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Molecular Psychiatry, ISSN 1359-4184, 10/2006, Volume 11, Issue 10, pp. 903 - 913
Previous research on adults has shown that a functional polymorphism in the promoter region of the monoamine oxidase A (MAOA) gene moderates the impact of... 
ADHD | Antisocial behavior | Monoamine oxidase A | Emotional problems | Maltreatment | Promoter polymorphism | Psychopathology | maltreatment | ASSOCIATION ANALYSIS | PSYCHIATRY | DEFICIT HYPERACTIVITY DISORDER | BIOCHEMISTRY & MOLECULAR BIOLOGY | promoter polymorphism | emotional problems | BEHAVIORAL DISTURBANCE | antisocial behavior | PHYSICAL MALTREATMENT | CHILDHOOD | NEUROSCIENCES | monoamine oxidase A | VIOLENCE | psychopathology | MONOAMINE-OXIDASE-A | PREFERENTIAL TRANSMISSION | COMPLEX DISEASES | Follow-Up Studies | Crime Victims - psychology | Humans | Middle Aged | Child, Preschool | Male | Child Behavior - psychology | Monoamine Oxidase - genetics | Promoter Regions, Genetic - genetics | Affective Symptoms - genetics | Antisocial Personality Disorder - genetics | Family Relations | Adult | Female | Attention Deficit and Disruptive Behavior Disorders - psychology | Child | Affective Symptoms - enzymology | Child Behavior Disorders - psychology | Genetic Predisposition to Disease | Chromosomes, Human, X - genetics | Antisocial Personality Disorder - psychology | Attention Deficit and Disruptive Behavior Disorders - enzymology | Violence - psychology | Child Behavior Disorders - enzymology | Polymorphism, Genetic | Regression Analysis | Affective Symptoms - psychology | Child Abuse - psychology | Adolescent | Environment | Child Behavior Disorders - genetics | Antisocial Personality Disorder - enzymology | Attention Deficit and Disruptive Behavior Disorders - genetics | Cohort Studies
Journal Article
Journal of Autism and Developmental Disorders, ISSN 0162-3257, 11/2016, Volume 46, Issue 11, pp. 3597 - 3606
Atypical responses to sensory stimuli are a new criterion in DSM-5 for the diagnosis of an autism spectrum disorder (ASD) but are also reported in other... 
Pediatrics | Child and School Psychology | Neurosciences | Public Health | DSM-5 | Behaviour | Diagnostic criteria | Psychology | Sensory interests | Sensory reactivity | Autism spectrum disorder | ABNORMALITIES | ANXIETY | PSYCHOLOGY, DEVELOPMENTAL | SYMPTOMS | STRENGTHS | DIFFICULTIES QUESTIONNAIRE | FEATURES | REPETITIVE BEHAVIORS | ASD | PROFILE | ASSOCIATION | Severity (of Disability) | Screening Tests | Preadolescents | Strengths and Difficulties Questionnaire | Autism | Comparative Analysis | Sensory Experience | Child Behavior | Special Needs Students | Behavior Problems | Pervasive Developmental Disorders | Questionnaires | Early Adolescents | Stimuli | Child Behavior Disorders - psychology | Diagnostic and Statistical Manual of Mental Disorders | Child Behavior Disorders - diagnosis | Education, Special | Humans | Sensation Disorders - psychology | Autism Spectrum Disorder - therapy | Male | Autism Spectrum Disorder - psychology | Case-Control Studies | Child Behavior Disorders - therapy | Neuropsychological Tests | Stereotyped Behavior | Adolescent | Sensation Disorders - therapy | Female | Sensation Disorders - diagnosis | Child | Autism Spectrum Disorder - diagnosis | Psychological aspects | Autistic children | Senses and sensation | Special needs children | Neurodevelopmental disorders | Sensory perception | Occupational therapy | Diagnosis | Behavior | Children | Communication | Emotional behavior | Emotional-Behavioural problems | Autistic spectrum disorders | Developmental disorders | Severity | Children & youth | Reactivity | Repetitive behaviour | Dysfunction | Educational needs | Behavioural problems | Intelligence quotient | Sensory stimuli | Child & adolescent psychiatry | language disability | Autism Diagnostic Interview Revised | major clinical study | Article | hearing impairment | movement (physiology) | sensory dysfunction | stereotypy | taste acuity | problem behavior | sensory stimulation | hearing | priority journal | female | disease severity | human | Social Sciences | conduct disorder | intellectual impairment | autism | behavior disorder | physical disability | Samhällsvetenskap | sensation | Wechsler intelligence scale for children | controlled study | chromosome disorder | adolescent | Psykologi | intelligence quotient | male | child
Journal Article
Journal of Intellectual Disability Research, ISSN 0964-2633, 02/2011, Volume 55, Issue 2, pp. 109 - 120
Background  Self‐injurious and aggressive behaviours are reported as components of some behavioural phenotypes but there are few studies comparing across... 
