Haploinsufficiency and triploinsensitivity of the same 6p25.1p24.3 region in a family

por Qi, Zhongxia, Jeng, Linda Jo Bone, Slavotinek, Anne, Yu, Jingwei
Publicado 2015

Challenges and disparities in the application of personalized genomic medicine to populations with African ancestry

por Kessler, Michael D., Yerges-Armstrong, Laura, Taub, Margaret A., Shetty, Amol C., Maloney, Kristin, Jeng, Linda Jo Bone, Ruczinski, Ingo, Levin, Albert M., Williams, L. Keoki, Beaty, Terri H., Mathias, Rasika A., Barnes, Kathleen C., O'Connor, Timothy D.
Publicado 2016

Human Disease Ontology 2018 update: classification, content and workflow expansion

por Schriml, Lynn M, Mitraka, Elvira, Munro, James, Tauber, Becky, Schor, Mike, Nickle, Lance, Felix, Victor, Jeng, Linda, Bearer, Cynthia, Lichenstein, Richard, Bisordi, Katharine, Campion, Nicole, Hyman, Brooke, Kurland, David, Oates, Connor Patrick, Kibbey, Siobhan, Sreekumar, Poorna, Le, Chris, Giglio, Michelle, Greene, Carol
Publicado 2019

KCNQ1 and Long QT Syndrome in 1/45 Amish: The Road From Identification to Implementation of Culturally Appropriate Precision Medicine

por Streeten, Elizabeth A., See, Vincent Y., Jeng, Linda B.J., Maloney, Kristin A., Lynch, Megan, Glazer, Andrew M., Yang, Tao, Roden, Dan, Pollin, Toni I., Daue, Melanie, Ryan, Kathleen A., Van Hout, Cristopher, Gosalia, Nehal, Gonzaga-Jauregui, Claudia, Economides, Aris, Perry, James A., O’Connell, Jeffrey, Beitelshees, Amber, Palmer, Kathleen, Mitchell, Braxton D., Shuldiner, Alan R
Publicado 2020