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Tourette International Collaborative Genetics (TIC Genetics) Study - NJCTS and NIMH

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De Novo Coding Variants Are Strongly Associated with Tourette Disorder

A. Willsey, T. Fernandez, Dongmei Yu, et al. (2017). Neuron. Cited 179 times. https://doi.org/10.1016/j.neuron.2017.04.024

The Inheritance of Tourette Disorder: A review.

D. Pauls, T. Fernandez, C. Mathews, et al. (2014). Journal of obsessive-compulsive and related disorders. Cited 77 times. https://doi.org/10.1016/J.JOCRD.2014.06.003

The Genetic Etiology of Tourette Syndrome: Large-Scale Collaborative Efforts on the Precipice of Discovery

John Vijay, Sagar Kommu, K. Maniadaki, et al. (2016). Frontiers in Neuroscience. Cited 54 times. https://doi.org/10.3389/fnins.2016.00351

The Tourette International Collaborative Genetics (TIC Genetics) study, finding the genes causing Tourette syndrome: objectives and methods

A. Dietrich, T. Fernandez, R. King, et al. (2014). European Child & Adolescent Psychiatry. Cited 50 times. https://doi.org/10.1007/s00787-014-0543-x

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

Sheng Wang, Jeffrey D. Mandell, Yogesh Kumar, et al. (2018). Cell reports. Cited 37 times. https://doi.org/10.1016/j.celrep.2018.08.082

Whole exome sequencing identifies genes associated with Tourette’s Disorder in multiplex families

Xiaolong Cao, Yeting Zhang, M. Abdulkadir, et al. (2021). Molecular psychiatry. Cited 27 times. https://doi.org/10.1038/s41380-021-01094-1

New Jersey Center for Tourette Syndrome Sharing Repository: methods and sample description

G. Heiman, R. King, J. Tischfield. (2008). BMC Medical Genomics. Cited 9 times. https://doi.org/10.1186/1755-8794-1-58