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

Assessing the association of common genetic variants in EPHB4 and RASA1 with phenotype severity in familial cerebral cavernous malformation

Molecular Genetics & Genomic Medicine(2021)10.1002/mgg3.1794Source: DataRank Database

Assessing the association of common genetic variants in EPHB4 and RASA1 with phenotype severity in familial cerebral cavernous malformation is a research paper published in Molecular Genetics & Genomic Medicine (2021). On theSindex it has a DataRank of 0. It has been cited 2 times.

N/A

0DataRank · unranked

Scored on demand from live citation data

Open Access2 citations

Download PDF

Cite:

Linked data & code

refsnp omim refseq igsr

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 (4 grants)OA: goldTopics (62)IDs (PubMed, PMC)Annotations (4)

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 (13)

Shantel Weinsheimer ORCID,Jeffrey Nelson ORCID,Ludmila Pawlikowska ORCID,Christine K. Fox ORCID,Atif Zafar ORCID

Live enrichment

PubMed:34491620 PMC:PMC8580075

National Institutes of Health

Grant: U54 NS065705

National Institutes of Health

Grant: U2CTR002818

National Institutes of Health

Grant: 5U54NS065705-05

Brain Vascular Malformation Consortium: Predictors of clinical course.

National Institutes of Health

Grant: 5U2CTR002818-03

Data Management and Coordinating Center: Rare Diseases Clinical Research Network

goldLicense: CC BY NC ND

publisherhttps://onlinelibrary.wiley.com/doi/pdf/10.1002/mgg3.1794

publisherhttps://onlinelibrary.wiley.com/doi/full-xml/10.1002/mgg3.1794

Unpaywallhttps://escholarship.org/uc/item/4w47f85x

Europe_PMChttps://europepmc.org/articles/PMC8580075

Europe_PMChttps://europepmc.org/articles/PMC8580075?pdf=render

Fields of Study

0301 basic medicine03 medical and health sciences0303 health sciences

MeSH Terms

HumansHemangioma, Cavernous, Central Nervous SystemGenetic Predisposition to DiseaseReceptor, EphB4p120 GTPase Activating ProteinSeverity of Illness IndexCross-Sectional StudiesPhenotypeMutationPolymorphism, Single NucleotideAllelesAdolescentAdultAgedAged, 80 and overMiddle AgedChildChild, PreschoolInfantFemaleMaleGenetic VariationYoung AdultGenetic Association StudiesSymptom Assessment

Keywords

Vascular malformationEphB4Cerebral Cavernous MalformationRasa1Ras-erk/ras-mapk SignalingAdultMaleRas‐Erk/Ras‐MAPK signalingHemangioma, Cavernous, Central Nervous SystemAdolescentClinical Sciences610Ras-MAPK signalingQH426-470Ras-ErkPolymorphism, Single NucleotideMedicinal and Biomolecular ChemistryGeneticsHumansGenetic Predisposition to DiseaseChildAllelesGenetic Association StudiesAgedAged, 80 and overGenetic VariationInfantOriginal ArticlesMiddle AgedCross-Sectional StudiesPhenotypeChild, PreschoolMutationFemale