrenia spectrum disorders in the German FOR2107 cohort. In EUROPEAN JOURNAL OF HUMAN GENETICS Vol. 31 (pp. 653). AUSTRIA, Vienna: SPRINGERNATURE. |
| 2023 | Beins, E., Hollstein, R., Ludwig, K., Hoffmann, P., Noethen, M. M., & Forstner, A. (2023). Generation and characterisation of induced pluripotent stem cell-derived microglia to study the influence of genetic risk for depression on microglial functions. In EUROPEAN JOURNAL OF HUMAN GENETICS Vol. 31 (pp. 483-484). AUSTRIA, Vienna: SPRINGERNATURE. |
| 2023 | Sindermann, L., Dannlowski, U., Meinert, S., Leehr, E. J., Waltemate, L., Lemke, H., . . . Forstner, A. (2023). Link of disorders in the schizo-affective spectrum and comorbidity with neurobiological correlates. In EUROPEAN JOURNAL OF HUMAN GENETICS Vol. 31 (pp. 480). AUSTRIA, Vienna: SPRINGERNATURE. |
| 2023 | Huenten, K., David, F., Sivalingam, S., Burger, B., Beins, E., Sirignano, L., . . . Forstner, A. (2023). Genetic characterization of patients with bipolar disorder and controls for the generation of induced pluripotent stem cells. In EUROPEAN JOURNAL OF HUMAN GENETICS Vol. 31 (pp. 195). AUSTRIA, Vienna: SPRINGERNATURE. |
| 2023 | Claus, I., Sivalingam, S., Hoffmann, P., Streit, F., Nenadic, I., Baune, B. T., . . . Degenhardt, F. (2023). ANALYSING THE GENETIC BURDEN OF RARE AND POTENTIALLY DAMAGING VARIANTS IN SCHIZOPHRENIA RISK-LOCUS XQ28,DISTAL USING HIGH-THROUGHPUT, MULTIPLEX TARGETED SEQUENCING. In EUROPEAN NEUROPSYCHOPHARMACOLOGY Vol. 75 (pp. S148). CANADA, Montreal: ELSEVIER. DOI |
| 2022 | Thirunavukkarasu, P., Fischer, S. B., Streit, F., Guzman-Parra, J., Rivas, F., Mayoral, F., . . . Cichon, S. (2022). TRANSCRIPTIONAL NETWORKS REGULATING THE EXPRESSION OF GENES SEGREGATING IN FAMILIES AFFECTED WITH BIPOLAR DISORDER: AN IN-SILICO ANALYSIS. In EUROPEAN NEUROPSYCHOPHARMACOLOGY Vol. 63 (pp. E179). ITALY, Florence: ELSEVIER. DOI |
| 2022 | Muehleisen, T. W., Zhao, L., Hilger, D., Burger, B., Forstner, A., Herms, S., . . . Palomero-Gallagher, N. (2022). Analysis of neurotransmitter gene expression and comparison with the receptor density in human hippocampal regions. In EUROPEAN JOURNAL OF HUMAN GENETICS Vol. 30 (pp. 437). SPRINGERNATURE. |
| 2021 | Fischer, S., Hoffmann, P., Reinbold, C., Burger, B., Herms, S., Streit, F., . . . Cichon, S. (2021). FOLLOW-UP OF 27 CANDIDATE GENES FROM A WHOLE-EXOME SEQUENCING STUDY IN LARGE FAMILIES WITH BIPOLAR DISORDER BY RESEQUENCING OF AN INDEPENDENT PATIENT-CONTROL COHORT. In EUROPEAN NEUROPSYCHOPHARMACOLOGY Vol. 51 (pp. E62-E63). ELECTR NETWORK: ELSEVIER. DOI |
| 2021 | Forstner, A. J., Karhoff, K., Maaser-Hecker, A., Streit, F., Sivalingam, S., Ludwig, K. U., . . . Noethen, M. M. (2021). Contribution of Rare Variants to Bipolar Disorder Susceptibility. In BIOLOGICAL PSYCHIATRY Vol. 89 (pp. S63-S64). ELSEVIER SCIENCE INC. |
| 2020 | Gottel, N., Rickenbacher, M., Reinbold, C. S., Herms, S., Hoffmann, P., Cichon, S., . . . Steiner, L. A. (2020). Genome-Wide Association Study of Postoperative Cognitive Dysfunction in older surgical patients. In EUROPEAN JOURNAL OF HUMAN GENETICS Vol. 28 (pp. 411-412). SPRINGERNATURE. |
| 2020 | Fischer, S. B., Fink, M., Ng, C. K. Y., Reinbold, C. S., Maaser-Hecker, A., Streit, F., . . . Cichon, S. (2020). A novel bioinformatic approach for the family-based genetic analysis of whole-genome sequencing data from 8 multigenerational Spanish families with bipolar disorder. In EUROPEAN JOURNAL OF HUMAN GENETICS Vol. 28 (pp. 423-424). SPRINGERNATURE. |
