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Common risk variants for epilepsy are enriched in families previously targeted for rare monogenic variant discovery

EBioMedicine(2022)10.1016/j.ebiom.2022.104079Source: DataRank Database

Common risk variants for epilepsy are enriched in families previously targeted for rare monogenic variant discovery is a research paper published in EBioMedicine (2022). On theSindex it has a DataRank of 0.561. It has been cited 41 times.

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0.561DataRank · unranked

Scored on demand from live citation data

Open Access41 citations

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datarank_citation_only_1hop_v6· scope data_onlyMethodology

Pipeline:MetadataData-paper checkEnrichmentCitation networkScoring

Enrichment:Funding (6 grants)OA: goldTopics (11)IDs (PubMed, PMC)

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Accessible (1/2)

Open Access

Interoperable (0/2)

Reusable (0/3)

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DataRank Breakdown

Base Score 100%Citation Network 0%

Base Score Contribution

0.561

From this paper's citation signal

Citation Network Contribution

Citation network not refreshed for this result

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Authors (17)

Colin A. Ellis ORCID,Ingrid E Scheffer ORCID,Shiva Ganesan ORCID,Costin Leu ORCID,Lynette G. Sadleir ORCID

Live enrichment

PubMed:35636315 PMC:PMC9156876

NINDS NIH HHS

Grant: U24 NS120854

NICHD NIH HHS

Grant: U54 HD086984

NINDS NIH HHS

Grant: U54 NS108874

NINDS NIH HHS

Grant: K23 NS121520

NCATS NIH HHS

Grant: UL1 TR001878

NINDS NIH HHS

Grant: K02 NS112600

goldLicense: cc-by-nc-nd

publisherhttp://www.thelancet.com/article/S2352396422002602/pdf

publisherhttps://api.elsevier.com/content/article/PII:S2352396422002602?httpAccept=text/xml

publisherhttps://api.elsevier.com/content/article/PII:S2352396422002602?httpAccept=text/plain

repositoryhttps://www.ncbi.nlm.nih.gov/pmc/articles/9156876

repositoryhttps://doaj.org/article/e6ab89744c3c49e6bb0fbb1187c051fd

MeSH Terms

HumansEpilepsyEpilepsy, GeneralizedGenetic Predisposition to DiseaseMultifactorial InheritanceGenome-Wide Association StudyEpileptic Syndromes

Keywords

Epilepsy GeneticsPolygenic Risk ScoresFamilial EpilepsiesCommon Genetic Variation

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