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1. Full Text Functional Magnetic Resonance Imaging During Planning Before and After Cognitive-Behavioral Therapy in Pediatric Obsessive-Compulsive Disorder
by Huyser, Chaim, M.D and Veltman, Dick J., M.D., Ph.D and Wolters, Lidewij H., M.Sc and de Haan, Else, M.Sc., Ph.D and Boer, Frits, M.D., Ph.D
Journal of the American Academy of Child & Adolescent Psychiatry, ISSN 0890-8567, 2010, Volume 49, Issue 12, pp. 1238 - 1248.e5
Objective Pediatric obsessive compulsive disorder (OCD) has been associated with cognitive abnormalities, in particular executive impairments, and dysfunction... 
Pediatrics | Psychiatry | cognitive behavioral therapy | executive functioning | obsessive compulsive disorder | functional magnetic resonance imaging | child | Functional magnetic resonance imaging | Obsessive compulsive disorder | Child | Executive functioning | Key Words | Cognitive behavioral therapy | LONDON TASK | SYMPTOM DIMENSIONS | PSYCHIATRY | PSYCHOLOGY, DEVELOPMENTAL | TOWER | CHILDHOOD | VOXEL-BASED MORPHOMETRY | CHILDREN | PAROXETINE | PEDIATRICS | BRAIN ACTIVATION | MATTER ABNORMALITIES | NEUROPSYCHOLOGICAL DEFICITS | Outcomes of Treatment | Therapy | Cognitive Processes | Brain Hemisphere Functions | Anxiety Disorders | Diagnostic Tests | Task Analysis | Measures (Individuals) | Cognitive Restructuring | Control Groups | Patients | Obsessive-Compulsive Disorder - physiopathology | Humans | Male | Reference Values | Parietal Lobe - physiopathology | Cerebral Cortex - physiopathology | Attention - physiology | Female | Nerve Net - physiopathology | Cognition Disorders - psychology | Cognition Disorders - physiopathology | Corpus Striatum - physiopathology | Brain - physiopathology | Frontal Lobe - physiopathology | Obsessive-Compulsive Disorder - therapy | Problem Solving - physiology | Reaction Time - physiology | Recruitment, Neurophysiological - physiology | Executive Function - physiology | Magnetic Resonance Imaging | Obsessive-Compulsive Disorder - psychology | Thalamus - physiopathology | Adolescent | Gyrus Cinguli - physiopathology | Cognitive Therapy | Cognition Disorders - therapy | Games, Experimental | Care and treatment | Usage | Cognitive therapy | Magnetic resonance imaging | Analysis | Executive function (Psychology) | Obsessive-compulsive disorder | Child psychopathology | Nuclear magnetic resonance--NMR | Behavior modification | Neuropsychology | Neuroses | Child & adolescent psychiatry
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2. Full Text Analysis of shared heritability in common disorders of the brain
by Anttila, Verneri and Bulik-Sullivan, Brendan and Finucane, Hilary K and Walters, Raymond K and Bras, Jose and Duncan, Laramie and Escott-Price, Valentina and Falcone, Guido J and Gormley, Padhraig and Malik, Rainer and Patsopoulos, Nikolaos A and Ripke, Stephan and Wei, Zhi and Yu, Dongmei and Lee, Phil H and Turley, Patrick and Grenier-Boley, Benjamin and Chouraki, Vincent and Kamatani, Yoichiro and Berr, Claudine and Letenneur, Luc and Hannequin, Didier and Amouyel, Philippe and Boland, Anne and Deleuze, Jean-François and Duron, Emmanuelle and Vardarajan, Badri N and Reitz, Christiane and Goate, Alison M and Huentelman, Matthew J and Ilyas Kamboh, M and Larson, Eric B and Rogaeva, Ekaterina and George-Hyslop, Peter St and Hakonarson, Hakon and Kukull, Walter A and Farrer, Lindsay A and Barnes, Lisa L and Beach, Thomas G and Yesim Demirci, F and Head, Elizabeth and Hulette, Christine M and Jicha, Gregory A and Kauwe, John S.K and Kaye, Jeffrey A and Leverenz, James B