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A burden of rare copy number variants in obsessive-compulsive disorder

UNC Libraries(2024)10.17615/sw39-vp58Source: DataRank Database

A burden of rare copy number variants in obsessive-compulsive disorder is a research paper published in UNC Libraries (2024). On theSindex it has a DataRank of 0.

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0DataRank · unranked

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Open Access0 citations

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›Methodology & internals

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Pipeline:MetadataData-paper checkEnrichmentCitation networkScoring

Enrichment:Funding (4 grants)Impact (FWCI 0.00)OA: greenTopics (27)IDs (PubMed, OpenAlex)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 (19)

Christian Rück ORCID,Nora I. Strom ORCID,Manuel Mattheisen ORCID,Matthew Halvorsen ORCID,Bengt T. Fundín ORCID

Live enrichment

PubMed:26207759 OpenAlex:https://openalex.org/W4404168708

National Institutes of Health

Grant: 5R01MH110427-02

OCD: Novel Comparative Genomic Approaches to Identify Disease and Treatment Mechanisms

National Institutes of Health

Grant: 5R01MH119084-03

Predicting Binge and Purge Episodes from Passive and Active Apple Watch Data Using a Dynamical Systems Approach

National Institutes of Health

Grant: 3U01MH109528-02S1

1/7 Psychiatric Genomics Consortium: Finding actionable variation

National Institutes of Health

Grant: 5R01MH120170-05

Eating Disorders Genetics Initiative (EDGI)

FWCI

0.00

Citation Percentile

0.2%

greenLicense: CC BY

repositoryhttps://doi.org/10.17615/sw39-vp58

https://doi.org/10.1038/s41380-024-02763-7

https://dx.doi.org/10.17615/sw39-vp58

https://pubmed.ncbi.nlm.nih.gov/39463448

http://dx.doi.org/10.1038/s41380-024-02763-7

Fields of Study

Genomic variations and chromosomal abnormalitiesAutism Spectrum Disorder ResearchPrenatal Screening and Diagnostics

Keywords

Obsessive compulsivePsychologyComputational biologyBiologyPsychiatryMaleSwedenAdult570Obsessive-Compulsive DisorderDNA Copy Number VariationsGenotypeNorway610Polymorphism, Single NucleotidePsykiatriMedicinsk genetik och genomikArticleMedical Genetics and GenomicsCase-Control StudiesHumansFemaleGenetic Predisposition to DiseaseGenome-Wide Association Study

Sustainable Development Goals

SDG 0: Gender equality