An Icelandic example of the impact of population structure on association studiesHELGASON, Agnar; YNGVADOTTIR, Bryndis; HRAFNKELSSON, Birgir et al.Nature genetics. 2005, Vol 37, Num 1, pp 90-95, issn 1061-4036, 6 p.Article

Assessing the signatures of selection in PRNP from polymorphism data : results support kreitman and Di Rienzo's opinionSOLDEVILA, Marta; CALAFELL, Francesc; HELGASON, Agnar et al.Trends in genetics (Regular ed.). 2005, Vol 21, Num 7, pp 389-391, issn 0168-9525, 3 p.Article

mtDNA and the islands of the North Atlantic: Estimating the proportions of norse and Gaelic ancestryHELGASON, Agnar; HICKEY, Eileen; GOODACRE, Sara et al.American journal of human genetics. 2001, Vol 68, Num 3, pp 723-737, issn 0002-9297Article

An Association Between the Kinship and Fertility of Human CouplesHELGASON, Agnar; PALSSON, Snaebjörn; GUÖBJARTSSON, Daniel F et al.Science (Washington, D.C.). 2008, Vol 319, Num 5864, pp 813-816, issn 0036-8075, 4 p.Article

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

A New Subclade of mtDNA Haplogroup C1 Found in Icelanders: Evidence of Pre-Columbian Contact?SUNNA EBENESERSDOTTIR, Sigríður; SIGURDSSON, Asgeir; SANCHEZ-QUINTO, Federico et al.American journal of physical anthropology. 2011, Vol 144, Num 1, pp 92-99, issn 0002-9483, 8 p.Article

Rate of de novo mutations and the importance of father's age to disease riskKONG, Augustine; FRIGGE, Michael L; WONG, Wendy S. W et al.Nature (London). 2012, Vol 488, Num 7412, pp 471-475, issn 0028-0836, 5 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

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

ASIP and TYR pigmentation variants associate with cutaneous melanoma and basal cell carcinomaGUDBJARTSSON, Daniel F; SULEM, Patrick; MAGNUSSON, Veronica et al.Nature genetics. 2008, Vol 40, Num 7, pp 886-891, issn 1061-4036, 6 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

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

A direct characterization of human mutation based on microsatellitesSUN, James X; HELGASON, Agnar; STEFANSSON, Kari et al.Nature genetics. 2012, Vol 44, Num 10, pp 1161-1165, issn 1061-4036, 5 p.Article

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

Two variants on chromosome 17 confer prostate cancer risk, and the one in TCF2 protects against type 2 diabetesGUDMUNDSSON, Julius; SULEM, Patrick; SIGURDSSON, Asgeir et al.Nature genetics. 2007, Vol 39, Num 8, pp 977-983, issn 1061-4036, 7 p.Article

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

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

Common variants near CAV1 and CAV2 are associated with primary open-angle glaucomaTHORLEIFSSON, Gudmar; BRAGI WALTERS, G; STEFANSSON, Hreinn et al.Nature genetics. 2010, Vol 42, Num 10, pp 906-909, issn 1061-4036, 4 p.Article

Fine-scale recombination rate differences between sexes, populations and individualsKONG, Augustine; THORLEIFSSON, Gudmar; GUDJONSSON, Sigurjon A et al.Nature (London). 2010, Vol 467, Num 7319, pp 1099-1103, issn 0028-0836, 5 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

Two newly identified genetic determinants of pigmentation in EuropeansSULEM, Patrick; GUDBJARTSSON, Daniel F; PALSSON, Snaebjörn et al.Nature genetics. 2008, Vol 40, Num 7, pp 835-837, issn 1061-4036, 3 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