Variants of uncertain clinical significance in hereditary breast and ovarian cancer genes: best practices in functional analysis for clinical annotation-Reference-Cited by-同舟云学术

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Variants of uncertain clinical significance in hereditary breast and ovarian cancer genes: best practices in functional analysis for clinical annotation

Published:2020-03-09 Issue:8 Volume:57 Page:509-518
ISSN:0022-2593
Container-title:Journal of Medical Genetics
language:en
Short-container-title:J Med Genet

Author:

Monteiro Alvaro N^ORCID,Bouwman Peter^ORCID,Kousholt Arne N^ORCID,Eccles Diana M^ORCID,Millot Gael A^ORCID,Masson Jean-Yves^ORCID,Schmidt Marjanka K^ORCID,Sharan Shyam K^ORCID,Scully Ralph^ORCID,Wiesmüller Lisa^ORCID,Couch Fergus^ORCID,Vreeswijk Maaike P G^ORCID

Funder

BIOKE

IDT

Netherlands Organization for Scientific Research

Royal Netherlands Academy of Arts and Sciences

Danish Counsil for Independent Research

Netherlands Cancer Institute

Publisher

BMJ

Subject

Genetics(clinical),Genetics

Reference75 articles.

1. A Strong Candidate for the Breast and Ovarian Cancer Susceptibility Gene BRCA1

2. Identification of the breast cancer susceptibility gene BRCA2

3. Gene-Panel Sequencing and the Prediction of Breast-Cancer Risk

4. Prevention and Management of Hereditary Breast Cancer

5. Hereditary breast cancer: new genetic developments, new therapeutic avenues

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1. Evaluating homologous recombination activity in tissues to predict the risk of hereditary breast and ovarian cancer and olaparib sensitivity;Scientific Reports;2024-04-08

2. Uncovering the clinical relevance of unclassified variants in DNA repair genes: a focus on BRCA negative Tunisian cancer families;Frontiers in Genetics;2024-01-19

3. Incorporating functional genomics into the pathology-supported genetic testing framework implemented in South Africa: A future view of precision medicine for breast carcinomas;Mutation Research - Reviews in Mutation Research;2024-01

4. AVENGERS: Analysis of Variant Effects using Next Generation sequencing to EnhanceBRCA2Stratification;2023-12-15

5. Prevalence of Variants of Uncertain Significance in Patients Undergoing Genetic Testing for Hereditary Breast and Ovarian Cancer and Lynch Syndrome;Cancers;2023-12-08

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