and Levey, Allan I and Lieberman, Andrew P and Pankratz, Vernon S and Poon, Wayne W and Quinn, Joseph F and Saykin, Andrew J and Schneider, Lon S and Smith, Amanda G and Sonnen, Joshua A and Stern, Robert A and Van Deerlin, Vivianna M and Van Eldik, Linda J and Harold, Denise and Russo, Giancarlo and Rubinsztein, David C and Bayer, Anthony and Tsolaki, Magda and Proitsi, Petra and Fox, Nick C and Hampel, Harald and Owen, Michael J and Mead, Simon and Passmore, Peter and Morgan, Kevin and Nöthen, Markus M and Rossor, Martin and Lupton, Michelle K and Hoffmann, Per and Kornhuber, Johannes and Lawlor, Brian and McQuillin, Andrew and Al-Chalabi, Ammar and Bis, Joshua C and Ruiz, Agustin and Boada, Mercè and Seshadri, Sudha and Beiser, Alexa and Rice, Kenneth and Van Der Lee, Sven J and De Jager, Philip L and Geschwind, Daniel H and Riemenschneider, Matthias and Riedel-Heller, Steffi and Rotter, Jerome I and Ransmayr, Gerhard and Hyman, Bradley T and Cruchaga, Carlos and Alegret, Montserrat and Winsvold, Bendik and Palta, Priit and Farh, Kai-How and Cuenca-Leon, Ester and Furlotte, Nicholas and Kurth, Tobias and ... and Brainstorm Consortium and The Brainstorm Consortium
Science, ISSN 0036-8075, 06/2018, Volume 360, Issue 6395, pp. 1313 - 1313
Disorders of the brain can exhibit considerable epidemiological comorbidity and often share symptoms, provoking debate about their etiologic overlap. We... 
ANOREXIA-NERVOSA | POPULATION-BASED TWIN | DEFICIT HYPERACTIVITY DISORDER | LONG-TERM SURVIVAL | ALZHEIMERS-DISEASE | MULTIDISCIPLINARY SCIENCES | GENETIC CORRELATIONS | BODY-MASS INDEX | MAJOR DEPRESSIVE DISORDER | BIPOLAR DISORDER | GENOME-WIDE ASSOCIATION | Genetic Variation | Mental Disorders - genetics | Genome-Wide Association Study | Phenotype | Brain Diseases - classification | Quantitative Trait, Heritable | Brain Diseases - diagnosis | Humans | Mental Disorders - classification | Risk Factors | Brain Diseases - genetics | Mental Disorders - diagnosis | Anorexia | Disorders | Cognitive ability | Bipolar disorder | Posttraumatic stress disorder | Mental depression | Epidemiology | Risk factors | Consortia | Proteins | Ischemia | Etiology | Classification | Gilles de la Tourette syndrome | Alzheimer's disease | Neurological disorders | Neurodegenerative diseases | Comorbidity | Behavior disorders | Anorexia nervosa | Risk analysis | Patients | Neurological diseases | Correlation analysis | Heritability | Attention deficit disorder | Headache | Mental disorders | Medical services | Schizophrenia | Risk sharing | Genomes | Heterogeneity | Biological effects | Risk assessment | Stroke | Phenotypes | Migraine | Attention deficit hyperactivity disorder | Eating disorders | Personality | Genetic diversity | Statistics | Activity patterns | Crohn's Disease | Population (statistical) | Scaffolding | Diagnostic systems | Alzheimers disease | Life Sciences | Human health and pathology | Mental Disorders | Neurons and Cognition | Brain Diseases | Genetics
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3. Full Text Developmental aspects of error and high-conflict-related brain activity in pediatric obsessive-compulsive disorder: a fMRI study with a Flanker task before and after CBT
by Huyser, Chaim and Veltman, Dick J and Wolters, Lidewij H and de Haan, Else and Boer, Frits
Journal of child psychology and psychiatry, and allied disciplines, ISSN 0021-9630, 2011, Volume 52, Issue 12, pp. 1251 - 1260
Heightened error and conflict monitoring are considered central mechanisms in obsessive-compulsive disorder (OCD) and are associated with anterior cingulate... 
