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Lancet, The, ISSN 0140-6736, 2013, Volume 381, Issue 9875, pp. 1371 - 1379
Summary Background Findings from family and twin studies suggest that genetic contributions to psychiatric disorders do not in all cases map to present... 
Internal Medicine | POPULATION | DEPRESSION | MEDICINE, GENERAL & INTERNAL | ATTENTION-DEFICIT/HYPERACTIVITY DISORDER | METAANALYSIS | GENE-EXPRESSION | SCHIZOPHRENIA | CACNA1C | AUTISM SPECTRUM DISORDERS | BIPOLAR DISORDER | ASSOCIATION | Child Development Disorders, Pervasive - epidemiology | Genome-Wide Association Study | Humans | Genetic Loci - genetics | Logistic Models | Bipolar Disorder - genetics | Depressive Disorder, Major - epidemiology | Schizophrenia - epidemiology | Calcium Channels, L-Type - genetics | Schizophrenia - genetics | Attention Deficit Disorder with Hyperactivity - genetics | Child Development Disorders, Pervasive - genetics | Depressive Disorder, Major - genetics | Age of Onset | Polymorphism, Single Nucleotide - genetics | Adult | Child | Bipolar Disorder - epidemiology | Attention Deficit Disorder with Hyperactivity - epidemiology | Physiological aspects | Genetic aspects | Research | Genetic variation | Mental illness | Risk factors | Medical research | Calcium channels | Genes | Depression, Mental | Genomics | Schizophrenia | Bipolar disorder | Child psychopathology | Quantitative genetics | Autism | Medicine, Experimental | Genetic research | Single nucleotide polymorphisms | Studies | Genetics | Children & youth | Attention deficit disorder | Enrichment | Brain | Calcium | Disease | Mental disorders | Hyperactivity | Mental health | Disorders | Genomes | Single-nucleotide polymorphism | Mental depression | Consortia | Datasets | Calcium signalling | Genetic effects | Signal transduction | Regression models | Autopsy | Classification | Psychopathology | Children | Chromosomes | Genotypes | Phenotypes | Channel gating | Attention deficit hyperactivity disorder | Calcium channels (voltage-gated) | Behavior disorders | Regression analysis | Risk analysis | Loci | Quantitative trait loci | Government grants | Calcium channels (L-type) | Diagnostic systems | Polygenic inheritance | Psychiatry | Polymorphism | Index Medicus | Abridged Index Medicus | Neurosciences | Calcium Channels | Pervasive | Attention Deficit Disorder with Hyperactivity | L-Type | Child Development Disorders | Depressive Disorder | Genetic Loci | Single Nucleotide | epidemiology | genetics | Bipolar Disorder | Major | Neurovetenskaper
Journal Article
Klinik Psikofarmakoloji Bulteni, ISSN 1017-7833, 01/2017, Volume 27, p. 277
Journal Article
Translational Psychiatry, ISSN 2158-3188, 12/2018, Volume 8, Issue 1, pp. 39 - 11
Journal Article
by Purcell, Shaun M and Wray, Naomi R and Stone, Jennifer L and Visscher, Peter M and O'Donovan, Michael C and Sullivan, Patrick F and Ruderfer, Douglas M and McQuillin, Andrew and Morris, Derek W and Oĝdushlaine, Colm T and Corvin, Aiden and Holmans, Peter A and Oĝdonovan, Michael C and MacGregor, Stuart and Gurling, Hugh and Blackwood, Douglas H. R and Craddock, Nick J and Gill, Michael and Hultman, Christina M and Kirov, George K and Lichtenstein, Paul and Muir, Walter J and Owen, Michael J and Pato, Carlos N and Scolnick, Edward M and St Clair, David and Williams, Nigel M and Georgieva, Lyudmila and Nikolov, Ivan and Norton, N and Williams, H and Toncheva, Draga and Milanova, Vihra and Thelander, Emma F and O'Dushlaine, Colm T and Kenny, Elaine and Quinn, Emma M and Choudhury, Khalid and Datta, Susmita and Pimm, Jonathan and Thirumalai, Srinivasa and Puri, Vinay and Krasucki, Robert and Lawrence, Jacob and Quested, Digby and Bass, Nicholas and Crombie, Caroline and Fraser, Gillian and Leh Kuan, Soh and Walker, Nicholas and McGhee, Kevin A and Pickard, Ben and Malloy, Pat and MacLean, Alan W and Van Beck, Margaret and Pato, Michele T and Medeiros, Helena and Middleton, Frank and Carvalho, Celia and Morley, Christopher and Fanous, Ayman and Conti, David and Knowles, James A and Paz Ferreira, Carlos and MacEdo, Antonio and Helena Azevedo, M and Kirby, Andrew N and Ferreira, Manuel A. R and Daly, Mark J and Chambert, Kimberly and Kuruvilla, Finny and Gabriel, Stacey B and Ardlie, Kristin and Moran, Jennifer L and Sklar, Pamela and International Schizophrenia Consortium and The International Schizophrenia Consortium and Medicinska fakulteten and Medicinska och farmaceutiska vetenskapsområdet and Uppsala universitet and Institutionen för neurovetenskap
Nature, ISSN 0028-0836, 08/2009, Volume 460, Issue 7256, pp. 748 - 752
Journal Article
Molecular Psychiatry, ISSN 1359-4184, 03/2018, Volume 23, Issue 3, pp. 666 - 673
Journal Article
Nature, ISSN 0028-0836, 11/2010, Volume 468, Issue 7321, pp. 263 - 269
Mutations in the X-linked MECP2 gene, which encodes the transcriptional regulator methyl-CpG-binding protein 2 (MeCP2), cause Rett syndrome and several... 
