Professor Lyle Palmer

Professor of Genetic Epidemiology

School of Public Health

College of Health

Eligible to supervise Masters and PhD - email supervisor to discuss availability.


Professor Lyle Palmer - Doctor of Philosophy with Distinction.Major Research Interests:1. Translational bioscience2. Machine learning applied to medicine3. Genetic epidemiology of complex diseases4. Population-based biobanking5. Life course genetic epidemiology

 

For details on projects available please view the following booklet: School of Public Health Student Projects

Date Position Institution name
2018 - ongoing Senior Research Fellow Australian Institute for Machine Learning
2017 - 2020 Chair, SA NT DataLink Steering Committee SA NT DataLink
2014 - ongoing Professor of Genetic Epidemiology University of Adelaide
2013 - 2014 Member The Ontario Vascular Health Knowledge Management Work Group
2012 - 2013 Member The Canadian Health Measures Survey Biobank Advisory Committee (CHMS-BAC)
2011 - 2014 Professor of Obstetrics and Gynecology University of Toronto
2010 - 2013 Member Arkansas Research Alliance
2010 - 2014 Executive Scientific Director The Ontario Health Study
2010 - 2014 Principal Investigator for Ontario The Canadian Partnership for Tomorrow Project
2010 - 2014 Senior Principal Investigator and Director of Genetic Epidemiology and Biostatistics Platform Ontario Institute for Cancer Research
2010 - 2014 Senior Investigator Samuel Lunenfeld Research Institute
2010 - 2014 Senior Scientist Cancer Care Ontario
2010 - 2014 Professor of Biostatistics and Professor of Epidemiology University of Toronto
2009 - ongoing Honorary Associate NHMRC Clinical Trials Centre, School of Public Heatlh
2009 - 2010 Winthrop Professor of Genetic Epidemiology University of Western Australia
2008 - 2010 Chair Australian Genomics and Clinical Outcomes of High Grade Glioma (AGOG) Project Executive Committee
2008 - 2010 Member of Management Committee Australian Cooperative Trials Group for Neuro-Oncology (COGNO)
2008 - 2010 Director University of Western Australia
2007 - 2011 Member, Scientific Advisory Board European Biobanking and Biomolecular Resources Infrastructure (BBMRI) Project
2007 - 2010 Member of Expert Reference Panel Australain Twins Register
2007 - 2010 Scientific Director The Busselton Healthy Ageing Study
2007 - 2007 Member of Biobanking Inventory Working Group WA Department of Health
2006 - 2010 Scientific Director University of Western Australia
2006 - 2010 Co-Director Universtiy of Westen Australia
2005 - ongoing Honourary Professorial Research Fellow, Genetic Epidemiology Bristol University
2005 - 2014 Member of Board of Directors International Public Population Project in Genomics (P3G)
2005 - 2010 Director University of Western Australia
2005 - 2009 Member, Western Australian Genetics Council WA Department of Health
2004 - 2010 Director University of Western Australia
2003 - 2009 Member of Program Committee International Genetic Epidemiology Society
2003 - ongoing Visiting Scientist Harvard T.H. Chan School of Public Health
2003 - 2010 Professor, Medicine University of Western Australia
2003 - 2010 Professor, Population Health University of Western Australia
2003 - 2010 Foundation Chair in Genetic Epidemiology [Endowed Chair] University of Western Australia
2003 - 2010 Director The Busselton Health Study Research Laboratory
2003 - 2009 Professor of Genetics, Epidemiology, Biostatistics (Adjunct) Case Western Reserve University
2003 - 2009 Scientific Director The Western Australian Genome Health Project
2002 - 2003 Member of Genetics, Molecular Biology and Epidemiology Committee American Academy of Asthma, Allergy and Inflammation
2002 - 2003 Member of Genetics Subcommittee Sleep Heart Health Study Steering Committee
2001 - 2006 Member of Education Committee International Genetic Epidemiology Society
2001 - 2004 Member of Assembly on Allergy, Immunology and Inflammation Program Committee American Thoracic Society (ATS)
2001 - 2003 Consultant Biostatistician Brigham and Women's Hospital
2000 - 2003 Director of Statistical Genomics and Project leader Harvard Medical School
2000 - 2003 Associate Epidemiologist Brigham and Women's Hospital
2000 - 2000 Visiting Fulbright Lecturer John Hopkins University
1999 - 2003 Assistant Professor of Medicine Harvard University
1999 - 2003 Principal Analyst International Consortium on Asthma Genetics (COAG)
1997 - 2010 Member, Board of Directors Busselton Population Research Foundation
1997 - 2010 Member, Scientific Advisory Committee Busselton Population Research Foundation
1997 - 2000 NHMRC Postdoctoral Research Fellow in Genetic Epidemiology Telethon Institute for Kids
1996 - 1999 Consultant Biostatistician University of Western Australia
1994 - 1994 President, Postgraduate Students Association University of Western Australia
1994 - 1994 Chair Council of Western Australian Postgraduate Associations

Date Type Title Institution Name Country Amount
2018 Achievement Listed as Highly Cited Researcher (Cross Field) Clarivate Analytics United States -
2011 Award Ori Rotstein Plenury Lecture University of Toronto - -
2008 Achievement Inaugural De La Salle College (Western Australia) Hall of Excellence Inductee. - - -
2007 Award Kevin Cullen Lecture - - -
2007 Award Named Inspirational Doctor Western Australian Medical Students' Society. - -
2007 Award Murray Clark Oration - - -
2007 Award Named as one of The Lord Mayor of Perth’s 2007 “One Hundred local champions.” - - -
2007 Award Fred Hollows Lecture - - -
2007 Award Vice Chancellors Research Prize University of Western Australia. - $10,000
2007 Achievement Biography included in Who’s Who in the World. - - -
2007 Achievement Biography included in Who’s Who in Australia. - - -
2007 Achievement Biography included in Who’s Who in Western Australia. - - -
2006 Award Awarded the Barbara Ell Lecture Victor Chang Cardiac Research Institute - -
2006 Award John Blandford Oration - - -
2005 Award Western Australian Business News “40 under 40” Award - - -
2005 Award Overall Winner, Western Australian Business News “40 under 40” Award. - - -
2005 Fellowship Leverhulme Visiting Fellowship Bristol University - -
2005 Award Named Lotterywest / Scoop Magazine 2005 Inspirational Western Australian. - - -
2005 Award Named Sunday Times 2005 Western Australian Leader - - -
2005 Nomination Nominated, Western Australian Citizen of the Year - - -
2003 Award Personal letter of congratulation on excellence of teaching for course Bio228 Harvard School of Public Health. - -
2002 Award Paper selected for showcasing as an “example of the focus and quality of the original research presented at the conference”, - - -
2002 Award Paper selected as one of 6 best papers published in Genetic Epidemiology in 2001 - - -
2001 Award Paper selected as one of 6 best papers published in 2000/2001 - - -
1999 Fellowship Churchill Fellowship - - -
1999 Fellowship Fulbright Fellowship (Postdoctoral) - - -
1998 Award Public Health Association of Australia (Western Australian Branch) Postgraduate Student Prize for Best Graduating Postgraduate Student, 1998 - - -
1997 Fellowship 1997-2000 National Health and Medical Research Council of Australia Postdoctoral Research Fellowship - - -
1996 Scholarship The Australian Lung Foundation/SensorMedics Travel Scholarship - - -
1996 Award The Allen & Hanburys Respiratory Medicine Research Award for Western Australia - - -
1995 Scholarship British Council Academic Exchange Scholar to Oxford University, UK - - -
1994 Award The Lillian Roxon Memorial Asthma Research Trust of Australia Award - - -
1994 Award Finalist, Royal Commonwealth of Nations Youth of the Year Award - - -
1993 Award Inaugural winner - - -
1993 Award National Health and Medical Research Council of Australia Postgraduate Medical Training Scholarship - - -
1993 Award The Convocation of the University of Western Australia Postgraduate Research Award - - -
1990 Award Malcolm Heywood McKenzie Cuff Prize in Anatomy - - -
1988 Award Archaeology Society of Western Australia Prize. - - -

Language Competency
English Can read, write, speak, understand spoken and peer review

Date Institution name Country Title
1998 University of Western Australia & Oxford University Australia/UK Doctor of Philosophy with Distinction - Genetic Epidemiology

Date Title Institution Country
1999 - 2000 Fulbright Fellow & Churchill Fellow Case Western Reserve University, Cleveland United States
1999 - 2000 Fulbright Fellow & Churchill Fellow Channing Laboratory, Harvard medical School United States
1997 - 2000 NHMRC Postdoctoral Research Fellow Telethon Kids Institute Australia