| 2020 | Herms, S., Bolukbas, I., Busmann, M., Lang, U., Walter, M., Wrege, J., . . . Euler, S. (2020). Borderline Personality Disorder - BION Study: Epigenetic changes observed after clinical intervention. In EUROPEAN JOURNAL OF HUMAN GENETICS Vol. 28 (pp. 985-986). SPRINGERNATURE. |
| 2020 | Vettiger, A., Fischer, S., Herms, S., Hoffmann, P., Cichon, S., Maaser, A., . . . Foerstner, P. (2020). Identification of rare risk variants in 12 multiply affected families with bipolar disorder. In EUROPEAN JOURNAL OF HUMAN GENETICS Vol. 28 (pp. 379). SPRINGERNATURE. |
| 2020 | Maj, C., Uellendahl-Werth, F., Borisov, O., Mucha, S., Bej, S., Wolfien, M., . . . Ellinghaus, D. (2020). Single and cross-tissue conditional transcriptome wide analyses reveal independent and shared susceptibility genes for psychiatric traits and inflammatory bowel diseases. In EUROPEAN JOURNAL OF HUMAN GENETICS Vol. 28 (pp. 675-676). SPRINGERNATURE. |
| 2020 | Jaeger, S., Cuadrat, R., Hoffmann, P., Wittenbecher, C., & Schulze, M. B. (2020). Evaluation of the causal effect of desaturase activity on the risk of type 2 diabetes and coronary artery disease. In EUROPEAN JOURNAL OF HUMAN GENETICS Vol. 28 (pp. 736). SPRINGERNATURE. |
| 2020 | Tremmel, R., van Eijck, B. A. C., Handin, N., Haag, M., Winter, S., Buettner, F., . . . Schaeffeler, E. (2020). A comprehensive multi-omics analysis of the key target of hepatitis viruses and bile acid and drug transporter NTCP. In NAUNYN-SCHMIEDEBERGS ARCHIVES OF PHARMACOLOGY Vol. 393 (pp. 45). GERMANY, Leipzig Univ, Leipzig: SPRINGER. |
| 2019 | Tremmel, R., Schaeffeler, E., Hoffmann, P., Noethen, M. M., Pereyra, V. M., Broders, I., . . . Ong, P. (2019). Assessment of Genetic Variants in European Patients With Coronary Spasm. In CIRCULATION Vol. 140 (pp. 2 pages). PA, Philadelphia: LIPPINCOTT WILLIAMS & WILKINS. |
| 2019 | Wenske, B., Marischen, L., Welzenbach, J., Heimbach, A., Hoffmann, P., Corbacioglu, S., . . . Troeger, A. (2019). Investigation of Cell-Contact Dependent Alterations in Immune Synapse Formation between T Cells and BCP-ALL Cells. In BLOOD Vol. 134 (pp. 4 pages). FL, Orlando: ELSEVIER. DOI |
| 2019 | Maj, C., Borisov, O., Weiss, A., Mucha, S., Bej, S., Uellendahl-Werth, F., . . . Ellinghaus, D. (2019). Cross-phenotype transcriptome-wide association study reveals shared susceptibility genes between schizophrenia and inflammatory bowel disease in gut-brain axis related tissues. In EUROPEAN JOURNAL OF HUMAN GENETICS Vol. 27 (pp. 1774-1775). SWEDEN, Gothenburg: NATURE PUBLISHING GROUP. |
| 2019 | Maaser, A., Strohmaier, J., Ludwig, K. U., Henschel, L., Streit, F., Degenhardt, F., . . . Forstner, A. J. (2019). Exome sequencing of multiplex bipolar disorder families and follow-up resequencing implicate rare variants in neuronal genes contributing to disease etiology. In EUROPEAN JOURNAL OF HUMAN GENETICS Vol. 27 (pp. 261-262). ITALY, Milan: NATURE PUBLISHING GROUP. |
| 2019 | Fischer, S. B., Ng, C. K. Y., Fink, M., Reinbold, C. S., Maaser, A., Streit, F., . . . Cichon, S. (2019). Comprehensive genetic analysis of whole genome sequencing data from 108 individuals of 8 multigenerational spanish families affected with bipolar disorder. In EUROPEAN JOURNAL OF HUMAN GENETICS Vol. 27 (pp. 1425-1426). SWEDEN, Gothenburg: NATURE PUBLISHING GROUP. |
