| 2026 |
Geleta, L. A., Doyle, C., Garton, F. C., Fowler, M., Carr, J. M., Akkari, P. A., . . . Benyamin, B. (2026). The roles of human endogenous retrovirus in neurodegenerative diseases: A systematic review. Brain Behavior and Immunity, 132, 13 pages. DOI Scopus1 WoS1 Europe PMC1 |
| 2026 |
Boomsma, A., Doyle, C., Sai, N., Rogers, M. -L., Lee, S. H., & Benyamin, B. (2026). The differences in sex ratio between sporadic and familial amyotrophic lateral sclerosis: a systematic review. Journal of Neurology, 273(2), 12 pages. DOI Scopus2 WoS2 Europe PMC1 |
| 2026 |
Momin, M. M., Zhou, X., Ahmed, M., Hypponen, E., Benyamin, B., & Lee, S. H. (2026). Cross-Ancestry Polygenic Prediction: Comparing Methods and Assessing Transferability Across Traits. Genetic Epidemiology, 50(1), e70029-1-e70029-13. DOI Scopus1 WoS1 Europe PMC2 |
| 2026 |
Fentaw, Z., Truong, B., Jayasinghe, D., Vedova, C. D., Hemani, G., Benyamin, B., . . . Lee, S. H. (2026). Leveraging polygenic risk scores to infer causal directions in genotype-by-environment interactions between complex traits. Human Genetics, 145(1), 19-1-19-16. DOI |
| 2026 |
Beyene, M. B., Visvanathan, R., Alemu, R., Theou, O., Beben, B., Cesari, M., . . . Amare, A. T. (2026). Associations and Interaction Effects of Socioeconomic, Lifestyle, and Genetic Factors on Intrinsic Capacity. The journals of gerontology. Series A, Biological sciences and medical sciences, 81(4), glag057-1-glag057-11. DOI |
| 2026 |
Chau, A. C. M., Ridding, M. C., Benyamin, B., & Hordacre, B. (2026). Plasticity is predicted by structural damage in sub-acute ischemic stroke. Neuroscience, 605, 11-18. DOI |
| 2026 |
Geleta, L. A., Doyle, C., Garton, F. C., Fowler, M., Carr, J. M., Akkari, P. A., . . . Benyamin, B. (2026). Reply to letter to editor “Clarifying exposure heterogeneity in a review of HERVs and neurodegenerative diseases”. Brain, Behavior, and Immunity, 137, 106834. DOI |
| 2026 |
Stacey, D., Reay, W. R., Veltman, L. J., Benyamin, B., Lee, S. H., & Hyppönen, E. (2026). Integrative genomic characterization of the FADS1-2-3 mood disorder risk locus: implications for the role of polyunsaturated fatty acids. Journal of Affective Disorders, 412, 8 pages. DOI |
| 2026 |
Henders, A. K., Ziser, L., Garton, F. C., Adams, L., Ernst, K., Furlong, S., . . . Wray, N. R. (2026). Strategic Amyotrophic Lateral Sclerosis Australia-Systems Genomics Consortium (SALSA-SGC): cohort profile. BMJ Open, 16(6), e110906-1-e110906-10. DOI |
| 2025 |
Byrne, S., Hypponen, E., Benyamin, B., & Boyle, T. (2025). Greater adherence to lifestyle recommendations after cancer diagnosis is associated with lower mortality in the UK Biobank. Cancer Epidemiology, Biomarkers and Prevention, 34(5), 669-675. DOI Scopus1 WoS1 |
| 2025 |
Stacey, D., Gaziano, L., Eldi, P., Toben, C., Benyamin, B., Lee, S. H., & Hyppönen, E. (2025). A Transcriptome-Wide Mendelian Randomization Study in Isolated Human Immune Cells Highlights Risk Genes Involved in Viral Infections and Potential Drug Repurposing Opportunities for Schizophrenia. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, 198(6), 19-31. DOI Scopus5 WoS5 Europe PMC4 |
| 2025 |
Dewau, R., Byrne, S., Hyppönen, E., Lee, S. H., & Benyamin, B. (2025). Genetic and Environmental Contributions to Child Height in Low- and Middle-Income Countries. American Journal of Human Biology, 37(9), e70134. DOI Europe PMC1 |
| 2025 |
