(Q34709103)

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An analysis of single nucleotide polymorphisms of 125 DNA repair genes in the Texas genome-wide association study of lung cancer with a replication for the XRCC4 SNPs

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scholarly article

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Europe PubMed Central

PubMed publication ID

4 August 2017

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An analysis of single nucleotide polymorphisms of 125 DNA repair genes in the Texas genome-wide association study of lung cancer with a replication for the XRCC4 SNPs (English)

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Europe PubMed Central

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4 August 2017

genome-wide association study

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single-nucleotide polymorphism

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based on heuristic

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Demetrius Albanes

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Demetrius Albanes

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Europe PubMed Central

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4 August 2017

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Thorunn Rafnar

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Richard Houlston

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Richard S Houlston

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Patrick Sulem

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Paul Brennan

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Kári Stefánsson

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Kari Stefansson

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4 August 2017

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Margaret R Spitz

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Christopher Amos

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Christopher I Amos

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Maria Teresa Landi

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Maria Teresa Landi

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Michael Thun

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author name string

Hongping Yu

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4 August 2017

Hui Zhao

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4 August 2017

Li-E Wang

3

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4 August 2017

Younghun Han

4

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4 August 2017

Wei V Chen

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Neil Caporaso

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James D McKay

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Yufei Wang

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Qingyi Wei

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4 August 2017

language of work or name

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publication date

5 February 2011

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10

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4 August 2017

4

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4 August 2017

398-407

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4 August 2017

describes a project that uses

genome-wide association study

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based on heuristic

inferred from title

Cancer statistics, 2010

1 reference

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A genome-wide association study of lung cancer identifies a region of chromosome 5p15 associated with risk for adenocarcinoma

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DNA repair: easy to visualize, difficult to elucidate

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DNA Damage, Aging, and Cancer

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Lung cancer susceptibility locus at 5p15.33

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Common 5p15.33 and 6p21.33 variants influence lung cancer risk

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The CHRNA5-A3 region on chromosome 15q24-25.1 is a risk factor both for nicotine dependence and for lung cancer

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Familial aggregation of common sequence variants on 15q24-25.1 in lung cancer

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Genetic susceptibility to cancer: the role of polymorphisms in candidate genes

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Genome-wide association scan of tag SNPs identifies a susceptibility locus for lung cancer at 15q25.1

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Common variants in the GDF5-UQCC region are associated with variation in human height

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Methods for meta-analysis in genetic association studies: a review of their potential and pitfalls

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Epidemiology of Lung Cancer

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A genome-wide association study of type 2 diabetes in Finns detects multiple susceptibility variants

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DNA double-strand break repair: from mechanistic understanding to cancer treatment

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Systematic review of the relationship between family history and lung cancer risk.

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USF1 and dyslipidemias: converging evidence for a functional intronic variant

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The cancer epidemiology of radiation

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An intronic SNP in a RUNX1 binding site of SLC22A4, encoding an organic cation transporter, is associated with rheumatoid arthritis

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12 December 2020

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10.1016/J.DNAREP.2011.01.005

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Europe PubMed Central

PubMed publication ID

4 August 2017

PMC publication ID

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Europe PubMed Central

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4 August 2017

PubMed publication ID

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Europe PubMed Central

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4 August 2017

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