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Genetic Risk Factors in Isolated Dystonia Escape Genome‐Wide Association Studies

Movement Disorders(2024)10.1002/mds.29968Source: DataRank Database

Genetic Risk Factors in Isolated Dystonia Escape Genome‐Wide Association Studies is a research paper published in Movement Disorders (2024). On theSindex it has a DataRank of 0. It has been cited 4 times.

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Open Access4 citations

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Enrichment:Funding (40 grants)Impact (FWCI 1.10)OA: hybridTopics (42)IDs (PubMed, PMC, OpenAlex)Annotations (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 (58)

Katja Lohmann ORCID,Eva‐Juliane Vollstedt ORCID,Tobias Reinberger ORCID,Lisa‐Marie Nuxoll ORCID,Gamze Kilic‐Berkmen ORCID

Live enrichment

PubMed:39287592 PMC:PMC11975433 OpenAlex:https://openalex.org/W4402557445

National Institutes of Health

Grant: NS065701

National Institutes of Health

Grant: NS095445

National Institutes of Health

Grant: NS116025

National Institutes of Health

Grant: P01NS087997

National Institutes of Health

Grant: R01DC011805

National Institutes of Health

Grant: R01DC012545

National Institutes of Health

Grant: R01NS026656

National Institutes of Health

Grant: R01NS088160

National Institutes of Health

Grant: TR001456

Deutsche Forschungsgemeinschaft

Grant: EXC2167

Deutsche Forschungsgemeinschaft

Grant: FOR2488

Bundesministerium für Bildung und Forschung

Grant: 01GM1514A

Bundesministerium für Bildung und Forschung

Grant: 01GM2302

National Institute for Neurological Research, Czech Republic

Grant: LX22NPO5107

NIA NIH HHS

Grant: R01 AG044546

NIDCD NIH HHS

Grant: R01 DC019353

NIDCR NIH HHS

Grant: R01 DE030464

NINDS NIH HHS

Grant: R01 NS121120

NINDS NIH HHS

Grant: R01 NS124228

NIA NIH HHS

Grant: RF1 AG053303

NIA NIH HHS

Grant: K23 AG059891

NINDS NIH HHS

Grant: R01 NS122943

NIA NIH HHS

Grant: R44 AG080861

NIA NIH HHS

Grant: RF1 AG058501

NIA NIH HHS

Grant: U01 AG058922

NINDS NIH HHS

Grant: U01 NS102035

NIA NIH HHS

Grant: P01 AG003991

NINDS NIH HHS

Grant: U54 NS065701

NINDS NIH HHS

Grant: U54 NS116025

NCATS NIH HHS

Grant: U54 TR001456

European Joint Programme on Rare Diseases

European Union

Technical University of Munich-Institute for Advanced Study

European Commission

Aligning Science Across Parkinson's

Technical University of Munich-Institute for Advanced Study

European Union

Aligning Science Across Parkinson's

European Joint Programme on Rare Diseases

FWCI

1.10

Citation Percentile

0.8%

Citation Trend

2025

2026

hybridLicense: cc-by-nc-nd

journalhttps://doi.org/10.1002/mds.29968

publisherhttps://doi.org/10.1002/mds.29968

publisherhttps://movementdisorders.onlinelibrary.wiley.com/doi/pdf/10.1002/mds.29968

repositoryhttps://pubmed.ncbi.nlm.nih.gov/39287592

repositoryhttp://nbn-resolving.de/urn:nbn:de:bvb:19-epub-123219-8

Fields of Study

Neurological disorders and treatmentsParkinson's Disease Mechanisms and TreatmentsGenetic Neurodegenerative DiseasesHumansGenome-Wide Association StudyPolymorphism, Single NucleotideMaleFemaleRisk FactorsGenetic Predisposition to DiseaseDystoniaAdultMiddle AgedDystonic Disorders

MeSH Terms

AdultDystoniaFemaleHumansMaleMiddle AgedRisk FactorsGenetic Predisposition to DiseasePolymorphism, Single NucleotideDystonic DisordersGenome-Wide Association Study

Keywords

Genome-wide association studyHeritabilityGenetic associationDystoniaMissing heritability problemSingle-nucleotide polymorphismGeneticsBiologyMedicinePsychiatryGenotypeGeneGwasCase–controlClinical ScoreAge At OnsetIsolated Dystonia