Association of gain-of-function EPHX2 polymorphism Lys55Arg with acute kidney injury following cardiac surgery. by Megan M Shuey, Frederic T Billings, Shouzou Wei, Ginger L Milne, Hui Nian, Chang Yu, Nancy J Brown

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430 Genome-wide meta-analysis identifies novel risk loci for uterine fibroids across multiple ancestry groups by Jeewoo Kim, Ariel Williams, Hannah Noh, Megan M. Shuey, Todd L. Edwards, Digna R. Velez Edwards, Jacklyn N. Hellwege

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Using Mendelian randomisation to identify opportunities for type 2 diabetes prevention by repurposing medications used for lipid management by Nikhil K. Khankari, Jacob M. Keaton, Venexia M. Walker, Kyung Min Lee, Megan M. Shuey, Shoa L. Clarke, Kent R. Heberer, Donald R. Miller, Peter D. Reaven, Julie A. Lynch, Marijana Vujkovic, Todd L. Edwards

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A genetically supported drug repurposing pipeline for diabetes treatment using electronic health recordsResearch in context by Megan M. Shuey, Kyung Min Lee, Jacob Keaton, Nikhil K. Khankari, Joseph H. Breeyear, Venexia M. Walker, Donald R. Miller, Kent R. Heberer, Peter D. Reaven, Shoa L. Clarke, Jennifer Lee, Julie A. Lynch, Marijana Vujkovic, Todd L. Edwards

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Comprehensive association analysis of speech recognition thresholds after cisplatin‐based chemotherapy in survivors of adult‐onset cancer by Mohammad Shahbazi, Xindi Zhang, Paul C. Dinh, Victoria A. Sanchez, Matthew R. Trendowski, Megan M. Shuey, Tessa Nguyen, Regeneron Genetics Center, Darren R. Feldman, David J. Vaughn, Chunkit Fung, Christian Kollmannsberger, Neil E. Martin, Lawrence H. Einhorn, Nancy J. Cox, Robert D. Frisina, Lois B. Travis, Mary Eileen Dolan

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Pharmacogenomics of cisplatin‐induced neurotoxicities: Hearing loss, tinnitus, and peripheral sensory neuropathy by Xindi Zhang, Matthew R. Trendowski, Emma Wilkinson, Mohammad Shahbazi, Paul C. Dinh, Megan M. Shuey, Regeneron Genetics Center, Darren R. Feldman, Robert J. Hamilton, David J. Vaughn, Chunkit Fung, Christian Kollmannsberger, Robert Huddart, Neil E. Martin, Victoria A. Sanchez, Robert D. Frisina, Lawrence H. Einhorn, Nancy J. Cox, Lois B. Travis, M. Eileen Dolan

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Genome-wide meta-analysis identifies novel risk loci for uterine fibroids within and across multiple ancestry groups by Jeewoo Kim, Ariel Williams, Hannah Noh, Elizabeth A. Jasper, Sarah H. Jones, James A. Jaworski, Megan M. Shuey, Edward A. Ruiz-Narváez, Lauren A. Wise, Julie R. Palmer, John Connolly, Jacob M. Keaton, Joshua C. Denny, Atlas Khan, Mohammad A. Abbass, Laura J. Rasmussen-Torvik, Leah C. Kottyan, Purnima Madhivanan, Karl Krupp, Wei-Qi Wei, Todd L. Edwards, Digna R. Velez Edwards, Jacklyn N. Hellwege

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Whole genome sequence analysis of apparent treatment resistant hypertension status in participants from the Trans-Omics for Precision Medicine program by Nicole D. Armstrong, Vinodh Srinivasasainagendra, Farah Ammous, Farah Ammous, Themistocles L. Assimes, Amber L. Beitelshees, Jennifer Brody, Brian E. Cade, Yii-Der Ida Chen, Han Chen, Han Chen, Paul S. de Vries, James S. Floyd, James S. Floyd, Nora Franceschini, Xiuqing Guo, Jacklyn N. Hellwege, Jacklyn N. Hellwege, John S. House, Chii-Min Hwu, Sharon L. R. Kardia, Ethan M. Lange, Leslie A. Lange, Caitrin W. McDonough, May E. Montasser, Jeffrey R. O’Connell, Megan M. Shuey, Megan M. Shuey, Xiao Sun, Rikki M. Tanner, Zhe Wang, Wei Zhao, Wei Zhao, April P. Carson, Todd L. Edwards, Todd L. Edwards, Tanika N. Kelly, Eimear E. Kenny, Charles Kooperberg, Ruth J. F. Loos, Alanna C. Morrison, Alison Motsinger-Reif, Bruce M. Psaty, Bruce M. Psaty, Bruce M. Psaty, Dabeeru C. Rao, Susan Redline, Stephen S. Rich, Jerome I. Rotter, Jennifer A. Smith, Jennifer A. Smith, Albert V. Smith, Marguerite R. Irvin, Donna K. Arnett

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