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Elizabeth C Chao

Showing results (21-30 of 36) with videos related to

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Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 20, 2019
Classification of variants of uncertain significance in BRCA1 and BRCA2 using personal and family history of cancer from individuals in a large hereditary cancer multigene panel testing cohortHongyan Li, Holly LaDuca, Tina Pesaran, et al.
JAMA Oncology|April 19, 2017
Associations Between Cancer Predisposition Testing Panel Genes and Breast CancerFergus J Couch, Hermela Shimelis, Chunling Hu, et al.
Journal of the National Cancer Institute|November 4, 2020
Racial and Ethnic Differences in Multigene Hereditary Cancer Panel Test Results for Women With Breast CancerSiddhartha Yadav, Holly LaDuca, Eric C Polley, et al.
Neurology|March 21, 2014
Congenital lethal motor neuron disease with a novel defect in ribosome biogenesisRussell J Butterfield, Tamara J Stevenson, Lingyan Xing, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 15, 2018
Misattributed parentage as an unanticipated finding during exome/genome sequencing: current clinical laboratory practices and an opportunity for standardizationCeleste Eno, Pinar Bayrak-Toydemir, Lora Bean, et al.
NPJ Genomic Medicine|August 25, 2022
Mutational and splicing landscape in a cohort of 43,000 patients tested for hereditary cancerCarolyn Horton, Ashley Cass, Blair R Conner, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 12, 2016
Candidate-gene criteria for clinical reporting: diagnostic exome sequencing identifies altered candidate genes among 8% of patients with undiagnosed diseasesKelly D Farwell Hagman, Deepali N Shinde, Cameron Mroske, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 1, 2017
Somatic TP53 variants frequently confound germ-line testing resultsJeffrey N Weitzel, Elizabeth C Chao, Bita Nehoray, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|February 2, 2018
Correction: Candidate-gene criteria for clinical reporting: diagnostic exome sequencing identifies altered candidate genes among 8% of patients with undiagnosed diseasesKelly D Farwell Hagman, Deepali N Shinde, Cameron Mroske, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|February 1, 2019
Comprehensive Paired Tumor/Germline Testing for Lynch Syndrome: Bringing Resolution to the Diagnostic ProcessMonalyn U Salvador, Melissa R F Truelson, Carla Mason, et al.
Pageof 4

Showing results (21-30 of 36) with videos related to

Sort By:
Pageof 4
Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 20, 2019
Classification of variants of uncertain significance in BRCA1 and BRCA2 using personal and family history of cancer from individuals in a large hereditary cancer multigene panel testing cohortHongyan Li, Holly LaDuca, Tina Pesaran, et al.
JAMA Oncology|April 19, 2017
Associations Between Cancer Predisposition Testing Panel Genes and Breast CancerFergus J Couch, Hermela Shimelis, Chunling Hu, et al.
Journal of the National Cancer Institute|November 4, 2020
Racial and Ethnic Differences in Multigene Hereditary Cancer Panel Test Results for Women With Breast CancerSiddhartha Yadav, Holly LaDuca, Eric C Polley, et al.
Neurology|March 21, 2014
Congenital lethal motor neuron disease with a novel defect in ribosome biogenesisRussell J Butterfield, Tamara J Stevenson, Lingyan Xing, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 15, 2018
Misattributed parentage as an unanticipated finding during exome/genome sequencing: current clinical laboratory practices and an opportunity for standardizationCeleste Eno, Pinar Bayrak-Toydemir, Lora Bean, et al.
NPJ Genomic Medicine|August 25, 2022
Mutational and splicing landscape in a cohort of 43,000 patients tested for hereditary cancerCarolyn Horton, Ashley Cass, Blair R Conner, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 12, 2016
Candidate-gene criteria for clinical reporting: diagnostic exome sequencing identifies altered candidate genes among 8% of patients with undiagnosed diseasesKelly D Farwell Hagman, Deepali N Shinde, Cameron Mroske, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 1, 2017
Somatic TP53 variants frequently confound germ-line testing resultsJeffrey N Weitzel, Elizabeth C Chao, Bita Nehoray, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|February 2, 2018
Correction: Candidate-gene criteria for clinical reporting: diagnostic exome sequencing identifies altered candidate genes among 8% of patients with undiagnosed diseasesKelly D Farwell Hagman, Deepali N Shinde, Cameron Mroske, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|February 1, 2019
Comprehensive Paired Tumor/Germline Testing for Lynch Syndrome: Bringing Resolution to the Diagnostic ProcessMonalyn U Salvador, Melissa R F Truelson, Carla Mason, et al.
Pageof 4