HaploReg v4: systematic mining of putative causal variants, cell types, regulators and target genes for human complex traits and disease (Q36435043)

14 August 2017

HaploReg v4: systematic mining of putative causal variants, cell types, regulators and target genes for human complex traits and disease (English)

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14 August 2017

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1

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14 August 2017

2

Manolis Kellis

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PMC publication ID

4702929

14 August 2017

language of work or name

English

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publication date

10 December 2015

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14 August 2017

Nucleic Acids Research

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14 August 2017

44

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14 August 2017

D1

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14 August 2017

D877-81

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Creative Commons Attribution-NonCommercial 4.0 International

14 August 2017

start time

15 November 2016

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April 2022 Public Data File from Crossref

copyright status

copyrighted

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cites work

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Integrative analysis of 111 reference human epigenomes

30 September 2017

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GRASP v2.0: an update on the Genome-Wide Repository of Associations between SNPs and phenotypes

30 September 2017

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The Mouse Genome Database (MGD): facilitating mouse as a model for human biology and disease

30 September 2017

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Genetic variability in the regulation of gene expression in ten regions of the human brain

30 September 2017

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GRASP: analysis of genotype-phenotype results from 1390 genome-wide association studies and corresponding open access database

30 September 2017

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Expression QTL-based analyses reveal candidate causal genes and loci across five tumor types

30 September 2017

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Genome-wide identification of expression quantitative trait loci (eQTLs) in human heart

30 September 2017

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Common genetic variants modulate pathogen-sensing responses in human dendritic cells

30 September 2017

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Innate immune activity conditions the effect of regulatory variants upon monocyte gene expression

30 September 2017

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Systematic discovery and characterization of regulatory motifs in ENCODE TF binding experiments

30 September 2017

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The NHGRI GWAS Catalog, a curated resource of SNP-trait associations

30 September 2017

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Functional interpretation of non-coding sequence variation: concepts and challenges

30 September 2017

1 reference

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Systems genetics approaches to understand complex traits

30 September 2017

1 reference

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Transcriptome and genome sequencing uncovers functional variation in humans

30 September 2017

1 reference

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

30 September 2017

1 reference

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Genome-wide association analysis of blood-pressure traits in African-ancestry individuals reveals common associated genes in African and non-African populations

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4702929

Identification of nine new susceptibility loci for testicular cancer, including variants near DAZL and PRDM14

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4702929

Meta-analysis identifies four new loci associated with testicular germ cell tumor

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4702929

Genome-wide meta-analyses of multiancestry cohorts identify multiple new susceptibility loci for refractive error and myopia

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4702929

Lung eQTLs to help reveal the molecular underpinnings of asthma

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4702929

Interpreting noncoding genetic variation in complex traits and human disease

30 September 2017

1 reference

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An integrated map of genetic variation from 1,092 human genomes

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4702929

Toward systems neuroscience of ADHD: a meta-analysis of 55 fMRI studies

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4702929

An integrated encyclopedia of DNA elements in the human genome

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4702929

Brain expression genome-wide association study (eGWAS) identifies human disease-associated variants

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4702929

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

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4702929

A high-resolution map of human evolutionary constraint using 29 mammals

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4702929

Human metabolic individuality in biomedical and pharmaceutical research

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4702929

Trans-eQTLs reveal that independent genetic variants associated with a complex phenotype converge on intermediate genes, with a major role for the HLA

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4702929

Global analysis of the impact of environmental perturbation on cis-regulation of gene expression

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4702929

Identifying a high fraction of the human genome to be under selective constraint using GERP .

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4702929

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

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4702929

Transcriptome genetics using second generation sequencing in a Caucasian population

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4702929

BEDTools: a flexible suite of utilities for comparing genomic features

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4702929

Molecular genetics of adult ADHD: converging evidence from genome-wide association and extended pedigree linkage studies

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4702929

Mapping the genetic architecture of gene expression in human liver

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4702929

Population genomics of human gene expression

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4702929

NCBI reference sequences (RefSeq): a curated non-redundant sequence database of genomes, transcripts and proteins

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4702929

GENCODE: producing a reference annotation for ENCODE

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4702929

dbSNP: the NCBI database of genetic variation

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4702929

Large-scale imputation of epigenomic datasets for systematic annotation of diverse human tissues

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4702929

30 September 2017

Identifiers

DOI

10.1093/NAR/GKV1340

1 reference

14 August 2017

1 reference

DBLP Dataset 2021-01-02

28 January 2021

1 reference

PMC publication ID

4702929

14 August 2017

PubMed publication ID

26657631

1 reference

PMC publication ID

4702929