Professor Lyle Palmer
Professor of Genetic Epidemiology
School of Public Health
Faculty of Health and Medical Sciences
Eligible to supervise Masters and PhD - email supervisor to discuss availability.
Professor Lyle Palmer - Doctor of Philosophy with Distinction.
Major Research Interests:
1. Translational bioscience
2. Machine learning applied to medicine
3. Genetic epidemiology of complex diseases
4. Population-based biobanking
5. Life course genetic epidemiology
- My Research
- Career
- Publications
- Grants and Funding
- Teaching
- Supervision
- Professional Activities
- Contact
For details on projects available please view the following booklet: School of Public Health Student Projects
-
Appointments
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 -
Awards and Achievements
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 Competencies
Language Competency English Can read, write, speak, understand spoken and peer review -
Education
Date Institution name Country Title 1998 University of Western Australia & Oxford University Australia/UK Doctor of Philosophy with Distinction - Genetic Epidemiology -
Postgraduate Training
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 -
Research Interests
Artificial Intelligence & Image Processing Bioinformatics Biostatistics Epidemiology Genetics Genetics & Heredity Medical Genetics Quantitative Genetics Ageing, Frailty and Mobility Cardiac, Respiratory and Vascular Health Early Origins of Health Men's Health Neuroscience, Behaviour and Brain Health Surgical and Health Systems Innovation Translational Health Outcomes
-
Journals
Year Citation 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 and Vasculature, 50, 9 pages.
Scopus1 Europe PMC12024 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. Clinical Rheumatology, 43(5), 1503-1512.
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), 10 pages.
Scopus1 Europe PMC12024 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 Neurology Open, 6(1), 8 pages.
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. The Lancet Digital Health, 5(12), e872-e881.
Scopus9 Europe PMC32023 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.
2023 Kirsh, V. A., Skead, K., McDonald, K., Kreiger, N., Little, J., Menard, K., . . . Awadalla, P. (2023). Cohort Profile: The Ontario Health Study (OHS). International Journal of Epidemiology, 52(2), E137-E151.
Scopus5 WoS2 Europe PMC32022 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.
Scopus7 WoS3 Europe PMC22022 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.
Scopus13 WoS7 Europe PMC52022 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.
Scopus4 WoS1 Europe PMC82022 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.
Scopus12022 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.
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.
Scopus5 WoS1 Europe PMC32022 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.
Scopus41 WoS18 Europe PMC252022 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.. The Medical journal of Australia, 216(11), 578-582.
Scopus1 Europe PMC12022 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.
Scopus205 WoS64 Europe PMC902022 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.
Scopus7 WoS2 Europe PMC42021 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.
Scopus110 WoS74 Europe PMC692021 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.
Scopus14 WoS8 Europe PMC132021 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.
Scopus4 WoS1 Europe PMC32021 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.
Scopus19 WoS8 Europe PMC132021 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.
Scopus92 WoS69 Europe PMC772021 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.
Scopus5 WoS2 Europe PMC42021 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.
Scopus22020 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.
Scopus36 WoS29 Europe PMC232020 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.
Scopus15 WoS11 Europe PMC92020 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.
Scopus20 WoS14 Europe PMC122020 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.
Scopus28 WoS16 Europe PMC182019 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.
Scopus8 WoS5 Europe PMC62019 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.
Scopus82 WoS57 Europe PMC612019 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.
Scopus1 Europe PMC12019 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.
Scopus5 WoS6 Europe PMC42019 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.
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.
Scopus26 WoS20 Europe PMC182018 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.
Scopus269 WoS210 Europe PMC2002018 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.
Scopus12 WoS7 Europe PMC42018 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.
Scopus65 WoS53 Europe PMC432018 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.
Scopus61 WoS52 Europe PMC392018 Mukherjee, S., Saxena, R., & Palmer, L. J. (2018). The genetics of obstructive sleep apnoea.. Respirology (Carlton, Vic.), 23(1), 18-27.
Scopus65 WoS35 Europe PMC362017 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.
Scopus7 Europe PMC52017 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.
Scopus34 WoS30 Europe PMC172017 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.
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.
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.
Scopus18 Europe PMC132017 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.
Scopus97 WoS78 Europe PMC662017 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.
Scopus140 WoS126 Europe PMC1222017 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.
Scopus146 WoS126 Europe PMC1032017 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.
Scopus120 WoS96 Europe PMC562017 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.
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.
Scopus50 WoS35 Europe PMC242017 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.
