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Jeffrey N Weitzel

Showing results (21-30 of 220) with videos related to

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Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 17, 2007
Selection of family members for communication of cancer risk and barriers to this communication before and after genetic cancer risk assessmentDeborah J MacDonald, Linda Sarna, Gwen van Servellen, et al.
Clinical Breast Cancer|December 17, 2008
BRCA mutations and the risk of angiosarcoma after breast cancer treatmentJohn G West, Jeffrey N Weitzel, May Lin Tao, et al.
Translational Gastroenterology and Hepatology|August 30, 2019
Genetics of gastric cancer: what do we know about the genetic risks?Thomas Paul Slavin, Jeffrey N Weitzel, Susan L Neuhausen, et al.
Journal of Health Communication|July 29, 2008
Comparison of Latina and non-Latina white women's beliefs about communicating genetic cancer risk to relativesDeborah J MacDonald, Linda Sarna, Joyce Newman Giger, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 18, 2005
Outcomes from intensive training in genetic cancer risk counseling for cliniciansKathleen R Blazer, Deborah J MacDonald, Charite Ricker, et al.
Archives of Surgery (Chicago, Ill. : 1960)|December 10, 2003
Effect of genetic cancer risk assessment on surgical decisions at breast cancer diagnosisJeffrey N Weitzel, Sarah M McCaffrey, Raluca Nedelcu, et al.
Familial Cancer|December 8, 2009
Evolving perspectives on genetic discrimination in health insurance among health care providersCarin R Huizenga, Katrina Lowstuter, Kimberly C Banks, et al.
Breast Cancer Research : BCR|September 20, 2019
Li-Fraumeni syndrome: not a straightforward diagnosis anymore-the interpretation of pathogenic variants of low allele frequency and the differences between germline PVs, mosaicism, and clonal hematopoiesisFelipe Batalini, Ellie G Peacock, Lindsey Stobie, et al.
Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association for Cancer Research, Cosponsored by the American Society of Preventive Oncology|July 21, 2005
Prevalence of BRCA mutations and founder effect in high-risk Hispanic familiesJeffrey N Weitzel, Veronica Lagos, Kathleen R Blazer, et al.
Gynecologic Oncology|November 3, 2011
BRCA1 and BRCA2 mutations among ovarian cancer patients from ColombiaAlexandra Ortiz Rodríguez, Marcia Llacuachaqui, Gonzalo Guevara Pardo, et al.
Pageof 22

Showing results (21-30 of 220) with videos related to

Sort By:
Pageof 22
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 17, 2007
Selection of family members for communication of cancer risk and barriers to this communication before and after genetic cancer risk assessmentDeborah J MacDonald, Linda Sarna, Gwen van Servellen, et al.
Clinical Breast Cancer|December 17, 2008
BRCA mutations and the risk of angiosarcoma after breast cancer treatmentJohn G West, Jeffrey N Weitzel, May Lin Tao, et al.
Translational Gastroenterology and Hepatology|August 30, 2019
Genetics of gastric cancer: what do we know about the genetic risks?Thomas Paul Slavin, Jeffrey N Weitzel, Susan L Neuhausen, et al.
Journal of Health Communication|July 29, 2008
Comparison of Latina and non-Latina white women's beliefs about communicating genetic cancer risk to relativesDeborah J MacDonald, Linda Sarna, Joyce Newman Giger, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 18, 2005
Outcomes from intensive training in genetic cancer risk counseling for cliniciansKathleen R Blazer, Deborah J MacDonald, Charite Ricker, et al.
Archives of Surgery (Chicago, Ill. : 1960)|December 10, 2003
Effect of genetic cancer risk assessment on surgical decisions at breast cancer diagnosisJeffrey N Weitzel, Sarah M McCaffrey, Raluca Nedelcu, et al.
Familial Cancer|December 8, 2009
Evolving perspectives on genetic discrimination in health insurance among health care providersCarin R Huizenga, Katrina Lowstuter, Kimberly C Banks, et al.
Breast Cancer Research : BCR|September 20, 2019
Li-Fraumeni syndrome: not a straightforward diagnosis anymore-the interpretation of pathogenic variants of low allele frequency and the differences between germline PVs, mosaicism, and clonal hematopoiesisFelipe Batalini, Ellie G Peacock, Lindsey Stobie, et al.
Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association for Cancer Research, Cosponsored by the American Society of Preventive Oncology|July 21, 2005
Prevalence of BRCA mutations and founder effect in high-risk Hispanic familiesJeffrey N Weitzel, Veronica Lagos, Kathleen R Blazer, et al.
Gynecologic Oncology|November 3, 2011
BRCA1 and BRCA2 mutations among ovarian cancer patients from ColombiaAlexandra Ortiz Rodríguez, Marcia Llacuachaqui, Gonzalo Guevara Pardo, et al.
Pageof 22