Beyene, M. B., Visvanathan, R., Alemu, R., Benyamin, B., Bhattacharjee, R., Beyene, H. B., . . . Amare, A. T. (2025). A genome-wide association study identified 10 novel genomic loci associated with intrinsic capacity. The Journals of Gerontology. Series A, Biological Sciences and Medical Sciences, 80(11), glaf196-1-glaf196-14. DOI Scopus2 WoS2 |
| 2025 |
Jayasinghe, D., Pham, V. V. H., Beckmann, K., Benyamin, B., & Lee, S. H. (2025). Analyzing complex traits and diseases using GxE PRS: genotype-environment interaction in polygenic risk score models. Journal of Human Genetics, 70(11), 547-556. DOI Scopus1 WoS3 Europe PMC3 |
| 2025 |
Harsono, I. W., Ariani, Y., Benyamin, B., Fadilah, F., Pujianto, D. A., Hafifah, C. N., & Prawitasari, T. (2025). Clinical phenotype and trio whole exome sequencing data from a patient with glycogen storage disease IV in Indonesia. Data in Brief, 58, 9 pages. DOI Europe PMC1 |
| 2024 |
Byrne, S., Boyle, T., Ahmed, M., Lee, S. H., Benyamin, B., & Hyppönen, E. (2024). Response to: Adherence to the World Cancer Research Fund lifestyle recommendations and incidence of prostate cancer in the UK Biobank.. Int J Epidemiol, 53(1), 1-2. DOI Scopus1 WoS1 Europe PMC1 |
| 2024 |
Beyene, M. B., Visvanathan, R., Ahmed, M., Benyamin, B., Beard, J. R., & Amare, A. T. (2024). Development and validation of an intrinsic capacity score in the UK Biobank study. Maturitas, 185(107976), 107976-1-107976-10. DOI Scopus22 WoS22 Europe PMC21 |
| 2024 |
Stacey, D., Benyamin, B., Lee, S. H., & Hyppönen, E. (2024). A metabolome-wide Mendelian randomization study identifies dysregulated arachidonic acid synthesis as a potential causal risk factor for bipolar disorder. Biological Psychiatry, 96(6), 455-462. DOI Scopus26 WoS25 Europe PMC20 |
| 2024 |
Stacey, D., Suppiah, V., Benyamin, B., Lee, S. H., & Hyppönen, E. (2024). In-silico functional analyses identify TMPRSS15-mediated intestinal absorption of lithium as a modulator of lithium response in bipolar disorder. Journal of Affective Disorders, 358, 416-421. DOI Scopus4 WoS4 Europe PMC3 |
| 2024 |
Duko, B., Mengistu, T. S., Stacey, D., Moran, L. J., Tessema, G., Pereira, G., . . . Hyppönen, E. (2024). Associations between maternal preconception and pregnancy adiposity and neuropsychiatric and behavioral outcomes in the offspring: a systematic review and meta-analysis. Psychiatry Research, 342(116149), 1-20. DOI Scopus11 WoS9 Europe PMC5 |
| 2024 |
Dewau, R., Boomsma, A., Doyle, C., Byrne, S., Hyppönen, E., Lee, S. H., & Benyamin, B. (2024). Meta-Analysis of the Heritability of Childhood Height From 560 000 Pairs of Relatives Born Between 1929 and 2004. American Journal of Human Biology, 37(1), e24188-1-e24188-15. DOI Scopus5 WoS5 Europe PMC3 |
| 2024 |
Jayasinghe, D., Eshetie, S., Beckmann, K., Benyamin, B., & Lee, S. H. (2024). Advancements and limitations in polygenic risk score methods for genomic prediction: a scoping review. Human Genetics, 143(12), 1401-1431. DOI Scopus20 WoS17 Europe PMC23 |
| 2024 |
Jayasinghe, D., Momin, M. M., Beckmann, K., Hyppönen, E., Benyamin, B., & Lee, S. H. (2024). Mitigating type 1 error inflation and power loss in GxE PRS: Genotype–environment interaction in polygenic risk score models. Genetic Epidemiology, 48(2), 85-100. DOI Scopus14 WoS14 Europe PMC14 |
| 2024 |
Allara, E., Bell, S., Smith, R., Keene, S. J., Gill, D., Gaziano, L., . . . Niemi, M. (2024). Novel loci and biomedical consequences of iron homoeostasis variation. Communications Biology, 7(1), 17 pages. DOI Scopus7 WoS7 Europe PMC9 |
| 2024 |
Eshetie, S., Choi, K. W., Hyppönen, E., Benyamin, B., & Lee, S. H. (2024). Integrative multi-omics analysis to gain new insights into COVID-19. Scientific Reports, 14(1), 14 pages. DOI Scopus4 WoS3 Europe PMC2 |
