Fast set-based association analysis using summary data from GWAS identifies novel gene loci for human complex traits (Q36125596)

12 August 2017

Fast set-based association analysis using summary data from GWAS identifies novel gene loci for human complex traits (English)

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genome-wide association study

12 August 2017

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1 reference

6

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31 May 2020

Andrew Bakshi

1

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31 May 2020

Zhihong Zhu

2

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31 May 2020

Anna Vinkhuyzen

3

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31 May 2020

Jian Yang

7

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31 May 2020

author name string

W David Hill

4

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31 May 2020

Allan F McRae

5

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31 May 2020

language of work or name

English

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publication date

8 September 2016

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12 August 2017

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31 May 2020

volume

6

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31 May 2020

page(s)

32894

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Creative Commons Attribution 4.0 International

31 May 2020

copyright license

start time

8 September 2016

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April 2022 Public Data File from Crossref

copyright status

copyrighted

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describes a project that uses

genome-wide association study

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based on heuristic

inferred from title

cites work

Fast and Rigorous Computation of Gene and Pathway Scores from SNP-Based Summary Statistics

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5015118

Adaptive gene- and pathway-trait association testing with GWAS summary statistics.

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5015118

The UK10K project identifies rare variants in health and disease

2 October 2017

1 reference

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Genetic variance estimation with imputed variants finds negligible missing heritability for human height and body mass index

2 October 2017

1 reference

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Genetic studies of body mass index yield new insights for obesity biology

2 October 2017

1 reference

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Partitioning heritability of regulatory and cell-type-specific variants across 11 common diseases

2 October 2017

1 reference

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Defining the role of common variation in the genomic and biological architecture of adult human height

2 October 2017

1 reference

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Brain-specific Foxp1 deletion impairs neuronal development and causes autistic-like behaviour

2 October 2017

1 reference

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Biological insights from 108 schizophrenia-associated genetic loci

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5015118

Increased gene expression of FOXP1 in patients with autism spectrum disorders

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5015118

All SNPs are not created equal: genome-wide association studies reveal a consistent pattern of enrichment among functionally annotated SNPs

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5015118

HYST: a hybrid set-based test for genome-wide association studies, with application to protein-protein interaction-based association analysis

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5015118

Fast and accurate genotype imputation in genome-wide association studies through pre-phasing

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5015118

Conditional and joint multiple-SNP analysis of GWAS summary statistics identifies additional variants influencing complex traits

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5015118

Permutation-based approaches do not adequately allow for linkage disequilibrium in gene-wide multi-locus association analysis

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5015118

Five years of GWAS discovery

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5015118

Genome partitioning of genetic variation for complex traits using common SNPs

2 October 2017

1 reference

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GATES: A Rapid and Powerful Gene-Based Association Test Using Extended Simes Procedure

2 October 2017

1 reference

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GCTA: a tool for genome-wide complex trait analysis

2 October 2017

1 reference

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A map of human genome variation from population-scale sequencing

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5015118

De novo mutations in FOXP1 in cases with intellectual disability, autism, and language impairment

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5015118

A versatile gene-based test for genome-wide association studies

2 October 2017

1 reference

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Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium: Design of prospective meta-analyses of genome-wide association studies from 5 cohorts

2 October 2017

1 reference

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A second generation human haplotype map of over 3.1 million SNPs

2 October 2017

1 reference

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

2 October 2017

1 reference

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2 October 2017

Identifiers

DOI

10.1038/SREP32894

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27604177 AND SRC:MED&resulttype=core&format=json

Dimensions Publication ID

31 May 2020

0 references

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27604177 AND SRC:MED&resulttype=core&format=json

31 May 2020

PubMed publication ID

27604177

1 reference