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De Novo Coding Variants Are Strongly Associated with Tourette Disorder

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References

2005Sequence Variants in SLITRK1 Are Associated with Tourette's Syndrome940 cited
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2011Rare Copy Number Variants in Tourette Syndrome Disrupt Genes in Histaminergic Pathways and Overlap with Autism208 cited

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2017Rare Copy Number Variants in NRXN1 and CNTN6 Increase Risk for Tourette Syndrome181 cited

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2021European clinical guidelines for Tourette syndrome and other tic disorders—version 2.0. Part I: assessment150 cited

2018De Novo Sequence and Copy Number Variants Are Strongly Associated with Tourette Disorder and Implicate Cell Polarity in Pathogenesis126 cited

2019De Novo Damaging DNA Coding Mutations Are Associated With Obsessive-Compulsive Disorder and Overlap With Tourette’s Disorder and Autism107 cited

2021Exome sequencing in obsessive–compulsive disorder reveals a burden of rare damaging coding variants84 cited

2025Genome-wide analyses identify 30 loci associated with obsessive–compulsive disorder82 cited

2018Ecopipam, a D1 receptor antagonist, for treatment of tourette syndrome in children: A randomized, placebo‐controlled crossover study82 cited

2018Tics and Tourette syndrome78 cited

2017Tourette syndrome: a disorder of the social decision-making network76 cited

2021Immunological Dysfunction in Tourette Syndrome and Related Disorders74 cited

2021Swearing and coprophenomena – A multidimensional approach36 cited