| 2024 |
Harsono, I. W., Ariani, Y., Benyamin, B., Fadilah, F., Pujianto, D. A., & Hafifah, C. N. (2024). IDeRare: a lightweight and extensible open-source phenotype and exome analysis pipeline for germline rare disease diagnosis. JAMIA Open, 7(2), 10 pages. DOI Scopus1 WoS1 Europe PMC1 |
| 2024 |
Momin, M. M., Zhou, X., Hyppönen, E., Benyamin, B., & Lee, S. H. (2024). Cross-ancestry genetic architecture and prediction for cholesterol traits. Human Genetics, 143(5), 635-648. DOI Scopus3 WoS4 Europe PMC5 |
| 2023 |
Byrne, S., Boyle, T., Ahmed, M., Lee, S. H., Benyamin, B., & Hyppönen, E. (2023). Lifestyle, genetic risk and incidence of cancer: a prospective cohort study of 13 cancer types.. International journal of epidemiology, 52(3), 817-826. DOI Scopus91 WoS85 Europe PMC70 |
| 2023 |
Hill, G., Johnson, F., Uy, J., Serrada, I., Benyamin, B., Van Den Berg, M., & Hordacre, B. (2023). Moderate intensity aerobic exercise may enhance neuroplasticity of the contralesional hemisphere after stroke: a randomised controlled study.. Scientific reports, 13(1), 1-11. DOI Scopus23 WoS21 Europe PMC15 |
| 2023 |
Lagou, V., Jiang, L., Ulrich, A., Zudina, L., González, K. S. G., Balkhiyarova, Z., . . . Prokopenko, I. (2023). GWAS of random glucose in 476,326 individuals provide insights into diabetes pathophysiology, complications and treatment stratification. Nature Genetics, 55(9), 1448-1461. DOI Scopus74 WoS79 Europe PMC93 |
| 2023 |
Eshetie, S., Jullian, P., Benyamin, B., & Lee, S. H. (2023). Host genetic determinants of COVID-19 susceptibility and severity: A systematic review and meta-analysis. Reviews in Medical Virology, 33(5), 12 pages. DOI Scopus11 WoS11 Europe PMC10 |
| 2023 |
Momin, M. M., Shin, J., Lee, S., Truong, B., Benyamin, B., & Lee, S. H. (2023). A method for an unbiased estimate of cross-ancestry genetic correlation using individual-level data. Nature Communications, 14(1), 13 pages. DOI Scopus16 WoS16 Europe PMC21 |
| 2022 |
Shin, J., Zhou, X., Tan, J. T. M., Hyppönen, E., Benyamin, B., & Lee, S. H. (2022). Lifestyle Modifies the Diabetes-Related Metabolic Risk, Conditional on Individual Genetic Differences. Frontiers in Genetics, 13(759309), 759309-1-759309-10. DOI Scopus8 WoS8 Europe PMC8 |
| 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. DOI Scopus1958 WoS1907 Europe PMC2419 |
| 2022 |
Neumann, A., Nolte, I. M., Pappa, I., Ahluwalia, T. S., Pettersson, E., Rodriguez, A., . . . Tiemeier, H. (2022). A genome-wide association study of total child psychiatric problems scores. Plos One, 17(8 August), 23 pages. DOI Scopus19 WoS18 Europe PMC26 |
| 2022 |
Jami, E. S., Hammerschlag, A. R., Ip, H. F., Allegrini, A. G., Benyamin, B., Border, R., . . . Middeldorp, C. M. (2022). Genome-wide Association Meta-analysis of Childhood and Adolescent Internalizing Symptoms. Journal of the American Academy of Child and Adolescent Psychiatry, 61(7), 934-945. DOI Scopus45 WoS39 Europe PMC57 |
| 2022 |
van Rheenen, W., van der Spek, R. A. A., Bakker, M. K., van Vugt, J. J. F. A., Hop, P. J., Zwamborn, R. A. J., . . . Kraft, J. (2022). Author Correction: Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology (Nature Genetics, (2021), 53, 12, (1636-1648), 10.1038/s41588-021-00973-1). Nature Genetics, 54(3), 361. DOI Scopus3 WoS2 Europe PMC5 |
| 2022 |
Shepheard, S. R., Karnaros, V., Benyamin, B., Schultz, D. W., Dubowsky, M., Wuu, J., . . . Rogers, M. L. (2022). Urinary neopterin: A novel biomarker of disease progression in amyotrophic lateral sclerosis. European Journal of Neurology, 29(4), 990-999. DOI Scopus27 WoS28 Europe PMC30 |
