Tagging single nucleotide polymorphisms in the BRIP1 gene and susceptibility to breast and ovarian cancer (Q33277172)

25 July 2017

title

Tagging single nucleotide polymorphisms in the BRIP1 gene and susceptibility to breast and ovarian cancer (English)

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single-nucleotide polymorphism

25 July 2017

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25 July 2017

Susanne Krüger Kjaer

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Susan J Ramus

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Paul D P Pharoah

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25 July 2017

Douglas F Easton

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25 July 2017

Alice S Whittemore

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25 July 2017

Simon A Gayther

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25 July 2017

Honglin Song

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25 July 2017

Estrid Hogdall

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25 July 2017

Richard A Dicioccio

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25 July 2017

Valerie McGuire

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25 July 2017

Claus Hogdall

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25 July 2017

Ian J Jacobs

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25 July 2017

Bruce A J Ponder

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25 July 2017

language of work or name

English

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publication date

7 March 2007

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25 July 2017

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25 July 2017

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25 July 2017

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25 July 2017

page(s)

e268

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Creative Commons Attribution 4.0 International

25 July 2017

start time

7 March 2007

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April 2022 Public Data File from Crossref

copyrighted

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cites work

A genome wide linkage search for breast cancer susceptibility genes

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BACH1 Ser919Pro variant and breast cancer risk

21 June 2018

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Mutation analysis of FANCD2, BRIP1/BACH1, LMO4 and SFN in familial breast cancer

21 June 2018

1 reference

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A haplotype map of the human genome

21 June 2018

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Efficiency and power in genetic association studies

21 June 2018

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The BRCA1-interacting helicase BRIP1 is deficient 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=1800910

Kin-cohort estimates for familial breast cancer risk in relation to variants in DNA base excision repair, BRCA1 interacting and growth factor genes

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1800910

The BRCA1-associated protein BACH1 is a DNA helicase targeted by clinically relevant inactivating 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=1800910

The BRCT Domain Is a Phospho-Protein Binding Domain

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1800910

Mutational analysis of the BRCA1-interacting genes ZNF350/ZBRK1 and BRIP1/BACH1 among BRCA1 and BRCA2-negative probands from breast-ovarian cancer families and among early-onset breast cancer cases and reference individuals

21 June 2018

1 reference

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The genetics of ovarian cancer

21 June 2018

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No mutations in the BACH1 gene in BRCA1 and BRCA2 negative breast-cancer families linked to 17q22

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1800910

BACH1, a novel helicase-like protein, interacts directly with BRCA1 and contributes to its DNA repair function

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1800910

How many more breast cancer predisposition genes are there?

21 June 2018

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Somatic mutations that contribute to breast cancer

21 June 2018

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Linkage of early-onset familial breast cancer to chromosome 17q21

21 June 2018

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THE GENETICS OF BREAST CANCER SUSCEPTIBILITY

21 June 2018

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https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0000268

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

21 January 2018

1 reference

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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.0000268

BACH1 517C-->T transition impairs protein translocation to nucleus: a role in breast cancer susceptibility?

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0000268

Testing association of statistically inferred haplotypes with discrete and continuous traits in samples of unrelated individuals.

21 January 2018

1 reference

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Common variants in mismatch repair genes and risk of invasive ovarian cancer.

21 January 2018

1 reference

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Genetics and ovarian carcinoma

31 October 2018

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Polymorphisms in DNA double-strand break repair genes and risk of breast cancer: two population-based studies in USA and Poland, and meta-analyses

31 October 2018

1 reference

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Allelic deletion mapping of putative tumor suppressor genes on 17q in sporadic ovarian cancer

31 October 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/17342202

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Risk models for familial ovarian and breast cancer

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/17342202

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1371/JOURNAL.PONE.0000268

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25 July 2017

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25 July 2017

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