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Genetic and phenotypic landscape of pediatric‐onset epilepsy in 142 Indian families: Counseling and therapeutic implications

Clinical Genetics(2024)10.1111/cge.14495Source: DataRank Database

Genetic and phenotypic landscape of pediatric‐onset epilepsy in 142 Indian families: Counseling and therapeutic implications is a research paper published in Clinical Genetics (2024). On theSindex it has a DataRank of 0. It has been cited 7 times.

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Open Access7 citations

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datarank_citation_only_1hop_v6· scope data_onlyMethodology

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Enrichment:Funding (7 grants)Impact (FWCI 2.75)OA: hybridTopics (74)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 (32)

Namanpreet Kaur,Selinda Mascarenhas,Lakshmi Priya Rao,Shruti Pande ORCID,Dhanya Lakshmi Narayanan ORCID

Live enrichment

PubMed:38374498 PMC:PMC7615923 OpenAlex:https://openalex.org/W4392782452

Wellcome Trust DBT India Alliance

Grant: IA/CRC/20/1/600002

National Institutes of Health

Grant: 1R01HD093570‐01A1

NICHD NIH HHS

Grant: R01 HD093570

NIH HHS

Grant: 1R01HD093570-01A1

Genetic Diagnosis of Neurodevelopmental Disorders in India

Wellcome Trust

Grant: unidentified

unidentified

Wellcome Trust

FWCI

2.75

Citation Percentile

0.9%

Citation Trend

2024

2025

hybridLicense: cc-by

journalhttps://onlinelibrary.wiley.com/doi/pdfdirect/10.1111/cge.14495

publisherhttps://onlinelibrary.wiley.com/doi/pdfdirect/10.1111/cge.14495

publisherhttps://onlinelibrary.wiley.com/doi/pdf/10.1111/cge.14495

journalhttps://doi.org/10.1111/cge.14495

repositoryhttps://pubmed.ncbi.nlm.nih.gov/38374498

Fields of Study

Genomics and Rare DiseasesGenetics and Neurodevelopmental DisordersGenomic variations and chromosomal abnormalities0301 basic medicine03 medical and health sciences0302 clinical medicineHumansEpilepsyIndiaMaleFemaleGenetic CounselingPhenotypeChildChild, PreschoolInfantGenetic Predisposition to DiseasePedigreeAge of OnsetGenetic Association StudiesAdolescentGenotypeDNA Copy Number Variations

MeSH Terms

AdolescentChildChild, PreschoolEpilepsyFemaleGenetic CounselingGenotypeHumansIndiaInfantMalePedigreePhenotypeAge of OnsetGenetic Predisposition to DiseaseGenetic Association StudiesDNA Copy Number Variations

Keywords

EpilepsyGenetic counselingEpilepsy syndromesGeneticsCopy-number variationPhenotypeMedicineDiseaseGenomic imprintingGenotype-phenotype distinctionIntellectual disabilityBioinformaticsBiologyPsychiatryGenePathologyGenomeIndiaGenetic TestingTherapeutic ImplicationsMaleAdolescentGenotypeDNA Copy Number VariationsInfantArticlePedigreeChild, PreschoolHumansFemaleGenetic Predisposition to DiseaseAge of OnsetChildGenetic Association Studies

Sustainable Development Goals

SDG 0: Good health and well-being

Genetic and phenotypic landscape of pediatric‐onset epilepsy in 142 Indian families: Counseling and therapeutic implications

FAIR Checklist

Authors (32)

Funding (7 grants)

Impact

Open Access

Topics

Annotations (Europe PMC)