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

Alun Thomas

Showing results (91-100 of 102) with videos related to

Pageof 11
Sort By:
American Journal of Human Genetics|June 6, 2022
Comprehensive evaluation and efficient classification of BRCA1 RING domain missense substitutionsKathleen A Clark, Andrew Paquette, Kayoko Tao, et al.
Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association for Cancer Research, Cosponsored by the American Society of Preventive Oncology|April 14, 2018
Reparameterization of PAM50 Expression Identifies Novel Breast Tumor Dimensions and Leads to Discovery of a Genome-Wide Significant Breast Cancer Locus at <i>12q15</i>Michael J Madsen, Stacey Knight, Carol Sweeney, et al.
Journal of the National Cancer Institute|April 17, 2018
A Nonsynonymous Variant in the GOLM1 Gene in Cutaneous Malignant MelanomaCraig C Teerlink, Chad Huff, Jeff Stevens, et al.
Breast Cancer Research : BCR|January 20, 2011
Rare, evolutionarily unlikely missense substitutions in CHEK2 contribute to breast cancer susceptibility: results from a breast cancer family registry case-control mutation-screening studyFlorence Le Calvez-Kelm, Fabienne Lesueur, Francesca Damiola, et al.
NPJ Precision Oncology|May 22, 2026
Molecular features unique to circulating tumor DNA enable the tumor-naïve liquid biopsy of glioblastomaHunter R Underhill, Drew L Sellers, Sabine Hellwig, et al.
BMC Proceedings|March 1, 2012
Identifying rare variants from exome scans: the GAW17 experienceSaurabh Ghosh, Heike Bickeböller, Julia Bailey, et al.
Human Mutation|September 6, 2012
Calibration of multiple in silico tools for predicting pathogenicity of mismatch repair gene missense substitutionsBryony A Thompson, Marc S Greenblatt, Maxime P Vallee, et al.
Plos Genetics|February 2, 2018
Novel pedigree analysis implicates DNA repair and chromatin remodeling in multiple myeloma riskRosalie G Waller, Todd M Darlington, Xiaomu Wei, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|August 14, 2023
Germline <i>EGFR</i> Mutations and Familial Lung CancerGeoffrey R Oxnard, Ruthia Chen, Jennifer C Pharr, et al.
American Journal of Human Genetics|September 29, 2009
Rare, evolutionarily unlikely missense substitutions in ATM confer increased risk of breast cancerSean V Tavtigian, Peter J Oefner, Davit Babikyan, et al.
Pageof 11

Showing results (91-100 of 102) with videos related to

Sort By:
Pageof 11
American Journal of Human Genetics|June 6, 2022
Comprehensive evaluation and efficient classification of BRCA1 RING domain missense substitutionsKathleen A Clark, Andrew Paquette, Kayoko Tao, et al.
Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association for Cancer Research, Cosponsored by the American Society of Preventive Oncology|April 14, 2018
Reparameterization of PAM50 Expression Identifies Novel Breast Tumor Dimensions and Leads to Discovery of a Genome-Wide Significant Breast Cancer Locus at <i>12q15</i>Michael J Madsen, Stacey Knight, Carol Sweeney, et al.
Journal of the National Cancer Institute|April 17, 2018
A Nonsynonymous Variant in the GOLM1 Gene in Cutaneous Malignant MelanomaCraig C Teerlink, Chad Huff, Jeff Stevens, et al.
Breast Cancer Research : BCR|January 20, 2011
Rare, evolutionarily unlikely missense substitutions in CHEK2 contribute to breast cancer susceptibility: results from a breast cancer family registry case-control mutation-screening studyFlorence Le Calvez-Kelm, Fabienne Lesueur, Francesca Damiola, et al.
NPJ Precision Oncology|May 22, 2026
Molecular features unique to circulating tumor DNA enable the tumor-naïve liquid biopsy of glioblastomaHunter R Underhill, Drew L Sellers, Sabine Hellwig, et al.
BMC Proceedings|March 1, 2012
Identifying rare variants from exome scans: the GAW17 experienceSaurabh Ghosh, Heike Bickeböller, Julia Bailey, et al.
Human Mutation|September 6, 2012
Calibration of multiple in silico tools for predicting pathogenicity of mismatch repair gene missense substitutionsBryony A Thompson, Marc S Greenblatt, Maxime P Vallee, et al.
Plos Genetics|February 2, 2018
Novel pedigree analysis implicates DNA repair and chromatin remodeling in multiple myeloma riskRosalie G Waller, Todd M Darlington, Xiaomu Wei, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|August 14, 2023
Germline <i>EGFR</i> Mutations and Familial Lung CancerGeoffrey R Oxnard, Ruthia Chen, Jennifer C Pharr, et al.
American Journal of Human Genetics|September 29, 2009
Rare, evolutionarily unlikely missense substitutions in ATM confer increased risk of breast cancerSean V Tavtigian, Peter J Oefner, Davit Babikyan, et al.
Pageof 11