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Genetic determinants of co-accessible chromatin regions in activated T cells across humans

Nature Genetics(2018)10.1038/s41588-018-0156-2Source: DataRank Database

Genetic determinants of co-accessible chromatin regions in activated T cells across humans is a research paper published in Nature Genetics (2018). On theSindex it has a DataRank of 0.799. It has been cited 205 times.

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0.799DataRank · unranked

Scored on demand from live citation data

Open Access205 citations

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›Methodology & internals

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Pipeline:MetadataData-paper checkEnrichmentCitation networkScoring

Enrichment:Funding (13 grants)Impact (FWCI 7.28)OA: closedTopics (68)Linked Datasets (12)DataCite Reuse (12)IDs (PubMed, PMC, OpenAlex)Annotations (2)SDGs (2)

FAIR Checklist

Context only (not used in score)

Findable (2/2)

Has DOI
Indexed in repositories

Accessible (1/2)

Open Access

Interoperable (2/2)

DataCite relations
Linked datasets

Reusable (0/3)

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DataRank Breakdown

Base Score 100%Citation Network 0%

Base Score Contribution

0.799

From this paper's citation signal

Citation Network Contribution

Citation network not refreshed for this result

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Authors (24)

Christine S. Cheng ORCID,Aviva P. Aiden,Atsede Siba,Marcin Tabaka ORCID,Dmytro Lituiev ORCID

Live enrichment

PubMed:29988122 PMC:PMC6097927 OpenAlex:https://openalex.org/W2837542075

NIAMS NIH HHS

Grant: R01 AR071522

NHGRI NIH HHS

Grant: U01 HG009380

NCI NIH HHS

Grant: F32 CA168253

NIDDK NIH HHS

Grant: F32 DK096822

NIAID NIH HHS

Grant: R21 AI133337

NHGRI NIH HHS

Grant: P50 HG007735

NIGMS NIH HHS

Grant: T32 GM067547

NHGRI NIH HHS

Grant: R01 HG007348

NHGRI NIH HHS

Grant: RM1 HG006193

NHGRI NIH HHS

Grant: U01 HG012192

National Institutes of Health

Grant: 1F32DK096822-01

Identification of mechanisms of diabetes predisposition in the 9p21 locus

National Institutes of Health

Grant: 5P50HG007735-02

Project 4

National Institutes of Health

Grant: 5R01AR071522-04

Fine mapping rheumatic disease variants using functional genomic sequencing

FWCI

7.28

Citation Percentile

1.0%

Influential Citations

Citation Trend

2018

2019

2020

2021

2022

2023

2024

2025

2026

closedLicense: Springer TDM

GREENhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6097927

publisherhttp://www.nature.com/articles/s41588-018-0156-2

publisherhttp://www.nature.com/articles/s41588-018-0156-2.pdf

journalhttps://doi.org/10.1038/s41588-018-0156-2

repositoryhttps://pubmed.ncbi.nlm.nih.gov/29988122

Fields of Study

Genomics and Chromatin DynamicsT-cell and B-cell Immunologyvaccines and immunoinformatics approachesMedicineBiology0301 basic medicine03 medical and health sciences0303 health sciencesAdultAutoimmune DiseasesCD4-Positive T-LymphocytesChromatinFemaleGene Expression RegulationGenotypeHumansMalePolymorphism, Single NucleotideRegulatory Sequences, Nucleic Acid

MeSH Terms

AdultAutoimmune DiseasesChromatinFemaleGene Expression RegulationGenotypeHumansMaleRegulatory Sequences, Nucleic AcidCD4-Positive T-LymphocytesPolymorphism, Single Nucleotide

Keywords

BiologyChromatinGeneGeneticsQuantitative trait locusTranscription factorGene expressionRegulatory sequenceExpression quantitative trait lociRegulation of gene expressionGenetic variationComputational biologySingle-nucleotide polymorphismGenotypeAdultCD4-Positive T-LymphocytesMaleAgricultural biotechnologyBioinformatics and Computational BiologyRegulatory Sequences, Nucleic AcidMedical and Health SciencesPolymorphism, Single NucleotideArticleAutoimmune DiseasesClinical Research2.1 Biological and endogenous factorsHumansAetiologyPolymorphismNucleic AcidHuman GenomeSingle NucleotideBiological SciencesStem Cell ResearchGene Expression RegulationFemaleRegulatory SequencesDevelopmental Biology

Sustainable Development Goals

SDG 3: 3. Good healthSDG 0: Good health and well-being

Additional file 1 of A systematic strategy for identifying causal single nucleotide polymorphisms and their target genes on Juvenile arthritis risk haplotypes

10.6084/m9.figshare.26289124.v1figshare

Additional file 1 of A systematic strategy for identifying causal single nucleotide polymorphisms and their target genes on Juvenile arthritis risk haplotypes

10.6084/m9.figshare.26289124figshare

Additional file 1 of Inferring cell-type-specific causal gene regulatory networks during human neurogenesis

10.6084/m9.figshare.26592962.v1figshare

Additional file 1 of Inferring cell-type-specific causal gene regulatory networks during human neurogenesis

10.6084/m9.figshare.26592962figshare

Additional file 5 of Inferring cell-type-specific causal gene regulatory networks during human neurogenesis

10.6084/m9.figshare.26592974.v1figshare

Additional file 5 of Inferring cell-type-specific causal gene regulatory networks during human neurogenesis

10.6084/m9.figshare.26592974figshare

Additional file 2 of Inferring cell-type-specific causal gene regulatory networks during human neurogenesis

10.6084/m9.figshare.26592965.v1figshare

Additional file 4 of Inferring cell-type-specific causal gene regulatory networks during human neurogenesis