| 2019 | Sivalingam, S., Forstner, A., Herms, S., Maaser, A., Koller, A., Reinbold, C., . . . Noethen, M. (2019). Integrated analysis of genetic and epigenetic data of healthy individuals with different risk factors for affective disorders. In EUROPEAN JOURNAL OF HUMAN GENETICS Vol. 27 (pp. 286-287). ITALY, Milan: NATURE PUBLISHING GROUP. |
| 2019 | Buettner, F., Meyerhoff, C., Kandabarau, S., Winter, S., Rausch, S., Stenzl, A., . . . Schaeffeler, E. (2019). Comprehensive genomic analyses of a case series of bilateral renal cell carcinoma. In CANCER RESEARCH Vol. 79 (pp. 2 pages). GA, Atlanta: AMER ASSOC CANCER RESEARCH. DOI |
| 2019 | Adorjan, K., Mekonnen, Z., Tessema, F., Ayana, M., Degenhardt, F., Hoffmann, P., . . . Mattheisen, M. (2019). GENOTYPE-PHENOTYPE FEASIBILITY STUDIES ON KHAT ABUSE, TRAUMATIC EXPERIENCES, AND PSYCHOSIS IN ETHIOPIA. In EUROPEAN NEUROPSYCHOPHARMACOLOGY Vol. 29 (pp. S265-S266). CA, Los Angeles: ELSEVIER. DOI |
| 2019 | Stavrum, A. -K., Polushina, T., Melle, I., Lagerberg, T. V., Ringen, P. A., Djurovic, S., . . . Le Hellard, S. (2019). IDENTIFICATION OF MOLECULAR MECHANISMS FOLLOWING CANNABIS EXPOSURE IN PATIENTS WITH PSYCHOSIS. In EUROPEAN NEUROPSYCHOPHARMACOLOGY Vol. 29 (pp. 1221-1222). SCOTLAND, Glasgow: ELSEVIER. DOI |
| 2019 | Maaser, A., Streit, F., Ludwig, K. U., Koller, A. C., Degenhardt, F., Thiele, H., . . . Forstner, A. J. (2019). WHOLE EXOME SEQUENCING OF MULTIPLEX BIPOLAR DISORDER FAMILIES AND FOLLOW-UP RESEQUENCING IMPLICATE RARE VARIANTS IN CELL ADHESION GENES CONTRIBUTING TO DISEASE ETIOLOGY. In EUROPEAN NEUROPSYCHOPHARMACOLOGY Vol. 29 (pp. 1088-1089). SCOTLAND, Glasgow: ELSEVIER. DOI |
| 2019 | Streit, F., Foo, J., Treutlein, J., Witt, S., Degenhardt, F., Forstner, A. J., . . . Frank, J. (2019). SHARED GENETIC ETIOLOGY BETWEEN ALCOHOL DEPENDENCE AND MAJOR DEPRESSIVE DISORDER. In EUROPEAN NEUROPSYCHOPHARMACOLOGY Vol. 29 (pp. 1186). SCOTLAND, Glasgow: ELSEVIER. DOI |
| 2019 | Fischer, S., Ng, C., Fink, M., Reinbold, C., Maaser, A., Streit, F., . . . Cichon, S. (2019). ANALYSIS OF WGS DATA FROM 108 INDIVIDUALS OF 8 SPANISH FAMILIES AFFECTED WITH BIPOLAR DISORDER. In EUROPEAN NEUROPSYCHOPHARMACOLOGY Vol. 29 (pp. 1283-1284). SCOTLAND, Glasgow: ELSEVIER. DOI |
| 2019 | Lardenoije, R., Roubroeks, J., Pishva, E., Leber, M., Wagner, H., Iatrou, A., . . . van den Hove, D. (2019). Alzheimer's Disease DNA (Hydroxy)Methylome in the Brain and Blood: Evidence for OXT Methylation as a Preclinical Marker. In BIOLOGICAL PSYCHIATRY Vol. 85 (pp. S144). IL, Chicago: ELSEVIER SCIENCE INC. DOI WoS1 |
| 2019 | Forstner, A. J., Maaser, A., Strohmaier, J., Ludwig, K. U., Degenhardt, F., Streit, F., . . . Noethen, M. M. (2019). EXOME SEQUENCING OF MULTIPLY AFFECTED BIPOLAR DISORDER FAMILIES AND FOLLOW-UP RESEQUENCING IMPLICATE RARE VARIANTS IN NEURONAL GENES CONTRIBUTING TO DISEASE ETIOLOGY. In EUROPEAN NEUROPSYCHOPHARMACOLOGY Vol. 29 (pp. S836-S837). FL, Orlando: ELSEVIER SCIENCE BV. DOI |
| 2019 | Thewes, M., Hoffmann, P., Vollmann, G., Kaundinya, I., & Lehan, A. (2019). Development of a cost model for a more exact estimation of the construction costs of tunnels. In Tunnels and Underground Cities Engineering and Innovation Meet Archaeology Architecture and Art Proceedings of the Wtc 2019 Ita Aites World Tunnel Congress (pp. 4606-4615). DOI |