Scopus50 WoS35 Europe PMC242016 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.
Scopus13 WoS10 Europe PMC92016 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.
Scopus389 WoS329 Europe PMC3192016 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.
Scopus34 WoS29 Europe PMC322016 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.
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.
Scopus1532 WoS1199 Europe PMC8362016 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.
Scopus57 WoS47 Europe PMC462015 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.
Scopus279 WoS255 Europe PMC2282015 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.
Scopus101 WoS66 Europe PMC552015 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.
Scopus46 WoS36 Europe PMC312015 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.
WoS12015 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.
Scopus328 WoS267 Europe PMC842015 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.
Scopus38 WoS33 Europe PMC182015 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.
Scopus101 WoS91 Europe PMC792015 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.
Scopus14 WoS13 Europe PMC132015 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.
Scopus1153 WoS1059 Europe PMC9192015 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.
Scopus2 WoS12014 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.
WoS22 Europe PMC182014 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.
Scopus35 Europe PMC232014 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.
Scopus50 WoS45 Europe PMC402014 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.
Scopus5 WoS5 Europe PMC52014 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.
Scopus5 WoS4 Europe PMC42014 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.
WoS275 Europe PMC2862014 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.
WoS275 Europe PMC2862014 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.
Scopus50 WoS46 Europe PMC412014 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.
Scopus92 WoS77 Europe PMC792014 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.
Scopus51 WoS34 Europe PMC322014 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.
Scopus11 WoS11 Europe PMC62014 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.
Scopus188 WoS155 Europe PMC1242013 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.
Scopus70 WoS62 Europe PMC522013 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.
Scopus45 WoS33 Europe PMC262013 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.
Scopus2 WoS2 Europe PMC12013 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.
Scopus764 WoS535 Europe PMC5092013 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.
Scopus391 WoS347 Europe PMC3082013 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.
Scopus106 WoS97 Europe PMC672013 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.
Scopus28 WoS24 Europe PMC152013 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.
Scopus69 WoS57 Europe PMC482013 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.
Scopus43 WoS36 Europe PMC192013 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.
Scopus66 WoS61 Europe PMC382013 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.
Scopus153 WoS132 Europe PMC1172013 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.
Scopus48 WoS35 Europe PMC242013 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.
Scopus108 WoS86 Europe PMC562013 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.
Scopus1 WoS1 Europe PMC22013 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.
Scopus59 WoS49 Europe PMC482013 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.
Scopus45 WoS43 Europe PMC352013 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.
Scopus26 WoS21 Europe PMC242013 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.
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.
Scopus1 WoS12012 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.
WoS20 Europe PMC132012 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.
Scopus9 WoS9 Europe PMC82012 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.
Scopus292 WoS249 Europe PMC1842012 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.
Scopus15 WoS13 Europe PMC132012 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.
Scopus2 WoS3 Europe PMC12012 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.
Scopus96 WoS106 Europe PMC992012 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.
Scopus308 WoS273 Europe PMC2422012 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.
Scopus15 WoS13 Europe PMC82012 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.
Scopus8 WoS7 Europe PMC32012 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.
Scopus9 WoS8 Europe PMC72012 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.
Scopus34 WoS27 Europe PMC232012 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.
Scopus331 WoS290 Europe PMC2752012 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.
Scopus49 WoS43 Europe PMC352012 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.
Scopus144 WoS128 Europe PMC1062012 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.
Scopus120 WoS110 Europe PMC732012 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.
WoS186 Europe PMC1832012 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.
Scopus637 WoS553 Europe PMC5642012 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.
Scopus94 WoS96 Europe PMC862012 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.
WoS6 Europe PMC32012 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.
Scopus122012 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.
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.
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.
WoS64 Europe PMC232011 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.
Scopus213 Europe PMC1592011 Chambers, J., & Palmer, L. (2011). Genome-wide association study identifies loci influencing concentrations of liver enzymes in plasma. Nature Genetics, 43(11), 1131-1138.
Scopus443 WoS416 Europe PMC3712011 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.
WoS691 Europe PMC5872011 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.
Scopus364 WoS315 Europe PMC3002011 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.
Scopus344 WoS288 Europe PMC2892011 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.
Scopus1698 WoS1509 Europe PMC12982011 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.
Scopus295 WoS258 Europe PMC2472011 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.
WoS133 Europe PMC1162011 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.
Scopus11 WoS9 Europe PMC62011 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.
Scopus155 WoS137 Europe PMC1252011 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.