ANTERIOR CINGULATE CORTEX | DECISION-MAKING | PSYCHIATRY | PERFORMANCE | PSYCHOLOGY, DEVELOPMENTAL | SCALE | PSYCHOLOGY | Therapy | Correlation | Diagnostic Tests | Task Analysis | Behavior Modification | Age Differences | Cognitive Restructuring | Control Groups | Patients | Brain Hemisphere Functions | Anxiety Disorders | Conflict | Attention Deficit Disorders | Psychopathology | Children | Adolescents | Error Patterns | Psychomotor Performance | Obsessive-Compulsive Disorder - physiopathology | Cognitive Therapy - methods | Brain - physiopathology | Humans | Obsessive-Compulsive Disorder - therapy | Aging - psychology | Male | Case-Control Studies | Neuropsychological Tests | Young Adult | Magnetic Resonance Imaging | Obsessive-Compulsive Disorder - psychology | Adolescent | Conflict (Psychology) | Gyrus Cinguli - physiopathology | Female | Child | Brain | Nuclear magnetic resonance--NMR | Neuroses | Children & youth
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4. Full Text F61. Long-Term Effects of Cognitive Behavioral Therapy on Planning and Prefrontal Cortex Function in Pediatric Obsessive-Compulsive Disorder
by van der Straten, Anouk and Huyser, Chaim and Wolters, Lidewij and Denys, Damiaan and van Wingen, Guido
Biological Psychiatry, ISSN 0006-3223, 05/2018, Volume 83, Issue 9, pp. S261 - S261
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5. Full Text De Novo Coding Variants Are Strongly Associated with Tourette Disorder
by Willsey, A. Jeremy and Fernandez, Thomas V and Yu, Dongmei and King, Robert A and Dietrich, Andrea and Xing, Jinchuan and Sanders, Stephan and Sanders, Stephan J and Mandell, Jeffrey D and Huang, Alden Y and Richer, Petra and Smith, Louw and Dong, Shan and Samocha, Kaitlin E and Abdulkadir, Mohamed and Bohnenpoll, Julia and Bromberg, Yana and Brown, Lawrence W and Cheon, Keun-Ah and Coffey, Barbara J and Deng, Li and Elzerman, Lonneke and Fründt, Odette and Garcia-Delgar, Blanca and Gedvilaite, Erika and Gilbert, Donald L and Grice, Dorothy E and Hagstrøm, Julie and Hedderly, Tammy and Heiman, Gary A and Heyman, Isobel and Hoekstra, Pieter J and Hong, Hyun Ju and Huyser, Chaim and Ibanez-Gomez, Laura and Kim, Young Key and Kim, Young-Shin and Koh, Yun-Joo and Kook, Sodahm and Kuperman, Samuel and Lamerz, Andreas and Leventhal, Bennett and Ludolph, Andrea G and Lühr da Silva, Claudia and Madruga-Garrido, Marcos and Maras, Athanasios and Mir, Pablo and Morer, Astrid and Münchau, Alexander and Murphy, Tara L and Nasello, Cara and Openneer, Thaïra J.C and Plessen, Kerstin J and Roessner, Veit and Shin, Eun-Young and Sival, Deborah A and Song, Jungeun and Song, Dong-Ho and State, Matthew W and Stolte, Anne Marie and Sun, Nawei and Tischfield, Jay A and Tübing, Jennifer and Visscher, Frank and Walker, Michael F and Wanderer, Sina and Wang, Shuoguo and Woods, Martin and Zhang, Yeting and Zhou, Anbo and Zinner, Samuel H and Barr, Cathy L and Batterson, James R and Berlin, Cheston and Bruun, Ruth D and Budman, Cathy L and Cath, Danielle C and Chouinard, Sylvain and Coppola, Giovanni and Cox, Nancy J and Darrow, Sabrina and Davis, Lea K and Dion, Yves and Freimer, Nelson B and Grados, Marco A and Hirschtritt, Matthew E and Illmann, Cornelia and Kurlan, Roger and Leckman, James F and Lyon, Gholson J and Malaty, Irene A and Mathews, Carol A and MaMahon, William M and Neale, Benjamin M and Okun, Michael S and Osiecki, Lisa and Pauls, David L and Posthuma, Danielle and Ramensky, Vasily and Robertson, Mary M and ... and Tourette Int Collaborative Genetic and Tourette Syndrome Assoc Int Consor and Tourette Syndrome Association International Consortium for Genetics (TSAICG) and Tourette International Collaborative Genetics (TIC Genetics)
Neuron, ISSN 0896-6273, 05/2017, Volume 94, Issue 3, pp. 486 - 499.e9
Whole-exome sequencing (WES) and de novo variant detection have proven a powerful approach to gene discovery in complex neurodevelopmental disorders. We have... 
