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The American journal of psychiatry, ISSN 0002-953X, 11/2010, Volume 167, Issue 11, pp. 1357 - 1363
Life Sciences & Biomedicine | Psychiatry | Science & Technology | Psychology. Psychoanalysis. Psychiatry | Infantile autism | Psychopathology. Psychiatry | Developmental disorders | Biological and medical sciences | Medical sciences | Child clinical studies | Twins, Dizygotic - psychology | Diseases in Twins - genetics | Twins, Monozygotic - genetics | Humans | Male | Motor Skills Disorders - genetics | Neurocognitive Disorders - psychology | Social Environment | Motor Skills Disorders - psychology | Twins, Monozygotic - psychology | Tic Disorders - diagnosis | Neurocognitive Disorders - genetics | Child Development Disorders, Pervasive - diagnosis | Learning Disorders - psychology | Female | Attention Deficit Disorder with Hyperactivity - diagnosis | Diseases in Twins - psychology | Child | Genetic Predisposition to Disease - psychology | Genetic Predisposition to Disease - genetics | Diseases in Twins - diagnosis | Quantitative Trait, Heritable | Comorbidity | Learning Disorders - diagnosis | Neurocognitive Disorders - diagnosis | Genotype | Tic Disorders - genetics | Twins, Dizygotic - genetics | Phenotype | Attention Deficit Disorder with Hyperactivity - genetics | Child Development Disorders, Pervasive - psychology | Child Development Disorders, Pervasive - genetics | Sex Factors | Attention Deficit Disorder with Hyperactivity - psychology | Polymorphism, Single Nucleotide - genetics | Learning Disorders - genetics | Genetic Variation - genetics | Models, Genetic | Motor Skills Disorders - diagnosis | Tic Disorders - psychology | Autism | Genetic aspects | Diagnosis | Research | Neuropsychiatry | Child psychopathology | Studies | Twins | Attention Deficit Hyperactivity Disorder | Children & youth | Index Medicus | Abridged Index Medicus | Delirium | Pervasive | Learning Disorders | Psychology | Genetic | Child Development Disorders | Single Nucleotide | Amnestic | Genetic Variation | Cognitive Disorders | Psykiatri | Genetics | Dizygotic | Monozygotic | Diseases in Twins | Genetic Predisposition to Disease | Motor Skills Disorders | Heritable | Attention Deficit Disorder with Hyperactivity | Tic Disorders | Models | Genetics Quantitative Trait | Dementia | Polymorphism
Journal Article
Psychiatric genetics, ISSN 0955-8829, 1990
Journal
Molecular psychiatry, ISSN 1359-4184, 1996
Journal
The journal of clinical psychiatry, ISSN 0160-6689, 02/2011, Volume 72, Issue 2, pp. 175 - 182
Psychology, Clinical | Social Sciences | Life Sciences & Biomedicine | Psychiatry | Psychology | Science & Technology | Chromosome fragility (bloom syndrome, ataxia telangiectasia, fanconi anemia, x-linked mental retardation...) | Miscellaneous | Anxiety disorders. Neuroses | Psychology. Psychoanalysis. Psychiatry | Adult and adolescent clinical studies | Psychopathology. Psychiatry | Medical genetics | Mood disorders | Biological and medical sciences | Medical sciences | Phobic Disorders - epidemiology | Mood Disorders - genetics | Humans | Middle Aged | Stress Disorders, Post-Traumatic - epidemiology | Anxiety Disorders - diagnosis | Male | Depressive Disorder, Major - epidemiology | Mood Disorders - epidemiology | DNA Mutational Analysis | Stress Disorders, Post-Traumatic - diagnosis | Phobic Disorders - diagnosis | Female | Phobic Disorders - genetics | Fragile X Syndrome - epidemiology | Fragile X Syndrome - genetics | Diagnostic and Statistical Manual of Mental Disorders | Genetic Predisposition to Disease - genetics | Cross-Sectional Studies | Comorbidity | RNA, Messenger - genetics | Anxiety Disorders - epidemiology | Phenotype | Depressive Disorder, Major - genetics | Panic Disorder - diagnosis | Mood Disorders - diagnosis | Panic Disorder - epidemiology | Anxiety Disorders - genetics | Aged | Fragile X Mental Retardation Protein - genetics | Depressive Disorder, Major - diagnosis | Stress Disorders, Post-Traumatic - genetics | Genetic Carrier Screening | Fragile X Syndrome - diagnosis | Panic Disorder - genetics | Index Medicus | Depressive Disorders | Panic Disorder | Phobia | Anxiety Disorders | Americans | Adults | Genetic Markers | Neurological Symptoms | Epidemiology | PTSD (DSM-IV) | Mood Disorders | mood disorders | fragile X-associated tremor | FXTAS | anxiety disorders | Fragile X syndrome | ataxia syndrome | FMR1 gene
