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Human Molecular Genetics|December 1, 2007
Susceptibility to coronary artery disease and diabetes is encoded by distinct, tightly linked SNPs in the ANRIL locus on chromosome 9pHelen M Broadbent, John F Peden, Stefan Lorkowski, et al.Proceedings of the National Academy of Sciences of the United States of America|June 27, 2007
Intergenic variants of HBS1L-MYB are responsible for a major quantitative trait locus on chromosome 6q23 influencing fetal hemoglobin levels in adultsSwee Lay Thein, Stephan Menzel, Xu Peng, et al.Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|August 21, 2007
European rational approach for the genetics of diabetic complications--EURAGEDIC: patient populations and strategyLise Tarnow, Per-Henrik Groop, Samy Hadjadj, et al.Diabetes|June 29, 2004
Polymorphisms in type II SH2 domain-containing inositol 5-phosphatase (INPPL1, SHIP2) are associated with physiological abnormalities of the metabolic syndromePamela J Kaisaki, Marc Delépine, Peng Y Woon, et al.Human Mutation|August 27, 2009
Seeing clearly: the dominant and recessive nature of FOXE3 in eye developmental anomaliesSibel Ugur Iseri, Robert J Osborne, Martin Farrall, et al.Journal of the American Society of Nephrology : JASN|July 3, 2010
HLA has strongest association with IgA nephropathy in genome-wide analysisJohn Feehally, Martin Farrall, Anne Boland, et al.Journal of the American Society of Nephrology : JASN|March 23, 2007
Association between angiotensin-converting enzyme gene polymorphisms and diabetic nephropathy: case-control, haplotype, and family-based study in three European populationsSamy Hadjadj, Lise Tarnow, Carol Forsblom, et al.Plos Genetics|May 20, 2006
Genome-wide mapping of susceptibility to coronary artery disease identifies a novel replicated locus on chromosome 17Martin Farrall, Fiona R Green, John F Peden, et al.Nature Genetics|January 26, 2021
Common genetic variants and modifiable risk factors underpin hypertrophic cardiomyopathy susceptibility and expressivityAndrew R Harper, Anuj Goel, Christopher Grace, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 18, 2016
Reassessment of Mendelian gene pathogenicity using 7,855 cardiomyopathy cases and 60,706 reference samplesRoddy Walsh, Kate L Thomson, James S Ware, et al.Pageof 17