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The Journal of Biological Chemistry|January 11, 2014
A large scale Huntingtin protein interaction network implicates Rho GTPase signaling pathways in Huntington diseaseCendrine Tourette, Biao Li, Russell Bell, et al.Obesity (Silver Spring, Md.)|October 4, 2021
From the clinic to the community: Can health system data accurately estimate population obesity prevalence?Stephen J Mooney, Lin Song, Adam Drewnowski, et al.Journal of Medical Internet Research|April 16, 2021
Forecasting Future Asthma Hospital Encounters of Patients With Asthma in an Academic Health Care System: Predictive Model Development and Secondary Analysis StudyYao Tong, Amanda I Messinger, Adam B Wilcox, et al.Nature Communications|December 9, 2022
A Multifaceted benchmarking of synthetic electronic health record generation modelsChao Yan, Yao Yan, Zhiyu Wan, et al.Journal of the American Medical Informatics Association : JAMIA|November 9, 2020
Information needs and priority use cases of population health researchers to improve preparedness for future hurricanes and floodsJimmy Phuong, Christina J Bandaragoda, Shefali Haldar, et al.Pacific Symposium on Biocomputing. Pacific Symposium on Biocomputing|November 30, 2016
PRECISION MEDICINE: DATA AND DISCOVERY FOR IMPROVED HEALTH AND THERAPYAlexander A Morgan, Dana C Crawford, Josh C Denny, et al.Proteins|February 27, 2008
An integrated approach to inferring gene-disease associations in humansPredrag Radivojac, Kang Peng, Wyatt T Clark, et al.Journal of Medical Internet Research|August 11, 2018
Using Mobile Apps to Assess and Treat Depression in Hispanic and Latino Populations: Fully Remote Randomized Clinical TrialAbhishek Pratap, Brenna N Renn, Joshua Volponi, et al.The Journal of Clinical Endocrinology and Metabolism|February 3, 2005
A novel recessive mutation in fibroblast growth factor-23 causes familial tumoral calcinosisTobias Larsson, Xijie Yu, Siobhan I Davis, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 6, 2016
CADD score has limited clinical validity for the identification of pathogenic variants in noncoding regions in a hereditary cancer panelCheryl A Mather, Sean D Mooney, Stephen J Salipante, et al.Pageof 13