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L Nathanson

Showing results (451-460 of 528) with videos related to

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Medrxiv : the Preprint Server for Health Sciences|August 20, 2025
Multi-Ancestry Transcriptome-wide Association Studies Uncover New Insights into Breast Cancer Genetics and BiologyJie Ping, Guochong Jia, Qiuyin Cai, et al.
Nature Genetics|January 3, 2025
Refining breast cancer genetic risk and biology through multi-ancestry fine-mapping analyses of 192 risk regionsGuochong Jia, Zhishan Chen, Jie Ping, et al.
Human Molecular Genetics|January 24, 2024
Novel breast cancer susceptibility loci under linkage peaks identified in African ancestry consortiaHeather M Ochs-Balcom, Leah Preus, Zhaohui Du, et al.
Nature Communications|May 30, 2026
Multi-ancestry transcriptome-wide association studies uncover insights into breast cancer genetics and biologyJie Ping, Guochong Jia, Qiuyin Cai, et al.
Breast Cancer Research : BCR|December 1, 2010
Evidence for SMAD3 as a modifier of breast cancer risk in BRCA2 mutation carriersLogan C Walker, Zachary S Fredericksen, Xianshu Wang, 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.
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.
British Journal of Cancer|April 19, 2023
Ovarian cancer pathology characteristics as predictors of variant pathogenicity in BRCA1 and BRCA2Denise G O'Mahony, Susan J Ramus, Melissa C Southey, et al.
Nature Communications|July 5, 2020
Assessment of polygenic architecture and risk prediction based on common variants across fourteen cancersYan Dora Zhang, Amber N Hurson, Haoyu Zhang, et al.
Breast Cancer Research : BCR|November 13, 2016
Inheritance of deleterious mutations at both BRCA1 and BRCA2 in an international sample of 32,295 womenTimothy R Rebbeck, Tara M Friebel, Nandita Mitra, et al.
Pageof 53

Showing results (451-460 of 528) with videos related to

Sort By:
Pageof 53
Medrxiv : the Preprint Server for Health Sciences|August 20, 2025
Multi-Ancestry Transcriptome-wide Association Studies Uncover New Insights into Breast Cancer Genetics and BiologyJie Ping, Guochong Jia, Qiuyin Cai, et al.
Nature Genetics|January 3, 2025
Refining breast cancer genetic risk and biology through multi-ancestry fine-mapping analyses of 192 risk regionsGuochong Jia, Zhishan Chen, Jie Ping, et al.
Human Molecular Genetics|January 24, 2024
Novel breast cancer susceptibility loci under linkage peaks identified in African ancestry consortiaHeather M Ochs-Balcom, Leah Preus, Zhaohui Du, et al.
Nature Communications|May 30, 2026
Multi-ancestry transcriptome-wide association studies uncover insights into breast cancer genetics and biologyJie Ping, Guochong Jia, Qiuyin Cai, et al.
Breast Cancer Research : BCR|December 1, 2010
Evidence for SMAD3 as a modifier of breast cancer risk in BRCA2 mutation carriersLogan C Walker, Zachary S Fredericksen, Xianshu Wang, 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.
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.
British Journal of Cancer|April 19, 2023
Ovarian cancer pathology characteristics as predictors of variant pathogenicity in BRCA1 and BRCA2Denise G O'Mahony, Susan J Ramus, Melissa C Southey, et al.
Nature Communications|July 5, 2020
Assessment of polygenic architecture and risk prediction based on common variants across fourteen cancersYan Dora Zhang, Amber N Hurson, Haoyu Zhang, et al.
Breast Cancer Research : BCR|November 13, 2016
Inheritance of deleterious mutations at both BRCA1 and BRCA2 in an international sample of 32,295 womenTimothy R Rebbeck, Tara M Friebel, Nandita Mitra, et al.
Pageof 53