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au.\*:("CHASMAN, Daniel I")

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Population-Based Genomewide Genetic Analysis of Common Clinical Chemistry AnalytesCHASMAN, Daniel I; PARE, Guillaume; RIDKER, Paul M et al.Clinical chemistry (Baltimore, Md.). 2009, Vol 55, Num 1, pp 39-51, issn 0009-9147, 13 p.Article

Genetic variants of 11 telomere-pathway gene loci and the risk of incident type 2 diabetes mellitus: The Women's Genome Health StudyZEE, Robert Y. L; RIDKER, Paul M; CHASMAN, Daniel I et al.Atherosclerosis. 2011, Vol 218, Num 1, pp 144-146, issn 0021-9150, 3 p.Article

Mitochondrial uncoupling protein gene cluster variation (UCP2―UCP3) and the risk of incident type 2 diabetes mellitus: The Women's Genome Health StudyZEE, Robert Y. L; RIDKER, Paul M; CHASMAN, Daniel I et al.Atherosclerosis. 2011, Vol 214, Num 1, pp 107-109, issn 0021-9150, 3 p.Article

Kinesin-Like Protein 6 (KIF6) Polymorphism and the Efficacy of Rosuvastatin in Primary PreventionRIDKER, Paul M; MACFADYEN, Jean G; GLYNN, Robert J et al.Circulation. Cardiovascular genetics (Print). 2011, Vol 4, Num 3, pp 312-317, issn 1942-325X, 6 p.Article

Tryptophanyl-tRNA synthetase gene polymorphisms and risk of incident myocardial infarctionZEE, Robert Y. L; HEGENER, Hillary H; CHASMAN, Daniel I et al.Atherosclerosis. 2005, Vol 181, Num 1, pp 137-141, issn 0021-9150, 5 p.Article

Common Variants in Mendelian Kidney Disease Genes and Their Association with Renal FunctionPARSA, Afshin; FUCHSBERGER, Christian; CHEN, Ming-Huei et al.Journal of the American Society of Nephrology. 2013, Vol 24, Num 12, pp 2105-2117, issn 1046-6673, 13 p.Article

Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studiesELKS, Cathy E; PERRY, John R. B; GUDBJARTSSON, Daniel F et al.Nature genetics. 2010, Vol 42, Num 12, pp 1077-1085, issn 1061-4036, 9 p.Article

A Kinesin Family Member 6 Variant Is Associated With Coronary Heart Disease in the Women's Health StudySHIFFMAN, Dov; CHASMAN, Daniel I; ZEE, Robert Y. L et al.Journal of the American College of Cardiology. 2008, Vol 51, Num 4, issn 0735-1097, 444-448, 456-458 [8 p.]Article

Polymorphisms of the HNF1A Gene Encoding Hepatocyte Nuclear Factor-1α are Associated with C-Reactive ProteinREINER, Alexander P; BARBER, Mathew J; DURDA, J. Peter et al.American journal of human genetics. 2008, Vol 82, Num 5, pp 1193-1201, issn 0002-9297, 9 p.Article

Integration of genome-wide association studies with biological knowledge identifies six novel genes related to kidney functionCHASMAN, Daniel I; FUCHSBERGER, Christian; MAN LI et al.Human molecular genetics (Print). 2012, Vol 21, Num 24, pp 5329-5343, issn 0964-6906, 15 p.Article

Genetic variants at 2q24 are associated with susceptibility to type 2 diabetesLU QI; CORNELIS, Marilyn C; QI SUN et al.Human molecular genetics (Print). 2010, Vol 19, Num 13, pp 2706-2715, issn 0964-6906, 10 p.Article

Multiple Genetic Loci Influence Serum Urate Levels and Their Relationship With Gout and Cardiovascular Disease Risk FactorsQIONG YANG; KÖTTGEN, Anna; LAUNER, Lenore et al.Circulation. Cardiovascular genetics (Print). 2010, Vol 3, Num 6, pp 523-530, issn 1942-325X, 8 p.Article

