Showing results (11-20 of 92) with videos related to

Sort By:
Pageof 10
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|December 9, 2020
Democratizing genomics: Leveraging software to make genetics an integral part of routine careMoran Snir, Shivani Nazareth, Emilie Simmons, et al.
Familial Cancer|October 8, 2021
Re-evaluating cancer risks associated with the CHEK2 p.Ser428Phe Ashkenazi Jewish founder pathogenic variantYael Laitman, Sarah M Nielsen, Kathryn E Hatchell, et al.
JAMA Oncology|February 8, 2019
Prevalence of Germline Variants in Prostate Cancer and Implications for Current Genetic Testing GuidelinesPiper Nicolosi, Elisa Ledet, Shan Yang, et al.
JCO Precision Oncology|July 11, 2024
Disparate Rates of Germline Variants in Cancer Predisposition Genes in African American/Black Compared With Non-Hispanic White Individuals Between 2015 and 2022Rachel B Wyatt Castillo, Sarah M Nielsen, Elaine Chen, et al.
JCO Precision Oncology|November 12, 2022
Multigene Panel Testing Yields High Rates of Clinically Actionable Variants Among Patients With Colorectal CancerSarah E Coughlin, Brandie Heald, Dana Farengo Clark, et al.
Annals of Surgical Oncology|July 13, 2018
Underdiagnosis of Hereditary Breast and Ovarian Cancer in Medicare Patients: Genetic Testing Criteria Miss the MarkShan Yang, Jennifer E Axilbund, Erin O'Leary, et al.
American Journal of Medical Genetics. Part A|March 26, 2018
Biallelic loss-of-function WNT5A mutations in an infant with severe and atypical manifestations of Robinow syndromeJohannes Birgmeier, Edward D Esplin, Karthik A Jagadeesh, et al.
Cancers|December 11, 2022
Ashkenazi Jewish and Other White APC I1307K Carriers Are at Higher Risk for Multiple CancersEsther Forkosh, Michael Bergel, Kathryn E Hatchell, et al.
Epilepsia Open|December 10, 2023
Early genetic testing in pediatric epilepsy: Diagnostic and cost implicationsShanna M Swartwood, Ana Morales, Kathryn E Hatchell, et al.
JCO Precision Oncology|September 29, 2021
Underdiagnosis of Hereditary Colorectal Cancers Among Medicare Patients: Genetic Testing Criteria for Lynch Syndrome Miss the MarkCharles Muller, Sarah M Nielsen, Kathryn E Hatchell, et al.
Pageof 10