Common variants on lp36 and lq42 are associated with cutaneous basal cell carcinoma but not with melanoma or pigmentation traitsSTACEY, Simon N; GUDBJARTSSON, Daniel F; THORISDOTTIR, Kristin et al.Nature genetics. 2008, Vol 40, Num 11, pp 1313-1318, issn 1061-4036, 6 p.Article

Genome-wide association study identifies a second prostate cancer susceptibility variant at 8q24GUDMUNDSSON, Julius; SULEM, Patrick; SIGURDSSON, Asgeir et al.Nature genetics. 2007, Vol 39, Num 5, pp 631-637, issn 1061-4036, 7 p.Article

Genome-wide association study identifies a sequence variant within the DAB2IP gene conferring susceptibility to abdominal aortic aneurysmGRETARSDOTTIR, Solveig; BAAS, Annette F; VAN RIJ, Andre M et al.Nature genetics. 2010, Vol 42, Num 8, pp 692-697, issn 1061-4036, 6 p.Article

Multiple Genetic Loci for Bone Mineral Density and FracturesSTYRKARSDOTTIR, Unnur; HALLDORSSON, Bjarni V; BAGGER, Yu et al.The New England journal of medicine. 2008, Vol 358, Num 22, pp 2355-2365, issn 0028-4793, 11 p.Article

Identification of low-frequency variants associated with gout and serum uric acid levelsSULEM, Patrick; GUDBJARTSSON, Daniel F; MAGNUSSON, Gisli et al.Nature genetics. 2011, Vol 43, Num 11, pp 1127-1130, issn 1061-4036, 4 p.Article

Variant in the sequence of the LINGO1 gene confers risk of essential tremorSTEFANSSON, Hreinn; STEINBERG, Stacy; BÖTTCHER, Yvonne et al.Nature genetics. 2009, Vol 41, Num 3, pp 277-279, issn 1061-4036, 3 p.Article

Risk Variants for Atrial Fibrillation on Chromosome 4q25 Associate with Ischemic StrokeGRETARSDOTTIR, Solveig; THORLEIFSSON, Gudmar; BJARNASON, Hjordis et al.Annals of neurology. 2008, Vol 64, Num 4, pp 402-409, issn 0364-5134, 8 p.Article

A rare variant in MYH6 is associated with high risk of sick sinus syndromeHOLM, Hilma; GUDBJARTSSON, Daniel F; STEFANSDOTTIR, Hrafnhildur et al.Nature genetics. 2011, Vol 43, Num 4, pp 316-320, issn 1061-4036, 5 p.Article

New sequence variants associated with bone minéral densitySTYRKARSDOTTIR, Unnur; HALLDORSSON, Bjarni V; NGUYEN, Tuan V et al.Nature genetics. 2009, Vol 41, Num 1, pp 15-17, issn 1061-4036, 3 p.Article

Common variants on chromosome 5pl2 confer susceptibility to estrogen receptor-positive breast cancerSTACEY, Simon N; MANOLESCU, Andrei; STROBBE, Luc J et al.Nature genetics. 2008, Vol 40, Num 6, pp 703-706, issn 1061-4036, 4 p.Article

Variant of transcription factor 7-like 2 (TCF7L2) gene confers risk of type 2 diabetesGRANT, Struan F. A; THORLEIFSSON, Gudmar; STYRKARSDOTTIR, Unnur et al.Nature genetics. 2006, Vol 38, Num 3, pp 320-323, issn 1061-4036, 4 p.Article

New common variants affecting susceptibility to basal cell carcinomaSTACEY, Simon N; SULEM, Patrick; THORISDOTTIR, Kristin et al.Nature genetics. 2009, Vol 41, Num 8, pp 909-914, issn 1061-4036, 6 p.Article

A variant associated with nicotine dependence, lung cancer and peripheral arterial diseaseTHORGEIRSSON, Thorgeir E; GELLER, Frank; STACEY, Simon N et al.Nature (London). 2008, Vol 452, Num 7187, pp 638-641, issn 0028-0836, 4 p.Article

Common variants on chromosomes 2q35 and 16q12 confer susceptibility to estrogen receptor-positive breast cancerSTACEY, Simon N; MANOLESCU, Andrei; ABEN, Katja K et al.Nature genetics. 2007, Vol 39, Num 7, pp 865-869, issn 1061-4036, 5 p.Article

Localization of a susceptibility gene for type 2 diabetes to chromosome 5q34-q35.2REYNISDOTTIR, Inga; THORLEIFSSON, Gudmar; HALLDORSSON, Skarphedinn et al.American journal of human genetics. 2003, Vol 73, Num 2, pp 323-335, issn 0002-9297, 13 p.Article