Overexpression of the myeloid leukemia-associated Hoxa9 gene in bone marrow cells induces stem cell expansionTHORSTEINSDOTTIR, Unnur; MAMO, Aline; KROON, Evert et al.Blood. 2002, Vol 99, Num 1, pp 121-129, issn 0006-4971Article

Loss of heterozygosity at the FHIT gene in different solid human tumours and its association with survival in colorectal cancer patientsPETURSDOTTIR, Thorgunnur Eyfjord; HAFSTEINSDOTTIR, Sigridur H; JONASSON, Jon G et al.Anticancer research. 2002, Vol 22, Num 6A, pp 3205-3212, issn 0250-7005, 8 p.Article

Common variants near FRK/COL10A1 and VEGFA are associated with advanced age-related macular degenerationYI YU; BHANGALE, Tushar R; REYNOLDS, Robyn et al.Human molecular genetics (Print). 2011, Vol 20, Num 18, pp 3699-3709, issn 0964-6906, 11 p.Article

Association of JAG 1 with Bone Mineral Density and Osteoporotic Fractures: A Genome-wide Association Study and Follow-up Replication StudiesKUNG, Annie W. C; XIAO, Su-Mei; ZHANG, Min-Jia et al.American journal of human genetics. 2010, Vol 86, Num 2, pp 229-239, issn 0002-9297, 11 p.Article

Genetic variation in the prostate stem cell antigen gene PSCA confers susceptibility to urinary bladder cancerXIFENG WU; YUANQING YE; DINNEY, Colin P et al.Nature genetics. 2009, Vol 41, Num 9, pp 991-995, issn 1061-4036, 5 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

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

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

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

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

Shared Genetic Susceptibility to Ischemic Stroke and Coronary Artery Disease: A Genome-Wide Analysis of Common VariantsDICHGANS, Martin; MALIK, Rainer; O'DONNELL, Christopher J et al.Stroke (1970). 2014, Vol 45, Num 1, pp 24-36, issn 0039-2499, 13 p.Article

Common variants at 6p21.1 are associated with large artery atherosclerotic strokeHOLLIDAY, Elizabeth G; MAGUIRE, Jane M; MALIK, Rainer et al.Nature genetics. 2012, Vol 44, Num 10, pp 1147-1151, issn 1061-4036, 5 p.Article

Plasma HDL cholesterol and risk of myocardial infarction: a mendelian randomisation studyVOIGHT, Benjamin F; PELOSO, Gina M; SCHUNKERT, Heribert et al.Lancet (British edition). 2012, Vol 380, Num 9841, pp 572-580, issn 0140-6736, 9 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

Genetic evidence that raised sex hormone binding globulin (SHBG) levels reduce the risk of type 2 diabetesPERRY, John R. B; WEEDON, Michael N; PAOLISSO, Giuseppe et al.Human molecular genetics (Print). 2010, Vol 19, Num 3, pp 535-544, issn 0964-6906, 10 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