behavioural phenotype | impulsivity | challenging behaviour | hyperactivity | autism spectrum disorder | affect | Behavioural phenotype | Impulsivity | Challenging behaviour | Hyperactivity | Affect | Autism spectrum disorder | POPULATION | MENTAL-RETARDATION | INTELLECTUAL DISABILITIES PREVALENCE | ADULTS | MALADAPTIVE BEHAVIOR | EDUCATION, SPECIAL | CHILDREN | SMITH-MAGENIS-SYNDROME | FRAGILE-X-SYNDROME | REHABILITATION | DE-LANGE-SYNDROME | PRADER-WILLI-SYNDROME | Intervention | At Risk Persons | Emotional Response | Self Destructive Behavior | Genetic Disorders | Incidence | Phenomenology | Comparative Analysis | Behavior Problems | Pervasive Developmental Disorders | Questionnaires | Genetics | Injuries | Prader-Willi Syndrome - epidemiology | Chromosome Disorders - epidemiology | Angelman Syndrome - psychology | Prevalence | Humans | Middle Aged | Child, Preschool | Male | Genetic Diseases, Inborn - epidemiology | De Lange Syndrome - epidemiology | Case-Control Studies | Smith-Magenis Syndrome - epidemiology | Chromosome Disorders - psychology | Young Adult | Prader-Willi Syndrome - psychology | Oculocerebrorenal Syndrome - psychology | Self-Injurious Behavior - epidemiology | Abnormalities, Multiple - epidemiology | Adult | Female | Child | Abnormalities, Multiple - genetics | Fragile X Syndrome - epidemiology | Behavioral Symptoms - psychology | Child Development Disorders, Pervasive - epidemiology | Aggression | Comorbidity | Self-Injurious Behavior - psychology | Angelman Syndrome - epidemiology | Behavioral Symptoms - epidemiology | Cri-du-Chat Syndrome - epidemiology | Abnormalities, Multiple - psychology | Genetic Diseases, Inborn - psychology | Syndrome | Behavioral Symptoms - genetics | Child Development Disorders, Pervasive - psychology | Smith-Magenis Syndrome - psychology | Fragile X Syndrome - psychology | Adolescent | Cri-du-Chat Syndrome - psychology | Intellectual Disability - psychology | De Lange Syndrome - psychology | Oculocerebrorenal Syndrome - epidemiology | Prader-Willi syndrome | Genetic research | Prevalence studies (Epidemiology) | Genotype & phenotype | Autism | Comparative analysis | Self destructive behavior | Risk factors | Aggressiveness
Journal Article
by D’Angelo, Debra and Lebon, Sébastien and Chen, Qixuan and Martin-Brevet, Sandra and Snyder, LeeAnne Green and Hippolyte, Loyse and Hanson, Ellen and Maillard, Anne M and Faucett, W. Andrew and Macé, Aurélien and Pain, Aurélie and Bernier, Raphael and Chawner, Samuel J. R. A and David, Albert and Andrieux, Joris and Aylward, Elizabeth and Baujat, Genevieve and Caldeira, Ines and Conus, Philippe and Ferrari, Carrina and Forzano, Francesca and Gérard, Marion and Goin-Kochel, Robin P and Grant, Ellen and Hunter, Jill V and Isidor, Bertrand and Jacquette, Aurélia and Jønch, Aia E and Keren, Boris and Lacombe, Didier and Le Caignec, Cédric and Martin, Christa Lese and Männik, Katrin and Metspalu, Andres and Mignot, Cyril and Mukherjee, Pratik