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Frequent inactivating germline mutations in DNA repair genes in patients with Ewing sarcoma

Genetics in medicine, 2017-08, Vol.19 (8), p.955-958

2017

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Genetic Counseling Considerations for Military Beneficiaries

Military medicine, 2021-12, Vol.187 (Supplement_1), p.36-39

2021

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Germline mutation landscape of DNA damage repair genes in African Americans with prostate cancer highlights potentially targetable RAD genes

Nature communications, 2022-03, Vol.13 (1), p.1361-1361, Article 1361

2022

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Computational in silico genetic variant prediction tools in cardiovascular disease

Annals of noninvasive electrocardiology, 2023-09, Vol.28 (5), p.e13079-n/a

2023

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Whole-exome sequencing reveals germline-mutated small cell lung cancer subtype with favorable response to DNA repair-targeted therapies

Science translational medicine, 2021-01, Vol.13 (578)

2021

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Eligibility, uptake and response to germline genetic testing in women with DCIS

Frontiers in oncology, 2022-08, Vol.12, p.918757

2022

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Genetic testing in Non-Hispanic Black women with breast cancer treated within an equal-access healthcare system

Genetics in medicine, 2022-01, Vol.24 (1), p.232-237

2022

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Cancer Previvors in an Active Duty Service Women Population: An Opportunity for Prevention and Increased Force Readiness

Military medicine, 2021-07, Vol.186 (7-8), p.e737-e742

2021

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A Review of the Hereditary Component of Triple Negative Breast Cancer: High- and Moderate-Penetrance Breast Cancer Genes, Low-Penetrance Loci, and the Role of Nontraditional Genetic Elements

Journal of oncology, 2019, Vol.2019 (2019), p.1-10

2019

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The ClinSeq Project: piloting large-scale genome sequencing for research in genomic medicine

Genome Research, 2009-09, Vol.19 (9), p.1665-1674

2009

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Applying Pharmacogenomic Guidelines to Combat Medical Care

Military medicine, 2022-01, Vol.187 (Supplement_1), p.18-24

2022

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Heritability of Low ER Staining/HER2-Breast Tumors: Are We Missing an Opportunity for Germline Testing?

Genes, 2020-12, Vol.11 (12), p.1469

2020

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Frequency and spectrum of mutations across 94 cancer predisposition genes in African American women with invasive breast cancer

Familial cancer, 2021-07, Vol.20 (3), p.181-187

2021

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Should Genetic Testing for Cancer Predisposition Be Standard-of-Care for Women with Invasive Breast Cancer? The Murtha Cancer Center Experience

Cancers, 2020-01, Vol.12 (1), p.234

2020

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Toward Personalized Medicine Implementation: Survey of Military Medicine Providers in the Area of Pharmacogenomics

Military medicine, 2020-03, Vol.185 (3-4), p.336-340

2020

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Exercise Dose Associated With Military Service: Implications for the Clinical Management of Inherited Risk for Arrhythmogenic Right Ventricular Cardiomyopathy

Military medicine, 2020-09, Vol.185 (9-10), p.e1447-e1452

2020

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Using a pilot-centric, qualitative drug risk assessment model to identify opportunities for implementing pharmacogenetics

Future journal of pharmaceutical sciences, 2022-09, Vol.8 (1), p.1-8, Article 37

2022

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De novo missense variants in PPP1CB are associated with intellectual disability and congenital heart disease

Human genetics, 2016-12, Vol.135 (12), p.1399-1409

2016

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Military genomics: a perspective on the successes and challenges of genomic medicine in the Armed Services

Molecular genetics & genomic medicine, 2017-11, Vol.5 (6), p.617-620

2017

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O09: Phenome-wide studies of hereditary transthyretin amyloidosis in the All of Us research program

Genetics in Medicine Open, 2024, Vol.2, p.101013, Article 101013

2024

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Management of Incidental Findings in the Era of Next-generation Sequencing

Current genomics, 2015-06, Vol.16 (3), p.159-174

2015

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Abstract P3-14-04: Genetic testing in non-Hispanic Black women with breast cancer treated within an equal-access healthcare system

Cancer research (Chicago, Ill.), 2022-02, Vol.82 (4_Supplement), p.P3-P3-14-04

2022

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Abstract 4624: Should genetic testing for cancer predisposition be standard-of-care for women with invasive breast cancer: The Murtha Cancer Center experience

Cancer research (Chicago, Ill.), 2020-08, Vol.80 (16_Supplement), p.4624-4624

2020

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Small Fiber Neuropathy and Multiple Endocrinopathies with COX6A1 Gene Deletion (P2.113)

Neurology, 2018-04, Vol.90 (15_supplement)

2018

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Frequent inactivating germline mutations in DNA repair genes in patients with Ewing sarcoma

Genetic Counseling Considerations for Military Beneficiaries

Germline mutation landscape of DNA damage repair genes in African Americans with prostate cancer highlights potentially targetable RAD genes

Computational in silico genetic variant prediction tools in cardiovascular disease

Whole-exome sequencing reveals germline-mutated small cell lung cancer subtype with favorable response to DNA repair-targeted therapies

Eligibility, uptake and response to germline genetic testing in women with DCIS

Genetic testing in Non-Hispanic Black women with breast cancer treated within an equal-access healthcare system

Cancer Previvors in an Active Duty Service Women Population: An Opportunity for Prevention and Increased Force Readiness

A Review of the Hereditary Component of Triple Negative Breast Cancer: High- and Moderate-Penetrance Breast Cancer Genes, Low-Penetrance Loci, and the Role of Nontraditional Genetic Elements

EIF2S3 Mutations Associated with Severe X‐Linked Intellectual Disability Syndrome MEHMO

The ClinSeq Project: piloting large-scale genome sequencing for research in genomic medicine

Applying Pharmacogenomic Guidelines to Combat Medical Care

Heritability of Low ER Staining/HER2-Breast Tumors: Are We Missing an Opportunity for Germline Testing?

Frequency and spectrum of mutations across 94 cancer predisposition genes in African American women with invasive breast cancer

Should Genetic Testing for Cancer Predisposition Be Standard-of-Care for Women with Invasive Breast Cancer? The Murtha Cancer Center Experience

Toward Personalized Medicine Implementation: Survey of Military Medicine Providers in the Area of Pharmacogenomics

Exercise Dose Associated With Military Service: Implications for the Clinical Management of Inherited Risk for Arrhythmogenic Right Ventricular Cardiomyopathy

Using a pilot-centric, qualitative drug risk assessment model to identify opportunities for implementing pharmacogenetics

De novo missense variants in PPP1CB are associated with intellectual disability and congenital heart disease

Military genomics: a perspective on the successes and challenges of genomic medicine in the Armed Services

O09: Phenome-wide studies of hereditary transthyretin amyloidosis in the All of Us research program

Management of Incidental Findings in the Era of Next-generation Sequencing

Abstract P3-14-04: Genetic testing in non-Hispanic Black women with breast cancer treated within an equal-access healthcare system

Abstract 4624: Should genetic testing for cancer predisposition be standard-of-care for women with invasive breast cancer: The Murtha Cancer Center experience

Small Fiber Neuropathy and Multiple Endocrinopathies with COX6A1 Gene Deletion (P2.113)

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