Year Citation
2025 Bampton, T. J., Chen, J. W., Brown, A., Barnett, M. I., Coates, P. T., & Palmer, L. J. (2025). Epidemiology and burden of adult chronic pancreatitis in South Australia: a 20-year data linkage study. BMJ Open, 15(3), e089297-1-e089297-7.
DOI
2025 Orsmond, A., Krishnan, G., Palmer, L. J., De Sousa, S. M. C., & McCormack, A. (2025). FGFR1 variation in the divergent settings of congenital hypopituitarism and pituitary tumours.. Pituitary, 28(2), 39.
DOI Scopus2 WoS2 Europe PMC1
2025 Whitbread, L., Laurenz, S., Palmer, L. J., & Jenkinson, M. (2025). Deep-Diffeomorphic Networks for Conditional Brain Templates. Human Brain Mapping, 46(8), e70229-1-e70229-18.
DOI
2025 Bird, A., Oakden-Rayner, L., Chakradeo, K., Thomas, R., Gupta, D., Jain, S., . . . Palmer, L. J. (2025). AI automated radiographic scoring in rheumatoid arthritis: Shedding light on barriers to implementation through comprehensive evaluation. Seminars in Arthritis and Rheumatism, 74, 152761.
DOI Scopus2 WoS1
2025 Otieno, L., Henderson, P., Khanna, S., Spurrier, N., Palmer, L. J., Hendrie, G., . . . Ryder, C. (2025). Co-designing a public health data analytics platform. . Nature medicine, 2 pages.
DOI
2025 Clark, S. R., Toben, C., Jawahar, M. C., Amare, A. T., Palmer, L. J., & Schubert, K. O. (2025). Infection, inflammation, and personalisation: time for an integrated approach to clozapine monitoring. Lancet Psychiatry, 12(9), 620-621.
DOI
2025 Nagarajan, P., Kurniansyah, N., Lee, J., Gharib, S. A., Xu, Y., Zhang, Y., . . . Wang, H. (2025). Genome-wide Gene by Sleepiness Interaction Analysis for Sleep Apnea.. Sleep, zsaf212.
DOI
2025 Pipicella, J. L., Gu, B., McNamara, J., Wilson, W., Palmer, L. J., Connor, S. J., & Andrews, J. M. (2025). Proposal and exploration of a novel score to quantify patient-perceived burden of inflammatory bowel disease under routine care.. Intern Med J, 55(4), 589-598.
DOI
2025 Chiam, T. L., Perkins, H., Hughes, T., Palmer, L., & Higgins, D. (2025). Palatal Morphology: A Systematic Review of the Association of Palatal Shape with Genetic Ancestry, Sex and Age. Archives of Oral Biology, 175, 106275-1-106275-22.
DOI
2025 Giri, J., Gurr, A., Bockmann, M., Palmer, L., Brook, A., & Hughes, T. (2025). Genetic and environmental contributions to the development of dental arch traits – a longitudinal twin study. European Journal of Orthodontics, 47(2), cjaf018-1-cjaf018-11.
DOI Scopus1 WoS1 Europe PMC1
2025 McCradden, M. D., London, A. J., Gichoya, J. W., Sendak, M., Erdman, L., Stedman, I., . . . Liu, X. (2025). CANAIRI: the Collaboration for Translational Artificial Intelligence Trials in healthcare.. Nat Med, 31(1), 9-11.
DOI Scopus7 WoS7 Europe PMC5
2025 Chiam, T., Gurr, A., Hughes, T., Palmer, L., & Higgins, D. (2025). Variation in the three-dimensional shape of the human hard palate and its association with population affinity: a geometric morphometrics study. Forensic Science International.
2025 Giri, J., Gurr, A., Bockmann, M., Palmer, L., Brook, A., & Hughes, T. (2025). Genetic and environmental influences on dental arch shape during childhood: a longitudinal twin study. Orthodontics and Craniofacial Research.
2025 Berry, J. G., Taranath, A., Goetti, R., Farrar, M. A., Fiori, S., Pham, H. -D., . . . van Eyk, C. L. (2025). Genetic diagnostic yield by MRI pattern in children with cerebral palsy: a population-based study.. EBioMedicine, 122, 106013.
DOI
2025 Mordaunt, D. A., Johnson, N., Verghese, S., Parker, R., Gibb, K., & Palmer, L. J. (2025). Navigating medication safety with electronic medical records: insights from a dual-phase implementation in paediatric, neonatal and maternity care. Australian Health Review A Publication of the Australian Hospital Association, 49(6), AH24344.
DOI
2025 Wang, X., Bampton, T. J., Dharmaprani, D., Mahajan, R., & Palmer, L. J. (2025). Machine learning and deep learning predictive models for prognosis in patients with atrial fibrillation: a systematic review and meta-analysis. BMJ Digital Health & AI, 1(1), e000154.
DOI
2024 Bird, A., Oakden-Rayner, L., Smith, L. A., Zeng, M., Ray, S., Proudman, S., & Palmer, L. J. (2024). Prognostic modeling in early rheumatoid arthritis: reconsidering the predictive role of disease activity scores.. Clin Rheumatol, 43(5), 1503-1512.
DOI
2024 Condon, J. J. J., Trinh, V., Hall, K. A., Reintals, M., Holmes, A. S., Oakden-Rayner, L., & Palmer, L. J. (2024). Impact of Transfer Learning Using Local Data on Performance of a Deep Learning Model for Screening Mammography.. Radiology. Artificial intelligence, 6(4), e230383.
DOI Scopus3 WoS3 Europe PMC3
2024 Giri, J., Bockmann, M., Brook, A., Gurr, A., Brook O'Donnell, M., & Hughes, T. (2024). Relative contributions of genetic and environmental factors to palatal morphology: a longitudinal twin study. European Journal of Orthodontics, 47(1), cjae076-1-cjae076-10.
DOI Scopus1 WoS1 Europe PMC1
2024 Nagarajan, P., Kurniansyah, N., Lee, J., Gharib, S. A., Xu, Y., Zhang, Y., . . . Wang, H. (2024). Gene-Excessive Sleepiness Interactions Suggest Treatment Targets for Obstructive Sleep Apnea Subtype.. medRxiv.
DOI
2024 Zeng, M., Smith, L., Bird, A., Trinh, V. Q. -N., Bacchi, S., Harvey, J., . . . Palmer, L. J. (2024). Predictions for functional outcome and mortality in acute ischaemic stroke following successful endovascular thrombectomy.. BMJ Neurol Open, 6(1), e000707.
DOI Scopus3 WoS3 Europe PMC2
2024 McMichael, G., Cusack, L., Andina Munawar, D., Boyd, M., Palmer, L., Lim, H. S., & Mahajan, R. (2024). Atrial Fibrillation Health Literacy Questionnaire (AFHLQ): The development of an AF-specific health literacy questionnaire. IJC Heart & Vasculature, 50, 101322.
DOI Scopus2 Europe PMC2
2023 Crawford, G. B., Lakhani, A., Palmer, L., Sebalj, M., & Rolan, P. (2023). A systematic review of qualitative research exploring patient and health professional perspectives of breakthrough cancer pain.. Supportive care in cancer : official journal of the Multinational Association of Supportive Care in Cancer, 31(12), 1-10.
DOI Scopus6 WoS5 Europe PMC3
2023 Smith, L. A., Oakden-Rayner, L., Bird, A., Zeng, M., To, M. -S., Mukherjee, S., & Palmer, L. J. (2023). Machine learning and deep learning predictive models for long-term prognosis in patients with chronic obstructive pulmonary disease: a systematic review and meta-analysis.. Lancet Digit Health, 5(12), e872-e881.
DOI Scopus58 WoS47 Europe PMC41
2022 Bird, A., Oakden-Rayner, L., McMaster, C., Smith, L. A., Zeng, M., Wechalekar, M. D., . . . Palmer, L. J. (2022). Artificial intelligence and the future of radiographic scoring in rheumatoid arthritis: a viewpoint. Arthritis Research & Therapy, 24(1), 1-10.
DOI Scopus24 WoS22 Europe PMC14
2022 Chun, S., Akle, S., Teodosiadis, A., Cade, B. E., Wang, H., Sofer, T., . . . Sunyaev, S. R. (2022). Leveraging pleiotropy to discover and interpret GWAS results for sleep-associated traits.. PLoS genetics, 18(12), 34 pages.
DOI Scopus10 WoS9 Europe PMC16
2022 Bampton, T. J., Couper, R. T. L., Khurana, S., Moore, D. J., Brown, A., Drogemuller, C. J., . . . Palmer, L. J. (2022). The epidemiology and burden of childhood chronic pancreatitis in South Australia. Journal of Pediatrics, 242, 93-98.
DOI Scopus2 WoS1 Europe PMC1
2022 Thompson, P. L., Hui, J., Beilby, J., Palmer, L. J., Watts, G. F., West, M. J., . . . Tonkin, A. M. (2022). Common genetic variants do not predict recurrent events in coronary heart disease patients. BMC Cardiovascular Disorders, 22(1), 1-9.
DOI Scopus1 WoS1 Europe PMC1
2022 Marriott, R. J., McArdle, N., Singh, B., King, S., Ling, I., Ward, K., . . . Cadby, G. (2022). The changing profile of obstructive sleep apnea: long term trends in characteristics of patients presenting for diagnostic polysomnography. Sleep Science, 15(Spec 1), 28-40.
DOI Scopus7 WoS4 Europe PMC4
2022 Oakden-Rayner, L., Gale, W., Bonham, T. A., Lungren, M. P., Carneiro, G., Bradley, A. P., & Palmer, L. J. (2022). Validation and algorithmic audit of a deep learning system for the detection of proximal femoral fractures in patients in the emergency department: a diagnostic accuracy study.. Lancet Digit Health, 4(5), e351-e358.
DOI Scopus68 WoS62 Europe PMC49
2022 Wu, D., Bampton, T. J., Scott, H. S., Brown, A., Kassahn, K., Drogemuller, C., . . . Coates, P. T. (2022). The clinical and genetic features of hereditary pancreatitis in South Australia.. Medical Journal of Australia, 216(11), 578-582.
DOI Scopus7 WoS5 Europe PMC4
2022 Gichoya, J. W., Banerjee, I., Bhimireddy, A. R., Burns, J. L., Celi, L. A., Chen, L. -C., . . . Zhang, H. (2022). AI recognition of patient race in medical imaging: a modelling study.. The Lancet. Digital health, 4(6), E406-E414.
DOI Scopus394 WoS312 Europe PMC243
2022 Liang, J., Wang, H., Cade, B. E., Kurniansyah, N., He, K. Y., Lee, J., . . . TOPMed Sleep Working Group. (2022). Targeted Genome Sequencing Identifies Multiple Rare Variants in Caveolin-1 Associated with Obstructive Sleep Apnea.. Am J Respir Crit Care Med, 206(10), 1271-1280.
DOI Scopus10 WoS7 Europe PMC8
2022 Kirsh, V. A., Skead, K., McDonald, K., Kreiger, N., Little, J., Menard, K., . . . Awadalla, P. (2022). Cohort Profile: The Ontario Health Study (OHS).. Int J Epidemiol, 52(2), E137-E151.
DOI Scopus6 WoS8 Europe PMC7
2022 Zeng, M., Oakden-Rayner, L., Bird, A., Smith, L., Wu, Z., Scroop, R., . . . Palmer, L. J. (2022). Pre-thrombectomy prognostic prediction of large-vessel ischemic stroke using machine learning: A systematic review and meta-analysis. Frontiers in Neurology, 13, 14 pages.
DOI Scopus13 WoS14 Europe PMC10
2021 Lagou, V., Mägi, R., Hottenga, J. -J., Grallert, H., Perry, J. R. B., Bouatia-Naji, N., . . . Meta-Analyses of Glucose and Insulin-related traits Consortium (MAGIC). (2021). Sex-dimorphic genetic effects and novel loci for fasting glucose and insulin variability.. Nature communications, 12(1), 24.
DOI Scopus121 WoS124 Europe PMC117
2021 Lagou, V., Mägi, R., Hottenga, J. -J., Grallert, H., Perry, J. R. B., Bouatia-Naji, N., . . . Meta-Analyses of Glucose and Insulin-related traits Consortium (MAGIC). (2021). Publisher Correction: Sex-dimorphic genetic effects and novel loci for fasting glucose and insulin variability.. Nature communications, 12(1), 995.
DOI Scopus5 WoS6 Europe PMC6
2021 Scheetz, J., Rothschild, P., McGuinness, M., Hadoux, X., Soyer, H. P., Janda, M., . . . van Wijngaarden, P. (2021). A survey of clinicians on the use of artificial intelligence in ophthalmology, dermatology, radiology and radiation oncology. Scientific Reports, 11(1), 5193-1-5193-10.
DOI Scopus164 WoS153 Europe PMC135
2021 Wang, H., Noordam, R., Cade, B. E., Schwander, K., Winkler, T. W., Lee, J., . . . van Heemst, D. (2021). Multi-ancestry genome-wide gene-sleep interactions identify novel loci for blood pressure.. Molecular psychiatry, 26(11), 6293-6304.
DOI Scopus21 WoS17 Europe PMC19
2021 Bampton, T. J., Holmes-Walker, D. J., Drogemuller, C. J., Radford, T., Anderson, P., Etherton, C., . . . Australian Islet Consortium. (2021). Australian experience with total pancreatectomy with islet autotransplantation to treat chronic pancreatitis. ANZ Journal of Surgery, 91(12), 2663-2668.
DOI Scopus6 WoS4 Europe PMC5
2021 Condon, J. J. J., Oakden-Rayner, L., Hall, K. A., Reintals, M., Holmes, A., Carneiro, G., & Palmer, L. J. (2021). Replication of an open-access deep learning system for screening mammography: Reduced performance mitigated by retraining on local data.
DOI
2021 Banerjee, I., Bhimireddy, A. R., Burns, J. L., Celi, L. A., Chen, L. -C., Correa, R., . . . Gichoya, J. W. (2021). Reading Race: AI Recognises Patient's Racial Identity In Medical Images.. CoRR, abs/2107.10356.
2021 Cade, B. E., Lee, J., Sofer, T., Wang, H., Zhang, M., Chen, H., . . . TOPMed Sleep Working Group. (2021). Whole-genome association analyses of sleep-disordered breathing phenotypes in the NHLBI TOPMed program. Genome Med, 13(1), 136-1-136-17.
DOI Scopus21 WoS22 Europe PMC24
2021 Shenoy, B., Singh, B., Dhaliwal, S. S., King, S., Rea, S. C., Ling, I. T., . . . McArdle, N. (2021). Cohort profile: The Western Australian Sleep health study, a prospective sleep clinic cohort study. Sleep Epidemiology, 1, 100010.
DOI Scopus3
2020 Loffler, K. A., Heeley, E., Freed, R., Meng, R., Bittencourt, L. R., Gonzaga Carvalho, C. C., . . . SAVE Substudy Investigators. (2020). Continuous positive airway pressure treatment, glycemia, and diabetes risk in obstructive sleep apnea and comorbid cardiovascular disease. Diabetes Care, 43(8), 1-9.
DOI Scopus43 WoS39 Europe PMC34
2020 Singh, M., Hall, K. A., Reynolds, A., Palmer, L. J., & Mukherjee, S. (2020). The Relationship of Sleep Duration with Ethnicity and Chronic Disease in a Canadian General Population Cohort. NATURE AND SCIENCE OF SLEEP, 12, 239-251.
DOI Scopus20 WoS15 Europe PMC14
2020 Pham, R., Mol, B. W., Gecz, J., MacLennan, A. H., MacLennan, S. C., Corbett, M. A., . . . Berry, J. G. (2020). Definition and diagnosis of cerebral palsy in genetic studies: a systematic review. Developmental Medicine and Child Neurology, 62(9), 1024-1030.
DOI Scopus31 WoS31 Europe PMC28
2020 Hall, K. A., Singh, M., Mukherjee, S., & Palmer, L. J. (2020). Physical Activity is Associated With Reduced Prevalence of Self-Reported Obstructive Sleep Apnea in a Large, General Population Cohort Study.. Journal of clinical sleep medicine : JCSM : official publication of the American Academy of Sleep Medicine, 16(7), 1179-1187.
DOI Scopus34 WoS30 Europe PMC36
2019 Liang, J., Cade, B. E., He, K. Y., Wang, H., Lee, J., Sofer, T., . . . Zhu, X. (2019). Sequencing Analysis at 8p23 Identifies Multiple Rare Variants in DLC1 Associated with Sleep-Related Oxyhemoglobin Saturation Level. American Journal of Human Genetics, 105(5), 1057-1068.
DOI Scopus9 WoS7 Europe PMC7
2019 Alves, A. C., De Silva, N. M. G., Karhunen, V., Sovio, U., Das, S., Rob Taal, H., . . . Järvelin, M. R. (2019). GWAS on longitudinal growth traits reveals different genetic factors influencing infant, child, and adult BMI. Science Advances, 5(9), 1-17.
DOI Scopus100 WoS92 Europe PMC105
2019 Smith, G., Gujari, D., Russell, O., Palmer, L., Toews, M., Wong, G., . . . Coates, P. T. (2019). International travel by Australians for overseas transplantation. Medical Journal of Australia, 211(10), 460.
DOI Scopus1 WoS1 Europe PMC1
2019 Cade, B. E., Chen, H., Stilp, A. M., Louie, T., Ancoli-Israel, S., Arens, R., . . . Redline, S. (2019). Associations of variants in the hexokinase 1 and interleukin 18 receptor regions with oxyhemoglobin saturation during sleep. PLoS Genetics, 15(4), 31 pages.
DOI Scopus31 WoS26 Europe PMC34
2019 Liu, C. T., Merino, J., Rybin, D., DiCorpo, D., Benke, K. S., Bragg-Gresham, J. L., . . . Bouatia-Naji, N. (2019). Genome-wide Association Study of Change in Fasting Glucose over time in 13,807 non-diabetic European Ancestry Individuals. Scientific Reports, 9(1), 9439-1-9439-8.
DOI Scopus5 WoS6 Europe PMC5
2019 Akle, S., Chun, S., Teodosiadis, A., Cade, B., Wang, H., Sofer, T., . . . Sunyaev, S. (2019). Leveraging pleiotropy to discover and interpret GWAS results for sleep-associated traits.
DOI
2018 Gale, W., Oakden-Rayner, L., Carneiro, G., Bradley, A. P., & Palmer, L. J. (2018). Producing radiologist-quality reports for interpretable artificial intelligence.. CoRR, abs/1806.00340.
2018 Ligthart, S., Vaez, A., Võsa, U., Stathopoulou, M. G., de Vries, P. S., Prins, B. P., . . . Morris, A. P. (2018). Genome Analyses of >200,000 Individuals Identify 58 Loci for Chronic Inflammation and Highlight Pathways that Link Inflammation and Complex Disorders. American Journal of Human Genetics, 103(5), 691-706.
DOI Scopus318 WoS311 Europe PMC341
2018 Oakden-Rayner, L., Beam, A. L., & Palmer, L. J. (2018). Medical journals should embrace preprints to address the reproducibility crisis. International Journal of Epidemiology, 47(5), 1363-1365.
DOI Scopus13 WoS8 Europe PMC6
2018 Dummer, T. J. B., Awadalla, P., Boileau, C., Craig, C., Fortier, I., Goel, V., . . . Zawati, M. (2018). The Canadian Partnership for Tomorrow Project: A pan-Canadian platform for research on chronic disease prevention. CMAJ, 190(23), E710-E717.
DOI Scopus84 WoS81 Europe PMC77
2018 Chen, H., Cade, B., Gleason, K., Bjonnes, A., Stilp, A., Sofer, T., . . . Redline, S. (2018). Multi-ethnic Meta-analysis Identifies RAI1 as a Possible Obstructive Sleep Apnea Related Quantitative Trait Locus in Men.. American journal of respiratory cell and molecular biology, 58(3), 391-401.
DOI Scopus74 WoS67 Europe PMC66
2018 Mukherjee, S., Saxena, R., & Palmer, L. J. (2018). The genetics of obstructive sleep apnoea.. Respirology (Carlton, Vic.), 23(1), 18-27.
DOI Scopus81 WoS62 Europe PMC58
2017 Graff, M., Scott, R. A., Justice, A. E., Young, K. L., Feitosa, M. F., Barata, L., . . . Faul, J. D. (2017). Erratum: Correction: Genome-wide physical activity interactions in adiposity - A meta-analysis of 200,452 adults (PLoS genetics (2017) 13 4 (e1006528)). Plos Genetics, 13(8), e1006972.
DOI Scopus7 Europe PMC4
2017 Loffler, K., Heeley, E., Freed, R., Anderson, C., Brockway, B., Corbett, A., . . . McEvoy, R. (2017). Effect of obstructive sleep apnea treatment on renal function in patients with cardiovascular disease. American journal of respiratory and critical care medicine, 196(11), 1456-1462.
DOI Scopus38 WoS37 Europe PMC28
2017 Robinson, M. R., Kleinman, A., Graff, M., Vinkhuyzen, A. A., Couper, D., Miller, M. B., . . . Visscher, P. M. (2017). Genetic evidence of assortative mating in humans. Nature Human Behaviour, 1(1), 0016.
DOI
2017 Winkler, T., Justice, A., Cupples, L., Kronenberg, F., Kutalik, Z., & Heid, I. (2017). Approaches to detect genetic effects that differ between two strata in genome-wide meta-analyses: Recommendations based on a systematic evaluation. PLOS ONE, 12(7), e0181038.
DOI
2017 Shungin, D., Deng, W., Varga, T., Luan, J., Mihailov, E., Metspalu, A., . . . Franks, P. (2017). Ranking and characterization of established BMI and lipid associated loci as candidates for gene-environment interactions. PLOS Genetics, 13(6), 1-15.
DOI Scopus21 Europe PMC24
2017 Gale, W., Oakden-Rayner, L., Carneiro, G., Bradley, A. P., & Palmer, L. J. (2017). Detecting hip fractures with radiologist-level performance using deep neural networks.. CoRR, abs/1711.06504.
2017 Song, C., Burgess, S., Eicher, J., O'Donnell, C., Johnson, A., Huang, J., . . . Smith, A. (2017). Causal effect of plasminogen activator inhibitor type 1 on coronary heart disease. Journal of the American Heart Association, 6(6), e004918-1-e004918-24.
DOI Scopus108 WoS104 Europe PMC87
2017 Justice, A., Winkler, T., Feitosa, M., Graff, M., Fisher, V., Young, K., . . . Cupples, L. (2017). Genome-wide meta-analysis of 241,258 adults accounting for smoking behaviour identifies novel loci for obesity traits. Nature Communications, 8(1), 14977-1-14977-19.
DOI Scopus152 WoS155 Europe PMC161
2017 Graff, M., Scott, R., Justice, A., Young, K., Feitosa, M., Barata, L., . . . Adair, L. (2017). Genome-wide physical activity interactions in adiposity ― A meta-analysis of 200,452 adults. PLoS Genetics, 13(4), e1006528-1-e1006528-26.
DOI Scopus163 WoS152 Europe PMC147
2017 Oakden-Rayner, L., Carneiro, G., Bessen, T., Nascimento, J., Bradley, A., & Palmer, L. (2017). Precision Radiology: Predicting longevity using feature engineering and deep learning methods in a radiomics framework. Scientific Reports, 7(1), 13 pages.
DOI Scopus126 WoS105 Europe PMC82
2017 De Silva, M., Sebert, S., Alves, A. C., Sovio, U., Das, S., Taal, R., . . . Järvelin, M. -R. (2017). Genetic architecture of early childhood growth phenotypes gives insights into their link with later obesity. biorxiv, 40 pages.
DOI
2017 Hinney, A., Kesselmeier, M., Jall, S., Volckmar, A. -L., Foecker, M., Antel, J., . . . Hebebrand, J. (2017). Evidence for three genetic loci involved in both anorexia nervosa risk and variation of body mass index. Molecular Psychiatry, 22(2), 192-201.
DOI Scopus54 WoS39 Europe PMC34
2017 Hinney, A., Kesselmeier, M., Jall, S., Volckmar, A. -L., Foecker, M., Antel, J., . . . Hebebrand, J. (2017). Evidence for three genetic loci involved in both anorexia nervosa risk and variation of body mass index. Molecular Psychiatry, 22(2), 192-201.
DOI Scopus54 WoS39 Europe PMC34
2016 Winkler, T. W., Justice, A. E., Graff, M., Barata, L., Feitosa, M. F., Chu, S., . . . Loos, R. J. (2016). The Influence of Age and Sex on Genetic Associations with Adult Body Size and Shape: A Large-Scale Genome-Wide Interaction Study (vol 11, e1005378, 2015). PLOS GENETICS, 12(6), 1-3.
DOI Scopus13 WoS12 Europe PMC11
2016 Pattaro, C., Teumer, A., Gorski, M., Chu, A., Li, M., Mijatovic, V., . . . Ernst, F. (2016). Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function. Nature Communications, 7(1), 1-19.
DOI Scopus425 WoS418 Europe PMC415
2016 Parmar, P. G., Taal, H. R., Timpson, N. J., Thiering, E., Lehtimäki, T., Marinelli, M., . . . Palmer, L. J. (2016). International genome-wide association study consortium identifies novel loci associated with blood pressure in children and adolescents. Circulation: Cardiovascular Genetics, 9(3), 266-278.
DOI Scopus36 WoS34 Europe PMC36
2016 Shrine, N., Tobin, M., Schurmann, C., Artigas, M., Hui, J., Lehtimäki, T., . . . Wain, L. (2016). Genome-wide association study of copy number variation with lung function identifies a novel signal of association near BANP for forced vital capacity. BMC Genetics, 17(1), 8 pages.
DOI
2016 McEvoy, R., Antic, N., Heeley, E., Luo, Y., Ou, Q., Zhang, X., . . . Anderson, C. (2016). CPAP for prevention of cardiovascular events in obstructive sleep apnea. New England Journal of Medicine, 375(10), 919-931.
DOI Scopus1749 WoS1537 Europe PMC1314
2016 Ried, J., Jeff, J., Chu, A., Bragg-Gresham, J., Van Dongen, J., Huffman, J., . . . Campbell, H. (2016). A principal component meta-analysis on multiple anthropometric traits identifies novel loci for body shape. Nature Communications, 7(1), 13357-1-13357-11.
DOI Scopus64 WoS62 Europe PMC67
2015 Winkler, T., Justice, A., Graff, M., Barata, L., Feitosa, M., Chu, S., . . . Kleber, M. (2015). The influence of age and sex on genetic associations with adult body size and shape: a large-scale genome-wide interaction study. PLoS Genetics, 11(10), e1005378-1-e1005378-42.
DOI Scopus311 WoS305 Europe PMC305
2015 Edwards, C., Mukherjee, S., Simpson, L., Palmer, L., Almeida, O., & Hillman, D. (2015). Depressive symptoms before and after treatment of obstructive sleep apnea in men and women. Journal of Clinical Sleep Medicine, 11(9), 1029-1038.
DOI Scopus117 WoS99 Europe PMC87
2015 Simpson, L., McArdle, N., Eastwood, P., Ward, K., Cooper, M., Wilson, A., . . . Mukherjee, S. (2015). Physical inactivity is associated with moderate-severe obstructive sleep apnea. Journal of Clinical Sleep Medicine, 11(10), 1091-1099A.
DOI Scopus50 WoS46 Europe PMC40
2015 Matullo, G., Guarrera, S., Betti, M., Fiorito, G., Ferrante, D., Voglino, F., . . . Dianzani, I. (2015). Erratum: Genetic variants associated with increased risk of malignant pleural mesothelioma: A genome-wide association study (PLoS ONE (2015) 8:4 (e61253) DOI: 10.1371/journal.pone.0061253). Plos One, 10(6), 2 pages.
DOI WoS1 Europe PMC1
2015 Kardan, O., Gozdyra, P., Misic, B., Moola, F., Palmer, L., Paus, T., & Berman, M. (2015). Neighborhood greenspace and health in a large urban center. Scientific Reports, 5(1), 11610-1-11610-14.
DOI Scopus376 WoS324 Europe PMC123
2015 Ward, K., McArdle, N., James, A., Bremner, A., Simpson, L., Cooper, M., . . . Hillman, D. (2015). A comprehensive evaluation of a two-channel portable monitor to "rule in" obstructive sleep apnea. Journal of Clinical Sleep Medicine, 11(4), 433-444.
DOI Scopus38 WoS34 Europe PMC30
2015 Warrington, N., Howe, L., Paternoster, L., Kaakinen, M., Herrala, S., Huikari, V., . . . Palmer, L. (2015). A genome-wide association study of body mass index across early life and childhood. International Journal of Epidemiology, 44(2), 700-712.
DOI Scopus108 WoS104 Europe PMC103
2015 Hansen, J. G., Gao, W., Dupuis, J., O'Connor, G. T., Tang, W., Kowgier, M., . . . Cassano, P. A. (2015). Association of 25-Hydroxyvitamin D status and genetic variation in the vitamin D metabolic pathway with FEV(1) in the Framingham Heart Study. Respiratory Research, 16(1), 81-1-81-8.
DOI Scopus15 WoS13 Europe PMC15
2015 Shungin, D., Winkler, T. W., Croteau-Chonka, D. C., Ferreira, T., Locke, A. E., Mägi, R., . . . Zhang, W. (2015). New genetic loci link adipose and insulin biology to body fat distribution. Nature, 518(7538), 187-197.
DOI Scopus1266 WoS1238 Europe PMC1250
2015 Ward, S., Dowty, J., Webster, R., Cadby, G., Glasson, E., Heyworth, J., . . . Palmer, L. (2015). The aggregation of early-onset melanoma in young Western Australian families. Cancer Epidemiology, 39(3), 346-352.
DOI Scopus2 WoS2 Europe PMC1
2015 Palmer, L., Briggs, C., McFadden, S., Zini, G., Burthem, J., Rozenberg, G., . . . Machin, S. J. (2015). ICSH recommendations for the standardization of nomenclature and grading of peripheral blood cell morphological features. INTERNATIONAL JOURNAL OF LABORATORY HEMATOLOGY, 37(3), 287-303.
DOI WoS190
2014 Palmer, L. J., Dias, D. A., Boughton, B., Roessner, U., Graham, R. D., & Stangoulis, J. C. R. (2014). Metabolite profiling of wheat (Triticum aestivum L.) phloem exudate. PLANT METHODS, 10(1), 9 pages.
DOI WoS31 Europe PMC22
2014 de Zeeuw, E., van Beijsterveldt, C., Glasner, T., Bartels, M., Ehli, E., Davies, G., . . . Joshi, P. (2014). Polygenic scores associated with educational attainment in adults predict educational achievement and ADHD symptoms in children. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, 165(6), 510-520.
DOI Scopus37 Europe PMC30
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 Scopus53 WoS50 Europe PMC49
2014 Saeed, S., Golfam, M., Beall, R., Ashbury, F., Palmer, L., & Little, J. (2014). Effectiveness of individual-focused interventions to prevent chronic disease. European Journal of Clinical Investigation, 44(9), 882-890.
DOI Scopus5 WoS5 Europe PMC5
2014 Ashbury, F. D., Little, J., Ioannidis, J. P. A., Kreiger, N., Palmer, L. J., Relton, C., & Taylor, P. (2014). A vision for chronic disease prevention and intervention research: report from a workshop. Canadian Journal of Public Health, 105(2), e150-e153.
DOI Scopus5 WoS4 Europe PMC4
2014 Winkler, T. W., Day, F. R., Croteau-Chonka, D. C., Wood, A. R., Locke, A. E., Maegi, R., . . . Loos, R. J. F. (2014). Quality control and conduct of genome-wide association meta-analyses. Nature Protocols, 9(5), 1192-1212.
DOI WoS344 Europe PMC394
2014 Winkler, T. W., Day, F. R., Croteau-Chonka, D. C., Wood, A. R., Locke, A. E., Maegi, R., . . . Loos, R. J. F. (2014). Quality control and conduct of genome-wide association meta-analyses. Nature Protocols, 9(5), 1192-1212.
DOI WoS344 Europe PMC394
2014 Tang, W., Kowgier, M., Loth, D., Soler Artigas, M., Joubert, B., Hodge, E., . . . Strachan, D. (2014). Large-scale genome-wide association studies and meta-analyses of longitudinal change in adult lung function. PLoS One, 9(7), e100776-1-e100776-13.
DOI Scopus53 WoS49 Europe PMC49
2014 Simino, J., Shi, G., Bis, J., Chasman, D., Ehret, G., Gu, X., . . . Rao, D. (2014). Gene-age interactions in blood pressure regulation: a large-scale investigation with the CHARGE, global BPgen, and ICBP consortia. American Journal of Human Genetics, 95(1), 24-38.
DOI Scopus97 WoS94 Europe PMC93
2014 Benke, K., Nivard, M., Velders, F., Walters, R., Pappa, I., Scheet, P., . . . Middeldorp, C. (2014). A genome-wide association meta-analysis of preschool internalizing problems. Journal of the American Academy of Child & Adolescent Psychiatry, 53(6), 667-676.e7.
DOI Scopus53 WoS44 Europe PMC40
2014 Cadby, G., Ward, S., Cole, J., Moses, E., Millward, M., & Palmer, L. (2014). The association of host and genetic melanoma risk factors with Breslow thickness in the Western Australian Melanoma Health Study. British Journal of Dermatology, 170(4), 851-857.
DOI Scopus12 WoS12 Europe PMC9
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 Scopus204 WoS185 Europe PMC179
2013 Adams, L., White, S., Marsh, J., Lye, S., Connor, K., Maganga, R., . . . Pennell, C. (2013). Association between liver-specific gene polymorphisms and their expression levels with nonalcoholic fatty liver disease. Hepatology, 57(2), 590-600.
DOI Scopus73 WoS66 Europe PMC58
2013 Cadby, G., Mukherjee, S., Musk, A., Reid, A., Garlepp, M., Dick, I., . . . Palmer, L. (2013). A genome-wide association study for malignant mesothelioma risk. Lung Cancer, 82(1), 1-8.
DOI Scopus46 WoS39 Europe PMC36
2013 Benke, K., Wu, Y., Fallin, D., Maher, B., & Palmer, L. (2013). Strategy to control type I error increases power to identify genetic variation using the full biological trajectory. Genetic Epidemiology, 37(5), 419-430.
DOI Scopus2 WoS2 Europe PMC1
2013 Vimaleswaran, K., & Palmer, L. (2013). Causal relationship between obesity and vitamin D status: bi-directional Mendelian randomization analysis of multiple cohorts. PLoS Medicine, 10(2), 1001383-1-1001383-1 3.
DOI Scopus823 WoS611 Europe PMC659
2013 Dastani, Z., & Palmer, L. (2013). Novel loci for adiponectin levels and their influence on type 2 diabetes and metabolic traits: A multi-ethnic meta-analysis of 45,891 individuals. PLoS Genetics, 8(3), e1002607.1-e1002607.23.
DOI Scopus407 WoS382 Europe PMC375
2013 Simpson, L., Hillman, D., Cooper, M., Ward, K., Hunter, M., Cullen, S., . . . Eastwood, P. (2013). High prevalence of undiagnosed obstructive sleep apnoea in the general population and methods for screening for representative controls. Sleep and Breathing, 17(3), 967-973.
DOI Scopus117 WoS112 Europe PMC103
2013 Warrington, N., Wu, Y., Pennell, C., Marsh, J., Beilin, L., Palmer, L., . . . Briollais, L. (2013). Modelling BMI trajectories in children for genetic association studies. PLoS One, 8(1), e53897-1-e53897-12.
DOI Scopus29 WoS26 Europe PMC24
2013 Peters, K., Beilby, J., Cadby, G., Warrington, N., Bruce, D., Davis, W., . . . Hung, J. (2013). A comprehensive investigation of variants in genes encoding adiponectin (ADIPOQ) and its receptors (ADIPOR1/R2), and their association with serum adiponectin, type 2 diabetes, insulin resistance and the metabolic syndrome. BMC Medical Genetics, 14(1), 15-1-15-12.
DOI Scopus70 WoS63 Europe PMC58
2013 de Klerk, N., Alfonso, H., Olsen, N., Reid, A., Sleith, J., Palmer, L., . . . Musk, A. (2013). Familial aggregation of malignant mesothelioma in former workers and residents of Wittenoom, Western Australia. International Journal of Cancer, 132(6), 1423-1428.
DOI Scopus44 WoS38 Europe PMC28
2013 Melen, E., & Palmer, L. (2013). Genome-wide association study of body mass index in 23 000 individuals with and without asthma. Clinical and Experimental Allergy, 43(4), 463-474.
DOI Scopus68 WoS64 Europe PMC50
2013 Cousminer, D., Berry, D., Timpson, N., Ang, W., Thiering, E., Byrne, E., . . . Palmer, L. (2013). Genome-wide association and longitudinal analyses reveal genetic loci linking pubertal height growth, pubertal timing and childhood adiposity. Human Molecular Genetics, 22(13), 2735-2747.
DOI Scopus165 WoS156 Europe PMC152
2013 James, A., Hunter, M., Straker, L., Beilby, J., Bucks, R., Davis, T., . . . Busselton Healthy Ageing Study (BHAS) Investigator Group. (2013). Rationale, design and methods for a community-based study of clustering and cumulative effects of chronic disease processes and their effects on ageing: the Busselton healthy ageing study. BMC Public Health, 13(1), 1-12.
DOI Scopus59 WoS57 Europe PMC49
2013 Ward, K., Hillman, D., James, A., Bremner, A., Simpson, L., Cooper, M., . . . Mukherjee, S. (2013). Excessive daytime sleepiness increases the risk of motor vehicle crash in obstructive sleep apnea. Journal of Clinical Sleep Medicine, 9(10), 1013-1021.
DOI Scopus121 WoS110 Europe PMC83
2013 Parmar, P., Marsh, J., Rob Taal, H., Kowgier, M., Uitterlinden, A., Rivadeneira, F., . . . Pennell, C. (2013). Polymorphisms in genes within the IGF-axis influence antenatal and postnatal growth. Journal of Developmental Origins of Health and Disease, 4(2), 157-169.
DOI Scopus1 WoS1 Europe PMC2
2013 Evans, D., Brion, M., Paternoster, L., Kemp, J., McMahon, G., Munafo, M., . . . Smith, G. (2013). Mining the human phenome using allelic scores that index biological intermediates. PLoS Genetics, 9(10), e1003919-1-e1003919-15.
DOI Scopus60 WoS52 Europe PMC62
2013 Warrington, N., Howe, L., Wu, Y., Timpson, N., Tilling, K., Pennell, C., . . . Briollais, L. (2013). Association of a body mass index genetic risk score with growth throughout childhood and adolescence. PLoS One, 8(11), e79547-1-e79547-10.
DOI Scopus49 WoS48 Europe PMC48
2013 Howe, L., Parmar, P., Paternoster, L., Warrington, N., Kemp, J., Briollais, L., . . . Lawlor, D. (2013). Genetic influences on trajectories of systolic blood pressure across childhood and adolescence. Circulation: Cardiovascular Genetics, 6(6), 608-614.
DOI Scopus29 WoS27 Europe PMC29
2013 Ikram, M. A., Fornage, M., Smith, A. V., Seshadri, S., Schmidt, R., Debette, S., . . . DeCarli, C. (2013). Erratum: Common variants at 6q22 and 17q21 are associated with intracranial volume (Nature Genetics (2012) 44 (539-544)). Nature Genetics, 45(6), 713.
DOI
2013 Taal, H. R., St Pourcain, B., Thiering, E., Das, S., Mook-Kanamori, D. O., Warrington, N. M., . . . Jaddoe, V. W. V. (2013). Erratum: Common variants at 12q15 and 12q24 are associated with infant head circumference (Nature Genetics (2012) 44 (532-538)). Nature Genetics, 45(6), 713.
DOI Scopus1 WoS1
2013 Le-Niculescu, H., Levey, D. F., Ayalew, M., Palmer, L., Gavrin, L. M., Jain, N., . . . Niculescu, A. B. (2013). Discovery and validation of blood biomarkers for suicidality. MOLECULAR PSYCHIATRY, 18(12), 1249-1264.
DOI WoS139
2012 Hamilton, G., Killick, R., Lambert, J. -C., Amouyel, P., Carrasquillo, M. M., Pankratz, V. S., . . . Wade-Martins, R. (2012). Functional and genetic analysis of haplotypic sequence variation at the nicastrin genomic locus. NEUROBIOLOGY OF AGING, 33(8), 13 pages.
DOI WoS6 Europe PMC4
2012 Ikram, M. A., Fornage, M., Smith, A. V., Seshadri, S., Schmidt, R., Debette, S., . . . Decarli, C. (2012). Erratum: Common variants at 6q22 and 17q21 are associated with intracranial volume (Nature Genetics (2012) 44 (539-544)). Nature Genetics, 44(6), 732.
DOI Scopus12
2012 Ikram, M. A., Fornage, M., Smith, A. V., Seshadri, S., Schmidt, R., Debette, S., . . . DeCarli, C. (2012). Common variants at 6q22 and 17q21 are associated with intracranial volume (vol 44, pg 539, 2012). NATURE GENETICS, 44(6), 732.
DOI
2012 Palmer, L., Hogan, N., & van den Heuvel, M. (2012). Phylogenetic analysis and molecular methods for the detection of lymphocystis disease virus from yellow perch, Perca flavescens (Mitchell). JOURNAL OF FISH DISEASES, 35(9), 661-670.
DOI WoS23 Europe PMC17
2012 Marsh, J., Pennell, C., Warrington, N., Mook-Kanamori, D., Briollais, L., Lye, S., . . . Palmer, L. (2012). Fat mass and obesity-associated obesity-risk genotype is associated with lower foetal growth: an effect that is reversed in the offspring of smoking mothers. Journal of Developmental Origins of Health and Disease, 3(1), 10-20.
DOI Scopus10 WoS10 Europe PMC9
2012 Paternoster, L., & Palmer, L. (2012). Meta-analysis of genome-wide association studies identifies three new risk loci for atopic dermatitis. Nature Genetics, 44(2), 187-192.
DOI Scopus303 WoS271 Europe PMC232
2012 Mukherjee, S., Hillman, D., Lee, J., Fedson, A., Simpson, L., Ward, K., . . . Palmer, L. (2012). Cohort profile: the Western Australian Sleep Health Study. Sleep and Breathing, 16(1), 205-215.
DOI Scopus15 WoS14 Europe PMC15
2012 Boraska, V., & Palmer, L. (2012). Genome-wide association study to identify common variants associated with brachial circumference: a meta-analysis of 14 cohorts. PLoS One, 7(3), e31369-1-e31369-10.
DOI Scopus2 WoS3 Europe PMC1
2012 Ikram, M., Fornage, M., Smith, A., Seshadri, S., Schmidt, R., Debette, S., . . . Uitterlinden, A. (2012). Common variants at 6q22 and 17q21 are associated with intracranial volume. Nature Genetics, 44(5), 539-544.
DOI Scopus100 WoS112 Europe PMC114
2012 Bradfield, J., Taal, H., Timpson, N., Scherag, A., Lecoeur, C., Warrington, N., . . . St Pourcain, B. (2012). A genome-wide association meta-analysis identifies new childhood obesity loci. Nature Genetics, 44(5), 526-531.
DOI Scopus341 WoS322 Europe PMC312
2012 Louise, S., Warrington, N., McCaskie, P., Oddy, W., Zubrick, S., Hands, B., . . . Beilin, L. (2012). Associations between anxious-depressed symptoms and cardiovascular risk factors in a longitudinal childhood study. Preventive Medicine, 54(5), 345-350.
DOI Scopus18 WoS17 Europe PMC15
2012 Ward, S., Cadby, G., Heyworth, J., Fear, M., Wallace, H., Cole, J., . . . Palmer, L. (2012). Association of TGFβ1 and clinical factors with scar outcome following melanoma excision. Archives of Dermatological Research, 304(5), 343-351.
DOI Scopus9 WoS8 Europe PMC3
2012 Louise, S., Warrington, N., McCaskie, P., Oddy, W., Zubrick, S., Hands, B., . . . Beilin, L. (2012). Associations between aggressive behaviour scores and cardiovascular risk factors in childhood. Pediatric Obesity, 7(4), 319-328.
DOI Scopus10 WoS9 Europe PMC10
2012 Adams, L., Marsh, J., Ayonrinde, O., Olynyk, J., Ang, W., Beilin, L., . . . Pennell, C. (2012). Cholesteryl ester transfer protein gene polymorphisms increase the risk of fatty liver in females independent of adiposity. Journal of Gastroenterology and Hepatology, 27(9), 1520-1527.
DOI Scopus37 WoS33 Europe PMC30
2012 Yang, J., Loos, R., Powell, J., Medland, S., Speliotes, E., Chasman, D., . . . Wang, S. (2012). FTO genotype is associated with phenotypic variability of body mass index. Nature, 490(7419), 267-273.
DOI Scopus348 WoS323 Europe PMC347
2012 Patel, S., Goodloe, R., De, G., Kowgier, M., Weng, J., Buxbaum, S., . . . Redline, S. (2012). Association of genetic loci with sleep apnea in European Americans and African-Americans: the Candidate Gene Association resource (CARe). PLoS One, 7(11), e48836-1108-e48836-1117.
DOI Scopus57 WoS54 Europe PMC47
2012 Palmer, N., McDonough, C., Hicks, P., Roh, B., Wing, M., Sandy An, S., . . . Adeyemo, A. (2012). A genome-wide association search for type 2 diabetes genes in African Americans. PLoS One, 7(1), e29202-1-e29202-14.
DOI Scopus149 WoS133 Europe PMC120
2012 Harris, J., Burton, P., Knoppers, B., Lindpaintner, K., Bledsoe, M., Brookes, A., . . . Zatloukal, K. (2012). Toward a roadmap in global biobanking for health. European Journal of Human Genetics, 20(11), 1105-1111.
DOI Scopus130 WoS121 Europe PMC93
2012 Palmer, L., Fox, C. S., Liu, Y., White, C. C., Feitosa, M., Smith, A. V., . . . Garcia, M. (2012). Genome-wide association for abdominal subcutaneous and visceral adipose reveals a novel locus for visceral fat in women. PLoS Genetics, 8(5), e1002695-1-e1002695-14.
DOI WoS216 Europe PMC213
2012 Palmer, L., Manning, A. K., Hivert M-, F., Scott, R. A., Grimsby, J. L., Bouatia-Naji, N., . . . Lahti, J. (2012). A genome-wide approach accounting for body mass index identifies genetic variants influencing fasting glycemic traits and insulin resistance. Nature Genetics, 44(6), 659-669.
DOI Scopus667 WoS647 Europe PMC659
2012 Taal, H., St Pourcain, B., Thiering, E., Das, S., Mook-Kanamori, D., Warrington, N., . . . Chawes, B. (2012). Common variants at 12q15 and 12q24 are associated with infant head circumference. Nature Genetics, 44(5), 532-538.
DOI Scopus99 WoS102 Europe PMC107
2011 Chambers, J., & Palmer, L. (2011). Genome-wide association study identifies loci influencing concentrations of liver enzymes in plasma. Nature Genetics, 43(11), 1131-1138.
DOI Scopus466 WoS449 Europe PMC448
2011 Zhu, H., Shyh-Chang, N., Segre, A., Shinoda, G., Shah, S., Einhorn, W., . . . Daley, G. (2011). The Lin28/let-7 axis regulates glucose metabolism. Cell, 147(1), 81-94.
DOI WoS762 Europe PMC707
2011 Wain, L., Verwoert, L., O'Reilly, P., Shi, G., Johnson, T., Johnson, A., . . . Jackson, A. (2011). Genome-wide association study identifies six new loci influencing pulse pressure and mean arterial pressure. Nature Genetics, 43(10), 1005-1011.
DOI Scopus373 WoS342 Europe PMC335
2011 Artigas, M., Loth, D., Wain, L., Gharib, S., Obeidat, M., Tang, W., . . . Barroso, I. (2011). Genome-wide association and large-scale follow up identifies 16 new loci influencing lung function. Nature Genetics, 43(11), 1082-1090.
DOI Scopus358 WoS311 Europe PMC331
2011 International Consortium for Blood Pressure Genome-Wide Association Studies. (2011). Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk. Nature, 478(7367), 103-109.
DOI Scopus1763 WoS1623 Europe PMC1512
2011 Strawbridge, R., Dupuis, J., Prokopenko, I., Barker, A., Ahlqvist, E., Rybin, D., . . . Palmer, L. (2011). Genome-wide association identifies nine common variants associated with fasting proinsulin levels and provides new insights into the pathophysiology of type 2 diabetes. Diabetes, 60(10), 2624-2634.
DOI Scopus306 WoS286 Europe PMC277
2011 Fox, E., Young, J., Li, Y., Dreisbach, A., Keating, B., Musani, S., . . . Levy, D. (2011). Association of genetic variation with systolic and diastolic blood pressure among African Americans: the Candidate Gene Association Resource Study. Human Molecular Genetics, 20(11), 2273-2284.
DOI WoS135 Europe PMC126
2011 Jamrozik, E., Warrington, N., McClenaghan, J., Hui, J., Musk, A., James, A., . . . Palmer, L. (2011). Functional haplotypes in the PTGDR gene fail to associate with asthma in two Australian populations. Respirology, 16(2), 359-366.
DOI Scopus11 WoS10 Europe PMC7
2011 Sovio, U., Mook-Kanamori, D., Warrington, N., Lawrence, R., Briollais, L., Palmer, C., . . . Early Growth Genetics Consortium. (2011). Association between common variation at the FTO locus and changes in body mass index from infancy to late childhood: the complex nature of genetic association through growth and development. PLoS Genetics, 7(2), e1001307-1-e1001307-13.
DOI Scopus164 WoS150 Europe PMC151
2011 C Reactive Protein Coronary Heart Disease Genetics Collaboration (CCGC). (2011). Association between C reactive protein and coronary heart disease: mendelian randomisation analysis based on individual participant data. BMJ, 342(7794), d548-1-d548-8.
DOI Scopus266 WoS495 Europe PMC474
2011 Golledge, J., Biros, E., Warrington, N., Jones, G., Cooper, M., van Rij, A., . . . Norman, P. (2011). A population-based study of polymorphisms in genes related to sex hormones and abdominal aortic aneurysm. European Journal of Human Genetics, 19(3), 363-366.
DOI Scopus6 WoS6 Europe PMC6
2011 Kilpelainen, T., den Hoed, M., Ong, K., Grontved, A., Brage, S., Early Growth Genetics Consortium., . . . Loos, R. (2011). Obesity-susceptibility loci have a limited influence on birth weight: A meta-analysis of up to 28,219 individuals. American Journal of Clinical Nutrition, 93(4), 851-860.
DOI Scopus55 WoS51 Europe PMC43
2011 Mook-Kanamori, D., Marsh, J., Warrington, N., Taal, H., Newnham, J., Beilin, L., . . . Jaddoe, V. (2011). Variants near CCNL1/LEKR1 and in ADCY5 and fetal growth characteristics in different trimesters. Journal of Clinical Endocrinology and Metabolism, 96(5), 810-815.
DOI Scopus19 WoS19 Europe PMC20
2011 Obeidat, M., Wain, L., Shrine, N., Kalsheker, N., Soler Artigas, M., Repapi, E., . . . Hadley, D. (2011). A comprehensive evaluation of potential lung function associated genes in the SpiroMeta general population sample. PLoS One, 6(5), e19382-online.
DOI Scopus51 WoS50 Europe PMC41
2011 Barker, A., Sharp, S., Timpson, N., Bouatia-Naji, N., Warrington, N., Kanoni, S., . . . Ntalla, I. (2011). Association of genetic loci with glucose levels in childhood and adolescence: a meta-analysis of over 6,000 children. Diabetes, 60(6), 1805-1812.
DOI Scopus102 WoS97 Europe PMC92
2011 Richardson, C., Hogan, A., Bucks, R., Baya, A., Virues-Ortega, J., Holloway, J., . . . Baldeweg, T. (2011). Neurophysiological evidence for cognitive and brain functional adaptation in adolescents living at high altitude. Clinical Neurophysiology, 122(9), 1726-1734.
DOI Scopus40 WoS37 Europe PMC33
2011 Ward, S., Cadby, G., Lee, A., Cole, J., Heyworth, J., Millward, M., . . . Palmer, L. (2011). The Western Australian Melanoma Health Study: study design and participant characteristics. Cancer Epidemiology, 35(5), 423-431.
DOI Scopus10 WoS10 Europe PMC10
2011 Artigas, M., Wain, L., Repapi, E., Obeidat, M., Sayers, I., Burton, P., . . . Barroso, I. (2011). Effect of five genetic variants associated with lung function on the risk of chronic obstructive lung disease, and their joint effects on lung function. American Journal of Respiratory and Critical Care Medicine, 184(7), 786-795.
DOI Scopus125 WoS123 Europe PMC117
2011 Gracie, S., Pennell, C., Ekman-Ordeberg, G., Lye, S., McManaman, J., Williams, S., . . . Gravett, M. (2011). An integrated systems biology approach to the study of preterm birth using "-omic" technology - a guideline for research. BMC Pregnancy and Childbirth, 11(71), 71-1-71-12.
DOI Scopus64 WoS54 Europe PMC49
2011 Musk, A., Knuiman, M., Hunter, M., Hui, J., Palmer, L., Beilby, J., . . . James, A. (2011). Patterns of airway disease and the clinical diagnosis of asthma in the Busselton population. European Respiratory Journal, 38(5), 1053-1059.
DOI Scopus14 WoS13 Europe PMC13
2011 Webster, R., Carter, K., Warrington, N., Loh, A., Zaloumis, S., Kuijpers, T., . . . Burgner, D. (2011). Hospitalisation with infection, asthma and allergy in Kawasaki disease patients and their families: Genealogical analysis using linked population data. PLoS One, 6(11), e28004-1-e28004-7.
DOI Scopus27 WoS25 Europe PMC20
2011 Heid, I. M., Jackson, A. U., Randall, J. C., Winkler, T. W., Qi, L., Steinthorsdottir, V., . . . Tammesoo, M. L. (2011). Erratum: Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution (Nature Genetics (2010) 42 (949-960)). Nature Genetics, 43(11), 1164.
DOI Scopus9 WoS9
2011 Brion, M. -J. A., Robinson, M., Matijasevich, A., Steer, C., Anselimi, L., Menezes, A. M. B., . . . Lawlor, D. A. (2011). Maternal Prenatal Smoking and Child Aggression: Exploring Intrauterine Effects in UK, Australian and Brazilian Cohorts. JOURNAL OF DEVELOPMENTAL ORIGINS OF HEALTH AND DISEASE, 2, S43.
2011 Fortier, I., Doiron, D., Little, J., Ferretti, V., L'Heureux, F., Stolk, R. P., . . . Burton, P. R. (2011). Is rigorous retrospective harmonization possible? Application of the DataSHaPER approach across 53 large studies. INTERNATIONAL JOURNAL OF EPIDEMIOLOGY, 40(5), 1314-1328.
DOI WoS73 Europe PMC70
2011 Ferreira, M. A. R., Matheson, M. C., Duffy, D. L., Marks, G. B., Hui, J., Le Souëf, P., . . . Kemp, A. S. (2011). Identification of IL6R and chromosome 11q13.5 as risk loci for asthma. Lancet, 378(9795), 1006-1014.
DOI Scopus325 WoS313 Europe PMC288
2011 Ferreira, M. A. R., Matheson, M. C., Duffy, D. L., Marks, G. B., Hui, J., Le Souëf, P., . . . Kemp, A. S. (2011). Identification of IL6R and chromosome 11q13.5 as risk loci for asthma. Lancet, 378(9795), 1006-1014.
DOI Scopus325 WoS313 Europe PMC288
2011 Groves, M. D., DeGroot, J., Tremont, I., Forman, A., Kang, S., Pei, B. -L., . . . Bachoo, R. (2011). ONGOING CLINICAL TRIALS. Neuro-oncology, 13(Suppl 3), iii85-iii91.
DOI Europe PMC1
2011 Kraja, A. T., Vaidya, D., Pankow, J. S., Goodarzi, M. O., Assimes, T. L., Kullo, I. J., . . . Borecki, I. B. (2011). A bivariate genome-wide approach to metabolic syndrome: STAMPEED Consortium. Diabetes, 60(4), 1329-1339.
DOI Scopus221 Europe PMC181
2011 Beauchamp, J. P., Cesarini, D., Johannesson, M., van der Loos, M. J. H. M., Koellinger, P. D., Groenen, P. J. F., . . . Christakis, N. A. (2011). Molecular Genetics and Economics. JOURNAL OF ECONOMIC PERSPECTIVES, 25(4), 57-82.
DOI WoS72 Europe PMC30
2010 Köttgen, A., Pattaro, C., Böger, C. A., Fuchsberger, C., Olden, M., Glazer, N. L., . . . Vitart, V. (2010). New loci associated with kidney function and chronic kidney disease. Nature Genetics, 42(5), 376-384.
DOI Scopus717 Europe PMC653
2010 Levy, D., Neuhausen, S. L., Hunt, S. C., Kimura, M., Hwang, S. J., Chen, W., . . . Aviv, A. (2010). Genome-wide association identifies OBFC1 as a locus involved in human leukocyte telomere biology. Proceedings of the National Academy of Sciences of the United States of America, 107(20), 9293-9298.
DOI Scopus235 Europe PMC210
2010 Dupuis, J., Langenberg, C., Prokopenko, I., Saxena, R., Soranzo, N., Jackson, A. U., . . . Hadjadj, S. (2010). Erratum: New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk (Nature Genetics (2010) 42 (105-116)). Nature Genetics, 42(5), 464.
DOI Scopus16 WoS7
2010 Moffatt, M. F., Gut, I. G., Demenais, F., Strachan, D. P., Bouzigon, E., Heath, S., . . . Cookson, W. O. (2010). A Large-Scale, Consortium-Based Genomewide Association Study of Asthma. NEW ENGLAND JOURNAL OF MEDICINE, 363(13), 1211-1221.
DOI WoS1593 Europe PMC1465
2010 Moran, C., Clancy, P., Biros, E., Blanco-Martin, B., McCaskie, P., Palmer, L., . . . Golledge, J. (2010). Association of PPARγ allelic variation, osteoprotegerin and abdominal aortic aneurysm. Clinical Endocrinology, 72(1), 128-132.
DOI Scopus29 WoS28 Europe PMC26
2010 Sofat, R., Hingorani, A., Smeeth, L., Humphries, S., Talmud, P., Cooper, J., . . . Van Gilst, W. (2010). Separating the mechanism-based and off-target actions of cholesteryl ester transfer protein inhibitors with CETP gene polymorphisms. Circulation, 121(1), 52-62.
DOI Scopus84 WoS81 Europe PMC77
2010 Repapi, E., Sayers, I., Wain, L., Burton, P., Johnson, T., Obeidat, M., . . . Loos, R. (2010). Genome-wide association study identifies five loci associated with lung function. Nature Genetics, 42(1), 36-44.
DOI Scopus492 WoS470 Europe PMC439
2010 James, A., Knuiman, M., Divitini, M., Hui, J., Hunter, M., Palmer, L., . . . Musk, A. (2010). Changes in the prevalence of asthma in adults since 1966: the Busselton health study. European Respiratory Journal, 35(2), 273-278.
DOI Scopus74 WoS69 Europe PMC58
2010 Chandler, D., Dragovic, M., Cooper, M., Badcock, J., Mullin, B., Faulkner, D., . . . Jablensky, A. (2010). Impact of Neuritin 1 (NRN1) polymorphisms on fluid intelligence in schizophrenia. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, 153(2), 428-437.
DOI Scopus27 WoS27 Europe PMC22
2010 Golledge, J., Biros, E., Cooper, M., Warrington, N., Palmer, L., & Norman, P. (2010). Apolipoprotein E genotype is associated with serum C-reactive protein but not abdominal aortic aneurysm. Atherosclerosis, 209(2), 487-491.
DOI Scopus25 WoS23 Europe PMC18
2010 Simpson, L., Mukherjee, S., Cooper, M., Ward, K., Lee, J., Fedson, A., . . . Kirkness, J. (2010). Sex differences in the association of regional fat distribution with the severity of obstructive sleep apnea. Sleep, 33(4), 467-474.
DOI Scopus155 WoS139 Europe PMC114
2010 Eastwood, P., Malhotra, A., Palmer, L., Kezirian, E., Horner, R., Ip, M., . . . Hillman, D. (2010). Obstructive sleep apnoea: from pathogenesis to treatment: current controversies and future directions. Respirology, 15(4), 587-595.
DOI Scopus91 WoS71 Europe PMC60
2010 Freathy, R., Mook-Kanamori, D., Sovio, U., Prokopenko, I., Timpson, N., Berry, D., . . . Bennett, A. (2010). Variants in ADCY5 and near CCNL1 are associated with fetal growth and birth weight. Nature Genetics, 42(5), 430-435.
DOI Scopus206 WoS195 Europe PMC179
2010 Hogan, A., Virues-Ortega, J., Botti, A., Bucks, R., Holloway, J., Rose-Zerilli, M., . . . Kirkham, F. (2010). Development of aptitude at altitude. Developmental Science, 13(3), 533-544.
DOI Scopus42 WoS40 Europe PMC35
2010 Thompson, S., Burgess, S., & CRP CHD Genetics Collaboration. (2010). Bayesian methods for meta-analysis of causal relationships estimated using genetic instrumental variables. Statistics in Medicine, 29(12), 1298-1311.
DOI Scopus23 WoS22 Europe PMC16
2010 Biros, E., Cooper, M., Palmer, L., Walker, P., Norman, P., & Golledge, J. (2010). Association of an allele on chromosome 9 and abdominal aortic aneurysm. Atherosclerosis, 212(2), 539-542.
DOI Scopus27 WoS22 Europe PMC21
2010 Fortier, I., Burton, P., Robson, P., Ferretti, V., Little, J., L'Heureux, F., . . . Parker, L. (2010). Quality, quantity and harmony: The DataSHaPER approach to integrating data across bioclinical studies. International Journal of Epidemiology, 39(5), 1383-1393.
DOI Scopus157 WoS132 Europe PMC124
2010 Webster, R., Warrington, N., Beilby, J., Frayling, T., & Palmer, L. (2010). The longitudinal association of common susceptibility variants for type 2 diabetes and obesity with fasting glucose level and BMI. BMC Medical Genetics, 11(1), 140-1-140-10.
DOI Scopus17 WoS16 Europe PMC12
