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Revisiting the Relative Contribution of Common and Rare Genetic Variants to Attention-Deficit/Hyperactivity Disorder Among Diverse Populations

Biological Psychiatry(2024)10.1016/j.biopsych.2024.02.1007Source: DataRank Database

Revisiting the Relative Contribution of Common and Rare Genetic Variants to Attention-Deficit/Hyperactivity Disorder Among Diverse Populations is a research paper published in Biological Psychiatry (2024). On theSindex it has a DataRank of 0.

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datarank_citation_only_1hop_v6· scope data_onlyMethodology

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Enrichment:Funding (4 grants)Impact (FWCI 0.00)OA: greenTopics (21)IDs (PubMed, OpenAlex)

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 (3)

Brisa S. Fernandes ORCID,Zhongming Zhao ORCID,Yulin Dai ORCID

Live enrichment

PubMed:38599708 OpenAlex:https://openalex.org/W4394567820

National Institute of Dental and Craniofacial Research

Grant: R01DE029818

National Institute of Dental and Craniofacial Research

Grant: R01DE030122

National Institute on Aging

Grant: U01AG079847

National Library of Medicine

Grant: R01LM012806

FWCI

0.00

Citation Percentile

0.0%

greenLicense: https://www.elsevier.com/legal/tdmrep-license

repositoryhttps://pmc.ncbi.nlm.nih.gov/articles/PMC13343490/pdf/nihms-2187602.pdf

publisherhttps://api.elsevier.com/content/article/PII:S0006322324011272?httpAccept=text/xml

publisherhttps://api.elsevier.com/content/article/PII:S0006322324011272?httpAccept=text/plain

repositoryhttps://pmc.ncbi.nlm.nih.gov/articles/PMC13343490/

Fields of Study

Genomic variations and chromosomal abnormalitiesGenetics and Neurodevelopmental DisordersGenetic Associations and Epidemiology

MeSH Terms

Attention Deficit Disorder with HyperactivityHumansGenetic Predisposition to Disease

Keywords

Polygenic risk scoreAttention deficit hyperactivity disorderCopy-number variationMedical geneticsPersonalized medicineGeneticsGenetic variantsPrecision medicineGeneBiologyMedicinePsychiatryGenomeGenotypeSingle-nucleotide polymorphism