| 2018 | Maaser, A., Strohmaier, J., Ludwig, K. U., Degenhardt, F., Streit, F., Schenk, L. M., . . . Forstner, A. J. (2018). Exome sequencing of multiply affected bipolar disorder families and follow-up resequencing implicate rare variants in neuronal genes contributing to disease etiology. In EUROPEAN JOURNAL OF HUMAN GENETICS Vol. 26 (pp. 373-374). DENMARK, Copenhagen: NATURE PUBLISHING GROUP. |
| 2018 | Forstner, A. J., Verhaert, A., Maaser, A., Fricker, N., Strohmaier, J., Degenhardt, F., . . . Noethen, M. M. (2018). Resequencing study of five microRNAs suggests an involvement of <i>MIR2113</i> and <i>MIR499</i> in the development of bipolar disorder. In EUROPEAN JOURNAL OF HUMAN GENETICS Vol. 26 (pp. 373). DENMARK, Copenhagen: NATURE PUBLISHING GROUP. |
| 2017 | Muehleisen, T., Teumer, A., Wittfeld, K., Jockwitz, C., van der Auwera, S., Herms, S., . . . Cichon, S. (2017). GENOME-WIDE ASSOCIATION STUDY IMPLICATES LOW-FREQUENCY AND COMMON VARIANTS IN BRAIN FOLDING. In EUROPEAN NEUROPSYCHOPHARMACOLOGY Vol. 27 (pp. S230). CANADA, Toronto: ELSEVIER SCIENCE BV. |
| 2017 | Fischer, S., Herms, S., Muehleisen, T., Strohmaier, J., Borrmann-Hassenbach, M., Streit, F., . . . Hoffmann, P. (2017). DELINEATION OF THE MUTATIONAL SPECTRUM IN TWO SUSCEPTIBILITY GENES FOR BIPOLAR DISORDER, NEUROCAN (NCAN) AND ADENYLATE CYCLASE 2 (ADCY2). In EUROPEAN NEUROPSYCHOPHARMACOLOGY Vol. 27 (pp. S211). CANADA, Toronto: ELSEVIER SCIENCE BV. |
| 2017 | Forstner, A. J., Hecker, J., Hofmann, A., Maaser, A., Reinbold, C. S., Mühleisen, T. W., . . . Nöthen, M. M. (2017). Identification of shared risk loci and pathways for bipolar disorder and schizophrenia. In Plos One Vol. 12. DOI Scopus69 Europe PMC66 |
| 2017 | Forstner, A. J., Maaser, A., Sumer, S., Khudayberdiev, S., Muehleisen, T. W., Leber, M., . . . Noethen, M. M. (2017). Genome-wide association analysis implicates microRNAs in bipolar affective disorder. In EUROPEAN NEUROPSYCHOPHARMACOLOGY Vol. 27 (pp. S536-S537). FRANCE, Paris: ELSEVIER. DOI |
| 2017 | Sud, A., Thomsen, H., Law, P., Foersti, A., da Silva Filho, M. I., Holroyd, A., . . . Houlston, R. (2017). GENOME-WIDE ASSOCIATION STUDY OF HODGKIN LYMPHOMA IDENTIFIES HISTOLOGY-SPECIFIC ASSOCIATIONS AND TRANSCRIPTIONAL REGULATORS OF DISEASE SUSCEPTIBILITY. In HAEMATOLOGICA Vol. 102 (pp. 91). SPAIN, Madrid: FERRATA STORTI FOUNDATION. |
| 2016 | Jamil, M. A., Pezeshkpoor, B., Hoffmann, A., Hoffmann, P., Heilmann, S., Noethen, M., . . . El-Maarri, O. (2016). DNA methylation of Factor VIII secreting endothelial cells and several other endothelial cells in comparison to blood. In HAEMOPHILIA Vol. 22 (pp. 20). WILEY-BLACKWELL. |
| 2016 | Weber, S., Hofmann, A., Naumann, A., Hoffmann, P., & Doerfler, W. (2016). Epigenetic alterations upon the insertion of foreign DNA into mammalian Genomes: Oncogenesis and evolution. In Epigenetics and Human Health (pp. 123-143). DOI Scopus1 WoS2 |
| 2016 | Reynolds, T., François, A., Riesen, N., Turvey, M., Nicholls, S., Hoffmann, P., & Monro, T. (2016). Using whispering gallery mode micro lasers for biosensing within undiluted serum. In M. Hutchinson, & E. Goldys (Eds.), Proceedings: SPIE BioPhotonics Australasia Vol. 10013 (pp. 100132X-1-100132X-8). US: SPIE. DOI Scopus2 WoS2 |
