Antihypertensive Medications: Benefits of BP Lowering and Hazards of Metabolic Effects

Por Karnes, Jason H., Cooper-DeHoff, Rhonda M.
Publicado em 2009

Clinical and Genetic Factors Associated With Cutaneous Squamous Cell Carcinoma in Kidney and Heart Transplant Recipients

Por Sanders, M. Lee, Karnes, Jason H., Denny, Josh C., Roden, Dan M., Ikizler, T. Alp, Birdwell, Kelly A.
Publicado no Transplant Direct (2015)

Factors Influencing Blood Pressure Response to Trandolapril Add-On Therapy in Patients Taking Verapamil SR (from the International Verapamil SR/Trandolapril [INVEST] Study)

Por Brunner, Martin, Cooper-DeHoff, Rhonda M., Gong, Yan, Karnes, Jason H., Langaee, Taimour Y., Pepine, Carl J., Johnson, Julie A.
Publicado em 2007

Using Systems Approaches to Address Challenges for Clinical Implementation of Pharmacogenomics

Por Karnes, Jason H, Van Driest, Sara, Bowton, Erica A, Weeke, Peter E, Mosley, Jonathan D, Peterson, Josh F, Denny, Joshua C, Roden, Dan M
Publicado em 2013

Alteration in Fasting Glucose after Prolonged Treatment with a Thiazide Diuretic

Por Karnes, Jason H, Gong, Yan, Arwood, Meghan J, Gums, John G, Hall, Karen, Limacher, Marian C, Johnson, Julie A, Cooper-DeHoff, Rhonda M
Publicado em 2014

IMPACT OF TCF7L2 SINGLE NUCLEOTIDE POLYMORPHISMS ON HYDROCHLOROTHIAZIDE-INDUCED DIABETES

Por Karnes, Jason H, Gong, Yan, Pacanowski, Michael A, McDonough, Caitrin W, Arwood, Meghan J, Langaee, Taimour Y, Pepine, Carl J, Johnson, Julie A, Cooper-DeHoff, Rhonda M
Publicado em 2013

Comparison of HLA allelic imputation programs

Por Karnes, Jason H., Shaffer, Christian M., Bastarache, Lisa, Gaudieri, Silvana, Glazer, Andrew M., Steiner, Heidi E., Mosley, Jonathan D., Mallal, Simon, Denny, Joshua C., Phillips, Elizabeth J., Roden, Dan M.
Publicado no PLoS One (2017)

Lack of association of the <it>HMGA1</it> IVS5-13insC variant with type 2 diabetes in an ethnically diverse hypertensive case control cohort

Por Karnes Jason H, Langaee Taimour Y, McDonough Caitrin W, Chang Shin-Wen, Ramos Miguel, Catlin Jr James R, Casanova Octavio E, Gong Yan, Pepine Carl J, Johnson Julie A, Cooper-DeHoff Rhonda M
Publicado em 2013-01-01

Lack of association of the HMGA1 IVS5-13insC variant with type 2 diabetes in an ethnically diverse hypertensive case control cohort

Por Karnes, Jason H, Langaee, Taimour Y, McDonough, Caitrin W, Chang, Shin-Wen, Ramos, Miguel, Catlin Jr, James R, Casanova, Octavio E, Gong, Yan, Pepine, Carl J, Johnson, Julie A, Cooper-DeHoff, Rhonda M
Publicado em 2013

PROX1 GENE VARIANT IS ASSOCIATED WITH FASTING GLUCOSE CHANGE AFTER ANTIHYPERTENSIVE TREATMENT

Por Gong, Yan, McDonough, Caitrin W, Beitelshees, Amber L, Karnes, Jason H, O’Connell, Jeffrey R., Turner, Stephen T, Chapman, Arlene B, Gums, John G, Bailey, Kent R, Boerwinkle, Eric, Johnson, Julie A, Cooper-DeHoff, Rhonda M
Publicado em 2013

