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The ZFHX3 GGC Repeat Expansion Underlying Spinocerebellar Ataxia Type 4 has a Common Ancestral Founder

Movement Disorders(2024)10.1002/mds.30077Source: DataRank Database

The ZFHX3 GGC Repeat Expansion Underlying Spinocerebellar Ataxia Type 4 has a Common Ancestral Founder is a research paper published in Movement Disorders (2024). On theSindex it has a DataRank of 0. It has been cited 5 times.

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Open Access5 citations

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datarank_citation_only_1hop_v6· scope data_onlyMethodology

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Enrichment:Funding (16 grants)Impact (FWCI 0.96)OA: hybridTopics (68)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 (0/3)

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Authors (24)

Pilar Álvarez Jerez ORCID,Claire Anderson ORCID,Martin Paucar ORCID,Jasmaine Lee,Daniel Nilsson ORCID

Live enrichment

PubMed:39635987 PMC:PMC11832790 OpenAlex:https://openalex.org/W4405075471

Intramural NIH HHS

Grant: ZIA AG000538

Wellcome Trust

Grant: 221951

Intramural NIH HHS

Grant: ZIA AG000542

Wellcome Trust

Grant: unidentified

unidentified

National Institutes of Health

Grant: 1ZIAAG000542-01

Long-read DNA sequencing of Parkinson's disease and related disorders

National Institutes of Health

Grant: 1ZIAAG000538-03

Long-read DNA sequencing of Alzheimers Disease and Related Dementias cases

National Institutes of Health

Wellcome Trust

Medical Research Council

Michael J. Fox Foundation for Parkinson's Research

NIH HHS

Medical Research Council

Michael J. Fox Foundation for Parkinson's Research

NIH HHS

Wellcome Trust

FWCI

0.96

Citation Percentile

0.7%

Citation Trend

2025

2026

hybridLicense: cc-by

journalhttps://onlinelibrary.wiley.com/doi/pdfdirect/10.1002/mds.30077

publisherhttps://onlinelibrary.wiley.com/doi/pdfdirect/10.1002/mds.30077

publisherhttps://movementdisorders.onlinelibrary.wiley.com/doi/pdf/10.1002/mds.30077

journalhttps://doi.org/10.1002/mds.30077

repositoryhttps://pubmed.ncbi.nlm.nih.gov/39635987

Fields of Study

Genetic Neurodegenerative DiseasesGenomics and Rare DiseasesUbiquitin and proteasome pathways0301 basic medicine03 medical and health sciences0303 health sciencesHumansSpinocerebellar AtaxiasMaleFemaleSwedenTrinucleotide Repeat ExpansionPedigreeMiddle AgedUtahAdultIowa

MeSH Terms

AdultFemaleHaplotypesHumansIowaMaleMiddle AgedPedigreeSwedenUtahMachado-Joseph DiseaseHomeodomain ProteinsFounder EffectTrinucleotide Repeat ExpansionSpinocerebellar Ataxias

Keywords

Spinocerebellar ataxiaTrinucleotide repeat expansionHaplotypeFounder effectGeneticsPopulationBiologyEvolutionary biologyMedicineGenotypeGeneAlleleAtaxiaRepeat Expansion DisorderLong‐read SequencingSpinocerebellar Ataxia Type 4MaleAdultClinical SciencesNeurodegenerativeRare DiseasesUtahHumansSpinocerebellar AtaxiasSwedenNeurology & NeurosurgeryBiomedical and Clinical SciencesBrief ReportNeurosciencesHuman Movement and Sports SciencesMiddle AgedIowaBrain DisordersPedigreelong-read sequencingFemale

Sustainable Development Goals

SDG 0: Partnerships for the goals