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The genetics of Tourette syndrome: A review
Open accessAbstract
Objectives This article summarizes and evaluates recent advances in the genetics of Gilles de la Tourette syndrome (GTS).Methods This is a review of recent literature focusing on (1) the genetic etiology of GTS; (2) common genetic components of GTS, attention deficit hyperactivity disorder (ADHD), and obsessive compulsive disorder (OCD); (3) recent linkage studies of GTS; (4) chromosomal translocations in GTS; and (5) candidate gene studies.Results Family, twin, and segregation studies provide strong evidence for the genetic nature of GTS. GTS is a heterogeneous disorder with complex inheritance patterns and phenotypic manifestations. Family studies of GTS and OCD indicate that an early-onset form of OCD is likely to share common genetic factors with GTS. While there apparently is an etiological relationship between GTS and ADHD, it appears that the common form of ADHD does not share genetic factors with GTS. The largest genome wide linkage study to date observed evidence for linkage on chromosome 2p23.2 (P=3.8x10(-5)). No causative candidate genes have been identified, and recent studies suggest that the newly identified candidate gene SLITRK1 is not a significant risk gene for the majority of individuals with GTS.Conclusion The genetics of GTS are complex and not well understood. The Genome Wide Association Study (GWAS) design can hopefully overcome the limitations of linkage and candidate gene studies. However, large-scale collaborations are needed to provide enough power to utilize the GWAS design for discovery of causative mutations. Knowledge of susceptibility mutations and biological pathways involved should eventually lead to new treatment paradigms for GTS.
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“a rare mutation in the gene SLITRK1 is associated with human TS [613,614].”
From Reward circuitry dysfunction in psychiatric and neurodevelopmental disorders and genetic syndromes: animal models and clinical findings (2012) · cites this paper as [614]
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Items 101–200 of 212
Association study of the SLITRK5 gene and Tourette syndrome
Zhang, K., Feng, Y., Wigg, K. G., Sandor, P., & Barr, C. L. (2014) · Psychiatric Genetics · doi:10.1097/ypg.0000000000000067 · Cited by 10
“Three self-administered instruments were used to obtain the information: about mood and anxiety and other psychiatric symptoms SCL90, OC symptoms (OCD inventory derived from Leyton Obsessive–Compulsive inventory) and ADHD symptoms (Conner’s Parent Rating Scale for children younger than 16 years of age).”
BackgroundInfluentialAssociation between Tourette Syndrome and the Dopamine D3 Receptor Gene Rs6280
He, F., Zheng, Y., Huang, H., Cheng, Y.-H., & Wang, C. (2015) · Chinese Medical Journal · doi:10.4103/0366-6999.151665 · Cited by 10
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Self-citationLRRTM4 Terminal Exon Duplicated in Family with Tourette Syndrome, Autism and ADHD
Clarke, R. A., & Eapen, V. (2021) · Genes · doi:10.3390/genes13010066 · Cited by 9
“Twin studies suggest a monozygotic to dizygotic concordance of 77 to 23%, and family studies have consistently shown a 10- to 100-fold increase in the rates of TS in first-degree relatives [4].”
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“However, the susceptible genes or relevant DNA sequence variations that might be involved in the pathogenesis of TD have not been identified [13,14].”
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“Several twin and family studies have indicated that TS is highly heritable and very likely to be genetically related [6].”
BackgroundRepublished review: Tourette's syndrome and other tic disorders
Rickards, H. E. (2011) · Postgraduate Medical Journal · doi:10.1136/pgmj.2010.223685rep · Cited by 8
“Family studies show that it is to a large extent heritable alongside an early onset form of OCD; large family pedigree studies have indicated that these two disorders cluster together but the commonest form of ADHD does not share genetic factors with Tourette's syndrome.”
