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Amanda B Spurdle

Showing results (161-170 of 398) with videos related to

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Gynecologic Oncology|December 3, 2014
Incidence, risk factors and estimates of a woman's risk of developing secondary lower limb lymphedema and lymphedema-specific supportive care needs in women treated for endometrial cancerVanessa L Beesley, Ingrid J Rowlands, Sandi C Hayes, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|March 4, 2008
Molecular, pathologic, and clinical features of early-onset endometrial cancer: identifying presumptive Lynch syndrome patientsMichael D Walsh, Margaret C Cummings, Daniel D Buchanan, et al.
Clinical Epigenetics|April 2, 2021
Correction to: The MLH1 polymorphism rs1800734 and risk of endometrial cancer with microsatellite instabilityHolly Russell, Katarzyna Kedzierska, Daniel D Buchanan, et al.
Iscience|May 11, 2023
Multi-trait genome-wide association study identifies a novel endometrial cancer risk locus that associates with testosterone levelsXuemin Wang, Pik Fang Kho, Dhanya Ramachandran, et al.
European Journal of Human Genetics : EJHG|November 30, 2006
Stability of BAT26 in Lynch syndrome colorectal tumoursLesley Jaskowski, Joanne Young, Leigh Jackson, et al.
Twin Research and Human Genetics : the Official Journal of the International Society for Twin Studies|July 27, 2011
CHEK2, MGMT, SULT1E1 and SULT1A1 polymorphisms and endometrial cancer riskTracy A O'Mara, Kaltin Ferguson, Paul Fahey, et al.
Human Genetics|November 10, 2014
Rare germline copy number deletions of likely functional importance are implicated in endometrial cancer predispositionGemma L Moir-Meyer, John F Pearson, Felicity Lose, et al.
Breast Cancer Research and Treatment|June 11, 2008
No evidence that CDKN1B (p27) polymorphisms modify breast cancer risk in BRCA1 and BRCA2 mutation carriersAmanda B Spurdle, Andrew J Deans, David Duffy, et al.
Molecular Carcinogenesis|December 5, 2013
Consequences of germline variation disrupting the constitutional translational initiation codon start sites of MLH1 and BRCA2: Use of potential alternative start sites and implications for predicting variant pathogenicityMichael T Parsons, Phillip J Whiley, Jonathan Beesley, et al.
American Journal of Human Genetics|June 6, 2025
Insights on improving accessibility and usability of functional data to unlock their potential for variant interpretationMin Seon Park, Runjun D Kumar, Cristian Ovadiuc, et al.
Pageof 40

Showing results (161-170 of 398) with videos related to

Sort By:
Pageof 40
Gynecologic Oncology|December 3, 2014
Incidence, risk factors and estimates of a woman's risk of developing secondary lower limb lymphedema and lymphedema-specific supportive care needs in women treated for endometrial cancerVanessa L Beesley, Ingrid J Rowlands, Sandi C Hayes, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|March 4, 2008
Molecular, pathologic, and clinical features of early-onset endometrial cancer: identifying presumptive Lynch syndrome patientsMichael D Walsh, Margaret C Cummings, Daniel D Buchanan, et al.
Clinical Epigenetics|April 2, 2021
Correction to: The MLH1 polymorphism rs1800734 and risk of endometrial cancer with microsatellite instabilityHolly Russell, Katarzyna Kedzierska, Daniel D Buchanan, et al.
Iscience|May 11, 2023
Multi-trait genome-wide association study identifies a novel endometrial cancer risk locus that associates with testosterone levelsXuemin Wang, Pik Fang Kho, Dhanya Ramachandran, et al.
European Journal of Human Genetics : EJHG|November 30, 2006
Stability of BAT26 in Lynch syndrome colorectal tumoursLesley Jaskowski, Joanne Young, Leigh Jackson, et al.
Twin Research and Human Genetics : the Official Journal of the International Society for Twin Studies|July 27, 2011
CHEK2, MGMT, SULT1E1 and SULT1A1 polymorphisms and endometrial cancer riskTracy A O'Mara, Kaltin Ferguson, Paul Fahey, et al.
Human Genetics|November 10, 2014
Rare germline copy number deletions of likely functional importance are implicated in endometrial cancer predispositionGemma L Moir-Meyer, John F Pearson, Felicity Lose, et al.
Breast Cancer Research and Treatment|June 11, 2008
No evidence that CDKN1B (p27) polymorphisms modify breast cancer risk in BRCA1 and BRCA2 mutation carriersAmanda B Spurdle, Andrew J Deans, David Duffy, et al.
Molecular Carcinogenesis|December 5, 2013
Consequences of germline variation disrupting the constitutional translational initiation codon start sites of MLH1 and BRCA2: Use of potential alternative start sites and implications for predicting variant pathogenicityMichael T Parsons, Phillip J Whiley, Jonathan Beesley, et al.
American Journal of Human Genetics|June 6, 2025
Insights on improving accessibility and usability of functional data to unlock their potential for variant interpretationMin Seon Park, Runjun D Kumar, Cristian Ovadiuc, et al.
Pageof 40