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

Kenneth Offit

Showing results (201-210 of 429) with videos related to

Pageof 43
Sort By:
Genome Medicine|August 15, 2022
Diagnostic yield and clinical relevance of expanded genetic testing for cancer patientsOzge Ceyhan-Birsoy, Gowtham Jayakumaran, Yelena Kemel, et al.
Plos One|January 12, 2016
A Germline Variant on Chromosome 4q31.1 Associates with Susceptibility to Developing Colon Cancer MetastasisSanford D Markowitz, Nora L Nock, Stephanie L Schmit, et al.
JAMA Oncology|July 25, 2024
BRCA1, BRCA2, and Associated Cancer Risks and Management for Male Patients: A ReviewHeather H Cheng, Jeffrey W Shevach, Elena Castro, et al.
Plos Genetics|January 26, 2013
Susceptibility loci associated with specific and shared subtypes of lymphoid malignanciesJoseph Vijai, Tomas Kirchhoff, Kasmintan A Schrader, et al.
HGG Advances|January 5, 2025
Biologically targeted discovery-replication scan identifies G×G interaction in relation to risk of Barrett's esophagus and esophageal adenocarcinomaLi Yan, Qianchuan He, Shiv P Verma, et al.
Neuron|March 23, 2021
Novel ultra-rare exonic variants identified in a founder population implicate cadherins in schizophreniaTodd Lencz, Jin Yu, Raiyan Rashid Khan, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 23, 2022
A validation of models for prediction of pathogenic variants in mismatch repair genesCathy Shyr, Amanda L Blackford, Theodore Huang, et al.
Plos Genetics|September 7, 2013
A recessive founder mutation in regulator of telomere elongation helicase 1, RTEL1, underlies severe immunodeficiency and features of Hoyeraal Hreidarsson syndromeBari J Ballew, Vijai Joseph, Saurav De, et al.
JCO Precision Oncology|January 29, 2026
Age-Related Germline Landscape of Endometrial Cancer: Focus on Early-Onset CasesJudy J Wang, Juliet Milani, Sarah Kane, et al.
Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association for Cancer Research, Cosponsored by the American Society of Preventive Oncology|April 21, 2021
Circulating Levels of Testosterone, Sex Hormone Binding Globulin and Colorectal Cancer Risk: Observational and Mendelian Randomization AnalysesNiki Dimou, Nagisa Mori, Sophia Harlid, et al.
Pageof 43

Showing results (201-210 of 429) with videos related to

Sort By:
Pageof 43
Genome Medicine|August 15, 2022
Diagnostic yield and clinical relevance of expanded genetic testing for cancer patientsOzge Ceyhan-Birsoy, Gowtham Jayakumaran, Yelena Kemel, et al.
Plos One|January 12, 2016
A Germline Variant on Chromosome 4q31.1 Associates with Susceptibility to Developing Colon Cancer MetastasisSanford D Markowitz, Nora L Nock, Stephanie L Schmit, et al.
JAMA Oncology|July 25, 2024
BRCA1, BRCA2, and Associated Cancer Risks and Management for Male Patients: A ReviewHeather H Cheng, Jeffrey W Shevach, Elena Castro, et al.
Plos Genetics|January 26, 2013
Susceptibility loci associated with specific and shared subtypes of lymphoid malignanciesJoseph Vijai, Tomas Kirchhoff, Kasmintan A Schrader, et al.
HGG Advances|January 5, 2025
Biologically targeted discovery-replication scan identifies G×G interaction in relation to risk of Barrett's esophagus and esophageal adenocarcinomaLi Yan, Qianchuan He, Shiv P Verma, et al.
Neuron|March 23, 2021
Novel ultra-rare exonic variants identified in a founder population implicate cadherins in schizophreniaTodd Lencz, Jin Yu, Raiyan Rashid Khan, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 23, 2022
A validation of models for prediction of pathogenic variants in mismatch repair genesCathy Shyr, Amanda L Blackford, Theodore Huang, et al.
Plos Genetics|September 7, 2013
A recessive founder mutation in regulator of telomere elongation helicase 1, RTEL1, underlies severe immunodeficiency and features of Hoyeraal Hreidarsson syndromeBari J Ballew, Vijai Joseph, Saurav De, et al.
JCO Precision Oncology|January 29, 2026
Age-Related Germline Landscape of Endometrial Cancer: Focus on Early-Onset CasesJudy J Wang, Juliet Milani, Sarah Kane, et al.
Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association for Cancer Research, Cosponsored by the American Society of Preventive Oncology|April 21, 2021
Circulating Levels of Testosterone, Sex Hormone Binding Globulin and Colorectal Cancer Risk: Observational and Mendelian Randomization AnalysesNiki Dimou, Nagisa Mori, Sophia Harlid, et al.
Pageof 43