| 2016 | Klantsataya, E., François, A., Sciacca, B., Zuber, A., Ebendorff-Heidepriem, H., Hoffmann, P., & Monro, T. (2016). Exploiting surface plasmon scattering on optical fibers. In M. Hutchinson, & E. Goldys (Eds.), Proceedings: SPIE BioPhotonics Australasia Vol. 10013 (pp. 1001319-1-1001319-9). US: SPIE. DOI |
| 2015 | François, A., Sciacca, B., Klantsataya, E., Zuber, A., Hoffmann, P., Klinger-Hoffmann, M., & Monro, T. (2015). Surface plasmon scattering: An alternative approach for optical fibers biosensors. In B. Lee, S. Lee, & Y. Rao (Eds.), Proceedings of SPIE - The International Society for Optical Engineering Vol. 9655 (pp. 4 pages). US: SPIE-INT SOC OPTICAL ENGINEERING. DOI |
| 2015 | El-Maarri, O., Jamil, M. A., Pezeshkpoor, B., Nuesgen, N., Hofmann, A., Hoffmann, P., . . . Oldenburg, J. (2015). Molecular Characterization of F8 Secreting Cell. In BLOOD Vol. 126 (pp. 3 pages). FL, Orlando: AMER SOC HEMATOLOGY. |
| 2015 | El-Maarri, O., Jamil, A., Nuesgen, N., Sharma, A., Pezeshkpoor, B., Hofmann, A., . . . Oldenburg, J. (2015). Molecular signature of LSECS: a F8 secreting endothelial cells. In JOURNAL OF THROMBOSIS AND HAEMOSTASIS Vol. 13 (pp. 825). WILEY-BLACKWELL. |
| 2013 | Johnson, D. C., Weinhold, N., Meissner, T., Walker, B. A., Broderick, P., Chen, B., . . . Morgan, G. J. (2013). Expression Quantitative Trait Loci Reveal Regulatory Regions Important In The Pathogenesis of Multiple Myeloma. In BLOOD Vol. 122 (pp. 2 pages). LA, New Orleans: AMER SOC HEMATOLOGY. DOI WoS1 |
| 2013 | von Spiczak, S., Lal, D., Reinthaler, E. M., Steiner, I., Nothnagel, M., Laube, B., . . . Lemke, J. R. (2013). MUTATIONS IN <i>GRIN2A</i> CAUSE IDIOPATHIC FOCAL EPILEPSY WITH ROLANDIC SPIKES. In EPILEPSIA Vol. 54 (pp. 344). CANADA, Montreal: WILEY-BLACKWELL. |
| 2013 | Sheppard, A. L., Wolffsohn, J. S., Bhatt, U., Hoffmann, P. C., Scheider, A., Huetz, W. W., & Shah, S. (2013). Clinical outcomes after implantation of a new hydrophobic acrylic toric IOL during routine cataract surgery. In JOURNAL OF CATARACT AND REFRACTIVE SURGERY Vol. 39 (pp. 41-47). AUSTRIA, Vienna: ELSEVIER SCIENCE INC. DOI WoS36 |
| 2013 | Rowland, K., François, A., Hoffmann, P., & Monro, T. (2013). Sub-wavelength fluorescent polymer coatings to convert standard glass capillaries into robust microfluidic refractometric sensors. In Proceedings of SPIE Vol. 8570 (pp. 1-7). Online: SPIE. DOI |
| 2012 | Sciacca, B., François, A., Penno, M., Brazzatti, J., Klingler-Hoffmann, M., Hoffmann, P., & Monro, T. (2012). Radiative-SPR platform for the detection of apolipoprotein E for use in medical diagnostics. In Progress in Biomedical Optics and Imaging - Proceedings of SPIE Vol. 8234 (pp. 1-8). US: SPIE. DOI Scopus1 |
| 2012 | Nowak, M., Kraemer, B., Haupt, M., Papapanou, P. N., Kebschull, J., Hoffmann, P., . . . Kebschull, M. (2012). Activation of invariant natural killer T-cells in periodontitis lesions. In IMMUNOLOGY Vol. 137 (pp. 465). SCOTLAND, Glasgow: WILEY-BLACKWELL. WoS1 |
| 2011 | François, A., Courtney, J., Penno, M., Hoffmann, P., & Monro, T. (2011). A novel optical-fiber based surface plasmon resonance sensing architecture and its application to gastric cancer diagnostics. In W. Bock, J. Albert, & X. Bao (Eds.), Proceedings of SPIE Vol. 7753 (pp. 1-4). Ottawa, Canada: SPIE. DOI Scopus3 WoS1 |
| 2010 | Mattheisen, M., Becker, T., Herold, C., Nowak, S., Becker, J., Herberz, R., . . . Knapp, M. (2010). Lessons We Have Learned from Genome-wide Haplotype Analysis (GWHA). In GENETIC EPIDEMIOLOGY Vol. 34 (pp. 948-949). MA, Boston: WILEY. |