and Owen, Michael J and Passeggeri, Marzia and Rooryck-Thambo, Caroline and Rosenfeld, Jill A and Spence, Sarah J and Steinman, Kyle J and Tjernagel, Jennifer and Van Haelst, Mieke and Shen, Yiping and Draganski, Bogdan and Sherr, Elliott H and Ledbetter, David H and van den Bree, Marianne B. M and Beckmann, Jacques S and Spiro, John E and Reymond, Alexandre and Jacquemont, Sébastien and Chung, Wendy K and Cardiff Univ Experiences Children and Simons Variation Individuals Proje and 16p112 European Consortium and Simons Variation in Individuals Project (VIP) Consortium and 16p11.2 European Consortium and Cardiff University Experiences of Children With Copy Number Variants (ECHO) Study and for the Cardiff University Experiences of Children With Copy Number Variants (ECHO) Study, the 16p11.2 European Consortium, and the Simons Variation in Individuals Project (VIP) Consortium
JAMA Psychiatry, ISSN 2168-622X, 01/2016, Volume 73, Issue 1, pp. 20 - 30
IMPORTANCE: The 16p11.2 BP4-BP5 duplication is the copy number variant most frequently associated with autism spectrum disorder (ASD), schizophrenia, and... 
DE-NOVO | INFANTILE SPASMS | AUTISM | PSYCHIATRY | COPY NUMBER VARIATIONS | SCHIZOPHRENIA | DISORDERS | PHENOTYPES | SPECTRUM | ASSOCIATION | DELETION | Chromosome Disorders - epidemiology | Microcephaly - genetics | Chromosome Duplication | Humans | Middle Aged | Child, Preschool | Male | Cognition | Developmental Disabilities - genetics | Cerebellum - abnormalities | Schizophrenic Psychology | Microcephaly - epidemiology | Case-Control Studies | Chromosome Disorders - psychology | DNA Copy Number Variations | Epilepsy - epidemiology | Intellectual Disability - genetics | Young Adult | Schizophrenia - genetics | Autism Spectrum Disorder - epidemiology | Adult | Epilepsy - genetics | Female | Nervous System Malformations - genetics | Child | Chromosomes, Human, Pair 16 - genetics | Intellectual Disability - epidemiology | Autistic Disorder - genetics | Chromosome Deletion | Autism Spectrum Disorder - genetics | Comorbidity | Autism Spectrum Disorder - psychology | Autistic Disorder - epidemiology | Schizophrenia - epidemiology | Autistic Disorder - psychology | Nervous System Malformations - epidemiology | Developmental Disabilities - epidemiology | Adolescent | Intellectual Disability - psychology | Chromosome Disorders - genetics | Cohort Studies | Body mass index | Genetic aspects | Analysis | Risk factors | Pervasive developmental disorders
Journal Article
Journal of the American Academy of Child and Adolescent Psychiatry, ISSN 0890-8567, 09/2006, Volume 45, Issue 9, pp. 1104 - 1113
Journal Article
JAMA Psychiatry, ISSN 2168-622X, 04/2015, Volume 72, Issue 4, pp. 377 - 385
Journal Article
Nature Genetics, ISSN 1061-4036, 2017, Volume 49, Issue 11, pp. 1584 - 1592
Persistent insomnia is among the most frequent complaints in general practice. To identify genetic factors for insomnia complaints, we performed a genome-wide... 