gene discovery | TIC Genetics | de novo variants | Tourette disorder | Tourette syndrome | TSAICG | whole-exome sequencing | INTELLECTUAL DISABILITY | PSYCHIATRIC-DISORDERS | FUNCTIONAL GENOMICS EXPERIMENTS | TIC DISORDERS | MUTATIONS | AUTISM SPECTRUM DISORDERS | COPY NUMBER VARIANTS | DNA-SEQUENCING DATA | NEUROSCIENCES | OBSESSIVE-COMPULSIVE DISORDER | LANGE-SYNDROME | Tourette Syndrome - genetics | Genetic Predisposition to Disease | Humans | Parents | Male | Phosphoproteins - genetics | Sequence Analysis, DNA | Genetic Variation | Proteins - genetics | Adult | Female | Fibronectins - genetics | Mutation | Cadherins - genetics | Odds Ratio | Child | Intracellular Signaling Peptides and Proteins - genetics | Cohort Studies | Receptors, Cell Surface - genetics | Tourette's syndrome | Fibronectins | Epidermal growth factor | Genes | Attention deficit disorder | Obsessive compulsive disorder | Neurosciences | Pathogenesis | Genomics | Genomes | Cadherin | Neurodevelopmental disorders | Fibronectin | Studies | Consortia | Celsr3 protein | Signal transduction | Autism | Coding | Quality control | Genetics | Gilles de la Tourette syndrome | Siblings
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6. Full Text Mapping cortical brain asymmetry in 17,141 healthy individuals worldwide via the ENIGMA consortium
by Kong, Xiang-Zhen and Mathias, Samuel R and Guadalupe, Tulio and Abé, Christoph and Agartz, Ingrid and Akudjedu, Theophilus N and Aleman, Andre and Alhusaini, Saud and Allen, Nicholas B and Ames, David and Andreassen, Ole A and Vasquez, Alejandro Arias and Armstrong, Nicola J and Bergo, Felipe and Bastin, Mark E and Batalla, Albert and Bauer, Jochen and Baune, Bernhard T and Baur-Streubel, Ramona and Biederman, Joseph and Blaine, Sara K and Boedhoe, Premika and Bøen, Erlend and Bose, Anushree and Bralten, Janita and Brandeis, Daniel and Brem, Silvia and Brodaty, Henry and Yüksel, Dilara and Brooks, Samantha J and Buitelaar, Jan and Bürger, Christian and Bülow, Robin and Calhoun, Vince and Calvo, Anna and Canales-Rodríguez, Erick Jorge and Canive, Jose M and Cannon, Dara M and Caparelli, Elisabeth C and Castellanos, Francisco X and Cavalleri, Gianpiero L and Cendes, Fernando and Chaim-Avancini, Tiffany Moukbel and Chantiluke, Kaylita and Chen, Qun-Lin and Chen, Xiayu and Cheng, Yuqi and Christakou, Anastasia and Clark, Vincent P and Coghill, David and Connolly, Colm G and Conzelmann, Annette and Córdova-Palomera, Aldo and Cousijn, Janna and Crow, Tim and Cubillo, Ana and Dale, Anders and Dannlowski, Udo and De Bruttopilo, Sara Ambrosino and De Zeeuw, Patrick and Deary, Ian J and Delanty, Norman and Demeter, Damion V and Di Martino, Adriana and Dickie, Erin W and Dietsche, Bruno and Doan, N. Trung and Doherty, Colin P and Doyle, Alysa and Durston, Sarah and Earl, Eric and Ehrlich, Stefan and Ekman, Carl Johan and Elvsåshagen, Torbjørn and Epstein, Jeffery N and Fair, Damien A and Faraone, Stephen