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Otolaryngology--Head and Neck Surgery : Official Journal of American Academy of Otolaryngology-Head and Neck Surgery|August 2, 2019
Clinical Practice Guideline: Sudden Hearing Loss (Update)Sujana S Chandrasekhar, Betty S Tsai Do, Seth R Schwartz, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 14, 2013
Stakeholder engagement: a key component of integrating genomic information into electronic health recordsAndrea Hartzler, Catherine A McCarty, Luke V Rasmussen, et al.
Research Square|April 6, 2021
Maternal-Fetal Immune Responses in Pregnant Women Infected with SARS-CoV-2Valeria Garcia-Flores, Roberto Romero, Yi Xu, et al.
Health Affairs (Project Hope)|May 8, 2018
Patient-Centered Precision Health In A Learning Health Care System: Geisinger's Genomic Medicine ExperienceMarc S Williams, Adam H Buchanan, F Daniel Davis, et al.
Nature Communications|January 19, 2022
Maternal-fetal immune responses in pregnant women infected with SARS-CoV-2Valeria Garcia-Flores, Roberto Romero, Yi Xu, et al.
American Journal of Human Genetics|August 14, 2018
A Model for Genome-First Care: Returning Secondary Genomic Findings to Participants and Their Healthcare Providers in a Large Research CohortMarci L B Schwartz, Cara Zayac McCormick, Amanda L Lazzeri, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 8, 2013
The Electronic Medical Records and Genomics (eMERGE) Network: past, present, and futureOmri Gottesman, Helena Kuivaniemi, Gerard Tromp, et al.
Journal of Medical Genetics|October 12, 2012
A 600 kb deletion syndrome at 16p11.2 leads to energy imbalance and neuropsychiatric disordersFlore Zufferey, Elliott H Sherr, Noam D Beckmann, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 21, 2017
Early cancer diagnoses through BRCA1/2 screening of unselected adult biobank participantsAdam H Buchanan, Kandamurugu Manickam, Michelle N Meyer, et al.
American Journal of Human Genetics|May 15, 2010
Consensus statement: chromosomal microarray is a first-tier clinical diagnostic test for individuals with developmental disabilities or congenital anomaliesDavid T Miller, Margaret P Adam, Swaroop Aradhya, et al.
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