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

A sequence variant on 17p21 is associated with age at onset and severity of asthmaHALAPI, Eva; GUDBJARTSSON, Daniel F; JONASDOTTIR, Aslaug et al.European journal of human genetics. 2010, Vol 18, Num 8, pp 902-908, issn 1018-4813, 7 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

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

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

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

Meta-analyses identify 13 loci associated with age at menopause and highlight DNA repair and immune pathwaysSTOLK, Lisette; PERRY, John R. B; ESKO, Tõnu et al.Nature genetics. 2012, Vol 44, Num 3, pp 260-268, issn 1061-4036, 9 p.Article

Sequence variants affecting eosinophil numbers associate with asthma and myocardial infarctionGUDBJARTSSON, Daniel F; BJORNSDOTTIR, Unnur S; WILLIAMS, Carolyn et al.Nature genetics. 2009, Vol 41, Num 3, pp 342-347, issn 1061-4036, 6 p.Article

Sequence Variants in the RNF212 Gene Associate with Genome-Wide Recombination RateKONG, Augustine; THORLEIFSSON, Gudmar; JONASDOTTIR, Aslaug et al.Science (Washington, D.C.). 2008, Vol 319, Num 5868, pp 1398-1401, issn 0036-8075, 4 p.Article

Genetic determinants of hair, eye and skin pigmentation in EuropeansSULEM, Patrick; GUDBJARTSSON, Daniel F; JAKOBSDOTTIR, Margret et al.Nature genetics. 2007, Vol 39, Num 12, pp 1443-1452, issn 1061-4036, 10 p.Article

A variant of the gene encoding leukotriene A4 hydrolase confers ethnicity-specific risk of myocardial infarctionHELGADOTTIR, Anna; MANOLESCU, Andrei; JONSSON, Thorlakur et al.Nature genetics. 2006, Vol 38, Num 1, pp 68-74, issn 1061-4036, 7 p.Article

The inheritance of rheumatoid arthritis in IcelandGRANT, Struan F. A; THORLEIFSSON, Gudmar; JONSSON, Helgi et al.Arthritis and rheumatism. 2001, Vol 44, Num 10, pp 2247-2254, issn 0004-3591Article

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

Genome-Wide Significant Association Between a Sequence Variant at 15q15.2 and Lung Cancer RiskRAFNAR, Thorunn; SULEM, Patrick; BJARNASON, Hjordis et al.Cancer research (Chicago, Ill.). 2011, Vol 71, Num 4, pp 1356-1361, issn 0008-5472, 6 p.Article

A germline variant in the TP53 polyadenylation signal confers cancer susceptibilitySTACEY, Simon N; SULEM, Patrick; RAGNARSSON, Rafn et al.Nature genetics. 2011, Vol 43, Num 11, pp 1098-1103, issn 1061-4036, 6 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

Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studiesELKS, Cathy E; PERRY, John R. B; GUDBJARTSSON, Daniel F et al.Nature genetics. 2010, Vol 42, Num 12, pp 1077-1085, issn 1061-4036, 9 p.Article

Detection of sharing by descent, long-range phasing and haplotype imputationKONG, Augustine; MASSON, Gisli; SULEM, Patrick et al.Nature genetics. 2008, Vol 40, Num 9, pp 1068-1075, issn 1061-4036, 8 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

A study based on whole-genome sequencing yields a rare variant at 8q24 associated with prostate cancerGUDMUNDSSON, Julius; SULEM, Patrick; JOHANNSDOTTIR, Hrefna et al.Nature genetics. 2012, Vol 44, Num 12, pp 1326-1329, issn 1061-4036, 4 p.Article

A sequence variant at 4p16.3 confers susceptibility to urinary bladder cancerKIEMENEY, Lambertus A; SULEM, Patrick; KOSTIC, Jelena et al.Nature genetics. 2010, Vol 42, Num 5, pp 415-419, issn 1061-4036, 5 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

Genome-wide association and replication studies identify four variants associated with prostate cancer susceptibilityGUDMUNDSSON, Julius; SULEM, Patrick; STACEY, Simon N et al.Nature genetics. 2009, Vol 41, Num 10, pp 1122-1126, issn 1061-4036, 5 p.Article

Parental origin of sequence variants associated with complex diseasesKONG, Augustine; STEINTHORSDOTTIR, Valgerdur; FRIGGE, Michael L et al.Nature (London). 2009, Vol 462, Num 7275, pp 868-874, issn 0028-0836, 7 p.Article