A strong familiality of ankylosing spondylitis through several generationsGEIRSSON, Arni Jon; KRISTJANSSON, Kristleifur; GUDBJORNSSON, Bjorn et al.Annals of the rheumatic diseases. 2010, Vol 69, Num 7, pp 1346-1348, issn 0003-4967, 3 p.Article

Impact of Genetics on Low Bone Mass in AdultsSIGURDSSON, Gunnar; HALLDORSSON, Bjarni V; STYRKARSDOTTIR, Unnur et al.Journal of bone and mineral research (Print). 2008, Vol 23, Num 10, pp 1584-1590, issn 0884-0431, 7 p.Article

The Adult Reading History Questionnaire (ARHQ) in Icelandic: Psychometric Properties and Factor StructureBJORNSDOTTIR, Gyda; HALLDORSSON, Jonas G; STEINBERG, Stacy et al.Journal of learning disabilities. 2014, Vol 47, Num 6, pp 532-542, issn 0022-2194, 11 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

Effects of a 5-lipoxygenase -activating protein inhibitor on biomarkers associated with risk of myocardial infarction : A randomized trialHAKONARSON, Hakon; THORVALDSSON, Sverrir; THORGEIRSSON, Gestur et al.JAMA, the journal of the American Medical Association. 2005, Vol 293, Num 18, pp 2245-2256, issn 0098-7484, 12 p.Article

Familial aggregation of atrial fibrillation in icelandARNAR, David O; THORVALDSSON, Sverrir; MANOLIO, Teri A et al.European heart journal. 2006, Vol 27, Num 6, pp 708-712, issn 0195-668X, 5 p.Article

Psychometric properties of the Icelandic NEO-FFI in a general population sample compared to a sample recruited for a study on the genetics of addictionBJORNSDOTTIR, Gyda; JONSSON, Fridrik H; HANSDOTTIR, Ingunn et al.Personality and individual differences. 2014, Vol 58, pp 71-75, issn 0191-8869, 5 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

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

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

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

Linkage of essential hypertension to chromosome 18qKRISTJANSSON, Kristleifur; MANOLESCU, Andrei; STEFANSSON, Kari et al.Hypertension (Dallas, Tex. 1979). 2002, Vol 39, Num 6, pp 1044-1049, issn 0194-911XArticle

Allelic frequencies and patterns of single-nucleotide polymorphisms in candidate genes for asthma and atopy in IcelandHAKONARSON, Hakon; BJORNSDOTTIR, Unnur S; GISLASON, David et al.American journal of respiratory and critical care medicine. 2001, Vol 164, Num 11, pp 2036-2044, issn 1073-449XArticle

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

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

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

Subclinical intestinal inflammation: An inherited abnormality in Crohn's disease relatives?THJODLEIFSSON, Bjarni; SIGTHORSSON, Gudmundur; SHERWOOD, Roy et al.Gastroenterology (New York, NY. 1943). 2003, Vol 124, Num 7, pp 1728-1737, issn 0016-5085, 10 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

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