2010 Elks, C., Perry, J., Sulem, P., Chasman, D., Franceschini, N., He, C., . . . Palmer, L. (2010). Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies. Nature Genetics, 42(12), 1077-1085.
DOI Scopus444 WoS412 Europe PMC363
2010 Speliotes, E., & Palmer, L. (2010). Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index. Nature Genetics, 42(11), 937-948.
DOI Scopus2475 WoS2275 Europe PMC2193
2010 Heid, I., Jackson, A., Randall, J., Winkler, T., Qi, L., Steinthorsdottir, V., . . . Moffatt, M. (2010). Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution. Nature Genetics, 42(11), 949-960.
DOI Scopus819 WoS751 Europe PMC737
2010 Allen, H., Estrada, K., Lettre, G., Berndt, S., Weedon, M., Rivadeneira, F., . . . Winkler, T. (2010). Hundreds of variants clustered in genomic loci and biological pathways affect human height. Nature, 467(7317), 832-838.
DOI Scopus1600 WoS1499 Europe PMC1426
2010 Dupuis, J., & Palmer, L. (2010). New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk. Nature Genetics, 42(2), 105-116.
DOI Scopus1862 WoS1766 Europe PMC1701
2009 Webster, R., Warrington, N., Weedon, M., Hattersley, A., McCaskie, P., Beilby, J., . . . Frayling, T. (2009). The association of common genetic variants in the APOA5, LPL and GCK genes with longitudinal changes in metabolic and cardiovascular traits. Diabetologia, 52(1), 106-114.
DOI Scopus28 WoS26 Europe PMC25
2009 Daly, D., Lemire, M., Akhabir, L., Chan-Yeung, M., He, J., McDonald, T., . . . Hudson, T. (2009). Analyses of associations with asthma in four asthma population samples from Canada and Australia. Human Genetics, 125(4), 445-459.
DOI Scopus102 WoS98 Europe PMC89
2009 Gudbjartsson, D., Bjornsdottir, U., Halapi, E., Helgadottir, A., Sulem, P., Jonsdottir, G., . . . Wheatley, A. (2009). Sequence variants affecting eosinophil numbers associate with asthma and myocardial infarction. Nature Genetics, 41(3), 342-347.
DOI Scopus667 WoS618 Europe PMC577
2009 Golledge, J., Clancy, P., Jones, G., Cooper, M., Palmer, L., van Rij, A., & Norman, P. (2009). Possible association between genetic polymorphisms in transforming growth factor β receptors, serum transforming growth factor β1 concentration and abdominal aortic aneurysm. British Journal of Surgery, 96(6), 628-632.
DOI Scopus26 WoS25 Europe PMC20
2009 McClenaghan, J., Warrington, N., Jamrozik, E., Hui, J., Beilby, J., Hansen, J., . . . Palmer, L. (2009). The PHF11 gene is not associated with asthma or asthma phenotypes in two independent populations. Thorax, 64(7), 620-625.
DOI Scopus8 WoS7 Europe PMC7
2009 Smallwood, L., Warrington, N., Allcock, R., van Bockxmeer, F., Palmer, L., Iacopetta, B., . . . Norman, P. (2009). Matrix metalloproteinase-2 gene variants and abdominal aortic aneurysm. European Journal of Vascular and Endovascular Surgery, 38(2), 169-171.
DOI Scopus10 WoS10 Europe PMC8
2009 Feng, X., Xiao, J., Longville, B., Tan, A., Wu, X., Cooper, M., . . . Constable, I. (2009). Complement factor H Y402H and C-reactive protein polymorphism and photodynamic therapy response in age-related macular degeneration. Ophthalmology, 116(10), 1908-1912.e1.
DOI Scopus57 WoS44 Europe PMC39
2009 Bosse, Y., Lemire, M., Poon, A., Daly, D., He, J., Stanford, A., . . . Laprise, C. (2009). Asthma and genes encoding components of the vitamin D pathway. Respiratory Research, 10(1), 98-1-98-21.
DOI Scopus124 WoS114 Europe PMC100
2009 Golledge, J., Biros, E., Clancy, P., Cooper, M., Palmer, L., & Norman, P. (2009). A single-nucleotide polymorphism in the gene encoding osteoprotegerin is associated with diastolic blood pressure in older men. American Journal of Hypertension, 22(11), 1167-1170.
DOI Scopus7 WoS6 Europe PMC5
2009 Ferreira, M., Hottenga, J., Warrington, N., Medland, S., Willemsen, G., Lawrence, R., . . . Boomsma, D. (2009). Sequence variants in three loci influence monocyte counts and erythrocyte volume. American Journal of Human Genetics, 85(5), 745-749.
DOI Scopus70 WoS68 Europe PMC66
2009 Heard-Costa, N. L., Carola Zillikens, M., Monda, K. L., Johansson, A., Harris, T. B., Fu, M., . . . North, K. E. (2009). NRXN3Is a novel locus for waist circumference: A genome-wide association study from the CHARGE consortium. Plos Genetics, 5(6), e1000539.
DOI Scopus235 Europe PMC198
2009 Zhang, Q., Ding, L., Larson, D. E., Koboldt, D. C., McLellan, M. D., Chen, K., . . . Province, M. A. (2009). CMDS: A population-based method for identifying recurrent DNA copy number aberrations in cancer from high-resolution data. Bioinformatics, 26(4), 464-469.
DOI Scopus55 Europe PMC46
2009 Srinivasan, B. S., Chen, J., Cheng, C., Conti, D., Duan, S., Fridley, B. L., . . . Ritchie, M. D. (2009). Methods for analysis in pharmacogenomics: Lessons from the Pharmacogenetics Research Network Analysis group. Pharmacogenomics, 10(2), 243-251.
DOI Scopus10 Europe PMC7
2009 Perez-Martinez, P., Corella, D., Shen, J., Arnett, D. K., Yiannakouris, N., Tai, E. S., . . . Ordovas, J. M. (2009). Association between glucokinase regulatory protein (GCKR) and apolipoprotein A5 (APOA5) gene polymorphisms and triacylglycerol concentrations in fasting, postprandial, and fenofibrate-treated states. American Journal of Clinical Nutrition, 89(1), 391-399.
DOI Scopus52 Europe PMC39
2008 Kimura, M., Cherkas, L. F., Kato, B. S., Demissie, S., Hjelmborg, J. B., Brimacombe, M., . . . Aviv, A. (2008). Offspring's leukocyte telomere length, paternal age, and telomere elongation in sperm. Plos Genetics, 4(2), e37.
DOI Scopus231 Europe PMC191
2008 Ding, L., Getz, G., Wheeler, D. A., Mardis, E. R., McLellan, M. D., Cibulskis, K., . . . Wilson, R. K. (2008). Somatic mutations affect key pathways in lung adenocarcinoma. Nature, 455(7216), 1069-1075.
DOI Scopus2357 Europe PMC1980
2008 CRP CHD Genetics Collaboration., Danesh, J., Hingorani, A., Wensley, F., Casas, J., & Smeeth, L. (2008). Collaborative pooled analysis of data on C-reactive protein gene variants and coronary disease: judging causality by Mendelian randomization. European Journal of Epidemiology, 23(8), 531-540.
DOI WoS45 Europe PMC42
2008 Smallwood, L., Allcock, R., van Bockxmeer, F., Warrington, N., Palmer, L., Iacopetta, B., & Norman, P. (2008). Polymorphisms of the interleukin-6 gene promoter and abdominal aortic aneurysm. European Journal of Vascular and Endovascular Surgery, 35(1), 31-36.
DOI Scopus37 WoS31 Europe PMC26
2008 Glasson, E., de Klerk, N., Bass, A., Rosman, D., Palmer, L., & Holman, C. (2008). Cohort profile: the Western Australian Family Connections Genealogical Project. International Journal of Epidemiology, 37(1), 30-35.
DOI Scopus45 WoS40 Europe PMC30
2008 Musk, A., James, A., Palmer, L., Ryan, G., Lake, F., Golledge, C., & de Klerk, N. (2008). Respiratory infections and lung function in an Australian Aboriginal community. Respirology, 13(2), 257-262.
DOI Scopus10 WoS10 Europe PMC9
2008 Hui, J., Oka, A., James, A., Palmer, L., Musk, A., Beilby, J., & Inoko, H. (2008). A genome-wide association scan for asthma in a general Australian population. Human Genetics, 123(3), 297-306.
DOI Scopus16 WoS15 Europe PMC14
2008 Wiltshire, S., Powell, B., Jennens, M., McCaskie, P., Carter, K., Palmer, L., . . . Beilby, J. (2008). Investigating the association between K198N coding polymorphism in EDN1 and hypertension, lipoprotein levels, the metabolic syndrome and cardiovascular disease. Human Genetics, 123(3), 307-313.
DOI Scopus15 WoS12 Europe PMC13
2008 Loh, A., Wiltshire, S., Emery, J., Carter, K., & Palmer, L. (2008). Celestial3D: a novel method for 3D visualization of familial data. Bioinformatics, 24(9), 1210-1211.
DOI Scopus8 WoS10 Europe PMC3
2008 Gallego, P., Shephard, N., Bulsara, M., van Bockxmeer, F., Powell, B., Beilby, J., . . . Choong, C. (2008). Angiotensinogen gene T235 variant: a marker for the development of persistent microalbuminuria in children and adolescents with type 1 diabetes mellitus. Journal of Diabetes and Its Complications, 22(3), 191-198.
DOI Scopus20 WoS16 Europe PMC13
2008 McCaskie, P., Beilby, J., Hung, J., Chapman, C., McQuillan, B., Powell, B., . . . Palmer, L. (2008). 15-lipoxygenase gene variants are associated with carotid plaque but not carotid intima-media thickness. Human Genetics, 123(5), 445-453.
DOI Scopus15 WoS15 Europe PMC14
2008 Xiao, J., Zhang, F., Wiltshire, S., Hung, J., Jennens, M., Beilby, J., . . . Powell, B. (2008). The apolipoprotein AII rs5082 variant is associated with reduced risk of coronary artery disease in an Australian male population. Atherosclerosis, 199(2), 333-339.
DOI Scopus32 WoS28 Europe PMC23
2008 Carter, K., Hung, J., Powell, B., Wiltshire, S., Foo, B., Leow, Y., . . . Palmer, L. (2008). Association of Interleukin-1 gene polymorphisms with central obesity and metabolic syndrome in a coronary heart disease population. Human Genetics, 124(3), 199-206.
DOI Scopus37 WoS33 Europe PMC23
2008 Powell, B., Wiltshire, S., Arscott, G., McCaskie, P., Hung, J., McQuillan, B., . . . Beilby, J. (2008). Association of PARL rs3732581 genetic variant with insulin levels, metabolic syndrome and coronary artery disease. Human Genetics, 124(3), 263-270.
DOI Scopus5 WoS6 Europe PMC5
2008 Smallwood, L., Allcock, R., van Bockxmeer, F., Warrington, N., Palmer, L., Iacopetta, B., . . . Norman, P. (2008). Polymorphisms of the matrix metalloproteinase 9 gene and abdominal aortic aneurysm. British Journal of Surgery, 95(10), 1239-1244.
DOI Scopus27 WoS23 Europe PMC20
2008 Peters, K., Wiltshire, S., Henders, A., Dragovic, M., Badcock, J., Chandler, D., . . . Jablensky, A. (2008). Comprehensive analysis of tagging sequence variants in DTNBP1 shows no association with schizophrenia or with its composite neurocognitive endophenotypes. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, 147(7), 1159-1166.
DOI Scopus30 WoS26 Europe PMC25
2008 Carter, K., McCaskie, P., & Palmer, L. (2008). SimHap GUI: an intuitive graphical user interface for genetic association analysis. BMC Bioinformatics, 9(1), 557-1-557-6.
DOI Scopus34 WoS34 Europe PMC28
2008 Lawlor, D., Harbord, R., Timpson, N., Lowe, G., Rumley, A., Gaunt, T., . . . Davey-Smith, G. (2008). The association of C-reactive protein and CRP genotype with coronary heart disease: findings from five studies with 4610 cases amongst 18637 participants. PLoS One, 3(8), 1-14.
DOI Scopus90 WoS77 Europe PMC71
2007 Golledge, J., Muller, J., Shephard, N., Clancy, P., Smallwood, L., Moran, C., . . . Norman, P. E. (2007). Association between osteopontin and human abdominal aortic aneurysm. Arteriosclerosis Thrombosis and Vascular Biology, 27(3), 655-660.
DOI Scopus122 WoS116 Europe PMC98
2007 Palmer, L. J. (2007). UK Biobank: bank on it. Lancet, 369(9578), 1980-1982.
DOI Scopus303 WoS290 Europe PMC256
2007 Carter, K. W., Pluzhnikov, A., Timms, A. E., Miceli-Richard, C., Bourgain, C., Wordsworth, B. P., . . . Brown, M. A. (2007). Combined analysis of three whole genome linkage scans for Ankylosing Spondylitis. Rheumatology, 46(5), 763-771.
DOI Scopus56 WoS49 Europe PMC44
2007 McCaskie, P. A., Beilby, J. P., Chapman, C. M. L., Hung, J., McQuillan, B. M., Thompson, P. L., & Palmer, L. J. (2007). Cholesteryl ester transfer protein gene haplotypes, plasma high-density lipoprotein levels and the risk of coronary heart disease. Human Genetics, 121(3-4), 401-411.
DOI Scopus32 WoS27 Europe PMC20
2007 Bulsara, M. K., Holman, C. D. J., Van Bockxmeer, F. M., Davis, E. A., Gallego, P. H., Beilby, J. P., . . . Jones, T. W. (2007). The relationship between ACE genotype and risk of severe hypoglycaemia in a large population-based cohort of children and adolescents with type 1 diabetes. Diabetologia, 50(5), 965-971.
DOI Scopus20 WoS14 Europe PMC16
2007 Pierce, R., White, D., Malhotra, A., Edwards, J. K., Kleverlaan, D., Palmer, L., & Trinder, J. (2007). Upper airway collapsibility, dilator muscle activation and resistance in sleep apnoea. European Respiratory Journal, 30(2), 345-353.
DOI Scopus64 WoS52 Europe PMC44
2007 Clarke, G. M., Carter, K. W., Palmer, L. J., Morris, A. P., & Cardon, L. R. (2007). Fine mapping versus replication in whole-genome association studies. American Journal of Human Genetics, 81(5), 995-1005.
DOI Scopus51 WoS45 Europe PMC37
2007 Huang, R. C., Burke, V., Newnham, J. P., Stanley, F. J., Kendall, G. E., Landau, L. I., . . . Beilin, L. J. (2007). Perinatal and childhood origins of cardiovascular disease. International Journal of Obesity, 31(2), 236-244.
DOI Scopus121 WoS107 Europe PMC95
2007 Chanock, S. J., Manolio, T., Boehnke, M., Boerwinkle, E., Hunter, D. J., Thomas, G., . . . Collins, F. S. (2007). Replicating genotype-phenotype associations. Nature, 447(7145), 655-660.
DOI Scopus1211 WoS1121 Europe PMC988
2007 Saunders, C. L., Chiodini, B. D., Sham, P., Lewis, C. M., Abkevich, V., Adeyemo, A. A., . . . Collier, D. A. (2007). Meta-analysis of genome-wide linkage studies in BMI and obesity. Obesity, 15(9), 2263-2275.
DOI Scopus125 WoS104 Europe PMC90
2006 Willwerth, B. M., Schaub, B., Tantisira, K. G., Gold, D. R., Palmer, L. J., Litonjua, A. A., . . . Finn, P. W. (2006). Prenatal, perinatal, and heritable influences on cord blood immune responses. Annals of Allergy Asthma and Immunology, 96(3), 445-453.
DOI Scopus31 WoS30 Europe PMC24
2006 Schaeffer, L., Gohlke, H., Müller, M., Heid, I. M., Palmer, L. J., Kompauer, I., . . . Heinrich, J. (2006). Common genetic variants of the FADS1 FADS2 gene cluster and their reconstructed haplotypes are associated with the fatty acid composition in phospholipids. Human Molecular Genetics, 15(11), 1745-1756.
DOI Scopus477 WoS455 Europe PMC402
2006 Kim, S. H., Oh, J. M., Kim, Y. S., Palmer, L. J., Suh, C. H., Nahm, D. H., & Park, H. S. (2006). Cysteinyl leukotriene receptor 1 promoter polymorphism is associated with aspirin-intolerant asthma in males. Clinical and Experimental Allergy, 36(4), 433-439.
DOI Scopus90 WoS81 Europe PMC65
2006 Lee, J. D. Y., & Palmer, L. J. (2006). The Western Australian Twin Register: A population-based register of adult and child multiples. Twin Research and Human Genetics, 9(6), 712-717.
DOI Scopus2 WoS2 Europe PMC2
2006 McCaskie, P. A., Cadby, G., Hung, J., McQuillan, B. M., Chapman, C. M. L., Carter, K. W., . . . Beilby, J. P. (2006). The C-480T hepatic lipase polymorphism is associated with HDL-C but not with risk of coronary heart disease. Clinical Genetics, 70(2), 114-121.
DOI Scopus34 WoS31 Europe PMC28
2006 Carter, K. W., McCaskie, P. A., & Palmer, L. J. (2006). JLIN: A java based linkage disequilibrium plotter. BMC Bioinformatics, 7(1), 3 pages.
DOI Scopus103 WoS103 Europe PMC94
2006 Gold, D. R., Willwerth, B. M., Tantisira, K. G., Finn, P. W., Schaub, B., Perkins, D. L., . . . Weiss, S. T. (2006). Associations of cord blood fatty acids with lymphocyte proliferation, IL-13, and IFN-γ. Journal of Allergy and Clinical Immunology, 117(4), 931-938.
DOI Scopus35 WoS32 Europe PMC28
2006 Smith, G. D., Gwinn, M., Ebrahim, S., Palmer, L. J., & Khoury, M. J. (2006). Make it HuGE: Human genome epidemiology reviews, population health, and the IJE. International Journal of Epidemiology, 35(3), 507-510.
DOI Scopus7 WoS6 Europe PMC6
2006 Hui, J., Palmer, L. J., James, A. L., Musk, A. W., & Beilby, J. P. (2006). AluyMICB dimorphism within the class I region of the major histocompatibility complex is associated with asthma and airflow obstruction in the Busselton population. Clinical and Experimental Allergy, 36(6), 728-734.
DOI Scopus8 WoS8 Europe PMC7
2006 Lee, J. D. Y., & Palmer, L. J. (2006). The Western Australian Twin Register: A Population-Based Register of Adult and Child Multiples. Twin Research and Human Genetics, 9(6), 712-717.
DOI
2005 Wu, J., Kraja, A. T., Oberman, A., Lewis, C. E., Ellison, R. C., Arnett, D. K., . . . Rao, D. C. (2005). A summary of the effects of antihypertensive medications on measured blood pressure. American Journal of Hypertension, 18(7), 935-942.
DOI Scopus108 Europe PMC101
2005 Feitosa, M. F., Borecki, I. B., Rankinen, T., Rice, T., Després, J. P., Chagnon, Y. C., . . . Rao, D. C. (2005). Evidence of QTLs on chromosomes 1q42 and 8q24 for LDL-cholesterol and apoB levels in the HERITAGE family study. Journal of Lipid Research, 46(2), 281-286.
DOI Scopus14 Europe PMC13
2005 Kraja, A. T., Rao, D. C., Weder, A. B., Cooper, R., Curb, J. D., Hanis, C. L., . . . Province, M. A. (2005). Two major QTLs and several others relate to factors of metabolic syndrome in the family blood pressure program. Hypertension, 46(4), 751-757.
DOI Scopus33 Europe PMC27
2005 Smith, G. D., Ebrahim, S., Lewis, S., Hansell, A. L., Palmer, L. J., & Burton, P. R. (2005). Genetic epidemiology and public health: Hope, hype, and future prospects. Lancet, 366(9495), 1484-1498.
DOI Scopus256 WoS207 Europe PMC163
2005 Palmer, L., & Cardon, L. (2005). Shaking the tree: Mapping complex disease genes with linkage disequilibrium. Lancet, 366(9492), 1223-1234.
DOI Scopus187 WoS150 Europe PMC117
2005 Larkin, E. K., Elston, R. C., Patel, S. R., Tishler, P. V., Palmer, L. J., Jenny, N. S., & Redline, S. (2005). Linkage of serum leptin levels in families with sleep apnea. International Journal of Obesity, 29(3), 260-267.
DOI Scopus10 WoS7 Europe PMC5
2005 McCaskie, P. A., Carter, K. W., McCaskie, S. R., & Palmer, L. J. (2005). The effect of missing data on linkage disequilibrium mapping and haplotype association analysis in the GAW14 simulated datasets. BMC Genetics, 6(SUPPL.1), 6 pages.
DOI Scopus7 WoS7 Europe PMC7
2005 Turner, S. W., Palmer, L. J., Rye, P. J., Gibson, N. A., Young, S., Goldblatt, J., . . . Le Souëf, P. N. (2005). Determinants of airway responsiveness to histamine in children. European Respiratory Journal, 25(3), 462-467.
DOI Scopus19 WoS19 Europe PMC15
2005 Levy, B. D., Bonnans, C., Silverman, E. S., Palmer, L. J., Marigowda, C., & Israel, E. (2005). Diminished lipoxin biosynthesis in severe asthma. American Journal of Respiratory and Critical Care Medicine, 172(7), 824-830.
DOI Scopus245 WoS221 Europe PMC188
2005 Beilby, J. P., Chapman, C. M. L., Palmer, L. J., McQuillan, B. M., Thompson, P. L., & Hung, J. (2005). Stromelysin-1 (MMP-3) gene 5A/6A promoter polymorphism is associated with blood pressure in a community population. Journal of Hypertension, 23(3), 537-542.
DOI Scopus22 WoS21 Europe PMC17
2005 Burton, P. R., Scurrah, K. J., Tobin, M. D., & Palmer, L. J. (2005). Covariance components models for longitudinal family data. International Journal of Epidemiology, 34(5), 1063-1077.
DOI Scopus27 WoS22 Europe PMC18
2005 Timpson, N. J., Lawlor, D. A., Harbord, R. M., Gaunt, T. R., Day, I. N., Palmer, L. J., . . . Smith, G. D. (2005). C-reactive protein and its role in metabolic syndrome: Mendelian randomisation study. Lancet, 366(9501), 1954-1959.
DOI Scopus290 WoS279 Europe PMC248
2005 Mukherjee, S., Rodrigues, E., Aeschliman, D. B., Houk, R. S., Palmer, L. J., Woodin, M. A., . . . Christiani, D. C. (2005). Urinary metal and polycyclic aromatic hydrocarbon biomarkers in boilermakers exposed to metal fume and residual oil fly ash. American Journal of Industrial Medicine, 47(6), 484-493.
DOI Scopus10 WoS10 Europe PMC9
2005 Lilly, C. M., & Palmer, L. J. (2005). The role of prostaglandin D receptor gene in asthma pathogenesis. American Journal of Respiratory Cell and Molecular Biology, 33(3), 224-226.
DOI Scopus11 WoS9 Europe PMC7
2005 Turner, S. W., Palmer, L. J., Gibson, N. A., Rye, P. J., Goldblatt, J., Landau, L. I., & Le Souëf, P. N. (2005). The effect of age on the relationship between birth order and immunoglobulin E sensitization. Clinical and Experimental Allergy, 35(5), 630-634.
DOI Scopus9 WoS8 Europe PMC6
2005 James, A. L., Palmer, L. J., Kick, E., Maxwell, P. S., Lagan, S. E., Ryan, G. F., & Musk, A. W. (2005). Decline in lung function in the Busselton health study: The effects of asthma and cigarette smoking. American Journal of Respiratory and Critical Care Medicine, 171(2), 109-114.
DOI Scopus377 WoS330 Europe PMC285
2005 Bollerslev, J., Wilson, S. G., Dick, I. M., Islam, F. M. A., Ueland, T., Palmer, L., . . . Prince, R. L. (2005). LRP5 gene polymorphisms predict bone mass and incident fractures in elderly Australian women. Bone, 36(4), 599-606.
DOI Scopus77 WoS66 Europe PMC62
2005 Morita, H., Nagai, R., Deykin, A., Lilly, C. M., & Palmer, L. J. (2005). Prostanoid DP receptor variants and asthma [3] (multiple letters). New England Journal of Medicine, 352(8), 837-838.
DOI Scopus2 Europe PMC1
2005 Carter, K. W., McCaskie, P. A., & Palmer, L. J. (2005). Genome-wide linkage and association mapping of disease genes with the GAW14 simulated datasets. BMC Genetics, 6(SUPPL.1), 5 pages.
DOI Scopus1 WoS1 Europe PMC1
2005 Pawitan, Y., Reilly, M., Nilsson, E., Cnattingius, S., Lichtenstein, P., Scurrah, K., . . . Burton, P. (2005). Estimation of genetic and environmental factors for binary traits using family data (multiple letters) [3]. Statistics in Medicine, 24(10), 1613-1617.
DOI WoS2 Europe PMC1
2004 Palmer, L. J., Valinsky, L., Pikora, T., & Landau, L. I. (2004). Do regular check ups and preventive drug use reduce asthma severity in school children?. Australian Family Physician, 33(7), 573-576.
Scopus8 Europe PMC4
2004 Palmer, L. J., Buxbaum, S. G., Larkin, E. K., Patel, S. R., Elston, R. C., Tishler, P. V., & Redline, S. (2004). Whole genome scan for obstructive sleep apnea and obesity in African-American families. American Journal of Respiratory and Critical Care Medicine, 169(12), 1314-1321.
DOI Scopus151 WoS114 Europe PMC95
2004 Palmer, L. J. (2004). The new epidemiology: Putting the pieces together in complex disease aetiology. International Journal of Epidemiology, 33(5), 925-928.
DOI Scopus7 WoS6 Europe PMC2
2004 Tantisira, K., Klimecki, W. T., Lazarus, R., Palmer, L. J., Raby, B. A., Kwiatkowski, D. J., . . . Weiss, S. T. (2004). Toll-like receptor 6 gene (TLR6): Single-nucleotide polymorphism frequencies and preliminary association with the diagnosis of asthma. Genes and Immunity, 5(5), 343-346.
DOI Scopus90 WoS82 Europe PMC68
2004 Pack, A. I., Gislason, T., Hakonarson, H., Palmer, L. J., Larkin, E. K., Elston, R. C., . . . Tishler, P. V. (2004). Linkage to apnea-hypopnea index across the life-span: Is this a viable strategy? (multiple letters). American Journal of Respiratory and Critical Care Medicine, 170(11), 1260-1261.
DOI Scopus1 WoS1 Europe PMC1
2004 Silverman, E. S., Palmer, L. J., Subramaniam, V., Hallock, A., Mathew, S., Vallone, J., . . . Shore, S. A. (2004). Transforming Growth Factor-β1 Promoter Polymorphism C-509T Is Associated with Asthma. American Journal of Respiratory and Critical Care Medicine, 169(2), 214-219.
DOI Scopus232 WoS216 Europe PMC181
2004 Tantisira, K. G., Lake, S., Silverman, E. E., Palmer, L. J., Lazarus, R., Silverman, E. K., . . . Weiss, S. T. (2004). Corticosteroid pharmacogenetics: Association of sequence variants in CRHR1 with inproved lung function in asthmatics treated with inhaled corticosteroids. Human Molecular Genetics, 13(13), 1353-1359.
DOI Scopus297 WoS254 Europe PMC208
2004 Turner, S. W., Palmer, L. J., Rye, P. J., Gibson, N. A., Judge, P. K., Cox, M., . . . Le Souëf, P. N. (2004). The relationship between infant airway function, childhood airway responsiveness, and asthma. American Journal of Respiratory and Critical Care Medicine, 169(8), 921-927.
DOI Scopus193 WoS172 Europe PMC136
2004 Schroeter, C. H., Schaub, B., Gold, D. R., Contreras, P. J., Manrique, O., Gillman, M. W., . . . Finn, P. W. (2004). Nuclear factor kappa B activation in human cord blood mononuclear cells. Pediatric Research, 56(2), 212-218.
DOI Scopus6 WoS4 Europe PMC6
2004 Patel, S. R., Palmer, L. J., Larkin, E. K., Jenny, N. S., White, D. P., & Redline, S. (2004). Relationship between obstructive sleep apnea and diurnal leptin rhythms. Sleep, 27(2), 235-239.
DOI Scopus71 WoS59 Europe PMC42
2004 Celedón, J. C., Lange, C., Raby, B. A., Litonjua, A. A., Palmer, L. J., DeMeo, D. L., . . . Silverman, E. K. (2004). The transforming growth factor-β1 (TGFB1) gene is associated with chronic obstructive pulmonary disease (COPD). Human Molecular Genetics, 13(15), 1649-1656.
DOI Scopus209 WoS183 Europe PMC164
2004 Oguma, T., Palmer, L. J., Birben, E., Sonna, L. A., Asano, K., & Lilly, C. M. (2004). Role of prostanoid DP receptor variants in susceptibility to asthma. New England Journal of Medicine, 351(17), 1752-1763.
DOI Scopus130 WoS116 Europe PMC89
2004 Mukherjee, S., Palmer, L. J., Kim, J. Y., Aeschliman, D. B., Houk, R. S., Woodin, M. A., & Christiani, D. C. (2004). Smoking status and occupational exposure affects oxidative DNA injury in boilermakers exposed to metal fume and residual oil fly ash. Cancer Epidemiology Biomarkers and Prevention, 13(3), 454-460.
DOI Scopus29 WoS26 Europe PMC17
2004 Turner, S. W., Khoo, S. K., Laing, I. A., Palmer, L. J., Gibson, N. A., Rye, P., . . . Le Souëf, P. N. (2004). β2 adrenoceptor Arg16Gly polymorphism, airway responsiveness, lung function and asthma in infants and children. Clinical and Experimental Allergy, 34(7), 1043-1048.
DOI Scopus51 WoS49 Europe PMC36
2004 Ceyhan, B. B., Burgos, A., Palmer, L. J., & Drazen, J. (2004). Lack of association of NAT2 (N-acetyl transferase 2) gene polymorphism with atopic asthma in Turkish subjects. Indian Journal of Human Genetics, 10(2), 65-69.
2003 Palmer, L. J., Celedón, J. C., Chapman, H. A., Speizer, F. E., Weiss, S. T., & Silverman, E. K. (2003). Erratum: Genome-wide linkage analysis of bronchodilator responsiveness and post-bronchodilator spirometric phenotypes in chronic obstructive pulmonary disease (Human Molecular Genetics (2003) vol. 12 (1199-1210)). Human Molecular Genetics, 12(16), 2085.
DOI WoS1
2003 Djoussé, L., Hunt, S. C., Arnett, D. K., Province, M. A., Eckfeldt, J. H., & Ellison, R. C. (2003). Dietary linolenic acid is inversely associated with plasma triacylglycerol: The National Heart, Lung, and Blood Institute Family Heart Study. American Journal of Clinical Nutrition, 78(6), 1098-1102.
DOI Scopus73 Europe PMC48
2003 Cannon, S. B., McCombie, W. R., Sato, S., Tabata, S., Denny, R., Palmer, L., . . . Stacey, G. (2003). Evolution and microsynteny of the apyrase gene family in three legume genomes. MOLECULAR GENETICS AND GENOMICS, 270(4), 347-361.
DOI WoS45
2003 Chapman, C. M. L., Beilby, J. P., Humphries, S. E., Palmer, L. J., Thompson, P. L., & Hung, J. (2003). Association of an allelic variant of interleukin-6 with subclinical carotid atherosclerosis in an Australian community population. European Heart Journal, 24(16), 1494-1499.
DOI Scopus58 WoS55 Europe PMC45
2003 Cardon, L. R., & Palmer, L. J. (2003). Population stratification and spurious allelic association. Lancet, 361(9357), 598-604.
DOI Scopus1032 WoS945 Europe PMC822
2003 Palmer, L. J., Scurrah, K. J., Tobin, M., Patel, S. R., Celedon, J. C., Burton, P. R., & Weiss, S. T. (2003). Genome-wide linkage analysis of longitudinal phenotypes using sigma2A random effects (SSARs) fitted by Gibbs sampling.. BMC Genetics, 4 Suppl 1(S1), S674-S679.
DOI Scopus5 WoS5 Europe PMC7
2003 Palmer, L. J., & Redline, S. (2003). Genomic approaches to understanding obstructive sleep apnea. Respiratory Physiology and Neurobiology, 135(2-3), 187-205.
DOI Scopus74 WoS53 Europe PMC43
2003 Tian, W., Boggs, D. A., Uko, G., Essiet, A., Inyama, M., Banjoko, B., . . . Fraser, P. A. (2003). MICA, HLA-B haplotypic variation in five population groups of sub-Saharan African ancestry. Genes and Immunity, 4(7), 500-505.
DOI Scopus37 WoS25 Europe PMC26
2003 Grasemann, H., Van's Gravesande, K. S., Büscher, R., Knauer, N., Silverman, E. S., Palmer, L. J., . . . Ratjen, F. (2003). Endothelial nitric oxide synthase variants in cystic fibrosis lung disease. American Journal of Respiratory and Critical Care Medicine, 167(3), 390-394.
DOI Scopus60 WoS50 Europe PMC39
2003 Patel, S. R., Celedon, J. C., Weiss, S. T., & Palmer, L. J. (2003). Lack of reproducibility of linkage results in serially measured blood pressure data.. BMC Genetics, 4 Suppl 1(Suppl 1), 6 pages.
DOI Scopus3 WoS3 Europe PMC2
2003 Lazarus, R., Klimecki, W. T., Raby, B. A., Vercelli, D., Palmer, L. J., Kwiatkowski, D. J., . . . Weiss, S. T. (2003). Single-nucleotide polymorphisms in the Toll-like receptor 9 gene (TLR9): Frequencies, pairwise linkage disequilibrium, and haplotypes in three U.S. ethnic groups and exploratory case-control disease association studies. Genomics, 81(1), 85-91.
DOI Scopus205 WoS189 Europe PMC151
2003 Almasy, L., Amos, C. I., Bailey-Wilson, J. E., Cantor, R. M., Jaquish, C. E., Martinez, M., . . . Maccluer, J. W. (2003). Genetic analysis workshop 13: Analysis of longitudinal family data for complex diseases and related risk factors - art. no. S1. BMC GENETICS, 4(Suppl 1), 3 pages.
DOI WoS9 Europe PMC9
2003 Van's Gravesande, K. S., Wechsler, M. E., Grasemann, H., Silverman, E. S., Le, L., Palmer, L. J., & Drazen, J. M. (2003). Association of a missense mutation in the NOS3 gene with exhaled nitric oxide levels. American Journal of Respiratory and Critical Care Medicine, 168(2), 228-231.
DOI Scopus59 WoS28 Europe PMC41
2003 Palmer, L. J., Scurrah, K. J., Tobin, M., Patel, S. R., Celedon, J. C., Burton, P. R., & Weiss, S. T. (2003). Genome-wide linkage analysis of longitudinal phenotypes using σ<SUP>2</SUP><sub>A</sub> random effects (SSARs) fitted by Gibbs sampling -: art. no. S12. BMC GENETICS, 4(Suppl 1), 5 pages.
DOI WoS8 Europe PMC7
2003 Beilby, J. P., Hunt, C. C. J., Palmer, L. J., Chapman, C. M. L., Burley, J. P., McQuillan, B. M., . . . Hung, J. (2003). Apolipoprotein E gene polymorphisms are associated with carotid plaque formation but not with intima-media wall thickening: Results from the Perth Carotid Ultrasound Disease Assessment Study (CUDAS). Stroke, 34(4), 869-874.
DOI Scopus46 WoS44 Europe PMC36
2003 Palmer, L. J., Buxbaum, S. G., Larkin, E., Patel, S. R., Elston, R. C., Tishler, P. V., & Redline, S. (2003). A whole-genome scan for obstructive sleep apnea and obesity. American Journal of Human Genetics, 72(2), 340-350.
DOI Scopus197 WoS158 Europe PMC128
2003 Palmer, L. J. (2003). Loosening the cuff: Important new advances in modeling antihypertensive treatment effects in genetic studies of hypertension. Hypertension, 41(2), 197-198.
DOI Scopus10 WoS15 Europe PMC13
2003 Palmer, L. J., Celedón, J. C., Chapman, H. A., Speizer E., F. E., Weiss, S. T., & Silverman, E. K. (2003). Genome-wide linkage analysis of bronchodilator responsiveness and post-bronchodilator spirometric phenotypes in chronic obstructive pulmonary disease. Human Molecular Genetics, 12(10), 1199-1210.
DOI Scopus98 WoS84 Europe PMC78
2002 Bennett, J. A., Palmer, L. J., Musk, A. W., & Erber, W. N. (2002). Gene frequencies of human platelet antigens 1-5 in indigenous Australians in Western Australia. Transfusion Medicine, 12(3), 199-203.
DOI Scopus26 WoS18 Europe PMC15
2002 Witte, J. S., Palmer, L. J., O’connor, R. D., Hopkins, P. J., & Hall, J. M. (2002). Relation between tumour necrosis factor polymorphism TNFα-308 and risk of asthma. European Journal of Human Genetics, 10(1), 82-85.
DOI Scopus114 WoS101 Europe PMC80
2002 Silverman, E. S., Baron, R. M., Palmer, L. J., Le, L., Hallock, A., Subramaniam, V., . . . Weiss, S. T. (2002). Constitutive and cytokine-induced expression of the ETS transcription factor ESE-3 in the lung. American Journal of Respiratory Cell and Molecular Biology, 27(6), 697-704.
DOI Scopus41 WoS43 Europe PMC39
2002 Lazarus, R., Vercelli, D., Palmer, L. J., Klimecki, W. J., Silverman, E. K., Richter, B., . . . Kwiatkowski, D. J. (2002). Single nucleotide polymorphisms in innate immunity genes: Abundant variation and potential role in complex human disease. Immunological Reviews, 190(1), 9-25.
DOI Scopus185 WoS172 Europe PMC154
2002 Silverman, E. K., Mosley, J. D., Palmer, L. J., Barth, M., Senter, J. M., Brown, A., . . . Weiss, S. T. (2002). Genome-wide linkage analysis of severe, early-onset chronic obstructive pulmonary disease: Airflow obstruction and chronic bronchitis phenotypes. Human Molecular Genetics, 11(6), 623-632.
DOI Scopus106 WoS85 Europe PMC81
2002 Turner, S. W., Palmer, L. J., Rye, P. J., Gibson, N. A., Judge, P. K., Young, S., . . . Le Souëf, P. N. (2002). Infants with flow limitation at 4 weeks: Outcome at 6 and 11 years. American Journal of Respiratory and Critical Care Medicine, 165(9), 1294-1298.
DOI Scopus93 WoS84 Europe PMC61
2002 Hjoberg, J., Drazen, J. M., Palmer, L. J., Weiss, S. T., & Silverman, E. S. (2002). The pharmacogenetics of asthma and allergic disease. Immunology and Allergy Clinics of North America, 22(2), 223-241.
DOI Scopus3 WoS2
2002 McDermott, B. M., & Palmer, L. J. (2002). Postdisaster emotional distress, depression and event-related variables: Finding across child and adolescent development stages. Australian and New Zealand Journal of Psychiatry, 36(6), 754-761.
DOI Scopus81 WoS64 Europe PMC44
2002 Palmer, L. J., Schnell, A. H., Witte, J. S., & Elston, R. C. (2002). Parametric linkage analysis.. Methods in molecular biology (Clifton, N.J.), 195, 13-35.
DOI Scopus2 Europe PMC1
2002 Raby, B. A., Klimecki, W. T., Laprise, C., Renaud, Y., Faith, J., Lemire, M., . . . Weiss, S. T. (2002). Polymorphisms in toll-like receptor 4 are not associated with asthma or atopy-related phenotypes. American Journal of Respiratory and Critical Care Medicine, 166(11), 1449-1456.
DOI Scopus155 WoS133 Europe PMC107
2002 Burton, P. R., Palmer, L. J., Keen, K. J., Olson, J. M., & Elston, R. C. (2002). Response to epstein et al. [2]. American Journal of Human Genetics, 71(2), 441-442.
DOI Scopus2 WoS2 Europe PMC2
2002 Lazarus, R., Klimecki, W. T., Palmer, L. J., Kwiatkowski, D. J., Silverman, E. K., Brown, A., . . . Weiss, S. T. (2002). Single-nucleotide polymorphisms in the interleukin-10 gene: Differences in frequencies, linkage disequilibrium patterns, and haplotypes in three United States ethnic groups. Genomics, 80(2), 223-228.
DOI Scopus68 WoS65 Europe PMC51
2002 Silverman, E. K., Palmer, L. J., Mosley, J. D., Barth, M., Senter, J. M., Brown, A., . . . Weiss, S. T. (2002). Genomewide linkage analysis of quantitative spirometric phenotypes in severe early-onset chronic obstructive pulmonary disease. American Journal of Human Genetics, 70(5), 1229-1239.
DOI Scopus162 WoS129 Europe PMC118
2002 Mukherjee, S., Rodrigues, E., Weker, R., Palmer, L. J., & Christiani, D. C. (2002). 1-Hydroxypyrene as a biomarker of occupational exposure to polycyclic aromatic hydrocarbons (PAH) in boilermakers. Journal of Occupational and Environmental Medicine, 44(12), 1119-1125.
DOI Scopus14 WoS14 Europe PMC12
2002 Palmer, L. J., Silverman, E. S., Weiss, S. T., & Drazen, J. M. (2002). Pharmacogenetics of asthma. American Journal of Respiratory and Critical Care Medicine, 165(7), 861-866.
DOI Scopus124 WoS90 Europe PMC69
2002 Celedón, J. C., Soto-Quiros, M. E., Palmer, L. J., Senter, J., Mosley, J., Silverman, E. K., & Weiss, S. T. (2002). Lack of association between a polymorphism in the interleukin-13 gene and total serum immunoglobulin E level among nuclear families in Costa Rica. Clinical and Experimental Allergy, 32(3), 387-390.
DOI Scopus30 WoS24 Europe PMC22
2002 Baron, R. M., Palmer, L. J., Tantisira, K., Gabriel, S., Sonna, L. A., Le, L., . . . Silverman, E. S. (2002). DNA sequence variants in epithelium-specific ETS-2 and ETS-3 are not associated with asthma. American Journal of Respiratory and Critical Care Medicine, 166(7), 927-932.
DOI Scopus14 WoS14 Europe PMC15
2002 Palmer, L. J., Celedón, J. C., Weiss, S. T., Wang, B., Fang, Z., & Xu, X. (2002). Ascaris lumbricoides infection is associated with increased risk of childhood asthma and atopy in rural China. American Journal of Respiratory and Critical Care Medicine, 165(11), 1489-1493.
DOI Scopus186 WoS165 Europe PMC135
2002 Boerwinkle, E., Brown, C. A., Carrejo, M., Ferrell, R., Hanis, C., Hutchinson, R., . . . Savage, P. (2002). Multi-center genetic study of hypertension: The Family blood pressure program (FBPP). Hypertension, 39(1), 3-9.
DOI Scopus172 Europe PMC144
2001 Palmer, L. J. (2001). Linkages and associations to intermediate phenotypes underlying asthma and allergic disease. Current Opinion in Allergy and Clinical Immunology, 1(5), 393-398.
DOI
2001 Godfrey, S., Palmer, L., Burton, P., & Cookson, W. (2001). Independent inheritance of serum immunoglobulin E concentrations and airway responsiveness [1] (multiple letters). American Journal of Respiratory and Critical Care Medicine, 163(4), 1030.
DOI Scopus1
2001 Turner, S., Rye, P., Gibson, N., Judgc, V., Palmer, L., Young, S., . . . Souëf, P. L. (2001). Pulmonary function at four weeks correlates with pulmonary function at 6 and 12 years. Respirology, 6(SUPPL. 1), A47.
2001 Xu, X., Palmer, L. J., Horvath, S., & Wei, L. J. (2001). Combining multiple phenotypic traits optimally for detecting linkage with sib-pair observations. GENETIC EPIDEMIOLOGY, 21(S1), S479-S483.
DOI WoS1
2001 Celedón, J. C., Palmer, L. J., Weiss, S. T., Wang, B., Fang, Z., & Xu, X. (2001). Asthma, rhinitis, and skin test reactivity to aeroallergens in families of asthmatic subjects in Anqing, China. American Journal of Respiratory and Critical Care Medicine, 163(5), 1108-1112.
DOI Scopus61 WoS46 Europe PMC38
2001 Celedón, J. C., Palmer, L. J., Litonjua, A. A., Weiss, S. T., Wang, B., Fang, Z., & Xu, X. (2001). Body mass index and asthma in adults in families of subjects with asthma in Anqing, China. American Journal of Respiratory and Critical Care Medicine, 164(10 I), 1835-1840.
DOI Scopus152 WoS137 Europe PMC115
2001 Horvath, S., Wei, E., Xu, X., Palmer, L. J., & Baur, M. (2001). Family-based association test method: Age of onset traits and covariates. Genetic Epidemiology, 21(SUPPL. 1), S403-S408.
Scopus31 WoS30 Europe PMC19
2001 Lance, R. S., Dinney, C. P. N., Swanson, D., Babaian, R. J., Pisters, L. L., Palmer, L. J., & Grossman, H. B. (2001). Radical cystectomy for invasive bladder cancer in the octogenarian. ONCOLOGY REPORTS, 8(4), 723-726.
DOI WoS39 Europe PMC32
2001 Bennett, J. A., Palmer, L. J., Musk, A. W., & Erber, W. N. (2001). Prevalence of factor V Leiden and prothrombin 20210A mutations in indigenous Australians. Thrombosis and Haemostasis, 86(6), 1592-1593.
DOI Scopus15 WoS13 Europe PMC7
2001 Celedón, J. C., Palmer, L. J., Xu, X., Wang, B., Fang, Z., & Weiss, S. T. (2001). Sensitization to silk and childhood asthma in rural China.. Pediatrics, 107(5), E80.
DOI Scopus34 WoS30 Europe PMC27
2001 Palmer, L. J., Rye, P. J., Gibson, N. A., Burton, P. R., Landau, L. I., & LeSouëf, P. N. (2001). Airway responsiveness in early infancy predicts asthma, lung function, and respiratory symptoms by school age. American Journal of Respiratory and Critical Care Medicine, 163(1), 37-42.
DOI Scopus182 WoS147 Europe PMC126
2001 Weiss, S. T., Silverman, E. K., & Palmer, L. J. (2001). Case-Control Association Studies in Pharmacogenetics. Pharmacogenomics Journal, 1(3), 157-158.
DOI Scopus69 Europe PMC46
2001 Palmer, L. J., Jacobs, K. B., Scurrah, K. J., Xu, X., Horvath, S., & Weiss, S. T. (2001). Genome-wide linkage analysis in a general population sample using σA2 random effects (SSARS) fitted by Gibbs sampling. Genetic Epidemiology, 21(SUPPL. 1), S674-S679.
DOI Scopus2
2001 Palmer, L. J., & Elston, R. C. (2001). Introduction: Linkage analyses of single regions. Genetic Epidemiology, 21(SUPPL. 1), S79-S80.
DOI
2001 Palmer, L. J. (2001). Linkages and associations to intermediate phenotypes underlying asthma and allergic disease.. Current Opinion in Allergy and Clinical Immunology, 1(5), 393-398.
DOI Scopus14 WoS13 Europe PMC9
2001 Frazer, F. L., Palmer, L. J., Clarey, A., Thonell, S., & Byrne, G. C. (2001). Relationship between renal volume and increased albumin excretion rates in children and adolescents with type 1 diabetes mellitus. Journal of Pediatric Endocrinology and Metabolism, 14(7), 875-881.
DOI Scopus7 WoS6 Europe PMC4
2001 Palmer, L. J., Knuiman, M. W., Divitini, M. L., Burton, P. R., James, A. L., Bartholomew, H. C., . . . Musk, A. W. (2001). Familial aggregation and heritability of adult lung function: Results from the Busselton health study. European Respiratory Journal, 17(4), 696-702.
DOI Scopus87 WoS73 Europe PMC65
2001 Jacobs, K. B., Burton, P. R., Iyengar, S. K., Elston, R. C., & Palmer, L. J. (2001). Pooling data and linkage analysis in the chromosome 5q candidate region for asthma. Genetic Epidemiology, 21(SUPPL. 1), S103-S108.
DOI Scopus6 WoS7 Europe PMC5
2001 Chapman, C. M. L., Palmer, L. J., McQuillan, B. M., Hung, J., Burley, J., Hunt, C., . . . Beilby, J. P. (2001). Polymorphisms in the angiotensinogen gene are associated with carotid intimal-medial thickening in females from a community-based population. Atherosclerosis, 159(1), 209-217.
DOI Scopus52 WoS43 Europe PMC36
2001 Iyengar, S. K., Jacobs, K. B., & Palmer, L. J. (2001). Improved evidence for linkage on 6p and 5p with retrospective pooling of data from three asthma genome screens. Genetic Epidemiology, 21(SUPPL. 1), S130-S135.
DOI Scopus5 WoS5 Europe PMC2
2001 Altmüller, J., Palmer, L. J., Fischer, G., Scherb, H., & Wjst, M. (2001). Genomewide scans of complex human diseases: True linkage is hard to find. American Journal of Human Genetics, 69(5), 936-950.
DOI Scopus446 WoS388 Europe PMC314
2001 Mukherjee, S., Nelson, D., Loh, S., Van Bruggen, I., Palmer, L. J., Leong, C., . . . Robinson, B. W. S. (2001). The immune anti-tumor effects of GM-CSF and B7-1 gene transfection are enhanced by surgical debulking of tumor. Cancer Gene Therapy, 8(8), 580-588.
DOI Scopus37 WoS34 Europe PMC29
2001 Palmer, L. J., Barnes, K. C., Burton, P. R., Chen, H., Cookson, W. O. C. M., Beaty, T., . . . Wjst, M. (2001). Meta-analysis for linkage to asthma and atopy in the chromosome 5q31-33 candidate region. Human Molecular Genetics, 10(8), 891-899.
DOI Scopus12 WoS15 Europe PMC10
2001 Palmer, L. J., & Cookson, W. O. C. M. (2001). Using single nucleotide polymorphisms as a means to understanding the pathophysiology of asthma. Respiratory Research, 2(2), 102-112.
DOI Scopus46 WoS41 Europe PMC23
2001 Palmer, L. J., Cookson, W. O. C. M., Deichmann, K. A., Holloway, J. W., & Laitinen, T. (2001). Single region linkage analyses of asthma: Description of data sets. Genetic Epidemiology, 21(SUPPL. 1), S9-S15.
DOI Scopus1 WoS1 Europe PMC1
2001 Schnell, A. H., Palmer, L. J., & Elston, R. C. (2001). Segregation analysis of asthma and respiratory allergy in population-based samples of families. Genetic Epidemiology, 21(SUPPL. 1), S30-S35.
DOI Scopus3 WoS1 Europe PMC1
2001 Palmer, L. J., Lonjou, C., Barnes, K., Chen, H., Cookson, W. O. C. M., Deichmann, K. A., . . . Morton, N. E. (2001). A retrospective collaboration on chromosome 5 by the International Consortium on Asthma Genetics (COAG). Clinical and Experimental Allergy, 31(1), 152-154.
DOI Scopus10 WoS11 Europe PMC8
2001 Palmer, L. J., Cookson, W. O. C. M., James, A. L., William Musk, A., & Burton, P. R. (2001). Gibbs sampling-based segregation analysis of asthma-associated quantitative traits in a population-based sample of nuclear families. Genetic Epidemiology, 20(3), 356-372.
DOI Scopus27 WoS25 Europe PMC18
2000 Silverman, E. K., & Palmer, L. J. (2000). Case-control association studies for the genetics of complex respiratory diseases. American Journal of Respiratory Cell and Molecular Biology, 22(6), 645-648.
DOI Scopus139 WoS121 Europe PMC92
2000 Turner, J., Batik, M., Palmer, L. J., Forbes, D., & McDermott, B. M. (2000). Detection and importance of laxative use in adolescents with anorexia nervosa. Journal of the American Academy of Child and Adolescent Psychiatry, 39(3), 378-385.
DOI Scopus36 WoS22 Europe PMC18
2000 Palmer, L. J., Jacobs, K. B., & Elston, R. C. (2000). Haseman and Elston revisited: The effects of ascertainment and residual familial correlations on power to detect linkage. GENETIC EPIDEMIOLOGY, 19(4), 456-460.
DOI WoS23 Europe PMC19
2000 Huang, R. C., Palmer, L. J., & Forbes, D. A. (2000). Prevalence and pattern of childhood abdominal pain in an Australian general practice. Journal of Paediatrics and Child Health, 36(4), 349-353.
DOI Scopus53 WoS46 Europe PMC34
2000 Mukherjee, S., De Klerk, N., Palmer, L. J., Olsen, N. J., Pang, S. C., & Musk, A. W. (2000). Chest pain in asbestos-exposed individuals with benign pleural and parenchymal disease. American Journal of Respiratory and Critical Care Medicine, 162(5), 1807-1811.
DOI Scopus35 WoS31 Europe PMC23
2000 Palmer, L. J., & Burton, P. R. (2000). Familial aggregation and segregation analysis of eosinophil levels [1] (multiple letters). American Journal of Respiratory and Critical Care Medicine, 162(2 I), 759-760.
DOI Scopus2 Europe PMC2
2000 Palmer, L. J., & Burton, P. R. (2000). Familial aggregation and segregation analysis of eosinophil levels. AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 162(2), 759.
DOI WoS2
2000 Scurrah, K. J., Palmer, L. J., & Burton, P. R. (2000). Variance components analysis for pedigree-based censored survival data using generalized linear mixed models (GLMMs) and Gibbs sampling in BUGS. Genetic Epidemiology, 19(2), 127-148.
DOI Scopus48 WoS51 Europe PMC40
2000 Palmer, L. J., & Cookson, W. O. C. M. (2000). Genomic approaches to understanding asthma. Genome Research, 10(9), 1280-1287.
DOI Scopus87 WoS67 Europe PMC54
2000 Lonjou, C., Barnes, K., Chen, H., Cookson, W. O. C. M., Deichmann, K. A., Hall, I. P., . . . Morton, N. E. (2000). A first trial of retrospective collaboration for positional cloning in complex inheritance: Assay of the cytokine region on chromosome 5 by the Consortium on Asthma Genetics (COAG). Proceedings of the National Academy of Sciences of the United States of America, 97(20), 10942-10947.
DOI Scopus39 WoS38 Europe PMC28
2000 Palmer, L. J., Burton, P. R., Faux, J. A., James, A. L., Musk, A. W., & Cookson, W. O. C. M. (2000). Independent inheritance of serum Immunoglobulin E concentrations and airway responsiveness. American Journal of Respiratory and Critical Care Medicine, 161(6), 1836-1843.
DOI Scopus106 WoS99 Europe PMC84
2000 Palmer, L. J., Burton, P. R., James, A. L., Musk, A. W., & Cookson, W. O. C. M. (2000). Familial aggregation and heritability of asthma-associated quantitative traits in a population-based sample of nuclear families. European Journal of Human Genetics, 8(11), 853-860.
DOI Scopus66 WoS59 Europe PMC45
2000 Burton, P. R., Palmer, L. J., Jacobs, K., Keen, K. J., Olson, J. M., & Elston, R. C. (2000). Ascertainment adjustment: Where does it take us?. American Journal of Human Genetics, 67(6), 1505-1514.
DOI Scopus48 WoS46 Europe PMC35
2000 Palmer, L. J., Jacobs, K. B., & Elston, R. C. (2000). Haseman and Elston revisited: The effects of ascertainment and residual familial correlations on power to detect linkage [1]. Genetic Epidemiology, 19(4), 456-460.
DOI Scopus30
2000 Waring, J. A., Wood, M., Acquarola, N., De Klerk, N. H., Palmer, L., & Musk, W. (2000). Screening for mycobacterial infections in a remote Australian aboriginal community using the QuantiFERON-TB assay. Thorax, 55(SUPPL. 3).
2000 Bailey-Wilson, J., Baron, J., Cawthon, R., Christian, J. C., Corder, E. H., Franceschi, C., . . . Hadley, E. (2000). Genetic epidemiologic studies on age-specified traits. American Journal of Epidemiology, 152(11), 1003-1008.
DOI Scopus30 Europe PMC20
2000 Bouchard, C., Rankinen, T., Chagnon, Y. C., Rice, T., Pérusse, L., Gagnon, J., . . . Rao, D. C. (2000). Genomic scan for maximal oxygen uptake and its response to training in the HERITAGE family study. Journal of Applied Physiology, 88(2), 551-559.
DOI Scopus172 Europe PMC97
1999 Burton, P. R., Tiller, K. J., Gurrin, L. C., Cookson, W. O. C. M., Musk, A. W., & Palmer, L. J. (1999). Genetic variance components analysis for binary phenotypes using generalized linear mixed models (GLMMs) and Gibbs sampling. Genetic Epidemiology, 17(2), 118-140.
DOI Scopus89 WoS87 Europe PMC69
1999 Palmer, L. J., Tiller, K. J., & Burton, P. R. (1999). Genome-wide linkage analysis using genetic variance components of alcohol dependency-associated censored and continuous traits. Genetic Epidemiology, 17(SUPPL. 1), S283-S288.
DOI Scopus18 WoS21 Europe PMC15
1999 Palmer, L. J., Valinsky, I. J., Pikora, T., Zubrick, S. R., & Landau, L. I. (1999). Environmental factors and asthma and allergy in schoolchildren from Western Australia. European Respiratory Journal, 14(6), 1351-1357.
DOI Scopus14 WoS12 Europe PMC7
1999 Burton, P. R., Tiller, K. J., Gurrin, L. C., Cookson, W. O., Musk, A. W., & Palmer, L. J. (1999). Genetic variance components analysis for binary phenotypes using generalized linear mixed models (GLMMs) and Gibbs sampling. Genetic Epidemiology, 17(2), 118-140.
DOI
1999 Palmer, L. J., Rye, P. J., Gibson, N. A., Moffatt, M. F., Goldblatt, J., Burton, P. R., . . . Lesouëf, P. N. (1999). Association of FcεR1-β polymorphisms with asthma and associated traits in Australian asthmatic families. Clinical and Experimental Allergy, 29(11), 1555-1562.
DOI Scopus23 WoS18 Europe PMC17
1999 McDermott, B. M. C., & Palmer, L. J. (1999). Post-disaster service provision following proactive identification of children with emotional distress and depression. Australian and New Zealand Journal of Psychiatry, 33(6), 855-863.
DOI Scopus31 WoS24 Europe PMC18
1998 Palmer, L. J., Daniels, S. E., Rye, P. J., Gibson, N. A., Tay, G. K., Cookson, W. O. C. M., . . . Lesouëf, P. N. (1998). Linkage of chromosome 5q and 11q gene markers to asthma-associated quantitative traits in Australian children. American Journal of Respiratory and Critical Care Medicine, 158(6), 1825-1830.
DOI Scopus93 WoS77 Europe PMC63
1998 Leong, J. W., Dore, N. D., Shelley, K., Holt, E. J., Laing, I. A., Palmer, L. J., & LeSouef, P. N. (1998). The elimination half-life of urinary cotinine in children of tobacco-smoking mothers. Pulmonary Pharmacology and Therapeutics, 11(4), 287-290.
DOI Scopus46 WoS40 Europe PMC35
1998 Cookson, W., & Palmer, L. (1998). Investigating the asthma phenotype. Clinical and Experimental Allergy, 28(Suppl. 1), 88-89.
DOI Scopus23 WoS19 Europe PMC12
1998 Albuquerque, R. V., Hayden, C. M., Palmer, L. J., Laing, I. A., Rye, P. J., Gibson, N. A., . . . Lesouëf, P. N. (1998). Association of polymorphisms within the tumour necrosis factor (TNF) genes and childhood asthma. Clinical and Experimental Allergy, 28(5), 578-584.
DOI Scopus138 WoS119 Europe PMC91
1998 Laing, I. A., Goldblatt, J., Eber, E., Hayden, C. M., Rye, P. J., Gibson, N. A., . . . Le Souëf, P. N. (1998). A polymorphism of the CC16 gene is associated with an increased risk of asthma. Journal of Medical Genetics, 35(6), 463-467.
DOI Scopus106 WoS98 Europe PMC80
1997 Palmer, L. J., Paré, P. D., Faux, J. A., Moffatt, M. F., Daniels, S. E., LeSouëf, P. N., . . . Cookson, W. O. C. M. (1997). Fc(ε)R1-β polymorphism and total serum IgE levels in endemically parasitized Australian aborigines. American Journal of Human Genetics, 61(1), 182-188.
DOI Scopus79
1997 Palmer, L. J., Pare, P. D., Faux, J. A., Moffatt, M. F., Daniels, S. E., LeSouef, P. N., . . . Cookson, W. O. C. M. (1997). Fc(epsilon)R1-beta polymorphism and total serum IgE levels in endemically parasitized Australian aborigines. AMERICAN JOURNAL OF HUMAN GENETICS, 61(1), 182-188.
DOI WoS73 Europe PMC52
1997 Hayden, C., Pereira, E., Rye, P., Palmer, L., Gibson, N., Palenque, M., . . . Lesouëf, P. (1997). Mutation screening of interferon-gamma (ifnγ) as a candidate gene for asthma. Clinical and Experimental Allergy, 27(12), 1412-1416.
DOI Scopus50 Europe PMC32
1997 Hayden, C., Pereira, E., Rye, P., Palmer, L., Gibson, N., Palenque, M., . . . LeSouëf, P. (1997). Mutation screening of interferon-gamma (IFNγ) as a candidate gene for asthma. CLINICAL AND EXPERIMENTAL ALLERGY, 27(12), 1412-1416.
DOI WoS37
1996 Blair, E., Palmer, L., Stanley, F., Nelson, K. B., & Grether, J. (1996). Cerebral palsy in very low birth weight infants, pre-eclampsia and magnesium sulphate [4]. Pediatrics, 97(5), 780-782.
DOI Scopus19 WoS16 Europe PMC9
1995 Palmer, L., Blairt, E., Petterson, B., & Burton, P. (1995). Antenatal antecedents of moderate and severe cerebral palsy. Paediatric and Perinatal Epidemiology, 9(2), 171-184.
DOI Scopus64 WoS40 Europe PMC37
1995 Upham, J. W., Holt, B. J., Baron-Hay, M. J., Yabuhara, A., Hales, B. J., Thomas, W. R., . . . Holt, P. G. (1995). Inhalant allergen-specific T-cell reactivity is detectable in close to 100% of atopic and normal individuals: Covert responses are unmasked by serum-free medium. Clinical and Experimental Allergy, 25(7), 634-642.
DOI Scopus118 WoS110 Europe PMC88
1994 Palmer, L., Petterson, B., Blair, E., & Burton, P. (1994). FAMILY PATTERNS OF GESTATIONAL AGE AT DELIVERY AND GROWTH IN UTERO IN MODERATE AND SEVERE CEREBRAL PALSY. Developmental Medicine &amp; Child Neurology, 36(12), 1108-1119.
DOI Scopus9 WoS7 Europe PMC6

