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Exome sequencing identifies novel genes underlying primary congenital glaucoma in the National Birth Defects Prevention Study

Birth Defects Research(2024)10.1002/bdr2.2384Source: DataRank Database

Exome sequencing identifies novel genes underlying primary congenital glaucoma in the National Birth Defects Prevention Study is a research paper published in Birth Defects Research (2024). On theSindex it has a DataRank of 0. It has been cited 2 times.

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0DataRank · unranked

Scored on demand from live citation data

Open Access2 citations

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›Methodology & internals

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Pipeline:MetadataData-paper checkEnrichmentCitation networkScoring

Enrichment:Funding (23 grants)Impact (FWCI 0.83)OA: greenTopics (47)IDs (PubMed, PMC, OpenAlex)Annotations (1)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)

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Authors (24)

Kristin J. Moore ORCID,K.E. North,Tania A. Desrosiers ORCID,Suzan L. Carmichael ORCID,Janson J. White ORCID

Live enrichment

PubMed:38990107 PMC:PMC11245170 OpenAlex:https://openalex.org/W4400540382

National Human Genome Research Institute

Grant: U01 HG011744

National Human Genome Research Institute

Grant: UM1 HG006493

National Human Genome Research Institute

Grant: U24 HG011746

National Human Genome Research Institute

Grant: U24 HG008956