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Public Health Genomics and Precision Health Knowledge Base (v9.0)
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Precision Health Database|Search|Public Health Genomics and Precision Health Knowledge Base (PHGKB)
Last data update: Apr 25, 2024
. (Total: 63675 Documents since 2012)
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Cancer genetic counselling for hereditary breast cancer in the era of precision oncology.
M Pensabene et al. Cancer Treat Rev 2024 125102702
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Influence of family history on penetrance of hereditary cancers in a population setting.
Leigh Jackson et al. EClinicalMedicine 2023 64102159
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Which Patients Do We Need to Test for BRCA1/2 Mutation? Feasibility of Adjuvant Olaparib Treatment in Early Breast Cancer-Real-World Data from Two Large German Breast Centers.
Dominik Dannehl et al. Cancers (Basel) 2023 15(15)
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A comprehensive study on surveillance outcomes of a male population followed at a hereditary breast cancer high-risk consultation at a Portuguese tertiary hospital.
Maria João Oliveira et al. J Cancer Res Clin Oncol 2023
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Genetic testing for hereditary breast cancer in Poland: 1998-2022.
Jacek Gronwald et al. Hered Cancer Clin Pract 2023 21(1) 9
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Effect on Germline Mutation Rate in a High-Risk Chinese Breast Cancer Cohort after Compliance with The National Comprehensive Cancer Network (NCCN) 2023 v.1 Testing Criteria.
Ava Kwong et al. Cancers (Basel) 2023 15(9)
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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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Systematic review of reported association studies of monogenic genes and bladder cancer risk and confirmation analysis in a large population cohort.
Abrar Mian et al. BJUI compass 2023 4(2) 156-163
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Cancer screening and breast cancer family history in Spanish-speaking Hispanic/Latina women in California.
Tamayo Lizeth I et al. Frontiers in oncology 2022 12940162
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Systematic mapping review of guidelines for BRCA1/2 genetic testing globally: investigating geographic and regional disparities in health equity for women and families at risk for hereditary ovarian cancer.
Hughes Brittany N et al. International journal of gynecological cancer : official journal of the International Gynecological Cancer Society 2022
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Hereditary Ovarian Cancer: Towards a Cost-Effective Prevention Strategy.
Ghose Aruni et al. International journal of environmental research and public health 2022 19(19)
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Ovarian cancer risk management in BRCA-mutation carriers: A comparison of six international and national guidelines.
Matan Liat S et al. European journal of obstetrics, gynecology, and reproductive biology 2022 278166-171
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Precise, Genotype-First Breast Cancer Prevention: Experience With Transferring Monogenic Findings From a Population Biobank to the Clinical Setting.
Jürgens Hannes et al. Frontiers in genetics 2022 13881100
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Training promotores to lead virtual hereditary breast cancer education sessions for Spanish-speaking individuals of Latin American heritage in California.
Reyna Micaela et al. BMC women's health 2022 22(1) 336
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Hereditary ovarian cancer risk reduction: a retrospective evaluation of patient perspectives and service provision at a regional hereditary gynaecologic cancer clinic 2006-2016.
Adolph Lauren et al. BMC women's health 2022 22(1) 263
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Mother and Daughter Perspectives on Genetic Counseling and Testing of Adolescents for Hereditary Breast Cancer Risk.
Jennings Catherine et al. The Journal of pediatrics 2022
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Pilot study of a culturally sensitive intervention to promote genetic counseling for breast cancer risk.
Henderson Vida et al. BMC health services research 2022 22(1) 826
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Development, Implementation and Initial Results of CDSS Recommendations for Patients at Risk of Hereditary Breast Cancer.
Rosa Juan et al. Studies in health technology and informatics 2022 290340-344
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How does re-classification of variants of unknown significance (VUS) impact the management of patients at risk for hereditary breast cancer?
Kwong Ava et al. BMC medical genomics 2022 15(1) 122
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Assessing Breast Cancer Risks to Improve Care for an Increased-Risk Population within Eastern North Carolina.
Shelton Charles H et al. North Carolina medical journal 2022 83(3) 221-228
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Histological and Immunohistochemical Characteristics for Hereditary Breast Cancer Risk in a Cohort of Brazilian Women.
de Freitas Renata Mendes et al. Revista brasileira de ginecologia e obstetricia : revista da Federacao Brasileira das Sociedades de Ginecologia e Obstetricia 2022
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Genetic Testing for All: Overcoming Disparities in Ovarian Cancer Genetic Testing.
Frey Melissa K et al. American Society of Clinical Oncology educational book. American Society of Clinical Oncology. Annual Meeting 2022 421-12
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"You Always Have It in the Back of Your Mind"-Feelings, Coping, and Support Needs of Women with Pathogenic Variants in Moderate-Risk Genes for Hereditary Breast Cancer Attending Genetic Counseling in Germany: A Qualitative Interview Study.
Stracke Claudia et al. International journal of environmental research and public health 2022 19(6)
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Evaluation of hereditary/familial breast cancer patients with multigene targeted next generation sequencing panel and MLPA analysis in Turkey.
Bora Elcin et al. Cancer genetics 2022 262-263118-133
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DrABC: deep learning accurately predicts germline pathogenic mutation status in breast cancer patients based on phenotype data.
Liu Jiaqi et al. Genome medicine 2022 14(1) 21
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Hereditary Ovarian Carcinoma: Cancer Pathogenesis Looking beyond BRCA1 and BRCA2.
Samuel David et al. Cells 2022 11(3)
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Challenges and opportunities in the establishment of a hereditary breast cancer clinic at an academic medical center in a low-middle income country.
Ehsan Lubaina et al. Journal of genetic counseling 2022
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An overview of genetic services delivery for hereditary breast cancer.
Reid Sonya et al. Breast cancer research and treatment 2022
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Should all patients undergoing genetic testing for hereditary breast cancer syndromes be offered a multigene panel?
Silver Erica L et al. Current opinion in obstetrics & gynecology 2021 34(1) 36-40
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Detection of BRCA1/2 Mutation and Analysis of Clinicopathological Characteristics in 141 Cases of Ovarian Cancer.
Li Ling et al. Computational and mathematical methods in medicine 2021 20214854282
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Page last reviewed:
Feb 1, 2024
Page last updated:
Apr 25, 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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