(Q33807900)

29 July 2017

A unified framework for multi-locus association analysis of both common and rare variants (English)

1 reference

29 July 2017

Daniel Shriner

1

0 references

author name string

Laura Kelly Vaughan

series ordinal

2

1 reference

PubMed ID

21281506

29 July 2017

language of work or name

English

0 references

publication date

31 January 2011

1 reference

29 July 2017

1 reference

29 July 2017

12

1 reference

29 July 2017

89

1 reference

https://scigraph.springernature.com/pub.10.1186/1471-2164-12-89

29 July 2017

0 references

cites work

Powerful SNP-set analysis for case-control genome-wide association studies

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3040731

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

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3040731

Genomewide association study for susceptibility genes contributing to familial Parkinson disease

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3040731

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

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3040731

A powerful and flexible multilocus association test for quantitative traits

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3040731

Shifting paradigm of association studies: value of rare single-nucleotide polymorphisms

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3040731

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

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3040731

Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3040731

Multiple roles of auxilin and hsc70 in clathrin-mediated endocytosis

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3040731

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

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3040731

Regional admixture mapping and structured association testing: conceptual unification and an extensible general linear model

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3040731

Linkage disequilibrium for different scales and applications

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3040731

Multiple rare variants in different genes account for multifactorial inherited susceptibility to colorectal adenomas

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3040731

Multiple Rare Alleles Contribute to Low Plasma Levels of HDL Cholesterol

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3040731

The allelic architecture of human disease genes: common disease-common variant... or not?

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3040731

Patterns of linkage disequilibrium in the human genome

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3040731

Genomic control for association studies

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3040731

Complexity and power in case-control association studies

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3040731

PNG1, a yeast gene encoding a highly conserved peptide:N-glycanase

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3040731

A third member of the synapsin gene family

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3040731

The power of independent types of genetic information to detect association in a case-control study design

4 July 2018

1 reference

Crossref

https://api.crossref.org/works/10.1186%2F1471-2164-12-89

Genomic control for association studies under various genetic models

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/21281506

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifying interacting SNPs using Monte Carlo logic regression

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/21281506

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Genomewide SNP assay reveals mutations underlying Parkinson disease

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/21281506

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1186/1471-2164-12-89

1 reference

PubMed ID

21281506

Dimensions Publication ID

29 July 2017

1 reference

https://scigraph.springernature.com/pub.10.1186/1471-2164-12-89

9 September 2019

1 reference

29 July 2017

1 reference

PubMed ID

21281506