检索结果 - Taylor, Kent D.

Variants in the HMG-CoA Reductase (HMGCR) Gene Influence Component Phenotypes in Polycystic Ovary Syndrome 由 Xu, Ning, Taylor, Kent D., Azziz, Ricardo, Goodarzi, Mark O.

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Linkage analysis of high-density SNPs confirms keratoconus locus at 5q chromosomal region 由 Bykhovskaya, Yelena, Li, Xiaohui, Taylor, Kent D., Haritunians, Talin, Rotter, Jerome I., Rabinowitz, Yaron S.

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Association of Androgen Receptor CAG Repeat Polymorphism and Polycystic Ovary Syndrome 由 Shah, Nissar A., Antoine, Heath J., Pall, Marita, Taylor, Kent D., Azziz, Ricardo, Goodarzi, Mark O.

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High Frequency Haplotypes in the X Chromosome Locus TLR8 are Associated with Both CD and UC in Females 由 Saruta, Masayuki, Targan, Stephan R., Mei, Ling, Ippoliti, Andrew F., Taylor, Kent D., Rotter, Jerome I.

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Association of the Kir6.2 E23K Variant with Reduced Acute Insulin Response in African-Americans 由 Palmer, Nicholette D., Langefeld, Carl D., Bryer-Ash, Michael, Rotter, Jerome I., Taylor, Kent D., Bowden, Donald W.

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A Genome-Wide Association Study of Vertical Cup-Disc Ratio in a Latino Population 由 Nannini, Drew R., Torres, Mina, Chen, Yii-Der I., Taylor, Kent D., Rotter, Jerome I., Varma, Rohit, Gao, Xiaoyi

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Deleterious Effect of Butyrylcholinesterase K-variant in donepezil treatment of mild cognitive impairment 由 Sokolow, Sophie, Li, Xiaohui, Chen, Lucia, Taylor, Kent D., Rotter, Jerome I., Rissman, Robert A., Aisen, Paul S., Apostolova, Liana G.

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IL23R Haplotypes Provide A Large Population Attributable Risk for Crohn’s Disease 由 Taylor, Kent D., Targan, Stephan R., Mei, Ling, Ippoliti, Andrew F., McGovern, Dermot, Mengesha, Emebet, King, Lily, Rotter, Jerome I.

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A Multinomial Ordinal Probit Model with Singular Value Decomposition Method for a Multinomial Trait 由 Kwon, Soonil, Goodarzi, Mark O., Taylor, Kent D., Cui, Jinrui, Chen, Y.-D. Ida, Rotter, Jerome I., Hsueh, Willa, Guo, Xiuqing

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Native American Ancestry Is Associated With Severe Diabetic Retinopathy in Latinos 由 Gao, Xiaoyi, Gauderman, W. James, Marjoram, Paul, Torres, Mina, Chen, Yii-Der I., Taylor, Kent D., Rotter, Jerome I., Varma, Rohit

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A novel method for testing association of multiple genetic markers with a multinomial trait 由 Kwon, Soonil, Goodarzi, Mark O., Taylor, Kent D., Cui, Jinrui, Chen, Y-D. Ida, Rotter, Jerome I., Hsueh, Willa, Guo, Xiuqing

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Improved imputation accuracy in Hispanic/Latino populations with larger and more diverse reference panels: applications in the Hispanic Community Health Study/Study of Latinos (HCH... 由 Nelson, Sarah C., Stilp, Adrienne M., Papanicolaou, George J., Taylor, Kent D., Rotter, Jerome I., Thornton, Timothy A., Laurie, Cathy C.

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The HMG-CoA reductase gene and lipid and lipoprotein levels: the Multi-Ethnic Study of Atherosclerosis 由 Chen, Yi-Chun, Chen, Yii-Der I., Li, Xiaohui, Post, Wendy, Herrington, David, Polak, Joseph F., Rotter, Jerome I., Taylor, Kent D.

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Genotype Imputation for Latinos Using the HapMap and 1000 Genomes Project Reference Panels 由 Gao, Xiaoyi, Haritunians, Talin, Marjoram, Paul, Mckean-Cowdin, Roberta, Torres, Mina, Taylor, Kent D., Rotter, Jerome I., Gauderman, William J., Varma, Rohit

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Associations of Candidate Genes to Age-related Macular Degeneration Among Racial/Ethnic Groups in the Multi-Ethnic Study of Atherosclerosis 由 Klein, Ronald, Li, Xiaohui, Kuo, Jane Z., Klein, Barbara E. K., Cotch, Mary Frances, Wong, Tien Y., Taylor, Kent D., Rotter, Jerome I.

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A genome-wide association study identifies a potential novel gene locus for keratoconus, one of the commonest causes for corneal transplantation in developed countries 由 Li, Xiaohui, Bykhovskaya, Yelena, Haritunians, Talin, Siscovick, David, Aldave, Anthony, Szczotka-Flynn, Loretta, Iyengar, Sudha K., Rotter, Jerome I., Taylor, Kent D., Rabinowitz, Yaron S.

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Associations of SNPs in ADIPOQ and subclinical cardiovascular disease in the Multi-Ethnic Study of Atherosclerosis (MESA) 由 Wassel, Christina L., Pankow, James S., Rasmussen-Torvik, Laura J., Li, Na, Taylor, Kent D., Guo, Xiuqing, Goodarzi, Mark O., Palmas, Walter R., Post, Wendy S.

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Individual and combined associations of genetic variants in CYP3A4, CYP3A5, and SLCO1B1 with simvastatin and simvastatin acid plasma concentrations 由 Luzum, Jasmine A., Theusch, Elizabeth, Taylor, Kent D., Wang, Ann, Sadee, Wolfgang, Binkley, Philip F., Krauss, Ronald M., Medina, Marisa W., Kitzmiller, Joseph P.

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Systems Genetics Reveals the Functional Context of PCOS Loci and Identifies Genetic and Molecular Mechanisms of Disease Heterogeneity 由 Jones, Michelle R., Brower, Meredith A., Xu, Ning, Cui, Jinrui, Mengesha, Emebet, Chen, Yii-Der I., Taylor, Kent D., Azziz, Ricardo, Goodarzi, Mark O.

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A Coronary Heart Disease (CHD) Genetic Risk Score (GRS) Predicts Cardiovascular Disease Risk in Men, Not Women: The Multi-Ethnic Study of Atherosclerosis 由 Hajek, Catherine, Guo, Xiuqing, Yao, Jie, Hai, Yang, Johnson, Craig, Frazier-Wood, Alexis C., Post, Wendy S., Psaty, Bruce M., Taylor, Kent D., Rotter, Jerome I.

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