Year Citation
2011 Palmer, L., Burton, P., & Smith, G. (Eds.) (2011). An Introduction to genetic epidemiology. Bristol, UK: The Policy Press.
DOI Scopus7
2002 Elston, R. C., Olson, J. M., & Palmer, L. (2002). Biostatistical Genetics and Genetic Epidemiology. John Wiley & Sons.

Year Citation
2024 Palmer, L. J., & Cookson, W. O. C. M. (2024). Atopy and asthma. In Analysis of Multifactorial Disease (pp. 215-238). Garland Science.
DOI Scopus12
2019 Oakden-Rayner, L., & Palmer, L. J. (2019). Artificial intelligence in medicine: Validation and study design. In E. R. Ranschaert, S. Morozov, & P. R. Algra (Eds.), Artificial Intelligence in Medical Imaging: Opportunities, Applications and Risks (pp. 83-104). Cham, Switzerland: Springer.
DOI Scopus9
2016 Kardan, O., Gozdyra, P., Misic, B., Moola, F., Palmer, L. J., Paus, T., & Berman, M. G. (2016). Neighborhood Greenspace and Health in a Large Urban Center. In Urban Forests: Ecosystem Services and Management (pp. 59-90).
Scopus1
2011 Smith, G., Ebrahim, S., Lewis, S., & Palmer, L. (2011). Population health aspects of genetic epidemiology: genomic profiling, personalised medicine, and Mendelian randomisation. In L. Palmer, G. Smith, & P. Burton (Eds.), An Introduction to Genetic Epidemiology (pp. 175-216). Bristol, UK: The Policy Press.
2011 Burton, P., Fortier, I., Deschenes, M., Hansell, A., & Palmer, L. (2011). Biobanks and biobank harmonisation. In L. Palmer, G. Smith, & P. Burton (Eds.), An Introduction to Genetic Epidemiology (pp. 155-174). Bristol, UK: The Policy Press.
Scopus2
2011 Palmer, L., Timpson, N., Evans, D., Smith, G., & Cardon, L. (2011). Mapping complex disease genes using linkage disequilibrium and genome-wide association scans. In L. Palmer, G. Smith, & P. Burton (Eds.), An Introduction to Genetic Epidemiology (pp. 91-130). Bristol, UK: The Policy Press.
2009 Pennell Dr, C., Palmer, L., Knight, B., Relton, C., & Lye, S. (2009). Approaches to evaluate gene-environment interactions underlying the developmental origins of health and disease. In J. Newnham, & M. Ross (Eds.), Early life origins of human health and disease (pp. 205-217). S. Karger AG.
DOI Scopus4
2003 Silverman, E. S., Hjoberg, J., Palmer, L. J., Weiss, S. T., & Drazen, J. M. (2003). Application of pharmacogenetics to the therapeutics of asthma. In Therapeutic Targets in Airway Inflammation (pp. 823-838).
Scopus6
2003 Palmer, L. J., Silverman, E. S., Drazen, J. M., & Weiss, S. T. (2003). Pharmacogenomics of Asthma Treatment. In Pharmacogenomics the Search for Individualized Therapies (pp. 215-234). Wiley.
DOI Scopus3
2002 Palmer, L. J., & McDermott, B. M. C. (2002). Helping Children Cope with Disasters and Terrorism. In A. M. L. Greca (Ed.), Helping Children Cope with Disasters and Terrorism (pp. 139-174). Amer Psychological Assn.
2000 Palmer, L. J. (2000). Analysis of Multifactorial Disease. In D. T. Bishop, & P. C. Sham (Eds.), Analysis of Multifactorial Disease (pp. 215-237). Academic Press.
1993 Palmer, L. J. (1993). Archaeometry. In B. Fankhauser, & J. R. Bird (Eds.), Archaeometry (pp. 28-37).