SLEEP DISTURBANCE | HUMAN HEIGHT | POPULATION | METAANALYSIS | RESTLESS LEGS SYNDROME | MYOCARDIAL-INFARCTION | VARIANTS | GENETICS & HEREDITY | SEX-DIFFERENCES | PERSISTENT INSOMNIA | EPIDEMIOLOGY | Humans | Type D Personality | Male | Educational Status | Genetic Loci | Gene Regulatory Networks | Restless Legs Syndrome - genetics | Restless Legs Syndrome - metabolism | Adult | Female | Quality of Life - psychology | Neoplasm Proteins - genetics | Sleep Initiation and Maintenance Disorders - metabolism | Gene Expression | Genetic Predisposition to Disease | Genome-Wide Association Study | Restless Legs Syndrome - physiopathology | Gene Frequency | Chromosome Mapping | Homeodomain Proteins - genetics | Protein Interaction Mapping | Restless Legs Syndrome - psychology | Alleles | Sex Factors | Sleep Initiation and Maintenance Disorders - genetics | Sleep Initiation and Maintenance Disorders - physiopathology | Polymorphism, Single Nucleotide | Myeloid Ecotropic Viral Integration Site 1 Protein | Genome, Human | Sleep Initiation and Maintenance Disorders - psychology | Care and treatment | Genome-wide association studies | Insomnia | Development and progression | Genotype | Genetic aspects | Health aspects | Methods | Legs | Psychological factors | Genes | Association analysis | Gender differences | Genomes | Metabolism | Loci | Independent sample | Studies | Restless legs syndrome | Sleep disorders | Pleiotropy | Sexes | Genetic factors | Bioinformatics
Journal Article
Journal of Autism and Developmental Disorders, ISSN 0162-3257, 8/2016, Volume 46, Issue 8, pp. 2734 - 2748
The 16p11.2 duplication (BP4–BP5) is associated with Autism Spectrum Disorder (ASD), although significant heterogeneity exists. Quantitative ASD, behavioral... 
Pediatrics | Autism | Child and School Psychology | Neurosciences | Public Health | Neuropsychological | Intellectual disability | Psychology | 16p11.2 duplication | Genetics | Cognitive | MICRODELETION | DIAGNOSTIC INTERVIEW | PSYCHOLOGY, DEVELOPMENTAL | CANDIDATE GENES | PHENOTYPE | SCHIZOPHRENIA | RISK | REARRANGEMENTS | DE-NOVO MUTATIONS | COPY NUMBER VARIANTS | ASSOCIATION | Developmental Disabilities | Ecological Factors | Diagnostic Tests | Control Groups | Genetic Disorders | Experimental Groups | Behavior Rating Scales | Pervasive Developmental Disorders | Adults | Neuropsychology | Children | Psychiatry | Statistical Analysis | Clinical Diagnosis | Autistic Disorder - genetics | Chromosome Deletion | Autism Spectrum Disorder - genetics | Humans | Child, Preschool | Infant | Male | Autism Spectrum Disorder - psychology | Autistic Disorder - psychology | Chromosome Disorders - psychology | Intellectual Disability - genetics | Phenotype | Intellectual Disability - diagnosis | Adolescent | Chromosome Disorders - diagnosis | Gene Duplication - genetics | Adult | Female | Intellectual Disability - psychology | Autistic Disorder - diagnosis | Child | Autism Spectrum Disorder - diagnosis | Chromosome Disorders - genetics | Chromosomes, Human, Pair 16 - genetics | Genetic aspects | Pervasive developmental disorders | Diagnosis | Phenotypes | Intellectual disabilities | Attention deficit hyperactivity disorder | Variability | Autistic spectrum disorders | Autistic children | Risk factors | Carriers | Disability | Clonal deletion | Learning disabilities | Anxiety
Journal Article
Biological Psychiatry, ISSN 0006-3223, 2015, Volume 77, Issue 9, pp. 785 - 793
Journal Article