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Hereditary Breast and Ovarian Cancer: An Updated Primer for OB/GYNs

Obstetrics and gynecology clinics of North America, 2022-03, Vol.49 (1), p.117-147

Bellcross, Cecelia A

2022

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Awareness and Utilization of BRCA1/2 Testing Among U.S. Primary Care Physicians

American journal of preventive medicine, 2011, Vol.40 (1), p.61-66

2011

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Validation of Version 3.0 of the Breast Cancer Genetics Referral Screening Tool (B-RST™)

Genetics in medicine, 2019-01, Vol.21 (1), p.181-184

2019

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Prevalence and Healthcare Actions of Women in a Large Health System with a Family History Meeting the 2005 USPSTF Recommendation for BRCA Genetic Counseling Referral

Cancer epidemiology, biomarkers & prevention, 2013-04, Vol.22 (4), p.728-735

2013

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Screening for Individuals at Risk for Hereditary Breast and Ovarian Cancer: A Statewide Initiative, Georgia, 2012–2020

American journal of public health (1971), 2022-09, Vol.112 (9), p.1249-1252

2022

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Willingness to decrease mammogram frequency among women at low risk for hereditary breast cancer

Scientific reports, 2019-07, Vol.9 (1), p.9599-10, Article 9599

2019

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Do Women who Receive a Negative BRCA1/2 Risk Result Understand the Implications for Breast Cancer Risk?

Public health genomics, 2019, Vol.22 (3/4), p.102-109

2019

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Evaluation of a breast/ovarian cancer genetics referral screening tool in a mammography population

Genetics in medicine, 2009-11, Vol.11 (11), p.783-789

2009

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Characteristics associated with genetic counseling referral and BRCA1/2 testing among women in a large integrated health system

Genetics in medicine, 2015-01, Vol.17 (1), p.43-50

2015

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Evaluating Differences in the Disease Experiences of Minority Adults With Cystic Fibrosis

Journal of patient experience, 2022, Vol.9, p.237437352211126-23743735221112629

2022

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Direct-to-consumer personal genome testing and cancer risk prediction

The cancer journal (Sudbury, Mass.), 2012-07, Vol.18 (4), p.293

2012

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Hereditary breast/ovarian cancer syndrome: a primer for obstetricians/gynecologists

Obstetrics and gynecology clinics of North America, 2013-09, Vol.40 (3), p.475-512

2013

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Implementing a Screening Tool for Identifying Patients at Risk for Hereditary Breast and Ovarian Cancer: A Statewide Initiative

Annals of surgical oncology, 2014-10, Vol.21 (10), p.3342-3347

2014

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Implementing screening for Lynch syndrome among patients with newly diagnosed colorectal cancer: summary of a public health/clinical collaborative meeting

Genetics in medicine, 2012-01, Vol.14 (1), p.152-162

2012

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The Impact of Genetic Counseling Educational Tools on Patients’ Knowledge of Molecular Testing Terminology

Journal of cancer education, 2020-10, Vol.35 (5), p.864-870

2020

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The changing landscape of genetic testing for hereditary breast and ovarian cancer

Current problems in cancer, 2014-11, Vol.38 (6), p.209-215

Bellcross, Cecelia A., PhD, MS, CGC

2014

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Evaluation and comparison of hereditary Cancer guidelines in the population

Hereditary cancer in clinical practice, 2021-07, Vol.19 (1), p.31-31, Article 31

2021

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Hereditary Breast and Ovarian Cancer

Obstetrics and gynecology clinics of North America, 2022-03, Vol.49 (1), p.117-147

Bellcross, Cecelia A.

2022

Volltextzugriff (PDF)

Georgia Primary Care Providers’ Knowledge of Hereditary Breast and Ovarian Cancer Syndrome

Journal of cancer education, 2017-03, Vol.32 (1), p.119-124

2017

Volltextzugriff (PDF)

Infrastructure and Educational Needs of Newborn Screening Short-Term Follow-Up Programs within the Southeast Regional Newborn Screening & Genetics Collaborative: A Pilot Survey

Healthcare (Basel), 2015-10, Vol.3 (4), p.964-972

2015

Volltextzugriff (PDF)

Automated Clinical Practice Guideline Recommendations for Hereditary Cancer Risk Using Chatbots and Ontologies: System Description

JMIR cancer, 2022-01, Vol.8 (1), p.e29289-e29289

2022

Volltextzugriff (PDF)

Genetic Counseling Considerations in the Evaluation of Families for Lynch Syndrome—A Review

Journal of genetic counseling, 2011-02, Vol.20 (1), p.5-19

2011

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Further development and evaluation of a breast/ovarian cancer genetics referral screening tool

Genetics in medicine, 2010-04, Vol.12 (4), p.240-240

Bellcross, Cecelia

2010

Volltextzugriff (PDF)

Hereditary Breast/Ovarian Cancer Syndrome

Obstetrics and gynecology clinics of North America, 2013-09, Vol.40 (3), p.475-512

2013

Volltextzugriff (PDF)

Genetic counselors' perceptions of student supervision across service delivery models

Journal of genetic counseling, 2023-12, Vol.32 (6), p.1314-1324

2023

Volltextzugriff (PDF)

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Hereditary Breast and Ovarian Cancer: An Updated Primer for OB/GYNs

Awareness and Utilization of BRCA1/2 Testing Among U.S. Primary Care Physicians

Validation of Version 3.0 of the Breast Cancer Genetics Referral Screening Tool (B-RST™)

Prevalence and Healthcare Actions of Women in a Large Health System with a Family History Meeting the 2005 USPSTF Recommendation for BRCA Genetic Counseling Referral

Screening for Individuals at Risk for Hereditary Breast and Ovarian Cancer: A Statewide Initiative, Georgia, 2012–2020

Willingness to decrease mammogram frequency among women at low risk for hereditary breast cancer

Do Women who Receive a Negative BRCA1/2 Risk Result Understand the Implications for Breast Cancer Risk?

Evaluation of a breast/ovarian cancer genetics referral screening tool in a mammography population

Characteristics associated with genetic counseling referral and BRCA1/2 testing among women in a large integrated health system

Evaluating Differences in the Disease Experiences of Minority Adults With Cystic Fibrosis

Direct-to-consumer personal genome testing and cancer risk prediction

Hereditary breast/ovarian cancer syndrome: a primer for obstetricians/gynecologists

Implementing a Screening Tool for Identifying Patients at Risk for Hereditary Breast and Ovarian Cancer: A Statewide Initiative

Implementing screening for Lynch syndrome among patients with newly diagnosed colorectal cancer: summary of a public health/clinical collaborative meeting

The Impact of Genetic Counseling Educational Tools on Patients’ Knowledge of Molecular Testing Terminology

The changing landscape of genetic testing for hereditary breast and ovarian cancer

Evaluation and comparison of hereditary Cancer guidelines in the population

Hereditary Breast and Ovarian Cancer

Georgia Primary Care Providers’ Knowledge of Hereditary Breast and Ovarian Cancer Syndrome

Infrastructure and Educational Needs of Newborn Screening Short-Term Follow-Up Programs within the Southeast Regional Newborn Screening & Genetics Collaborative: A Pilot Survey

Automated Clinical Practice Guideline Recommendations for Hereditary Cancer Risk Using Chatbots and Ontologies: System Description

Genetic Counseling Considerations in the Evaluation of Families for Lynch Syndrome—A Review

Further development and evaluation of a breast/ovarian cancer genetics referral screening tool

Hereditary Breast/Ovarian Cancer Syndrome

Genetic counselors' perceptions of student supervision across service delivery models

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