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

Apolipoprotein(a) Genetic Sequence Variants Associated With Systemic Atherosclerosis and Coronary Atherosclerotic Burden But Not With Venous ThromboembolismHELGADOTTIR, Anna; GRETARSDOTTIR, Solveig; TREGOUET, David-Alexandre et al.Journal of the American College of Cardiology. 2012, Vol 60, Num 8, pp 722-729, issn 0735-1097, 8 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

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

Plasma HDL cholesterol and risk of myocardial infarction: a mendelian randomisation studyVOIGHT, Benjamin F; PELOSO, Gina M; SCHUNKERT, Heribert et al.Lancet (British edition). 2012, Vol 380, Num 9841, pp 572-580, issn 0140-6736, 9 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

Several common variants modulate heart rate, PR interval and QRS durationHOLM, Hilma; GUDBJARTSSON, Daniel F; NYRNES, Audhild et al.Nature genetics. 2010, Vol 42, Num 2, pp 117-122, issn 1061-4036, 6 p.Article

Common variants on 9q22.33 and 14q13.3 predispose to thyroid cancer in European populationsGUDMUNDSSON, Julius; SULEM, Patrick; MAGNUSDOTTIR, Droplaug N et al.Nature genetics. 2009, Vol 41, Num 4, pp 460-464, issn 1061-4036, 5 p.Article

Large-scale association analysis identifies 13 new susceptibility loci for coronary artery diseaseSCHUNKERT, Heribert; KÖNIG, Inke R; ABSHER, Devin et al.Nature genetics. 2011, Vol 43, Num 4, pp 333-338, issn 1061-4036, 6 p.Article

Sequence variants at CYP1A1―CYP1A2 and AHR associate with coffee consumptionSULEM, Patrick; GUDBJARTSSON, Daniel F; MÄGI, Reedik et al.Human molecular genetics (Print). 2011, Vol 20, Num 10, pp 2071-2077, issn 0964-6906, 7 p.Article

Genome-wide association study identifies loci influencing concentrations of liver enzymes in plasmaCHAMBERS, John C; WEIHUA ZHANG; COIN, Lachlan J et al.Nature genetics. 2011, Vol 43, Num 11, pp 1131-1138, issn 1061-4036, 8 p.Article

Design of the Coronary ARtery Disease Genome-Wide Replication And Meta-Analysis (CARDIoGRAM) Study A Genome-Wide Association Meta-analysis Involving More Than 22 000 Cases and 60 000 ControlsPREUSS, Michael; KÖNIG, Inke R; HALL, Alistair S et al.Circulation. Cardiovascular genetics (Print). 2010, Vol 3, Num 5, pp 475-483, issn 1942-325X, 9 p.Article

Lack of Association Between the Trp719Arg Polymorphism in Kinesin-Like Protein-6 and Coronary Artery Disease in 19 Case-Control StudiesASSIMES, Themistocles L; HOLM, Hilma; PATTERSON, Chris C et al.Journal of the American College of Cardiology. 2010, Vol 56, Num 19, pp 1552-1563, issn 0735-1097, 12 p.Article

Sequence variants in the CLDN14 gene associate with kidney stones and bone mineral densityTHORLEIFSSON, Gudmar; HOLM, Hilma; DEN HEIJER, Martin et al.Nature genetics. 2009, Vol 41, Num 8, pp 926-930, issn 1061-4036, 5 p.Article

Discovery of common variants associated with low TSH levels and thyroid cancer riskGUDMUNDSSON, Julius; SULEM, Patrick; HELGADOTTIR, Hafdis Th et al.Nature genetics. 2012, Vol 44, Num 3, pp 319-322, issn 1061-4036, 4 p.Article

Seventy―five genetic loci influencing the human red blood cellDER HARST, Pim Van; WEIHUA ZHANG; RADHAKRISHNAN, Aparna et al.Nature (London). 2012, Vol 492, Num 7429, pp 369-375, issn 0028-0836, 7 p.Article

The chromosome 9p21 risk locus is associated with angiographic severity and progression of coronary artery diseasePATEL, Riyaz S; SHAOYONG SU; WADDY, Salina et al.European heart journal. 2010, Vol 31, Num 24, pp 3017-3023, issn 0195-668X, 7 p.Article

A sequence variant in ZFHX3 on 16q22 associates with atrial fibrillation and ischemic strokeGUDBJARTSSON, Daniel F; HOLM, Hilma; WILSGAARD, Tom et al.Nature genetics. 2009, Vol 41, Num 8, pp 876-878, issn 1061-4036, 3 p.Article

Genome-wide association study identifies sequence variants on 6q21 associated with age at menarcheSULEM, Patrick; GUDBJARTSSON, Daniel F; ABEN, Katja K et al.Nature genetics. 2009, Vol 41, Num 6, pp 734-738, issn 1061-4036, 5 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

Variants conferring risk of atrial fibrillation on chromosome 4q25GUDBJARTSSON, Daniel F; ARNAR, David O; PALSSON, Arnar et al.Nature (London). 2007, Vol 448, Num 7151, pp 353-357, issn 0028-0836, 5 p.Article