Rare mutations in XRCC2 increase the risk of breast cancer (Q28730692)

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scientific article (publication date: 6 April 2012)

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Language	Label	Description	Also known as
English	Rare mutations in XRCC2 increase the risk of breast cancer	scientific article (publication date: 6 April 2012)

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scholarly article

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title

Rare mutations in XRCC2 increase the risk of breast cancer (English)

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author

Tu Nguyen-Dumont

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T Nguyen-Dumont

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3

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Fabienne Lesueur

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F Lesueur

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2

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Ana Osorio

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A Osorio

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21

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Nicoline Hoogerbrugge

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N Hoogerbrugge

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19

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Susan L Neuhausen

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7

object named as

S L Neuhausen

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Graham Giles

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24

object named as

G G Giles

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John Hopper

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27

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J L Hopper

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Peter Devilee

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25

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P Devilee

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Irene L Andrulis

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9

object named as

I L Andrulis

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Javier Benitez

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26

object named as

J Benitez

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Melissa C. Southey

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30

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M C Southey

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David Goldgar

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29

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D E Goldgar

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author name string

D J Park

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1

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M Pertesi

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4

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F Odefrey

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5

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F Hammet

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6

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E M John

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8

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M B Terry

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10

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M Daly

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11

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S Buys

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12

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F Le Calvez-Kelm

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13

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A Lonie

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14

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B J Pope

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15

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H Tsimiklis

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16

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C Voegele

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17

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F M Hilbers

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18

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A Barroso

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20

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S V Tavtigian

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28

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language of work or name

English

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publication date

6 April 2012

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published in

American Journal of Human Genetics

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volume

90

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issue

4

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page(s)

734-9

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cites work

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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

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

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Involvement of Rad51C in two distinct protein complexes of Rad51 paralogs in human cells

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The XRCC2 DNA repair gene from human and mouse encodes a novel member of the recA/RAD51 family

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Brca1 controls homology-directed DNA repair

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BRCA2 is required for homology-directed repair of chromosomal breaks

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7 April 2017

Rare germline mutations in PALB2 and breast cancer risk: a population-based study

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20 June 2018

Gene-gene interactions in breast cancer susceptibility

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20 June 2018

Rare variants in the ATM gene and risk of breast cancer

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20 June 2018

A role for XRCC2 gene polymorphisms in breast cancer risk and survival

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Germline mutations in PALB2 in African-American breast cancer cases

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The importance of XRCC2 in RAD51-related DNA damage repair.

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20 June 2018

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

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20 June 2018

Genetic predisposition to breast cancer: past, present, and future

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20 June 2018

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Homologous recombination deficiency leads to profound genetic instability in cells derived from Xrcc2-knockout mice

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Exome sequencing reveals a novel Fanconi group defined by XRCC2 mutation

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27 November 2018

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

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27 November 2018

The Melbourne Collaborative Cohort Study

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27 November 2018

A potential role for the XRCC2 R188H polymorphic site in DNA-damage repair and breast cancer

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27 November 2018

Mammalian recombination-repair genes XRCC2 and XRCC3 promote correct chromosome segregation

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retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/22464251

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

DOI

10.1016/J.AJHG.2012.02.027

1 reference

stated in

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

984922

OpenCitations bibliographic resource ID

984922

1 reference

stated in

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

984922

PMC publication ID

3322233

1 reference

stated in

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

984922

PubMed publication ID

22464251

1 reference

stated in

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

984922

ResearchGate publication ID

223992832

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