(Q42263943)

19 October 2017

A rapid method for combined analysis of common and rare variants at the level of a region, gene, or pathway (English)

1 reference

19 October 2017

David Curtis

1

1 reference

19 October 2017

24 July 2012

1 reference

Advances and Applications in Bioinformatics and Chemistry

19 October 2017

1 reference

19 October 2017

5

1 reference

19 October 2017

1-9

1 reference

Creative Commons Attribution-NonCommercial 3.0 Unported

19 October 2017

start time

1 July 2012

1 reference

April 2022 Public Data File from Crossref

copyright status

copyrighted

0 references

cites work

Finding disease variants in Mendelian disorders by using sequence data: methods and applications

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3413013

A simple method for assessing the strength of evidence for association at the level of the whole gene

26 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3413013

GATES: a rapid and powerful gene-based association test using extended Simes procedure

26 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3413013

CCRaVAT and QuTie-enabling analysis of rare variants in large-scale case control and quantitative trait association studies

26 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3413013

An evaluation of statistical approaches to rare variant analysis in genetic association studies

26 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3413013

A groupwise association test for rare mutations using a weighted sum statistic

26 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3413013

Methods for detecting associations with rare variants for common diseases: application to analysis of sequence data

26 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3413013

CARD15/NOD2 mutational analysis and genotype-phenotype correlation in 612 patients with inflammatory bowel disease

26 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3413013

Bias due to selection of rare variants using frequency in controls.

26 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3413013

17 August 2018

Identifiers

DOI

10.2147/AABC.S33049

1 reference

19 October 2017

1 reference

PMC publication ID

3413013

19 October 2017

PubMed publication ID

22888262

1 reference

PMC publication ID

3413013