Scopus252 WoS443 Europe PMC3762011 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.
Scopus5 WoS5 Europe PMC52011 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.
Scopus53 WoS48 Europe PMC372011 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.
Scopus18 WoS18 Europe PMC162011 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.
Scopus50 WoS49 Europe PMC382011 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.
Scopus95 WoS87 Europe PMC822011 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.
Scopus37 WoS33 Europe PMC232011 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.
Scopus9 WoS9 Europe PMC92011 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.
Scopus118 WoS117 Europe PMC1012011 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.
Scopus59 WoS48 Europe PMC402011 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.
Scopus13 WoS12 Europe PMC92011 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.
Scopus26 WoS22 Europe PMC152011 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.
Scopus9 WoS92011 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.
WoS60 Europe PMC612011 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. The Lancet, 378(9795), 1006-1014.
Scopus310 WoS289 Europe PMC2342011 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. The Lancet, 378(9795), 1006-1014.
Scopus310 WoS289 Europe PMC2342010 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.
Scopus16 WoS62010 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.
WoS1473 Europe PMC11872010 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.
Scopus28 WoS28 Europe PMC232010 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.
Scopus78 WoS74 Europe PMC622010 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.
Scopus477 WoS438 Europe PMC3802010 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.
Scopus70 WoS63 Europe PMC422010 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.
Scopus23 WoS20 Europe PMC162010 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.
Scopus25 WoS23 Europe PMC162010 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.
Scopus145 WoS118 Europe PMC922010 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.
Scopus85 WoS66 Europe PMC482010 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.
Scopus199 WoS188 Europe PMC1572010 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.
Scopus38 WoS33 Europe PMC252010 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.
Scopus23 WoS22 Europe PMC162010 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.
Scopus26 WoS22 Europe PMC172010 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.
Scopus149 WoS111 Europe PMC1072010 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.
Scopus17 WoS16 Europe PMC92010 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.
Scopus429 WoS383 Europe PMC2952010 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.
Scopus2386 WoS2157 Europe PMC18722010 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.
Scopus775 WoS695 Europe PMC6342010 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.
Scopus1548 WoS1432 Europe PMC12462010 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.
Scopus1789 WoS1574 Europe PMC14982010 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.
Scopus228 Europe PMC1842010 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.
Scopus686 Europe PMC5702009 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.
Scopus55 Europe PMC382009 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.
Scopus10 Europe PMC62009 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.
Scopus52 Europe PMC342009 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.
Scopus27 WoS24 Europe PMC222009 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.
Scopus102 WoS96 Europe PMC812009 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.
Scopus655 WoS589 Europe PMC5072009 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.
Scopus26 WoS24 Europe PMC192009 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.
Scopus7 WoS6 Europe PMC52009 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.
Scopus10 WoS10 Europe PMC82009 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.
Scopus57 WoS43 Europe PMC322009 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.
Scopus123 WoS112 Europe PMC922009 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.
Scopus7 WoS6 Europe PMC52009 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.
Scopus70 WoS62 Europe PMC602009 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.
Scopus226 Europe PMC1792008 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.
WoS45 Europe PMC352008 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.
Scopus36 WoS30 Europe PMC222008 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.
Scopus43 WoS34 Europe PMC222008 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.
Scopus9 WoS8 Europe PMC42008 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.
Scopus16 WoS15 Europe PMC132008 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.
Scopus15 WoS12 Europe PMC112008 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.
Scopus8 WoS10 Europe PMC32008 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.
Scopus19 WoS16 Europe PMC92008 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.
Scopus15 WoS15 Europe PMC132008 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.
Scopus30 WoS25 Europe PMC212008 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.
Scopus35 WoS30 Europe PMC192008 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.
Scopus4 WoS5 Europe PMC42008 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.
Scopus28 WoS23 Europe PMC182008 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.
Scopus30 WoS26 Europe PMC222008 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.
Scopus34 WoS34 Europe PMC252008 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.
Scopus89 WoS75 Europe PMC612008 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.
Scopus218 Europe PMC1522008 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.
Scopus2297 Europe PMC17182007 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.
Scopus117 WoS110 Europe PMC812007 Palmer, L. J. (2007). UK Biobank: bank on it. Lancet, 369(9578), 1980-1982.
Scopus236 WoS167 Europe PMC1332007 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.
Scopus54 WoS49 Europe PMC372007 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.
Scopus30 WoS27 Europe PMC182007 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.
Scopus20 WoS14 Europe PMC132007 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.
