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Amanda Gammon

Showing results (11-20 of 34) with videos related to

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Research Square|May 27, 2024
Newborn Screening for Li-Fraumeni Syndrome: Patient PerspectivesMakenna Beigh, Jennie Vagher, Rachel Codden, et al.
JCO Precision Oncology|February 1, 2022
Comparison of Somatic and Germline Variant Interpretation in Hereditary Cancer GenesEmily W Moody, Jennie Vagher, Whitney Espinel, et al.
Journal of Genetic Counseling|September 25, 2023
Applying the practice-based competencies to evaluate and characterize the contracting process within genetic counseling sessionsEmma Baldry, Bonnie J Baty, Kimberly A Kaphingst, et al.
Diseases of the Colon and Rectum|October 10, 2013
Serrated polyposis: colonic phenotype, extracolonic features, and familial risk in a large cohortKory W Jasperson, Priyanka Kanth, Anne C Kirchhoff, et al.
Journal of Genetic Counseling|June 15, 2019
Female family members lack understanding of indeterminate negative BRCA1/2 test results shared by probandsDeborah O Himes, Deborah K Gibbons, Wendy C Birmingham, et al.
Health Communication|October 17, 2025
Clinical and Family Conversations Regarding Genetic Testing: A Case Study of Uncertainty ManagementHeather E Canary, Brianne M Daly, Sarah Roberts, et al.
Health Communication|November 22, 2022
Communication About Negative and Uncertain Results: Interactional Dilemmas During a Genetic Telehealth ConsultWayne A Beach, Heather E Canary, Yea-Wen Chen, et al.
Familial Cancer|August 13, 2013
Role of rapid sequence whole-body MRI screening in SDH-associated hereditary paraganglioma familiesKory W Jasperson, Wendy Kohlmann, Amanda Gammon, et al.
Human Mutation|October 13, 2011
Classification of missense substitutions in the BRCA genes: a database dedicated to Ex-UVsMaxime P Vallée, Tiana C Francy, Megan K Judkins, et al.
Cancer|January 14, 2017
A study of over 35,000 women with breast cancer tested with a 25-gene panel of hereditary cancer genesSaundra S Buys, John F Sandbach, Amanda Gammon, et al.
Pageof 4

Showing results (11-20 of 34) with videos related to

Sort By:
Pageof 4
Research Square|May 27, 2024
Newborn Screening for Li-Fraumeni Syndrome: Patient PerspectivesMakenna Beigh, Jennie Vagher, Rachel Codden, et al.
JCO Precision Oncology|February 1, 2022
Comparison of Somatic and Germline Variant Interpretation in Hereditary Cancer GenesEmily W Moody, Jennie Vagher, Whitney Espinel, et al.
Journal of Genetic Counseling|September 25, 2023
Applying the practice-based competencies to evaluate and characterize the contracting process within genetic counseling sessionsEmma Baldry, Bonnie J Baty, Kimberly A Kaphingst, et al.
Diseases of the Colon and Rectum|October 10, 2013
Serrated polyposis: colonic phenotype, extracolonic features, and familial risk in a large cohortKory W Jasperson, Priyanka Kanth, Anne C Kirchhoff, et al.
Journal of Genetic Counseling|June 15, 2019
Female family members lack understanding of indeterminate negative BRCA1/2 test results shared by probandsDeborah O Himes, Deborah K Gibbons, Wendy C Birmingham, et al.
Health Communication|October 17, 2025
Clinical and Family Conversations Regarding Genetic Testing: A Case Study of Uncertainty ManagementHeather E Canary, Brianne M Daly, Sarah Roberts, et al.
Health Communication|November 22, 2022
Communication About Negative and Uncertain Results: Interactional Dilemmas During a Genetic Telehealth ConsultWayne A Beach, Heather E Canary, Yea-Wen Chen, et al.
Familial Cancer|August 13, 2013
Role of rapid sequence whole-body MRI screening in SDH-associated hereditary paraganglioma familiesKory W Jasperson, Wendy Kohlmann, Amanda Gammon, et al.
Human Mutation|October 13, 2011
Classification of missense substitutions in the BRCA genes: a database dedicated to Ex-UVsMaxime P Vallée, Tiana C Francy, Megan K Judkins, et al.
Cancer|January 14, 2017
A study of over 35,000 women with breast cancer tested with a 25-gene panel of hereditary cancer genesSaundra S Buys, John F Sandbach, Amanda Gammon, et al.
Pageof 4