Germline mutation in the RAD51B gene confers predisposition to breast cancer (Q33591622)

28 July 2017

title

Germline mutation in the RAD51B gene confers predisposition to breast cancer (English)

1 reference

28 July 2017

author

Dominique Stoppa-Lyonnet

15

Dominique Stoppa-Lyonnet

0 references

Virginie Caux-Moncoutier

2

Virginie Caux-Moncoutier

0 references

Xavier Sastre-Garau

12

Xavier Sastre-Garau

0 references

Grégoire Davy

Grégoire Davy

3

0 references

Marc-Henri Stern

Marc-Henri Stern

13

0 references

Claude Houdayer

14

Claude Houdayer

1 reference

28 July 2017

7

Dorothée Michaux

1 reference

28 July 2017

1

Lisa Golmard

1 reference

28 July 2017

6

Carole Tirapo

1 reference

28 July 2017

Essam Al Ageeli

4

1 reference

28 July 2017

Brigitte Poirot

5

1 reference

28 July 2017

Catherine Barbaroux

8

1 reference

28 July 2017

Catherine Dubois d'Enghien

9

1 reference

28 July 2017

André Nicolas

10

1 reference

28 July 2017

Laurent Castéra

11

1 reference

28 July 2017

language of work or name

English

0 references

publication date

19 October 2013

1 reference

28 July 2017

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28 July 2017

volume

13

1 reference

28 July 2017

page(s)

484

1 reference

Rare variants in XRCC2 as breast cancer susceptibility alleles

28 July 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4016303

Genome-wide association study identifies a common variant in RAD51B associated with male breast cancer risk

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4016303

Guidelines for splicing analysis in molecular diagnosis derived from a set of 327 combined in silico/in vitro studies on BRCA1 and BRCA2 variants

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4016303

Rare mutations in XRCC2 increase the risk of breast cancer

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4016303

Germline mutations in RAD51D confer susceptibility to ovarian cancer

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4016303

RAD51 paralogs: roles in DNA damage signalling, recombinational repair and tumorigenesis

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4016303

21 June 2018

Global cancer statistics

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4016303

Germline mutations in breast and ovarian cancer pedigrees establish RAD51C as a human cancer susceptibility gene

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4016303

A method and server for predicting damaging missense mutations

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4016303

Rare variants create synthetic genome-wide associations

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4016303

Predicting the effects of coding non-synonymous variants on protein function using the SIFT algorithm

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4016303

A multistage genome-wide association study in breast cancer identifies two new risk alleles at 1p11.2 and 14q24.1 (RAD51L1).

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4016303

Inherited susceptibility to common cancers

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4016303

Biallelic mutations in PALB2 cause Fanconi anemia subtype FA-N and predispose to childhood cancer

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4016303

PALB2, which encodes a BRCA2-interacting protein, is a breast cancer susceptibility gene

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4016303

Haploinsufficiency of RAD51B causes centrosome fragmentation and aneuploidy in human cells

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4016303

Comprehensive statistical study of 452 BRCA1 missense substitutions with classification of eight recurrent substitutions as neutral

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4016303

Interferon regulatory factor 6 (IRF6) gene variants and the risk of isolated cleft lip or palate

21 June 2018

1 reference

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Biallelic inactivation of BRCA2 in Fanconi anemia

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4016303

Allelic knockout of novel splice variants of human recombination repair gene RAD51B in t(12;14) uterine leiomyomas

21 June 2018

1 reference

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Identification of the breast cancer susceptibility gene BRCA2

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4016303

A specific translocation, t(12;14)(q14-15;q23-24), characterizes a subgroup of uterine leiomyomas

21 June 2018

1 reference

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Genetic analysis of breast cancer in the cancer and steroid hormone study

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4016303

A strong candidate for the breast and ovarian cancer susceptibility gene BRCA1

21 June 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2407-13-484

Ten genes for inherited breast cancer.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2407-13-484

Truncating mutations in the Fanconi anemia J gene BRIP1 are low-penetrance breast cancer susceptibility alleles

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2407-13-484

The DNA helicase BRIP1 is defective in Fanconi anemia complementation group J

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2407-13-484

Mutation of the RAD51C gene in a Fanconi anemia-like disorder

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2407-13-484

Exome sequencing reveals a novel Fanconi group defined by XRCC2 mutation

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2407-13-484

Association between the XRCC3 polymorphisms and breast cancer risk: meta-analysis based on case-control studies.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2407-13-484

Germline RAD51C mutations confer susceptibility to ovarian cancer

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2407-13-484

Polygenes, risk prediction, and targeted prevention of breast cancer

21 January 2018

1 reference

12 December 2020

EMMA, a cost- and time-effective diagnostic method for simultaneous detection of point mutations and large-scale genomic rearrangements: application to BRCA1 and BRCA2 in 1,525 patients

1 reference

12 December 2020

Mutation analysis of RAD51L1 (RAD51B/REC2) in multiple-case, non-BRCA1/2 breast cancer families

1 reference

12 December 2020

A HRM-based screening method detects RAD51C germ-line deleterious mutations in Spanish breast and ovarian cancer families

1 reference

12 December 2020

Analysis of RAD51C germline mutations in high-risk breast and ovarian cancer families and ovarian cancer patients

1 reference

12 December 2020

Identifiers

DOI

10.1186/1471-2407-13-484

1 reference

Dimensions Publication ID

28 July 2017

0 references

1 reference

28 July 2017

1 reference