| 2010 | Schulte-Koerne, G., Bruder, J., Neuhoff, N., Roeske, D., Hoffmann, P., Ludwig, K., . . . Mueller-Myhsok, B. (2010). Brain gene interactions in dyslexia. In INTERNATIONAL JOURNAL OF PSYCHOPHYSIOLOGY Vol. 77 (pp. 229-230). HUNGARY, Budapest: ELSEVIER SCIENCE BV. DOI WoS1 |
| 2008 | Monro, T., Ruan, Y., Ebendorff-Heidepriem, H., Foo, H., Hoffmann, P., & Moore, R. (2008). Antibody immobilization within glass microstructured fibers: a route to sensitive and selective biosensors. In D. Sampson, S. Collins, K. Oh, & R. Yamauchi (Eds.), Proceedings of SPIE 7004 Vol. 7004 (pp. 70046Q-1-70046Q-4). Perth, W. Aust.: Society of Photo-Optical Instrumentation Engineers. DOI Scopus3 WoS1 |
| 2007 | Schartner, E., Ruan, Y., Hoffmann, P., & Monro, T. (2007). An optical fibre protein sensor. In Proceedings of COIN ACOFT (pp. 1-4). Australia: IEEE. DOI Scopus4 |
| 2006 | Cichon, S., Muehleisen, T., Hillmer, A., Fuerst, R., Abou Jamra, R., Schumacher, J., . . . Noethen, M. M. (2006). A systematic HAPMAP-based survey of schizophrenia candidate genes in the German population. In AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS Vol. 141B (pp. 731-732). ITALY, Cagliari: WILEY-LISS. |
| 2003 | Hoffmann, P., Alberti, S., Gonzalez-Carmona, M. A., Hoehfeld, J., & Caselmann, W. H. (2003). Co-chaperone chip induces stimulation of HBV replication in vitro. In JOURNAL OF HEPATOLOGY Vol. 38 (pp. 7). TURKEY, ISTANBUL: ELSEVIER SCIENCE BV. DOI |
| 1995 | HUETZ, W. W., HOFFMANN, P. C., & ECKHARDT, H. B. (1995). THE EXCENTRIC ASTIGMATISM PRK, A PHOTOREFRACTIVE METHOD TO CORRECT CORNEAL ASTIGMATISM USING THE 193-NM EXCIMER-LASER. In VISION RESEARCH Vol. 35 (pp. 3111). PERGAMON-ELSEVIER SCIENCE LTD. |
| Year | Citation |
|---|---|
| 2017 | Schubert, O., Stacey, D., Air, T., Arentz, G., Hoffmann, P., & Baune, B. T. (2017). USING AN INTEGRATED SYSTEMS BIOLOGY APROACH TO CHARACTERIZE THE MOLECULAR PROFILE OF COGNITIVE DYSFUNCTION IN PEOPLE WITH REMITTED MAJOR DEPRESSIVE DISORDER. Poster session presented at the meeting of AUSTRALIAN AND NEW ZEALAND JOURNAL OF PSYCHIATRY. SAGE PUBLICATIONS LTD. |
| 2015 | Lokman, N. A., Elder, A. S. F., Ween, M. P., Pyragius, C. E., Hoffmann, P., Ruszkiewicz, A., . . . Ricciardelli, C. (2015). Annexin A2 a potential prognostic marker for serous ovarian cancer promotes ovarian cancer metastasis. Poster session presented at the meeting of CLINICAL & EXPERIMENTAL METASTASIS. SPRINGER. WoS1 |
| 2015 | Schubert, K. O., Stacey, D., Arentz, G., Hoffmann, P., & Baune, B. T. (2015). Peripheral blood gene expression and proteomic analysis implicates B-cell development and ribosomal proteins in cognitive dysfunction in people with remitted Major Depression. Poster session presented at the meeting of Society for Mental Health Research Conference 2015. Brisbane. |
| 2014 | Lokman, N. A., Elder, A. S. F., Ween, M. P., Pyragius, C. E., Hoffmann, P., Ruszkiewicz, A., . . . Oehler, M. K. (2014). ANNEXIN A2 A POTENTIAL PROGNOSTIC MARKER FOR SEROUS OVARIAN CANCER PROMOTES OVARIAN CANCER METATASIS. Poster session presented at the meeting of INTERNATIONAL JOURNAL OF GYNECOLOGICAL CANCER. LIPPINCOTT WILLIAMS & WILKINS. |
| 2014 | Hoffmann, P., Gustafsson, J. O. R., Zhang, C., Mitall, P., Klingler-Hoffmann, M., & Oehler, M. K. (2014). PEPTIDE IMAGING MASS SPECTROMETRY ON FORMALIN FIXED PARAFFIN EMBEDDED TISSUE IN GYNAECOLOGICAL CANCER. Poster session presented at the meeting of INTERNATIONAL JOURNAL OF GYNECOLOGICAL CANCER. LIPPINCOTT WILLIAMS & WILKINS. |
