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Randomized Noninferiority Trial of Telephone vs In-Person Genetic Counseling for Hereditary Breast and Ovarian Cancer: A 12-Month Follow-Up.
JNCI Cancer Spectr
15
2017
Hereditary Breast and Ovarian Cancer, TC, UC, cancer, patient, women
Author NameAffiliation
Morgan SimilukGeorgetown Lombardi Comprehensive Cancer Center (MKI, MDS) and Jess and Mildred Fisher Center for Hereditary Cancer and Clinical Genomics Research (MKI, Georgetown University, Icahn School of Medicine at Mount Sinai, Reykjavik University, Iceland (HBV) School of Medicine, University of Maryland, MD (RN) National Institute of Allergy and Infectious Diseases, National Institutes of Health, Inova Translational Medicine Institute, Inova Health System, TN (GH) Familial Cancer Program of the Vermont Cancer Center, University of Vermont College of Medicine, WM) Center for Cancer Genetics and Prevention, Dana-Farber Cancer Institute-Harvard Medical School, SM) Center for Cancer Risk Assessment, Massachusetts General Hospital Cancer Center, MA (SM) Carol G. Simon Cancer Center, Atlantic Health Services, NJ (JH) University of Utah School of Medicine and Huntsman Cancer Institute, University of New Mexico Cancer Center
Claudine IsaacsGeorgetown Lombardi Comprehensive Cancer Center (MKI, MDS) and Jess and Mildred Fisher Center for Hereditary Cancer and Clinical Genomics Research (MKI, Georgetown University, Icahn School of Medicine at Mount Sinai, Reykjavik University, Iceland (HBV) School of Medicine, University of Maryland, MD (RN) National Institute of Allergy and Infectious Diseases, National Institutes of Health, Inova Translational Medicine Institute, Inova Health System, TN (GH) Familial Cancer Program of the Vermont Cancer Center, University of Vermont College of Medicine, WM) Center for Cancer Genetics and Prevention, Dana-Farber Cancer Institute-Harvard Medical School, SM) Center for Cancer Risk Assessment, Massachusetts General Hospital Cancer Center, MA (SM) Carol G. Simon Cancer Center, Atlantic Health Services, NJ (JH) University of Utah School of Medicine and Huntsman Cancer Institute, University of New Mexico Cancer Center
Judy E GarberGeorgetown Lombardi Comprehensive Cancer Center (MKI, MDS) and Jess and Mildred Fisher Center for Hereditary Cancer and Clinical Genomics Research (MKI, Georgetown University, Icahn School of Medicine at Mount Sinai, Reykjavik University, Iceland (HBV) School of Medicine, University of Maryland, MD (RN) National Institute of Allergy and Infectious Diseases, National Institutes of Health, Inova Translational Medicine Institute, Inova Health System, TN (GH) Familial Cancer Program of the Vermont Cancer Center, University of Vermont College of Medicine, WM) Center for Cancer Genetics and Prevention, Dana-Farber Cancer Institute-Harvard Medical School, SM) Center for Cancer Risk Assessment, Massachusetts General Hospital Cancer Center, MA (SM) Carol G. Simon Cancer Center, Atlantic Health Services, NJ (JH) University of Utah School of Medicine and Huntsman Cancer Institute, University of New Mexico Cancer Center
Stephen M SchwartzGeorgetown Lombardi Comprehensive Cancer Center (MKI, MDS) and Jess and Mildred Fisher Center for Hereditary Cancer and Clinical Genomics Research (MKI, Georgetown University, Icahn School of Medicine at Mount Sinai, Reykjavik University, Iceland (HBV) School of Medicine, University of Maryland, MD (RN) National Institute of Allergy and Infectious Diseases, National Institutes of Health, Inova Translational Medicine Institute, Inova Health System, TN (GH) Familial Cancer Program of the Vermont Cancer Center, University of Vermont College of Medicine, WM) Center for Cancer Genetics and Prevention, Dana-Farber Cancer Institute-Harvard Medical School, SM) Center for Cancer Risk Assessment, Massachusetts General Hospital Cancer Center, MA (SM) Carol G. Simon Cancer Center, Atlantic Health Services, NJ (JH) University of Utah School of Medicine and Huntsman Cancer Institute, University of New Mexico Cancer Center
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