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Developmental Neurobiology, ISSN 1932-8451, 02/2014, Volume 74, Issue 2, pp. 113 - 122
Journal Article
Journal Article
Current Opinion in Neurobiology, ISSN 0959-4388, 2015, Volume 36, pp. 118 - 127
Journal Article
Nature Neuroscience, ISSN 1097-6256, 02/2015, Volume 18, Issue 2, pp. 182 - 184
Human chromosome 16p11.2 microdeletion is the most common gene copy number variation in autism, but the synaptic pathophysiology caused by this mutation is... 
DEPRESSION | AUTISM | INHIBITION | FRAGILE-X-SYNDROME | ARC/ARG3.1 | MICE | PHENOTYPES | TRANSLATION | PROTEIN-SYNTHESIS | NEUROSCIENCES | DELETION SYNDROME | Memory Disorders - physiopathology | Autistic Disorder - physiopathology | Autistic Disorder - metabolism | Memory Disorders - metabolism | Neuronal Plasticity - drug effects | Male | Intellectual Disability - genetics | Intellectual Disability - metabolism | Receptor, Metabotropic Glutamate 5 - genetics | Neuronal Plasticity - genetics | Neuronal Plasticity - physiology | Receptor, Metabotropic Glutamate 5 - physiology | Behavior, Animal - drug effects | Chromosome Disorders - physiopathology | Chromosomes, Human, Pair 16 - genetics | Disease Models, Animal | Autistic Disorder - genetics | Chromosome Deletion | Chromosome Disorders - metabolism | Chromosomes, Human, Pair 16 - metabolism | Mice, Inbred C57BL | Behavior, Animal - physiology | Mice, Transgenic | Imidazoles - pharmacology | Signal Transduction - genetics | Receptor, Metabotropic Glutamate 5 - metabolism | Chromosomes, Mammalian | Intellectual Disability - physiopathology | Hippocampus - metabolism | Animals | Memory Disorders - drug therapy | Signal Transduction - drug effects | Signal Transduction - physiology | Mice | Pyridines - pharmacology | Hippocampus - physiopathology | Chromosome Disorders - genetics | Neuroplasticity | Cell receptors | Chromosome mapping | Brain research | Genetic research | Genetic aspects | Research | Properties
Journal Article
Journal of the American Academy of Child & Adolescent Psychiatry, ISSN 0890-8567, 2009, Volume 48, Issue 1, pp. 35 - 41
Abstract Objective There are no published nationally representative prevalence estimates of enuresis among children in the United States using standardized... 
Pediatrics | Psychiatry | prevalence | ADHD | health care use | comorbidities | enuresis | Prevalence | Comorbidities | Enuresis | Health care use | PSYCHIATRY | PSYCHOLOGY, DEVELOPMENTAL | ADULTS | DEFICIT-HYPERACTIVITY DISORDER | ADOLESCENCE | CHINESE CHILDREN | PRIMARY NOCTURNAL ENURESIS | BEHAVIORAL-PROBLEMS | CHILDHOOD ENURESIS | ENURETIC CHILDREN | PSYCHIATRIC-DISORDERS | PEDIATRICS | EPIDEMIOLOGY | Gender Differences | Correlation | Attention Deficit Hyperactivity Disorder | Human Body | Children | Incidence | Symptoms (Individual Disorders) | Gene Duplication | Chromosome Disorders - epidemiology | Attention Deficit Disorder with Hyperactivity - physiopathology | Autistic Disorder - physiopathology | Humans | Child Development Disorders, Pervasive - physiopathology | Enuresis - genetics | Cerebral Cortex - physiopathology | Schizophrenia - genetics | Schizophrenia - physiopathology | Enuresis - epidemiology | Child | Chromosome Disorders - physiopathology | Autistic Disorder - genetics | Chromosome Deletion | Child Development Disorders, Pervasive - epidemiology | Diagnosis, Differential | Diagnostic and Statistical Manual of Mental Disorders | Genetic Predisposition to Disease - genetics | Cross-Sectional Studies | Comorbidity | Brain - physiopathology | Genotype | Chromosome Mapping | Autistic Disorder - epidemiology | Schizophrenia - epidemiology | Attention Deficit Disorder with Hyperactivity - genetics | Child Development Disorders, Pervasive - genetics | Enuresis - physiopathology | Chromosome Disorders - genetics | Attention Deficit Disorder with Hyperactivity - epidemiology | Diagnosis | Attention-deficit hyperactivity disorder | Prevalence studies (Epidemiology) | Attention deficit disorder | Medical personnel | Medical screening | Medical disorders | Children & youth
Journal Article
Proceedings of the National Academy of Sciences, ISSN 0027-8424, 10/2013, Volume 110, Issue 42, pp. E4016 - E4025
Journal Article
Biological Psychiatry, ISSN 0006-3223, 2015, Volume 77, Issue 9, pp. 785 - 793
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 Neuroscience, ISSN 0270-6474, 12/2015, Volume 35, Issue 49, pp. 16282 - 16294
Journal Article
Journal Article