| 2022 |
Restuadi, R., Garton, F. C., Benyamin, B., Lin, T., Williams, K. L., Vinkhuyzen, A., . . . McRae, A. F. (2022). Polygenic risk score analysis for amyotrophic lateral sclerosis leveraging cognitive performance, educational attainment and schizophrenia. European Journal of Human Genetics, 30(5), 532-539. DOI Scopus20 WoS20 Europe PMC24 |
| 2021 |
Byrne, S., Boyle, T., Benyamin, B., Lee, S. H., Ahmed, M., & Hypponen, E. (2021). Do associations between a healthy lifestyle and incidence of cancer differ by genetic risk?. INTERNATIONAL JOURNAL OF EPIDEMIOLOGY, 50(Supplement_1), 40. DOI |
| 2021 |
van Rheenen, W., van der Spek, R. A. A., Bakker, M. K., van Vugt, J. J. F. A., Hop, P. J., Zwamborn, R. A. J., . . . Kraft, J. (2021). Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology. Nature Genetics, 53(12), 1636-1648. DOI Scopus380 WoS374 Europe PMC481 |
| 2021 |
Julián-Serrano, S., Yuan, F., Wheeler, W., Benyamin, B., Machiela, M. J., Arslan, A. A., . . . Stolzenberg-Solomon, R. Z. (2021). Hepcidin-regulating iron metabolism genes and pancreatic ductal adenocarcinoma: A pathway analysis of genome-wide association studies. American Journal of Clinical Nutrition, 114(4), 1408-1417. DOI Scopus21 WoS17 Europe PMC12 |
| 2020 |
Shin, J., Zhou, X., Tan, J., Hyppönen, E., Benyamin, B., & Lee, H. (2020). Lifestyle modifies the diabetes-related metabolic risk, conditional on individual genetic differences. DOI |
| 2020 |
Nabais, M. F., Lin, T., Benyamin, B., Williams, K. L., & Wray, N. R. (2020). Significant out-of-sample classification from methylation profile scoring for amyotrophic lateral sclerosis. npj Genomic Medicine, 5(1), 1-9. DOI Scopus26 WoS25 Europe PMC26 |
| 2019 |
Lam, M., Chen, C. Y., Li, Z., Martin, A. R., Benyamin, B., & Huang, H. (2019). Comparative genetic architectures of schizophrenia in East Asian and European populations. Nature Genetics, 51(12), 1670-1678. DOI Scopus540 WoS814 Europe PMC577 |
| 2019 |
Gill, D., Benyamin, B., Moore, L. S. P., Monori, G., Zhou, A., Koskeridis, F., . . . Tzoulaki, I. (2019). Associations of genetically determined iron status across the phenome: a mendelian randomization study. PLOS medicine, 16(6, article no. e1002833), 1-16. DOI Scopus53 WoS49 Europe PMC56 |
| 2019 |
Eirich, A., Biermann, T., Müller, C. P., Kornhuber, J., Benyamin, B., Hulse, G. K., . . . Schwab, S. G. (2019). Association of CamK2A genetic variants with transition time from occasional to regular heroin use in a sample of heroin-dependent individuals. Psychiatric genetics, 29(1), 18-25. DOI Scopus5 WoS4 Europe PMC3 |
| 2019 |
Tarr, I. S., McCann, E. P., Benyamin, B., Peters, T. J., Twine, N. A., Zhang, K. Y., . . . Williams, K. L. (2019). Monozygotic twins and triplets discordant for amyotrophic lateral sclerosis display differential methylation and gene expression. Scientific Reports, 9(1), 17 pages. DOI Scopus44 WoS39 Europe PMC35 |
| 2017 |
Mills, N., Maier, R., Whitfield, J., Wright, M., Colodro-Conde, L., Byrne, E., . . . Benyamin, B. (2017). Investigating the relationship between iron and depression. Journal of Psychiatric Research, 94, 148-155. DOI Scopus17 WoS12 Europe PMC12 |
| 2017 |
Lupton, M. K., Benyamin, B., Proitsi, P., Nyholt, D. R., & Whitfield, J. B. (2017). No genetic overlap between circulating Iron Levels and Alzheimer's disease. Journal of Alzheimer's disease, 59(1), 85-99. DOI Scopus13 WoS13 Europe PMC13 |
| 2017 |
