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

Differences in Sex‐Specific Frequency of Glucocerebrosidase Variant Carriers and Familial Parkinsonism

Movement Disorders(2022)10.1002/mds.29197Source: DataRank Database

Differences in Sex‐Specific Frequency of Glucocerebrosidase Variant Carriers and Familial Parkinsonism is a research paper published in Movement Disorders (2022). On theSindex it has a DataRank of 0. It has been cited 25 times.

N/A

0DataRank · unranked

Scored on demand from live citation data

Open Access25 citations

Download PDF

Cite:

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 (5 grants)Impact (FWCI 2.31)OA: greenTopics (33)IDs (PubMed, PMC, 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)

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 (12)

Susan Bressman ORCID,Deborah Raymond ORCID,Laurie J. Ozelius ORCID,Viktoriya Katsnelson,Katherine Leaver

Live enrichment

PubMed:36054306 PMC:PMC9669136 OpenAlex:https://openalex.org/W4293354860

National Institutes of Health

Grant: U01NS107016‐01A1

National Institutes of Health

Grant: U01NS094148‐01

NINDS NIH HHS

Grant: U01 NS107016

NINDS NIH HHS

Grant: U01 NS094148

Michael J. Fox Foundation for Parkinson's Research

FWCI

2.31

Citation Percentile

0.9%

Citation Trend

2023

2024

2025

2026

greenLicense: http://onlinelibrary.wiley.com/termsAndConditions#vor

repositoryhttps://www.ncbi.nlm.nih.gov/pmc/articles/9669136

publisherhttps://onlinelibrary.wiley.com/doi/pdf/10.1002/mds.29197

publisherhttps://onlinelibrary.wiley.com/doi/full-xml/10.1002/mds.29197

publisherhttps://movementdisorders.onlinelibrary.wiley.com/doi/pdf/10.1002/mds.29197

Fields of Study

Lysosomal Storage Disorders ResearchParkinson's Disease Mechanisms and TreatmentsGlycogen Storage Diseases and MyoclonusFemaleMaleHumansGlucosylceramidaseLeucine-Rich Repeat Serine-Threonine Protein Kinase-2MutationHeterozygoteParkinson Disease

MeSH Terms

Leucine-Rich Repeat Serine-Threonine Protein Kinase-2FemaleGlucosylceramidaseHeterozygoteHumansMaleMutationParkinson Disease

Keywords

GlucocerebrosidaseParkinsonismGeneticsMedicineNeuroscienceBiologyInternal medicineGeneDiseaseSexFamily HistoryParkinson'sLrrk2Gba

Sustainable Development Goals

SDG 0: Good health and well-being