Cancer incidence among Icelandic deck officers in a population-based studySULEM, Patrick; RAFNSSON, Vilhjalmur.Scandinavian journal of work, environment & health. 2003, Vol 29, Num 2, pp 100-105, issn 0355-3140, 6 p.Article

A mutation in APP protects against Alzheimer's disease and age-related cognitive declineJONSSON, Thorlakur; ATWAL, Jasvinder K; HOYTE, Kwame et al.Nature (London). 2012, Vol 488, Num 7409, pp 96-99, issn 0028-0836, 4 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 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

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

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 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

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

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

European genome-wide association study identifies SLC14A1 as a new urinary bladder cancer susceptibility geneRAFNAR, Thorunn; VERMEULEN, Sita H; GUDBJARTSSON, Daniel et al.Human molecular genetics (Print). 2011, Vol 20, Num 21, pp 4268-4281, issn 0964-6906, 14 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

Mutations in BRIP1 confer high risk of ovarian cancerRAFNAR, Thorunn; GUDBJARTSSON, Daniel F; MAGNUSSON, Olafur T et al.Nature genetics. 2011, Vol 43, Num 11, pp 1104-1107, issn 1061-4036, 4 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

Many sequence variants affecting diversity of adult human heightGUDBJARTSSON, Daniel F; WALTERS, G. Bragi; HELGADOTTIR, Anna et al.Nature genetics. 2008, Vol 40, Num 5, pp 609-615, issn 1061-4036, 7 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

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