(Q51852805)

14 April 2018

title

A practical case-control association test for detecting a susceptibility allele at a copy number variation locus. (English)

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14 April 2018

author name string

Jun Ohashi

series ordinal

1

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14 April 2018

publication date

6 February 2009

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Journal of Human Genetics

published in

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14 April 2018

volume

54

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14 April 2018

issue

3

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page(s)

169-173

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14 April 2018

https://scigraph.springernature.com/pub.10.1038/jhg.2009.8

exact match

0 references

cites work

Structural variation in the human genome

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2009.8

FCGR3B copy number variation is associated with susceptibility to systemic, but not organ-specific, autoimmunity

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2009.8

The influence of CCL3L1 gene-containing segmental duplications on HIV-1/AIDS susceptibility

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2009.8

Copy number variants and common disorders: filling the gaps and exploring complexity in genome-wide association studies

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2009.8

An algorithm for inferring complex haplotypes in a region of copy-number variation

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2009.8

MOCSphaser: a haplotype inference tool from a mixture of copy number variation and single nucleotide polymorphism data

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2009.8

Association test algorithm between a qualitative phenotype and a haplotype or haplotype set using simultaneous estimation of haplotype frequencies, diplotype configurations and diplotype-based penetrances

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2009.8

A haplotype map of the human genome

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2009.8

A second generation human haplotype map of over 3.1 million SNPs

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2009.8

Integrated detection and population-genetic analysis of SNPs and copy number variation

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2009.8

21 January 2018

Identifiers

DOI

10.1038/JHG.2009.8

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14 April 2018

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14 April 2018