(Q34623703)

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An international initiative to identify genetic modifiers of cancer risk in BRCA1 and BRCA2 mutation carriers: the Consortium of Investigators of Modifiers of BRCA1 and BRCA2 (CIMBA)

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

3 August 2017

An international initiative to identify genetic modifiers of cancer risk in BRCA1 and BRCA2 mutation carriers: the Consortium of Investigators of Modifiers of BRCA1 and BRCA2 (CIMBA) (English)

1 reference

Europe PubMed Central

PubMed publication ID

3 August 2017

1 reference

based on heuristic

inferred from title

1 reference

based on heuristic

inferred from title

Georgia Chenevix-Trench

1

object named as

Georgia Chenevix-Trench

0 references

Douglas F. Easton

5

object named as

Douglas F Easton

1 reference

Europe PubMed Central

PubMed publication ID

3 August 2017

Fergus J. Couch

4

object named as

Fergus J Couch

1 reference

Europe PubMed Central

PubMed publication ID

3 August 2017

2

object named as

Roger L Milne

1 reference

Europe PubMed Central

PubMed publication ID

3 August 2017

Antonis C Antoniou

3

object named as

Antonis C Antoniou

1 reference

Europe PubMed Central

PubMed publication ID

3 August 2017

6

object named as

David E Goldgar

1 reference

Europe PubMed Central

PubMed publication ID

3 August 2017

author name string

CIMBA

7

1 reference

Europe PubMed Central

PubMed publication ID

3 August 2017

publication date

1 January 2007

1 reference

Europe PubMed Central

PubMed publication ID

3 August 2017

Breast Cancer Research

1 reference

Europe PubMed Central

PubMed publication ID

3 August 2017

9

1 reference

Europe PubMed Central

PubMed publication ID

3 August 2017

2

1 reference

Europe PubMed Central

PubMed publication ID

3 August 2017

104

1 reference

Europe PubMed Central

PubMed publication ID

3 August 2017

https://scigraph.springernature.com/pub.10.1186/bcr1670

0 references

Familial clustering of site-specific cancer risks associated with BRCA1 and BRCA2 mutations in the Ashkenazi Jewish population

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1868919

7 July 2018

Prediction of BRCA1 status in patients with breast cancer using estrogen receptor and basal phenotype

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1868919

7 July 2018

The androgen receptor CAG repeat polymorphism and modification of breast cancer risk in BRCA1 and BRCA2 mutation carriers

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1868919

7 July 2018

Genome-wide association studies for common diseases and complex traits

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1868919

7 July 2018

Association studies for finding cancer-susceptibility genetic variants

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1868919

7 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1868919

7 July 2018

Average risks of breast and ovarian cancer associated with BRCA1 or BRCA2 mutations detected in case Series unselected for family history: a combined analysis of 22 studies

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1868919

7 July 2018

CAG and GGC repeat polymorphisms in the androgen receptor gene and breast cancer susceptibility in BRCA1/2 carriers and non-carriers

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1868919

7 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1868919

7 July 2018

Modification of BRCA1-associated breast cancer risk by the polymorphic androgen-receptor CAG repeat

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1868919

7 July 2018

Multifactorial analysis of differences between sporadic breast cancers and cancers involving BRCA1 and BRCA2 mutations

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1868919

7 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1868919

7 July 2018

Breast and ovarian cancer incidence in BRCA1-mutation carriers. Breast Cancer Linkage Consortium.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1868919

7 July 2018

Heritability of mammographic density, a risk factor for breast cancer.

1 reference

https://api.crossref.org/works/10.1186%2FBCR1670

21 January 2018

Mammographic density and breast cancer risk in BRCA1 and BRCA2 mutation carriers.

1 reference

https://api.crossref.org/works/10.1186%2FBCR1670

21 January 2018

Polyglutamine repeat length in theAIB1 gene modifies breast cancer susceptibility inBRCA1 carriers

1 reference

https://api.crossref.org/works/10.1186%2FBCR1670

21 January 2018

The AIB1 Polyglutamine Repeat Does Not Modify Breast Cancer Risk in BRCA1 and BRCA2 Mutation Carriers

1 reference

https://api.crossref.org/works/10.1186%2FBCR1670

21 January 2018

A common coding variant in CASP8 is associated with breast cancer risk

1 reference

https://api.crossref.org/works/10.1186%2FBCR1670

21 January 2018

Modification of BRCA1- and BRCA2-associated breast cancer risk by AIB1 genotype and reproductive history.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1868919

26 October 2018

CGH-targeted linkage analysis reveals a possible BRCA1 modifier locus on chromosome 5q

1 reference

https://api.crossref.org/works/10.1186%2FBCR1670

21 January 2018

A single nucleotide polymorphism in the 5' untranslated region of RAD51 and risk of cancer among BRCA1/2 mutation carriers

1 reference

https://pubmed.ncbi.nlm.nih.gov/17466083

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Androgen receptor CAG repeat length in Jewish Israeli women who are BRCA1/2 mutation carriers: association with breast/ovarian cancer phenotype

1 reference

https://pubmed.ncbi.nlm.nih.gov/17466083

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A weighted cohort approach for analysing factors modifying disease risks in carriers of high-risk susceptibility genes

1 reference

https://pubmed.ncbi.nlm.nih.gov/17466083

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Breast cancer risk inBRCA1 andBRCA2 mutation carriers and polyglutamine repeat length in theAIB1 gene

1 reference

https://pubmed.ncbi.nlm.nih.gov/17466083

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1186/BCR1670

1 reference

Europe PubMed Central

PubMed publication ID

3 August 2017

Dimensions Publication ID

0 references

PMC publication ID

1 reference

Europe PubMed Central

PubMed publication ID

3 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

3 August 2017

ResearchGate publication ID

0 references

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