Massively parallel sequencing in hereditary prostate cancer families reveals a rare risk variant in the DNA repair gene, RAD51C-Reference-Cited by-同舟云学术

Massively parallel sequencing in hereditary prostate cancer families reveals a rare risk variant in the DNA repair gene, RAD51C

Published:2021-12 Issue: Volume:159 Page:52-55
ISSN:0959-8049
Container-title:European Journal of Cancer
language:en
Short-container-title:European Journal of Cancer

Author:

Marthick James R.,Raspin Kelsie^ORCID,Foley Georgea R.^ORCID,Blackburn Nicholas B.^ORCID,Banks Annette^ORCID,Donovan Shaun,Malley Roslyn C.,Field Matthew A.,Stanford Janet L.^ORCID,Ostrander Elaine A.,FitzGerald Liesel M.^ORCID,Dickinson Joanne L.^ORCID

Publisher

Elsevier BV

Subject

Cancer Research,Oncology

Reference10 articles.

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5. Impact of the G84E variant on HOXB13 gene and protein expression in formalin-fixed, paraffin-embedded prostate tumours;FitzGerald;Sci Rep,2017

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1. Germline Sequencing of DNA Damage Repair Genes in Two Hereditary Prostate Cancer Cohorts Reveals New Disease Risk-Associated Gene Variants;Cancers;2024-07-07

2. Association of a novel BRCA2 mutation with prostate cancer risk further supports germline genetic testing;European Journal of Cancer;2023-02

3. Identification of a novel recurrent EEF2 gene amplification in familial prostate tumors;Genes, Chromosomes and Cancer;2022-12-23

4. Germline sequencing of DNA-damage-repair genes in two hereditary prostate cancer cohorts reveals new disease risk-associated gene variants;2022-04-13