Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Steven N Hart

Showing results (71-80 of 124) with videos related to

Pageof 13
Sort By:
Cancer Research|December 18, 2015
Integrated Genomic Analysis of Pancreatic Ductal Adenocarcinomas Reveals Genomic Rearrangement Events as Significant Drivers of DiseaseStephen J Murphy, Steven N Hart, Geoffrey C Halling, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|June 23, 2022
Classification of BRCA2 Variants of Uncertain Significance (VUS) Using an ACMG/AMP Model Incorporating a Homology-Directed Repair (HDR) Functional AssayChunling Hu, Lisa R Susswein, Maegan E Roberts, et al.
American Journal of Human Genetics|May 7, 2016
Evaluation of ACMG-Guideline-Based Variant Classification of Cancer Susceptibility and Non-Cancer-Associated Genes in Families Affected by Breast CancerKara N Maxwell, Steven N Hart, Joseph Vijai, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 14, 2019
A clinical guide to hereditary cancer panel testing: evaluation of gene-specific cancer associations and sensitivity of genetic testing criteria in a cohort of 165,000 high-risk patientsHolly LaDuca, Eric C Polley, Amal Yussuf, et al.
Journal of Pathology Informatics|December 9, 2021
A Pathologist-Annotated Dataset for Validating Artificial Intelligence: A Project Description and Pilot StudySarah N Dudgeon, Si Wen, Matthew G Hanna, et al.
Plos One|December 24, 2015
Mutational Landscapes of Sequential Prostate Metastases and Matched Patient Derived Xenografts during Enzalutamide TherapyManish Kohli, Liguo Wang, Fang Xie, et al.
Cancer Research Communications|November 28, 2023
Polygenic Risk Score Modifies Prostate Cancer Risk of Pathogenic Variants in Men of African AncestryRaymond W Hughley, Marco Matejcic, Ziwei Song, et al.
Biorxiv : the Preprint Server for Biology|January 3, 2024
Saturation genome editing-based functional evaluation and clinical classification of BRCA2 single nucleotide variantsHuaizhi Huang, Chunling Hu, Jie Na, et al.
Scientific Reports|November 5, 2021
Design considerations for workflow management systems use in production genomics research and the clinicAzza E Ahmed, Joshua M Allen, Tajesvi Bhat, et al.
Frontiers in Oncology|June 2, 2012
Deep Sequence Analysis of Non-Small Cell Lung Cancer: Integrated Analysis of Gene Expression, Alternative Splicing, and Single Nucleotide Variations in Lung Adenocarcinomas with and without Oncogenic KRAS MutationsKrishna R Kalari, David Rossell, Brian M Necela, et al.
Pageof 13

Showing results (71-80 of 124) with videos related to

Sort By:
Pageof 13
Cancer Research|December 18, 2015
Integrated Genomic Analysis of Pancreatic Ductal Adenocarcinomas Reveals Genomic Rearrangement Events as Significant Drivers of DiseaseStephen J Murphy, Steven N Hart, Geoffrey C Halling, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|June 23, 2022
Classification of BRCA2 Variants of Uncertain Significance (VUS) Using an ACMG/AMP Model Incorporating a Homology-Directed Repair (HDR) Functional AssayChunling Hu, Lisa R Susswein, Maegan E Roberts, et al.
American Journal of Human Genetics|May 7, 2016
Evaluation of ACMG-Guideline-Based Variant Classification of Cancer Susceptibility and Non-Cancer-Associated Genes in Families Affected by Breast CancerKara N Maxwell, Steven N Hart, Joseph Vijai, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 14, 2019
A clinical guide to hereditary cancer panel testing: evaluation of gene-specific cancer associations and sensitivity of genetic testing criteria in a cohort of 165,000 high-risk patientsHolly LaDuca, Eric C Polley, Amal Yussuf, et al.
Journal of Pathology Informatics|December 9, 2021
A Pathologist-Annotated Dataset for Validating Artificial Intelligence: A Project Description and Pilot StudySarah N Dudgeon, Si Wen, Matthew G Hanna, et al.
Plos One|December 24, 2015
Mutational Landscapes of Sequential Prostate Metastases and Matched Patient Derived Xenografts during Enzalutamide TherapyManish Kohli, Liguo Wang, Fang Xie, et al.
Cancer Research Communications|November 28, 2023
Polygenic Risk Score Modifies Prostate Cancer Risk of Pathogenic Variants in Men of African AncestryRaymond W Hughley, Marco Matejcic, Ziwei Song, et al.
Biorxiv : the Preprint Server for Biology|January 3, 2024
Saturation genome editing-based functional evaluation and clinical classification of BRCA2 single nucleotide variantsHuaizhi Huang, Chunling Hu, Jie Na, et al.
Scientific Reports|November 5, 2021
Design considerations for workflow management systems use in production genomics research and the clinicAzza E Ahmed, Joshua M Allen, Tajesvi Bhat, et al.
Frontiers in Oncology|June 2, 2012
Deep Sequence Analysis of Non-Small Cell Lung Cancer: Integrated Analysis of Gene Expression, Alternative Splicing, and Single Nucleotide Variations in Lung Adenocarcinomas with and without Oncogenic KRAS MutationsKrishna R Kalari, David Rossell, Brian M Necela, et al.
Pageof 13