Modulators of normal ECG intervals identified in a large electronic medical record

Por Ramirez, Andrea H, Schildcrout, Jonathan S, Blakemore, Dana L, Masys, Dan R, Pulley, Jill M, Basford, Melissa A, Roden, Dan M, Denny, Joshua C
Publicado em 2010

Genetic Determinants of Variability in Warfarin Response after the Dose-Titration Phase

Por Iwuchukwu, Otito F, Ramirez, Andrea H, Shi, Yaping, Bowton, Erica A, Kawai, Vivian K, Schildcrout, Jonathan S, Roden, Dan M, Denny, Joshua C, Stein, C. Michael
Publicado no Pharmacogenet Genomics (2016)

Novel Rare Variants in Congenital Cardiac Arrhythmia Genes are Frequent in Drug-induced Torsades de Pointes

Por Ramirez, Andrea H., Shaffer, Christian M., Delaney, Jessica T., Sexton, David P., Levy, Shawn E., Rieder, Mark J., Nickerson, Deborah A., George, Alfred L., Roden, Dan M.
Publicado em 2012

Identification of Genomic Predictors of Atrioventricular Conduction: Using Electronic Medical Records as a Tool for Genome Science

Por Denny, Joshua C., Ritchie, Marylyn D., Crawford, Dana C., Schildcrout, Jonathan S., Ramirez, Andrea H., Pulley, Jill M., Basford, Melissa A., Masys, Daniel R., Haines, Jonathan L., Roden, Dan M.
Publicado em 2010

Robust Replication of Genotype-Phenotype Associations across Multiple Diseases in an Electronic Medical Record

Por Ritchie, Marylyn D., Denny, Joshua C., Crawford, Dana C., Ramirez, Andrea H., Weiner, Justin B., Pulley, Jill M., Basford, Melissa A., Brown-Gentry, Kristin, Balser, Jeffrey R., Masys, Daniel R., Haines, Jonathan L., Roden, Dan M.
Publicado em 2010

Robust Replication of Genotype-Phenotype Associations across Multiple Diseases in an Electronic Medical Record

Por Ritchie, Marylyn D., Denny, Joshua C., Crawford, Dana C., Ramirez, Andrea H., Weiner, Justin B., Pulley, Jill M., Basford, Melissa A., Brown-Gentry, Kristin, Balser, Jeffrey R., Masys, Daniel R., Haines, Jonathan L., Roden, Dan M.
Publicado em 2010

The effect of novel promoter variants in MATE1 and MATE2 on the pharmacokinetics and pharmacodynamics of metformin

Por Stocker, Sophie L., Morrissey, Kari M., Yee, Sook Wah, Castro, Richard A., Xu, Lu, Dahlin, Amber, Ramirez, Andrea H., Roden, Dan M., Wilke, Russ A., McCarty, Cathy A., Davis, Robert L., Brett, Claire M., Giacomini, Kathleen M.
Publicado em 2012

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

Facilitating pharmacogenetic studies using electronic health records and natural-language processing: a case study of warfarin

Por Xu, Hua, Jiang, Min, Oetjens, Matt, Bowton, Erica A, Ramirez, Andrea H, Jeff, Janina M, Basford, Melissa A, Pulley, Jill M, Cowan, James D, Wang, Xiaoming, Ritchie, Marylyn D, Masys, Daniel R, Roden, Dan M, Crawford, Dana C, Denny, Joshua C
Publicado em 2011

Generalization of Variants Identified by Genome-wide Association Studies for Electrocardiographic Traits in African Americans

Por Jeff, Janina M., Ritchie, Marylyn D., Denny, Joshua C., Kho, Abel N., Ramirez, Andrea H., Crosslin, David, Armstrong, Loren, Basford, Melissa A., Wolf, Wendy A., Pacheco, Jennifer A., Chisholm, Rex L., Roden, Dan M., Hayes, M. Geoffrey, Crawford, Dana C.
Publicado em 2013

Optimizing drug outcomes through pharmacogenetics: A case for preemptive genotyping

Por Schildcrout, Jonathan S., Denny, Joshua C., Bowton, Erica, Gregg, William, Pulley, Jill M., Basford, Melissa A., Cowan, James D., Xu, Hua, Ramirez, Andrea H., Crawford, Dana C., Ritchie, Marylyn D., Peterson, Josh F., Masys, Daniel R., Wilke, Russell A., Roden, Dan M.
Publicado em 2012

Predicting warfarin dosage in European–Americans and African–Americans using DNA samples linked to an electronic health record

Por Ramirez, Andrea H, Shi, Yaping, Schildcrout, Jonathan S, Delaney, Jessica T, Xu, Hua, Oetjens, Matthew T, Zuvich, Rebecca L, Basford, Melissa A, Bowton, Erica, Jiang, Min, Speltz, Peter, Zink, Raquel, Cowan, James, Pulley, Jill M, Ritchie, Marylyn D, Masys, Daniel R, Roden, Dan M, Crawford, Dana C, Denny, Joshua C
Publicado em 2012

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

Operational implementation of prospective genotyping for personalized medicine: The design of the Vanderbilt PREDICT project

