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Early‐Onset and Severe Complex Hereditary Spastic Paraplegia Caused by De Novo Variants in SPAST

Movement Disorders(2022)10.1002/mds.29225Source: DataRank Database

Early‐Onset and Severe Complex Hereditary Spastic Paraplegia Caused by De Novo Variants in SPAST is a research paper published in Movement Disorders (2022). On theSindex it has a DataRank of 0. It has been cited 21 times.

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Open Access21 citations

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datarank_citation_only_1hop_v6· scope data_onlyMethodology

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Enrichment:Funding (20 grants)Impact (FWCI 1.66)OA: greenTopics (64)IDs (PubMed, PMC, OpenAlex)Annotations (1)SDGs (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)

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Authors (18)

Afshin Saffari ORCID,Melanie Kellner,Marion Döbler‐Neumann,Catherine Jordan ORCID,Siddharth Srivastava ORCID

Live enrichment

PubMed:36103453 PMC:PMC10062395 OpenAlex:https://openalex.org/W4295758813

Deutsche Forschungsgemeinschaft

Grant: SA 4171/1‐1

National Institute of Neurological Disorders and Stroke

Grant: 1K08NS123552‐01

National Institute of Neurological Disorders and Stroke

Grant: K23NS119666

National Institute of Neurological Disorders and Stroke

Grant: R25 NS070682

National Institutes of Health

Grant: NIH P50 HD105351

NINDS NIH HHS

Grant: K08 NS123552

NICHD NIH HHS

Grant: P50 HD105351

NHGRI NIH HHS

Grant: U01 HG011758

NINDS NIH HHS

Grant: R01 NS072248

NINDS NIH HHS

Grant: 1K08NS123552-01

Development of a Translational Research Platform to Understand and treat Defective Protein Trafficking in Childhood-Onset Hereditary Spastic Paraplegia

National Institutes of Health

Grant: 1K23NS119666-01A1

Investigating the Genetic Landscape of Cerebral Palsy

National Institutes of Health

Grant: 5P50HD105351-02

Boston Children's Hospital/HMS Intellectual and Developmental Disabilities Research Center

Deutsche Forschungsgemeinschaft

Grant: unidentified

unidentified

European Commission

Grant: 779257

Solving the unsolved Rare Diseases

National Institutes of Health

Grant: 3R25NS070682-04S1

CH/BIDMC/Harvard Medical School Neurology Resident Research Education Program

European Commission

Grant: 825575

European Joint Programme on Rare Diseases

National Human Genome Research Institute

Manton Center for Orphan Disease Research, Boston Children's Hospital

Spastic Paraplegia Foundation

NIH Clinical Center

FWCI

1.66

Citation Percentile

0.8%

Citation Trend

2023

2024

2025

2026

greenLicense: Wiley Online Library User Agreement

repositoryhttps://pmc.ncbi.nlm.nih.gov/articles/PMC10062395/pdf/nihms-1882517.pdf

publisherhttps://onlinelibrary.wiley.com/doi/pdf/10.1002/mds.29225

publisherhttps://onlinelibrary.wiley.com/doi/full-xml/10.1002/mds.29225

publisherhttps://movementdisorders.onlinelibrary.wiley.com/doi/pdf/10.1002/mds.29225

Fields of Study

Hereditary Neurological DisordersAmyotrophic Lateral Sclerosis ResearchGenomics and Rare Diseases0301 basic medicine03 medical and health sciences0302 clinical medicineChild, PreschoolHumansCross-Sectional StudiesMuscle SpasticityMutationPhenotypeSpastic Paraplegia, HereditarySpastinChildAdolescentYoung AdultAdult

MeSH Terms

SpastinAdolescentAdultChildChild, PreschoolCross-Sectional StudiesHumansMuscle SpasticityMutationPhenotypeSpastic Paraplegia, HereditaryYoung Adult

Keywords

Hereditary spastic paraplegiaMedicineSpasticityDystoniaInterquartile rangePediatricsSpasticAge of onsetPhenotypeCerebral palsyInternal medicinePhysical therapyGeneticsBiologyDiseasePsychiatryNeurogeneticsSpastChildhood-onset Movement DisordersAdultSpastinAdolescentSpastic Paraplegia, HereditarySpastic Paraplegia, Hereditary: diagnosisSpastic Paraplegia, Hereditary: geneticsYoung AdultSpastin: geneticsCross-Sectional StudiesMuscle SpasticityChild, PreschoolMutationHumansChildinfo:eu-repo/classification/ddc/610

Sustainable Development Goals

SDG 3: 3. Good healthSDG 0: Good health and well-being

Early‐Onset and Severe Complex Hereditary Spastic Paraplegia Caused by De Novo Variants in SPAST

FAIR Checklist

Authors (18)

Funding (20 grants)

Impact

Open Access

Topics

Annotations (Europe PMC)