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

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

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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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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Hoyeraal-Hreidarsson Syndrome due to PARN Mutations: Fourteen Years of Follow-Up

Pediatric neurology, 2016-03, Vol.56, p.62-68.e1

2016

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Hypogammaglobulinemia and impaired antibody response in a child with chromosome 2p15-16.1 microdeletion syndrome

Annals of allergy, asthma, & immunology, 2015-08, Vol.115 (2), p.153-155

2015

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Prevalence of Heart Failure Stages in a Universal Health Care System: The Military Health System Experience

The American journal of medicine, 2023-11, Vol.136 (11), p.1079-1086.e1

2023

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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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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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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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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, p.4382606-10

2019

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Influence of germline test results on surgical decision making in women with invasive breast cancer

Cancer genetics, 2022-08, Vol.266-267, p.81-85

2022

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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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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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Diagnosis of Bardet-Biedl Syndrome in Consecutive Pregnancies Affected with Echogenic Kidneys and Polydactyly in a Consanguineous Couple

Case reports in genetics, 2013-01, Vol.2013, p.159143-3

2013

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Impact of germline mutations on surgical decision-making in women with DCIS

Journal of clinical oncology, 2022-06, Vol.40 (16_suppl), p.10576-10576

2022

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Trisomy 9 mosaicism and XX sex reversal

American journal of medical genetics. Part A, 2007-11, Vol.143A (22), p.2688-2691

2007

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Abstract 5893: Comprehensive proteogenomic analysis and classification of lung adenocarcinoma

Cancer research (Chicago, Ill.), 2020-08, Vol.80 (16_Supplement), p.5893-5893

2020

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Prevalence of Heart Failure Stages in a Universal Healthcare System The Military Health System Experience

The American journal of medicine, 2023-07

2023

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

Genetics in medicine, 2017-01, Vol.19 (8), p.955-958

2017

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Hypogammaglobulinemia and impaired antibody response in a child with chromosome 2p15-16.1 microdeletion syndrome

Annals of allergy, asthma & immunology : official publication of the American College of Allergy, Asthma, & Immunology, 2015, Vol.115 (2), p.153-155

2015

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Trisomy 9 mosaicism and XX sex reversal

American Journal of Medical Genetics Part A, 2007, Vol.143A (22), p.2688-2691

2007

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

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

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

Hoyeraal-Hreidarsson Syndrome due to PARN Mutations: Fourteen Years of Follow-Up

Hypogammaglobulinemia and impaired antibody response in a child with chromosome 2p15-16.1 microdeletion syndrome

Prevalence of Heart Failure Stages in a Universal Health Care System: The Military Health System Experience

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

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

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

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

Influence of germline test results on surgical decision making in women with invasive breast cancer

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

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

Diagnosis of Bardet-Biedl Syndrome in Consecutive Pregnancies Affected with Echogenic Kidneys and Polydactyly in a Consanguineous Couple

Impact of germline mutations on surgical decision-making in women with DCIS

Trisomy 9 mosaicism and XX sex reversal

Abstract 5893: Comprehensive proteogenomic analysis and classification of lung adenocarcinoma

Prevalence of Heart Failure Stages in a Universal Healthcare System The Military Health System Experience

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

EIF2S3 Mutations Associated with Severe X-Linked Intellectual Disability Syndrome MEHMO: HUMAN MUTATION

De Novo Missense Variants in PPP1CB Are Associated with Intellectual Disabilities and Congenital Heart Disease

Hypogammaglobulinemia and impaired antibody response in a child with chromosome 2p15-16.1 microdeletion syndrome

Trisomy 9 mosaicism and XX sex reversal

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