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BMC Pregnancy and Childbirth|May 4, 2018
Adverse obstetric and neonatal outcomes complicated by psychosis among pregnant women in the United StatesQiu-Yue Zhong, Bizu Gelaye, Gregory L Fricchione, et al.The Journal of Pediatrics|February 19, 2020
Identifying Patients at Lowest Risk for Streptococcal Pharyngitis: A National Validation StudyDaniel J Shapiro, Yuval Barak-Corren, Mark I Neuman, et al.CMAJ : Canadian Medical Association Journal = Journal De L'Association Medicale Canadienne|September 21, 2011
Effect of expanded US recommendations for seasonal influenza vaccination: comparison of two pediatric emergency departments in the United States and CanadaAnne Gatewood Hoen, David L Buckeridge, Katia M L Charland, et al.Journal of the American Medical Informatics Association : JAMIA|April 27, 2007
A self-scaling, distributed information architecture for public health, research, and clinical careAndrew J McMurry, Clint A Gilbert, Ben Y Reis, et al.AMIA Joint Summits on Translational Science Proceedings. AMIA Joint Summits on Translational Science|December 5, 2013
Development of a scalable pharmacogenomic clinical decision support serviceVincent A Fusaro, Catherine Brownstein, Wendy Wolf, et al.Genome Research|December 8, 2011
Disclosing pathogenic genetic variants to research participants: quantifying an emerging ethical responsibilityChristopher A Cassa, Sarah K Savage, Patrick L Taylor, et al.Scientific Reports|May 23, 2020
Nonlinear Analysis of Visually Normal EEGs to Differentiate Benign Childhood Epilepsy with Centrotemporal Spikes (BECTS)Aarti Sathyanarayana, Rima El Atrache, Michele Jackson, et al.Annals of the American Thoracic Society|December 8, 2016
Accelerating Scientific Advancement for Pediatric Rare Lung Disease Research. Report from a National Institutes of Health-NHLBI Workshop, September 3 and 4, 2015Lisa R Young, Bruce C Trapnell, Kenneth D Mandl, et al.Human Mutation|November 7, 2019
The Clinical Genome and Ancestry Report: An interactive web application for prioritizing clinically implicated variants from genome sequencing data with ancestry compositionIn-Hee Lee, Jose A Negron, Carles Hernandez-Ferrer, et al.Science (New York, N.Y.)|February 3, 2022
How NFTs could transform health information exchangeKristin Kostick-Quenet, Kenneth D Mandl, Timo Minssen, et al.Pageof 44