Rezultati - Taylor, Kent D.

Variants in the HMG-CoA Reductase (HMGCR) Gene Influence Component Phenotypes in Polycystic Ovary Syndrome od 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 od 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 od 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 od 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 od 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 od 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 od 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 od 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 od 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 od 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 od 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... od 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 od 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 od 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 od 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 od 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) od 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 od 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 od 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 od 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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