Scopus58 WoS48 Europe PMC312007 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.
Scopus51 WoS45 Europe PMC362007 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.
Scopus116 WoS101 Europe PMC722007 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.
Scopus1196 WoS1101 Europe PMC9052007 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.
Scopus122 WoS102 Europe PMC852006 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.
Scopus30 WoS29 Europe PMC182006 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.
Scopus458 WoS429 Europe PMC3342006 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.
Scopus90 WoS81 Europe PMC602006 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.
Scopus2 WoS2 Europe PMC22006 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.
Scopus32 WoS31 Europe PMC242006 Carter, K. W., McCaskie, P. A., & Palmer, L. J. (2006). JLIN: A java based linkage disequilibrium plotter. BMC Bioinformatics, 7(1), 3 pages.
Scopus102 WoS103 Europe PMC872006 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.
Scopus34 WoS30 Europe PMC262006 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.
Scopus7 WoS6 Europe PMC62006 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.
Scopus6 WoS7 Europe PMC62006 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.
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.
Scopus102 Europe PMC802005 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.
Scopus14 Europe PMC122005 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.
Scopus33 Europe PMC252005 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.
Scopus253 WoS202 Europe PMC1402005 Palmer, L., & Cardon, L. (2005). Shaking the tree: Mapping complex disease genes with linkage disequilibrium. Lancet, 366(9492), 1223-1234.
Scopus182 WoS147 Europe PMC1042005 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.
Scopus10 WoS6 Europe PMC32005 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.
Scopus7 WoS7 Europe PMC62005 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.
Scopus19 WoS19 Europe PMC132005 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.
Scopus233 WoS205 Europe PMC1602005 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.
Scopus22 WoS21 Europe PMC142005 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.
Scopus26 WoS22 Europe PMC172005 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.
Scopus280 WoS265 Europe PMC2202005 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.
Scopus10 WoS10 Europe PMC72005 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.
Scopus10 WoS9 Europe PMC72005 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.
Scopus9 WoS8 Europe PMC62005 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.
Scopus371 WoS317 Europe PMC2322005 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.
Scopus75 WoS65 Europe PMC552005 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.
Scopus2 Europe PMC12005 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.
Scopus1 WoS1 Europe PMC12005 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.
WoS2 Europe PMC12004 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 PMC42004 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.
Scopus148 WoS110 Europe PMC822004 Palmer, L. J. (2004). The new epidemiology: Putting the pieces together in complex disease aetiology. International Journal of Epidemiology, 33(5), 925-928.
Scopus7 WoS6 Europe PMC22004 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.
Scopus87 WoS77 Europe PMC582004 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.
Scopus1 Europe PMC12004 Silverman, E. S., Palmer, L. J., Subramaniam, V., Hallock, A., Mathew, S., Vallone, J., . . . Shore, S. A. (2004). Transforming Growth Factor-β<inf>1</inf> Promoter Polymorphism C-509T Is Associated with Asthma. American Journal of Respiratory and Critical Care Medicine, 169(2), 214-219.
Scopus230 WoS213 Europe PMC1582004 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.
Scopus293 WoS249 Europe PMC1912004 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.
Scopus189 WoS169 Europe PMC1142004 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.
Scopus6 WoS4 Europe PMC62004 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.
Scopus69 WoS56 Europe PMC362004 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.
Scopus207 WoS180 Europe PMC1482004 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.
Scopus130 WoS114 Europe PMC762004 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.
Scopus28 WoS25 Europe PMC122004 Turner, S. W., Khoo, S. K., Laing, I. A., Palmer, L. J., Gibson, N. A., Rye, P., . . . Le Souëf, P. N. (2004). β<inf>2</inf> adrenoceptor Arg16Gly polymorphism, airway responsiveness, lung function and asthma in infants and children. Clinical and Experimental Allergy, 34(7), 1043-1048.
Scopus51 WoS49 Europe PMC352004 Ceyhan, B., Burgos, A., Palmer, L., & 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.
WoS12003 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.
Scopus72 Europe PMC372003 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.
Scopus58 WoS55 Europe PMC392003 Cardon, L. R., & Palmer, L. J. (2003). Population stratification and spurious allelic association. Lancet, 361(9357), 598-604.
Scopus1010 WoS914 Europe PMC7222003 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.
Scopus5 WoS5 Europe PMC62003 Palmer, L. J., & Redline, S. (2003). Genomic approaches to understanding obstructive sleep apnea. Respiratory Physiology and Neurobiology, 135(2-3), 187-205.
