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Results 1 to 25 of 43

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Quantitative trait loci for fasting glucose in young europeans replicate previous findings for type 2 diabetes in 2q23-24 and other locationsFRADIN, Delphine; HEATH, Simon; LATHROP, Mark et al.Diabetes (New York, NY). 2007, Vol 56, Num 6, pp 1742-1745, issn 0012-1797, 4 p.Article

Epigenomic analysis detects widespread gene-body DNA hypomethylation in chronic lymphocytic leukemiaKULIS, Marta; HEATH, Simon; BARBERAN-SOLER, Sergio et al.Nature genetics. 2012, Vol 44, Num 11, pp 1236-1242, issn 1061-4036, 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

Identification of distinct quantitative trait loci affecting length or weight variability at birth in humansFRADIN, Delphine; HEATH, Simon; LEPERCQ, Jacques et al.The Journal of clinical endocrinology and metabolism. 2006, Vol 91, Num 10, pp 4164-4170, issn 0021-972X, 7 p.Article

Whole-genome sequencing identifies recurrent mutations in chronic lymphocytic leukaemiaPUENTE, Xose S; PINYOL, Magda; BASSAGANYAS, Laia et al.Nature (London). 2011, Vol 475, Num 7354, pp 101-105, issn 0028-0836, 5 p.Article

Genome-wide association study identifies variants at CLU and CR1 associated with Alzheimer's diseaseLAMBERT, Jean-Charles; HEATH, Simon; LETENNEUR, Luc et al.Nature genetics. 2009, Vol 41, Num 10, pp 1094-1099, issn 1061-4036, 6 p.Article

Confirmation of psoriasis susceptibility loci on chromosome 6p21 and 20p13 in french familiesLESUEUR, Fabienne; LEFEVRE, Caroline; HEATH, Simon et al.Journal of investigative dermatology. 2007, Vol 127, Num 6, pp 1403-1409, issn 0022-202X, 7 p.Article

Exome sequencing identifies recurrent mutations of the splicing factor SF3B1 gene in chronic lymphocytic leukemiaQUESADA, Victor; CONDE, Laura; LOPEZ-GUERRA, Mónica et al.Nature genetics. 2012, Vol 44, Num 1, pp 47-52, issn 1061-4036, 6 p.Article

A Large-Scale, Consortium-Based Genomewide Association Study of AsthmaMOFFATT, Miriam F; GUT, Ivo G; DEMENAIS, Florence et al.The New England journal of medicine. 2010, Vol 363, Num 13, pp 1211-1221, issn 0028-4793, 11 p.Article

Interferon y receptor 2 gene variants are associated with liver fibrosis in patients with chronic hepatitis C infectionNALPAS, Bertrand; LAVIALLE-MEZIANI, Roubila; FONTAINE, Hélène et al.Gut. 2010, Vol 59, Num 8, pp 1120-1126, issn 0017-5749, 7 p.Article

A QTL influencing F cell production maps to a gene encoding a zinc-finger protein on chromosome 2p15MENZEL, Stephan; GARNER, Chad; BEST, Steve et al.Nature genetics. 2007, Vol 39, Num 10, pp 1197-1199, issn 1061-4036, 3 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

A Follow-Up Study of a Genome-wide Association Scan Identifies a Susceptibility Locus for Venous Thrombosis on Chromosome 6p24.1MORANGE, Pierre-Emmanuel; BEZEMER, Irene; GALAN, Pilar et al.American journal of human genetics. 2010, Vol 86, Num 4, pp 592-595, issn 0002-9297, 4 p.Article

A locus for bilateral occipital polymicrogyria maps to chromosome 6q16-q22BEN CHEIKH, Bouchra Ouled Amar; BAULAC, Stéphanie; HEATH, Simon et al.Neurogenetics (Oxford. Print). 2009, Vol 10, Num 1, pp 35-42, issn 1364-6745, 8 p.Article

Common susceptibility alleles are unlikely to contribute as strongly as the FV and ABO loci to VTE risk: results from a GWAS approachTREGOUËT, David-Alexandre; HEATH, Simon; ALESSI, Marie-Christine et al.Blood. 2009, Vol 113, Num 21, pp 5298-5303, issn 0006-4971, 6 p.Article

G/T Substitution in Intron 1 of the UNC13B Gene Is Associated With Increased Risk of Nephropathy in Patients With Type 1 DiabetesTREGOUET, David-Alexandre; GROOP, Per-Henrik; NICAUD, Viviane et al.Diabetes (New York, NY). 2008, Vol 57, Num 10, pp 2843-2850, issn 0012-1797, 8 p.Article

Three Genome-wide Association Studies and a Linkage Analysis Identify HERC2 as a Human Iris Color GeneKAYSER, Manfred; FAN LIU; VAN IJCKEN, Wilfred F. J et al.American journal of human genetics. 2008, Vol 82, Num 2, pp 411-423, issn 0002-9297, 13 p.Article

Systematic Analysis of Glutamatergic Neurotransmission Genes in Alcohol Dependence and Adolescent Risky Drinking BehaviorSCHUMANN, Gunter; JOHANN, Monika; KRAUSE, Kristina et al.Archives of general psychiatry. 2008, Vol 65, Num 7, pp 826-838, issn 0003-990X, 13 p.Article

A transmission/Disequilibrium test that allows for genotyping errors in the analysis of single-nucleotide polymorphism dataGORDON, Derek; HEATH, Simon C; XIN LIU et al.American journal of human genetics. 2001, Vol 69, Num 2, pp 371-380, issn 0002-9297Article

Association between a 15q25 gene variant, smoking quantity and tobacco-related cancers among 17 000 individualsLIPS, Esther H; GABORIEAU, Valerie; RUDNAI, Peter et al.International journal of epidemiology. 2010, Vol 39, Num 2, pp 563-577, issn 0300-5771, 15 p.Article

HLA Has Strongest Association with IgA Nephropathy in Genome-Wide AnalysisFEEHALLY, John; FARRALL, Martin; PADMANABHAN, Sandosh et al.Journal of the American Society of Nephrology. 2010, Vol 21, Num 10, pp 1791-1797, issn 1046-6673, 7 p.Article

An Association Study of 22 Candidate Genes in Psoriasis Families Reveals Shared Genetic Factors with Other Autoimmune and Skin DisordersOUDOT, Tiphaine; LESUEUR, Fabienne; FISCHER, Judith et al.Journal of investigative dermatology. 2009, Vol 129, Num 11, pp 2637-2645, issn 0022-202X, 9 p.Article

Mutations of the FHL1 Gene Cause Emery-Dreifuss Muscular DystrophyGUENEAU, Lucie; BERTRAND, Anne T; TRANCHANT, Christine et al.American journal of human genetics. 2009, Vol 85, Num 3, pp 338-353, issn 0002-9297, 16 p.Article

Lung cancer susceptibility locus at 5p15.33MCKAY, James D; HUNG, Rayjean J; RUDNAI, Peter et al.Nature genetics. 2008, Vol 40, Num 12, pp 1404-1406, issn 1061-4036, 3 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

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