RAD51 and breast cancer susceptibility: no evidence for rare variant association in the Breast Cancer Family Registry study (Q34540638)

2 August 2017

RAD51 and breast cancer susceptibility: no evidence for rare variant association in the Breast Cancer Family Registry study (English)

1 reference

2 August 2017

1 reference

Maxime P Vallée

8

0 references

Javier Oliver

Javier Oliver

2

0 references

Fabienne Lesueur

Fabienne Lesueur

16

0 references

Melissa C. Southey

Melissa C Southey

12

0 references

Graham Byrnes

Graham Byrnes

9

0 references

John Hopper

11

John L Hopper

1 reference

2 August 2017

13

Irene L Andrulis

1 reference

2 August 2017

14

Esther M John

1 reference

2 August 2017

Florence Le Calvez-Kelm

1

1 reference

2 August 2017

Francesca Damiola

3

1 reference

2 August 2017

Nathalie Forey

4

1 reference

2 August 2017

Nivonirina Robinot

5

1 reference

2 August 2017

Geoffroy Durand

6

1 reference

2 August 2017

Catherine Voegele

7

1 reference

2 August 2017

Breast Cancer Family Registry

10

1 reference

2 August 2017

Sean V Tavtigian

15

1 reference

2 August 2017

language of work or name

English

0 references

publication date

27 December 2012

1 reference

2 August 2017

1 reference

2 August 2017

7

1 reference

2 August 2017

12

1 reference

2 August 2017

e52374

1 reference

Creative Commons Attribution 4.0 International

2 August 2017

start time

27 December 2012

1 reference

April 2022 Public Data File from Crossref

copyright status

copyrighted

0 references

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Rare, evolutionarily unlikely missense substitutions in CHEK2 contribute to breast cancer susceptibility: results from a breast cancer family registry case-control mutation-screening study

7 July 2018

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A PALB2 mutation associated with high risk of breast cancer

7 July 2018

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Enhancement of RAD51 recombinase activity by the tumor suppressor PALB2.

7 July 2018

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RAD51C germline mutations in breast and ovarian cancer patients

7 July 2018

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Screening RAD51C nucleotide alterations in patients with a family history of breast and ovarian cancer

7 July 2018

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

7 July 2018

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A method and server for predicting damaging missense mutations

7 July 2018

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Rare, evolutionarily unlikely missense substitutions in ATM confer increased risk of breast cancer

7 July 2018

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Description and validation of high-throughput simultaneous genotyping and mutation scanning by high-resolution melting curve analysis

7 July 2018

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Determining the effectiveness of High Resolution Melting analysis for SNP genotyping and mutation scanning at the TP53 locus

7 July 2018

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In silico analysis of missense substitutions using sequence-alignment based methods

7 July 2018

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Penetrance analysis of the PALB2 c.1592delT founder mutation

7 July 2018

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Identification of a novel human Rad51 variant that promotes DNA strand exchange

7 July 2018

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RAD51 135G-->C modifies breast cancer risk among BRCA2 mutation carriers: results from a combined analysis of 19 studies

7 July 2018

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A Laboratory Information Management System (LIMS) for a high throughput genetic platform aimed at candidate gene mutation screening

7 July 2018

1 reference

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

7 July 2018

1 reference

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ATM mutations that cause ataxia-telangiectasia are breast cancer susceptibility alleles

7 July 2018

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Variation in the RAD51 gene and familial breast cancer

7 July 2018

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M-Coffee: combining multiple sequence alignment methods with T-Coffee

7 July 2018

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The Breast Cancer Family Registry: an infrastructure for cooperative multinational, interdisciplinary and translational studies of the genetic epidemiology of breast cancer

7 July 2018

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A single-nucleotide polymorphism in the RAD51 gene modifies breast cancer risk in BRCA2 carriers, but not in BRCA1 carriers or noncarriers

7 July 2018

1 reference

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Full-length archaeal Rad51 structure and mutants: mechanisms for RAD51 assembly and control by BRCA2