Year Citation
2024 Pipicella, J. L., Gu, B., Palmer, L., Connor, S. J., Wilson, W., & Andrews, J. M. (2024). Assessing patient-perceived burden of disease in Crohn's disease: a novel scoring approach in a real-world Australasian cohort. In JOURNAL OF CROHNS & COLITIS Vol. 18 (pp. I1035-I1037). OXFORD UNIV PRESS.
2024 Gu, B., Pipicella, J. L., Palmer, L. J., Connor, S. J., Wilson, W. E., & Andrews, J. M. (2024). ASSESSING PATIENT-PERCEIVED BURDEN OF DISEASE IN ULCERATIVE COLITIS: A NOVEL SCORING APPROACH IN A REAL-WORLD AUSTRALASIAN COHORT. In GASTROENTEROLOGY Vol. 166 (pp. S1444). DC, Washington: W B SAUNDERS CO-ELSEVIER INC.
2024 Pipicella, J. L., Gu, B., Palmer, L. J., Connor, S. J., Wilson, W. E., & Andrews, J. M. (2024). ASSESSING PATIENT-PERCEIVED BURDEN OF DISEASE IN CROHN'S DISEASE: A NOVEL SCORING APPROACH IN A REAL-WORLD AUSTRALASIAN COHORT. In GASTROENTEROLOGY Vol. 166 (pp. S1444-S1445). DC, Washington: W B SAUNDERS CO-ELSEVIER INC.
2023 Zeng, M., Xie, Y., To, M. S., Oakden-Rayner, L., Whitbread, L., Bacchi, S., . . . Jenkinson, M. (2023). Improved Flexibility and Interpretability of Large Vessel Stroke Prognostication Using Image Synthesis and Multi-task Learning. In H. Greenspan, A. Madabhushi, P. Mousavi, S. Salcudean, J. Duncan, T. Syeda-Mahmood, & R. Taylor (Eds.), Lecture Notes in Computer Science Including Subseries Lecture Notes in Artificial Intelligence and Lecture Notes in Bioinformatics Vol. 14224 LNCS (pp. 696-705). CANADA, Vancouver: SPRINGER INTERNATIONAL PUBLISHING AG.
DOI Scopus2 WoS2
2022 Pham, R., Marshall, H., Kolovos, A., Qassim, A., Mullany, S., Saks, D., . . . Palmer, L. J. (2022). Associations between deep learning segmented macular optical coherence tomography cell layer thicknesses and primary open-angle glaucoma outcomes in the PROGRESSA study. In CLINICAL AND EXPERIMENTAL OPHTHALMOLOGY Vol. 49 (pp. 913-914). WILEY.
2022 Shenoy, B., Singh, B., Cadby, G., Hung, J., Walsh, J., McQuillan, B., . . . McArdle, N. (2022). Association of conventional polysomnographic metrics of obstructive sleep apnea with major adverse cardiovascular events: a prospective sleep clinic cohort study. In JOURNAL OF SLEEP RESEARCH Vol. 31 (pp. 2 pages). WILEY.
2019 Shenoy, B., Younes, M., Dhaliwal, S., King, S., Rea, C., Hatch, K., . . . Mcardle, N. (2019). CROSS-SECTIONAL ASSOCIATION OF TRADITIONAL AND NOVEL POLYSOMNOGRAPHY METRICS WITH ATHEROSCLEROSIS IN OBSTRUCTIVE SLEEP APNOEA. In SLEEP MEDICINE Vol. 64 (pp. S249). ELSEVIER.
2019 Singh, B., McArdle, N., Marriott, R., Darcey, E., Bond-Smith, D., King, S., . . . Cadby, G. (2019). Association between hypoxemia in OSA and cancer incidence in a large sleep clinic cohort. In JOURNAL OF SLEEP RESEARCH Vol. 28 (pp. 1 page). AUSTRALIA, Sydney: WILEY.
2019 Huseini, T., Dhillon, S., Lu, C. L., McArdle, N., Ling, I., Dhaliwal, S., . . . Singh, B. (2019). Relationship between obstructive sleep apnoea, other cardiovascular risk factors and cardiovascular disease. In JOURNAL OF SLEEP RESEARCH Vol. 28 (pp. 1 page). AUSTRALIA, Sydney: WILEY.
2019 Singh, B., Marriott, R., McArdle, N., Darcey, E., Bond-Smith, D., King, S., . . . Cadby, G. (2019). Age-related differences in association of OSA with cancer incidence in a large sleep clinic cohort. In JOURNAL OF SLEEP RESEARCH Vol. 28 (pp. 1 page). AUSTRALIA, Sydney: WILEY.
2019 Cade, B. E., Lee, J., Gharib, S. A., Gottlieb, D. J., He, K. Y., Hillman, D. R., . . . Redline, S. (2019). Shared Genetic Architecture Between Sleep and Blood Pressure Traits in Humans. In AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE Vol. 199 (pp. 2 pages). TX, Dallas: AMER THORACIC SOC.
2019 Gale, W., Oakden-Rayner, L., Carneiro, G., Palmer, L. J., & Bradley, A. P. (2019). Producing radiologist quality reports for interpretable deep learning. In Proceedings of the 2019 IEEE 16th International Symposium on Biomedical Imaging Vol. 2019-April (pp. 1275-1279). online: IEEE.
DOI Scopus40 WoS33
2018 Lu, C., McArdle, N., Ling, I., Dhaliwal, S., Kosky, C., Hillman, D., . . . Singh, B. (2018). RELATIONSHIP BETWEEN OBSTRUCTIVE SLEEP APNOEA, OTHER CARDIOVASCULAR RISK FACTORS AND CARDIOVASCULAR DISEASE. In RESPIROLOGY Vol. 23 (pp. 38). WILEY.
2018 Singh, B., Marriott, R., Cadby, G., King, S., Ward, K., Darcey, E., . . . McArdle, N. (2018). Association of OSA with the prevalence and incidence of malignant cancers in Western Australia. In JOURNAL OF SLEEP RESEARCH Vol. 27 (pp. 1 page). Brisbane, AUSTRALIA: WILEY.
2018 Ching, D., Abeyweera, P., Singh, B., Ling, I., Kosky, C., Buswell, J., . . . McArdle, N. (2018). CPAP acceptance and adherence in Aboriginal Australians with obstructive sleep apnoea. In JOURNAL OF SLEEP RESEARCH Vol. 27 (pp. 2 pages). Brisbane, AUSTRALIA: WILEY.
2018 Tran, T., Pham, T., Carneiro, G., Palmer, L., & Reid, I. (2018). A Bayesian data augmentation approach for learning deep models. In Advances in Neural Information Processing Systems 30 (NIPS 2017) Vol. 2017-December (pp. 1-10). Long Beach, CA: Neural Information Processing Systems Foundation.
Scopus172 WoS50
2018 De Silva, M., Sebert, S., Alves, A. C., Sovio, U., Das, S., Taal, R. H., . . . Jarvelin, M. (2018). Genetic architecture of early growth phenotypes gives insights into their link with later obesity. In EUROPEAN JOURNAL OF HUMAN GENETICS Vol. 26 (pp. 222-223). DENMARK, Copenhagen: NATURE PUBLISHING GROUP.
2017 Carneiro, G., Oakden-Rayner, L., Bradley, A., Nascimento, J., & Palmer, L. (2017). Automated 5-year mortality prediction using deep learning and radiomics features from chest computed tomography. In Proceedings of the IEEE 14th International Symposium on Biomedical Imaging (ISBI 2017) Vol. abs/1607.00267 (pp. 130-134). Online: IEEE.
DOI Scopus20 WoS12
2017 Singh, B., Bond-Smith, D., Mcardle, N., Ward, K., King, S., Noffsinger, W., . . . Cadby, G. (2017). CHANGING TRENDS OF OBSTRUCTIVE SLEEP APNOEA IN WESTERN AUSTRALIA FROM 1988 TO 2014. In JOURNAL OF SLEEP RESEARCH Vol. 26 (pp. 61-62). Auckland, NEW ZEALAND: WILEY.
DOI
2015 Murphy, S., Palmer, L., & Larkum, M. (2015). Transcranial magnetic stimulation (tms) generates GABAβ-mediated inhibition in layer 5 dendrites. In JOURNAL OF NEUROCHEMISTRY Vol. 134 (pp. 239). AUSTRALIA, Cairns: WILEY-BLACKWELL.
WoS1
2015 Micallef, A., & Palmer, L. (2015). Sensory discrimination in dendrites. In JOURNAL OF NEUROCHEMISTRY Vol. 134 (pp. 239). AUSTRALIA, Cairns: WILEY-BLACKWELL.
2011 Mukherjee, S., Cadby, G., Robinson, B. W., Musk, B., de Klerk, N., & Palmer, L. (2011). A Genome-Wide Association Scan For Malignant Mesothelioma. In AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE Vol. 183 (pp. 1 page). AMER THORACIC SOC.
2011 Musk, A. W., Knuiman, M., Hunter, M., Hui, J., Palmer, L., Beilby, J., . . . James, A. (2011). Patterns Of Airway Disease And The Clinical Diagnosis Of Asthma In The Busselton Population. In AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE Vol. 183 (pp. 1 page). AMER THORACIC SOC.
2011 Ward, K., Palmer, L., Mukherjee, S., Lee, J., Love, G., Fedson, A., . . . Hillman, D. (2011). Validation of a portable monitoring device for investigation of obstructive sleep apnoea (OSA). In JOURNAL OF SLEEP RESEARCH Vol. 20 (pp. 57). Sydney, AUSTRALIA: WILEY-BLACKWELL.
2011 Wu, X. N., Ang, A., Khan, J., Tan, A., Constable, I., & Palmer, L. (2011). CARDIOVASCULAR RISK FACTORS AND AGE-RELATED MACULAR DEGENERATION: LARGE CASE-CONTROL STUDY USING A COMPREHENSIVE LONG-TERM ADMINISTRATIVE DATABASE. In CLINICAL AND EXPERIMENTAL OPHTHALMOLOGY Vol. 39 (pp. 34). WILEY-BLACKWELL.
2011 de Klerk, N., Alfonso, H., Olsen, N., Reid, A., Sleith, J., Hansen, J., . . . Musk, B. (2011). FAMILIAL ASSOCIATIONS FOR MALIGNANT MESOTHELIOMA AFTER EXPOSURE TO BLUE ASBESTOS. In JOURNAL OF THORACIC ONCOLOGY Vol. 6 (pp. S14). Melbourne, AUSTRALIA: ELSEVIER SCIENCE INC.
2011 Marsh, J., McDonald, K., Wheeler, H., Teo, C., Martin, L., Palmer, L., . . . Nowak, A. K. (2011). AUSTRALIAN GENOMICS AND CLINICAL OUTCOMES OF GLIOMA: CHARACTERIZING A RESEARCH POPULATION. In NEURO-ONCOLOGY Vol. 13 (pp. 87). OXFORD UNIV PRESS INC.
2010 Wain, L. V., Shrine, N. R. G., Shaw, C., Powell, J. F., Hardy, J., Shaw, P., . . . Tobin, M. D. (2010). The Role of Common Copy Number Variation in Amyotrophic Lateral Sclerosis (ALS). In GENETIC EPIDEMIOLOGY Vol. 34 (pp. 929-930). Boston, MA: WILEY-BLACKWELL.
2010 Liew, Y. M., Ward, S., McLaughlin, R. A., Wood, F., Palmer, L., & Sampson, D. S. (2010). VISUALIZATION OF SUB-SURFACE STRUCTURES IN SCAR TISSUE USING OPTICAL COHERENCE TOMOGRAPHY. In WOUND REPAIR AND REGENERATION Vol. 18 (pp. A67). WILEY-BLACKWELL.
2010 Adams, L. A., Ang, W. Q., Ayonrinde, O. T., Olynyk, J. K., Beilin, L. J., Palmer, L. J., . . . Pennell, C. P. (2010). Lipid metabolism gene polymorphisms and risk of fatty liver in adolescents: a population cohort study. In JOURNAL OF GASTROENTEROLOGY AND HEPATOLOGY Vol. 25 (pp. A109). WILEY-BLACKWELL PUBLISHING, INC.
2010 Fedson, A., Cooper, M., Lee, J., Ward, K., Simpson, L., Edwards, C., . . . Palmer, L. J. (2010). OBSTRUCTIVE SLEEP APNEA IS INDEPENDENTLY ASSOCIATED WITH INSULIN RESISTANCE AND CARDIOVASCULAR SINGLE NUCLEOTIDE POLYMORPHISMS. In SLEEP Vol. 33 (pp. A180). OXFORD UNIV PRESS INC.
2010 Pennell, C. E., Ang, Q. W., van Eekelen, J. A. M., Marsh, J. A., Briollais, L., Newhnam, J. P., . . . Lye, S. J. (2010). Polymorphisms in Genes That Regulate HPAAxis Function Are Associated with Antenatal Fetal Growth Trajectories and Postnatal HPA Axis. In REPRODUCTIVE SCIENCES Vol. 17 (pp. 108A). Orlando, FL: SAGE PUBLICATIONS INC.
2010 Huang, R. C., Pennell, C. E., Ang, Q. W., Mori, T. A., Stanley, F. J., Lye, S. J., . . . Beilin, L. J. (2010). ASSOCIATION OF HYPOTHALAMIC PITUITARY AXIS GENES WITH LONGITUDINAL CHILDHOOD SYSTOLIC BLOOD PRESSURE. In HYPERTENSION Vol. 55 (pp. 1499-1500). Sydney, AUSTRALIA: LIPPINCOTT WILLIAMS & WILKINS.
2010 Golledge, J., Biros, E., Warrington, N., Jones, G., Cooper, M., van Rij, A., . . . Norman, P. (2010). A Population-Based Study of Polymorphisms in Genes Related to Sex Hormones and Abdominal Aortic Aneurysm. In JOURNAL OF VASCULAR SURGERY Vol. 51 (pp. 92S). Boston, MA: MOSBY-ELSEVIER.
DOI
2010 Cadby, G., Ward, S. V., Cole, J. M., Millward, M., & Palmer, L. J. (2010). Association of Candidate SNPs with Melanoma Susceptibility in Australian Adults. In GENETIC EPIDEMIOLOGY Vol. 34 (pp. 966). Boston, MA: WILEY-BLACKWELL.
2010 Fedson, A., Lam, E., Ward, K., Cooper, M., Lee, J., Simpson, L., . . . Palmer, L. J. (2010). CARDIOVASCULAR AND ASSOCIATED MORBIDITY COMPARISONS BETWEEN OBSTRUCTIVE SLEEP APNEA PATIENTS AND GENERAL POPULATION CONTROLS USING WESTERN AUSTRALIAN LINKED HEALTH DATA. In SLEEP Vol. 33 (pp. A117). OXFORD UNIV PRESS INC.
2010 Freathy, R. M., Mook-Kanamori, D. O., Sovio, U., Prokopenko, I., Timpson, N. J., Berry, D. J., . . . Mccarthy, M. I. (2010). Identification of Novel Genetic Loci Associated with Birth Weight Confirms Genetic Links between Fetal Growth and Type 2 Diabetes. In DIABETES Vol. 59 (pp. A36). Orlando, FL: AMER DIABETES ASSOC.
2010 Adams, L. A., Ang, W. Q., Ayonrinde, O. T., Olynyk, J. K., Beilin, L. J., Mori, T. A., . . . Penne, C. E. (2010). LIPID METABOLISM GENE POLYMORPHISMS AND RISK OF FATTY LIVER IN ADOLESCENTS: A POPULATION BASED COHORT STUDY. In HEPATOLOGY Vol. 52 (pp. 451A-452A). Boston, MA: WILEY-BLACKWELL.
2010 Ang, Q. W., Pennell, C. E., Ayonrinde, O. T., Olynyk, J. K., Warrington, N. M., Palmer, L. J., . . . Adams, L. A. (2010). Gene-Environment Interactions Underlying the Development of Non-Alcoholic Fatty Liver Disease (NAFLD) in Adolescence. In REPRODUCTIVE SCIENCES Vol. 17 (pp. 287A). Orlando, FL: SAGE PUBLICATIONS INC.
2009 Cooper, M. N., Cadby, G., Lee, J. D., Fedson, A. C., Simpson, L., Ward, K. L., . . . Palmer, L. J. (2009). Using Mendelian Randomisation to Investigate the Relationship Between Blood Pressure and The Severity of Bbstructive Sleep Apnea. In GENETIC EPIDEMIOLOGY Vol. 33 (pp. 778-779). Honolulu, HI: WILEY-LISS.
2009 Musk, A. W., Hui, J., Knuiman, M. W., Divitini, M. L., Maier, G., Hunter, M., . . . James, A. L. (2009). Increased Doctor-Diagnosed Asthma in Busselton Adults: Is It Really Asthma?.. In AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE Vol. 179 (pp. 1 page). AMER THORACIC SOC.
2009 Ayonrinde, O. T., Olynyk, J. K., Pennell, C. E., Warrington, N. M., Palmer, L. J., Beilin, L. J., . . . Adams, L. A. (2009). Polymorphisms in adiponectin gene are associated with non-alcoholic fatty liver disease (NAFLD) in Western Australian adolescents. In JOURNAL OF GASTROENTEROLOGY AND HEPATOLOGY Vol. 24 (pp. A295). WILEY-BLACKWELL PUBLISHING, INC.
2009 Pennell, C. E., Marsh, J. A., Warrington, N. M., Beilin, L. J., Newnham, J. P., Lye, S. J., & Palmer, L. J. (2009). Polymorphism in <i>FTO</i> Links Fetal Growth Trajectories to Childhood BMI. In REPRODUCTIVE SCIENCES Vol. 16 (pp. 98A). Glasgow, SCOTLAND: SAGE PUBLICATIONS INC.
2009 Lam, E., Webster, R. J., Emery, J., & Palmer, L. J. (2009). Celestial3D: Designing a Tool for 3D Visualization of Familial Data from a Bioinformatics Perspective. In GENETIC EPIDEMIOLOGY Vol. 33 (pp. 820). Honolulu, HI: WILEY-LISS.
2009 Ayonrinde, O. T., Olynyk, J. K., Pennell, C. E., Beilin, L. J., Mori, T. A., Oddy, W. H., . . . Adams, L. (2009). GENE-ENVIRONMENT INTERACTIONS UNDERLYING THE DEVELOPMENT OF NON-ALCOHOLIC FATTY LIVER DISEASE IN ADOLESCENCE ARE INFLUENCED BY GENDER. In HEPATOLOGY Vol. 50 (pp. 770A). Boston, MA: JOHN WILEY & SONS INC.
2009 Marsh, J. A., Warrington, N. M., Pennell, C. E., Newnham, J. P., Baddeley, A. J., & Palmer, L. J. (2009). Weighing up the Evidence: a Comparison of Antenatal Growth Trajectories and Birth Weight in Genetic Analyses. In GENETIC EPIDEMIOLOGY Vol. 33 (pp. 803-804). Honolulu, HI: WILEY-LISS.
2009 Ayonrinde, O. T., Olynyk, J. K., Pennell, C. E., Ang, W., Warrington, N. M., Palmer, L. J., . . . Adams, L. A. (2009). Polymorphisms in the C-reactive protein (CRP) gene are associated with non-alcoholic fatty liver disease (NAFLD) in Western Australian adolescents independent of insulin resistance. In JOURNAL OF GASTROENTEROLOGY AND HEPATOLOGY Vol. 24 (pp. A295). WILEY-BLACKWELL PUBLISHING, INC.
2009 He, J., Bosse, Y., Laprise, C., Pare, P., Sandford, A., Kozyrskyj, A., . . . Daley, D. (2009). Novel Associations of Genetic Polymorphisms in the Interleukin-1 receptor/Toll-like Receptor Signaling Pathways with Atopy and Atopic Asthma. In JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY Vol. 123 (pp. S167). Washington, DC: MOSBY-ELSEVIER.
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2009 An, P., Mukherjee, O., Chanda, P., Yao, L., Engelman, C. D., Huang, C. H., . . . Province, M. A. (2009). The challenge of detecting epistasis (G x G interactions): Genetic analysis workshop 16. In Genetic Epidemiology Vol. 33 (pp. S58-S67). United States: Wiley.
DOI Scopus17 Europe PMC16
2009 Ward, S. V., Cadby, G., Cole, J. M., Wood, F. M., Millward, M., & Palmer, L. J. (2009). The Western Australian Melanoma Health Study (WAMHS). In GENETIC EPIDEMIOLOGY Vol. 33 (pp. 787). Honolulu, HI: WILEY-LISS.
2009 Warrington, N. M., Briollais, L., Marsh, J. A., Pennell, C. E., Lye, S. J., & Palmer, L. J. (2009). Modelling Complex Longitudinal Data in Genetic Association analyses. In GENETIC EPIDEMIOLOGY Vol. 33 (pp. 803). Honolulu, HI: WILEY-LISS.
2009 Cadby, G., Carter, K. W., Wiltshire, S., & Palmer, L. J. (2009). Investigating Aspects of Statistical Power in Meta-Analysis of Complex Traits. In GENETIC EPIDEMIOLOGY Vol. 33 (pp. 791). Honolulu, HI: WILEY-LISS.
2009 Webster, R. J., Warrington, N. M., Weedon, M. N., Hattersley, A. T., Beilby, J. P., Frayling, T. M., & Palmer, L. J. (2009). The Longitudinal Association of Common Susceptibility Variants for Type 2 Diabetes and Obesity with Fasting Plasma Glucose and BMI. In GENETIC EPIDEMIOLOGY Vol. 33 (pp. 803). Honolulu, HI: WILEY-LISS.
2008 Longville, B. A. C., Xiao, J., Tan, A. X. J., Feng, X., Wu, X., Adams, C. J., . . . Palmer, L. J. (2008). C2 and CFB Genes in Severity of Age-related Macular Degeneration. In GENETIC EPIDEMIOLOGY Vol. 32 (pp. 704). St Louis, MO: WILEY-LISS.
2008 Huang, R. C., Mori, T. A., Burke, V., Newnham, J. P., Stanley, F. J., Landau, L. I., . . . Beilin, L. J. (2008). FACTORS PREDISPOSING TO INFLAMMATION AND ALTERED LIVER FUNCTION IN 13 YEAR OLDS WITH FEATURES OF THE METABOLIC SYNDROME. In HYPERTENSION Vol. 52 (pp. 168). Adelaide, AUSTRALIA: LIPPINCOTT WILLIAMS & WILKINS.
2008 Huang, R. C., Mori, T. A., Newnham, J. P., Kendall, G., Stanley, F. J., Landau, L. I., . . . Beilin, L. J. (2008). POSTNATAL GROWTH TRAJECTORIES, BIRTHWEIGHT AND MATERNAL SMOKING CAN PREDICT CARDIOVASCULAR RISK IN ADOLESCENCE. In HYPERTENSION Vol. 52 (pp. 169). Adelaide, AUSTRALIA: LIPPINCOTT WILLIAMS & WILKINS.
2008 Palmer, L., Economou, P., Huntington, J., Cruz, D., McLennon, S. M., Maris, M., . . . Gross, M. (2008). The relationship between fatigue, emotional functioning, neurocognitive functions, and learning disabilities in college students. In CLINICAL NEUROPSYCHOLOGIST Vol. 22 (pp. 757). TAYLOR & FRANCIS INC.
2008 Huang, R. -C., Mori, T., Newnham, J., Kendall, G., Stanley, F., Landau, L., . . . Beilin, L. (2008). Antenatal and postnatal growth trajectories predict hsCRP in adolescence. In JOURNAL OF HYPERTENSION Vol. 26 (pp. S323). Berlin, GERMANY: LIPPINCOTT WILLIAMS & WILKINS.
2008 Huang, R. -C., Mori, T., Newnham, J., Kendall, G., Stanley, F., Landau, L., . . . Beilin, L. (2008). Antenatal and postnatal growth trajectories predict systolic blood pressure in adolescence. In JOURNAL OF HYPERTENSION Vol. 26 (pp. S239-S240). Berlin, GERMANY: LIPPINCOTT WILLIAMS & WILKINS.
2008 Huang, R. -C., Mori, T., Newnham, J., Kendall, G., Stanley, F., Landau, L., . . . Beilin, L. (2008). Postnatal growth trajectories predict cardiovascular risk in adolescence. In JOURNAL OF HYPERTENSION Vol. 26 (pp. S240). Berlin, GERMANY: LIPPINCOTT WILLIAMS & WILKINS.
2007 Allen, R. P., Calloway, M. O., Kwong, W. J., & Palmer, L. (2007). Prevalence of Restless legs syndrome in a primary-care population. In MOVEMENT DISORDERS Vol. 22 (pp. S273). Istanbul, TURKEY: WILEY-LISS.
2007 Allen, R. P., Kwong, W. J., Calloway, M. O., & Palmer, L. (2007). Burden of illness associated with Restless legs syndrome: Findings from patients visiting primary care settings in the US. In MOVEMENT DISORDERS Vol. 22 (pp. S272). Istanbul, TURKEY: WILEY-LISS.
2007 Huang, R. C., Mori, T. A., Newnham, J. P., Kendal, G., Doherty, D., Stanley, F. J., . . . Beilin, L. J. (2007). Antenatal growth trajectories are associated with postnatal growth trajectories and cardiovascular outcomes. In EARLY HUMAN DEVELOPMENT Vol. 83 (pp. S74). ELSEVIER IRELAND LTD.
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2007 Huang, R. C., Mori, T. A., Newnham, J. R., Kendall, G., Doherty, D., Stanley, F. J., . . . Beilin, L. J. (2007). Postnatal growth trajectories can predict cardiovascular risk in adolescence. In EARLY HUMAN DEVELOPMENT Vol. 83 (pp. S90). ELSEVIER IRELAND LTD.
2007 Huang, R. C., Mori, T. A., Newnham, J. P., Kendall, G., Sloan, N., Stanley, F. J., . . . Beilin, L. J. (2007). Inflammation and altered liver function is present in 13 year old children with features of the metabolic syndrome. In EARLY HUMAN DEVELOPMENT Vol. 83 (pp. S67-S68). ELSEVIER IRELAND LTD.
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2007 McCaskie, P. A., Chapman, C. M. L., Beilby, J. P., Hung, J., McQuillan, B. M., Carter, K. W., . . . Palmer, L. J. (2007). SNPs and haplotypes in the 15-LOX gene are associated with intermediate phenotypes but not risk of coronary heart disease. In GENETIC EPIDEMIOLOGY Vol. 31 (pp. 488). St Petersburg, FL: WILEY-BLACKWELL.
2007 Huang, R. C., Mori, T. A., Newnham, J. P., Kendall, G., Doherty, D., Stanley, F. J., . . . Beilin, L. J. (2007). The definition of postnatal growth trajectories. In EARLY HUMAN DEVELOPMENT Vol. 83 (pp. S90). ELSEVIER IRELAND LTD.
2007 Huang, R. C., Mori, T. A., Newnham, J. P., Kendall, G., Doherty, D., Stanley, F. J., . . . Beilin, L. J. (2007). The definition of antenatal growth trajectories. In EARLY HUMAN DEVELOPMENT Vol. 83 (pp. S90-S91). ELSEVIER IRELAND LTD.
2007 Huang, R. C., Mori, T. A., Stanley, F. J., Kendall, G., Palmer, L. J., Oddy, W. H., . . . Beilin, L. J. (2007). Inflammation and altered liver function is present in 13 year olds with features of the metabolic syndrome. In HYPERTENSION Vol. 49 (pp. 1463-1464). Brisbane, AUSTRALIA: LIPPINCOTT WILLIAMS & WILKINS.
2007 McCaskie, P. A., & Palmer, L. J. (2007). Too correlated to be true? Complete separation and the problem of "bouncing betas". In GENETIC EPIDEMIOLOGY Vol. 31 (pp. 489). St Petersburg, FL: WILEY-BLACKWELL.
2007 Palmer, L. J. (2007). Human genome epidemiology, biobanks, and DOHaD. In EARLY HUMAN DEVELOPMENT Vol. 83 (pp. S36). ELSEVIER IRELAND LTD.
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2007 Clarkel, G. M., Carter, K., Palmer, L. J., Morris, A. P., & Cardon, L. R. (2007). Replication strategies for whole genome association (WGA) studies. In GENETIC EPIDEMIOLOGY Vol. 31 (pp. 456-457). St Petersburg, FL: WILEY-LISS.
2006 Huang, R. -C., Mori, T. A., Stanley, F. J., Kendal, G., Palmer, L. J., Oddy, W. H., . . . Beilin, L. J. (2006). Inflammation and altered liver function is present in 13 year olds with features of the metabolic syndrome. In JOURNAL OF HYPERTENSION Vol. 24 (pp. 36). Fukuoka, JAPAN: LIPPINCOTT WILLIAMS & WILKINS.
2006 de Klerk, N., Alfonso, H., Reid, A., Ambrosini, G., Olsen, N., Berry, G., . . . Palmer, L. (2006). Familial clustering of mesothelioma in subjects exposed to crocidolite at Wittenoom. In LUNG CANCER Vol. 54 (pp. S1). ELSEVIER IRELAND LTD.
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2005 Beilin, L., Huang, R., Burke, V., Palmer, L., Kendall, G., Blake, K., . . . Stanley, F. (2005). Predicted birthweight and postnatal weight gain and the risk of metabolic syndrome at 8 years of age. In JOURNAL OF HYPERTENSION Vol. 23 (pp. S133). Milan, ITALY: LIPPINCOTT WILLIAMS & WILKINS.
2005 Beilin, L. J., Huang, R. C., Burke, V., Palmer, L. J., Kendall, G., Blake, K., . . . Stanley, F. (2005). Predicted birthweight and postnatal weight gain and the risk of metabolic syndrome at 8 years of age. In CLINICAL AND EXPERIMENTAL PHARMACOLOGY AND PHYSIOLOGY Vol. 32 (pp. A8). Sydney, AUSTRALIA: WILEY-BLACKWELL.
2005 Carter, K. W., Pluznhnikov, A., Timms, A. E., Miceli-Richard, C., Jin, L., Wordsworth, B. P., . . . Brown, M. A. (2005). Meta-analysis in ankylosing spondylitis (AS) - Genomewide linkage map including 589 affected sibling pairs.. In ARTHRITIS AND RHEUMATISM Vol. 52 (pp. S241). San Diego, CA: WILEY-BLACKWELL.
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2005 Kushmerick, M. J., Shankland, E., Rusk, J., & Palmer, L. (2005). Energetics of fast and slow muscle are not different. In FASEB JOURNAL Vol. 19 (pp. A1124). CA, San Diego: FEDERATION AMER SOC EXP BIOL.
2005 Carter, K. W., Pluzhnikov, A., Timms, A. E., Miceli-Richard, C., Jin, L., Wordsworth, B. P., . . . Brown, M. A. (2005). Meta-analysis in ankylosing spondylitis (AS) - Genomewide linkage map including 589 affected sibling pairs. In TISSUE ANTIGENS Vol. 66 (pp. 368-369). Melbourne, AUSTRALIA: BLACKWELL PUBLISHING.
2005 McCaskie, P. A., Carter, K. W., & Palmer, L. J. (2005). SimHap: A comprehensive modeling framework and simulation-based approach to haplotype analysis for population data. In GENETIC EPIDEMIOLOGY Vol. 29 (pp. 268). Park City, UT: WILEY-LISS.
2004 Association between haplotypes in the cholesteryl ester transfer protein (CETP) gene and high density lipoprotein (HDL) levels: Results from three separate populations (2004). In GENETIC EPIDEMIOLOGY Vol. 27 (pp. 285). WILEY-LISS.
2004 Regulatory promoter variants of the PTGDR gene are protective for asthma (2004). In GENETIC EPIDEMIOLOGY Vol. 27 (pp. 309). WILEY-LISS.
2003 Celedon, J. C., Raby, B., Palmer, L., Sylvia, J., Kwiatkowski, D., Chapman, H., . . . Silverman, E. K. (2003). Linkage and association analysis of COPD-related phenotypes on chromosome 19.. In AMERICAN JOURNAL OF HUMAN GENETICS Vol. 73 (pp. 505). LOS ANGELES, CALIFORNIA: UNIV CHICAGO PRESS.
2003 Palmer, L. J., Buxbaum, S. G., Larkin, E. K., Patel, S. R., Elston, R. C., Tishler, P. V., & Redline, S. (2003). A whole genome scan for obstructive sleep apnea and obesity in African-American families. In SLEEP Vol. 26 (pp. A419). CHICAGO, ILLINOIS: AMER ACADEMY SLEEP MEDICINE.
2003 Turner, S. W., Palmer, L. J., Rye, P. J., Gibson, N. A., Judge, P. K., Young, S., . . . Le Souëf, P. N. (2003). Longitudinal analyses of airway responsiveness from infancy to mid-childhood. In THORAX Vol. 58 (pp. 12). LONDON, ENGLAND: B M J PUBLISHING GROUP.
2002 Raby, B. A., Klimecki, W. T., Laprise, C., Renaud, Y., Faith, J., Lemire, M., . . . Weiss, S. T. (2002). Common functional polymorphisms in toll-like receptor 4 (TLR4) are not associated with asthma or atopy-related phenotypes.. In AMERICAN JOURNAL OF HUMAN GENETICS Vol. 71 (pp. 465). BALTIMORE, MARYLAND: UNIV CHICAGO PRESS.
2002 Turner, S. W., Palmer, L. J., Rye, P. J., Gibson, N. A., Judge, P. K., Young, S., . . . Le Souëf, P. N. (2002). The complex relationship between asthma and airway responsiveness throughout childhood. In THORAX Vol. 57 (pp. 1 page). LONDON, ENGLAND: BRITISH MED JOURNAL PUBL GROUP.
2002 Celedon, J. C., Palmer, L. J., Raby, B., Seriter, J. M., Drazen, J. M., Kwiatkowski, D. J., . . . Silverman, E. K. (2002). Fine mapping linkage analysis of COPD-related phenotypes on chromosome 19.. In AMERICAN JOURNAL OF HUMAN GENETICS Vol. 71 (pp. 465). BALTIMORE, MARYLAND: UNIV CHICAGO PRESS.
2000 Palmer, L. J., Jones, T. W., Davies, E. A., & Burton, P. R. (2000). The familial aggregation of age-of-onset of childhood-onset type-1 diabetes in a population-based diabetes register from Western Australia.. In AMERICAN JOURNAL OF HUMAN GENETICS Vol. 67 (pp. 215). UNIV CHICAGO PRESS.
2000 Palmer, L., Farrar, A., & Schmitt, B. (2000). The impact of psychological trauma on language in school age children. In ARCHIVES OF CLINICAL NEUROPSYCHOLOGY Vol. 15 (pp. 798). PERGAMON-ELSEVIER SCIENCE LTD.
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2000 Chapman, C. M., McQuillan, B. M., Hung, J., Beilby, J. P., & Palmer, L. J. (2000). Polymorphisms in the angiotensinogen gene are associated with intima-medial wall thickening in females from a community based population.. In AMERICAN JOURNAL OF HUMAN GENETICS Vol. 67 (pp. 344). UNIV CHICAGO PRESS.
1999 Palmer, L. J., Tiller, K. J., Musk, A. W., Cookson, W. O. C. M., & Burton, P. R. (1999). Major gene focusing: A novel technique for high efficiency linkage analysis and genomic screening for complex traits such as asthma. In AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE Vol. 159 (pp. A646). AMER LUNG ASSOC.
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1999 Palmer, L. J., Tiller, K. J., Jacobs, K. B., Musk, A. W., James, A. L., Elston, R. C., . . . Cookson, W. O. C. M. (1999). Genome wide linkage analysis using genetic variance effects of asthma-associated binary, censored and continuous traits.. In AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE Vol. 159 (pp. A646). AMER LUNG ASSOC.
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1999 Palmer, L. J., Rye, P. J., Gibson, N. A., Judge, V., Young, S., Burton, P. R., . . . LeSouëf, P. N. (1999). Airway responsiveness (AR) and lung function at 1 month of age predict airway responsiveness, lung function, asthma and ATCPY at 6 years of age.. In AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE Vol. 159 (pp. A150). AMER LUNG ASSOC.
1996 Palmer, L., Saha, B., Hodes, R., & Abe, R. (1996). Immune-mediated responses against mouse mammary tumor virus (MMTV) in CD28-deficient mice.. In FASEB JOURNAL Vol. 10 (pp. 2639). FEDERATION AMER SOC EXP BIOL.