Willems, S. M., Wright, D. J., Day, F. R., Trajanoska, K., Benyamin, B., & Scott, R. A. (2017). Large-scale GWAS identifies multiple loci for hand grip strength providing biological insights into muscular fitness. Nature communications, 8(16015), 1-12. DOI Scopus178 WoS162 Europe PMC166 |
| 2017 |
Gratten, J., Zhao, Q., Benyamin, B., Garton, F., & Fan, D. (2017). Whole-exome sequencing in amyotrophic lateral sclerosis suggests NEK1 is a risk gene in Chinese. Genome medicine, 9(1), 1-9. DOI Scopus29 WoS28 Europe PMC23 |
| 2017 |
Benyamin, B., He, J., Zhao, Q., Gratten, J., & Fan, D. (2017). Cross-ethnic meta-analysis identifies association of the GPX3-TNIP1 locus with amyotrophic lateral sclerosis. Nature communications, 8(1), 1-7. DOI Scopus78 WoS76 Europe PMC82 |
| 2017 |
Benyamin, B., Maihofer, A. X., Schork, A. J., Hamilton, B. A., Rao, F., Schmid Schönbein, G. W., . . . O'Connor, D. T. (2017). Identification of novel loci affecting circulating chromogranins and related peptides. Human molecular genetics, 26(1), 233-242. DOI Scopus15 WoS14 Europe PMC12 |
| 2017 |
Del Greco, F. M., Foco, L., Pichler, I., Eller, P., Eller, K., Benyamin, B., . . . Minelli, C. (2017). Serum iron level and kidney function: a Mendelian randomization study. Nephrology dialysis transplantation, 32(2), 273-278. DOI Scopus41 WoS38 Europe PMC31 |
| 2017 |
Garton, F. C., Benyamin, B., Zhao, Q., Liu, Z., Gratten, J., Henders, A. K., . . . McCombe, P. A. (2017). Whole exome sequencing and DNA methylation analysis in a clinical amyotrophic lateral sclerosis cohort. Molecular Genetics and Genomic Medicine, 5(4), 418-428. DOI Scopus14 WoS15 Europe PMC14 |
| 2017 |
Benyamin, B., & Kasbawati. (2017). Preface: Symposium on Biomathematics 2016. Aip Conference Proceedings, 1825, 010001. DOI |
| 2016 |
Chen, G. B., Lee, S. H., Zhu, Z. X., Benyamin, B., & Robinson, M. R. (2016). EigenGWAS: finding loci under selection through genome-wide association studies of eigenvectors in structured populations. Heredity, 117(1), 51-61. DOI Scopus67 WoS69 Europe PMC72 |
| 2015 |
Fall, T., Hägg, S., Ploner, A., Mägi, R., Benyamin, B., & Ingelsson, E. (2015). Age- and sex-specific causal effects of adiposity on cardiovascular risk factors. Diabetes, 64(5), 1841-1852. DOI Scopus64 WoS62 Europe PMC61 |
| 2015 |
Hägg, S., Fall, T., Ploner, A., Mägi, R., Benyamin, B., & Ingelsson, E. (2015). Adiposity as a cause of cardiovascular disease: a Mendelian randomization study. International journal of epidemiology, 44(2), 578-586. DOI Scopus129 WoS116 Europe PMC116 |
| 2015 |
He, J., Tang, L., Benyamin, B., Shah, S., Hemani, G., Liu, R., . . . Fan, D. (2015). C9orf72 hexanucleotide repeat expansions in Chinese sporadic amyotrophic lateral sclerosis. Neurobiology of aging, 36(9), 1-8. DOI Scopus51 WoS47 Europe PMC46 |
| 2015 |
Galesloot, T. E., Janss, L. L., Burgess, S., Kiemeney, L. A. L. M., den Heijer, M., de Graaf, J., . . . Vermeulen, S. H. (2015). Iron and hepcidin as risk factors in atherosclerosis: what do the genes say?. BMC genetics, 16(1, article no. 79), 1-12. DOI Scopus31 WoS30 Europe PMC25 |
| 2015 |
Bui, M., Benyamin, B., Shah, S., Henders, A. K., Martin, N. G., Montgomery, G. W., & McRae, A. F. (2015). Sharing a placenta is associated with a greater similarity in DNA methylation in monochorionic versus dichorionic twin pars in blood at age 14. Twin research and human genetics, 18(6), 680-685. DOI Scopus7 WoS6 Europe PMC6 |
| 2015 |
Polderman, T. J. C., Benyamin, B., De Leeuw, C. A., Sullivan, P. F., Van Bochoven, A., Visscher, P. M., & Posthuma, D. (2015). Meta-analysis of the heritability of human traits based on fifty years of twin studies. Nature genetics, 47(7), 702-709. DOI Scopus1785 WoS1612 Europe PMC1382 |
