(Q45960056)

English

Comprehensive association testing of common genetic variation in DNA repair pathway genes in relationship with breast cancer risk in multiple populations.

scientific article published on 3 December 2007

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scholarly article

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Europe PubMed Central

PubMed publication ID

18 December 2017

http://europepmc.org/abstract/MED/18056155

Comprehensive association testing of common genetic variation in DNA repair pathway genes in relationship with breast cancer risk in multiple populations. (English)

1 reference

Europe PubMed Central

PubMed publication ID

18 December 2017

http://europepmc.org/abstract/MED/18056155

genetic variation

1 reference

based on heuristic

inferred from title

12

1 reference

Europe PubMed Central

PubMed publication ID

18 December 2017

http://europepmc.org/abstract/MED/18056155

Melissa A Frasco

object named as

Melissa Frasco

4

0 references

Loic Le Marchand

9

object named as

Loic Le Marchand

1 reference

Europe PubMed Central

PubMed publication ID

18 December 2017

Christopher A. Haiman

1

object named as

Christopher A Haiman

1 reference

Europe PubMed Central

PubMed publication ID

18 December 2017

Brian E. Henderson

18

object named as

Brian E Henderson

1 reference

Europe PubMed Central

PubMed publication ID

18 December 2017

David Van Den Berg

6

object named as

David Van Den Berg

1 reference

Europe PubMed Central

PubMed publication ID

18 December 2017

http://europepmc.org/abstract/MED/18056155

David J. Hunter

15

object named as

David J Hunter

1 reference

Europe PubMed Central

PubMed publication ID

18 December 2017

http://europepmc.org/abstract/MED/18056155

Susan E. Hankinson

10

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Susan E Hankinson

1 reference

Europe PubMed Central

PubMed publication ID

18 December 2017

16

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Anna H Wu

1 reference

Europe PubMed Central

PubMed publication ID

18 December 2017

http://europepmc.org/abstract/MED/18056155

Laurence N Kolonel

8

object named as

Laurence N Kolonel

1 reference

Europe PubMed Central

PubMed publication ID

18 December 2017

http://europepmc.org/abstract/MED/18056155

author name string

Chris Hsu

2

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Europe PubMed Central

PubMed publication ID

18 December 2017

http://europepmc.org/abstract/MED/18056155

Paul I W de Bakker

3

1 reference

Europe PubMed Central

PubMed publication ID

18 December 2017

http://europepmc.org/abstract/MED/18056155

Xin Sheng

5

1 reference

Europe PubMed Central

PubMed publication ID

18 December 2017

http://europepmc.org/abstract/MED/18056155

John T Casagrande

7

1 reference

Europe PubMed Central

PubMed publication ID

18 December 2017

http://europepmc.org/abstract/MED/18056155

Jiali Han

11

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Europe PubMed Central

PubMed publication ID

18 December 2017

http://europepmc.org/abstract/MED/18056155

Karen A Pooley

13

1 reference

Europe PubMed Central

PubMed publication ID

18 December 2017

http://europepmc.org/abstract/MED/18056155

Matthew L Freedman

14

1 reference

Europe PubMed Central

PubMed publication ID

18 December 2017

http://europepmc.org/abstract/MED/18056155

Daniel O Stram

17

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Europe PubMed Central

PubMed publication ID

18 December 2017

http://europepmc.org/abstract/MED/18056155

publication date

3 December 2007

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Europe PubMed Central

PubMed publication ID

18 December 2017

http://europepmc.org/abstract/MED/18056155

Human Molecular Genetics

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Europe PubMed Central

PubMed publication ID

18 December 2017

http://europepmc.org/abstract/MED/18056155

17

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Europe PubMed Central

PubMed publication ID

18 December 2017

http://europepmc.org/abstract/MED/18056155

6

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Europe PubMed Central

PubMed publication ID

18 December 2017

http://europepmc.org/abstract/MED/18056155

825-834

1 reference

Europe PubMed Central

PubMed publication ID

18 December 2017

http://europepmc.org/abstract/MED/18056155

Online Mendelian Inheritance in Man (OMIM).

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM354

21 January 2018

DNA repair capacity of lymphoblastoid cell lines from sisters discordant for breast cancer

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM354

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM354

21 January 2018

Ten genes for inherited breast cancer.

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM354

21 January 2018

Many amino acid substitution variants identified in DNA repair genes during human population screenings are predicted to impact protein function

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM354

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM354

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM354

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM354

21 January 2018

Genetic polymorphisms in base-excision repair pathway genes and risk of breast cancer.

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM354

21 January 2018

A haplotype map of the human genome

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM354

21 January 2018

High-resolution haplotype structure in the human genome

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM354

21 January 2018

Multiple regions within 8q24 independently affect risk for prostate cancer

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM354

21 January 2018

Human DNA repair genes

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM354

21 January 2018

A multiethnic cohort in Hawaii and Los Angeles: baseline characteristics

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM354

21 January 2018

Efficiency and power in genetic association studies

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM354

21 January 2018

Principal components analysis corrects for stratification in genome-wide association studies

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM354

21 January 2018

Body size, hormone therapy and risk of breast cancer in Asian-American women

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM354

21 January 2018

Allelic association of the human homologue of the mouse modifier Ptprj with breast cancer

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM354

21 January 2018

Predicting the effects of amino acid substitutions on protein function

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM354

21 January 2018

Human non-synonymous SNPs: server and survey

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM354

21 January 2018

PALB2, which encodes a BRCA2-interacting protein, is a breast cancer susceptibility gene

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM354

21 January 2018

Truncating mutations in the Fanconi anemia J gene BRIP1 are low-penetrance breast cancer susceptibility alleles

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM354

21 January 2018

Emergence of a DNA-damage response network consisting of Fanconi anaemia and BRCA proteins

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM354

21 January 2018

Localization of a breast cancer susceptibility gene, BRCA2, to chromosome 13q12-13.

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM354

21 January 2018

Multiple rare variants in different genes account for multifactorial inherited susceptibility to colorectal adenomas

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM354

21 January 2018

Genome-wide association study identifies novel breast cancer susceptibility loci

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM354

21 January 2018

A genome-wide association study identifies alleles in FGFR2 associated with risk of sporadic postmenopausal breast cancer

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM354

21 January 2018

Common variants on chromosomes 2q35 and 16q12 confer susceptibility to estrogen receptor-positive breast cancer

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM354

21 January 2018

Genome-wide strategies for detecting multiple loci that influence complex diseases.

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM354

21 January 2018

The EPIC Project: rationale and study design. European Prospective Investigation into Cancer and Nutrition

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM354

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM354

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM354

21 January 2018

Computational prediction of the effects of non-synonymous single nucleotide polymorphisms in human DNA repair genes.

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM354

21 January 2018

Counting potentially functional variants in BRCA1, BRCA2 and ATM predicts breast cancer susceptibility

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM354

21 January 2018

Haplotype tagging for the identification of common disease genes

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM354

21 January 2018

Identifiers

10.1093/HMG/DDM354

1 reference

Europe PubMed Central

PubMed publication ID

18 December 2017

http://europepmc.org/abstract/MED/18056155

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

18 December 2017

http://europepmc.org/abstract/MED/18056155

ResearchGate publication ID

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