Publication
An RCT of Rapid Genomic Sequencing among Seriously Ill Infants Results in High Clinical Utility, Changes in Management, and Low Perceived Harm
David P. Dimmock, Michelle M. Clark, Mary Gaughran, Julie A. Cakici, Sara A. Caylor, Christina Clarke, Michele Feddock, Shimul Chowdhury, Lisa Salz, Cynthia Cheung, Lynne M. Bird, Charlotte Hobbs, Kristen Wigby, Lauge Farnaes, Cinnamon S. Bloss, Stephen F. Kingsmore, Matthew N. Bainbridge, Jaime Barea, Sergey Batalov, Zaira Bezares, Lynne M. Bird, Cinnamon S. Bloss, Joshua J.A. Braun, Julie A. Cakici, Miguel Del Campo, Jeanne Carroll, Cynthia Cheung, Casey Cohenmeyer, Nicole G. Coufal, Carlos Diaz, Yan Ding, Katarzyna Ellsworth, Marva Evans, Annette Feigenbaum, Jennifer Friedman, Joe Gleeson, Christian Hansen, Jose Honold, Kiely James, Marilyn C. Jones, Amy Kimball, Gail Knight, Lucitia Van Der Kraan, Brian Lane, Jennie Le, Sandra Leibel, Jerica Lenberg, Dana Mashburn, Laurel Moyer, Patrick Mulrooney, Shareef Nahas, Daeheon Oh, Daniken Orendain, Albert Oriol, Maria Ortiz-Arechiga, Lance Prince, Seema Rego, Iris Reyes, Erica Sanford, Charles Sauer, Leila Schwanemann, Mark Speziale, Denise Suttner, Nathaly Sweeney, Richard Song, Mari Tokita, Narayanan Veeraraghavan, Kelly Watkins, Terence Wong, Meredith S. Wright, Catherine Yamada
The American Journal of Human Genetics, November 2020, Elsevier
DOI: 10.1016/j.ajhg.2020.10.003