| 2015 |
Benyamin, B., Esko, T., Ried, J. S., Radhakrishnan, A., Vermeulen, S. H., Traglia, M., . . . Whitfield, J. B. (2015). Corrigendum: Novel loci affecting iron homeostasis and their effects in individuals at risk for hemochromatosis. Nature Communications, 6(1), 1 page. DOI Scopus10 WoS3 Europe PMC3 |
| 2015 |
Rietveld, C. A., Esko, T., Davies, G., Pers, T. H., Turley, P., Benyamin, B., . . . Koellinger, P. D. (2015). Erratum: Common genetic variants associated with cognitive performance identified using the proxy-phenotype method (Proc Natl Acad Sci USA (2014) 111 (13790-13794) DOI: 10.1073/pnas.1404623111). Proceedings of the National Academy of Sciences of the United States of America, 112(4), e380. DOI Scopus2 WoS4 Europe PMC1 |
| 2014 |
Benyamin, B., St Pourcain, B., Davis, O., Davies, G., Hansell, N., Brion, M., . . . Visscher, P. (2014). Childhood intelligence is heritable, highly polygenic and associated with FNBP1L. Molecular Psychiatry, 19(2), 253-258. DOI Scopus212 WoS190 Europe PMC193 |
| 2014 |
Hoggart, C., Venturini, G., Mangino, M., Gomez, F., Ascari, G., Zhao, J., . . . Kutalik, Z. (2014). Novel approach identifies SNPs in SLC2A10 and KCNK9 with evidence for parent-of-origin effect on Body Mass Index. PLoS Genetics, 10(7), e1004508-1-e1004508-12. DOI Scopus54 WoS51 Europe PMC52 |
| 2014 |
Rietveld, C. A., Esko, T., Davies, G., Pers, T. H., Benyamin, B., & Koellinger, P. D. (2014). Common genetic variants associated with cognitive performance identified using the proxy-phenotype method. Proceedings of the National Academy of Sciences of the United States of America, 111(38), 13790-13794. DOI Scopus201 WoS188 Europe PMC181 |
| 2014 |
Benyamin, B., Esko, T., Ried, J. S., Radhakrishnan, A., & Whitfield, J. B. (2014). Novel loci affecting iron homeostasis and their effects in individuals at risk for hemochromatosis. Nature communications, 5(5926), 1-10. DOI Scopus237 WoS237 Europe PMC229 |
| 2014 |
Brion, M. J. A., Benyamin, B., Visscher, P. M., & Smith, G. D. (2014). Beyond the single SNP: emerging developments in Mendelian randomization in the 'omics' era. Current epidemiological reports, 1(4), 228-236. DOI |
| 2013 |
Fall, T., Hagg, S., Magi, R., Ploner, A., Benyamin, B., Hypponen, E. T., & Pokoppenko, I. (2013). The role of adiposity in cardiometabolic traits: a Mendelian randomization analysis. PLoS medicine, 10(6), 1-16. DOI Scopus179 WoS160 Europe PMC166 |
| 2013 |
Verweij, K. J. H., Vinkhuyzen, A. A. E., Benyamin, B., Lynskey, M. T., Quaye, L., Agrawal, A., . . . Medland, S. E. (2013). The genetic aetiology of cannabis use initiation: a meta-analysis of genome-wide association studies and a SNP-based heritability estimation. Addiction biology, 18(5), 846-850. DOI Scopus46 WoS42 Europe PMC45 |
| 2013 |
Schwab, S. G., Kusumawardhani, A. A. A. A., Dai, N., Qin, W. W., Benyamin, B., & Wildenauer, D. B. (2013). Association of rs1344706 in the ZNF804A gene with schizophrenia in a case/control sample from Indonesia. Schizophrenia research, 147(1), 46-52. DOI Scopus30 WoS28 Europe PMC25 |
| 2013 |
Pichler, I., Del Greco M, F., Gögele, M., Lill, C. M., Benyamin, B., & Minelli, C. (2013). Serum iron levels and the risk of Parkinson Disease: a Mendelian randomization study. PLoS medicine, 10(6, article no. e1001462), 1-13. DOI Scopus137 WoS132 Europe PMC108 |
| 2013 |
