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

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References

2000An international perspective on Tourette syndrome: selected findings from 3500 individuals in 22 countries925 cited
2014Population prevalence of Tourette syndrome: A systematic review and meta‐analysis375 cited
2008The prevalence and epidemiology of Gilles de la Tourette syndrome369 cited
1985A Twin Study of Tourette Syndrome349 cited
2003Cntnap2 is disrupted in a family with gilles de la tourette syndrome and obsessive compulsive disorder234 cited
2009Prevalence of Diagnosed Tourette Syndrome in Persons Aged 6-17 Years - United States, 2007225 cited
2012Genome-wide association study of Tourette's syndrome211 cited
2011Rare Copy Number Variants in Tourette Syndrome Disrupt Genes in Histaminergic Pathways and Overlap with Autism208 cited
2017De Novo Coding Variants Are Strongly Associated with Tourette Disorder187 cited
2017Rare Copy Number Variants in NRXN1 and CNTN6 Increase Risk for Tourette Syndrome181 cited
2014Copy Number Variation in Obsessive-Compulsive Disorder and Tourette Syndrome: A Cross-Disorder Study141 cited
1981Familial Pattern and Transmission of Gilles de la Tourette Syndrome and Multiple Tics137 cited
2018Current Approaches and New Developments in the Pharmacological Management of Tourette Syndrome131 cited

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

107 cited

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