BackgroundPharmacological Treatment of Tics
Cavanna, A. E. (2020) · Cambridge University Press eBooks · doi:10.1017/9781108186599 · Cited by 8
How do daily routines and situational factors affect the severity of obsessive-compulsive disorder?
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“To date, the precise etiology of TS is still unknown, but there is evidence demonstrating that the etiology of TS may be associated with genetic (O’Rourke et al., 2009) and environmental (Conelea and Woods, 2008) factors.”
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“Although an etiological relationship is evident between Tourette syndrome and ADHD, no genetic factors are shared between the most common forms of these disorders.(7) Based on the above background, we aim to use a questionnaire survey to analyze the correlation of Tourette syndrome with four major allergic diseases (a…”
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“Numerous gene (dopaminergic, serotonergic, and glutamatergic) mutations have been associated with TC (Georgitsi et al., 2016; O’Rourke, Scharf, Yu, & Pauls, 2009 In a systematic review of 22 studies, TS was associated with prenatal (maternal smoking, alcohol exposure and pregnancy complications),…”
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“To the best of our knowledge, there have been only 2 studies that have examined smooth pursuit eye movements of children with TS.13,18 Bollen et al13 reported normal smooth pursuit eye movements among children with TS, although it lacked formal statistical analyses and a normal comparison group.”
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“chronic tics, and OCD in first-degree relatives and the high estimated rate (80–90%) of heritability in twin studies (O’Rourke et al., 2009).”
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Gong, H., Du, X., Su, A., & Du, Y.-W. (2023) · Neurological Sciences · doi:10.1007/s10072-023-07172-2 · Cited by 4
The Developmental Neurobiology of Repetitive Behavior
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Association of poly(ADP-ribose) polymerase-1 polymorphism with Tourette syndrome
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“The genetic contribution to OCD and CTD has been well established for decades 8,9 , but the identification of specific risk genes and alleles has so far had limited impact on treatment development or the understanding and clinical management of these syndromes.”
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Yang, C., Yang, N., Hao, Z., Yu, D., & Zhang, L. (2025) · Journal of Psychiatric Research · doi:10.1016/j.jpsychires.2025.02.047 · Cited by 3
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A case of Gilles de la Tourette's syndrome
Prakash, J., Singh, P., Bhat, P. S., Srivastava, K., & Gupta, V. S. (2015) · Industrial Psychiatry Journal · doi:10.4103/0972-6748.181727 · Cited by 3
“Individual had GTS with associated OCD.”
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Genetics of Tourette syndrome and tic disorders
Jain, P., Paschou, P., & Topaloudi, A. (2026) · Handbook of clinical neurology · doi:10.1016/b978-0-443-13554-5.00020-1 · Cited by 2
The Phenomenology of Obsessive–Compulsive Symptoms in Tourette Syndrome
Ferrão, Y. A., de Alvarenga, P. G., Hounie, A. G., de Mathis, M. A., Farhat, L. C., do Rosário, M. C., & Miguel, E. C. (2022) · Oxford University Press eBooks · doi:10.1093/med/9780197543214.003.0004 · Cited by 2
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Genetics of obsessive-compulsive disorder and Tourette disorder
Burton, C. L., Barta, C., Cath, D. C., GELLER, D. A., van den Heuvel, O. A., Shugart, Y. Y., Eapen, V., Grünblatt, E., & Zai, G. C. (2019) · Elsevier eBooks · doi:10.1016/b978-0-12-813176-3.00020-1 · Cited by 2
Tourette syndrome in children and adolescents: aetiology, presentation and treatment
Robertson, M. M. (2016) · BJPsych Advances · doi:10.1192/apt.bp.114.014092 · Cited by 3
“For full reviews of the genetics of Tourette syndrome see O’Rourke et al (2009) and Deng et al (2012).”
