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FANCD2 genome binding is nonrandom and is enriched at large transcriptionally active neural genes prone to copy number variation

Functional & Integrative Genomics(2024)10.1007/s10142-024-01453-5Source: DataRank Database

FANCD2 genome binding is nonrandom and is enriched at large transcriptionally active neural genes prone to copy number variation is a research paper published in Functional & Integrative Genomics (2024). On theSindex it has a DataRank of 0. It has been cited 2 times.

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0DataRank · unranked

Scored on demand from live citation data

Open Access2 citations

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›Methodology & internals

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Pipeline:MetadataData-paper checkEnrichmentCitation networkScoring

Enrichment:Funding (3 grants)Impact (FWCI 0.77)OA: hybridTopics (28)IDs (PubMed, OpenAlex)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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Authors (3)

Jada L. Garzon ORCID,Niall G. Howlett ORCID,Justin L. Blaize

Live enrichment

PubMed:39365306 OpenAlex:https://openalex.org/W4403139322

National Institutes of Health

Grant: R01 HL149907

National Institutes of Health

Grant: 3R01HL149907-03S1

Chromatin State Alterations in Fanconi Anemia Hematologic Disease and Bone Marrow Failure

National Institutes of Health

Grant: 2P20GM103430-14

Bioinformatics Core

FWCI

0.77

Citation Percentile

0.8%

Citation Trend

2025

2026

hybridLicense: cc-by

journalhttps://link.springer.com/content/pdf/10.1007/s10142-024-01453-5.pdf

publisherhttps://link.springer.com/content/pdf/10.1007/s10142-024-01453-5.pdf

publisherhttps://link.springer.com/article/10.1007/s10142-024-01453-5/fulltext.html

journalhttps://doi.org/10.1007/s10142-024-01453-5

repositoryhttps://pubmed.ncbi.nlm.nih.gov/39365306

Fields of Study

Genomic variations and chromosomal abnormalitiesDNA Repair MechanismsGenomics and Chromatin Dynamics0303 health sciences03 medical and health sciences

MeSH Terms

DNA ReplicationFanconi AnemiaHumansNeuronsProtein BindingTranscription Initiation SiteFanconi Anemia Complementation Group D2 ProteinDNA Copy Number Variations

Keywords

BiologyGeneticsGeneCopy-number variationGenomeFanconi anemiaDNA repairNeuronsDNA ReplicationDNA Copy Number VariationsResearchFanconi Anemia Complementation Group D2 ProteinHumansTranscription Initiation SiteProtein Binding

Sustainable Development Goals

SDG 0: Good health and well-being