Pilot corpus: NIH-funded biomedical datasets. Any DOI can be scored on demand — network effects sharpen as coverage grows.

Pentanucleotide Repeat Insertions in RAI1 Cause Benign Adult Familial Myoclonic Epilepsy Type 8

Movement Disorders(2023)10.1002/mds.29654Source: DataRank Database

Pentanucleotide Repeat Insertions in RAI1 Cause Benign Adult Familial Myoclonic Epilepsy Type 8 is a research paper published in Movement Disorders (2023). On theSindex it has a DataRank of 0. It has been cited 24 times.

N/A

0DataRank · unranked

Scored on demand from live citation data

Open Access24 citations

Download PDF

Cite:

Linked data & code

refsnp doi

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 (4 grants)Impact (FWCI 4.55)OA: hybridTopics (34)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 (0/3)

FAIR checklist signals are shown for context only and do not affect DataRank scoring.

Run a calibrated FAIR evaluation for this paper →

We only score data papers we can read in full — never from an abstract alone.

Authors (20)

Mohamed E. Dembélé,Monnat Pongpanich ORCID,Lassana Cissé ORCID,Chalurmpon Srichomthong,Alassane Baneye Maīga ORCID

Live enrichment

PubMed:37994247 PMC:PMC10872918 OpenAlex:https://openalex.org/W4388952110

Health Systems Research Institute

Grant: 65‐040

National Institute of Neurological Disorders and Stroke

Grant: U01HG007044 administered by the National Human Gen

NHGRI NIH HHS

Grant: U01 HG007044

NINDS NIH HHS

Grant: R01 NS118522

FWCI

4.55

Citation Percentile

1.0%

Citation Trend

2024

2025

2026

hybridLicense: public-domain

journalhttps://onlinelibrary.wiley.com/doi/pdfdirect/10.1002/mds.29654

publisherhttps://onlinelibrary.wiley.com/doi/pdfdirect/10.1002/mds.29654

publisherhttps://movementdisorders.onlinelibrary.wiley.com/doi/pdf/10.1002/mds.29654

journalhttps://doi.org/10.1002/mds.29654

repositoryhttps://pubmed.ncbi.nlm.nih.gov/37994247

Fields of Study

Glycogen Storage Diseases and MyoclonusEpilepsy research and treatmentGenetic Neurodegenerative DiseasesAdultHumansEpilepsies, MyoclonicIntronsMicrosatellite RepeatsRNASeizuresTrans-Activators

MeSH Terms

AdultEpilepsies, MyoclonicHumansIntronsRNASeizuresTrans-ActivatorsMicrosatellite Repeats

Keywords

HaploinsufficiencyEpilepsyGeneticsGeneBiologyDiseaseMutationTrinucleotide repeat expansionMedicineInternal medicineNeuroscienceRai1Long-read SequencingTttca Repeat InsertionsBafme8