GENOMIZER: an integrated analysis system for genome-wide association data (Q31038986)

28 June 2017

title

GENOMIZER: an integrated analysis system for genome-wide association data (English)

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genome-wide association study

28 June 2017

main subject

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Peter Nürnberg

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28 June 2017

Michael Krawczak

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28 June 2017

Stefan Schreiber

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28 June 2017

Andre Franke

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28 June 2017

Michael Wittig

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28 June 2017

Andreas Wollstein

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28 June 2017

Markus Teuber

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28 June 2017

Tim Lu

series ordinal

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28 June 2017

Katrin Hoffmann

series ordinal

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28 June 2017

Jochen Hampe

series ordinal

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28 June 2017

publication date

1 June 2006

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28 June 2017

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inferred from page(s)

published in

Human Mutation

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28 June 2017

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28 June 2017

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28 June 2017

page(s)

583-588

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A single-nucleotide polymorphism tagging set for human drug metabolism and transport

28 June 2017

cites work

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https://api.crossref.org/works/10.1002%2FHUMU.20306

7 January 2021

The power of genomic control

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https://api.crossref.org/works/10.1002%2FHUMU.20306

7 January 2021

Unbiased application of the transmission/disequilibrium test to multilocus haplotypes

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20306

7 January 2021

Pedigree disequilibrium tests for multilocus haplotypes.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20306

7 January 2021

Parallel genotyping of human SNPs using generic high-density oligonucleotide tag arrays

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https://api.crossref.org/works/10.1002%2FHUMU.20306

7 January 2021

Genome scans and candidate gene approaches in the study of common diseases and variable drug responses

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https://api.crossref.org/works/10.1002%2FHUMU.20306

7 January 2021

An integrated system for high throughput TaqManTM based SNP genotyping

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20306

7 January 2021

Genome-wide association studies for common diseases and complex traits

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https://api.crossref.org/works/10.1002%2FHUMU.20306

7 January 2021

Mathematical multi-locus approaches to localizing complex human trait genes

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20306

7 January 2021

Efficiency and consistency of haplotype tagging of dense SNP maps in multiple samples.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20306

7 January 2021

The human genome browser at UCSC

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20306

7 January 2021

Complement factor H polymorphism in age-related macular degeneration

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20306

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20306

7 January 2021

Genotyping over 100,000 SNPs on a pair of oligonucleotide arrays.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20306

7 January 2021

Tests and estimates of allelic association in complex inheritance

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20306

7 January 2021

The optimal measure of allelic association

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20306

7 January 2021

The future of genetic studies of complex human diseases

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20306

7 January 2021

Genome-wide association studies: theoretical and practical concerns

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20306

7 January 2021

A note on exact tests of Hardy-Weinberg equilibrium

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https://api.crossref.org/works/10.1002%2FHUMU.20306

7 January 2021

Identifiers

DOI

10.1002/HUMU.20306

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28 June 2017

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