Identifying genetically driven clinical phenotypes using linear mixed models

Por Mosley, Jonathan D., Witte, John S., Larkin, Emma K., Bastarache, Lisa, Shaffer, Christian M., Karnes, Jason H., Stein, C. Michael, Phillips, Elizabeth, Hebbring, Scott J., Brilliant, Murray H., Mayer, John, Ye, Zhan, Roden, Dan M., Denny, Joshua C.
Publicado no Nat Commun (2016)

Biobanks and Electronic Medical Records: Enabling Cost-Effective Research

Por Bowton, Erica, Field, Julie R., Wang, Sunny, Schildcrout, Jonathan S., Van Driest, Sara L., Delaney, Jessica T., Cowan, James, Weeke, Peter, Mosley, Jonathan D., Wells, Quinn S., Karnes, Jason H., Shaffer, Christian, Peterson, Josh F., Denny, Joshua C., Roden, Dan M., Pulley, Jill M.
Publicado no Sci Transl Med (2014)

Phenome-wide scanning identifies multiple diseases and disease severity phenotypes associated with HLA variants

Por Karnes, Jason H, Bastarache, Lisa, Shaffer, Christian M, Gaudieri, Silvana, Xu, Yaomin, Glazer, Andrew, Mosley, Jonathan D, Zhao, Shilin, Raychaudhuri, Soumya, Mallal, Simon, Ye, Zhan, Mayer, John G, Brilliant, Murray H, Hebbring, Scott J, Roden, Dan M, Phillips, Elizabeth J, Denny, Joshua C
Publicado no Sci Transl Med (2017)

Exome Sequencing Implicates an Increased Burden of Rare Potassium Channel Variants in the Risk of Drug Induced Long QT Syndrome

Por Weeke, Peter, Mosley, Jonathan D., Hanna, David, Delaney, Jessica T., Shaffer, Christian, Wells, Quinn S., Van Driest, Sara, Karnes, Jason H., Ingram, Christie, Guo, Yan, Shyr, Yu, Norris, Kris, Kannankeril, Prince J., Ramirez, Andrea H., Smith, Joshua D., Mardis, Elaine R., Nickerson, Deborah, George, Alfred L., Roden, Dan M.
Publicado em 2014

A genome-wide association study of heparin-induced thrombocytopenia using an electronic medical record

Por Karnes, Jason H, Cronin, Robert M, Rollin, Jerome, Teumer, Alexander, Pouplard, Claire, Shaffer, Christian M, Blanquicett, Carmelo, Bowton, Erica A, Cowan, James D, Mosley, Jonathan D, Van Driest, Sara L, Weeke, Peter E, Wells, Quinn S, Bakchoul, Tamam, Denny, Joshua C, Greinacher, Andreas, Gruel, Yves, Roden, Dan M
Publicado no Thromb Haemost (2014)

Mechanistic Phenotypes: An Aggregative Phenotyping Strategy to Identify Disease Mechanisms Using GWAS Data

Por Mosley, Jonathan D., Van Driest, Sara L., Larkin, Emma K., Weeke, Peter E., Witte, John S., Wells, Quinn S., Karnes, Jason H., Guo, Yan, Bastarache, Lisa, Olson, Lana M., McCarty, Catherine A., Pacheco, Jennifer A., Jarvik, Gail P., Carrell, David S., Larson, Eric B., Crosslin, David R., Kullo, Iftikhar J., Tromp, Gerard, Kuivaniemi, Helena, Carey, David J., Ritchie, Marylyn D., Denny, Josh C., Roden, Dan M.
Publicado em 2013

Genome-wide association and pathway analysis of left ventricular function after anthracycline exposure in adults

Por Wells, Quinn S., Veatch, Olivia J., Fessel, Joshua P., Joon, Aron Y., Levinson, Rebecca T., Mosley, Jonathan D., Held, Elizabeth P., Lindsay, Chase S., Shaffer, Christian M., Weeke, Peter E., Glazer, Andrew M., Bersell, Kevin R., Van Driest, Sara L., Karnes, Jason H., Blair, Marcia A., Lagrone, Lore W., Su, Yan R., Bowton, Erica A., Feng, Ziding, Ky, Bonnie, Lenihan, Daniel J., Fisch, Michael J., Denny, Joshua C., Roden, Dan M.
Publicado no Pharmacogenet Genomics (2017)