A simple method for assessing the strength of evidence for association at the level of the whole gene (Q38364027)

2 September 2017

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

1 reference

2 September 2017

Jo Knight

3

0 references

author name string

David Curtis

series ordinal

1

1 reference

PMC publication ID

3169937

2 September 2017

Anna E Vine

series ordinal

2

1 reference

2 September 2017

17 November 2008

1 reference

Advances and Applications in Bioinformatics and Chemistry

2 September 2017

1 reference

2 September 2017

1

1 reference

2 September 2017

115-120

1 reference

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

2 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3169937

One degree of freedom for dominance in indirect association studies

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3169937

Genome-wide genotyping in Parkinson's disease and neurologically normal controls: first stage analysis and public release of data

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3169937

Loss of function mutations in the gene encoding Omi/HtrA2 in Parkinson's disease

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3169937

Use of unphased multilocus genotype data in indirect association studies

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3169937

The future of association studies: gene-based analysis and replication

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3169937

Efficient computation of significance levels for multiple associations in large studies of correlated data, including genomewide association studies

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3169937

Assessing the probability that a positive report is false: an approach for molecular epidemiology studies

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3169937

Trimming, weighting, and grouping SNPs in human case-control association studies

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3169937

CLUMPHAP: a simple tool for performing haplotype-based association analysis

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3169937

A sliding-window weighted linkage disequilibrium test.

31 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3169937

Resampling-based multiple hypothesis testing procedures for genetic case-control association studies.

31 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3169937

Detecting disease associations due to linkage disequilibrium using haplotype tags: a class of tests and the determinants of statistical power

31 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3169937

Assessing optimal neural network architecture for identifying disease-associated multi-marker genotypes using a permutation test, and application to calpain 10 polymorphisms associated with diabetes.

31 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3169937

A note on calculation of empirical P values from Monte Carlo procedure

31 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3169937

GENECOUNTING: haplotype analysis with missing genotypes

31 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3169937

Truncated product method for combining P-values.

31 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3169937

Investigation of the Ability of Haplotype Association and Logistic Regression to Identify Associated Susceptibility Loci

31 August 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/21918610

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Program Report: GENECOUNTING Support Programs

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/21918610

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Omnibus permutation tests of the association of an ensemble of genetic markers with disease in case-control studies

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/21918610

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.2147/AABC.S4095

1 reference

2 September 2017

1 reference

PMC publication ID

3169937

2 September 2017

PubMed publication ID

21918610

1 reference

PMC publication ID

3169937