Tourette syndrome phenotype

Aliases: Gilles de la Tourette syndrome, TD, TS, Tourette, Tourette cases, Tourette diagnosis, Tourette’s syndrome, tics

Evidence from: primary | all sources

Related entities (16)

Subject	Relation	Object	p-value	Evidence
CELSR3	risk_factor_for	Tourette syndrome	0.3	1
copy number variation	associated_with	Tourette syndrome	—	1
de novo variant	risk_factor_for	Tourette syndrome	0.03	1
dopamine	risk_factor_for	Tourette syndrome	—	1
FN1	risk_factor_for	Tourette syndrome	0.3	1
histamine	associated_with	Tourette syndrome	—	1
histamine	risk_factor_for	Tourette syndrome	—	1
indel	risk_factor_for	Tourette syndrome	—	1
probands	associated_with	Tourette syndrome	—	1
serotonin	associated_with	Tourette syndrome	—	1
TIC Genetics	associated_with	Tourette syndrome	—	1
Tourette syndrome	associated_with	anxiety	—	1
Tourette syndrome	associated_with	attention deficit hyperactivity disorder	—	1
Tourette syndrome	associated_with	mood disorders	—	1
Tourette syndrome	associated_with	obsessive-compulsive disorder	—	1
Tourette syndrome	associated_with	trichotillomania	—	1

Mentioned in (35)

Papers in which this entity is mentioned.

Mapping the genetic landscape across 14 psychiatric disorders. (2026)
Massively parallel reporter assay investigates shared genetic variants of eight psychiatric disorders. (2025)
Genome-wide analyses identify 30 loci associated with obsessive-compulsive disorder. (2025)
Pervasive Downward Bias in Estimates of Liability-Scale Heritability in Genome-wide Association Study Meta-analysis: A Simple Solution. (2023)
Genetic Influences on the Developing Young Brain and Risk for Neuropsychiatric Disorders. (2023)
Genetic architecture of 11 major psychiatric disorders at biobehavioral, functional genomic and molecular genetic levels of analysis. (2022)
Shared genetic architecture across psychiatric disorders. (2021)
Whole-genome analysis reveals the contribution of non-coding de novo transposon insertions to autism spectrum disorder. (2021)
Toward a neurocircuit-based taxonomy to guide treatment of obsessive-compulsive disorder. (2021)
ENIGMA and global neuroscience: A decade of large-scale studies of the brain in health and disease across more than 40 countries. (2020)
De Novo Damaging DNA Coding Mutations Are Associated With Obsessive-Compulsive Disorder and Overlap With Tourette's Disorder and Autism. (2020)
Defining the Genetic, Genomic, Cellular, and Diagnostic Architectures of Psychiatric Disorders. (2019)
Sex differences in the genetic architecture of obsessive-compulsive disorder. (2019)
Interrogating the Genetic Determinants of Tourette's Syndrome and Other Tic Disorders Through Genome-Wide Association Studies. (2019)
Sex differences in the developing brain: insights from multimodal neuroimaging. (2019)
Neural cell adhesion molecule Negr1 deficiency in mouse results in structural brain endophenotypes and behavioral deviations related to psychiatric disorders. (2019)
Heritability enrichment of specifically expressed genes identifies disease-relevant tissues and cell types. (2018)
Psychiatric Genomics: An Update and an Agenda. (2018)
Elevated polygenic burden for autism is associated with differential DNA methylation at birth. (2018)
Cortical Abnormalities Associated With Pediatric and Adult Obsessive-Compulsive Disorder: Findings From the ENIGMA Obsessive-Compulsive Disorder Working Group. (2018)
Assembly of functionally integrated human forebrain spheroids. (2017)
De Novo Coding Variants Are Strongly Associated with Tourette Disorder. (2017)
Sex differences and stress across the lifespan. (2015)
Genome-wide association study in obsessive-compulsive disorder: results from the OCGAS. (2015)
Use of resting-state functional MRI to study brain development and injury in neonates. (2015)
Genetics and genomics of psychiatric disease. (2015)
Effects of methylphenidate in children with attention deficit hyperactivity disorder: a near-infrared spectroscopy study with CANTAB®. (2014)
Genetic influences on brain developmental trajectories on neuroimaging studies: from infancy to young adulthood. (2014)
The aggregate effect of dopamine genes on dependence symptoms among cocaine users: cross-validation of a candidate system scoring approach. (2012)
A longitudinal study of the long-term consequences of drinking during pregnancy: heavy in utero alcohol exposure disrupts the normal processes of brain development. (2012)
Normal development of brain circuits. (2010)
The neuropathology of autism: defects of neurogenesis and neuronal migration, and dysplastic changes. (2010)
Neuroimaging studies of normal brain development and their relevance for understanding childhood neuropsychiatric disorders. (2008)
Genetic and environmental factors in complex neurodevelopmental disorders. (2007)

Merged raw entities (6)

All extracted name/type variants the normalize job merged into this entity. Use this to spot wrong merges, or aliases that should be split off.

Raw name	Type	Papers	Mentions
tourette syndrome	phenotype	32	73
tourette	phenotype	2	6
tourette disorder	phenotype	2	14
gilles de la tourette syndrome	phenotype	—	—
tourette cases	phenotype	—	—
tourette diagnosis	phenotype	—	—