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Journal of Pathology Informatics|March 28, 2014
The 2013 symposium on pathology data integration and clinical decision support and the current state of fieldJason M Baron, Anand S Dighe, Ramy Arnaout, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 19, 2021
One in seven pathogenic variants can be challenging to detect by NGS: an analysis of 450,000 patients with implications for clinical sensitivity and genetic test implementationStephen E Lincoln, Tina Hambuch, Justin M Zook, et al.
Human Mutation|October 13, 2018
Scaling resolution of variant classification differences in ClinVar between 41 clinical laboratories through an outlier approachSteven M Harrison, Jill S Dolinksy, Wenjie Chen, et al.
Journal of the American Medical Informatics Association : JAMIA|July 5, 2015
CSER and eMERGE: current and potential state of the display of genetic information in the electronic health recordBrian H Shirts, Joseph S Salama, Samuel J Aronson, et al.
Contemporary Clinical Trials|August 11, 2019
Clinical exome sequencing vs. usual care for hereditary colorectal cancer diagnosis: A pilot comparative effectiveness studyXin Niu, Laura M Amendola, Ragan Hart, et al.
American Journal of Respiratory and Critical Care Medicine|May 17, 2012
An official multi-society statement: the role of clinical research results in the practice of critical care medicineMark R Tonelli, J Randall Curtis, Kalpalatha K Guntupalli, et al.
American Journal of Human Genetics|September 24, 2013
Actionable, pathogenic incidental findings in 1,000 participants' exomesMichael O Dorschner, Laura M Amendola, Emily H Turner, et al.
European Urology|December 5, 2021
Inherited TP53 Variants and Risk of Prostate CancerKara N Maxwell, Heather H Cheng, Jacquelyn Powers, et al.
JCO Precision Oncology|July 12, 2021
Prospective Statewide Study of Universal Screening for Hereditary Colorectal Cancer: The Ohio Colorectal Cancer Prevention InitiativeRachel Pearlman, Wendy L Frankel, Benjamin J Swanson, et al.
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