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Proteome-wide assessment of differential missense variant clustering in neurodevelopmental disorders and cancer

Cell Genomics(2025)10.1016/j.xgen.2025.100807Source: DataRank Database

Proteome-wide assessment of differential missense variant clustering in neurodevelopmental disorders and cancer is a research paper published in Cell Genomics (2025). On theSindex it has a DataRank of 0.241. It has been cited 4 times.

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0.241DataRank · unranked

Scored on demand from live citation data

Open Access4 citations

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›Methodology & internals

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Pipeline:MetadataData-paper checkEnrichmentCitation networkScoring

Enrichment:Funding (15 grants)Impact (FWCI 3.57)OA: goldTopics (43)IDs (PubMed, PMC, OpenAlex)Annotations (2)SDGs (1)

FAIR Checklist

Context only (not used in score)

Findable (1/2)

Has DOI

Accessible (1/2)

Open Access

Interoperable (0/2)

Reusable (0/3)

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DataRank Breakdown

Base Score 100%Citation Network 0%

Base Score Contribution

0.241

From this paper's citation signal

Citation Network Contribution

Citation network not refreshed for this result

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Authors (12)

Yilin Chen ORCID,Titilope M. Akinwe ORCID,Hillary B. Heins ORCID,Elvisa Mehinovic ORCID,Yoonhoo Chang ORCID

Live enrichment

PubMed:40073865 PMC:PMC12008811 OpenAlex:https://openalex.org/W4408330447

National Institutes of Health National Cancer Institute

Grant: U24CA258393

National Institute of Child Health and Human Development

Grant: P50HD103525

National Institute of Mental Health

Grant: R00MH117165

National Institute of Mental Health

Grant: R01MH126933

Simons Foundation Autism Research Initiative

Grant: 734069

National Institutes of Health

Grant: 5P50HD103525-03

Washington University Intellectual and Developmental Disabilities Research Center

National Institutes of Health

Grant: 1R01MH126933-01A1

Noncoding mutations in neurodevelopmental disorders

National Institutes of Health

Grant: 5U24CA258393-02

OpenCRAVAT: Informatics Tools for High-Throughput Analysis of Cancer Mutations

National Institutes of Health

Grant: 4R00MH117165-02

Nature and contribution of noncoding, regulatory mutations in neurodevelopmental disorders

Intellectual and Developmental Disabilities Research Center, School of Medicine, Washington University in St. Louis

National Institutes of Health

Instituto Tecnológico de Costa Rica

McDonnell Center for Cellular and Molecular Neurobiology, Washington University in St. Louis

Intellectual and Developmental Disabilities Research Center

Simons Foundation

FWCI

3.57

Citation Percentile

0.9%

Citation Trend

2025

2026

goldLicense: CC BY NC ND

journalhttps://doi.org/10.1016/j.xgen.2025.100807

publisherhttps://doi.org/10.1016/j.xgen.2025.100807

publisherhttps://api.elsevier.com/content/article/PII:S2666979X25000631?httpAccept=text/xml

publisherhttps://api.elsevier.com/content/article/PII:S2666979X25000631?httpAccept=text/plain

repositoryhttps://pubmed.ncbi.nlm.nih.gov/40073865

Fields of Study

Genetics and Neurodevelopmental DisordersGenomics and Rare DiseasesEpigenetics and DNA Methylation0303 health sciences03 medical and health sciencesHumansMutation, MissenseNeurodevelopmental DisordersNeoplasmsProteomeCluster Analysis

MeSH Terms

HumansNeoplasmsCluster AnalysisMutation, MissenseProteomeNeurodevelopmental Disorders

Keywords

Missense mutationProteomeComputational biologyCancerCluster analysisBioinformaticsBiologyMedicineGeneticsNeuroscienceComputer scienceMutationGeneArtificial intelligenceProteinClustering algorithmMissenseSomaticNeurodevelopmental DisordersDe NovoVariant Interpretation3D Protein Structure ModelsNeoplasmsMutation, MissenseHumansArticle

Sustainable Development Goals

SDG 0: Zero hunger