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

Georgia L Wiesner

Showing results (11-20 of 71) with videos related to

Pageof 8
Sort By:
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|November 8, 2006
Validation of a self-administered, computerized tool for collecting and displaying the family history of cancerLouise S Acheson, Stephen J Zyzanski, Kurt C Stange, et al.
Journal of Empirical Research on Human Research Ethics : JERHRE|March 19, 2010
Attitudes toward genetic research review: results from a national survey of professionals involved in human subjects protectionAmy A Lemke, Susan B Trinidad, Karen L Edwards, et al.
Primary Care|August 28, 2004
Clinical consult: developmental delay/fragile X syndromeGeorgia L Wiesner, Suzanne B Cassidy, Sarah J Grimes, et al.
Annals of Diagnostic Pathology|July 29, 2018
Subsequent breast and high grade serous carcinomas after risk-reducing salpingo-oophorectomy in BRCA mutation carriers and patients with history of breast cancerMelissa M Straub, Mirna B Podoll, Stephanie N David, et al.
Molecular Genetics & Genomic Medicine|April 25, 2020
Patient perspectives on variant reclassification after cancer susceptibility testingColin M E Halverson, Laurie M Connors, Bronson C Wessinger, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 8, 2018
The impact of variant classification on the clinical management of hereditary cancer syndromesScott A Turner, Smita K Rao, R Hayes Morgan, et al.
Journal of Community Genetics|January 3, 2021
Increased ease of access to genetic counseling for low-income women with breast cancer using a point of care screening toolSmita K Rao, Kimberly A Thomas, Rajbir Singh, et al.
Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association for Cancer Research, Cosponsored by the American Society of Preventive Oncology|May 18, 2007
Is TGFBR1*6A a susceptibility allele for nonsyndromic familial colorectal neoplasia?Denise Daley, Wendi Morgan, Susan Lewis, et al.
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|April 22, 2003
Duty to warn at-risk relatives for genetic disease: genetic counselors' clinical experienceR Beth Dugan, Georgia L Wiesner, Eric T Juengst, et al.
Cancer|January 23, 2020
Breast cancer screening implications of risk modeling among female relatives of ATM and CHEK2 carriersAnne E Weidner, Mariel E Liggin, Brenda I Zuniga, et al.
Pageof 8

Showing results (11-20 of 71) with videos related to

Sort By:
Pageof 8
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|November 8, 2006
Validation of a self-administered, computerized tool for collecting and displaying the family history of cancerLouise S Acheson, Stephen J Zyzanski, Kurt C Stange, et al.
Journal of Empirical Research on Human Research Ethics : JERHRE|March 19, 2010
Attitudes toward genetic research review: results from a national survey of professionals involved in human subjects protectionAmy A Lemke, Susan B Trinidad, Karen L Edwards, et al.
Primary Care|August 28, 2004
Clinical consult: developmental delay/fragile X syndromeGeorgia L Wiesner, Suzanne B Cassidy, Sarah J Grimes, et al.
Annals of Diagnostic Pathology|July 29, 2018
Subsequent breast and high grade serous carcinomas after risk-reducing salpingo-oophorectomy in BRCA mutation carriers and patients with history of breast cancerMelissa M Straub, Mirna B Podoll, Stephanie N David, et al.
Molecular Genetics & Genomic Medicine|April 25, 2020
Patient perspectives on variant reclassification after cancer susceptibility testingColin M E Halverson, Laurie M Connors, Bronson C Wessinger, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 8, 2018
The impact of variant classification on the clinical management of hereditary cancer syndromesScott A Turner, Smita K Rao, R Hayes Morgan, et al.
Journal of Community Genetics|January 3, 2021
Increased ease of access to genetic counseling for low-income women with breast cancer using a point of care screening toolSmita K Rao, Kimberly A Thomas, Rajbir Singh, et al.
Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association for Cancer Research, Cosponsored by the American Society of Preventive Oncology|May 18, 2007
Is TGFBR1*6A a susceptibility allele for nonsyndromic familial colorectal neoplasia?Denise Daley, Wendi Morgan, Susan Lewis, et al.
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|April 22, 2003
Duty to warn at-risk relatives for genetic disease: genetic counselors' clinical experienceR Beth Dugan, Georgia L Wiesner, Eric T Juengst, et al.
Cancer|January 23, 2020
Breast cancer screening implications of risk modeling among female relatives of ATM and CHEK2 carriersAnne E Weidner, Mariel E Liggin, Brenda I Zuniga, et al.
Pageof 8