Splice Variants of mIAP1 Have an Enhanced Ability to Inhibit Apoptosis

Por Mosley, Jonathan D., Keri, Ruth A.
Publicado em 2006

Cell cycle correlated genes dictate the prognostic power of breast cancer gene lists

Por Mosley, Jonathan D, Keri, Ruth A
Publicado em 2008

Intrinsic bias in breast cancer gene expression data sets

Por Mosley, Jonathan D, Keri, Ruth A
Publicado em 2009

Validation and Enhancement of a Computable Medication Indication Resource (MEDI) Using a Large Practice-based Dataset

Por Wei, Wei-Qi, Mosley, Jonathan D., Bastarache, Lisa, Denny, Joshua C.
Publicado em 2013

Rapamycin Inhibits Multiple Stages of c-Neu/ErbB2-induced Tumor Progression in a Transgenic Mouse Model of HER2 Positive Breast Cancer

Por Mosley, Jonathan D., Poirier, John T., Seachrist, Darcie D., Landis, Melissa D., Keri, Ruth A.
Publicado em 2007

Letter to the Editor, in response to: “Iron Homeostasis and Pulmonary Hypertension: Iron Deficiency Leads to Pulmonary Vascular Remodeling in the Rat”

Por Mosley, Jonathan D., Brittain, Evan L., Loyd, James E., Denny, Joshua C., Austin, Eric D., Larkin, Emma K.
Publicado no Circ Res (2015)

Screening for Acute I(Kr) Block is Insufficient to Detect Torsades de Pointes Liability: Role of Late Sodium Current

Por Yang, Tao, Chun, Young Wook, Stroud, Dina M., Mosley, Jonathan D., Knollmann, Bjorn C., Hong, Charles, Roden, Dan M.
Publicado em 2014

QT variability during initial exposure to sotalol: experience based on a large electronic medical record

Por Weeke, Peter, Delaney, Jessica, Mosley, Jonathan D., Wells, Quinn, Van Driest, Sara, Norris, Kris, Kucera, Gayle, Stubblefield, Tanya, Roden, Dan M.
Publicado em 2013

Integrating EMR-Linked and In Vivo Functional Genetic Data to Identify New Genotype-Phenotype Associations

Por Mosley, Jonathan D., Van Driest, Sara L., Weeke, Peter E., Delaney, Jessica T., Wells, Quinn S., Bastarache, Lisa, Roden, Dan M., Denny, Josh C.
Publicado em 2014

Whole-exome sequencing in familial atrial fibrillation

Por Weeke, Peter, Muhammad, Raafia, Delaney, Jessica T., Shaffer, Christian, Mosley, Jonathan D., Blair, Marcia, Short, Laura, Stubblefield, Tanya, Roden, Dan M., Darbar, Dawood
Publicado em 2014

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

Combined SFK/mTOR inhibition prevents rapamycin-induced feedback activation of AKT and elicits efficient tumor regression

Por Yori, Jennifer L., Lozada, Kristen L., Seachrist, Darcie D., Mosley, Jonathan D., Abdul-Karim, Fadi W., Booth, Christine N., Flask, Chris A., Keri, Ruth A.
Publicado em 2014

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)

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)

FOXA1 is an essential determinant of ERα expression and mammary ductal morphogenesis

Por Bernardo, Gina M., Lozada, Kristen L., Miedler, John D., Harburg, Gwyndolen, Hewitt, Sylvia C., Mosley, Jonathan D., Godwin, Andrew K., Korach, Kenneth S., Visvader, Jane E., Kaestner, Klaus H., Abdul-Karim, Fadi W., Montano, Monica M., Keri, Ruth A.
Publicado em 2010

Whole Exome Sequencing Identifies a Causal RBM20 Mutation in a Large Pedigree with Familial Dilated Cardiomyopathy

Por Wells, Quinn S., Becker, Jason R., Su, Yan R., Mosley, Jonathan D., Weeke, Peter, D'Aoust, Laura, Ausborn, Natalie L., Ramirez, Andrea H., Pfotenhauer, Jean P., Naftilan, Allen J., Markham, Larry, Exil, Vernat, Roden, Dan M., Hong, Charles C.
Publicado em 2013

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)

Genomewide Linkage Analysis of Quantitative Spirometric Phenotypes in Severe Early-Onset Chronic Obstructive Pulmonary Disease

Por Silverman, Edwin K., Palmer, Lyle J., Mosley, Jonathan D., Barth, Matthew, Senter, Jody M., Brown, Alison, Drazen, Jeffrey M., Kwiatkowski, David J., Chapman, Harold A., Campbell, Edward J., Province, Michael A., Rao, D. C., Reilly, John J., Ginns, Leo C., Speizer, Frank E., Weiss, Scott T.
Publicado em 2002

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)