(Q24798716)

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

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scholarly article

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

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Nilanjan Chatterjee

3

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object named as

Joni L Rutter

6

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Jeffery Struewing

object named as

Jeffery P Struewing

7

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Michael Hauptmann

object named as

Michael Hauptmann

2

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Alice J Sigurdson

1

object named as

Alice J Sigurdson

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author name string

Bruce H Alexander

4

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Michele Morin Doody

5

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language of work or name

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publication date

12 March 2004

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4

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1

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9

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Genes other than BRCA1 and BRCA2 involved in breast cancer susceptibility

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=408462

7 April 2017

How many more breast cancer predisposition genes are there?

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=408462

7 April 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=408462

7 April 2017

Nonconservative amino acid substitution variants exist at polymorphic frequency in DNA repair genes in healthy humans

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=408462

7 April 2017

Challenges and complexities in estimating both the functional impact and the disease risk associated with the extensive genetic variation in human DNA repair genes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=408462

28 September 2017

Polymorphisms of XRCC1 and XRCC3 genes and susceptibility to breast cancer

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=408462

28 September 2017

Polymorphisms in DNA repair genes and associations with cancer risk

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=408462

28 September 2017

Central role for the XRCC1 BRCT I domain in mammalian DNA single-strand break repair

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=408462

28 September 2017

Association between the T29-->C polymorphism in the transforming growth factor beta1 gene and breast cancer among elderly white women: The Study of Osteoporotic Fractures.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=408462

28 September 2017

Breast cancer genetics: what we know and what we need

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=408462

28 September 2017

Kin-cohort designs for gene characterization

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=408462

28 September 2017

XRCC1 keeps DNA from getting stranded

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=408462

28 September 2017

Heritability of cellular radiosensitivity: a marker of low-penetrance predisposition genes in breast cancer?

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=408462

28 September 2017

Life without DNA repair

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=408462

28 September 2017

Cancer experience in the relatives of an unselected series of breast cancer patients.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=408462

28 September 2017

Variation in DNA repair is a factor in cancer susceptibility: a paradigm for the promises and perils of individual and population risk estimation?

1 reference

https://api.crossref.org/works/10.1186%2F1471-2407-4-9

21 January 2018

A marginal likelihood approach for estimating penetrance from kin-cohort designs

1 reference

https://api.crossref.org/works/10.1186%2F1471-2407-4-9

21 January 2018

Kin-cohort evaluation of relative risks of genetic variants

1 reference

https://api.crossref.org/works/10.1186%2F1471-2407-4-9

21 January 2018

The HER2 I655V polymorphism and breast cancer risk in Ashkenazim

1 reference

https://api.crossref.org/works/10.1186%2F1471-2407-4-9

21 January 2018

XRCC1 genetic polymorphism and breast cancer risk.

1 reference

https://api.crossref.org/works/10.1186%2F1471-2407-4-9

21 January 2018

Polymorphic variation at the -202 locus in IGFBP3: Influence on serum levels of insulin-like growth factors, interaction with plasma retinol and vitamin D and breast cancer risk

1 reference

https://api.crossref.org/works/10.1186%2F1471-2407-4-9

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1186%2F1471-2407-4-9

21 January 2018

Family history of cancer in patients with glioma: a validation study of accuracy.

1 reference

https://api.crossref.org/works/10.1186%2F1471-2407-4-9

21 January 2018

A sharper Bonferroni procedure for multiple tests of significance

1 reference

https://api.crossref.org/works/10.1186%2F1471-2407-4-9

21 January 2018

The Kin-Cohort Study for Estimating Penetrance

1 reference

https://api.crossref.org/works/10.1186%2F1471-2407-4-9

21 January 2018

BRCA2 arg372hispolymorphism and epithelial ovarian cancer risk

1 reference

https://api.crossref.org/works/10.1186%2F1471-2407-4-9

21 January 2018

A population-based case-control study of the Arg399Gln polymorphism in DNA repair gene XRCC1 and risk of breast cancer.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=408462

28 November 2018

Combination of DNA repair gene single nucleotide polymorphisms and increased levels of DNA adducts in a population-based study.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=408462

28 November 2018

A transforming growth factorbeta1 signal peptide variant increases secretion in vitro and is associated with increased incidence of invasive breast cancer.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=408462

28 November 2018

Identification of 127 amino acid substitution variants in screening 37 DNA repair genes in humans.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=408462

28 November 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=408462

28 November 2018

Polymorphisms in the DNA repair gene XRCC1 and breast cancer

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=408462

28 November 2018

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

1 reference

https://api.crossref.org/works/10.1186%2F1471-2407-4-9

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1186%2F1471-2407-4-9

21 January 2018

Evidence for further breast cancer susceptibility genes in addition to BRCA1 and BRCA2 in a population-based study

1 reference

https://api.crossref.org/works/10.1186%2F1471-2407-4-9

21 January 2018

Polygenic susceptibility to breast cancer and implications for prevention

1 reference

https://api.crossref.org/works/10.1186%2F1471-2407-4-9

21 January 2018

Amino acid substitution variants of APE1 and XRCC1 genes associated with ionizing radiation sensitivity

1 reference

https://api.crossref.org/works/10.1186%2F1471-2407-4-9

21 January 2018

Polymorphisms of the transforming growth factor-beta 1 gene in relation to myocardial infarction and blood pressure. The Etude Cas-Témoin de l'Infarctus du Myocarde (ECTIM) Study

1 reference

https://api.crossref.org/works/10.1186%2F1471-2407-4-9

21 January 2018

Polymorphisms in the DNA repair gene XRCC1, breast cancer risk, and response to radiotherapy

1 reference

https://pubmed.ncbi.nlm.nih.gov/15113441

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

DNA-repair genetic polymorphisms and breast cancer risk

1 reference

https://pubmed.ncbi.nlm.nih.gov/15113441

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Insulin-like growth factor-I in relation to premenopausal ductal carcinoma in situ of the breast

1 reference

https://pubmed.ncbi.nlm.nih.gov/15113441

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

XRCC1 polymorphisms: effects on aflatoxin B1-DNA adducts and glycophorin A variant frequency

1 reference

https://pubmed.ncbi.nlm.nih.gov/15113441

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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10.1186/1471-2407-4-9

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