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Random allelic expression in the adult human body

Cell Reports(2023)10.1016/j.celrep.2022.111945Source: DataRank Database

Random allelic expression in the adult human body is a dataset published in Cell Reports (2023). On theSindex it has a DataRank of 0.994, placing it in the top 20.4% of the data-sharing corpus. It has been cited 44 times, with 44 citing works in its 1-hop citation network.

Top 20%percentile

0.994DataRank

Ranks in the top 20% for downstream scientific impact

Data paper Open Access44 citations · 44 citing works in its network

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Linked data & code

dbgap

DataRank reads this dataset's downstream impact straight off the citation graph — no black box, no proprietary weighting. How is this computed?

›Methodology & internals

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Pipeline:MetadataData-paper checkEnrichmentCitation networkScoring

Enrichment:Funding (14 grants)Impact (FWCI 4.10)OA: goldTopics (47)IDs (PubMed, PMC, OpenAlex)Annotations (1)SDGs (1)

FAIR Checklist

Context only (not used in score)

Findable (1/2)

Has DOI

Accessible (1/2)

Open Access

Interoperable (0/2)

Reusable (1/3)

Dataset classification

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DataRank Breakdown

Base Score 57%Citation Network 43%

Base Score Contribution

0.571

From this paper's citation signal

Citation Network Contribution

0.423

From 26 citing papers with measurable signal

Learn more about DataRank methodology →

Top 5 citers driving the network score

Ranked by each citer's contribution to N(p) — log1p(C_q) divided by its reference count — out of 44 citers.

Early detection and stratification of colorectal cancer using plasma cell-free DNA fragmentomic profiling
Genomics20249 citations47 referencesContributes 0.049
Opportunities and tradeoffs in single-cell transcriptomic technologies
Trends in Genetics202351 citations90 referencesContributes 0.044
Mcam inhibits macrophage-mediated development of mammary gland through non-canonical Wnt signaling
Nature Communications202410 citations64 referencesContributes 0.037
Characterization of Loss-of-Imprinting in Breast Cancer at the Cellular Level by Integrating Single-Cell Full-Length Transcriptome with Bulk RNA-Seq Data
Biomolecules20242 citations32 referencesContributes 0.034
The Spectrum of the Heterozygous Effect in Biallelic Mendelian Diseases—The Symptomatic Heterozygote Issue
Genes202322 citations93 referencesContributes 0.034

Authors (6)

Elliott Ferris ORCID,Michael I. Love ORCID,Alun Thomas ORCID,Aaron R. Quinlan ORCID,Christopher Gregg ORCID

Live enrichment

PubMed:36640362 PMC:PMC10484211 OpenAlex:https://openalex.org/W4313549727

National Institutes of Health

Grant: R01AG064013

National Institutes of Health

Grant: R01HG012252

National Institutes of Health

Grant: R01MH109577

National Institutes of Health

Grant: R21MH118570

National Institutes of Health

Grant: R21MH120468

National Center for Advancing Translational Sciences

Grant: UL1TR002538

National Institutes of Health

Grant: 5R21MH120468-02

Functions and Mechanisms of Epigenetic Allelic Effects in the Brain

National Institutes of Health

Grant: 5R01MH109577-08

The Nature and Function of Genomic Imprinting in Monoaminergic Neurons

National Institutes of Health

Grant: 5R21MH118570-02

Allelic regulatory mechanisms in the brain

National Institutes of Health

Grant: 5R01HG012252-04

New algorithms and tools for large-scale genomic analyses

National Institutes of Health

Grant: 3UL1TR002538-01S1

Utah Center for Clinical and Translational Science

National Institutes of Health

Grant: 5R01AG064013-03

Noncoding Elements Shaping Brain Aging

Wellcome Trust

Grant: unidentified

unidentified

University of Utah

FWCI

4.10

Citation Percentile

1.0%

Citation Trend

2023

2024

2025

2026

goldLicense: cc-by

journalhttp://www.cell.com/article/S2211124722018460/pdf

publisherhttp://www.cell.com/article/S2211124722018460/pdf

publisherhttps://api.elsevier.com/content/article/PII:S2211124722018460?httpAccept=text/xml

publisherhttps://api.elsevier.com/content/article/PII:S2211124722018460?httpAccept=text/plain

journalhttps://doi.org/10.1016/j.celrep.2022.111945

Fields of Study

Genomics and Chromatin DynamicsGenetic Syndromes and ImprintingEpigenetics and DNA Methylation0301 basic medicine0303 health sciences03 medical and health sciencesHumansAdultAllelesHuman BodyChromosomesPhenotypeCell Line

MeSH Terms

AdultAllelesCell LineChromosomesHumansPhenotypeHuman Body

Keywords

GeneBiologyPhenotypeGeneticsAlleleHuman genomeGenomeNeurodegenerationComputational biologyDiseaseAgingCancerGene regulationDementiaGene ExpressionAllele-specific ExpressionRandom Monoallelic ExpressionCp: Molecular BiologyAdultHuman BodyQH301-705.5ArticleChromosomesCell LineHumansBiology (General)Alleles

Sustainable Development Goals

SDG 0: Good health and well-being

Related Papers (1)

HGNChelper: identification and correction of invalid gene symbols for human and mouse

N/A

1.3DataRank · unranked

F1000Research(2022)

co-cited

10.12688/f1000research.28033.2

Random allelic expression in the adult human body

FAIR Checklist

DataRank Breakdown

Top 5 citers driving the network score

Authors (6)

Funding (14 grants)

Impact

Open Access

Topics

Annotations (Europe PMC)

Related Papers (1)