INTERSNP: genome-wide interaction analysis guided by a priori information (Q58273647)

1

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F. F. Brockschmidt

3

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M. P. Baur

4

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T. Becker

Genetic mapping in human disease

5

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language of work or name

English

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publication date

16 October 2009

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number of pages

7

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based on heuristic

inferred from page(s)

published in

Bioinformatics

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volume

25

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issue

24

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page(s)

3275-3281

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cites work

1 reference

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Joint analysis of tightly linked SNPs in screening step of genome-wide association studies leads to increased power

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Testing for association on the X chromosome

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A unified stepwise regression procedure for evaluating the relative effects of polymorphisms within a gene using case/control or family data: application to HLA in type 1 diabetes

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Genomic Control to the extreme

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The SNP ratio test: pathway analysis of genome-wide association datasets

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Susceptibility variants for male-pattern baldness on chromosome 20p11.

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From genomics to chemical genomics: new developments in KEGG

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Personal genomes: The case of the missing heritability

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

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Epistasis--the essential role of gene interactions in the structure and evolution of genetic systems

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

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PLINK: a tool set for whole-genome association and population-based linkage analyses

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The future of genetic studies of complex human diseases

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Genome-wide haplotype association study identifies the SLC22A3-LPAL2-LPA gene cluster as a risk locus for coronary artery disease

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10.1093/BIOINFORMATICS/BTP596

21 January 2018

Identifiers

DOI

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DBLP publication ID

journals/bioinformatics/HeroldSBBB09

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DBLP Dataset 2021-01-02