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The Journal of Applied Laboratory Medicine|February 27, 2021
A Paradigm Shift: Considerations in Prenatal Cell-Free DNA ScreeningJennifer N Dines, Ashley M Eckel, Edith Y Cheng, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 9, 2020
Systematic misclassification of missense variants in BRCA1 and BRCA2 "coldspots"Jennifer N Dines, Brian H Shirts, Thomas P Slavin, et al.
American Journal of Medical Genetics. Part A|December 5, 2018
Expanding clinical phenotype in CACNA1C related disorders: From neonatal onset severe epileptic encephalopathy to late-onset epilepsyXiuhua Bozarth, Jennifer N Dines, Qian Cong, et al.
American Journal of Human Genetics|November 18, 2021
Closing the gap: Systematic integration of multiplexed functional data resolves variants of uncertain significance in BRCA1, TP53, and PTENShawn Fayer, Carrie Horton, Jennifer N Dines, et al.
Genome Medicine|December 22, 2019
Recommendations for the collection and use of multiplexed functional data for clinical variant interpretationHannah Gelman, Jennifer N Dines, Jonathan Berg, et al.
American Journal of Medical Genetics. Part A|July 12, 2019
Expanding phenotype with severe midline brain anomalies and missense variant supports a causal role for FOXA2 in 20p11.2 deletion syndromeJennifer N Dines, Yajuan J Liu, Whitney Neufeld-Kaiser, et al.
Nature Genetics|May 23, 2018
Multiplex assessment of protein variant abundance by massively parallel sequencingKenneth A Matreyek, Lea M Starita, Jason J Stephany, et al.
American Journal of Human Genetics|December 6, 2024
A missense variant effect map for the human tumor-suppressor protein CHK2Marinella Gebbia, Daniel Zimmerman, Rosanna Jiang, et al.
Frontiers in Neuroinformatics|February 13, 2016
Using Make for Reproducible and Parallel Neuroimaging Workflow and Quality-AssuranceMary K Askren, Trevor K McAllister-Day, Natalie Koh, et al.
Clinical Infectious Diseases : an Official Publication of the Infectious Diseases Society of America|May 6, 2022
Clinical Validation of a Novel T-Cell Receptor Sequencing Assay for Identification of Recent or Prior Severe Acute Respiratory Syndrome Coronavirus 2 InfectionSudeb C Dalai, Jennifer N Dines, Thomas M Snyder, et al.
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