Year Citation
2024 Gu, B., Pipicella, J. L., Palmer, L., Connor, S. J., Wilson, W., & Andrews, J. M. (2024). Assessing patient-perceived burden of disease in Ulcerative Colitis: a novel scoring approach in a real-world Australasian cohort. Poster session presented at the meeting of JOURNAL OF CROHNS & COLITIS. OXFORD UNIV PRESS.
2023 Bhattacharjya, R., Bampton, T. J., Barnett, M., Palmer, L. J., & Coates, T. P. (2023). Demand prevalence on health care services by type 1 and 2 diabetes mellitus in an Australian population - a data linkage analysis. Poster session presented at the meeting of TRANSPLANTATION. CA, San Diego: LIPPINCOTT WILLIAMS & WILKINS.
DOI
2022 Wu, D., Drogemuller, C., Couper, R., Torpy, D., Scott, H., Palmer, L., . . . Coates, P. T. (2022). The Genetic Epidemiology of Hereditary Pancreatitis in Australia and Its Effect on Patients of Total Pancreatectomy and Islet Auto Translation (TP-IAT). Poster session presented at the meeting of TRANSPLANTATION. ELECTR NETWORK: LIPPINCOTT WILLIAMS & WILKINS.
2020 Wu, D., Coates, P. T. H., & Palmer, L. (2020). PHENOTYPIC AND GENOTYPIC ANALYSIS OF HEREDITARY PANCREATITIS IN PATIENTS AND POTENTIAL CANDIDATES FOR TOTAL PANCREATECTOMY WITH ISLET AUTOTRANSPLANTATION (TP-IAT). Poster session presented at the meeting of TRANSPLANTATION. ELECTR NETWORK: LIPPINCOTT WILLIAMS & WILKINS.
2017 Carneiro, G., Oakden-Rayner, L., Bradley, A. P., Nascimento, J. C., & Palmer, L. J. (2017). Automated 5-year mortality prediction using deep learning and radiomics features from chest computed tomography.. Poster session presented at the meeting of ISBI. IEEE.
2014 Palmer, L. J. (2014). Challenges Of Congenital Central Hypoventilation Syndrome For An Adult Patient Presenting With An Acute Abdominal Catastrophe. Poster session presented at the meeting of AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE. AMER THORACIC SOC.
2014 Singh, M., Kowgier, M., Filate, W., Palmer, L. J., & Mukherjee, S. (2014). Sleep Patterns In The Ontario Health Study: Ethnic Variations In Sleep Duration. Poster session presented at the meeting of AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE. AMER THORACIC SOC.
2013 Kowgier, M., Mukherjee, S., Redline, S. S., Patel, S. R., Cade, B. E., Hillman, D., & Palmer, L. J. (2013). A Genome-Wide Association Study Of Obstructive Sleep Apnea In Non-Obese Subjects From The Western Australian Sleep Health Study. Poster session presented at the meeting of AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE. AMER THORACIC SOC.
2012 Benke, K. S., Wu, Y., & Palmer, L. J. (2012). Power Considerations for a GWA of Linear Mixed Effects Models. Poster session presented at the meeting of GENETIC EPIDEMIOLOGY. Stevenson, WA: WILEY-BLACKWELL.
2012 Louise, S., Briollais, L., Mori, T. A., Mattes, E., McCaskie, P. A., Pennell, C. E., . . . Beilin, L. J. (2012). THE PLEIOTROPHIC EFFECT OF LEPTIN AND LEPTIN RECEPTOR GENES ON BMI AND AGGRESSION SCORES IN ADOLESCENTS. Poster session presented at the meeting of HYPERTENSION. Perth, AUSTRALIA: LIPPINCOTT WILLIAMS & WILKINS.
2012 Pennell, C. E., Marsh, J. A., Ang, Q. W., Taal, H. R., Palmer, L. J., Lye, S. J., . . . Newnham, J. P. (2012). Maternal and Fetal Genotype Is Required To Understand the Full Impact of Genetics on Fetal Growth.. Poster session presented at the meeting of REPRODUCTIVE SCIENCES. SAGE PUBLICATIONS INC.
2012 Ward, S. V., Wallace, H. J., Cadby, G., Heyworth, J. S., Fear, M. W., Cole, J. M., . . . Palmer, L. J. (2012). ASSOCIATION OF WOUND REPAIR AND PIGMENTATION GENES WITH SCAR OUTCOME FOLLOWING SUCCESSFUL PRIMARY CLOSURE OF SKIN TUMOR EXCISION. Poster session presented at the meeting of WOUND REPAIR AND REGENERATION. WILEY-BLACKWELL.
2011 Louise, S., Briollais, L., Mattes, E., McCaskie, P., Oddy, W. H., Mori, T., . . . Palmer, L. J. (2011). MONOAMINE OXIDASE A (MAOA) IS ASSOCIATED WITH DEPRESSIVE SYMPTOM SCORES AND BLOOD PRESSURE IN ADOLESCENT BOYS BUT NOT GIRLS. Poster session presented at the meeting of HYPERTENSION. Melbourne, AUSTRALIA: LIPPINCOTT WILLIAMS & WILKINS.
2011 Parmar, P. G., Marsh, J. A., Taal, R. H., Newnham, J. P., Uitterlinden, A. G., Briollais, L., . . . Pennell, C. E. (2011). Polymorphisms in Genes within the IGF-Axis Influence Antenatal and Postnatal Growth. Poster session presented at the meeting of JOURNAL OF DEVELOPMENTAL ORIGINS OF HEALTH AND DISEASE. CAMBRIDGE UNIV PRESS.
2011 Mukherjee, S., Cadby, G., Reid, A., Garlepp, M., Robinson, B. W. S., de Klerk, N., . . . Palmer, L. J. (2011). A GENOME WIDE ASSOCIATION SCAN FOR MALIGNANT MESOTHELIOMA. Poster session presented at the meeting of JOURNAL OF THORACIC ONCOLOGY. Melbourne, AUSTRALIA: ELSEVIER SCIENCE INC.
WoS1
2011 White, S. W., Wa, N. M., Marsh, J. A., Beilin, L. J., Newnham, J. P., Palmer, L. J., . . . Pennell, C. E. (2011). Genetic Variants Associated with Adult Glucose Homeostasis Are Associated with Fetal Growth Trajectories and Adolescent Insulin Resistance. Poster session presented at the meeting of REPRODUCTIVE SCIENCES. SAGE PUBLICATIONS INC.
2011 Warrington, N., Mook-Kanamori, D., Marsh, J., Taal, H., Newnham, J., Beilin, L., . . . Jaddoe, V. (2011). Variants near CCNL1/LEKR1 and in ADCY5 and fetal growth characteristics in different trimesters. Poster session presented at the meeting of Abstracts of the 58th Annual Scientific Meeting of the Society for Gynecologic Investigation, as published in Reproductive Sciences. Miami Beach, FL.: SAGE Publications.
DOI
2011 Pennell, C. E., Warrington, N. M., Mook-Kanamori, D., Lye, S. J., Newnham, J. P., Palmer, L. J., . . . Frayling, T. M. (2011). Genetic Basis for Gestation Length. Poster session presented at the meeting of REPRODUCTIVE SCIENCES. SAGE PUBLICATIONS INC.
2011 Marsh, J. A., White, S. W., Warrington, N. M., Lye, S. J., Smith, G. D., Newnham, J. P., . . . Pennell, C. E. (2011). Feeding the Epidemic of Childhood Obesity. Poster session presented at the meeting of JOURNAL OF DEVELOPMENTAL ORIGINS OF HEALTH AND DISEASE. CAMBRIDGE UNIV PRESS.
2011 Pennell, C. E., Marsh, J. A., Ang, Q. W., Taal, H. R., Palmer, L. J., Lye, S. J., . . . Newnham, J. P. (2011). Maternal and Fetal Genotype Is Required to Understand the Full Impact of Genetics on Fetal Growth. Poster session presented at the meeting of JOURNAL OF DEVELOPMENTAL ORIGINS OF HEALTH AND DISEASE. CAMBRIDGE UNIV PRESS.

