Enhancing neuroimaging genetics through meta-analysis for Tourette syndrome (ENIGMA-TS): A worldwide platform for collaboration

The thalamus and its subnuclei—a gateway to obsessive-compulsive disorder

(2022) Cees J. Weeland et al.   Translational Psychiatry

Investigating shared genetic basis across Tourette Syndrome and comorbid neurodevelopmental disorders along the impulsivity-compulsivity spectrum

(2021) Zhiyu Yang et al.   BIOLOGICAL PSYCHIATRY

Synaptic processes and immune-related pathways implicated in Tourette syndrome

(2021) Fotis Tsetsos et al.   Translational Psychiatry

Analysis of structural brain asymmetries in attention‐deficit/hyperactivity disorder in 39 datasets

(2021) Merel C. Postema et al.   JOURNAL OF CHILD PSYCHOLOGY AND PSYCHIATRY

Gray matter abnormalities in Tourette Syndrome: a meta-analysis of voxel-based morphometry studies

(2021) Xinyue Wan et al.   Translational Psychiatry

Thalamic Subregions and Obsessive-Compulsive Symptoms in 2,500 Children From the General Population

(2021) Cees J. Weeland et al.   JOURNAL OF THE AMERICAN ACADEMY OF CHILD AND ADOLESCENT PSYCHIATRY

An overview of the first 5 years of the ENIGMA obsessive–compulsive disorder working group: The power of worldwide collaboration

(2020) Odile A. Heuvel et al.   HUMAN BRAIN MAPPING

Consortium neuroscience of attention deficit/hyperactivity disorder and autism spectrum disorder: The ENIGMA adventure

(2020) Martine Hoogman et al.   HUMAN BRAIN MAPPING

Brain structural abnormalities in obesity: relation to age, genetic risk, and common psychiatric disorders

(2020) Nils Opel et al.   MOLECULAR PSYCHIATRY

The genetic architecture of the human cerebral cortex

(2020) Katrina L. Grasby et al.   SCIENCE

ENIGMA and global neuroscience: A decade of large-scale studies of the brain in health and disease across more than 40 countries

(2020) Paul M. Thompson et al.   Translational Psychiatry

Shared genetic etiology between obsessive-compulsive disorder, obsessive-compulsive symptoms in the population, and insulin signaling

(2020) Janita Bralten et al.   Translational Psychiatry

Subcortical Brain Volume, Regional Cortical Thickness, and Cortical Surface Area Across Disorders: Findings From the ENIGMA ADHD, ASD, and OCD Working Groups

(2020) Premika S.W. Boedhoe et al.   AMERICAN JOURNAL OF PSYCHIATRY

Hippocampal Volume in Provisional Tic Disorder Predicts Tic Severity at 12-Month Follow-up

(2020) Soyoung Kim et al.   Journal of Clinical Medicine

White matter abnormalities across different epilepsy syndromes in adults: an ENIGMA-Epilepsy study

(2020) Sean N Hatton et al.   BRAIN

Brain Morphology Associated With Obsessive-Compulsive Symptoms In 2,551 Children From the General Population

(2020) Cees J. Weeland et al.   JOURNAL OF THE AMERICAN ACADEMY OF CHILD AND ADOLESCENT PSYCHIATRY

An Empirical Comparison of Meta- and Mega-Analysis With Data From the ENIGMA Obsessive-Compulsive Disorder Working Group

(2019) Premika S. W. Boedhoe et al.   Frontiers in Neuroinformatics

Concordance of genetic variation that increases risk for tourette syndrome and that influences its underlying neurocircuitry

(2019) Mary Mufford et al.   Translational Psychiatry

Interrogating the Genetic Determinants of Tourette’s Syndrome and Other Tic Disorders Through Genome-Wide Association Studies

(2019) Dongmei Yu et al.   AMERICAN JOURNAL OF PSYCHIATRY

Brain Imaging of the Cortex in ADHD: A Coordinated Analysis of Large-Scale Clinical and Population-Based Samples

(2019) Martine Hoogman et al.   AMERICAN JOURNAL OF PSYCHIATRY

Genomic structural equation modelling provides insights into the multivariate genetic architecture of complex traits

(2019) Andrew D. Grotzinger et al.   Nature Human Behaviour

Mutations in ASH1L confer susceptibility to Tourette syndrome

(2019) Shiguo Liu et al.   MOLECULAR PSYCHIATRY

Genetic architecture of subcortical brain structures in 38,851 individuals

(2019) Claudia L. Satizabal et al.   NATURE GENETICS

Cortical and Subcortical Brain Morphometry Differences Between Patients With Autism Spectrum Disorder and Healthy Individuals Across the Lifespan: Results From the ENIGMA ASD Working Group