| 2014 | Martin, K., Hoffmann, P., & Oehler, M. K. (2014). AUTOANTIBODY BIOMARKERS FOR THE EARLY DETECTION OF OVARIAN CANCER. Poster session presented at the meeting of INTERNATIONAL JOURNAL OF GYNECOLOGICAL CANCER. LIPPINCOTT WILLIAMS & WILKINS. |
| 2012 | McColl, S. R., Turvey, M., Koudelka, T., Carroll, W., Bernard, C., Greer, J., & Hoffmann, P. (2012). Quantitative analysis of the spinal cord CD4+T lymphocyte proteome in EAE. Poster session presented at the meeting of MULTIPLE SCLEROSIS JOURNAL. Melbourne, AUSTRALIA: SAGE PUBLICATIONS LTD. |
| 2009 | Jaehne, E., Colella, A., Hoffmann, P., & Irvine, R. J. (2009). A behavioural, neurochemical and proteomic analysis after treatment with MDMA and methamphetamine. Poster session presented at the meeting of Abstracts of the MDMA Conference, as published in Neuropsychobiology. Melbourne, Australia: Karger. DOI |
| 2006 | Olayioye, M., Buchholz, M., Schmid, S., Hoffmann, P., & Pomorski, T. (2006). Phosphorylation of StarD10 on serine 284 regulates lipid transfer activity. Poster session presented at the meeting of EUROPEAN JOURNAL OF CELL BIOLOGY. Braunschweig, GERMANY: ELSEVIER GMBH, URBAN & FISCHER VERLAG. |
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Program 3: Modulating grain oil content of oats to improve suitability for milling and food/beverage ingredient development, SA Research and Development Institute (SARDI), 31/05/2024 - 31/03/2028
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Understanding herbicide residues on challenging soil types within the southern region, Grains Research and Development Corporation, 28/03/2025 - 30/03/2027
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Assessment of current best practice techniques for handling pesticides in forestry applications, Forest and Wood Products Australia, 15/06/2023 - 31/07/2026
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Nanoparticle regulation of DNA replication and repair pathways, ARC - Discovery Projects, 21/01/2019 - 29/06/2023
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Enabling personalised medicine for patients with ovarian cancer, Tour de Cure Ltd, 01/11/2021 - 31/12/2022
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Ovarian Blood Markers of Ovarian Cancer (phase 1 transfer in), Ovarian Cancer Research Foundation Inc, 04/12/2017 - 30/06/2018
| Date | Role | Research Topic | Program | Degree Type | Student Load | Student Name |
|---|---|---|---|---|---|---|
| 2025 | External Supervisor | Shining a light on the dark proteome of ovarian cancer | Doctor of Philosophy | Doctorate | Full Time | Ms Paula González Menéndez |
| Date | Role | Research Topic | Program | Degree Type | Student Load | Student Name |
|---|---|---|---|---|---|---|
| 2018 - 2022 | Co-Supervisor | Effects of mitochondrial DNA haplotype on conceptus phenotype in cattle at midgestation | Doctor of Philosophy | Doctorate | Full Time | Mrs Hanh Thi Hong Nguyen |
| 2016 - 2023 | Co-Supervisor | Characterisation of Ovarian Cancer Development, Progression and Treatment Resistance Through Mass Spectrometry Analysis | Doctor of Philosophy | Doctorate | Full Time | Mr Mitchell Aidan Acland |
