(Q33638511)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24844982%20AND%20SRC:MED&resulttype=core&format=json

18 March 2020

title

A Bayesian method to incorporate hundreds of functional characteristics with association evidence to improve variant prioritization (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24844982%20AND%20SRC:MED&resulttype=core&format=json

18 March 2020

1 reference

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24844982%20AND%20SRC:MED&resulttype=core&format=json

18 March 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24844982%20AND%20SRC:MED&resulttype=core&format=json

18 March 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24844982%20AND%20SRC:MED&resulttype=core&format=json

18 March 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24844982%20AND%20SRC:MED&resulttype=core&format=json

18 March 2020

Sarah A Gagliano

1 reference

PubMed publication ID

24844982

28 July 2017

language of work or name

English

0 references

publication date

20 May 2014

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24844982%20AND%20SRC:MED&resulttype=core&format=json

18 March 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24844982%20AND%20SRC:MED&resulttype=core&format=json

18 March 2020

volume

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24844982%20AND%20SRC:MED&resulttype=core&format=json

18 March 2020

issue

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24844982%20AND%20SRC:MED&resulttype=core&format=json

18 March 2020

page(s)

e98122

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24844982%20AND%20SRC:MED&resulttype=core&format=json

Creative Commons Attribution 4.0 International

18 March 2020

start time

20 May 2014

1 reference

April 2022 Public Data File from Crossref

copyrighted

0 references

cites work

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

14 July 2018

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The genomic signature of trait-associated variants.

14 July 2018

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14 July 2018

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Annotation of functional variation in personal genomes using RegulomeDB

14 July 2018

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14 July 2018

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14 July 2018

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Systematic localization of common disease-associated variation in regulatory DNA

14 July 2018

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Incorporating prior information into association studies

14 July 2018

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SNPnexus: a web server for functional annotation of novel and publicly known genetic variants (2012 update).

14 July 2018

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HaploReg: a resource for exploring chromatin states, conservation, and regulatory motif alterations within sets of genetically linked variants

14 July 2018

1 reference

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Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk

14 July 2018

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Quality control parameters on a large dataset of regionally dissected human control brains for whole genome expression studies

14 July 2018

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The variant call format and VCFtools

14 July 2018

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Using Functional Annotation for the Empirical Determination of Bayes Factors for Genome-Wide Association Study Analysis

14 July 2018

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A user's guide to the encyclopedia of DNA elements (ENCODE)

14 July 2018

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Promise and pitfalls of the Immunochip

14 July 2018

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A map of human genome variation from population-scale sequencing

14 July 2018

1 reference

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A genome-wide association study identifies new psoriasis susceptibility loci and an interaction between HLA-C and ERAP1.

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4028284

Hundreds of variants clustered in genomic loci and biological pathways affect human height

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4028284

Regularization Paths for Generalized Linear Models via Coordinate Descent

14 July 2018

1 reference

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Abundant quantitative trait loci exist for DNA methylation and gene expression in human brain

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4028284

Trait-associated SNPs are more likely to be eQTLs: annotation to enhance discovery from GWAS

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4028284

Transcriptome genetics using second generation sequencing in a Caucasian population

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4028284

Bayesian statistical methods for genetic association studies

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4028284

Common polygenic variation contributes to risk of schizophrenia and bipolar disorder

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4028284

Potential etiologic and functional implications of genome-wide association loci for human diseases and traits

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4028284

Mapping the genetic architecture of gene expression in human liver

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4028284

A Bayesian measure of the probability of false discovery in genetic epidemiology studies

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4028284

Relative impact of nucleotide and copy number variation on gene expression phenotypes

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4028284

ROCR: visualizing classifier performance in R

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4028284

Conserved seed pairing, often flanked by adenosines, indicates that thousands of human genes are microRNA targets

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4028284

The UCSC Table Browser data retrieval tool

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4028284

"Chip"ping away at heart failure

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4028284

GENOVA: gene overlap analysis of GWAS results

30 October 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/24844982

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1371/JOURNAL.PONE.0098122

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24844982%20AND%20SRC:MED&resulttype=core&format=json

18 March 2020

0 references

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24844982%20AND%20SRC:MED&resulttype=core&format=json

18 March 2020

PubMed publication ID

24844982

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24844982%20AND%20SRC:MED&resulttype=core&format=json