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Public Health Genomics and Precision Health Knowledge Base (v8.8)
PHGKB
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Public Health Genomics Branch
Genomics and Precision Health Update
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Last data update: Nov 29, 2023
. (Total: 62229 Documents since 2012)
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all[original query]>>Hereditary Cancer[Category]
Public Awareness and Acceptability of PGT-M in Cancer Predisposition Syndromes.
Davide Calosci et al. Genes (Basel) 2023 14(11)
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Impact of genetic counselling strategy on diagnostic yield and workload for genome sequencing-based tumour diagnostics.
Roelof Koster et al. Genet Med 2023 101032
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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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Chatbot Artificial Intelligence for Genetic Cancer Risk Assessment and Counseling: A Systematic Review and Meta-Analysis.
Emily M Webster et al. JCO Clin Cancer Inform 2023 7e2300123
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Referral, Uptake, and Outcome of Genetic Counseling and Testing in Patients With Early-Onset Colorectal Cancer.
Hareem Syed et al. J Natl Compr Canc Netw 2023 21(11) 1156-1163.e5
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Diagnostic Outcomes of Concurrent DNA and RNA Sequencing in Individuals Undergoing Hereditary Cancer Testing.
Carolyn Horton et al. JAMA Oncol 2023
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Prognosis of CDKN2A germline mutation in patients with familial melanoma: a systematic review and meta-analysis.
Ana Taibo et al. Melanoma Res 2023
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Patient decisions regarding cancer gene panel testing: An exploratory study.
Margaret M Emmet et al. J Genet Couns 2023
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An analysis of the impact of annual cancer genetic testing guideline updates on a past patient population.
Jordan Johnson et al. J Genet Couns 2023
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Experiences of Family Communication and Cascade Genetic Testing for Hereditary Cancer in Medically Underserved Populations-A Qualitative Study.
Erica M Bednar et al. Cancer Prev Res (Phila) 2023
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Pathogenic germline variants in BRCA1/2 and p53 identified by real-world comprehensive cancer genome profiling tests in Asian patients.
Tomoyuki Satake et al. Cancer Res Commun 2023
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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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Parent Quality of Life After Disclosure of Pediatric Oncology Germline Sequencing Results.
Katianne M Howard Sharp et al. JCO Precis Oncol 2023 7e2300159
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Screening and testing practices for Lynch syndrome in Nova Scotians with endometrial cancer: a descriptive study.
Marianne Levesque et al. CMAJ Open 2023 11(5) E1012-E1019
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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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Screening uptake of colonoscopy versus fecal immunochemical testing in first-degree relatives of patients with non-syndromic colorectal cancer: A multicenter, open-label, parallel-group, randomized trial (ParCoFit study).
Natalia González-López et al. PLoS Med 2023 20(10) e1004298
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Implementation, Evolution, and Laboratory Performance of Methods-Based Proficiency Testing for Next-Generation Sequencing Detection of Germline Sequence Variants.
Karen D Tsuchiya et al. Arch Pathol Lab Med 2023
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Implementation of a dedicated cascade testing clinic for patients at risk for hereditary cancer syndromes.
Michelle F Jacobs et al. J Genet Couns 2023
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Province-Wide Ascertainment of Lynch Syndrome in Manitoba.
Heidi Rothenmund et al. Clin Gastroenterol Hepatol 2023
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Colorectal Cancer Screening for Persons With a Positive Family History—Evaluation of the FARKOR Program for the Secondary Prevention of Colorectal Cancer in Persons Aged 25 to 50.
Alexander Crispin et al. Dtsch Arztebl Int 2023 (Forthcoming)
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NCCN Guidelines® Insights: Genetic/Familial High-Risk Assessment: Breast, Ovarian, and Pancreatic, Version 2.2024.
Mary B Daly et al. J Natl Compr Canc Netw 2023 21(10) 1000-1010
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The diagnostic yield of genetic testing in patients with multiple colorectal adenomas: a specialist centre cohort study.
Sau Mak et al. Clin Transl Gastroenterol 2023
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Management of Women at High Risk for Breast Cancer.
Lashika Yogendran et al. J Am Board Fam Med 2023
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Current practice of cancer predisposition testing in pediatric patients with CNS tumors in the United States.
Baylee Roy et al. Pediatr Blood Cancer 2023 e30725
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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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Family History and Risk of Renal Cell Carcinoma: A National Multi-Register Case-Control Study.
Rasmus G Jakobsson et al. J Urol 2023 101097JU0000000000003765
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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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Less is more: rethinking colorectal cancer resection strategies in Lynch syndrome.
Bryson W Katona et al. Lancet Gastroenterol Hepatol 2023
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Exploring Stakeholders' Perspectives on Implementing Universal Germline Testing for Colorectal Cancer: Findings From a Clinical Practice Survey.
Linda Rodgers-Fouche et al. JCO Precis Oncol 2023 7e2300440
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Tumor Testing and Genetic Analysis to Identify Lynch Syndrome Patients in an Italian Colorectal Cancer Cohort.
Antonino Pantaleo et al. Cancers (Basel) 2023 15(20)
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Page last reviewed:
Oct 1, 2023
Page last updated:
Nov 29, 2023
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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