7 July 2018

1 reference

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Molecular views of recombination proteins and their control

7 July 2018

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Insights into DNA recombination from the structure of a RAD51-BRCA2 complex

7 July 2018

1 reference

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Low-penetrance susceptibility to breast cancer due to CHEK2(*)1100delC in noncarriers of BRCA1 or BRCA2 mutations

7 July 2018

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Accounting for human polymorphisms predicted to affect protein function

7 July 2018

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A single nucleotide polymorphism in the RAD51 gene modifies cancer risk in BRCA2 but not BRCA1 carriers

7 July 2018

1 reference

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DNA double-strand breaks: signaling, repair and the cancer connection

7 July 2018

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Over-expression of wild-type Rad51 correlates with histological grading of invasive ductal breast cancer

7 July 2018

1 reference

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Abnormal expression of BRCA1 and BRCA1-interactive DNA-repair proteins in breast carcinomas

7 July 2018

1 reference

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The BRC repeats in BRCA2 are critical for RAD51 binding and resistance to methyl methanesulfonate treatment

7 July 2018

1 reference

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Genetic heterogeneity and penetrance analysis of the BRCA1 and BRCA2 genes in breast cancer families. The Breast Cancer Linkage Consortium

7 July 2018

1 reference

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RAD51 interacts with the evolutionarily conserved BRC motifs in the human breast cancer susceptibility gene brca2

7 July 2018

1 reference

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Improved splice site detection in Genie

7 July 2018

1 reference

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Association of BRCA1 with Rad51 in mitotic and meiotic cells

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3531476

A mutation in mouse rad51 results in an early embryonic lethal that is suppressed by a mutation in p53

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3531476

Targeted disruption of the Rad51 gene leads to lethality in embryonic mice

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3531476

p53 is linked directly to homologous recombination processes via RAD51/RecA protein interaction

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3531476

Risks of cancer in BRCA1-mutation carriers. Breast Cancer Linkage Consortium

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3531476

Basic local alignment search tool

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3531476

Germ line p53 mutations in a familial syndrome of breast cancer, sarcomas, and other neoplasms

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3531476

Abnormal expression of BRCA1 and BRCA1-interactive DNA-repair proteins in breast carcinomas

7 July 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0052374

RAD51 G135C polymorphism is associated with breast cancer susceptibility: a meta-analysis involving 22,399 subjects

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0052374

RAD51 135G>C does not modify breast cancer risk in non-BRCA1/2 mutation carriers: evidence from a meta-analysis of 12 studies

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0052374

Is RAD51 135G>C polymorphism really associated with breast cancer in general population? Biased design and results lead to inappropriate conclusion.

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0052374

Screening for RAD51 and BRCA2 BRC repeat mutations in breast and ovarian cancer families.

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0052374

Altered DNA binding by the human Rad51-R150Q mutant found in breast cancer patients.

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0052374

Maximum entropy modeling of short sequence motifs with applications to RNA splicing signals.

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0052374

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/10.1371%2FJOURNAL.PONE.0052374

Identification of Rad51 alteration in patients with bilateral breast cancer

21 January 2018

1 reference

12 December 2020

RAD51 135G>C polymorphism contributes to breast cancer susceptibility: a meta-analysis involving 26,444 subjects

1 reference

12 December 2020

RAD51 135G/C polymorphism and breast cancer risk: a meta-analysis from 21 studies

1 reference

12 December 2020

Need for clarification of data in the recent meta-analysis about RAD51 135G>C polymorphism and breast cancer risk

1 reference

12 December 2020

BRCA2 germline mutations in male breast cancer cases and breast cancer families

1 reference

12 December 2020

10.1371/JOURNAL.PONE.0052374

Identifiers

DOI

1 reference

release_xhyjm4wjyzgk5br5u5vit3swmy

2 August 2017

0 references

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/xhyjm4wjyzgk5br5u5vit3swmy

24 November 2022

mapped directly with Wikidata item

PMCID

3531476

1 reference

2 August 2017

1 reference