Scopus72 WoS50 Europe PMC352003 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.
Scopus37 WoS25 Europe PMC232003 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.
Scopus57 WoS47 Europe PMC332003 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.
Scopus3 WoS3 Europe PMC22003 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.
Scopus201 WoS185 Europe PMC1412003 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. BMC GENETICS, 4(Suppl 1), 3 pages.
WoS9 Europe PMC82003 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.
Scopus59 WoS28 Europe PMC362003 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.
WoS8 Europe PMC72003 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.
Scopus46 WoS43 Europe PMC332003 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.
Scopus194 WoS156 Europe PMC1142003 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.
Scopus10 WoS15 Europe PMC122003 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.
Scopus98 WoS83 Europe PMC702002 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.
Scopus24 WoS17 Europe PMC132002 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.
Scopus113 WoS99 Europe PMC732002 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.
Scopus41 WoS43 Europe PMC322002 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.
Scopus181 WoS167 Europe PMC1302002 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.
Scopus106 WoS85 Europe PMC682002 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.
Scopus93 WoS84 Europe PMC492002 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.
Scopus3 WoS22002 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.
Scopus76 WoS58 Europe PMC352002 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.
Scopus2 Europe PMC12002 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.
Scopus155 WoS132 Europe PMC972002 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.
Scopus2 WoS2 Europe PMC22002 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.
Scopus66 WoS62 Europe PMC472002 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.
Scopus160 WoS127 Europe PMC1012002 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.
Scopus14 WoS14 Europe PMC102002 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.
Scopus124 WoS90 Europe PMC622002 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.
Scopus30 WoS24 Europe PMC202002 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.
Scopus13 WoS13 Europe PMC102002 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.
Scopus184 WoS163 Europe PMC1222002 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.
Scopus171 Europe PMC1372001 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.
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.
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). 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.
WoS12001 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.
Scopus62 WoS45 Europe PMC342001 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.
Scopus149 WoS134 Europe PMC982001 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.
Scopus30 WoS30 Europe PMC192001 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.
WoS39 Europe PMC292001 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.
Scopus15 WoS13 Europe PMC82001 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), 4 pages.
Scopus30 WoS27 Europe PMC212001 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.
Scopus179 WoS142 Europe PMC1002001 Weiss, S. T., Silverman, E. K., & Palmer, L. J. (2001). Case-Control Association Studies in Pharmacogenetics. Pharmacogenomics Journal, 1(3), 157-158.
Scopus68 Europe PMC392001 Palmer, L., Jacobs, K., Scurrah, K., Xu, X., Horvath, S., & Weiss, S. (2001). Genome-wide linkage analysis in a general population sample using σ<inf>A</inf><sup>2</sup> random effects (SSARS) fitted by Gibbs sampling. Genetic Epidemiology, 21(SUPPL. 1).
Scopus22001 Palmer, L. J., & Elston, R. C. (2001). Introduction: Linkage analyses of single regions. Genetic Epidemiology, 21(SUPPL. 1), S79-S80.
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.
Scopus14 WoS13 Europe PMC92001 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.
Scopus7 WoS6 Europe PMC42001 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.
Scopus83 WoS67 Europe PMC542001 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.
Scopus6 WoS7 Europe PMC52001 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.
Scopus52 WoS43 Europe PMC352001 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.
Scopus5 WoS5 Europe PMC22001 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.
Scopus437 WoS386 Europe PMC2922001 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.
Scopus37 WoS33 Europe PMC242001 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.
Scopus12 WoS15 Europe PMC72001 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.
Scopus43 WoS41 Europe PMC222001 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.
Scopus1 WoS1 Europe PMC12001 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.
Scopus3 WoS1 Europe PMC12001 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.
Scopus10 WoS11 Europe PMC72001 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.
Scopus27 WoS25 Europe PMC162000 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.
Scopus137 WoS120 Europe PMC842000 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.
Scopus35 WoS22 Europe PMC142000 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.
WoS23 Europe PMC152000 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.
Scopus51 WoS44 Europe PMC272000 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.
Scopus33 WoS28 Europe PMC202000 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.
Scopus22000 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.
WoS22000 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.
Scopus48 WoS50 Europe PMC372000 Palmer, L. J., & Cookson, W. O. C. M. (2000). Genomic approaches to understanding asthma. Genome Research, 10(9), 1280-1287.
Scopus85 WoS66 Europe PMC522000 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.
