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Intercellular Adhesion Molecule 1 (ICAM1) Lys56Met and Gly241Arg Gene Variants, Plasma-Soluble ICAM1 Concentrations, and Risk of Incident Cardiovascular Events in 23 014 Initially Healthy White WomenZEE, Robert Y. L; CHENG, Suzanne; ERLICH, Henry A et al.Stroke (1970). 2007, Vol 38, Num 12, pp 3152-3157, issn 0039-2499, 6 p.Article

Association of phosphodiesterase 4D polymorphisms with ischemic stroke in a US population stratified by hypertension statusBROPHY, Victoria H; RO, Sunhee K; ERLICH, Henry A et al.Stroke (1970). 2006, Vol 37, Num 6, pp 1385-1390, issn 0039-2499, 6 p.Article

Susceptibility to type 1 diabetes is associated with ApoCIII gene haplotypesHOKANSON, John E; KINNEY, Gregory L; CHENG, Suzanne et al.Diabetes (New York, NY). 2006, Vol 55, Num 3, pp 834-838, issn 0012-1797, 5 p.Article

Effect of hepatic lipase -514C→T polymorphism and its interactions with apolipoprotein C3 -482C→T and apolipoprotein E exon 4 polymorphisms on the risk of nephropathy in chinese type 2 diabetic patientsBAUM, Larry; NG, Maggie C. Y; SO, Wing-Yee et al.Diabetes care. 2005, Vol 28, Num 7, pp 1704-1709, issn 0149-5992, 6 p.Article

Unique lipoprotein phenotype and genotype associated with exceptional longevityBARZILAI, Nir; ATZMON, Gil; SCHECHTER, Clyde et al.JAMA, the journal of the American Medical Association. 2003, Vol 290, Num 15, pp 2030-2040, issn 0098-7484, 11 p.Article

Use of a modeling framework to evaluate the effect of a modifier gene (MBL2) on variation in cystic fibrosisMCDOUGAL, Kathryn E; GREEN, Deanna M; CUTTING, Garry R et al.European journal of human genetics. 2010, Vol 18, Num 6, pp 680-684, issn 1018-4813, 5 p.Article

Polymorphism in the β₂-adrenergic receptor and lipoprotein lipase genes as risk determinants for idiopathic venous thromboembolism a multilocus, population-based, prospective genetic analysisZEE, Robert Y. L; COOK, Nancy R; CHENG, Suzanne et al.Circulation (New York, N.Y.). 2006, Vol 113, Num 18, pp 2193-2200, issn 0009-7322, 8 p.Article

Risks of human limb deficiency anomalies associated with 29 SNPs of genes involved in homocysteine metabolism, coagulation, cell-cell interactions, inflammatory response, and blood pressure regulationCARMICHAEL, Suzan L; SHAW, Gary M; IOVANNISCI, David M et al.American journal of medical genetics. Part A. 2006, Vol 140, Num 22, pp 2433-2440, issn 1552-4825, 8 p.Article

Impact of αENaC polymorphisms on the risk of ischemic cerebrovascular events : A multicenter case-control studyHSIEH, Kety; LALOUSCHEK, Wolfgang; SCHILLINGER, Martin et al.Clinical chemistry (Baltimore, Md.). 2005, Vol 51, Num 6, pp 952-956, issn 0009-9147, 5 p.Article

Are common disease susceptibility alleles the same in outbred and founder populations?NEWMAN, Dina L; HOFFJAN, Sabine; REYNOLDS, Rebecca et al.European journal of human genetics. 2004, Vol 12, Num 7, pp 584-590, issn 1018-4813, 7 p.Article

Genotypes and haplotypes predisposing to myocardial infarction: a multi locus case-control studyTOBIN, Martin D; BRAUND, Peter S; BURTON, Paul R et al.European heart journal. 2004, Vol 25, Num 6, pp 459-467, issn 0195-668X, 9 p.Article

