(Q35794359)

10 August 2017

title

Common variants in the ATM, BRCA1, BRCA2, CHEK2 and TP53 cancer susceptibility genes are unlikely to increase breast cancer risk (English)

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10 August 2017

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5

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10 August 2017

10

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10 August 2017

Serena Scollen

4

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Paul D P Pharoah

7

object named as

Paul D P Pharoah

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10 August 2017

8

Douglas F Easton

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10 August 2017

6

Deborah J Thompson

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10 August 2017

Caroline Baynes

1

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10 August 2017

Catherine S Healey

2

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10 August 2017

Karen A Pooley

3

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10 August 2017

Bruce A J Ponder

9

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10 August 2017

SEARCH breast cancer study

11

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10 August 2017

publication date

1 January 2007

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10 August 2017

published in

Breast Cancer Research

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10 August 2017

volume

9

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10 August 2017

issue

2

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10 August 2017

page(s)

R27

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https://scigraph.springernature.com/pub.10.1186/bcr1669

10 August 2017

exact match

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cites work

Commonly studied single-nucleotide polymorphisms and breast cancer: results from the Breast Cancer Association Consortium

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1868915

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

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1868915

Linkage disequilibrium mapping of CHEK2: common variation and breast cancer risk

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1868915

The ATM missense mutation p.Ser49Cys (c.146C>G) and the risk of breast cancer

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1868915

Haplotype analysis of common variants in the BRCA1 gene and risk of sporadic breast cancer

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1868915

CHEK2*1100delC and susceptibility to breast cancer: a collaborative analysis involving 10,860 breast cancer cases and 9,065 controls from 10 studies

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1868915

Choosing haplotype-tagging SNPS based on unphased genotype data using a preliminary sample of unrelated subjects with an example from the Multiethnic Cohort Study

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1868915

Polymorphisms in DNA repair genes and associations with cancer risk

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1868915

A comprehensive model for familial breast cancer incorporating BRCA1, BRCA2 and other genes

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1868915

Global analysis of ATM polymorphism reveals significant functional constraint

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1868915

No association between BRCA2 N372H and breast cancer risk

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1868915

Identification of target genes regulated by FOXC1 using nickel agarose-based chromatin enrichment

25 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1868915

Heterozygote excess is repeatedly observed in females at the BRCA2 locus N372H.

25 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1868915

The BRCA2 372 HH genotype is associated with risk of breast cancer in Australian women under age 60 years.

25 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1868915

A common variant in BRCA2 is associated with both breast cancer risk and prenatal viability

25 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1868915

Polygenic susceptibility to breast cancer and implications for prevention

25 September 2018

1 reference

12 December 2020

Common variation in BRCA2 and breast cancer risk: a haplotype-based analysis in the Multiethnic Cohort

1 reference

12 December 2020

Common BRCA1 variants and susceptibility to breast and ovarian cancer in the general population

1 reference

12 December 2020

Prevalence of BRCA1 and BRCA2 gene mutations in patients with early-onset breast cancer

1 reference

12 December 2020

A haplotype-based case-control study of BRCA1 and sporadic breast cancer risk

1 reference

12 December 2020

Prevalence and penetrance of BRCA1 and BRCA2 mutations in a population-based series of breast cancer cases. Anglian Breast Cancer Study Group

1 reference

12 December 2020

Identifiers

DOI

10.1186/BCR1669

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Dimensions Publication ID

10 August 2017

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10 August 2017

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