GLUTAMIC-ACID DECARBOXYLASE | GENE | 67 KDA | MULTIDISCIPLINARY SCIENCES | MOUSE MODEL | MUTATION | NEURONAL MECP2 | SCHIZOPHRENIA | MICE | CPG-BINDING PROTEIN-2 | YOUNG GIRLS | Autistic Disorder - physiopathology | gamma-Aminobutyric Acid - metabolism | Methyl-CpG-Binding Protein 2 - metabolism | Male | Psychomotor Disorders - complications | Methyl-CpG-Binding Protein 2 - deficiency | Compulsive Behavior - physiopathology | Neurons - metabolism | Disease Models, Animal | Autistic Disorder - genetics | Signal Transduction | Compulsive Behavior - genetics | Genotype | Mice, Transgenic | Survival Rate | Hippocampus - pathology | Rett Syndrome - physiopathology | Self-Injurious Behavior - genetics | Phenotype | Neuronal Plasticity | Long-Term Potentiation | Stereotypic Movement Disorder - genetics | Compulsive Behavior - complications | Glutamate Decarboxylase - metabolism | Mice | Hippocampus - physiopathology | Autistic Disorder - pathology | Rett Syndrome - complications | Neural Inhibition | Stereotypic Movement Disorder - pathology | Reflex, Startle - genetics | Electroencephalography | Methyl-CpG-Binding Protein 2 - genetics | Synaptic Transmission | Psychomotor Disorders - genetics | Self-Injurious Behavior - complications | Psychomotor Disorders - physiopathology | Inhibitory Postsynaptic Potentials | Stereotypic Movement Disorder - physiopathology | Brain - cytology | Homeodomain Proteins - genetics | Stereotypic Movement Disorder - complications | Self-Injurious Behavior - physiopathology | Animals | Rett Syndrome - pathology | Vesicular Inhibitory Amino Acid Transport Proteins - genetics | Presynaptic Terminals - metabolism | Autistic Disorder - complications | Respiration | Rett Syndrome - genetics | Autism | Care and treatment | Rett syndrome | Schizophrenia | GABA | Genetic aspects | Diagnosis | Cognition disorders | Seizures (Medicine) | Health aspects | Studies | Anxieties | Social interaction | Neurons | Rodents | Bipolar disorder | Behavior | Gene expression | Index Medicus
Journal Article
Journal of the American Academy of Child & Adolescent Psychiatry, ISSN 0890-8567, 12/2017, Volume 56, Issue 12, pp. 1073 - 1080
Bipolar disorder (BD) is one of the most heritable psychiatric conditions and is associated with high suicide risk. To explore the reasons for this link, this... 
bipolar disorder | traumatic stress | attempted | populations at risk | suicide | polygenic risk | CHILDHOOD ABUSE | PSYCHIATRY | PSYCHOLOGY, DEVELOPMENTAL | NONSUICIDAL SELF-INJURY | RELIABILITY | CHILDREN | REPLICATION | LONGITUDINAL DATA-ANALYSIS | LINKAGE ANALYSES | ADOLESCENTS | PEDIATRICS | BEHAVIORS | GENOME-WIDE ASSOCIATION | Follow-Up Studies | Humans | Psychological Trauma - psychology | Male | Suicidal Ideation | Self-Injurious Behavior - diagnosis | Psychological Trauma - diagnosis | Bipolar Disorder - diagnosis | Case-Control Studies | Young Adult | Psychiatric Status Rating Scales | Female | Retrospective Studies | Child | Genetic Predisposition to Disease | Risk Assessment | Self-Injurious Behavior - psychology | Risk Factors | Models, Statistical | Bipolar Disorder - genetics | Bipolar Disorder - psychology | Suicide, Attempted - psychology | Self-Injurious Behavior - genetics | Adolescent | Polymorphism, Single Nucleotide | Psychological Trauma - genetics | Bullying | Self injury | Demography | Mental disorders | Demographic aspects | Genetic susceptibility | Attempted | Bipolar disorder | Alcohol dependence | Suicidal ideation | Suicide | Alcohol use | Domestic violence | Demographics | Risk assessment | Suicides & suicide attempts | Traumatic life events | Sexual abuse | Psychological trauma | Young adults | Self-injury | Abuse | Aggression | Vulnerability | Trauma | Progeny | Mood | Polygenic inheritance | Traumatic stress | Substance abuse disorders | Index Medicus
Journal Article
Nature, ISSN 0028-0836, 05/2009, Volume 459, Issue 7246, pp. 528 - 533
Journal Article