Scopus38 WoS38 Europe PMC242000 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.
Scopus106 WoS98 Europe PMC712000 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.
Scopus64 WoS58 Europe PMC382000 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.
Scopus47 WoS45 Europe PMC342000 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.
Scopus292000 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.
Scopus30 Europe PMC112000 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.
Scopus168 Europe PMC841999 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.
Scopus86 WoS86 Europe PMC621999 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.
Scopus18 WoS21 Europe PMC121999 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.
Scopus14 WoS12 Europe PMC51999 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.
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.
Scopus23 WoS18 Europe PMC171999 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.
Scopus28 WoS22 Europe PMC161998 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.
Scopus92 WoS76 Europe PMC581998 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.
Scopus45 WoS38 Europe PMC271998 Cookson, W., & Palmer, L. (1998). Investigating the asthma phenotype. Clinical and Experimental Allergy, 28(Suppl. 1), 88-89.
Scopus22 WoS19 Europe PMC81998 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.
Scopus138 WoS118 Europe PMC841998 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.
Scopus106 WoS98 Europe PMC641997 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.
Scopus771997 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.
WoS73 Europe PMC501997 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.
Scopus50 Europe PMC301997 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.
WoS371996 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.
Scopus19 WoS16 Europe PMC91995 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.
Scopus62 WoS38 Europe PMC321995 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.
Scopus118 WoS110 Europe PMC811994 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 & Child Neurology, 36(12), 1108-1119.
Scopus9 WoS7 Europe PMC6 -
Books
Year Citation 2011 Palmer, L., Burton, P., & Smith, G. (Eds.) (2011). An Introduction to genetic epidemiology. Bristol, UK: The Policy Press.
DOI Scopus72002 Elston, R. C., Olson, J. M., & Palmer, L. (2002). Biostatistical Genetics and Genetic Epidemiology. John Wiley & Sons. -
Book Chapters
Year Citation 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 Scopus82016 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).
Scopus12011 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.
Scopus22011 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 Scopus42003 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).
Scopus62002 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). -
Conference Papers
Year Citation 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.
DOI2022 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. 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 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 Scopus31 WoS152019 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. 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 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 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.
Scopus147 WoS292017 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. 3361 (pp. 130-134). Online: IEEE.
DOI Scopus20 WoS112017 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.
DOI2011 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.
DOI2010 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.
DOI WoS12009 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 Scopus16 Europe PMC102009 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.
DOI2007 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.
DOI2007 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.
DOI2007 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.
DOI2005 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.
WoS12005 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.
DOI2000 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.
WoS11999 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.
WoS11999 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. -
Conference Items
Year Citation 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.
DOI2022 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.
WoS12011 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.
DOI2011 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. -
Report for External Bodies
-
Recorded/Rendered Creative Works
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. -
Preprint
Year Citation 2024 Whitbread, L., Lau, S., Palmer, L. J., & Jenkinson, M. (2024). Deep-diffeomorphic networks for conditional brain templates.
DOI2020 Wang, H., Noordam, R., Cade, B. E., Schwander, K., Winkler, T. W., 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 |
-
Current Higher Degree by Research Supervision (University of Adelaide)
Date Role Research Topic Program Degree Type Student Load Student Name 2024 Co-Supervisor A longitudinal study of the development of dental occlusion and facial profiles of monozygotic and dizygotic Australian twins, from the primary to the permanent dentition. Doctor of Philosophy Doctorate Full Time Mr Jamal Giri 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 Using deep learning methods to enhance cognitive outcomes in paediatric brain cancer. 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 Full Time Luke Thomas Whitbread 2021 Principal Supervisor Deep learning for the discovery of clinically relevant imaging biomarkers in the assessment of rheumatoid arthritis Doctor of Philosophy Doctorate Full Time Dr Alix Bird 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 2020 Principal Supervisor Prognostic prediction of large-vessel stroke using machine learning methods Doctor of Philosophy Doctorate Full Time Miss Minyan Zeng -
Past Higher Degree by Research Supervision (University of Adelaide)
Date Role Research Topic Program Degree Type Student Load Student Name 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 -
Other Supervision Activities
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
-
Board Memberships
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) - - -
Committee Memberships
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) - - -
Editorial Boards
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 - -
Offices Held
Date Office Name Institution Country 2019 - ongoing Leader, Precision Healthcare Flagship, Australian Alliance for AI in Healthcare Australian Alliance for AI in Healthcare Australia
Connect With Me
External Profiles