Exome-wide evaluation of rare coding variants using electronic health records identifies new gene–phenotype associations

Posted On: January 11, 2021

Exome-wide evaluation of rare coding variants using electronic health records identifies new gene–phenotype associations

Joseph Park, Anastasia M. Lucas, Xinyuan Zhang, Kumardeep Chaudhary, Judy H. Cho, Girish Nadkarni, Amanda Dobbyn, Geetha Chittoor, Navya S. Josyula, Nathan Katz, Joseph H. Breeyear, Shadi Ahmadmehrabi, Theodore G. Drivas, Venkata R. M. Chavali, Maria Fasolino, Hisashi Sawada, Alan Daugherty, Yanming Li, Chen Zhang, Yuki Bradford, JoEllen Weaver, Anurag Verma, Renae L. Judy, Rachel L. Kember, John D. Overton, Jeffrey G. Reid, Manuel A. R. Ferreira, Alexander H. Li, Aris Baras, Scott A. LeMaire, Ying H. Shen, Ali Naji, Klaus H. Kaestner, Golnaz Vahedi, Todd L. Edwards, Jinbo Chen, Scott M. Damrauer, Anne E. Justice, Ron Do, Marylyn D. Ritchie & Daniel J. Rader.

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