Paul, D. S., Albers, C. A., Rendon, A., Voss, K., Stephens, J., HaemGen Consortium., . . . Deloukas, P. (2013). Maps of open chromatin highlight cell type-restricted patterns of regulatory sequence variation at hematological trait loci.. Genome research, 23(7), 1130-1141. DOI Europe PMC31 |
| 2012 |
Middelberg, R. P., Benyamin, B., de Moor, M. H. M., Warrington, N. M., & Whitfield, J. B. (2012). Loci affecting gamma-glutamyl transferase in adults and adolescents show age × SNP interaction and cardiometabolic disease associations. Human molecular genetics, 21(2), 446-455. DOI Scopus26 WoS25 Europe PMC25 |
| 2012 |
Tielbeek, J. J., Medland, S. E., Benyamin, B., Byrne, E. M., Heath, A. C., Madden, P. A. F., . . . Verweij, K. J. H. (2012). Unraveling the genetic etiology of adult antisocial behavior: a genome-wide association study. PLoS ONE, 7(10), 1-7. DOI Scopus73 WoS55 Europe PMC42 |
| 2012 |
Van Der Harst, P., Zhang, W., Mateo Leach, I., Rendon, A., Benyamin, B., & Chambers, J. C. (2012). Seventy-five genetic loci influencing the human red blood cell. Nature, 492(7429), 369-375. DOI Scopus269 WoS264 Europe PMC289 |
| 2012 |
Rao, F., Chiron, S., Wei, Z., Fung, M. M., Chen, Y., Wen, G., . . . O'Connor, D. T. (2012). Genetic variation within a metabolic motif in the chromogranin a promoter: pleiotropic influence on cardiometabolic risk traits in twins. American journal of hypertension, 25(1), 29-40. DOI Scopus6 WoS6 Europe PMC6 |
| 2011 |
Benyamin, B., Middelberg, R. P., Lind, P. A., Valle, A. M., Gordon, S., Nyholt, D. R., . . . Whitfield, J. B. (2011). GWAS of butyrylcholinesterase activity identifies four novel loci, independent effects within BCHE and secondary associations with metabolic risk factors. Human molecular genetics, 20(22), 4504-4514. DOI Scopus53 WoS50 Europe PMC44 |
| 2011 |
Kutalik, Z., Benyamin, B., Bergmann, S., Mooser, V., Waeber, G., Montgomery, G. W., . . . Whitfield, J. B. (2011). Genome-wide association study identifies two loci strongly affecting transferrin glycosylation. Human molecular genetics, 20(18), 3710-3717. DOI Scopus32 WoS28 Europe PMC24 |
| 2011 |
Benyamin, B., Montgomery, G. W., Martin, N. G., & Whitfield, J. B. (2011). Transferrin saturation and mortality. Clinical chemistry, 57(6), 921-923. DOI Scopus2 WoS1 Europe PMC1 |
| 2011 |
Martin, N. W., Benyamin, B., Hansell, N. K., Montgomery, G. W., Martin, N. G., Wright, M. J., & Bates, T. C. (2011). Cognitive function in adolescence: testing for interactions between breast-feeding and FADS2 polymorphisms. Journal of the American Academy of Child and Adolescent Psychiatry, 50(1), 55-62. DOI Scopus29 WoS24 Europe PMC21 |
| 2010 |
Verweij, K. J. H., Zietsch, B. P., Medland, S. E., Gordon, S. D., Benyamin, B., Nyholt, D. R., . . . Wray, N. R. (2010). A genome-wide association study of Cloninger's temperament scales: implications for the evolutionary genetics of personality. Biological psychology, 85(2), 306-317. DOI Scopus91 WoS77 Europe PMC63 |
| 2010 |
Yang, J., Benyamin, B., McEvoy, B. P., Gordon, S., Henders, A. K., Nyholt, D. R., . . . Visscher, P. M. (2010). Common SNPs explain a large proportion of the heritability for human height. Nature genetics, 42(7), 565-569. DOI Scopus3396 WoS3235 Europe PMC3299 |
| 2009 |
Kettunen, J., Perola, M., Martin, N. G., Cornes, B. K., Benyamin, B., & Peltonen, L. (2009). Multicenter dizygotic twin cohort study confirms two linkage susceptibility loci for body mass index at 3q29 and 7q36 and identifies three further potential novel loci. International journal of obesity, 33(11), 1235-1242. DOI Scopus19 WoS20 Europe PMC16 |
| 2009 |
