(Q41380870)

30 September 2017

Constraints on eQTL Fine Mapping in the Presence of Multisite Local Regulation of Gene Expression (English)

1 reference

30 September 2017

Jian Yang

11

0 references

Grant W. Montgomery

object named as

Grant W Montgomery

6

0 references

Urko M Marigorta

object named as

Urko M Marigorta

4

0 references

Andres Metspalu

5

object named as

Andres Metspalu

1 reference

30 September 2017

7

Tonu Esko

1 reference

30 September 2017

12

Peter M Visscher

1 reference

30 September 2017

9

Arshed A Quyyumi

1 reference

30 September 2017

Biao Zeng

1

1 reference

30 September 2017

Luke R Lloyd-Jones

2

1 reference

30 September 2017

Alexander Holloway

3

1 reference

30 September 2017

Kenneth L Brigham

8

1 reference

30 September 2017

Youssef Idaghdour

10

1 reference

30 September 2017

Joseph E Powell

13

1 reference

30 September 2017

Greg Gibson

14

1 reference

30 September 2017

9 June 2017

1 reference

30 September 2017

1 reference

30 September 2017

7

1 reference

30 September 2017

8

1 reference

30 September 2017

2533-2544

1 reference

Fine-mapping inflammatory bowel disease loci to single-variant resolution

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5555460

Fast, scalable prediction of deleterious noncoding variants from functional and population genomic data

1 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5555460

The Genetic Architecture of Gene Expression in Peripheral Blood

1 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5555460

Colocalization of GWAS and eQTL Signals Detects Target Genes

1 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5555460

Trans-ethnic Meta-analysis and Functional Annotation Illuminates the Genetic Architecture of Fasting Glucose and Insulin

1 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5555460

Direct Identification of Hundreds of Expression-Modulating Variants using a Multiplexed Reporter Assay

1 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5555460

Efficient Integrative Multi-SNP Association Analysis via Deterministic Approximation of Posteriors

1 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5555460

A Burden of Rare Variants Associated with Extremes of Gene Expression in Human Peripheral Blood.

1 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5555460

FINEMAP: efficient variable selection using summary data from genome-wide association studies

1 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5555460

Genetic fine mapping and genomic annotation defines causal mechanisms at type 2 diabetes susceptibility loci

1 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5555460

Large-scale identification of sequence variants influencing human transcription factor occupancy in vivo

1 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5555460

Partitioning heritability by functional annotation using genome-wide association summary statistics

1 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5555460

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

1 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5555460

Leveraging Functional-Annotation Data in Trans-ethnic Fine-Mapping Studies

1 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5555460

Statistical colocalization of genetic risk variants for related autoimmune diseases in the context of common controls

1 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5555460

Fine Mapping Causal Variants with an Approximate Bayesian Method Using Marginal Test Statistics

1 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5555460

Cross-population joint analysis of eQTLs: fine mapping and functional annotation

1 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5555460

The role of regulatory variation in complex traits and disease

1 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5555460

Integrative analysis of 111 reference human epigenomes

1 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5555460

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

1 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5555460

GPA: a statistical approach to prioritizing GWAS results by integrating pleiotropy and annotation

1 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5555460

Genetic and epigenetic fine mapping of causal autoimmune disease variants

1 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5555460

Integrating functional data to prioritize causal variants in statistical fine-mapping studies

1 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5555460

Blood gene expression profiles suggest altered immune function associated with symptoms of generalized anxiety disorder

1 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5555460

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

1 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5555460

Identifying causal variants at loci with multiple signals of association

1 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5555460

Gene expression profiles associated with acute myocardial infarction and risk of cardiovascular death

1 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5555460

Bayesian test for colocalisation between pairs of genetic association studies using summary statistics

1 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5555460

Mapping the genetic architecture of gene regulation in whole blood

1 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5555460

Heritability and genomics of gene expression in peripheral blood

1 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5555460

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

1 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5555460

A general framework for estimating the relative pathogenicity of human genetic variants

1 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5555460

Transcriptome and genome sequencing uncovers functional variation in humans

1 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5555460

Systematic identification of trans eQTLs as putative drivers of known disease associations

1 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5555460

Congruence of additive and non-additive effects on gene expression estimated from pedigree and SNP data

1 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5555460

Polygenic modeling with bayesian sparse linear mixed models

1 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5555460

A cross-platform analysis of 14,177 expression quantitative trait loci derived from lymphoblastoid cell lines

1 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5555460

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

1 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5555460

Systematic localization of common disease-associated variation in regulatory DNA

1 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5555460

An integrated encyclopedia of DNA elements in the human genome

1 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5555460

Prioritizing genetic variants for causality on the basis of preferential linkage disequilibrium

1 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5555460

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

1 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5555460

The Brisbane Systems Genetics Study: genetical genomics meets complex trait genetics

1 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5555460

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

1 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5555460

Lessons from eQTL mapping studies: non-coding regions and their role behind natural phenotypic variation in plants

1 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5555460

From noncoding variant to phenotype via SORT1 at the 1p13 cholesterol locus

1 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5555460

Candidate causal regulatory effects by integration of expression QTLs with complex trait genetic associations

1 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5555460

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

1 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5555460

Rare variants create synthetic genome-wide associations

1 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5555460

Geographical genomics of human leukocyte gene expression variation in southern Morocco

1 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5555460

Imputation-based analysis of association studies: candidate regions and quantitative traits

1 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5555460

Limited statistical evidence for shared genetic effects of eQTLs and autoimmune-disease-associated loci in three major immune-cell types.

1 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5555460

Evaluating the power to discriminate between highly correlated SNPs in genetic association studies

11 June 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/28600440

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1534/G3.117.043752

1 reference

30 September 2017

1 reference

30 September 2017

PubMed publication ID

28600440

1 reference