References

References

1. Tinker, S.C., et al., Estimating the number of people with Tourette syndrome and persistent tic disorder in the United States. Psychiatr Res, 2022. 314.

2. Bitsko, R.H., et al., Health care needs of children with Tourette syndrome. J Child Neurol, 2013. 28(12): p. 1626-36.

3. Bitsko, R.H., et al., Indicators of social competence and social participation among U.S. children with Tourette syndrome. J Child Neurol, 2020. 35(9): p. 612-620.

4. Bitsko, R.H., et al., A national profile of Tourette syndrome, 2011–2012. J Dev Behav Pediatr, 2014. 35(5): p. 317–22.

5. Charania, S.N., et al., Bullying victimization and perpetration among us children with and without Tourette syndrome. J Dev Behav Pediatr, 2022. 43: p. 23-31.

6. Claussen, A.H., et al., Impact of Tourette syndrome on school measures in a nationally representative sample. J Dev Behav Pediatr 2018. 39(4): p. 335–342.

7. Ricketts, E.J., et al., Sleep Sufficiency in Pediatric and Adolescent Tourette's Disorder: National Survey of Children's Health. J Dev Behav Pediatr, 2018. 39(1): p. 72-76.

8. Robinson, L.R., et al., Tourette syndrome, parenting aggravation, and the contribution of co-occurring conditions among a nationally representative sample. Disabil Health J, 2013. 6(1): p. 26-35.

9. Ricketts, E.J., et al., Academic, interpersonal, recreational, and family impairment in children with Tourette syndrome and attention-deficit/hyperactivity disorder. Child Psychiatry & Human Development, 2022. 53(1): p. 3-15.

10. Ricketts, E.J., et al., Clinical characteristics of children with Tourette syndrome with and without sleep disorder. Pediatric Neurology, 2023. 141: p. 18-24.

11. Wolicki, S.B., et al., Children with Tourette syndrome in the United States: Parent-reported diagnosis, co-occurring disorders, severity, and influence of activities on tics. J Dev Behav Pediatr, 2019. 40(6): p. 407–414.

12. Wolicki, S.B., et al., Treatment use among children with Tourette syndrome living in the United States, 2014. Psychiatry Research, 2020. 293: p. 113400.

13. Augustine, E., et al., Design of a Multi-Site Study Assessing the Impact of Tic Disorders on Individuals, Families, and Communities. Pediatric Neurology, 2017. 68: p. 49-58.

14. Storch, E.A., et al., Suicidal Thoughts and Behaviors in Children and Adolescents with Chronic Tic Disorders. Depress Anxiety, 2015. 32(10): p. 744-53.

15. Yu, J. and H. Cooper, A Quantitative Review of Research Design Effects on Response Rates to Questionnaires. Journal of Marketing Research, 1983. 20(1): p. 36-44.