Por Pulley, Jill M., Denny, Joshua C., Peterson, Josh F., Bernard, Gordon R., Vnencak-Jones, Cindy L., Ramirez, Andrea H., Delaney, Jessica T., Bowton, Erica, Brothers, Kyle, Johnson, Kevin, Crawford, Dana C., Schildcrout, Jonathan, Masys, Daniel R., Dilks, Holli H., Russell, Wilke A., Clayton, Ellen Wright, Shultz, Ed, Laposata, Michael, McPherson, John, Jirjis, Jim N., Roden, Dan M.
Publicado em 2012

Electronic medical records and genomics (eMERGE) network exploration in cataract: Several new potential susceptibility loci

Por Ritchie, Marylyn D., Verma, Shefali S., Hall, Molly A., Goodloe, Robert J., Berg, Richard L., Carrell, Dave S., Carlson, Christopher S., Chen, Lin, Crosslin, David R., Denny, Joshua C., Jarvik, Gail, Li, Rongling, Linneman, James G., Pathak, Jyoti, Peissig, Peggy, Rasmussen, Luke V., Ramirez, Andrea H., Wang, Xiaoming, Wilke, Russell A., Wolf, Wendy A., Torstenson, Eric S., Turner, Stephen D., McCarty, Catherine A.
Publicado em 2014

Genome- and Phenome-Wide Analysis of Cardiac Conduction Identifies Markers of Arrhythmia Risk

Por Ritchie, Marylyn D., Denny, Joshua C., Zuvich, Rebecca L., Crawford, Dana C., Schildcrout, Jonathan S., Bastarache, Lisa, Ramirez, Andrea H., Mosley, Jonathan D., Pulley, Jill M., Basford, Melissa A., Bradford, Yuki, Rasmussen, Luke V., Pathak, Jyotishman, Chute, Christopher G., Kullo, Iftikhar J., McCarty, Catherine A., Chisholm, Rex L., Kho, Abel N., Carlson, Christopher S., Larson, Eric B., Jarvik, Gail P., Sotoodehnia, Nona, Manolio, Teri A., Li, Rongling, Masys, Daniel R., Haines, Jonathan L., Roden, Dan M.
Publicado em 2013

Variants Near FOXE1 Are Associated with Hypothyroidism and Other Thyroid Conditions: Using Electronic Medical Records for Genome- and Phenome-wide Studies

Por Denny, Joshua C., Crawford, Dana C., Ritchie, Marylyn D., Bielinski, Suzette J., Basford, Melissa A., Bradford, Yuki, Chai, High Seng, Bastarache, Lisa, Zuvich, Rebecca, Peissig, Peggy, Carrell, David, Ramirez, Andrea H., Pathak, Jyotishman, Wilke, Russell A., Rasmussen, Luke, Wang, Xiaoming, Pacheco, Jennifer A., Kho, Abel N., Hayes, M. Geoffrey, Weston, Noah, Matsumoto, Martha, Kopp, Peter A., Newton, Katherine M., Jarvik, Gail P., Li, Rongling, Manolio, Teri A., Kullo, Iftikhar J., Chute, Christopher G., Chisholm, Rex L., Larson, Eric B., McCarty, Catherine A., Masys, Daniel R., Roden, Dan M., de Andrade, Mariza
Publicado em 2011

Systematic comparison of phenome-wide association study of electronic medical record data and genome-wide association study data

Por Denny, Joshua C, Bastarache, Lisa, Ritchie, Marylyn D, Carroll, Robert J, Zink, Raquel, Mosley, Jonathan D, Field, Julie R, Pulley, Jill M, Ramirez, Andrea H, Bowton, Erica, Basford, Melissa A, Carrell, David S, Peissig, Peggy L, Kho, Abel N, Pacheco, Jennifer A, Rasmussen, Luke V, Crosslin, David R, Crane, Paul K, Pathak, Jyotishman, Bielinski, Suzette J, Pendergrass, Sarah A, Xu, Hua, Hindorff, Lucia A, Li, Rongling, Manolio, Teri A, Chute, Christopher G, Chisholm, Rex L, Larson, Eric B, Jarvik, Gail P, Brilliant, Murray H, McCarty, Catherine A, Kullo, Iftikhar J, Haines, Jonathan L, Crawford, Dana C, Masys, Daniel R, Roden, Dan M
Publicado em 2013

Genome-wide study of resistant hypertension identified from electronic health records

Por Dumitrescu, Logan, Ritchie, Marylyn D., Denny, Joshua C., El Rouby, Nihal M., McDonough, Caitrin W., Bradford, Yuki, Ramirez, Andrea H., Bielinski, Suzette J., Basford, Melissa A., Chai, High Seng, Peissig, Peggy, Carrell, David, Pathak, Jyotishman, Rasmussen, Luke V., Wang, Xiaoming, Pacheco, Jennifer A., Kho, Abel N., Hayes, M. Geoffrey, Matsumoto, Martha, Smith, Maureen E., Li, Rongling, Cooper-DeHoff, Rhonda M., Kullo, Iftikhar J., Chute, Christopher G., Chisholm, Rex L., Jarvik, Gail P., Larson, Eric B., Carey, David, McCarty, Catherine A., Williams, Marc S., Roden, Dan M., Bottinger, Erwin, Johnson, Julie A., de Andrade, Mariza, Crawford, Dana C.
Publicado no PLoS One (2017)