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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: Mar 28, 2024
. (Total: 63390 Documents since 2012)
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Ovarian cancer[original query]>>Original Studies[Product Type]
The history of families at-risk for hereditary breast and ovarian cancer: what are the impacts of genetic counseling and testing?
Natalia Campacci et al. Front Psychol 2024 151306388
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Clinical evaluation of a low-coverage whole-genome test for detecting homologous recombination deficiency in ovarian cancer.
Romain Boidot et al. Eur J Cancer 2024 202113978
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Cascade screening in HBOC and Lynch syndrome: guidelines and procedures in a UK centre.
D Gareth Evans et al. Fam Cancer 2024
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[Return of Individual Genomic Results to Germline Pathogenic Variant Carriers of Hereditary Cancer in Population Based Cohort Study].
Kinuko Ohneda et al. Gan To Kagaku Ryoho 2024 51(3) 231-236
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Delivery of hereditary cancer genetics services to patients newly diagnosed with ovarian and endometrial cancers at three gynecologic oncology clinics in the USA, Brazil, and Mexico.
Erica M Bednar et al. Int J Gynecol Cancer 2024
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Mainstream Model of Genetic Testing for Prostate Cancer at a Large Tertiary Cancer Centre.
Xin Wang et al. Clin Genitourin Cancer 2024 102052
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Young Women's Perspectives on Being Screened for Hereditary Breast and Ovarian Cancer Risk During Routine Primary Care.
Mady Head et al. Womens Health Issues 2024
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Implementing mainstream genetic counseling within the area-wide network of the German Consortium Hereditary Breast and Ovarian Cancer (GD-HBOC): Satisfaction of primary care providers with the provided state-of-the-art training by the Cologne Center.
Natalie Herold et al. J Genet Couns 2024
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Germline mutations of 4567 patients with hereditary breast-ovarian cancer spectrum in Thailand.
Chalermkiat Kansuttiviwat et al. NPJ Genom Med 2024 9(1) 9
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Development of an Electronic Decision Aid Tool to Facilitate Mainstream Genetic Testing in Ovarian Cancer Patients.
Kristen M Shannon et al. Oncologist 2024
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Age-specific breast and ovarian cancer risks associated with germline BRCA1 or BRCA2 pathogenic variants – an Asian study of 572 families
WK Ho et al, Lancet Regional Health, February 2024
Talking about Familial Breast and Ovarian Cancer Risk-Evaluation of a Psychosocial Training Module for Gynecologists in Germany.
Friederike Kendel et al. Cancers (Basel) 2024 16(2)
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Ten-Year Follow-Up of Women at High Risk for Familial Breast and Ovarian Cancer in Otago and Southland, New Zealand.
Simone Petrich et al. Asian Pac J Cancer Prev 2024 25(1) 3-7
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Clinical implications of VUS reclassification in a single-centre series from application of ACMG/AMP classification rules specified for BRCA1/2.
Giovanni Innella et al. J Med Genet 2023
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Risk-reducing decisions regarding germline BRCA pathogenic variant: focusing on the timing of genetic testing and RRSO.
Akiko Abe et al. J Med Genet 2023
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Recontact to return new or updated PALB2 genetic results in the clinical laboratory setting.
Seema Panchal et al. J Med Genet 2023
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Secondary (additional) findings from the 100,000 Genomes Project: disease manifestation, healthcare outcomes and costs of disclosure.
Joshua Nolan et al. Genet Med 2023 101051
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Development and testing of patient-centered education about hormone replacement therapy for women at high genetic risk of breast and ovarian cancer.
Katherine N Penvose et al. Gynecol Oncol 2023 18191-98
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Prevalence of Variants of Uncertain Significance in Patients Undergoing Genetic Testing for Hereditary Breast and Ovarian Cancer and Lynch Syndrome.
Pavlina Chrysafi et al. Cancers (Basel) 2023 15(24)
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Air quality and cancer risk in the All of Us Research Program.
Andrew Craver et al. Cancer Causes Control 2023
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Genomic instability analysis in DNA from Papanicolaou test provides proof-of-principle early diagnosis of high-grade serous ovarian cancer.
Lara Paracchini et al. Sci Transl Med 2023 15(725) eadi2556
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Serial circulating-tumor DNA analysis with a tumor naïve next-generation sequencing panel detects minimal residual disease and predicts outcome in ovarian cancer.
Jinho Heo et al. Cancer Res 2023
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Molecular landscape of ERBB2/HER2 gene amplification among patients with gynecologic malignancies; clinical implications and future directions.
Dimitrios Nasioudis et al. Gynecol Oncol 2023 1801-5
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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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A population-level digital histologic biomarker for enhanced prognosis of invasive breast cancer.
Mohamed Amgad et al. Nat Med 2023
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Development of a Hereditary Breast and Ovarian Cancer and Genetics Curriculum for Community Health Workers: KEEP IT (Keeping Each other Engaged Program via IT) Community Health Worker Training.
Caitlin G Allen et al. J Cancer Educ 2023
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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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"Out of the blue": A qualitative study exploring the experiences of women and next of kin receiving unexpected results from BRA-STRAP research gene panel testing.
April Morrow et al. J Genet Couns 2023
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Male awareness of prostate cancer risk remains poor in relatives of women with germline variants in DNA-repair genes.
Vittorio Fasulo et al. BJUI Compass 2023 4(6) 738-745
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Use of a multi-phased approach to identify and address facilitators and barriers to the implementation of a population-wide genomic screening program.
Caitlin G Allen et al. Implement Sci Commun 2023 4(1) 122
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Page last reviewed:
Feb 1, 2024
Page last updated:
Mar 28, 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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