V and Fernández, Guillén and Filho, Geraldo Busatto and Förster, Katharina and Fouche, Jean-Paul and Foxe, John J and Frodl, Thomas and Fuentes-Claramonte, Paola and Fullerton, Janice and Garavan, Hugh and Garcia, Danielle Do Santos and Gotlib, Ian H and Goudriaan, Anna E and Grabe, Hans Jörgen and Groenewold, Nynke A and Grotegerd, Dominik and Gruber, Oliver and Gurholt, Tiril and Haavik, Jan and Hahn, Tim and Hansell, Narelle K and Harris, Mathew A and Hartman, Catharina A and Hernández, Maria Del Carmen Valdés and ... and ENIGMA Laterality Working Grp and ENIGMA Laterality Working Group and Institute of Neuroscience and Physiology and Sahlgrenska akademin and Göteborgs universitet and Gothenburg University and Sahlgrenska Academy and Institutionen för neurovetenskap och fysiologi
Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 05/2018, Volume 115, Issue 22, pp. E5154 - E5163
Hemispheric asymmetry is a cardinal feature of human brain organization. Altered brain asymmetry has also been linked to some cognitive and neuropsychiatric... 
Brain asymmetry | Cortical thickness | Surface area | Lateralization | Meta-analysis | SURFACE-AREA | THICKNESS ASYMMETRY | cortical thickness | ALZHEIMERS-DISEASE | MULTIDISCIPLINARY SCIENCES | meta-analysis | surface area | lateralization | HUMAN CEREBRAL-CORTEX | PLANUM TEMPORALE | HEMISPHERIC ASYMMETRIES | LANGUAGE LATERALIZATION | SEX-DIFFERENCES | brain asymmetry | STRUCTURAL ASYMMETRY | SELECTIVE REGIONS | Neuroimaging - methods | Humans | Middle Aged | Databases, Factual - statistics & numerical data | Child, Preschool | Infant | Male | Cerebral Cortex - diagnostic imaging | Young Adult | Adolescent | Aged, 80 and over | Adult | Female | Aged | Child | Cerebral hemispheres | Physiological aspects | Brain research | Research | Cortical maps | Cerebral dominance | Dominància cerebral | Lateralitat | Laterality | Neuroscience | Cognitive science | Biological Sciences | PNAS Plus | Psykiatri | Psychiatry
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7. Full Text Brain volume in male patients with recent onset schizophrenia with and without cannabis use disorders
by Koenders, Laura, MSc and Machielsen, Marise W.J., MD, MSc and van der Meer, Floor J., MSc and van Gasselt, Angelique C.M., MSc and Meijer, Carin J., PhD and van den Brink, Wim, MD, PhD and Koeter, Maarten W.J., PhD and Cousijn, Janna, PhD and Rive, Maaike M., MD, MSc and Schene, Aart H., MD, PhD and Huyser, Chaim, MD, PhD and de Kwaasteniet, Bart P., MD, MSc and Veltman, Dick J., MD, PhD and de Haan, Lieuwe, MD, PhD and Caan, Matthan W.A., PhD and van de Giessen, Elsmarieke, MD, PhD and Braber, Anouk den, PhD and van ‘t Ent, Dennis, PhD
Journal of Psychiatry and Neuroscience, ISSN 1180-4882, 2015, Volume 40, Issue 3, pp. 197 - 206
Background Schizophrenia is highly comorbid with cannabis use disorders (CUDs), and this comorbidity is associated with an unfavourable course. Early onset or... 
