(Q30981389)

14 October 2017

Leveraging Functional-Annotation Data in Trans-ethnic Fine-Mapping Studies (English)

1 reference

14 October 2017

Bogdan Pasaniuc

2

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author name string

Gleb Kichaev

series ordinal

1

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14 October 2017

language of work or name

English

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publication date

16 July 2015

1 reference

American Journal of Human Genetics

14 October 2017

1 reference

14 October 2017

97

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14 October 2017

2

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14 October 2017

260-271

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describes a project that uses

14 October 2017

Bayes' theorem

1 reference

18 June 2022

https://europepmc.org/article/PMC/4573268

based on heuristic

inferred from PubMed Central ID database lookup

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21 June 2018

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21 June 2018

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21 June 2018

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21 June 2018

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21 June 2018

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21 June 2018

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21 June 2018

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21 June 2018

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21 June 2018

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21 June 2018

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21 June 2018

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21 June 2018

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Fast and accurate imputation of summary statistics enhances evidence of functional enrichment

21 June 2018

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Multi-ethnic fine-mapping of 14 central adiposity loci

21 June 2018

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Joint analysis of functional genomic data and genome-wide association studies of 18 human traits

21 June 2018

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21 June 2018

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Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibility

21 June 2018

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Comprehensive functional annotation of 77 prostate cancer risk loci

21 June 2018

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Genetics of rheumatoid arthritis contributes to biology and drug discovery

21 June 2018

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21 June 2018

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Fine-scale mapping of the FGFR2 breast cancer risk locus: putative functional variants differentially bind FOXA1 and E2F1.

21 June 2018

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21 June 2018

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Discovery and refinement of loci associated with lipid levels

21 June 2018

1 reference

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Analysis of immune-related loci identifies 48 new susceptibility variants for multiple sclerosis

21 June 2018

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High trans-ethnic replicability of GWAS results implies common causal variants.

21 June 2018

1 reference

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Genome-wide characterization of shared and distinct genetic components that influence blood lipid levels in ethnically diverse human populations

21 June 2018

1 reference

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21 June 2018

1 reference

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Meta-analysis methods for genome-wide association studies and beyond

21 June 2018

1 reference

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Chromatin marks identify critical cell types for fine mapping complex trait variants

21 June 2018

1 reference

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21 June 2018

1 reference

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Bayesian refinement of association signals for 14 loci in 3 common diseases

21 June 2018

1 reference

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Discovery and fine mapping of serum protein loci through transethnic meta-analysis

21 June 2018

1 reference

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Systematic localization of common disease-associated variation in regulatory DNA

21 June 2018

1 reference

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The accessible chromatin landscape of the human genome

21 June 2018

1 reference

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An integrated encyclopedia of DNA elements in the human genome

21 June 2018

1 reference

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Efficiency of trans-ethnic genome-wide meta-analysis and fine-mapping

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4573268

Five years of GWAS discovery

21 June 2018

1 reference

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Dense genotyping identifies and localizes multiple common and rare variant association signals in celiac disease

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4573268

Deep resequencing of GWAS loci identifies independent rare variants associated with inflammatory bowel disease

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4573268

Genome partitioning of genetic variation for complex traits using common SNPs

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4573268

Mapping and analysis of chromatin state dynamics in nine human cell types

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4573268

Integrating common and rare genetic variation in diverse human populations

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4573268

Ancestry-shift refinement mapping of the C6orf97-ESR1 breast cancer susceptibility locus

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4573268

Leveraging genetic variability across populations for the identification of causal variants.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4573268

A common FADS2 promoter polymorphism increases promoter activity and facilitates binding of transcription factor ELK1.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4573268

Genetic structure of Europeans: a view from the North-East

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4573268

FGFR2 variants and breast cancer risk: fine-scale mapping using African American studies and analysis of chromatin conformation

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4573268

Comparing methods for performing trans-ethnic meta-analysis of genome-wide association studies

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4573268

Transethnic meta-analysis of genomewide association studies

25 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4573268

HAPGEN2: simulation of multiple disease SNPs

25 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4573268

Identifying candidate causal variants via trans-population fine-mapping.

25 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4573268

10.1016/J.AJHG.2015.06.007

25 November 2018

Identifiers

DOI

1 reference

14 October 2017

1 reference

14 October 2017

PubMed publication ID

26189819

1 reference