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Pathogenic and likely pathogenic variant prevalence among the first 10,000 patients referred for next-generation cancer panel testing

Genetics in medicine, 2016-08, Vol.18 (8), p.823-832

2016

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The Evolution of Cancer Risk Assessment in the Era of Next Generation Sequencing

Journal of genetic counseling, 2014-08, Vol.23 (4), p.633-639

2014

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Cancer Genetic Counseling and Testing in an Era of Rapid Change

Journal of genetic counseling, 2017-12, Vol.26 (6), p.1244-1253

2017

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Accuracy of Perceived Breast Cancer Risk in Black and White Women with an Elevated Risk

Ethnicity & disease, 2022-04, Vol.32 (2), p.81-90

2022

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Urologists' Current Practices in Screening and Treating Men with a Family History of Prostate Cancer

Urology (Ridgewood, N.J.), 2017-01, Vol.99, p.180-185

2017

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Alcohol and Tobacco Lower the Age of Presentation in Sporadic Pancreatic Cancer in a Dose-Dependent Manner: A Multicenter Study

The American journal of gastroenterology, 2012-11, Vol.107 (11), p.1730-1739

2012

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Utilization of breast cancer risk prediction models by cancer genetic counselors in clinical practice predominantly in the United States

Journal of genetic counseling, 2021-12, Vol.30 (6), p.1737-1747

2021

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Initial clinical validation of Health Heritage, a patient-facing tool for personal and family history collection and cancer risk assessment

Familial cancer, 2016-04, Vol.15 (2), p.331-339

2016

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BRCA1 and BRCA2 Genetic Testing in Hispanic Patients: Mutation Prevalence and Evaluation of the BRCAPRO Risk Assessment Model

Journal of clinical oncology, 2007-10, Vol.25 (29), p.4635-4641

2007

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FDA Approval of PARP Inhibitors and the Impact on Genetic Counseling and Genetic Testing Practices

Journal of genetic counseling, 2018-02, Vol.27 (1), p.131-139

2018

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Monoallelic MUTYH pathogenic variants ascertained via multi-gene hereditary cancer panels are not associated with colorectal, endometrial, or breast cancer

Familial cancer, 2022-10, Vol.21 (4), p.415-422

2022

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Evaluation of laboratory perspectives on hereditary cancer panels

Familial cancer, 2016-10, Vol.15 (4), p.689-696

2016

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Family Physicians’ Awareness and Knowledge of the Genetic Information Non-Discrimination Act (GINA)

Journal of genetic counseling, 2012-04, Vol.21 (2), p.345-352

2012

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Learning to Say No

Journal of genetic counseling, 2012-04, Vol.21 (2), p.237-238

Vogel, Kristen J.

2012

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Cancer genetic testing panels for inherited cancer susceptibility: the clinical experience of a large adult genetics practice

Familial cancer, 2014-12, Vol.13 (4), p.527-536

2014

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Genetic counselors’ perspectives on population‐based screening for BRCA‐related hereditary breast and ovarian cancer and Lynch syndrome

Journal of genetic counseling, 2021-02, Vol.30 (1), p.158-169

2021

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Tu1874 Earlier Age of Presentation of Pancreatic Adenocarcinoma in Individuals With Chronic Pancreatitis

Gastroenterology (New York, N.Y. 1943), 2013-05, Vol.144 (5), p.S-869-S-869

2013

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10 rare tumors that warrant a genetics referral

Familial cancer, 2013-03, Vol.12 (1), p.1-18

2013

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Using a Family History Intervention to Improve Cancer Risk Perception in a Black Community

Journal of genetic counseling, 2011-12, Vol.20 (6), p.639-649

2011

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Accuracy of the BRCAPRO model among women with bilateral breast cancer

Cancer, 2009-02, Vol.115 (4), p.725-730

2009

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High prevalence of preinvasive lesions adjacent to BRCA1/2-associated breast cancers

Cancer prevention research (Philadelphia, Pa.), 2009-02, Vol.2 (2), p.122-127

2009

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The Use of Family Health Histories to Address Health Disparities in an African American Community

Health promotion practice, 2007-10, Vol.8 (4), p.350-357

2007

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PD35-07 PROSTATE CANCER RISKS IN MALE BRCA1/2 PATHOGENIC VARIANT CARRIERS

The Journal of urology, 2019-04, Vol.201 (Supplement 4)

2019

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Cancer risk assessment using an automated electronic patient-facing tool for the collection and evaluation of family history

Journal of clinical oncology, 2016-05, Vol.34 (15_suppl), p.e13055-e13055

2016

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Mosaic TP53 pathogenic variants on multi-gene hereditary cancer panel testing: Clinical characteristics and follow-up testing

Journal of clinical oncology, 2018-05, Vol.36 (15_suppl), p.1580-1580

2018

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Pathogenic and likely pathogenic variant prevalence among the first 10,000 patients referred for next-generation cancer panel testing

The Evolution of Cancer Risk Assessment in the Era of Next Generation Sequencing

Cancer Genetic Counseling and Testing in an Era of Rapid Change

Accuracy of Perceived Breast Cancer Risk in Black and White Women with an Elevated Risk

Urologists' Current Practices in Screening and Treating Men with a Family History of Prostate Cancer

Alcohol and Tobacco Lower the Age of Presentation in Sporadic Pancreatic Cancer in a Dose-Dependent Manner: A Multicenter Study

Utilization of breast cancer risk prediction models by cancer genetic counselors in clinical practice predominantly in the United States

Initial clinical validation of Health Heritage, a patient-facing tool for personal and family history collection and cancer risk assessment

BRCA1 and BRCA2 Genetic Testing in Hispanic Patients: Mutation Prevalence and Evaluation of the BRCAPRO Risk Assessment Model

FDA Approval of PARP Inhibitors and the Impact on Genetic Counseling and Genetic Testing Practices

Monoallelic MUTYH pathogenic variants ascertained via multi-gene hereditary cancer panels are not associated with colorectal, endometrial, or breast cancer

Evaluation of laboratory perspectives on hereditary cancer panels

Family Physicians’ Awareness and Knowledge of the Genetic Information Non-Discrimination Act (GINA)

Learning to Say No

Cancer genetic testing panels for inherited cancer susceptibility: the clinical experience of a large adult genetics practice

Genetic counselors’ perspectives on population‐based screening for BRCA‐related hereditary breast and ovarian cancer and Lynch syndrome

Tu1874 Earlier Age of Presentation of Pancreatic Adenocarcinoma in Individuals With Chronic Pancreatitis

10 rare tumors that warrant a genetics referral

Using a Family History Intervention to Improve Cancer Risk Perception in a Black Community

Accuracy of the BRCAPRO model among women with bilateral breast cancer

High prevalence of preinvasive lesions adjacent to BRCA1/2-associated breast cancers

The Use of Family Health Histories to Address Health Disparities in an African American Community

PD35-07 PROSTATE CANCER RISKS IN MALE BRCA1/2 PATHOGENIC VARIANT CARRIERS

Cancer risk assessment using an automated electronic patient-facing tool for the collection and evaluation of family history

Mosaic TP53 pathogenic variants on multi-gene hereditary cancer panel testing: Clinical characteristics and follow-up testing

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