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

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English	INTERSNP: genome-wide interaction analysis guided by a priori information	article

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scholarly article

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title

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

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author

Michael Steffens

object named as

M. Steffens

series ordinal

2

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author name string

C. Herold

series ordinal

1

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F. F. Brockschmidt

series ordinal

3

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M. P. Baur

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4

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T. Becker

series ordinal

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

Genetic mapping in human disease

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1093%2FBIOINFORMATICS%2FBTP596

retrieved

21 January 2018

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

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1093%2FBIOINFORMATICS%2FBTP596

retrieved

21 January 2018

Testing for association on the X chromosome

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1093%2FBIOINFORMATICS%2FBTP596

retrieved

21 January 2018

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

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1093%2FBIOINFORMATICS%2FBTP596

retrieved

21 January 2018

Genomic Control to the extreme

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1093%2FBIOINFORMATICS%2FBTP596

retrieved

21 January 2018

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

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1093%2FBIOINFORMATICS%2FBTP596

retrieved

21 January 2018

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

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1093%2FBIOINFORMATICS%2FBTP596

retrieved

21 January 2018

From genomics to chemical genomics: new developments in KEGG

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1093%2FBIOINFORMATICS%2FBTP596

retrieved

21 January 2018

Personal genomes: The case of the missing heritability

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1093%2FBIOINFORMATICS%2FBTP596

retrieved

21 January 2018

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

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1093%2FBIOINFORMATICS%2FBTP596

retrieved

21 January 2018

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

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1093%2FBIOINFORMATICS%2FBTP596

retrieved

21 January 2018

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

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1093%2FBIOINFORMATICS%2FBTP596

retrieved

21 January 2018

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

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1093%2FBIOINFORMATICS%2FBTP596

retrieved

21 January 2018

The future of genetic studies of complex human diseases

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1093%2FBIOINFORMATICS%2FBTP596

retrieved

21 January 2018

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

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1093%2FBIOINFORMATICS%2FBTP596

retrieved

21 January 2018

Identifiers

DOI

10.1093/BIOINFORMATICS/BTP596

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DBLP publication ID

journals/bioinformatics/HeroldSBBB09

1 reference

stated in

DBLP Dataset 2021-01-02

retrieved

28 January 2021

PubMed publication ID

19837719

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