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

K Bolla

Showing results (101-110 of 256) with videos related to

Pageof 26
Sort By:
Oncotarget|February 10, 2017
TP53-based interaction analysis identifies cis-eQTL variants for TP53BP2, FBXO28, and FAM53A that associate with survival and treatment outcome in breast cancerRainer Fagerholm, Sofia Khan, Marjanka K Schmidt, et al.
Ebiomedicine|August 20, 2015
Crowdsourcing the General Public for Large Scale Molecular Pathology Studies in CancerFrancisco J Candido Dos Reis, Stuart Lynn, H Raza Ali, et al.
The Journal of Pathology. Clinical Research|August 9, 2016
Performance of automated scoring of ER, PR, HER2, CK5/6 and EGFR in breast cancer tissue microarrays in the Breast Cancer Association ConsortiumWilliam J Howat, Fiona M Blows, Elena Provenzano, et al.
American Journal of Human Genetics|November 10, 2022
Genome- and transcriptome-wide association studies of 386,000 Asian and European-ancestry women provide new insights into breast cancer geneticsGuochong Jia, Jie Ping, Xiang Shu, et al.
Breast Cancer Research : BCR|April 13, 2022
Genome-wide and transcriptome-wide association studies of mammographic density phenotypes reveal novel lociHongjie Chen, Shaoqi Fan, Jennifer Stone, et al.
Oncotarget|August 29, 2015
SNP-SNP interaction analysis of NF-κB signaling pathway on breast cancer survivalMaral Jamshidi, Rainer Fagerholm, Sofia Khan, et al.
Nature Genetics|September 26, 2023
Author Correction: Exome sequencing identifies breast cancer susceptibility genes and defines the contribution of coding variants to breast cancer riskNaomi Wilcox, Martine Dumont, Anna González-Neira, et al.
Nature Genetics|August 17, 2023
Exome sequencing identifies breast cancer susceptibility genes and defines the contribution of coding variants to breast cancer riskNaomi Wilcox, Martine Dumont, Anna González-Neira, et al.
Breast Cancer Research : BCR|December 19, 2019
Prediction and clinical utility of a contralateral breast cancer risk modelDaniele Giardiello, Ewout W Steyerberg, Michael Hauptmann, et al.
Journal of the National Cancer Institute|March 26, 2021
Evaluating Polygenic Risk Scores for Breast Cancer in Women of African AncestryZhaohui Du, Guimin Gao, Babatunde Adedokun, et al.
Pageof 26

Showing results (101-110 of 256) with videos related to

Sort By:
Pageof 26
Oncotarget|February 10, 2017
TP53-based interaction analysis identifies cis-eQTL variants for TP53BP2, FBXO28, and FAM53A that associate with survival and treatment outcome in breast cancerRainer Fagerholm, Sofia Khan, Marjanka K Schmidt, et al.
Ebiomedicine|August 20, 2015
Crowdsourcing the General Public for Large Scale Molecular Pathology Studies in CancerFrancisco J Candido Dos Reis, Stuart Lynn, H Raza Ali, et al.
The Journal of Pathology. Clinical Research|August 9, 2016
Performance of automated scoring of ER, PR, HER2, CK5/6 and EGFR in breast cancer tissue microarrays in the Breast Cancer Association ConsortiumWilliam J Howat, Fiona M Blows, Elena Provenzano, et al.
American Journal of Human Genetics|November 10, 2022
Genome- and transcriptome-wide association studies of 386,000 Asian and European-ancestry women provide new insights into breast cancer geneticsGuochong Jia, Jie Ping, Xiang Shu, et al.
Breast Cancer Research : BCR|April 13, 2022
Genome-wide and transcriptome-wide association studies of mammographic density phenotypes reveal novel lociHongjie Chen, Shaoqi Fan, Jennifer Stone, et al.
Oncotarget|August 29, 2015
SNP-SNP interaction analysis of NF-κB signaling pathway on breast cancer survivalMaral Jamshidi, Rainer Fagerholm, Sofia Khan, et al.
Nature Genetics|September 26, 2023
Author Correction: Exome sequencing identifies breast cancer susceptibility genes and defines the contribution of coding variants to breast cancer riskNaomi Wilcox, Martine Dumont, Anna González-Neira, et al.
Nature Genetics|August 17, 2023
Exome sequencing identifies breast cancer susceptibility genes and defines the contribution of coding variants to breast cancer riskNaomi Wilcox, Martine Dumont, Anna González-Neira, et al.
Breast Cancer Research : BCR|December 19, 2019
Prediction and clinical utility of a contralateral breast cancer risk modelDaniele Giardiello, Ewout W Steyerberg, Michael Hauptmann, et al.
Journal of the National Cancer Institute|March 26, 2021
Evaluating Polygenic Risk Scores for Breast Cancer in Women of African AncestryZhaohui Du, Guimin Gao, Babatunde Adedokun, et al.
Pageof 26