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

J Couch

Showing results (511-520 of 697) with videos related to

Pageof 70
Sort By:
Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association for Cancer Research, Cosponsored by the American Society of Preventive Oncology|March 12, 2011
Common genetic variation at BARD1 is not associated with breast cancer risk in BRCA1 or BRCA2 mutation carriersAmanda B Spurdle, Louise Marquart, Lesley McGuffog, et al.
Breast Cancer Research : BCR|November 9, 2017
Reproductive profiles and risk of breast cancer subtypes: a multi-center case-only studyOlivier Brouckaert, Anja Rudolph, Annouschka Laenen, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|October 7, 2016
Genetic modifiers of CHEK2*1100delC-associated breast cancer riskTaru A Muranen, Dario Greco, Carl Blomqvist, et al.
American Journal of Human Genetics|November 14, 2007
RAD51 135G-->C modifies breast cancer risk among BRCA2 mutation carriers: results from a combined analysis of 19 studiesAntonis C Antoniou, Olga M Sinilnikova, Jacques Simard, et al.
Cancer Research|August 17, 2011
Common breast cancer susceptibility loci are associated with triple-negative breast cancerKristen N Stevens, Celine M Vachon, Adam M Lee, et al.
Breast Cancer Research : BCR|January 4, 2011
Assessing interactions between the associations of common genetic susceptibility variants, reproductive history and body mass index with breast cancer risk in the breast cancer association consortium: a combined case-control studyRoger L Milne, Mia M Gaudet, Amanda B Spurdle, et al.
Human Genetics|December 2, 2015
Genetic variation in the immunosuppression pathway genes and breast cancer susceptibility: a pooled analysis of 42,510 cases and 40,577 controls from the Breast Cancer Association ConsortiumJieping Lei, Anja Rudolph, Kirsten B Moysich, et al.
Human Molecular Genetics|December 21, 2013
DNA mismatch repair gene MSH6 implicated in determining age at natural menopauseJohn R B Perry, Yi-Hsiang Hsu, Daniel I Chasman, et al.
Scientific Reports|April 14, 2022
Genome-wide interaction analysis of menopausal hormone therapy use and breast cancer risk among 62,370 womenXiaoliang Wang, Pooja Middha Kapoor, Paul L Auer, et al.
American Journal of Human Genetics|March 22, 2008
Common breast cancer-predisposition alleles are associated with breast cancer risk in BRCA1 and BRCA2 mutation carriersAntonis C Antoniou, Amanda B Spurdle, Olga M Sinilnikova, et al.
Pageof 70

Showing results (511-520 of 697) with videos related to

Sort By:
Pageof 70
Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association for Cancer Research, Cosponsored by the American Society of Preventive Oncology|March 12, 2011
Common genetic variation at BARD1 is not associated with breast cancer risk in BRCA1 or BRCA2 mutation carriersAmanda B Spurdle, Louise Marquart, Lesley McGuffog, et al.
Breast Cancer Research : BCR|November 9, 2017
Reproductive profiles and risk of breast cancer subtypes: a multi-center case-only studyOlivier Brouckaert, Anja Rudolph, Annouschka Laenen, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|October 7, 2016
Genetic modifiers of CHEK2*1100delC-associated breast cancer riskTaru A Muranen, Dario Greco, Carl Blomqvist, et al.
American Journal of Human Genetics|November 14, 2007
RAD51 135G-->C modifies breast cancer risk among BRCA2 mutation carriers: results from a combined analysis of 19 studiesAntonis C Antoniou, Olga M Sinilnikova, Jacques Simard, et al.
Cancer Research|August 17, 2011
Common breast cancer susceptibility loci are associated with triple-negative breast cancerKristen N Stevens, Celine M Vachon, Adam M Lee, et al.
Breast Cancer Research : BCR|January 4, 2011
Assessing interactions between the associations of common genetic susceptibility variants, reproductive history and body mass index with breast cancer risk in the breast cancer association consortium: a combined case-control studyRoger L Milne, Mia M Gaudet, Amanda B Spurdle, et al.
Human Genetics|December 2, 2015
Genetic variation in the immunosuppression pathway genes and breast cancer susceptibility: a pooled analysis of 42,510 cases and 40,577 controls from the Breast Cancer Association ConsortiumJieping Lei, Anja Rudolph, Kirsten B Moysich, et al.
Human Molecular Genetics|December 21, 2013
DNA mismatch repair gene MSH6 implicated in determining age at natural menopauseJohn R B Perry, Yi-Hsiang Hsu, Daniel I Chasman, et al.
Scientific Reports|April 14, 2022
Genome-wide interaction analysis of menopausal hormone therapy use and breast cancer risk among 62,370 womenXiaoliang Wang, Pooja Middha Kapoor, Paul L Auer, et al.
American Journal of Human Genetics|March 22, 2008
Common breast cancer-predisposition alleles are associated with breast cancer risk in BRCA1 and BRCA2 mutation carriersAntonis C Antoniou, Amanda B Spurdle, Olga M Sinilnikova, et al.
Pageof 70