| 2015 - 2018 | Principal Supervisor | Painting a Picture of the Ovarian Cancer N-Glycome | Doctor of Philosophy | Doctorate | Full Time | Mr Matthew Thomas Briggs |
| 2014 - 2016 | Co-Supervisor | Clustering of Proteomics Imaging Mass Spectrometry Data | Master of Philosophy | Master | Full Time | Ms Annie Conway |
| 2014 - 2017 | Principal Supervisor | Molecular Characterization of Metastatic Endometrial Cancer by Mass Spectrometry | Doctor of Philosophy | Doctorate | Full Time | Ms Parul Mittal |
| 2014 - 2018 | Principal Supervisor | Proteomics characterization of HPV-independent Vulvar Cancer Tumor Progression and Metastasis by Mass Spectrometry | Doctor of Philosophy | Doctorate | Full Time | Mr Chao Zhang |
| 2013 - 2018 | Co-Supervisor | Examination of Placenta and Child Saliva Samples Associated with Childhood Allergy Development | Doctor of Philosophy | Doctorate | Full Time | Dr Nurul Hayati Mohamad Zainal |
| 2012 - 2015 | Co-Supervisor | The role and regulation of the p84 adaptor subunit in phosphatidylinositol 3-kinase gamma lipid-kinase signalling and the control of PI3Kgamma-dependent cell migration | Doctor of Philosophy | Doctorate | Full Time | Ms Michelle Elizabeth Turvey |
| 2012 - 2018 | Co-Supervisor | Role of Insulin Receptor Isoform A in Breast Cancer | Doctor of Philosophy | Doctorate | Full Time | Mr Liang Li |
| 2012 - 2016 | Co-Supervisor | Statistical Treatment of Proteomic Imaging Mass Spectrometry Data | Doctor of Philosophy | Doctorate | Full Time | Lyron Juan Winderbaum |
| 2010 - 2015 | Principal Supervisor | Utilising Quantitative Immunoproteomics To Reveal Differential Autoantibody Biomarker Panels In Serous Ovarian Cancer Patients | Doctor of Philosophy | Doctorate | Full Time | Mrs Karina Martin |
| 2009 - 2013 | Co-Supervisor | MOLECULAR MECHANISMS OF INSULIN RECEPTOR ISOFORM-A SIGNALLING | Doctor of Philosophy | Doctorate | Full Time | Mr Kolin Harinda Rajapaksha |
| 2008 - 2012 | Principal Supervisor | Molecular Characterization of Metastatic Ovarian Cancer by MALDI Imaging Mass Spectrometry | Doctor of Philosophy | Doctorate | Full Time | Mr Ove Gustafsson |
| 2008 - 2014 | Co-Supervisor | "Understanding the Apoptotic Signaling Pathway that Involve In Breast Cancer Using Microarray, Proteomics and Bioinformatics | Doctor of Philosophy | Doctorate | Full Time | Mr Ibrahim Oqla Alanazi |
| 2007 - 2011 | Co-Supervisor | The Differential Roles of p101 and p84, the Regulatory Subunits of Phosphoinositide 3-kinase Gamma, in Cell Migration | Doctor of Philosophy | Doctorate | Full Time | Miss Julie Brazzatti |
| 2006 - 2011 | Principal Supervisor | Development of Sensitive Proteomic Approaches for Protein Tyrosine Phosphorylation Detection | Doctor of Philosophy | Doctorate | Full Time | Mr Mark Condina |
| 2006 - 2011 | Co-Supervisor | Casein Proteins: Investigating Their Chaperone Activity And Amyloid Fibril Formation | Doctor of Philosophy | Doctorate | Full Time | Mr Tomas Koudelka |
| 2006 - 2012 | Co-Supervisor | Clinical and Biological Determinants of the Coronary Slow Flow Phenomenon | Doctor of Philosophy | Doctorate | Part Time | Miss Victoria Kopetz |
| 2006 - 2014 | Co-Supervisor | Characteristic Negative Ion Fragmentations of Deprotonated Peptides Containing Post-Translational Modifications | Doctor of Philosophy | Doctorate | Full Time | Ms Hayley Andreazza |
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