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

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

Association of Folate-Pathway Gene Polymorphisms with the Risk of Prostate Cancer: a Population-Based Nested Case-Control Study, Systematic Review, and Meta-analysisCOLLIN, Simon M; METCALFE, Chris; NEAL, David E et al.Cancer epidemiology, biomarkers & prevention. 2009, Vol 18, Num 9, pp 2528-2539, issn 1055-9965, 12 p.Article

Sequence variants at the TERT-CLPTM1L locus associate with many cancer typesRAFNAR, Thorunn; SULEM, Patrick; BLÖNDAL, Thorarinn et al.Nature genetics. 2009, Vol 41, Num 2, pp 221-227, issn 1061-4036, 7 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

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

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

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

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

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

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

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

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

A variant associated with nicotine dependence, lung cancer and peripheral arterial diseaseTHORGEIRSSON, Thorgeir E; GELLER, Frank; STACEY, Simon N et al.Nature (London). 2008, Vol 452, Num 7187, pp 638-641, issn 0028-0836, 4 p.Article

Common sequence variants on 2p15 and Xp11.22 confer susceptibility to prostate cancerGUDMUNDSSON, Julius; SULEM, Patrick; JAKOBSDOTTIR, Margret et al.Nature genetics. 2008, Vol 40, Num 3, pp 281-283, issn 1061-4036, 3 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