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Results 1 to 25 of 59

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Segmental duplication density decrease with distance to human-mouse breaks of syntenySAINZ, Jesus; ROVENSKY, Pavol; GUDJONSSON, Sigurjon A et al.European journal of human genetics. 2006, Vol 14, Num 2, pp 216-221, issn 1018-4813, 6 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

FTO genotype is associated with phenotypic variability of body mass indexJIAN YANG; LOOS, Ruth J. F; WAITE, Lindsay et al.Nature (London). 2012, Vol 490, Num 7419, pp 267-272, issn 0028-0836, 6 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

Meta-analysis of genome-wide association studies confirms a susceptibility locus for knee osteoarthritis on chromosome 7q22EVANGELOU, Evangelos; VALDES, Ana M; AKUNE, Toru et al.Annals of the rheumatic diseases. 2011, Vol 70, Num 2, pp 349-355, issn 0003-4967, 7 p.Article

Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distributionHEID, Iris M; JACKSON, Anne U; WORKALEMAHU, Tsegaselassie et al.Nature genetics. 2010, Vol 42, Num 11, pp 949-960, issn 1061-4036, 12 p.Article

Hundreds of variants clustered in genomic loci and biological pathways affect human heightALLEN, Hana Lango; ESTRADA, Karol; FERREIRA, Teresa et al.Nature (London). 2010, Vol 467, Num 7317, pp 832-838, issn 0028-0836, 7 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

Large-scale association analyses identify new loci influencing glycemic traits and provide insight into the underlying biological pathwaysSCOTT, Robert A; LAGOU, Vasiliki; KANONI, Stavroula et al.Nature genetics. 2012, Vol 44, Num 9, pp 991-1005, issn 1061-4036, 15 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

Genome-wide association study identifies loci influencing concentrations of liver enzymes in plasmaCHAMBERS, John C; WEIHUA ZHANG; COIN, Lachlan J et al.Nature genetics. 2011, Vol 43, Num 11, pp 1131-1138, issn 1061-4036, 8 p.Article

Design of the Coronary ARtery Disease Genome-Wide Replication And Meta-Analysis (CARDIoGRAM) Study A Genome-Wide Association Meta-analysis Involving More Than 22 000 Cases and 60 000 ControlsPREUSS, Michael; KÖNIG, Inke R; HALL, Alistair S et al.Circulation. Cardiovascular genetics (Print). 2010, Vol 3, Num 5, pp 475-483, issn 1942-325X, 9 p.Article

Lack of Association Between the Trp719Arg Polymorphism in Kinesin-Like Protein-6 and Coronary Artery Disease in 19 Case-Control StudiesASSIMES, Themistocles L; HOLM, Hilma; PATTERSON, Chris C et al.Journal of the American College of Cardiology. 2010, Vol 56, Num 19, pp 1552-1563, issn 0735-1097, 12 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

The same sequence variant on 9p21 associates with myocardial infarction, abdominal aortic aneurysm and intracranial aneurysmHELGADOTTIR, Anna; THORLEIFSSON, Gudmar; KYO, Yoshiki et al.Nature genetics. 2008, Vol 40, Num 2, pp 217-224, 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

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

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