MethodIncreased expression of genetically-regulated FLT3 implicated in Tourette’s SyndromePreprint
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Dopamine in Tourette syndrome: a 30-year bibliometric analysis of hotspot evolution
Liu, Q., Zhu, Z., Luo, F., Ding, Y., Wang, Y., Zhao, C., & Yuan, B. (2025) · Frontiers in Neurology · doi:10.3389/fneur.2025.1589842 · Cited by 1
“Family, twin studies provide evidence for the strong heritability of TS (39).”
Tourette Syndrome; Is It an Annoying Disorder or an Inspiring Companion??!!!
Zaky, E. A. (2017) · Journal of Child and Adolescent Behaviour · doi:10.4172/2375-4494.1000353 · Cited by 1
“In addition, it was found that gender plays a role in gene expression in cases of TS as males are more likely to manifest tics than females [14,15].”
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Introduction: The Long and Winding Road to Tourette Syndrome
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Behavioral Treatment of Tourette Disorder
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Lack of association between SLC5A7 polymorphisms and Tourette syndrome in a Chinese Han population
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“To date, many candidate genes have been studied such as dopamine receptors D1–D4, dopamine β–hydroxylase (DBH), monoamine oxidase A (MAOA), and serotonin receptor (5-HT2A) [19], but most of these candidate gene associations have not been”
Prenatal Risk Factors for Tourette Syndrome: a Systematic Review Update
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Evaluation and Differential Diagnosis of Tics and Related Disorders
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GENETIC ANIMAL MODELS OF TOURETTE SYNDROME: THE LONG AND WINDING ROAD
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Elia, J., Sackett, J. C., Kurtz, N., de Berardinis, R., Larsen, L., Tang, S.-C., Hakonarson, H. H., & Nissley‐Tsiopinis, J. (2013) · doi:10.2217/ebo.13.190
Cavanna, A. E. (2020) · Cambridge University Press eBooks · doi:10.1017/9781108186599.011
Bootes, K. R., & Himle, M. B. (2022) · Elsevier eBooks · doi:10.1016/b978-0-323-91497-0.00222-8
Mann, G. S., Gadelmawla, A. F., Dway, A., Fayaz, F. H., Kebede, E., Varadharaj, N. K., Akram, A., Khan, A., Azuwike, U. B., Sampangi, B. K., et al. (2026) · Neuroscience · doi:10.1016/j.neuroscience.2026.05.044
Ruggiero, S. M., & Helbig, I. (2025) · Elsevier eBooks · doi:10.1016/b978-0-443-10944-7.00051-2
Woods, D. W., Piacentini, J. C., Peterson, A. L., Scahill, L. D., & Walkup, J. T. (2025) · doi:10.1093/med-psych/9780199363346.001.0001
Woods, D. W., Piacentini, J. C., Peterson, A. L., Scahill, L. D., & Walkup, J. T. (2025) · Oxford University Press eBooks · doi:10.1093/med-psych/9780199363346.002.0005
(2025) · Oxford University Press eBooks · doi:10.1093/med-psych/9780199363346.002.0007
Woods, D. W., Piacentini, J. C., Peterson, A. L., Scahill, L. D., & Walkup, J. T. (2025) · Oxford University Press eBooks · doi:10.1093/med-psych/9780199363346.002.0004
Introductory Information for Therapists
Woods, D. W., Piacentini, J. C., Peterson, A. L., Scahill, L. D., & Walkup, J. T. (2025) · Oxford University Press eBooks · doi:10.1093/med-psych/9780199363346.003.0001
Behavioral Model of Tic Disorders and Mechanisms of Change
Woods, D. W., Piacentini, J. C., Peterson, A. L., Scahill, L. D., & Walkup, J. T. (2025) · Oxford University Press eBooks · doi:10.1093/med-psych/9780199363346.003.0003