Polymorphism in the apolipoprotein(a) gene, plasma lipoprotein(a), cardiovascular disease, and low-dose aspirin therapyCHASMAN, Daniel I; SHIFFMAN, Dov; ZEE, Robert Y. L et al.Atherosclerosis. 2009, Vol 203, Num 2, pp 371-376, issn 0021-9150, 6 p.Article

Purinergic receptor P2Y, G-protein coupled, 12 gene variants and risk of incident ischemic stroke, myocardial infarction, and venous thromboembolismZEE, Robert Y. L; MICHAUD, Sherri E; DIEHL, Kirsti A et al.Atherosclerosis. 2008, Vol 197, Num 2, pp 694-699, issn 0021-9150, 6 p.Article

Inactivating Mutations in NPC1L1 and Protection from Coronary Heart Disease: The Myocardial Infarction Genetics Consortium InvestigatorsSTITZIEL, Nathan O; WON, Hong-Hee; FARRALL, Martin et al.The New England journal of medicine. 2014, Vol 371, Num 22, pp 2072-2082, issn 0028-4793, 11 p.Article

Genetic Determinants of Statin-Induced Low-Density Lipoprotein Cholesterol Reduction: The Justification for the Use of Statins in Prevention: An Intervention Trial Evaluating Rosuvastatin (JUPITER) TrialCHASMAN, Daniel I; GIULIANINI, Franco; MACFADYEN, Jean et al.Circulation. Cardiovascular genetics (Print). 2012, Vol 5, Num 2, pp 257-264, issn 1942-325X, 8 p.Article

Genome-wide Linkage and Association Analyses Implicate FASN in Predisposition to Uterine LeiomyomataEGGERT, Stacey L; HUYCK, Karen L; TRELOAR, Susan A et al.American journal of human genetics. 2012, Vol 91, Num 4, pp 621-628, issn 0002-9297, 8 p.Article

A common variant at the TERT-CLPTM1L locus is associated with estrogen receptor―negative breast cancerHAIMAN, Christopher A; CHEN, Gary K; BAGLIETTO, Laura et al.Nature genetics. 2011, Vol 43, Num 12, pp 1210-1214, issn 1061-4036, 5 p.Article

The Fat-Mass and Obesity-Associated (FTO) gene, physical activity, and risk of incident cardiovascular events in white womenAHMAD, Tariq; CHASMAN, Daniel I; MORA, Samia et al.The American heart journal. 2010, Vol 160, Num 6, pp 1163-1169, issn 0002-8703, 7 p.Article

Genome-wide association studies identify loci associated with age at menarche and age at natural menopauseCHUNYAN HE; KRAFT, Peter; CHEN, Constance et al.Nature genetics. 2009, Vol 41, Num 6, pp 724-728, issn 1061-4036, 5 p.Article

Genome-wide meta-analysis of observational studies shows common genetic variants associated with macronutrient intakeTANAKA, Toshiko; NGWA, Julius S; MIKKILÄ, Vera et al.The American journal of clinical nutrition. 2013, Vol 97, Num 6, pp 1395-1402, issn 0002-9165, 8 p.Article

Pharmacogenetic Determinants of Statin-Induced Reductions in C-Reactive ProteinCHU, Audrey Y; GUILIANINI, Franco; BARRATT, Bryan J et al.Circulation. Cardiovascular genetics (Print). 2012, Vol 5, Num 1, pp 58-65, issn 1942-325X, 8 p.Article

A large-scale candidate gene association study of age at menarche and age at natural menopauseCHUNYAN HE; KRAFT, Peter; CHASMAN, Daniel I et al.Human genetics. 2010, Vol 128, Num 5, pp 515-527, issn 0340-6717, 13 p.Article

Cardiovascular Disease Risk Prediction With and Without Knowledge of Genetic Variation at Chromosome 9p21.3PAYNTER, Nina P; CHASMAN, Daniel I; BURING, Julie E et al.Annals of internal medicine. 2009, Vol 150, Num 2, issn 0003-4819, 65-72, 139-141 [11 p.]Article

Population Analysis of Large Copy Number Variants and Hotspots of Human Genetic DiseaseITSARA, Andy; COOPER, Gregory M; MEFFORD, Heather et al.American journal of human genetics. 2009, Vol 84, Num 2, pp 148-161, issn 0002-9297, 14 p.Article

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