Psychiatry | Medical Education | SUBSTANCE-ABUSE | STRUCTURAL ALTERATIONS | CORTICAL THICKNESS | SURFACE-AREA | GREY-MATTER DEFICITS | PSYCHIATRY | DRUG-ADDICTION | MENTAL-HEALTH | NEUROSCIENCES | GRAY-MATTER | 1ST-EPISODE SCHIZOPHRENIA | VOXEL-BASED MORPHOMETRY | Humans | Marijuana Abuse - pathology | Organ Size | Male | Schizophrenia - complications | Schizophrenia - pathology | Marijuana Abuse - complications | Brain - drug effects | Young Adult | Magnetic Resonance Imaging | Antipsychotic Agents - therapeutic use | Gray Matter - pathology | Smoking - pathology | Brain - pathology | Psychological aspects | Schizophrenia | Physiological aspects | Brain | Cannabis | Health aspects | Index Medicus | Research Paper
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8. Full Text Paediatric obsessive-compulsive disorder, a neurodevelopmental disorder? Evidence from neuroimaging
by Huyser, C and Veltman, D.J and Haan, E and Boer, F
Neuroscience and Biobehavioral Reviews, ISSN 0149-7634, 2009, Volume 33, Issue 6, pp. 818 - 830
Objective: To present an overview of neuroimaging data on paediatric obsessive-compulsive disorder (OCD) and discuss implications for further research. Method:... 
Neuroimaging | Development | Adolescence | Obsessive-compulsive disorder | Magnetic resonance imaging | Childhood | CEREBRAL GLUCOSE-METABOLISM | ANTERIOR CINGULATE CORTEX | BASAL GANGLIA | MAJOR DEPRESSION | NEUROSCIENCES | PREFRONTAL CORTEX | VOXEL-BASED MORPHOMETRY | MEDIAL THALAMIC CHOLINE | MAGNETIC-RESONANCE-SPECTROSCOPY | TOURETTES-SYNDROME | COGNITIVE-BEHAVIORAL THERAPY | BEHAVIORAL SCIENCES | Young Adult | Diagnostic Imaging | Obsessive-Compulsive Disorder - physiopathology | Brain - physiopathology | Humans | Adolescent | Adolescent Development | Brain Chemistry | Child Development | Brain - growth & development | Child
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9. Full Text Investigation of previously implicated genetic variants in chronic tic disorders: a transmission disequilibrium test approach
by Abdulkadir, Mohamed and Londono, Douglas and Gordon, Derek and Fernandez, Thomas V and Brown, Lawrence W and Cheon, Keun-Ah and Coffey, Barbara J and Elzerman, Lonneke and Fremer, Carolin and Fründt, Odette and Garcia-Delgar, Blanca and Gilbert, Donald L and Grice, Dorothy E and Hedderly, Tammy and Heyman, Isobel and Hong, Hyun Ju and Huyser, Chaim and Ibanez-Gomez, Laura and Jakubovski, Ewgeni and Kim, Young Key and Kim, Young Shin and Koh, Yun-Joo and Kook, Sodahm and Kuperman, Samuel and Leventhal, Bennett and Ludolph, Andrea G and Madruga-Garrido, Marcos and Maras, Athanasios and Mir, Pablo and Morer, Astrid and Müller-Vahl, Kirsten and Münchau, Alexander and Murphy, Tara L and Plessen, Kerstin J and Roessner, Veit and Shin, Eun-Young and Song, Dong-Ho and Song, Jungeun and Tübing, Jennifer and van den Ban, Els and Visscher, Frank and Wanderer, Sina and Woods, Martin and Zinner, Samuel H and King, Robert A and Tischfield, Jay A and Heiman, Gary A and Hoekstra, Pieter J and Dietrich, Andrea
European Archives of Psychiatry and Clinical Neuroscience, ISSN 0940-1334, 4/2018, Volume 268, Issue 3, pp. 301 - 316
Genetic studies in Tourette syndrome (TS) are characterized by scattered and poorly replicated findings. We aimed to replicate findings from candidate gene and... 
