UNSUPERVISED EMPIRICAL BAYESIAN MULTIPLE TESTING WITH EXTERNAL COVARIATESFERKINGSTAD, Egil; FRIGESSI, Arnoldo; RUE, Havard et al.The Annals of applied statistics. 2008, Vol 2, Num 2, pp 714-735, issn 1932-6157, 22 p.Article

Mapping cis- and trans-regulatory effects across multiple tissues in twinsGRUNDBERG, Elin; SMALL, Kerrin S; NISBETT, James et al.Nature genetics. 2012, Vol 44, Num 10, pp 1084-1089, 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

Support for involvement of the AHI1 locus in schizophreniaINGASON, Andres; SIGMUNDSSON, Thordur; STEFANSSON, Kari et al.European journal of human genetics. 2007, Vol 15, Num 9, pp 988-991, issn 1018-4813, 4 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

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

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

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

Variant in the sequence of the LINGO1 gene confers risk of essential tremorSTEFANSSON, Hreinn; STEINBERG, Stacy; BÖTTCHER, Yvonne et al.Nature genetics. 2009, Vol 41, Num 3, pp 277-279, issn 1061-4036, 3 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

Risk Variants for Atrial Fibrillation on Chromosome 4q25 Associate with Ischemic StrokeGRETARSDOTTIR, Solveig; THORLEIFSSON, Gudmar; BJARNASON, Hjordis et al.Annals of neurology. 2008, Vol 64, Num 4, pp 402-409, issn 0364-5134, 8 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

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

Genomewide scan for hand osteoarthritis: A novel mutation in matrilin-3STEFANSSON, Stefan Einar; JONSSON, Helgi; KONG, Augustine et al.American journal of human genetics. 2003, Vol 72, Num 6, pp 1448-1459, issn 0002-9297, 12 p.Article

Variant of TREM2 Associated with the Risk of Alzheimer's DiseaseJONSSON, Thorlakur; STEFANSSON, Hreinn; RUJESCU, Dan et al.The New England journal of medicine. 2013, Vol 368, Num 2, pp 107-116, issn 0028-4793, 10 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

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

Variants in MTNR1B influence fasting glucose levelsPROKOPENKO, Inga; LANGENBERG, Claudia; POTTER, Simon C et al.Nature genetics. 2009, Vol 41, Num 1, pp 77-81, 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

Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetesZEGGINI, Eleftheria; SCOTT, Laura J; DE BAKKER, Paul I. W et al.ZEGGINI, Eleftheria; SCOTT, Laura J; Nature genetics. 2008, Vol 40, Num 5, pp 638-645, issn 1061-4036, 8 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