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Racial disparities in BRCA testing and cancer risk management across a population‐based sample of young breast cancer survivors

Cancer, 2017-07, Vol.123 (13), p.2497-2505

2017

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Cancer risk management among female BRCA1/2, PALB2, CHEK2, and ATM carriers

Breast cancer research and treatment, 2020-07, Vol.182 (2), p.421-428

2020

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An overview of genetic services delivery for hereditary breast cancer

Breast cancer research and treatment, 2022-02, Vol.191 (3), p.491-500

2022

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International trends in the uptake of cancer risk reduction strategies in women with a BRCA1 or BRCA2 mutation

British journal of cancer, 2019-07, Vol.121 (1), p.15-21

2019

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Management of individuals with germline variants in PALB2: a clinical practice resource of the American College of Medical Genetics and Genomics (ACMG)

Genetics in medicine, 2021-08, Vol.23 (8), p.1416-1423

2021

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Overall Mortality After Diagnosis of Breast Cancer in Men vs Women

JAMA oncology, 2019-11, Vol.5 (11), p.1589

2019

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Current Insights: Evolving Principles and Controversies of Cancer Risk Assessment and Management of Hereditary Cancers

Journal of the National Comprehensive Cancer Network, 2020-07, Vol.18 (7.5), p.964-967

2020

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Diversity in cancer genomics research is a matter of equity and scientific discovery

Genetics in medicine, 2022-03, Vol.24 (3), p.549-551

Pal, Tuya

2022

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Impact of molecular subtype and race on HR+, HER2− breast cancer survival

Breast cancer research and treatment, 2021-10, Vol.189 (3), p.845-852

2021

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Enhancing Cancer care of rural dwellers through telehealth and engagement (ENCORE): protocol to evaluate effectiveness of a multi-level telehealth-based intervention to improve rural cancer care delivery

BMC cancer, 2021-11, Vol.21 (1), p.1262-1262, Article 1262

2021

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Systematic Review and Meta-analysis of Ovarian Cancers: Estimation of Microsatellite-High Frequency and Characterization of Mismatch Repair Deficient Tumor Histology

Clinical cancer research, 2008-11, Vol.14 (21), p.6847-6854

2008

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Disparities in BRCA counseling across providers in a diverse population of young breast cancer survivors

Genetics in medicine, 2020-06, Vol.22 (6), p.1088-1093

2020

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BRCA1 and BRCA2 mutations account for a large proportion of ovarian carcinoma cases

Cancer, 2005-12, Vol.104 (12), p.2807-2816

2005

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The Development and Evaluation of Novel Patient Educational Material for a Variant of Uncertain Significance (VUS) Result in Hereditary Cancer Genes

Current oncology (Toronto), 2024-06, Vol.31 (6), p.3361-3378

2024

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P070: Impact of genetic test result recall on adherence to cancer risk management recommendations

Genetics in Medicine Open, 2024, Vol.2, p.100952, Article 100952

2024

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IMProving care After inherited Cancer Testing (IMPACT) study: protocol of a randomized trial evaluating the efficacy of two interventions designed to improve cancer risk management and family communication of genetic test results

BMC cancer, 2021-10, Vol.21 (1), p.1099-1099, Article 1099

2021

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Impact of Genetic Testing on Risk-Management Behavior of Black Breast Cancer Survivors: A Longitudinal, Observational Study

Annals of surgical oncology, 2020-05, Vol.27 (5), p.1659-1670

2020

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Piloting a Spanish-Language Web-Based Tool for Hereditary Cancer Genetic Testing

Current oncology (Toronto), 2023-09, Vol.30 (9), p.8352-8362

2023

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A pooled case-only analysis of obesity and breast cancer subtype among Black women in the southeastern United States

Cancer causes & control, 2022-04, Vol.33 (4), p.515-524

2022

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P403: Reasons for pursuing germline genetic testing and family sharing of results among young Black women with breast cancer

Genetics in Medicine Open, 2023, Vol.1 (1), p.100439, Article 100439

2023

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Fertility in women with BRCA mutations: a case-control study

Fertility and sterility, 2010-04, Vol.93 (6), p.1805-1808

2010

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A review of the clinical relevance of mismatch‐repair deficiency in ovarian cancer

Cancer, 2008-08, Vol.113 (4), p.733-742

2008

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Breast cancer risk after age 60 among BRCA1 and BRCA2 mutation carriers

Breast cancer research and treatment, 2021-06, Vol.187 (2), p.515-523

2021

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Genetic/familial high-risk assessment: breast and ovarian, version 1.2014

Journal of the National Comprehensive Cancer Network, 2014-09, Vol.12 (9), p.1326-1338

2014

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Applying the framework for developing and evaluating complex interventions to increase family communication about hereditary cancer

PEC innovation, 2023-12, Vol.2, p.100133-100133, Article 100133

2023

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Racial disparities in BRCA testing and cancer risk management across a population‐based sample of young breast cancer survivors

Cancer risk management among female BRCA1/2, PALB2, CHEK2, and ATM carriers

An overview of genetic services delivery for hereditary breast cancer

International trends in the uptake of cancer risk reduction strategies in women with a BRCA1 or BRCA2 mutation

Management of individuals with germline variants in PALB2: a clinical practice resource of the American College of Medical Genetics and Genomics (ACMG)

Overall Mortality After Diagnosis of Breast Cancer in Men vs Women

Current Insights: Evolving Principles and Controversies of Cancer Risk Assessment and Management of Hereditary Cancers

Diversity in cancer genomics research is a matter of equity and scientific discovery

Impact of molecular subtype and race on HR+, HER2− breast cancer survival

Enhancing Cancer care of rural dwellers through telehealth and engagement (ENCORE): protocol to evaluate effectiveness of a multi-level telehealth-based intervention to improve rural cancer care delivery

Systematic Review and Meta-analysis of Ovarian Cancers: Estimation of Microsatellite-High Frequency and Characterization of Mismatch Repair Deficient Tumor Histology

Disparities in BRCA counseling across providers in a diverse population of young breast cancer survivors

BRCA1 and BRCA2 mutations account for a large proportion of ovarian carcinoma cases

The Development and Evaluation of Novel Patient Educational Material for a Variant of Uncertain Significance (VUS) Result in Hereditary Cancer Genes

P070: Impact of genetic test result recall on adherence to cancer risk management recommendations

IMProving care After inherited Cancer Testing (IMPACT) study: protocol of a randomized trial evaluating the efficacy of two interventions designed to improve cancer risk management and family communication of genetic test results

Impact of Genetic Testing on Risk-Management Behavior of Black Breast Cancer Survivors: A Longitudinal, Observational Study

Piloting a Spanish-Language Web-Based Tool for Hereditary Cancer Genetic Testing

A pooled case-only analysis of obesity and breast cancer subtype among Black women in the southeastern United States

P403: Reasons for pursuing germline genetic testing and family sharing of results among young Black women with breast cancer

Fertility in women with BRCA mutations: a case-control study

A review of the clinical relevance of mismatch‐repair deficiency in ovarian cancer

Breast cancer risk after age 60 among BRCA1 and BRCA2 mutation carriers

Genetic/familial high-risk assessment: breast and ovarian, version 1.2014

Applying the framework for developing and evaluating complex interventions to increase family communication about hereditary cancer

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