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Precision Health Database


Precision Health Database|Search|PHGKB

Last data update: Nov 29, 2023. (Total: 62229 Documents since 2012)
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Query Trace: 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)
Impact of genetic counselling strategy on diagnostic yield and workload for genome sequencing-based tumour diagnostics.
Roelof Koster et al. Genet Med 2023 101032
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
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
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
Diagnostic Outcomes of Concurrent DNA and RNA Sequencing in Individuals Undergoing Hereditary Cancer Testing.
Carolyn Horton et al. JAMA Oncol 2023
Prognosis of CDKN2A germline mutation in patients with familial melanoma: a systematic review and meta-analysis.
Ana Taibo et al. Melanoma Res 2023
Patient decisions regarding cancer gene panel testing: An exploratory study.
Margaret M Emmet et al. J Genet Couns 2023
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
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
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
Influence of family history on penetrance of hereditary cancers in a population setting.
Leigh Jackson et al. EClinicalMedicine 2023 64102159
Parent Quality of Life After Disclosure of Pediatric Oncology Germline Sequencing Results.
Katianne M Howard Sharp et al. JCO Precis Oncol 2023 7e2300159
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
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
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
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
Implementation of a dedicated cascade testing clinic for patients at risk for hereditary cancer syndromes.
Michelle F Jacobs et al. J Genet Couns 2023
Province-Wide Ascertainment of Lynch Syndrome in Manitoba.
Heidi Rothenmund et al. Clin Gastroenterol Hepatol 2023
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)
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
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
Management of Women at High Risk for Breast Cancer.
Lashika Yogendran et al. J Am Board Fam Med 2023
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
Hereditary cancer testing in a diverse sample across three breast imaging centers.
Laura Westbrook et al. Breast Cancer Res Treat 2023
Family History and Risk of Renal Cell Carcinoma: A National Multi-Register Case-Control Study.
Rasmus G Jakobsson et al. J Urol 2023 101097JU0000000000003765
"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
Less is more: rethinking colorectal cancer resection strategies in Lynch syndrome.
Bryson W Katona et al. Lancet Gastroenterol Hepatol 2023
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
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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