A common promoter polymorphism in the hepatic lipase gene (LIPC-480C>T) is associated with an increase in coronary calcification in type 1 diabetesHOKANSON, John E; CHENG, Suzanne; SNELL-BERGEON, Janet K et al.Diabetes (New York, NY). 2002, Vol 51, Num 4, pp 1208-1213, issn 0012-1797Article

Confirmation of an association between the TNF(-308) promoter polymorphism and stroke risk in children with sickle cell anemiaHOPPE, Carolyn; KLITZ, William; D'HARLINGUE, Katherine et al.Stroke (1970). 2007, Vol 38, Num 8, pp 2241-2246, issn 0039-2499, 6 p.Article

Homocysteine, 5,10-methylenetetrahydrofolate reductase 677C>T polymorphism, nutrient intake, and incident cardiovascular disease in 24 968 initially healthy womenZEE, Robert Y. L; MORA, Samia; CHENG, Suzanne et al.Clinical chemistry (Baltimore, Md.). 2007, Vol 53, Num 5, pp 845-851, issn 0009-9147, 7 p.Article

Genetic determinants of plasma HDL-cholesterol levels in familial hypercholesterolemiaVAN AALST-COHEN, Emily S; JANSEN, Angelique C. M; BOEKHOLDT, S. Matthijs et al.European journal of human genetics. 2005, Vol 13, Num 10, pp 1137-1142, issn 1018-4813, 6 p.Article

Matched case-control study on factor V Leiden and the prothrombin G20210A mutation in patients with ischemic stroke/transient ischemic attack up to the age of 60 yearsLALOUSCHEK, Wolfgang; SCHILLINGER, Martin; HSIEH, Kety et al.Stroke (1970). 2005, Vol 36, Num 7, pp 1405-1409, issn 0039-2499, 5 p.Article

Genetic determinants of cardiovascular disease risk in familial hypercholesterolemiaJANSEN, Angelique C. M; VAN AALST-COHEN, Emily S; TANCK, Michael W. T et al.Arteriosclerosis, thrombosis, and vascular biology. 2005, Vol 25, Num 7, pp 1475-1481, issn 1079-5642, 7 p.Article

Ethnic differences in the linkage disequilibrium and distribution of single-nucleotide polymorphisms in 35 candidate genes for cardiovascular diseasesNG, Maggie C. Y; YING WANG; SO, Wing-Yee et al.Genomics (San Diego, Calif.). 2004, Vol 83, Num 4, pp 559-565, issn 0888-7543, 7 p.Article

Familial studies on the genetics of cardiovascular diseases : the Stanislas cohortVISVIKIS, Sophie; SASS, Catherine; PALLAUD, Celine et al.Clinical chemistry and laboratory medicine. 2000, Vol 38, Num 9, pp 827-832, issn 1434-6621Conference Paper

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Association of 77 polymorphisms in 52 candidate genes with blood pressure progression and incident hypertension : the Women's Genome Health StudyCONEN, David; CHENG, Suzanne; STEINER, Lori L et al.Journal of hypertension. 2009, Vol 27, Num 3, pp 476-483, issn 0263-6352, 8 p.Article

Polymorphisms in Inflammatory Genes and the Risk of Ischemic Stroke and Transient Ischemic Attack : Results of a Multilocus Genotyping AssayGREISENEGGER, Stefan; ZEHETMAYER, Sonja; MANNHALTER, Christine et al.Clinical chemistry (Baltimore, Md.). 2009, Vol 55, Num 1, pp 134-138, issn 0009-9147, 5 p.Article

Polymorphisms of the renin-angiotensin system genes predict progression of subclinical coronary atherosclerosisKRETOWSKI, Adam; MCFANN, Kim; JIA LI et al.Diabetes (New York, NY). 2007, Vol 56, Num 3, pp 863-871, issn 0012-1797, 9 p.Article

The glu298asp polymorphism in the nitric oxide synthase 3 gene is associated with the risk of ischemic stroke in two large independent case-control studiesBERGER, Klaus; STÖGBAUER, Florian; FUNKE, Harald et al.Human genetics. 2007, Vol 121, Num 2, pp 169-178, issn 0340-6717, 10 p.Article