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au.\*:("LATHROP, G. Mark")

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Results 1 to 13 of 13

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Variation of gene-based SNPs and linkage disequilibrium patterns in the human genomeTSUNODA, Tatsuhiko; LATHROP, G. Mark; SEKINE, Akihiro et al.Human molecular genetics (Print). 2004, Vol 13, Num 15, pp 1623-1632, issn 0964-6906, 10 p.Article

Wolcott-rallison syndrome: Clinical, genetic, and functional study of EIF2AK3 mutations and suggestion of genetic heterogeneitySENEE, Valérie; VATTEM, Krishna M; MICHAUD, Jacques L et al.Diabetes (New York, NY). 2004, Vol 53, Num 7, pp 1876-1883, issn 0012-1797, 8 p.Article

Common variants at 30 loci contribute to polygenic dyslipidemiaKATHIRESAN, Sekar; WILLER, Cristen J; VOIGHT, Benjamin F et al.Nature genetics. 2009, Vol 41, Num 1, pp 56-65, issn 1061-4036, 10 p.Article

Genome-wide scan reveals association of psoriasis with IL-23 and NF-κB pathwaysNAIR, Rajan P; CALLIS DUFFIN, Kristina; RUETHER, Andreas et al.Nature genetics. 2009, Vol 41, Num 2, pp 199-204, issn 1061-4036, 6 p.Article

Haplotypes of the WNK1 gene associate with blood pressure variation in a severely hypertensive population from the british genetics of hypertension studyNEWHOUSE, Stephen J; WALLACE, Chris; CONNELL, John M et al.Human molecular genetics (Print). 2005, Vol 14, Num 13, pp 1805-1814, issn 0964-6906, 10 p.Article

Genome-wide association study identifies three loci associated with melanoma riskBISHOP, D. Timothy; DEMENAIS, Florence; BAKKER, Bert et al.Nature genetics. 2009, Vol 41, Num 8, pp 920-925, issn 1061-4036, 6 p.Article

Genetic variants regulating ORMDL3 expression contribute to the risk of childhood asthmaMOFFATT, Miriam F; KABESCH, Michael; HEINZMANN, Andrea et al.Nature (London). 2007, Vol 448, Num 7152, pp 470-473, issn 0028-0836, 4 p.Article

Linkage analysis using Co-phenotypes in the BRIGHT study reveals novel potential susceptibility loci for hypertensionWALLACE, Chris; XUE, Ming-Zhan; DOMINICZAK, Anna et al.American journal of human genetics. 2006, Vol 79, Num 2, pp 323-331, issn 0002-9297, 9 p.Article

A genomewide scan for loci predisposing to type 2 Diabetes in a U.K. population (the Diabetes UK Warren 2 repository) : Analysis of 573 pedigrees provides independent replication of a susceptibility locus on chromosome 1qWILTSHIRE, Teven; HATTERSLEY, Andrew T; BENNETT, Amanda et al.American journal of human genetics. 2001, Vol 69, Num 3, pp 553-569, issn 0002-9297Article

The Effect on Melanoma Risk of Genes Previously Associated With Telomere LengthILES, Mark M; BISHOP, D. Timothy; ANDRESEN, Per A et al.Journal of the National Cancer Institute. 2014, Vol 106, Num 10, issn 0027-8874, 267.1-267.5Article

Genome-wide Association Study Identifies Genes for Biomarkers of Cardiovascular Disease : Serum Urate and DyslipidemiaWALLACE, Chris; NEWHOUSE, Stephen J; BURTON, Paul et al.American journal of human genetics. 2008, Vol 82, Num 1, pp 139-149, issn 0002-9297, 11 p.Article

A genome-wide association study of global gene expressionDIXON, Anna L; LIMING LIANG; LATHROP, G. Mark et al.Nature genetics. 2007, Vol 39, Num 10, pp 1202-1207, issn 1061-4036, 6 p.Article

Two-dimensional genome-scan identifies novel epistatic loci for essential hypertensionTZENOVA BELL, Jordana; WALLACE, Chris; WEBSTER, John et al.Human molecular genetics (Print). 2006, Vol 15, Num 8, pp 1365-1374, issn 0964-6906, 10 p.Article

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