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Public Health Genomics and Precision Health Knowledge Base (v9.0)
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Public Health Genomics Branch
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Precision Health Database|Search|Public Health Genomics and Precision Health Knowledge Base (PHGKB)
Last data update: May 08, 2024
. (Total: 63790 Documents since 2012)
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Cost-effectiveness of BRCA1 testing at time of obstetrical prenatal carrier screening for cancer prevention.
Shayan M Dioun et al. Am J Obstet Gynecol 2024
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Population-based BRCA germline mutation screening in the Han Chinese identifies individuals at risk of BRCA mutation-related cancer: experience from a clinical diagnostic center from greater Shanghai area.
Zhiyuan Wu et al. BMC Cancer 2024 24(1) 411
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Challenges and opportunities for Lynch syndrome cascade testing in the United States.
Lauren E Passero et al. Fam Cancer 2024
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A Scoping Review of Personalized, Interactive, Web-Based Clinical Decision Tools Available for Breast Cancer Prevention and Screening in the United States.
Dalya Kamil et al. MDM Policy Pract 2024 9(1) 23814683241236511
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Efficacy of Community Health Worker-Delivered Family Health History-Based Breast Cancer Education and Services Among Chinese Americans.
Bertille Assoumou et al. J Cancer Educ 2024
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Cost-Effectiveness of Population-Based Multigene Testing for Breast and Ovarian Cancer Prevention.
Fangjian Guo et al. JAMA Netw Open 2024 7(2) e2356078
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Utilizing Human Genetics to Develop Chemoprevention for Cancer-Too Good an Opportunity to be Missed.
Ulrike Peters et al. Cancer Prev Res (Phila) 2024 17(1) 7-12
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Genetic Testing for Successful Cancer Treatment.
Desh Nidhi Singh et al. Cureus 2024 15(12) e49889
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Only 32.3% of Breast Cancer Families with Pathogenic Variants in Cancer Genes Utilized Cascade Genetic Testing.
Konstantinos Agiannitopoulos et al. Cancers (Basel) 2023 15(21)
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Cascade testing in Italian Hereditary Breast Ovarian Cancer families: a missed opportunity for cancer prevention?
Lucia Trevisan et al. Fam Cancer 2023
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Management of breast cancer patients with BRCA gene mutations in Jordan: perspectives and challenges.
Hikmat Abdel-Razeq et al. Hosp Pract (1995) 2023 1-8
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Hereditary cancer testing in a diverse sample across three breast imaging centers.
Laura Westbrook et al. Breast Cancer Res Treat 2023
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"There should be one spot that you can go:" BRCA mutation carriers' perspectives on cancer risk management and a hereditary cancer registry.
J Hynes et al. J Community Genet 2023
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Implementation of Risk-Stratified Breast Cancer Prevention With a Polygenic Risk Score Test in Clinical Practice.
Peeter Padrik et al. Breast Cancer (Auckl) 2023 1711782234231205700
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Germline Cancer Genetic Counseling: Clinical Care for Transgender and Nonbinary Individuals.
Suzanne M Mahon et al. Clin J Oncol Nurs 2023 27(4) 442-447
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Intentions of Patients With Cancer and Their Relatives to Use a Live Chat on Familial Cancer Risk: Results From a Cross-Sectional Web-Based Survey.
Paula Memenga et al. J Med Internet Res 2023 25e45198
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Opportunistic genetic screening increases the diagnostic yield and is medically valuable for care of patients and their relatives with hereditary cancer.
Sara Fernández-Castillejo et al. J Med Genet 2023
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A Community Health Worker Model to Support Hereditary Cancer Risk Assessment and Genetic Testing.
Leah Marsh et al. Obstet Gynecol 2023
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Germline mutations in 12 genes and risk of ovarian cancer in three population-based cohorts.
Joanne Kotsopoulos et al. Cancer Epidemiol Biomarkers Prev 2023
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Predicting Breast Cancer Risk for Women Veterans of African Ancestry in the Million Veteran Program.
Shiuh-Wen Luoh et al. Health Equity 2023 7(1) 303-306
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Privacy and utility of genetic testing in families with hereditary cancer syndromes living in three countries: the international cascade genetic screening experience.
Sivia Barnoy et al. Front Genet 2023 141109431
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Prediction of breast cancer risk for sisters of women attending screening.
Xinhe Mao et al. J Natl Cancer Inst 2023
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Extended Family Outreach in Hereditary Cancer Using Web-Based Genealogy, Direct-to-Consumer Ancestry Genetics, and Social Media: Mixed Methods Process Evaluation of the ConnectMyVariant Intervention.
Annie T Chen et al. JMIR Cancer 9e43126
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Breast cancer genetics and risk assessment: an overview for the clinician.
L Larkin et al. Climacteric : the journal of the International Menopause Society 2023 1-6
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Universal screening for Lynch syndrome in operated colorectal cancer by immunohistochemistry: a cohort of patients in Liaoning province, China.
Guangyue Zhao et al. European journal of cancer prevention : the official journal of the European Cancer Prevention Organisation (ECP) 2023
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Information needs on nutrition in link to cancer prevention among cancer patients, high-risk individuals and general population - A national cross-sectional study.
L Veron et al. Clinical nutrition ESPEN 2023 54421-429
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Communicating risk and the landscape of cancer prevention - an exploratory study that examines perceptions of cancer-related genetic counseling and testing among African Americans and Latinos in the Midwest.
Crystal Y Lumpkins et al. Journal of community genetics 2023 1-13
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Rare germline variants in pancreatic cancer and multiple primary cancers: an autopsy study.
Hiroo Fujitani et al. European journal of cancer prevention : the official journal of the European Cancer Prevention Organisation (ECP) 2023
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Validation of an abridged breast cancer risk prediction model for the general population.
Erika L Spaeth et al. Cancer prevention research (Philadelphia, Pa.) 2023
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Cancer Genetic Services in a Low- to Middle-Income Country: Cross-Sectional Survey Assessing Willingness to Undergo and Pay for Germline Genetic Testing.
Prisca O Adejumo et al. JCO global oncology 2023 9e2100140
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Page last reviewed:
Feb 1, 2024
Page last updated:
May 08, 2024
Content source:
Public Health Genomics Branch in the Division of Blood Disorders and Public Health Genomics
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National Center on Birth Defects and Developmental Disabilities
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