Year Citation
2007 Authors: Palmer LJ. Title: Analysis of SNP Haplotypes. In Christiani, D. and Fraser, P. (eds), Gene-Environment Interactions: Role in the Modulation of Pulmonary and Autoimmune Disease Risks, The Biomedical & Life Sciences Collection, Henry Stewart Talks Ltd, London [Online audiovisual talk]. Description: N/A. Extent: 57 minutes.

Year Citation
2024 Wang, H., Nagarajan, P., Kurniansyah, N., Lee, J., Gharib, S., Xu, Y., . . . Redline, S. (2024). Gene-Excessive Sleepiness Interactions Suggest Treatment Targets for Obstructive Sleep Apnea Subtype.
DOI
2024 Mordaunt, D., Johnson, N., Verghese, S., Parker, R., Gibb, K., & Palmer, L. (2024). Navigating Medication Safety with Electronic Medical Records: Insights from a Dual-Phase Implementation in Paediatric, Neonatal and Maternity Care.
DOI
2024 Whitbread, L., Laurenz, S., Palmer, L., Jenkinson, M., & the Alzheimer’s Disease Neuroimaging Initiative. (2024). Deep-diffeomorphic networks for conditional brain templates.
DOI
2024 Tikhomirov, L., Smith, L., Oakden-Rayner, L., Bird, A., Palmer, L., & Semmler, C. (2024). Large-Scale Evaluation of the Influence of AI-use on Radiologist Performance using Signal Detection Theory.
DOI
2024 Tikhomirov, L., Smith, L., Oakden-Rayner, L., Bird, A., Palmer, L., & Semmler, C. (2024). Greater disease detection, less AI rejection: Large-scale evaluation of the influence of AI-use on radiologist performance using signal detection theory.
DOI
2020 Wang, H., Noordam, R., Cade, B., Schwander, K., Winkler, T., Lee, J., . . . van Heemst, D. (2020). Multi-ancestry genome-wide gene-sleep interactions identify novel loci for blood pressure.
DOI

Competitive Research Funding

National Competitive Schemes

 

Date Project/No. Investigators Funding Body Amount
1993-1996 974301 - The genetic epidemiology of childhood asthma PI - Palmer. NHMRC AUD $90,000
1996 - 1997 A study of HLA and T cell receptor beta-chain DNA polymorphism within a cohort of patients with idiopathic arthritis of childhood Co-PI - Palmer, Manners. Rheumatology Research Trust Fund of Western Australia AUD $10,000
1999 Respiratory health in a remote tropical Aboriginal community Co-PI - Musk, et al. Health Department of Western Australia AUD $140,000
1997 - 2001 974301 - The genetic epidemiology of complex human diseases PI - Palmer. NHMRC AUD $200,000
2001 A whole genome screen for asthma in 387 families from Anqing Province, China. Co-I - Weiss, Xu Mammalian Genotyping Service, NHLBI, NIH, USA USD $200,000
2001 A collaboration to investigate simulated annealing in Gibbs sampler analyses of genetic data. PI - Palmer, Hurn. European Science Foundation €5,000 Euro
2000 - 2004 003209 - Epidemiological studies in maternal and child health Co-I (PI on Core) - Stanley, et al. NHMRC AUD $5,725,000
2000 - 2002 Combination of evidence in complex inheritance: consortium on asthma genetics (COAG) Co-I - Morton, Collins, Palmer. MRC, UK GBP £166,204
2000 - 2004 The Pharmacogenetics of Asthma Treatment Co-I - Weiss. NHLBI, NIH, USA ~USD $13,000,000
2000 - 2004 Innate immunity in Heart, Lung and Blood Disease Co-I - Weiss, Martinez. NHLBI, NIH, USA ~USD $12,800,000
2001 - 2005 The genetics of sleep apnea

Co-I (PI of sub-contract) - Redline

NHLBI, NIH, USA USD $2,206,330
2001 - 2006 Counter Regulatory Lipid-Derived Signals in Severe Asthma Co-I - Israel NHLBI, NIH, USA USD $3,018,406
2001 - 2005 Molecular Biology and Genetics of EGR-1 in Asthma Co-I - Silverman. NHLBI, NIH, USA USD $1,052,750
2002 - 2007 Asthma Coalition on Community, Environment and Stress Co-I - Wright. NHLBI, NIH, USA ~USD $8,000,000
2003 - 2004 Gene polymorphisms and environmental interactions on plasma HDL-C levels in the Busselton Health Study. Co-I - Beilby, Chapman, Thompson, Palmer. National Heart Foundation of Australia AUD $199,220
2004 Linux supercomputer cluster for high-end and high-availability computing, database, and web-server functions PI - Palmer, et al. UWA Small Bequests Infrastructure Funds AUD $31,440
2004 Ultracold freezers for the Busselton Health Study. Co-PI - Musk, James, Knuiman, Beilby, de Klerk, Olynyk, Hung, Palmer. UWA Small Bequests Infrastructure Funds AUD $32,000
2004 264515 - High-throughput PCR thermocycler & Plate Reader PI - Palmer, et al. NHMRC Equipment Grant AUD $107,000
2004 Infrastructure support PI - Palmer. NIRIS Award, Department of Health, Government of Western Australia AUD $15,000
2004 Sun Fire V20z High Performance Computing Cluster PI - Palmer, et al. Sun Microsystems Australia Equipment Grant AUD $77,455
2004 264652 - Sun Fire V20z High Performance Computing Cluster PI - Palmer, et al. NHMRC Equipment Grant AUD $77,455
2004 - 2005 303176 - Molecular and genetic risk factors for abdominal aortic aneurysms PI - Norman, van Bockxmeer, Palmer. NHMRC Project Grant AUD $220,163
2004 - 2005 Genetic Investigations of Asthma and Type 1 Diabetes. PI - Palmer. Nitric Oxide Analyser System. AUD $21,120
2005 NHMRC Equipment Grant/UWA Co-PI - Musk, James, Beilby, Palmer, Knuiman. UWA Small Bequest Seeding Grant

AUD $123,915

2005 Provision of new array-based Illumina technology for genetic and genomic studies of cancer aetiology.  PI - Palmer, Klinken, Leedman, Abraham, Millward, Swanson, Robinson, Iacopetta, Musk, Olynyk, Joseph, Zeps.  Cancer Council of Western Australia, Cancer Research Equipment Initiative. AUD $155,000
2006 Feasibility study for establishing an Interdisciplinary Bioethics Centre at UWA focusing on ELSI issues relating to genetic epidemiology Director - Palmer, et al. UWA Institute for Advanced Studies AUD $15,000
2005 - 2006 G 04P 1617 - Genetic polymorphisms and environmental factors that affect HDL metabolism Co-I - Beilby, Thompson, Chapman, Palmer. National Heart Foundation of Australia AUD $112,940
2006 Busselton Health Data Bases Bioinformatics and Pharmaceutical Development Visualisation PI - Palmer et al. Government of Western Australia Department of Industry and Resources: South-West Industry Assistance Scheme AUD $50,000
2002 - 2006 219169 - Strategies to optimise glycaemic control and prevent hypoglycaemia in children and adolescents with type 1 Diabetes.  Co-PI - Jones, Davis, Fournier, Foster, Stick, Palmer NHMRC/JDFI Program Grant

AUD

$2,500,000

2005 - 2007 353532 - The Changing Prevalence of Asthma and Chronic Obstructive Airway Disease in Australia Co-PI - Musk, James, Beilby, Palmer, Knuiman.  NHMRC Project Grant AUD $625,000
2005 - 2007 350908 - Genetic polymorphisms in genes controlling innate immunity as risk factors for childhood acute lymphoblastic leukemia Co-PI - Ashton, Armstrong, Palmer, Milne. NHMRC Project Grant AUD $229,234
2003 - 2008 Endowment: Chair in Genetic Epidemiology PI - Palmer Wind Over Water Foundation AUD $2,500,000
2006 - 2008 404009 - Novel statistical methods for genetic epidemiology PI - Palmer, Carter, Baddeley, Hazelton. NHMRC Project Grant. AUD $472,500
2006 - 2008 DP0663247 - Novel Bioinformatics approaches for genetics and data linkage. 

