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

Fibrillation and molecular characteristics are coherent with clinical and pathological features of 4-repeat tauopathy caused by MAPT variant G273R

Neurobiology of Disease(2020)10.1016/j.nbd.2020.105079Source: DataRank Database

Fibrillation and molecular characteristics are coherent with clinical and pathological features of 4-repeat tauopathy caused by MAPT variant G273R is a research paper published in Neurobiology of Disease (2020). On theSindex it has a DataRank of 0. It has been cited 8 times.

N/A

0DataRank · unranked

Scored on demand from live citation data

Open Access8 citations

Free full text

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 (16 grants)OA: goldTopics (39)IDs (PubMed)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 (17)

Helen Ling ORCID,Marla Gearing ORCID,Beth A. Dombroski ORCID,Laura B. Cantwell,Lea R’Bibo ORCID

Live enrichment

PubMed:32961270

Karin & Sten Mortstedt CBD Solutions

Grant: 512385

Swedish Research Council

Grant: 2015-04521

Swedish Research Council

Grant: 2019-04405

Goizueta Alzheimer's Disease Research Center

Grant: NIH P50 AG025688

Medical Research Council

Grant: MR/N026004/1

Understanding the genes for Parkinson's disease

Wellcome Trust

Grant: 202903/Z/16/Z

Medical Research Council

Grant: UKDRI-1009

NIA NIH HHS

Grant: P50 AG025688

National Institutes of Health

Grant: 2P50AG025688-11

A Proteogenomic Approach to Understanding AD GWAS Results

Wellcome Trust

Grant: 202903

BRAINEACv2: a resource for the interpretation of genetic variation in multiple regions of the adult human brain

Swedish Research Council

Grant: unidentified

unidentified

Medical Research Council

National Institute for Health Research (NIHR)

Alzheimer's Research UK

National Institute for Health Research (NIHR) Biomedical Research Centre(BRC) at University College London Hospitals NHS Foundation Trust and University College London

goldLicense: cc-by

publisherhttps://www.sciencedirect.com/science/article/pii/S0969996120303545/pdf

publisherhttps://api.elsevier.com/content/article/PII:S0969996120303545?httpAccept=text/xml

publisherhttps://api.elsevier.com/content/article/PII:S0969996120303545?httpAccept=text/plain

repositoryhttp://urn.kb.se/resolve?urn=urn:nbn:se:liu:diva-172199

repositoryhttps://doaj.org/article/f4fc7835db1b4223bcf2ec2d2ca9fce2

Fields of Study

0301 basic medicine03 medical and health sciences0303 health sciences

MeSH Terms

BrainNeurogliaNeuronsAnimalsDrosophilaBasal Ganglia DiseasesSupranuclear Palsy, ProgressiveTauopathiesMutation

Keywords

PathologyPSPTauopathyProgressive Supranuclear PalsyCBDMaptCorticobasal DegenerationAggregation Propensity4-Repeat TauG273r571572Neurosciences. Biological psychiatry. NeuropsychiatryMedical Genetics and GenomicsBasal Ganglia DiseasesAnimalsNeuronsMAPT; G273R; Pathology; 4-repeat tau; Tauopathy; Corticobasal degeneration; CBD; Progressive supranuclear palsy; PSP; Aggregation propensityBrainMedicinsk genetik och genomikTauopathies2808 NeurologyMutationDrosophilaSupranuclear Palsy, ProgressiveNeurogliaRC321-571

Sustainable Development Goals

SDG 3: 3. Good health