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Amanda B Spurdle

Showing results (191-200 of 398) with videos related to

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Carcinogenesis|December 15, 2010
Progesterone receptor gene variants and risk of endometrial cancerTracy A O'Mara, Paul Fahey, Kaltin Ferguson, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 23, 2020
Two integrated and highly predictive functional analysis-based procedures for the classification of MSH6 variants in Lynch syndromeMark Drost, Yvonne Tiersma, Dylan Glubb, et al.
Cancers|January 8, 2023
Results of PD-L1 Analysis of Women Treated with Durvalumab in Advanced Endometrial Carcinoma (PHAEDRA)Deborah Smith, Kristy P Robledo, Sonia Yip, et al.
BMC Cancer|April 5, 2011
A Kallikrein 15 (KLK15) single nucleotide polymorphism located close to a novel exon shows evidence of association with poor ovarian cancer survivalJyotsna Batra, Christina M Nagle, Tracy O'Mara, et al.
Communications Medicine|November 19, 2025
Pan-cancer prevalence, risk, and clinical and demographic characteristics of Lynch Syndrome-associated variants in BioBank JapanKeijiro Mizukami, Yoshiaki Usui, Yusuke Iwasaki, et al.
American Journal of Human Genetics|June 23, 2023
Using the ACMG/AMP framework to capture evidence related to predicted and observed impact on splicing: Recommendations from the ClinGen SVI Splicing SubgroupLogan C Walker, Miguel de la Hoya, George A R Wiggins, et al.
Breast Cancer Research : BCR|July 27, 2011
Rare variants in the ATM gene and risk of breast cancerDavid E Goldgar, Sue Healey, James G Dowty, et al.
Human Mutation|June 1, 2010
Detection of splicing aberrations caused by BRCA1 and BRCA2 sequence variants encoding missense substitutions: implications for prediction of pathogenicityLogan C Walker, Phillip J Whiley, Fergus J Couch, et al.
NPJ Genomic Medicine|February 27, 2018
Clinical testing of <i>BRCA1</i> and <i>BRCA2</i>: a worldwide snapshot of technological practicesAmanda Ewart Toland, Andrea Forman, Fergus J Couch, et al.
Human Mutation|June 3, 2020
Suggested application of HER2+ breast tumor phenotype for germline TP53 variant classification within ACMG/AMP guidelinesCristina Fortuno, Jessica Mester, Tina Pesaran, et al.
Pageof 40

Showing results (191-200 of 398) with videos related to

Sort By:
Pageof 40
Carcinogenesis|December 15, 2010
Progesterone receptor gene variants and risk of endometrial cancerTracy A O'Mara, Paul Fahey, Kaltin Ferguson, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 23, 2020
Two integrated and highly predictive functional analysis-based procedures for the classification of MSH6 variants in Lynch syndromeMark Drost, Yvonne Tiersma, Dylan Glubb, et al.
Cancers|January 8, 2023
Results of PD-L1 Analysis of Women Treated with Durvalumab in Advanced Endometrial Carcinoma (PHAEDRA)Deborah Smith, Kristy P Robledo, Sonia Yip, et al.
BMC Cancer|April 5, 2011
A Kallikrein 15 (KLK15) single nucleotide polymorphism located close to a novel exon shows evidence of association with poor ovarian cancer survivalJyotsna Batra, Christina M Nagle, Tracy O'Mara, et al.
Communications Medicine|November 19, 2025
Pan-cancer prevalence, risk, and clinical and demographic characteristics of Lynch Syndrome-associated variants in BioBank JapanKeijiro Mizukami, Yoshiaki Usui, Yusuke Iwasaki, et al.
American Journal of Human Genetics|June 23, 2023
Using the ACMG/AMP framework to capture evidence related to predicted and observed impact on splicing: Recommendations from the ClinGen SVI Splicing SubgroupLogan C Walker, Miguel de la Hoya, George A R Wiggins, et al.
Breast Cancer Research : BCR|July 27, 2011
Rare variants in the ATM gene and risk of breast cancerDavid E Goldgar, Sue Healey, James G Dowty, et al.
Human Mutation|June 1, 2010
Detection of splicing aberrations caused by BRCA1 and BRCA2 sequence variants encoding missense substitutions: implications for prediction of pathogenicityLogan C Walker, Phillip J Whiley, Fergus J Couch, et al.
NPJ Genomic Medicine|February 27, 2018
Clinical testing of <i>BRCA1</i> and <i>BRCA2</i>: a worldwide snapshot of technological practicesAmanda Ewart Toland, Andrea Forman, Fergus J Couch, et al.
Human Mutation|June 3, 2020
Suggested application of HER2+ breast tumor phenotype for germline TP53 variant classification within ACMG/AMP guidelinesCristina Fortuno, Jessica Mester, Tina Pesaran, et al.
Pageof 40