(2018) Daan van Rooij et al.   AMERICAN JOURNAL OF PSYCHIATRY

Genome-wide association analyses identify 44 risk variants and refine the genetic architecture of major depression

(2018) Naomi R. Wray et al.   NATURE GENETICS

Mapping cortical brain asymmetry in 17,141 healthy individuals worldwide via the ENIGMA Consortium

(2018) Xiang-Zhen Kong et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

The Adolescent Brain Cognitive Development (ABCD) study: Imaging acquisition across 21 sites

(2018) B.J. Casey et al.   Developmental Cognitive Neuroscience

Demographic, physical and mental health assessments in the adolescent brain and cognitive development study: Rationale and description

(2018) Deanna M. Barch et al.   Developmental Cognitive Neuroscience

The conception of the ABCD study: From substance use to a broad NIH collaboration

(2018) Nora D. Volkow et al.   Developmental Cognitive Neuroscience

Polygenic risk scores derived from a Tourette syndrome GWAS predict presence of tics in the Avon Longitudinal Study of Parents and Children (ALSPAC) cohort

(2018) Mohamed Abdulkadir et al.   BIOLOGICAL PSYCHIATRY

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

(2018) Sheng Wang et al.   Cell Reports

Genome-wide association studies of brain imaging phenotypes in UK Biobank

(2018) Lloyd T. Elliott et al.   NATURE

Discovery of the first genome-wide significant risk loci for attention deficit/hyperactivity disorder

(2018) Ditte Demontis et al.   NATURE GENETICS

Paediatric population neuroimaging and the Generation R Study: the second wave

(2017) Tonya White et al.   EUROPEAN JOURNAL OF EPIDEMIOLOGY

Autism spectrum disorders and autistic traits share genetics and biology

(2017) J Bralten et al.   MOLECULAR PSYCHIATRY

Harmonization of multi-site diffusion tensor imaging data

(2017) Jean-Philippe Fortin et al.   NEUROIMAGE

De Novo Coding Variants Are Strongly Associated with Tourette Disorder

(2017) A. Jeremy Willsey et al.   NEURON

Rare Copy Number Variants in NRXN1 and CNTN6 Increase Risk for Tourette Syndrome

(2017) Alden Y. Huang et al.   NEURON

Novel genetic loci associated with hippocampal volume

(2017) Derrek P. Hibar et al.   Nature Communications

Altered Spontaneous Brain Activity in Children with Early Tourette Syndrome: a Resting-state fMRI Study

(2017) Yue Liu et al.   Scientific Reports

No Association between Cortical Gyrification or Intrinsic Curvature and Attention-deficit/Hyperactivity Disorder in Adolescents and Young Adults

(2017) Natalie J. Forde et al.   Frontiers in Neuroscience

Gilles de la Tourette syndrome

(2017) Mary M. Robertson et al.   Nature Reviews Disease Primers

Editorial: The Neurobiology and Genetics of Gilles de la Tourette Syndrome: New Avenues through Large-Scale Collaborative Projects

(2017) Peristera Paschou et al.   Frontiers in Psychiatry

Pathological glutamatergic neurotransmission in Gilles de la Tourette syndrome

(2016) Ahmad Seif Kanaan et al.   BRAIN

Putting the Pieces Together in Gilles de la Tourette Syndrome: Exploring the Link Between Clinical Observations and the Biological Basis of Dysfunction

(2016) Rowshanak Hashemiyoon et al.   BRAIN TOPOGRAPHY

The Generation R Study: design and cohort update 2017

(2016) Marjolein N. Kooijman et al.   EUROPEAN JOURNAL OF EPIDEMIOLOGY

Cortical abnormalities in adults and adolescents with major depression based on brain scans from 20 cohorts worldwide in the ENIGMA Major Depressive Disorder Working Group

(2016) L Schmaal et al.   MOLECULAR PSYCHIATRY

Meta-analysis of genome-wide association studies of anxiety disorders

(2016) T Otowa et al.   MOLECULAR PSYCHIATRY

Brain structure in pediatric Tourette syndrome

(2016) D J Greene et al.   MOLECULAR PSYCHIATRY

Genetic risk for autism spectrum disorders and neuropsychiatric variation in the general population

(2016) Elise B Robinson et al.   NATURE GENETICS

Novel genetic loci underlying human intracranial volume identified through genome-wide association

(2016) Hieab H H Adams et al.   NATURE NEUROSCIENCE

Mild White Matter Changes in Un-medicated Obsessive-Compulsive Disorder Patients and Their Unaffected Siblings

(2016) Siyan Fan et al.   Frontiers in Neuroscience

TS-EUROTRAIN: A European-Wide Investigation and Training Network on the Etiology and Pathophysiology of Gilles de la Tourette Syndrome