 
PI - Carter, Palmer, Hopper, Hazelton, Baddeley. Australian Research Council. AUD $233,000
2007 - 2008 G 06P 2521 - Immunogenetic determinants of Kawasaki disease and atherosclerosis. Co-PI - Burgner, Mamotte, Palmer, Christiansen. National Heart Foundation. AUD $123,000
2008 Western Australian Genetic Epidemiology Resource: Computing Infrastructure PI - Palmer, et al. Ramaciotti Foundation AUD $30,000
2008 Enhancement of the WA DNA Bank (CryoBio High Security Storage System for Plasma and Serum) PI - Palmer, et al. NHMRC Equipment Grant AUD $65,000
2008 Genetics Education in the 21st Century. Co - Applicant - Venville, Dawson, Palmer. DEST Australian School Innovation in Science, Technology and Mathematics (ASISTM) Grant AUD $57,750
2004 - 2009 303312 - A National Population-based Genetic Epidemiology, Biospecimen and Bioinformatic Resource PI - Palmer, Holman, Stanley, deKlerk, Zeps, vanBockxmeer, Semmens, Smith.  NHMRC Enabling Grant (Special Facilities) AUD $2,900,000
2005 - 2009 RO1 HL080010-01 - Osteoprotegrin and osteopontin in aortic aneurysm Co-I - Golledge, Daugherty, Bruemmer, Norman, Palmer. NIH National Heart, Lung and Blood Institute USD $1,250,000
2005 - 2009 The Scott Kirkbride Melanoma Genetics Centre Scientific Director - Palmer. Bequest AUD $2,500,000
2006 - 2009 343020 - Australian Sleep Health Clinical Trials Network. Co-PI - Grunstein, McEvoy, Palmer, Marks, Pierce, Rogers NHMRC Enabling Grant (Clinical Trials). AUD $1,040,000
2006 - 2009 403981 - Childhood Precursors of Adult Cardiovascular Disease, Obesity and Diabetes- 16 year follow up of a Longitudinal Cohort Co-PI - Beilin, Palmer, Oddy, Mori, Kendall, Hands. NHMRC Project Grant. AUD $812,213
2007 - 2009 458520 - The Genetic Understanding of Asbestos-Related Disorders (GUARD). PI - Palmer, Musk, Garlepp, deKlerk, Reid, Robinson.  NHMRC National Asbestos Research Grants. AUD $543,600
2007 - 2009 458519 - Epidemiology and community consequences of asbestos exposure in WA. Co-PI - Musk, deKlerk, Palmer, Howat, Berry, Layman, Alfonso, Ambrosini, Lingren, Mackerras, Phillips, Reid, Smyth.  NHMRC National Asbestos Research Grants. AUD $836,385
2007 - 2009 166067 - Gene-Environment Interactions Underlying the Developmental Origins of Health and Disease. Co - Applicant - Lye, Briollais, Challis, Doherty, Matthews, Newnham, Ozcelik, Pennell, Simminovitch, Stanley, Palmer, Beilin, Zubrick, Van Eekelen. Canadian Institutes for Health Research. AUD $449,924
2006 - 2010 404025 - The Australian Medical Bioinformatics Resource (AMBeR) PI - Palmer, Hopper, Stanley, Armstrong, Baddeley, Eisman, Semmens. NHMRC Medical Bioinformatics, Genomics, Proteomics Program. AUD $2,185,000
2006 - 2010 404116 - The Western Australian DNA Bank. PI - Palmer, Beilby, van Bockxmeer, Zeps, Semmens, Stanley, Klinken, Constable, Christiansen.  NHMRC Enabling Grant (Special Facilities). AUD $1,375,000
2007 - 2010 Public Population Project in Genomics (P3G).

PIs: Knoppers and Hudson.

Co-I - Co-investigators: Burton, Deschênes, Ferretti, Fortier, Khoury, Laberge, Little, Metspalu, Ollier, Palmer, Peltonen.

Genome Canada and Genome Quebec International Consortium Initiative Canadian $5,489,552
2009 - 2011 572613 - A genome-wide search for genes underlying the developmental origins of health and disease PI - Palmer, Pennell, Beilin, Newnham, Lye, Davey Smith. NHMRC Project Grant. AUD $989,500
2009 - 2010 G 08P 3671 - An investigation of common genes influencing cardiovascular disease and cardiovascular disease in early life Co - Applicant - McCaskie, Beilin, Mattes, Palmer, Pennell, Davey-Smith. National Heart Foundation AUD $129,000
2007 - 2012 Causal Analyses in Translational Epidemiology Centre (CAiTE).

PIs: Davey-Smith, Thomas.

Co-Applicant -

Co-applicants: Lawlor, Day, Palmer, Donovan, Windmeijer, Green, Gaunt.

Medical Research Council of the UK Centre of Excellence in Translational Medicine. GBP ₤2,600,000
2008 - 2012 SRP 08-10 - Australian Genomics and Clinical Outcomes of High Grade Glioma: AGOG. PI - Palmer, Nowak, Teo, McDonald, Wheeler, Joseph, Robinson. Cancer Council of New South Wales AUD $1,238,114
2009 - 2013 The Ontario Health Study PI - Palmer Canadian Partnership Against Cancer / Ontario Institute for Cancer Research / Public Health Ontario Canadian $29,000,000
2009 - 2013 1001020 - National Centre for Asbestos Related Diseases Co-PI - Robinson, Creaney, Nowak, Lake, Musk, Fazekas de St Groth, Palmer, Simpson, Skates, Watkins NHMRC Centre for Research Excellence AUD $4,500,000
2010 - 2013 Genetic Epidemiology & Biostatistics Platform PI - Palmer Ontario Institute for Cancer Research Canadian $4,000,000
2011 - 2013 1010279 - Examining GWAS-identified loci of interest in predicting coronary events in subjects with known coronary heart disease: the LIPID Genetic Study Co-PI - Thompson, Tonkin, Kirby, White, Beilby, West, Palmer, Blankenberg. NHMRC Project Grant. AUD $632,524
2011 - 2013 1010279 - Developmental Trajectories: A University of Toronto System-Wide Initiative to Improve Health, Learning and Society. Co-PI - Lye, Barr, Briollais, Corter, Fleming, Jenkins, Kennedy, Lee, Levitan, Matthews, Palmer, Pascal, Sokolowski. Connaught Global Challenge (University of Toronto). Canadian $1,000,000
2013 Dissecting the genetic etiology of obstructive sleep apnoea. Co-I - Mukherjee, Palmer. McLaughlin Centre Accelerator Grant, University of Toronto Canadian $50,000
2013 - 2014 Bridge Grant 7487 - Sleep fragmentation and the risk of stroke and heart disease. Co-I - Lim, Palmer, Mukherjee, Ryan, Kowgier, Bennett, Buchman Heart and Stroke Foundation of Ontario (HSFO)

Canadian

$70,000

Current:

Date Project/No. Investigators Funding Body Amount
2010 - 2015 MOP-82893 - Gene Environment Interactions Underlying the Developmental Origins of Health and Disease Co-Applicant - Lye, Adams, Beilin, Briollais, Matthews, Newnham, Olynyk, Palmer, Pennell Canadian Institutes for Health Research. Canadian $876,530
2011 - 2016 260883 - Measuring and improving the quality of ambulatory care for people with cardiovascular risk factors and/or chronic cardiovascular diseases. Co-I - Tu, Alter, Atzema, Austin, Bhatia, Booth, Garg, Gershon, Glazier, Hillmer, Hogg, Kapral, Ko, Lee, Lewis, Manuel, Palmer, Stukel, Tu, Walton, Wijeysundera, You. Canadian Institutes for Health Research. Team Grant: Chronic Disease Risk and Intervention Strategies. Canadian $1,998,740
2013 - 2017 287194 - Identifying Genetic Determinants of Human Sleep and Circadian Rhythms. Co-I - Lim, Bennett, Buchman, Dejager, Kowgier, Mukherjee, Palmer, Paré, Ryan. Canadian Institutes of Health Research

Canadian $446,488

2013 - 2015 299333 - Canadian Fatty Acid Reference Ranges Co-PI - Ma, Palmer (co-PIs), Little, Stark Canadian Institutes of Health Research

Canadian $545,112

 

 

Teaching
1993

Tutor in Genetics and Anatomy, Department Anatomy & Human Biology, University of Western Australia

2 tutorials/week of 1 Anatomy hour/week and

3 Genetics and human variation hours/week

25 medical students (Anatomy) and 60 BS students (Genetics and human variation).  Prep time: 4 hours/week

2002   

 

Instructor, ‘Gene discovery in complex human disease’.  Five-day short course -    

Genomics, Society and Human Health Program, University of Western Australia.  25 students.  Prep time: 2 weeks.

2003

Instructor, ‘An introduction to genetic epidemiology.’  Five-day short course –       

School of Population Health Summer School, University of Western Australia.  18 students.  Prep time: 2 weeks.

2004 Instructor (with Dr Martin Hazelton), Biostatistics 4S2 (core unit for statistics honours students), School of Mathematics and Statistics, University of Western Australia.  Full-semester unit (6 points); 3 hrs/week for 5 months.

Honours students in Statistics / Statistics faculty / PhD students.
2004 Occasional lectures, Masters of Epidemiology Course, School of                 Population Health, University of Western Australia.  40 graduate students.
2004

Occasional lectures and Genetics PBL, Health Sciences Degree Program,   School of Population Health, University of Western Australia.

40 undergraduate (3rd year) students.

2004

Instructor, ‘Fundamentals of Genetic Epidemiology 750.742.’  School of Population Health, University of Western Australia.

Full-semester unit (6 points); 1 x 3hr lecture/week for 3 months.

10 Graduate students / Clinical Faculty.

2004 Lecturer, ‘Medical Genetics 970.320’, Bachelor of Science 3rd Year Program, Faculty of Life Sciences, University of Western Australia.
2004 Lecturer, ‘Genetic Epidemiology’, Neurogenetics Workshop, Australasian   Society for Psychiatric Research Annual Scientific          Meeting, Perth, Australia        (December 2004).
2004 Instructor, ‘Fundamentals of genetic epidemiology.’  Five-day short course –          School of Population Health Summer School, University of Western Australia.
2005

Occasional lectures and Genetics PBL, Health Sciences Degree Program,   School of Population Health, University of Western Australia.

40 undergraduate (3rd year) students.

2005 Tutorials in Medical Genomics, Bachelor of Medicine / Bachelor of Surgery 6th year course, University of Western Australia (4 x 1hr tutorials throughout year).
2006 Tutorials in Medical Genomics, Bachelor of Medicine / Bachelor of Surgery 6th year course, University of Western Australia (4 x 1hr tutorials throughout year).
2006 Contributed to design of new BSc (Bioinformatics) course in Faculty of Life Sciences, including new undergraduate unit in Genetic Epidemiology (PUBH8742).
2007

Occasional lectures, Masters of Epidemiology Course, School of Population Health, University of Western Australia.

40 graduate students.

2007 Tutorials in Medical Genomics, Bachelor of Medicine / Bachelor of Surgery 6th year course, University of Western Australia (4 x 1hr tutorials throughout year).
2007 PUBH8742 Fundamentals of Genetic Epidemiology (2nd year undergraduate unit taught as part of BSc Bioinformatics course in Faculty of Life Sciences).
2008 Tutorials in Medical Genomics, Bachelor of Medicine / Bachelor of Surgery 6th year course, University of Western Australia (4 x 1hr tutorials throughout year).
2009 Tutorials in Medical Genomics, Bachelor of Medicine / Bachelor of Surgery 6th year course, University of Western Australia (4 x 1hr tutorials throughout year).
2009

Instructor, ‘An introduction to genetic epidemiology.’  Five-day short course –       

School of Population Health Summer School, University of Western Australia.  12 students.  Prep time: 2 weeks.

2016

Course Coordinator, PUB HLTH 7075 Introduction to Epidemiology (MPH Unit), School of Public Health, University of Adelaide. Semester 1. 45 students.  Prep time: 4 hrs/week.

 

 

Student assessment

“Is an effective university teacher” =87.6% (broad agreement=100%)

 
Clinical (undergraduate) research projects
Vacation scholarships

Philip Tong.  The genetic epidemiology of metastatic melanoma.  Supervisors: LJ Palmer, M Millward, J Cole.

Award: UWA Faculty of Medicine and Dentistry Vacation Scholarship 2005.

Philip Tong. Pilot study evaluation: The Western Australian Melanoma Health Study. Supervisors: LJ Palmer, SV Ward.

Award: Western Australian Institute for Medical Research Vacation Scholarship Summer 2006 - 2007

Arya Gupta. The association of IL2RB with cardiovascular disease. Supervisors: LJ Palmer, R Webster. Summer 2007 – 2008.

Irwin Kashani.  The association of diabetic retinopathy with various co-morbidities in population-level health data. Supervisors: LJ Palmer.

Award: Western Australian Institute for Medical Research Vacation Scholarship Summer 2007 - 2008

2006 Med IV Research Projects (IMED)
Adam Mossenson, Sally Banfield, Jeremy Hill.  The Genetic Determinants of asthma and decline in lung function - PHF11 Gene.  Supervisors: LJ Palmer, A James, AW Musk.
Sherman Picardo, Amit Malik, Evonne Low.  The Genetic Determinants of asthma and decline in lung function - TGFB1 gene.  Supervisors: LJ Palmer, A James, AW Musk.
Jing Xiao, Fan Zhang.  Investigating genetic and environmental interactions of apolipoprotein polymorphisms with cardiovascular disease. Supervisors: BL Powell, J Hung, LJ Palmer.
Brendan Foo, Yuen Leow.  Investigating gene-gene and gene-environment interactions of Interleukin-1 gene polymorphisms with cardiovascular disease. Supervisors: KW Carter, B McQuillan, LJ Palmer.
Marie Hordijenko, Muntasser Islam, Janitha Jayawardena.  The Scott Kirkbride Melanoma Research Centre: Pilot Study implementation and evaluation. Supervisors: L McDonald, M Millward, LJ Palmer.
2007 Med IV Research Projects (IMED)
Jessica Kierath, Louise O’Halloran, Jennifer Watts.  The Western Australian Melanoma Health Project: Development and assessment of a scar assessment tool in melanoma patients. Supervisors: F Wood, LJ Palmer.
2008 Med IV Research Projects (IMED)
Anand Venkataraman.  Obstructive Sleep Apnea and Depression in the Western Australian Sleep Health Study.  Supervisors: S Mukherjee, LJ Palmer.
Prize: Research of greatest clinical significance. Students in Health & Medical Research Conference, WA Medical Students Society and Faculty of Medicine, Dentistry and Health Sciences, University of Western Australia (2008)
2009 Med IV Research Projects (IMED)
A total of 32 4th year medical students worked within our Centre on various projects during 2009.
Regional, national, or international contributions
1997   

 

Lecturer, Queensland Institute for Medical Research Postgraduate Course on Statistical Genetics, Brisbane

3 day workshop, 50 graduate students                                   

Prep time: 2 weeks

2000

Instructor for Short Course ‘Approaches to gene mapping in complex         human             diseases’, Pulmonary Division, Brigham and Women’s         Hospital, Boston MA.

Clinical faculty and fellows

Course given over 10 weeks, 50 participants.

Prep time: 6 hours/week.

2001

Lecturer on Genetics for American Academy of Allergy, Asthma and         Immunology (AAAAI) Board Review Course, Boston. 

Clinical fellows.  100 participants.  Prep time: 6 hours.

2001

Occasional lectures, Division of Health Sciences and Technology,   Harvard Medical School/MIT.

MD/PhD and PhD students.

2001

Instructor, Biostatistics 228b - Statistical Genetics in Complex Human       Disease’, Department of Biostatistics, Harvard School of Public Health          (Fall 2001).  2 x 2hr lectures/week for 2.5 months.  40 students.

Graduate students / clinical fellows / HMS and HSPH faculty.

Prep time: 30 hours/week.

Student assessment [http://www.hsph.harvard.edu/registrar/evaluations/index.shtml]

“Usefulness of content”=78.6%; “Advanced knowledge”= 85.7%; “Overall rating”=71.4%.

2002

Course Director (Co-director with Donata Vercelli) – ‘The Genetics            and Genomics        of Innate Immunity in Lung Disease.’  One-day short  course.  The Sheraton Hotel, Tucson, AZ.  90 participants.  Prep time: 2 weeks.

Average of student assessment: 82.3%.

2002

Instructor, Biostatistics 228 - ‘Statistical Genetics in Complex Human        Disease’, Department of Biostatistics, Harvard School of Public Health (Fall 2002).  2 x 2hr lectures/week for 2 months.  40 students.

Graduate students / clinical fellows / HMS and HSPH faculty.

Prep time: 10 hours/week.

Student assessment [http://www.hsph.harvard.edu/registrar/evaluations/index.shtml]

“Usefulness of content”=85.7%; “Advanced knowledge”= 85.7%; “Overall rating”=85.7%.

2003 Faculty, ‘Genomics and Genetic Epidemiology: General Principles and Applications to Disease Studies.’  Two-day short course. Department of Continuing Education, Harvard Medical School / Department of Medicine, Beth Israel Deaconess Medical Center (April 2003).
2003 Co-Chair (with William Cookson and Scott Weiss) – ‘Genetic association studies in complex lung disease’.  One-day Postgraduate Course, American Thoracic Society Annual Scientific Meeting 2003.
2003 Instructor – ‘An introduction to the genetic epidemiology of complex human disease.’ Two-day short course, Biostatistics and Clinicial & Molecular Profiling, Merck Research Laboratories, Bluebell, PA.  30 participants. 

Prep time: 1 week.

2004 Instructor, “Genetic Data Analysis”, Master of Science in Biostatistics Program, Center for Statistics, Limburgs Universitair Centrum, Belgium. 3-week course.  40 students.

Prep time: 2 weeks.
2004

Instructor – ‘An introduction to the genetic epidemiology of complex human disease.’ Two-day short course, Epidemiology, Merck Research Laboratories, Bluebell, PA, USA.  20 participants. 

Prep time: 1 week.

2004

Lecturer, Sleep Medicine Lecture Series (4 day short course), Woolcock Institute of Medical Research, Sydney, Australia.  60 participants.

Prep time: 1 week.

2005

Lecturer, Short course on genetic epidemiology, Department of Social Medicine, Bristol University, Bristol, UK.  30 participants.

Prep time: 1 week.

2005

Lecturer, Short course on genetic epidemiology, Department of Social Medicine, Bristol University, Bristol, UK.  30 participants.

Prep time: 1 week.

2011

Lecturer, Fundamentals of Genetic Epidemiology, Dalla Lana School of Public Health, University of Toronto, Toronto, Canada.  8 participants.

Prep time: 1 week.

2012

Lecturer / Module Presenter, ‘Cardiovasulcar Epidemiology’, Chronic Disease Epidemiology, Dalla Lana School of Public Health, University of Toronto, Toronto, Canada.  16 participants.

Prep time: 1 week.

Mentored fellows at Harvard (NIH K awards)

Kelan Tantisira MD MS.  KO8 project: STAT6 Polymorphisms and the Ontogeny of Asthma. 

Sanjay J. Patel MD.  K23 project: The Genetics of Hormonal Resistance in Sleep Apnea.

  

Summer student research projects (Ontario Health Study)
2010 - 2012 Rashida Brown. Summer student from Rutgers University, Master of Public Health Program.
2012 Cody Black. Summer student from McMaster University, Biology and Pharmacology.
2012 Lorraine Mangalit. Summer student from University of Waterloo, Health Studies.
2012 Amanda Manoharan. Summer student from University of Waterloo, Health Studies.
2012 - 2013 Jenny Hayhoe. Summer student from University of Waterloo, Biomedical Science.
2013 Tiffany Fitzpatrick MPH. Summer student from University of Toronto Dalla Lana School of Public Health, Master of Public Health Program

       

Date Role Research Topic Program Degree Type Student Load Student Name
2025 Principal Supervisor Enhancing Diagnostic and Prognostic Accuracy in Colorectal Cancer Screening through Multimodal Data Fusion of Medical Imaging and Clinical Records Doctor of Philosophy Doctorate Full Time Miss Mei Yang
2025 Co-Supervisor Ethics of AI in Healthcare Doctor of Philosophy Doctorate Full Time Mr Humphrey Thompson
2025 Principal Supervisor Cutting-Edge Artificial Intelligence for Prognostic Prediction of Major Amputation in Patients with Chronic Limb Threatening Ischaemia and Diabetes-related Foot Disease Doctor of Philosophy Doctorate Full Time Ms Lipin Guo
2024 Co-Supervisor Using palatal and arch shape analysis to inform human identity in forensic investigations Doctor of Philosophy Doctorate Full Time Mr Thao Liang Chiam
2024 Co-Supervisor Unraveling psychosis: Deep Learning Analysis of Structural Neuroimaging to Predict Clinical Outcomes in Schizophrenia. Doctor of Philosophy Doctorate Part Time Mr Tristan John Bampton
2024 Principal Supervisor Enhancing Diagnostic Accuracy through Multimodal Data Fusion of Electrocardiogram and Clinical Records Doctor of Philosophy Doctorate Full Time Miss Xiaoyi Wang
2024 Co-Supervisor Developing a clinician-informed model for predicting cognitive trajectories in individuals with schizophrenia using machine learning methods. Doctor of Philosophy Doctorate Full Time Miss Shamini Thirugnana Sambandam
2024 Principal Supervisor The development and application of machine learning diagnostic and prognostic systems for paediatric brain cancer. Doctor of Philosophy Doctorate Full Time Mr Jordan Cooper Vihermaki
2022 Co-Supervisor Using AI to predict clinical outcomes in dementia Doctor of Philosophy Doctorate Part Time Luke Whitbread
2021 Principal Supervisor Using deep learning and other artificial intelligence methods to determine COPD severity using medical imaging data. Doctor of Philosophy Doctorate Full Time Mr Luke Anthony Smith

Date Role Research Topic Program Degree Type Student Load Student Name
2024 - 2025 Co-Supervisor A longitudinal study of genetic and environmental influences on the development of the dental arches, palate, and soft tissue facial profile in Australian twins from primary to permanent dentition Doctor of Philosophy Doctorate Full Time Mr Jamal Giri
2021 - 2025 Principal Supervisor Artificial intelligence for the discovery of clinically relevant biomarkers in the assessment of rheumatoid arthritis Doctor of Philosophy Doctorate Full Time Dr Alix Bird
2020 - 2024 Principal Supervisor Prognostication of large-vessel ischaemic stroke treated with endovascular thrombectomy Doctor of Philosophy Doctorate Full Time Miss Minyan Zeng
2018 - 2022 Co-Supervisor Weakly Supervised Localisation for Censor Aware Survival Prediction from Medical Images Doctor of Philosophy Doctorate Full Time Mr Renato Hermoza Aragones
2016 - 2022 Principal Supervisor Closing the implementation gap in pre-deployment medical AI study design Doctor of Philosophy Doctorate Part Time Dr Lauren Oakden-Rayner

Date Role Research Topic Location Program Supervision Type Student Load Student Name
2021 - ongoing Principal Supervisor A project investigating the role of genetics in cerebral palsy patients with comparison to MRI scans The University of Adelaide Bachelor of Medicine, Bachelor of Surgery (MBBS) Honours in the School of Public Health Honours Full Time Huy-Dat Pham
2020 - ongoing Co-Supervisor AI Stroke Imaging Research The University of Adelaide Faculty of Health Sciences, School of Public Health Doctorate Full Time Ms Minyan Zeng
2018 - 2018 Co-Supervisor The role of genetic variants in cerebral palsy: A systematic review University of Adelaide Bachelor of Health and Medical Sciences (Honours) Honours Full Time Ryan Pham

Date Role Board name Institution name Country
2019 - ongoing Member Australian Alliance for AI in Healthcare (AAAIiH) Executive Committee Australian Alliance for AI in Healthcare (AAAIiH) Australia
2018 - 2020 Chair SA NT DataLink Steering Committee Government of South Australia Australia
2014 - 2015 - Faculty of Health Sciences Board University of Adelaide -
2005 - ongoing Member Board of Directors, International Public Population Project in Genomics (P3G) - -

Date Role Committee Institution Country
2020 - ongoing Member Human Research Ethics Committee The University of Adelaide Australia
2020 - ongoing Member Clinical Informatics Advisory Committee Department of Health and Wellbeing, Government of South Australia Australia
2019 - 2020 Member Vision 2020 Steering Committee Department of Health and Wellbeing, Government of South Australia Australia
2018 - ongoing Member Department for Health and Wellbeing Human Research Ethics Committee Government of South Australian Australia
2017 - ongoing Board Member SA-NT DataLink Steering Committee SA-NT DataLink Australia
2015 - 2021 Chair School of Public Health Research Committee University of Adelaide Australia
2014 - 2015 Member Executive Deans Advisory Committee Faculty of Health Sciences, University of Adelaide -
2014 - ongoing Member Leadership Group, The Centre for Research Excellence in Aboriginal Chronic Disease Knowledge Translation and Exchange, South Australian Health and Medical Research Institute. - -
2013 - 2014 Member The Ontario Vascular Health Knowledge Management Work Group. - -
2012 - 2013 Chair Ontario Health Study Scientific Steering Committee - -
2012 - 2013 Member The Canadian Health Measures Survey Biobank Advisory Committee (CHMS-BAC). - -
2010 - 2014 Member Senior Management Team Ontario Institute for Cancer Institute. -
2010 - 2013 Member Executive Committee Ontario Biospecimen Research Platform -
2010 - 2013 Member Steering Committee Canadian Partnership for Tomorrow Project -
2010 - 2013 Member National Task Force developing a Cancer Prevention Plan for Canada Canadian Cancer Research Alliance -
2009 - ongoing Member Australian Bone Marrow Donor Registry Ethics Committee - -
2008 - ongoing Member Australian Genomics and Clinical Outcomes of High Grade Glioma (AGOG) Project Executive Committee - -
2006 - ongoing Member Executive Committee, Australasian Sleep Trials Network - -
2006 - ongoing Member Executive Committee, Sleep Apnea CardioVascular Endpoints (SAVE) Study - -
2005 - ongoing Member Steering Committee, International Public Population Project in Genomics (P3G) - -

Date Role Editorial Board Name Institution Country
2018 - ongoing Associate Editor Nature Scientific Reports Scientific Reports United Kingdom
2014 - ongoing Editor International Journal of Epidemiology University of Bristol United Kingdom
2005 - ongoing Associate Editor Human Genetics - -
2004 - ongoing Editor The Encyclopedia of Biostatistics 2nd Edition, John Wiley & Sons: Chichester [In Press]. - -
2003 - ongoing Associate Editor Genetic Analysis Workshop 13 Proceedings. - -
2003 - ongoing Editor International Journal of Epidemiology - -
2002 - ongoing Editor Biostatistical Genetics and Genetic Epidemiology - -
1994 - ongoing Editor ‘Submission on quality of education in postgraduate research degrees at the University of Western Australia.’ Submitted to the University of Western Australia as a policy paper; subsequently used as a guide for revision of University regulations and distributed nationally. University of Western Australia -
1993 - ongoing Editor Postgraduate Insert, Pelican Magazine University of Western Australia -

Date Office Name Institution Country
2019 - ongoing Leader, Precision Healthcare Flagship, Australian Alliance for AI in Healthcare Australian Alliance for AI in Healthcare Australia

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