Candidate gene study | Neurology | Neurosciences | Medicine & Public Health | Transmission Disequilibrium Test | Obsessive–compulsive disorder | Attention-deficit/hyperactivity disorder | Tourette syndrome | Psychiatry | POPULATION | AUTISM | PSYCHIATRY | CROSS-DISORDER | FAMILY-BASED ASSOCIATION | CLINICAL NEUROLOGY | COMPREHENSIVE METAANALYSIS | LA-TOURETTE-SYNDROME | HISTIDINE-DECARBOXYLASE | SLITRK1 GENE | Obsessive-compulsive disorder | GENOME-WIDE ASSOCIATION | Severity of Illness Index | Genome-Wide Association Study | Microtubule-Associated Proteins - genetics | Humans | Middle Aged | Child, Preschool | Family Health | Genotype | Male | Tic Disorders - genetics | Linkage Disequilibrium | Tryptophan Hydroxylase - genetics | Young Adult | Adolescent | Polymorphism, Single Nucleotide - genetics | Adult | Female | Child | Genetic research | Analysis | Investigations | Attention deficit disorder | Obsessive compulsive disorder | Dopamine | Serotonin | Hyperactivity | Attention deficit hyperactivity disorder | Genes | Genomes | Single-nucleotide polymorphism | Autism | Genetic variance | Quality control | Gilles de la Tourette syndrome | Polymorphism | Attention-deficit | hyperactivity disorder | Original Paper
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10. Full Text European Multicentre Tics in Children Studies (EMTICS): protocol for two cohort studies to assess risk factors for tic onset and exacerbation in children and adolescents
by Schrag, Anette and Martino, Davide and Apter, Alan and Ball, Juliane and Bartolini, Erika and Benaroya-Milshtein, Noa and Buttiglione, Maura and Cardona, Francesco and Creti, Roberta and Efstratiou, Androulla and Gariup, Maria and Georgitsi, Marianthi and Hedderly, Tammy and Heyman, Isobel and Margarit, Immaculada and Mir, Pablo and Moll, Natalie and Morer, Astrid and Müller, Norbert and Müller-Vahl, Kirsten and Münchau, Alexander and Orefici, Graziella and Plessen, Kerstin J and Porcelli, Cesare and Paschou, Peristera and Rizzo, Renata and Roessner, Veit and Schwarz, Markus J and Steinberg, Tamar and Tagwerker Gloor, Friederike and Tarnok, Zsanett and Walitza, Susanne and Dietrich, Andrea and Hoekstra, Pieter J and EMTICS Collaborative Grp and EMTICS Collaborative Group
European Child & Adolescent Psychiatry, ISSN 1018-8827, 1/2019, Volume 28, Issue 1, pp. 91 - 109
Genetic predisposition, autoimmunity and environmental factors [e.g. pre- and perinatal difficulties, Group A Streptococcal (GAS) and other infections,... 
Longitudinal | Medicine & Public Health | Streptococcal infection | Child and Adolescent Psychiatry | Obsessive–compulsive disorder | Genetics | Tourette syndrome | Psychiatry | Stress | PSYCHOMETRIC PROPERTIES | LA-TOURETTE SYNDROME | PSYCHIATRY | PSYCHOLOGY, DEVELOPMENTAL | A STREPTOCOCCAL INFECTIONS | NEUROPSYCHIATRIC DISORDERS | GENE-EXPRESSION | HAIR CORTISOL | PEDIATRICS | Obsessive-compulsive disorder | QUALITY-OF-LIFE | PSYCHOSOCIAL STRESS | BLOOD | Autoimmunity | Medicine, Experimental | Medical research | Adolescence | Antigens | Tics | At risk | Immune response | Perinatal | Environmental aspects | Population studies | Vulnerability | Environmental factors | Risk factors | Studies | Cohort analysis | Social interactions | Streptococci infection | Multicentre | Risk assessment | Children | Psychosocial factors | Original Contribution
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