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

Por Xu, Ning, Taylor, Kent D., Azziz, Ricardo, Goodarzi, Mark O.
Publicado em 2009

Linkage analysis of high-density SNPs confirms keratoconus locus at 5q chromosomal region

Por Bykhovskaya, Yelena, Li, Xiaohui, Taylor, Kent D., Haritunians, Talin, Rotter, Jerome I., Rabinowitz, Yaron S.
Publicado em 2014

Association of Androgen Receptor CAG Repeat Polymorphism and Polycystic Ovary Syndrome

Por Shah, Nissar A., Antoine, Heath J., Pall, Marita, Taylor, Kent D., Azziz, Ricardo, Goodarzi, Mark O.
Publicado em 2008

High Frequency Haplotypes in the X Chromosome Locus TLR8 are Associated with Both CD and UC in Females

Por Saruta, Masayuki, Targan, Stephan R., Mei, Ling, Ippoliti, Andrew F., Taylor, Kent D., Rotter, Jerome I.
Publicado em 2009

Association of the Kir6.2 E23K Variant with Reduced Acute Insulin Response in African-Americans

Por Palmer, Nicholette D., Langefeld, Carl D., Bryer-Ash, Michael, Rotter, Jerome I., Taylor, Kent D., Bowden, Donald W.
Publicado em 2008

African ancestry is associated with higher intraocular pressure in Latinos

Por Nannini, Drew, Torres, Mina, Chen, Yii-Der I., Taylor, Kent D., Rotter, Jerome I., Varma, Rohit, Gao, Xiaoyi
Publicado no Ophthalmology (2015)

A Genome-Wide Association Study of Vertical Cup-Disc Ratio in a Latino Population

Por Nannini, Drew R., Torres, Mina, Chen, Yii-Der I., Taylor, Kent D., Rotter, Jerome I., Varma, Rohit, Gao, Xiaoyi
Publicado no Invest Ophthalmol Vis Sci (2017)

Deleterious Effect of Butyrylcholinesterase K-variant in donepezil treatment of mild cognitive impairment

Por Sokolow, Sophie, Li, Xiaohui, Chen, Lucia, Taylor, Kent D., Rotter, Jerome I., Rissman, Robert A., Aisen, Paul S., Apostolova, Liana G.
Publicado no J Alzheimers Dis (2017)

IL23R Haplotypes Provide A Large Population Attributable Risk for Crohn’s Disease

Por Taylor, Kent D., Targan, Stephan R., Mei, Ling, Ippoliti, Andrew F., McGovern, Dermot, Mengesha, Emebet, King, Lily, Rotter, Jerome I.
Publicado em 2008

A Multinomial Ordinal Probit Model with Singular Value Decomposition Method for a Multinomial Trait

Por Kwon, Soonil, Goodarzi, Mark O., Taylor, Kent D., Cui, Jinrui, Chen, Y.-D. Ida, Rotter, Jerome I., Hsueh, Willa, Guo, Xiuqing
Publicado em 2012

Native American Ancestry Is Associated With Severe Diabetic Retinopathy in Latinos

Por Gao, Xiaoyi, Gauderman, W. James, Marjoram, Paul, Torres, Mina, Chen, Yii-Der I., Taylor, Kent D., Rotter, Jerome I., Varma, Rohit
Publicado em 2014

A novel method for testing association of multiple genetic markers with a multinomial trait

Por Kwon, Soonil, Goodarzi, Mark O., Taylor, Kent D., Cui, Jinrui, Chen, Y-D. Ida, Rotter, Jerome I., Hsueh, Willa, Guo, Xiuqing
Publicado no Proc Am Stat Assoc (2010)

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...

Por Nelson, Sarah C., Stilp, Adrienne M., Papanicolaou, George J., Taylor, Kent D., Rotter, Jerome I., Thornton, Timothy A., Laurie, Cathy C.
Publicado no Hum Mol Genet (2016)

The HMG-CoA reductase gene and lipid and lipoprotein levels: the Multi-Ethnic Study of Atherosclerosis

Por Chen, Yi-Chun, Chen, Yii-Der I., Li, Xiaohui, Post, Wendy, Herrington, David, Polak, Joseph F., Rotter, Jerome I., Taylor, Kent D.
Publicado em 2009

Genotype Imputation for Latinos Using the HapMap and 1000 Genomes Project Reference Panels

Por Gao, Xiaoyi, Haritunians, Talin, Marjoram, Paul, Mckean-Cowdin, Roberta, Torres, Mina, Taylor, Kent D., Rotter, Jerome I., Gauderman, William J., Varma, Rohit
Publicado em 2012

Associations of Candidate Genes to Age-related Macular Degeneration Among Racial/Ethnic Groups in the Multi-Ethnic Study of Atherosclerosis

Por Klein, Ronald, Li, Xiaohui, Kuo, Jane Z., Klein, Barbara E. K., Cotch, Mary Frances, Wong, Tien Y., Taylor, Kent D., Rotter, Jerome I.
Publicado em 2013

A genome-wide association study identifies a potential novel gene locus for keratoconus, one of the commonest causes for corneal transplantation in developed countries

Por 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.
Publicado em 2012

Associations of SNPs in ADIPOQ and subclinical cardiovascular disease in the Multi-Ethnic Study of Atherosclerosis (MESA)

Por 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.
Publicado em 2010

Individual and combined associations of genetic variants in CYP3A4, CYP3A5, and SLCO1B1 with simvastatin and simvastatin acid plasma concentrations

Por Luzum, Jasmine A., Theusch, Elizabeth, Taylor, Kent D., Wang, Ann, Sadee, Wolfgang, Binkley, Philip F., Krauss, Ronald M., Medina, Marisa W., Kitzmiller, Joseph P.
Publicado no J Cardiovasc Pharmacol (2015)

Systems Genetics Reveals the Functional Context of PCOS Loci and Identifies Genetic and Molecular Mechanisms of Disease Heterogeneity

Por Jones, Michelle R., Brower, Meredith A., Xu, Ning, Cui, Jinrui, Mengesha, Emebet, Chen, Yii-Der I., Taylor, Kent D., Azziz, Ricardo, Goodarzi, Mark O.
Publicado no PLoS Genet (2015)