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A populationwide coalescent analysis of Icelandic matrilineal and patrilineal genealogies: Evidence for a faster evolutionary rate of mtDNA lineages than Y chromosomesHELGASON, Agnar; HRAFNKELSSON, Birgir; GULCHER, Jeffrey R et al.American journal of human genetics. 2003, Vol 72, Num 6, pp 1370-1388, issn 0002-9297, 19 p.Article

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A common inversion under selection in EuropeansSTEFANSSON, Hreinn; HELGASON, Agnar; DESNICA, Natasa et al.Nature genetics. 2005, Vol 37, Num 2, pp 129-137, issn 1061-4036, 9 p.Article

Familial Risk of lung carcinoma in the Icelandic populationJONSSON, Steinn; THORSTEINSDOTTIR, Unnur; AMUNDADOTTIR, Laufey T et al.JAMA, the journal of the American Medical Association. 2004, Vol 292, Num 24, pp 2977-2983, issn 0098-7484, 7 p.Article

A large icelandic family with early osteoarthritis of the hip associated with a susceptibility locus on chromosome 16pINGVARSSON, Thorvaldur; STEFANSSON, Stefan Einar; LOHMANDER, L. Stefan et al.Arthritis and rheumatism. 2001, Vol 44, Num 11, pp 2548-2555, issn 0004-3591Article

Refining the impact of TCF7L2 gene variants on type 2 diabetes and adaptive evolutionHELGASON, Agnar; PALSSON, Snaebjörn; BENEDIKTSSON, Rafn et al.Nature genetics. 2007, Vol 39, Num 2, pp 218-225, issn 1061-4036, 8 p.Article

A common variant associated with prostate cancer in European and African populationsAMUNDADOTTIR, Laufey T; SULEM, Patrick; JAKOBSDOTTIR, Margret et al.Nature genetics. 2006, Vol 38, Num 6, pp 652-658, issn 1061-4036, 7 p.Article

Recombination rate and reproductive success in humansKONG, Augustine; BARNARD, John; LAMB, Neil E et al.Nature genetics. 2004, Vol 36, Num 11, pp 1203-1206, issn 1061-4036, 4 p.Article

Genomewide scan for hand osteoarthritis: A novel mutation in matrilin-3STEFANSSON, Stefan Einar; JONSSON, Helgi; KONG, Augustine et al.American journal of human genetics. 2003, Vol 72, Num 6, pp 1448-1459, issn 0002-9297, 12 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

Genetics of gene expression and its effect on diseaseEMILSSON, Valur; THORLEIFSSON, Gudmar; MOUY, Magali et al.Nature (London). 2008, Vol 452, Num 7186, pp 423-428, issn 0028-0836, 6 p.Article

Sequence variant on 8q24 confers susceptibility to urinary bladder cancerKIEMENEY, Lambertus A; THORLACIUS, Steinunn; BLONDAL, Thorarinn et al.Nature genetics. 2008, Vol 40, Num 11, pp 1307-1312, issn 1061-4036, 6 p.Article

A common variant on chromosome 9p21 affects the risk of myocardial infarctionHELGADOTTIR, Anna; THORLEIFSSON, Gudmar; MASSON, Gisli et al.Science (Washington, D.C.). 2007, Vol 316, Num 5830, pp 1491-1493, issn 0036-8075, 3 p.Article

PDE4D and ALOX5AP genetic variants and risk for ischemic cerebrovascular disease in SwedenKOSTULAS, Konstantinos; GRETARSDOTTIR, Solveig; HILLERT, Jan et al.Journal of the neurological sciences. 2007, Vol 263, Num 1-2, pp 113-117, issn 0022-510X, 5 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

The gene encoding 5-lipoxygenase activating protein confers risk of myocardial infarction and strokeHELGADOTTIR, Anna; MANOLESCU, Andrei; SVEINBJORNSDOTTIR, Sigurlaug et al.Nature genetics. 2004, Vol 36, Num 3, pp 233-239, issn 1061-4036, 7 p.Article

Localization of a gene for Migraine without aura to chromosome 4q21BJÖRNSSON, Asgeir; GUDMUNDSSON, Grétar; GULCHER, Jeffrey R et al.American journal of human genetics. 2003, Vol 73, Num 5, pp 986-993, issn 0002-9297, 8 p.Article

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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

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

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