Benyamin, B., Visscher, P. M., & McRae, A. F. (2009). Family-based genome-wide association studies. Pharmacogenomics, 10(2), 181-190. DOI Scopus64 WoS59 Europe PMC51 |
| 2009 |
Benyamin, B., Ferreira, M. A. R., Willemsen, G., Gordon, S., Middelberg, R. P. S., McEvoy, B. P., . . . Whitfield, J. B. (2009). Common variants in TMPRSS6 are associated with iron status and erythrocyte volume. Nature genetics, 41(11), 1173-1175. DOI Scopus224 WoS214 Europe PMC201 |
| 2009 |
Benyamin, B., McRae, A. F., Zhu, G., Gordon, S., Henders, A. K., Palotie, A., . . . Visscher, P. M. (2009). Variants in TF and HFE explain ∼40% of genetic variation in serum-transferrin levels. American journal of human genetics, 84(1), 60-65. DOI Scopus153 WoS143 Europe PMC132 |
| 2008 |
Benyamin, B., Perola, M., Cornes, B. K., Madden, P. A. F., Palotie, A., Nyholt, D. R., . . . Visscher, P. M. (2008). Within-family outliers: segregating alleles or environmental effects? A linkage analysis of height from 5815 sibling pairs. European journal of human genetics, 16(4), 516-524. DOI Scopus11 WoS11 Europe PMC8 |
| 2008 |
Hasselbalch, A. L., Benyamin, B., Visscher, P. M., Heitmann, B. L., Kyvik, K. O., & Sørensen, T. I. A. (2008). Common genetic components of obesity traits and serum leptin. Obesity, 16(12), 2723-2729. DOI Scopus28 WoS26 Europe PMC25 |
| 2007 |
Visscher, P. M., Macgregor, S., Benyamin, B., Zhu, G., Gordon, S., Medland, S., . . . Martin, N. G. (2007). Genome partitioning of genetic variation for height from 11,214 sibling pairs. American Journal of Human Genetics, 81(5), 1104-1110. DOI Scopus121 WoS114 Europe PMC109 |
| 2007 |
Benyamin, B., Sørensen, T. I. A., Schousboe, K., Fenger, M., Visscher, P. M., & Kyvik, K. O. (2007). Are there common genetic and environmental factors behind the endophenotypes associated with the metabolic syndrome?. Diabetologia, 50(9), 1880-1888. DOI Scopus98 WoS99 Europe PMC87 |
| 2007 |
Fenger, M., Schousboe, K., Sorensen, T. I. A., & Kyvik, K. O. (2007). Variance decomposition of apolipoproteins and lipids in Danish twins. ATHEROSCLEROSIS, 191(1), 40-47. DOI WoS20 Europe PMC16 |
| 2007 |
Perola, M., Sammalisto, S., Hiekkalinna, T., Martin, N. G., Visscher, P. M., Montgomery, G. W., . . . Peltonen, L. (2007). Combined genome scans for body stature in 6,602 European twins: Evidence for common caucasian loci. Plos Genetics, 3(6), 1019-1028. DOI Scopus156 WoS145 Europe PMC124 |
| 2007 |
Benyamin, B., Martin, I. C. A., Cheung, C. C., Buckley, M. F., Thomson, P. C., Visscher, P. M., & Moran, C. (2007). Bodyweight QTL on mouse chromosomes 4 and 11 by selective genotyping: Regression v. maximum likelihood. Australian Journal of Experimental Agriculture, 47(6), 677-682. DOI Scopus1 WoS1 |
| 2006 |
Benyamin, B., Deary, I. J., & Visscher, P. M. (2006). Precision and bias of a normal finite mixture distribution model to analyze twin data when zygosity is unknown: simulations and application to IQ phenotypes on a large sample of twin pairs.. Behavior Genetics, 36(6), 935-946. DOI Scopus12 WoS9 Europe PMC10 |
| 2005 |
Benyamin, B., Wilson, V., Whalley, L. J., Visscher, P. M., & Deary, I. J. (2005). Large, consistent estimates of the heritability of cognitive ability in two entire populations of 11-year-old twins from Scottish Mental Surveys of 1932 and 1947. Behavior Genetics, 35(5), 525-534. DOI Scopus34 WoS36 Europe PMC27 |
| 2004 |
Visscher, P. M., Benyamin, B., & White, I. (2004). The use of linear mixed models to estimate variance components from data on twin pairs by maximum likelihood. Twin Research, 7(6), 670-674. DOI Scopus36 WoS36 Europe PMC36 |