(Q24813163)

4 July 2017

title

Characterization of the linkage disequilibrium structure and identification of tagging-SNPs in five DNA repair genes (English)

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4 July 2017

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linkage disequilibrium

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2

Nicola J Camp

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4 July 2017

Kristina Allen-Brady

1

1 reference

4 July 2017

language of work or name

English

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publication date

9 August 2005

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4 July 2017

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4 July 2017

volume

5

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4 July 2017

issue

1

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page(s)

99

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Common ataxia telangiectasia mutated haplotypes and risk of breast cancer: a nested case-control study

4 July 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1208870

7 April 2017

The Hallmarks of Cancer

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1208870

The International HapMap Project

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1208870

The structure of haplotype blocks in the human genome

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1208870

DNA double-strand breaks: signaling, repair and the cancer connection

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1208870

Dominant Negative ATM Mutations in Breast Cancer Families

7 April 2017

1 reference

https://api.crossref.org/works/10.1186/1471-2407-5-99

Selecting a maximally informative set of single-nucleotide polymorphisms for association analyses using linkage disequilibrium

22 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1208870

Linkage disequilibrium in the human genome

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1208870

A survey of haplotype variants at several disease candidate genes: the importance of rare variants for complex diseases.

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1208870

Finding haplotype tagging SNPs by use of principal components analysis

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1208870

Xeroderma pigmentosum: from symptoms and genetics to gene-based skin therapy

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1208870

Association analyses of DNA methyltransferase-1 (DNMT1) polymorphisms with systemic lupus erythematosus.

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1208870

The effects of scale: variation in the APOA1/C3/A4/A5 gene cluster

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1208870

A simple correction for multiple testing for single-nucleotide polymorphisms in linkage disequilibrium with each other

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1208870

Selection and evaluation of tagging SNPs in the neuronal-sodium-channel gene SCN1A: implications for linkage-disequilibrium gene mapping

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1208870

The hereditary nonpolyposis colorectal cancer syndrome: genetics and clinical implications

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1208870

Efficient selective screening of haplotype tag SNPs

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1208870

A dynamic programming algorithm for haplotype block partitioning

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1208870

Haplotypes at ATM identify coding-sequence variation and indicate a region of extensive linkage disequilibrium

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1208870

ATM-heterozygous germline mutations contribute to breast cancer-susceptibility

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1208870

Heterozygous ATM mutations do not contribute to early onset of breast cancer

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1208870

Allelic discrimination by nick-translation PCR with fluorogenic probes

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1208870

Cancers in 44 families with ataxia-telangiectasia

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1208870

Global analysis of ATM polymorphism reveals significant functional constraint

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1208870

Mortality and cancer incidence in 263 patients with ataxia-telangiectasia

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1208870

High-resolution haplotype structure in the human genome

30 May 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2407-5-99

Blocks of limited haplotype diversity revealed by high-resolution scanning of human chromosome 21.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2407-5-99

The impact of SNP density on fine-scale patterns of linkage disequilibrium

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2407-5-99

Selection of genetic markers for association analyses, using linkage disequilibrium and haplotypes.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2407-5-99

Principal component analysis for selection of optimal SNP-sets that capture intragenic genetic variation

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2407-5-99

HSD17B1 gene polymorphisms and risk of endometrial and breast cancer

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2407-5-99

Polymorphic variation in the CBLB gene in human type 1 diabetes.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2407-5-99

Cancer in patients with ataxia-telangiectasia and in their relatives in the nordic countries

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2407-5-99

Haplotype tagging single nucleotide polymorphisms and association studies.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2407-5-99

A first-generation linkage disequilibrium map of human chromosome 22

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2407-5-99

Chromosome-wide distribution of haplotype blocks and the role of recombination hot spots

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2407-5-99

Contributions of ATM mutations to familial breast and ovarian cancer.

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1208870

Haplotype tagging for the identification of common disease genes

28 November 2018

1 reference

12 December 2020

Incidence of cancer in 161 families affected by ataxia-telangiectasia

1 reference

12 December 2020

Neutral sequence variants and haplotypes at the 150 Kb ataxia-telangiectasia locus

1 reference

12 December 2020

The effect of SNP marker density on the efficacy of haplotype tagging SNPs--a warning

1 reference

12 December 2020

Characterization of linkage disequilibrium structure, mutation history, and tagging SNPs, and their use in association analyses:ELAC2 and familial early-onset prostate cancer

1 reference

12 December 2020

Identification of germline missense mutations and rare allelic variants in theATM gene in early-onset breast cancer

1 reference

12 December 2020

Identifiers

DOI

10.1186/1471-2407-5-99

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Dimensions Publication ID

4 July 2017

0 references

1 reference

4 July 2017

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