(2016) Natalie J. Forde et al.   Frontiers in Neuroscience

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

(2016) Marianthi Georgitsi et al.   Frontiers in Neuroscience

The Fallacy of Univariate Solutions to Complex Systems Problems

(2016) Christina N. Lessov-Schlaggar et al.   Frontiers in Neuroscience

Aripiprazole Improves Associated Comorbid Conditions in Addition to Tics in Adult Patients with Gilles de la Tourette Syndrome

(2016) Sarah Gerasch et al.   Frontiers in Neuroscience

Effect of Deep Brain Stimulation on Regional Cerebral Blood Flow in Patients with Medically Refractory Tourette Syndrome

(2016) Cathleen Haense et al.   Frontiers in Psychiatry

Subcortical brain alterations in major depressive disorder: findings from the ENIGMA Major Depressive Disorder working group

(2015) L Schmaal et al.   MOLECULAR PSYCHIATRY

Neuroimaging of tic genesis: Present status and future perspectives

(2015) Yulia Worbe et al.   MOVEMENT DISORDERS

Common genetic variants influence human subcortical brain structures

(2015) Derrek P. Hibar et al.   NATURE

Lifetime Prevalence, Age of Risk, and Genetic Relationships of Comorbid Psychiatric Disorders in Tourette Syndrome

(2015) Matthew E. Hirschtritt et al.   JAMA Psychiatry

Histidine Decarboxylase Deficiency Causes Tourette Syndrome: Parallel Findings in Humans and Mice

(2014) Lissandra Castellan Baldan et al.   NEURON

Support of the histaminergic hypothesis in Tourette Syndrome: association of the histamine decarboxylase gene in a large sample of families

(2013) Iordanis Karagiannidis et al.   JOURNAL OF MEDICAL GENETICS

The genetic basis of Gilles de la Tourette Syndrome

(2013) Peristera Paschou   NEUROSCIENCE AND BIOBEHAVIORAL REVIEWS

CNV Analysis in Tourette Syndrome Implicates Large Genomic Rearrangements in COL8A1 and NRXN1

(2013) Abhishek Nag et al.   PLoS One

Altered intrahemispheric structural connectivity in Gilles de la Tourette syndrome

(2013) Bastian Cheng et al.   NeuroImage-Clinical

Functional immaturity of cortico-basal ganglia networks in Gilles de la Tourette syndrome

(2012) Yulia Worbe et al.   BRAIN

Identification of common variants associated with human hippocampal and intracranial volumes

(2012) Jason L Stein et al.   NATURE GENETICS

The functional anatomy of Gilles de la Tourette syndrome

(2012) Christos Ganos et al.   NEUROSCIENCE AND BIOBEHAVIORAL REVIEWS

Thalamic shape and connectivity abnormalities in children with attention- deficit/hyperactivity disorder

(2012) Shugao Xia et al.   PSYCHIATRY RESEARCH-NEUROIMAGING

Replication of association between a SLITRK1 haplotype and Tourette Syndrome in a large sample of families

(2011) I Karagiannidis et al.   MOLECULAR PSYCHIATRY

Morphological Abnormalities of the Thalamus in Youths With Attention Deficit Hyperactivity Disorder

(2010) Iliyan Ivanov et al.   AMERICAN JOURNAL OF PSYCHIATRY

Enlargement of Thalamic Nuclei in Tourette Syndrome

(2010) Ann M. Miller et al.   ARCHIVES OF GENERAL PSYCHIATRY

Gray Matter Alterations in Adults with Attention-Deficit/Hyperactivity Disorder Identified by Voxel Based Morphometry

(2010) Larry J. Seidman et al.   BIOLOGICAL PSYCHIATRY

Distinct structural changes underpin clinical phenotypes in patients with Gilles de la Tourette syndrome

(2010) Yulia Worbe et al.   BRAIN

Multispectral brain morphometry in Tourette syndrome persisting into adulthood

(2010) Bogdan Draganski et al.   BRAIN

Tourette syndrome is associated with recurrent exonic copy number variants

(2010) S. K. Sundaram et al.   NEUROLOGY

L-Histidine Decarboxylase and Tourette's Syndrome

(2010) A. Gulhan Ercan-Sencicek et al.   NEW ENGLAND JOURNAL OF MEDICINE

Prefrontal and anterior cingulate cortex abnormalities in Tourette Syndrome: evidence from voxel-based morphometry and magnetization transfer imaging

(2009) Kirsten R Müller-Vahl et al.   BMC NEUROSCIENCE

Somatosensory–motor bodily representation cortical thinning in Tourette: Effects of tic severity, age and gender

(2009) Cherine Fahim et al.   CORTEX

Control networks in paediatric Tourette syndrome show immature and anomalous patterns of functional connectivity

(2008) Jessica A. Church et al.   BRAIN

Thinning of sensorimotor cortices in children with Tourette syndrome

(2008) Elizabeth R Sowell et al.   NATURE NEUROSCIENCE