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Elevated common variant genetic risk for tourette syndrome in a densely-affected pedigree

UCL Discovery (University College London)(2024)10.17615/hf6f-r758Source: DataRank Database

Elevated common variant genetic risk for tourette syndrome in a densely-affected pedigree is a research paper published in UCL Discovery (University College London) (2024). On theSindex it has a DataRank of 0.

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Enrichment:Funding (2 grants)OA: hybridTopics (11)IDs (PubMed)SDGs (1)

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Authors (12)

Carol A. Mathews ORCID,Jeremiah M. Scharf ORCID,Andrew McQuillin ORCID,Dongmei Yu ORCID,Jin Szatkiewicz ORCID

Live enrichment

PubMed:34526668

National Institutes of Health

Grant: 5R01MH105500-05

Genetic & Environmental Predictors of Tourette Syndrome & OCD in Denmark

National Institutes of Health

Grant: 5R01MH110427-02

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

hybridLicense: Springer TDM

https://doi.org/10.1038/s41380-021-01277-w

https://dx.doi.org/10.17615/hf6f-r758

https://pubmed.ncbi.nlm.nih.gov/34526668

http://dx.doi.org/10.1038/s41380-021-01277-w

https://hdl.handle.net/1871.1/643e071e-3b47-41cb-b0d5-a9d898addfe3

Fields of Study

0301 basic medicine0303 health sciences03 medical and health sciences

Keywords

Risk FactorsTic DisordersHumansHumans; Pedigree; Polymorphism, Single Nucleotide/genetics; Risk Factors; Tic Disorders; Tourette Syndrome/geneticsPolymorphism, Single NucleotideArticlePedigreeTourette Syndrome

Sustainable Development Goals

SDG 3: 3. Good health