Polymorphisms in DNA double-strand break repair genes and risk of breast cancer: two population-based studies in USA and Poland, and meta-analyses (Q57250685)

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

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scholarly article

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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 (English)

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based on heuristic

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Jolanta Lissowska

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Jolanta Lissowska

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Louise A. Brinton

4

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Louise A. Brinton

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Montserrat García-Closas

1

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Montserrat García-Closas

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Neonila Szeszenia-Dabrowska

10

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Neonila Szeszenia-Dabrowska

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Stephen Chanock

6

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Stephen Chanock

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Polly A Newcomb

3

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Polly A. Newcomb

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Beata Pepłońska

9

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Beata Peplonska

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Witold Zatoński

11

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Witold Zatonski

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Alicja Bardin-Mikolajczak

12

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Alicja Bardin-Mikolajczak

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Linda Titus-Ernstoff

5

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Linda Titus-Ernstoff

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author name string

Kathleen M. Egan

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Robert Welch

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Jeffery P. Struewing

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publication date

17 February 2006

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119

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4

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376-388

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https://scigraph.springernature.com/pub.10.1007/s00439-006-0135-z

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Functional characterization of polymorphisms in DNA repair genes using cytogenetic challenge assays

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https://api.crossref.org/works/10.1007%2FS00439-006-0135-Z

21 January 2018

Bias in meta-analysis detected by a simple, graphical test

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https://api.crossref.org/works/10.1007%2FS00439-006-0135-Z

21 January 2018

Radiation and other environmental exposures and breast cancer

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https://api.crossref.org/works/10.1007%2FS00439-006-0135-Z

21 January 2018

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

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https://pubmed.ncbi.nlm.nih.gov/16485136

12 December 2020

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No association between BRCA2 N372H and breast cancer risk

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https://pubmed.ncbi.nlm.nih.gov/16485136

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Polymorphisms in DNA double-strand break repair genes and breast cancer risk in the Nurses' Health Study

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https://pubmed.ncbi.nlm.nih.gov/16485136

12 December 2020

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Operating characteristics of a rank correlation test for publication bias

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https://pubmed.ncbi.nlm.nih.gov/16485136

12 December 2020

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Double-Strand Break Repair Gene Polymorphisms and Risk of Breast or Ovarian Cancer

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https://pubmed.ncbi.nlm.nih.gov/16485136

12 December 2020

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

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https://pubmed.ncbi.nlm.nih.gov/16485136

12 December 2020

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Chromosomal stability and the DNA double-stranded break connection

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https://pubmed.ncbi.nlm.nih.gov/16485136

12 December 2020

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

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https://pubmed.ncbi.nlm.nih.gov/16485136

12 December 2020

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HapScope: a software system for automated and visual analysis of functionally annotated haplotypes

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https://pubmed.ncbi.nlm.nih.gov/16485136

12 December 2020

based on heuristic

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SNP500Cancer: a public resource for sequence validation and assay development for genetic variation in candidate genes

1 reference

https://pubmed.ncbi.nlm.nih.gov/16485136

12 December 2020

based on heuristic

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Association of BRCA2 polymorphism at codon 784 (Met/Val) with breast cancer risk and prognosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/16485136

12 December 2020

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No association between the DNA repair gene XRCC3 T241M polymorphism and risk of skin cancer and breast cancer.

1 reference

https://pubmed.ncbi.nlm.nih.gov/16485136

12 December 2020

based on heuristic

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Variants in DNA double-strand break repair genes and breast cancer susceptibility

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https://pubmed.ncbi.nlm.nih.gov/16485136

12 December 2020

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/16485136

12 December 2020

based on heuristic

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Single nucleotide polymorphisms in breast cancer

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https://pubmed.ncbi.nlm.nih.gov/16485136

12 December 2020

based on heuristic

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Some statistical methods for combining experimental results

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https://pubmed.ncbi.nlm.nih.gov/16485136

12 December 2020

based on heuristic

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Breast cancer risk associated with genotypic polymorphism of the nonhomologous end-joining genes: a multigenic study on cancer susceptibility

1 reference

https://pubmed.ncbi.nlm.nih.gov/16485136

12 December 2020

based on heuristic

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Evaluating associations of haplotypes with traits

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https://pubmed.ncbi.nlm.nih.gov/16485136

12 December 2020

based on heuristic

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Polymorphisms of XRCC1 and XRCC3 genes and susceptibility to breast cancer

1 reference

https://pubmed.ncbi.nlm.nih.gov/16485136

12 December 2020

based on heuristic

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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

1 reference

https://pubmed.ncbi.nlm.nih.gov/16485136

12 December 2020

based on heuristic

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Polymorphisms XRCC1-R399Q and XRCC3-T241M and the risk of breast cancer at the Ontario site of the Breast Cancer Family Registry.

1 reference

https://pubmed.ncbi.nlm.nih.gov/16485136

12 December 2020

based on heuristic

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Identifying functional genetic variants in DNA repair pathway using protein conservation analysis

1 reference

https://pubmed.ncbi.nlm.nih.gov/16485136

12 December 2020

based on heuristic

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Collection of genomic DNA from adults in epidemiological studies by buccal cytobrush and mouthwash

1 reference

https://pubmed.ncbi.nlm.nih.gov/16485136

12 December 2020

based on heuristic

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DNA-repair genetic polymorphisms and breast cancer risk

1 reference

https://pubmed.ncbi.nlm.nih.gov/16485136

12 December 2020

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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://pubmed.ncbi.nlm.nih.gov/16485136

12 December 2020

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Identifiers

10.1007/S00439-006-0135-Z

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