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Novel Genetic Markers Associate With Atrial Fibrillation Risk in Europeans and JapaneseLUBITZ, Steven A; LUNETTA, Kathryn L; DÖRR, Marcus et al.Journal of the American College of Cardiology. 2014, Vol 63, Num 12, pp 1200-1210, issn 0735-1097, 11 p.Article

A genome-wide association study identifies a potential novel gene locus for keratoconus, one of the commonest causes for corneal transplantation in developed countriesXIAOHUI LI; BYKHOVSKAYA, Yelena; HARITUNIANS, Talin et al.Human molecular genetics (Print). 2012, Vol 21, Num 2, pp 421-429, issn 0964-6906, 9 p.Article

Metabolic and cardiovascular genes in polycystic ovary syndrome: A candidate-wide association study (CWAS)JONES, Michelle R; CHUA, Angela K; GOODARZI, Mark O et al.Steroids. 2012, Vol 77, Num 4, pp 317-322, issn 0039-128X, 6 p.Conference Paper

Genomewide Association Studies of StrokeARFAN IKRAM, M; SESHADRI, Sudha; BOS, Michiel J et al.The New England journal of medicine. 2009, Vol 360, Num 17, pp 1718-1728, issn 0028-4793, 11 p.Article

Carotid intima-media thickness (cIMT) cosegregates with blood pressure and renal function in hypertensive Hispanic familiesCHEN, Yi-Chun; XIUQING GUO; RAFFEL, Leslie J et al.Atherosclerosis. 2008, Vol 198, Num 1, pp 160-165, issn 0021-9150, 6 p.Article

Two-stage genome-wide linkage scan in keratoconus sib pair familiesXIAOHUI LI; RABINOWITZ, Yaron S; TANG, Yongming G et al.Investigative ophthalmology & visual science. 2006, Vol 47, Num 9, pp 3791-3795, issn 0146-0404, 5 p.Article

Lipoprotein lipase is a gene for insulin resistance in Mexican AmericansGOODARZI, Mark O; XIUQING GUO; TAYLOR, Kent D et al.Diabetes (New York, NY). 2004, Vol 53, Num 1, pp 214-220, issn 0012-1797, 7 p.Article

Replication of association of a novel insulin receptor gene polymorphism with polycystic ovary syndromeGOODARZI, Mark O; LOUWERS, Yvonne V; LAVEN, Joop S. E et al.Fertility and sterility. 2011, Vol 95, Num 5, pp 1736-1741, issn 0015-0282, 6 p.Article

Ulcerative colitis-risk loci on chromosomes lp36 and 12q15 found by genome-wide association studySILVERBERG, Mark S; CHO, Judy H; BARMADA, M. Michael et al.Nature genetics. 2009, Vol 41, Num 2, pp 216-220, issn 1061-4036, 5 p.Article

Genome-wide linkage scans for type ₂ diabetes mellitus in four ethnically diverse populations -significant evidence for linkage on chromosome ₄q in African Americans: the Family Investigation of Nephropathy and Diabetes Research GroupMALHOTRA, Alka; IGO, Robert P; GODDARD, Katrina A. B et al.Diabetes/metabolism research and reviews (Print). 2009, Vol 25, Num 8, pp 740-747, issn 1520-7552, 8 p.Article

Refined genomic localization and ethnic differences observed for the IBD5 association with Crohn's diseaseSILVERBERG, Mark S; DUERR, Richard H; TAYLOR, Kent D et al.European journal of human genetics. 2007, Vol 15, Num 3, pp 328-335, issn 1018-4813, 8 p.Article

A Search for Variants Associated With Young-Onset Type 2 Diabetes in American Indians in a 100K Genotyping Array. CommentaryTAYLOR, Kent D; NORRIS, Jill M; BENITEZ, Deb et al.Diabetes (New York, NY). 2007, Vol 56, Num 12, issn 0012-1797, 2844-2848, 3045-3052 [13 p.]Article

A genome-wide association study identifies IL23R as an inflammatory bowel disease geneDUERR, Richard H; TAYLOR, Kent D; DASSOPOULOS, Themistocles et al.Science (Washington, D.C.). 2006, Vol 314, Num 5804, pp 1461-1463, issn 0036-8075, 3 p.Article

A genome-wide scan for carotid artery intima-media thickness: The Mexican-American coronary artery disease family studyDAI WANG; HUIYING YANG; HSUEH, Willa A et al.Stroke (1970). 2005, Vol 36, Num 3, pp 540-545, issn 0039-2499, 6 p.Article

Mutations in NOD2 are associated with fibrostenosing disease in patients with crohn's diseaseABREU, Maria T; TAYLOR, Kent D; ROTTER, Jerome I et al.Gastroenterology (New York, NY. 1943). 2002, Vol 123, Num 3, pp 679-688, issn 0016-5085Article

Genome-wide meta-analysis points to CTC1 and ZNF676 as genes regulating telomere homeostasis in humansMANGINO, Massimo; HWANG, Shih-Jen; WEI CHEN et al.Human molecular genetics (Print). 2012, Vol 21, Num 24, pp 5385-5394, issn 0964-6906, 10 p.Article

Genome-wide association identifies multiple ulcerative colitis susceptibility lociMCGOVERN, Dermot P. B; GARDET, Agnès; GREEN, Todd et al.Nature genetics. 2010, Vol 42, Num 4, pp 332-337, issn 1061-4036, 6 p.Article

Replication of calpain-10 genetic association with carotid intima-media thicknessGOODARZI, Mark O; TAYLOR, Kent D; JONES, Michelle R et al.Atherosclerosis. 2009, Vol 205, Num 2, pp 503-505, issn 0021-9150, 3 p.Article

Association of Androgen Receptor CAG Repeat Polymorphism and Polycystic Ovary SyndromeSHAH, Nissar A; ANTOINE, Heath J; PALL, Marita et al.The Journal of clinical endocrinology and metabolism. 2008, Vol 93, Num 5, pp 1939-1945, issn 0021-972X, 7 p.Article

Deletion polymorphism upstream of IRGM associated with altered IRGM expression and Crohn's diseaseMCCARROLL, Steven A; HUETT, Alan; DUERR, Richard H et al.Nature genetics. 2008, Vol 40, Num 9, pp 1107-1112, issn 1061-4036, 6 p.Article

Association of the Kir6.2 E23K Variant with Reduced Acute Insulin Response in African-AmericansPALMER, Nicholette D; LANGEFELD, Carl D; BRYER-ASH, Michael et al.The Journal of clinical endocrinology and metabolism. 2008, Vol 93, Num 12, pp 4979-4983, issn 0021-972X, 5 p.Article

Association between angiotensinogen, angiotensin II receptor genes, and blood pressure response to an angiotensin-converting enzyme inhibitorXIAOWEN SU; LEE, Liming; KRAUSS, Ronald M et al.Circulation (New York, N.Y.). 2007, Vol 115, Num 6, pp 725-732, issn 0009-7322, 8 p.Article

The 3' untranslated region of the lipoprotein lipase gene : Haplotype structure and association with post-heparin plasma lipase activityGOODARZI, Mark O; WONG, Howard; QUINONES, Manuel J et al.The Journal of clinical endocrinology and metabolism. 2005, Vol 90, Num 8, pp 4816-4823, issn 0021-972X, 8 p.Article

Cerivastatin, genetic variants, and the risk of rhabdomyolysisMARCIANTE, Kristin D; DURDA, Jon P; KASPERA, Rudiger et al.Pharmacogenetics and genomics (Print). 2011, Vol 21, Num 5, pp 280-288, issn 1744-6872, 9 p.Article