Woods, D. W., Piacentini, J. C., Peterson, A. L., Scahill, L. D., & Walkup, J. T. (2025) · Oxford University Press eBooks · doi:10.1093/med-psych/9780199363346.003.0002
Woods, D. W., Piacentini, J. C., Peterson, A. L., Scahill, L. D., & Walkup, J. T. (2025) · Oxford University Press eBooks · doi:10.1093/med-psych/9780199363346.005.0001
Woods, D. W., Piacentini, J. C., Peterson, A. L., Scahill, L. D., & Walkup, J. T. (2025) · Oxford University Press eBooks · doi:10.1093/med-psych/9780199363346.003.0006
Comorbidity Management: It’s Not Just Tics
Lewin, A. B. (2025) · Oxford University Press eBooks · doi:10.1093/med-psych/9780199363346.003.0017
Bootes, K. R., Blount, T. H., Kudryk, K., & Himle, M. B. (2025) · Oxford University Press eBooks · doi:10.1093/med-psych/9780199363346.003.0015
Occupational Therapy, Tourette Disorder, and CBIT
Rowe, J., & Martin, H. S. (2025) · Oxford University Press eBooks · doi:10.1093/med-psych/9780199363346.003.0013
Assessment of Tourette Disorder
Woods, D. W., Piacentini, J. C., Peterson, A. L., Scahill, L. D., & Walkup, J. T. (2025) · Oxford University Press eBooks · doi:10.1093/med-psych/9780199363346.003.0004
Woods, D. W., Piacentini, J. C., Peterson, A. L., Scahill, L. D., & Walkup, J. T. (2025) · Oxford University Press eBooks · doi:10.1093/med-psych/9780199363346.003.0007
Functional Assessment and Function-Based Intervention
Woods, D. W., Piacentini, J. C., Peterson, A. L., Scahill, L. D., & Walkup, J. T. (2025) · Oxford University Press eBooks · doi:10.1093/med-psych/9780199363346.003.0005
Woods, D. W., Piacentini, J. C., Peterson, A. L., Scahill, L. D., & Walkup, J. T. (2025) · Oxford University Press eBooks · doi:10.1093/med-psych/9780199363346.003.0010
Metadata
- Authors
- O'Rourke, J. A., Scharf, J. M., Yu, D., & Pauls, D. L.
- Affiliations
- Harvard University (US)
- Corresponding author
- Pauls, David L.
- Venue
- Journal of Psychosomatic Research
- Publisher
- Elsevier BV
- Published
- 2009-12
- Volume
- 67
- Issue
- 6
- Pages
- 533-545
- ISSN
- 0022-3999 (ISSN-L)
- PMC
- PMC2778609
- OpenAlex
- W2041237576
- Cited by
- 212
- References
- 171
- Citations by year
- 2026: 3 · 2025: 31 · 2024: 2 · 2023: 4 · 2022: 6 · 2021: 10 · 2020: 16 · 2019: 6 · 2018: 5 · 2017: 10 · 2016: 9 · 2015: 13 · 2014: 13 · 2013: 21 · 2012: 23
- FWCI
- 2.74
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Journal of Psychosomatic Research (publishedVersion)
- PubMed (publishedVersion)
- Europe PMC (PubMed Central) (acceptedVersion)
- PubMed Central (acceptedVersion)
- Funders
- National Institute of Neurological Disorders and Stroke (NS40024, R01NS016648, U01NS040024, R01NS040024, NS-16648)
- Topics
- Social Sciences › Psychology › Clinical Psychology › Obsessive-Compulsive Spectrum Disorders
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Genetic Associations and Epidemiology
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Genetics and Neurodevelopmental Disorders
- Keywords
- Tourette syndrome, genetic etiology, attention deficit hyperactivity disorder, obsessive-compulsive disorder, linkage analysis, SLITRK1, chromosomal translocation, candidate genes, genome-wide association study, genetic heterogeneity
- MeSH terms
- Alleles, Attention Deficit Disorder with Hyperactivity, Genotype, Tourette Syndrome, Humans, Genetic Linkage, Obsessive-Compulsive Disorder, Genome-Wide Association Study
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