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A genome-wide spectrum of tandem repeat expansions in 338,963 humans

Cell(2024)10.1016/j.cell.2024.03.004Source: DataRank Database

A genome-wide spectrum of tandem repeat expansions in 338,963 humans is a dataset published in Cell (2024). On theSindex it has a DataRank of 1.1, placing it in the top 18% of the data-sharing corpus. It has been cited 39 times, with 38 citing works in its 1-hop citation network.

Top 18%percentile

1.1DataRank

Ranks in the top 18% for downstream scientific impact

Data paper Open Access39 citations · 38 citing works in its network

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Linked data & code

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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 (47 grants)Impact (FWCI 7.56)OA: hybridTopics (30)IDs (PubMed, PMC, OpenAlex)Annotations (2)

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 49%Citation Network 51%

Base Score Contribution

0.553

From this paper's citation signal

Citation Network Contribution

0.582

From 25 citing papers with measurable signal

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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 38 citers.

Novel Intermediate ATXN10 Alleles in the Healthy Peruvian Population: A Matter of Indigenous American Ethnic Origin
The Cerebellum20255 citations27 referencesContributes 0.066
Population-scale variability at short tandem repeat loci reveals pathogenicity signature
bioRxiv (Cold Spring Harbor Laboratory)202511 citations40 referencesContributes 0.062
Defining a tandem repeat catalog and variation clusters for genome-wide analyses
bioRxiv (Cold Spring Harbor Laboratory)202413 citations52 referencesContributes 0.051
Biallelic GGGCC repeat expansion leading to NAXE-related mitochondrial encephalopathy
npj Genomic Medicine20247 citations50 referencesContributes 0.042
Structural variation in 1,019 diverse humans based on long-read sequencing
Nature202556 citations107 referencesContributes 0.038

Authors (7)

Wenbin Ye ORCID,Jason Sheng Li ORCID,Jingyi Jessica Li ORCID,Éric Vilain ORCID,Tamer Sallam ORCID

Live enrichment

PubMed:38582080 PMC:PMC11065452 OpenAlex:https://openalex.org/W4393995286

National Human Genome Research Institute

Grant: U54 HG003067

National Institutes of Health

Grant: 1 OT2 OD025276

National Institutes of Health

Grant: 1 OT2 OD025337

National Institutes of Health

Grant: 1 U24 OD023163

National Institutes of Health

Grant: 3 OT2 OD023206

National Institutes of Health

Grant: 1 OT2 OD025277

National Institutes of Health

Grant: 3 OT2 OD023205

National Institutes of Health

Grant: 1 OT2 OD026555

National Institutes of Health

Grant: HHSN 263201600085U

National Institutes of Health

Grant: 1 U24 OD023121

National Institutes of Health

Grant: AOD 16037

National Institutes of Health

Grant: U24 OD023176

National Institutes of Health

Grant: 5UL1TR001414

National Institutes of Health

Grant: U01HG011745

National Institutes of Health

Grant: R01CA228140

National Institutes of Health

Grant: R01CA193466

National Institutes of Health

Grant: R01HG007538

NIH HHS

Grant: OT2 OD026550

NIH HHS

Grant: OT2 OD026553

NIH HHS

Grant: OT2 OD026557

NIH HHS

Grant: OT2 OD023205

NIH HHS

Grant: OT2 OD025277

NCI NIH HHS

Grant: T32 CA009054

NIH HHS

Grant: U24 OD023121

NHLBI NIH HHS

Grant: HHSN268201800001C

NIH HHS

Grant: OT2 OD026548

NIH HHS

Grant: U2C OD023196

NIH HHS

Grant: OT2 OD026551

NIH HHS

Grant: OT2 OD026552

NHLBI NIH HHS

Grant: R01 HL117626

NCATS NIH HHS

Grant: UL1 TR001414

NHLBI NIH HHS

Grant: HHSN268201100037C

NIH HHS

Grant: OT2 OD025337

NIH HHS

Grant: OT2 OD026556

NCI NIH HHS

Grant: P30 CA062203

NIH HHS

Grant: OT2 OD025276

NIH HHS

Grant: OT2 OD025315

NHLBI NIH HHS

Grant: U01 HL120393

NIH HHS

Grant: OT2 OD023206

NIH HHS

Grant: OT2 OD026554

NIH HHS

Grant: OT2 OD026555

NHLBI NIH HHS

Grant: R01 HL092577

NIH HHS

Grant: OT2 OD026549

NHLBI NIH HHS

Grant: R01 HL120393

NIH HHS

Grant: U24 OD023163

National Heart, Lung, and Blood Institute

Broad Institute

FWCI

7.56

Citation Percentile

1.0%

Influential Citations

Citation Trend

2024

2025

2026

hybridLicense: cc-by

journalhttp://www.cell.com/article/S0092867424002526/pdf

HYBRIDhttp://www.cell.com/article/S0092867424002526/pdf

publisherhttp://www.cell.com/article/S0092867424002526/pdf

publisherhttps://api.elsevier.com/content/article/PII:S0092867424002526?httpAccept=text/xml

publisherhttps://api.elsevier.com/content/article/PII:S0092867424002526?httpAccept=text/plain

Fields of Study

Genetic Neurodegenerative DiseasesMitochondrial Function and PathologyGenomics and Rare DiseasesMedicineBiology

MeSH Terms

Whole Genome SequencingHumansGenome, HumanTandem Repeat SequencesDatabases, GeneticDNA Repeat ExpansionGenome-Wide Association Study

Keywords

BiologyGenomeComputational biologyGeneticsTandemBroad spectrumEvolutionary biologyGeneHuman geneticsTandem repeatExpansionGwasRare DiseasesWhole Genome SequencingMissing HeritabilityAncestriesTr-gnomadGenome Aggregation