Journal Article
Science (American Association for the Advancement of Science), ISSN 0036-8075, 12/2012, Volume 338, Issue 6114, pp. 1619 - 1622
Exome | Genetic variation | Pervasive child development disorders | DNA | REPORTS | Cell lines | Genetic loci | Genomes | Genetic mutation | Sequencing | Cells | Science & Technology - Other Topics | Multidisciplinary Sciences | Science & Technology | Fundamental and applied biological sciences. Psychology | Classical genetics, quantitative genetics, hybrids | Human | Psychology. Psychoanalysis. Psychiatry | Infantile autism | Psychopathology. Psychiatry | Developmental disorders | Biological and medical sciences | Genetics of eukaryotes. Biological and molecular evolution | Medical sciences | Child clinical studies | Microcephaly - genetics | Humans | Child, Preschool | Male | Cephalometry | Receptors, N-Methyl-D-Aspartate - genetics | Protein-Tyrosine Kinases - genetics | Female | Nuclear Proteins - genetics | Child | Megalencephaly - genetics | DNA Probes | PTEN Phosphohydrolase - genetics | Genetic Predisposition to Disease | Genetic Association Studies | Protein-Serine-Threonine Kinases - genetics | Chromatin Assembly and Disassembly | Repressor Proteins - genetics | Receptors, Cytoplasmic and Nuclear - genetics | Transcription Factors - genetics | DNA-Binding Proteins - genetics | T-Box Domain Proteins - genetics | beta Catenin - metabolism | beta Catenin - genetics | Child Development Disorders, Pervasive - genetics | Mutation | Sequence Analysis, DNA - methods | Cohort Studies | Genetic aspects | Research | Nucleotide sequencing | Gene mutations | Pervasive developmental disorders | DNA sequencing | Autism | Genotype & phenotype | Genomics | Index Medicus | Multiplexing | Mutations | Genes | Inversions | Disorders | Online | Gene sequencing
Journal Article
JAMA psychiatry (Chicago, Ill.), ISSN 2168-622X, 01/2013, Volume 70, Issue 1, pp. 22 - 30
Journal Article
American journal of medical genetics. Part B, Neuropsychiatric genetics, ISSN 1552-4841, 06/2018, Volume 177, Issue 4, pp. 416 - 425
adolescence | psychotic‐like experiences | ALSPAC | GWAS | schizophrenia | psychotic-like experiences | Genetics & Heredity | Life Sciences & Biomedicine | Psychiatry | Science & Technology | Multifactorial Inheritance - genetics | European Continental Ancestry Group - genetics | Genetic Predisposition to Disease - genetics | Genome-Wide Association Study | Humans | Psychotic Disorders - psychology | Risk Factors | Linkage Disequilibrium - genetics | Anhedonia | Male | Bipolar Disorder - genetics | Genetic Testing - methods | Young Adult | Hallucinations - psychology | Paranoid Disorders | Psychotic Disorders - genetics | Schizophrenia - genetics | Depressive Disorder, Major - genetics | Adolescent | Polymorphism, Single Nucleotide - genetics | Female | Medical research | Depression, Mental | Genomics | Schizophrenia | Bipolar disorder | Youth | Child psychopathology | International cooperation | Paranoia | Analysis | Medicine, Experimental | Genetic research | Teenagers | Single nucleotide polymorphisms | Emotional behavior | Mental disorders | Linkage disequilibrium | Cognitive ability | Genomes | Single-nucleotide polymorphism | Behavior disorders | Mental depression | Psychosis | Child development | Hedonic response | Hallucinations | Heritability | Adolescents | Polygenic inheritance | Index Medicus | childhood | association | young adulthood | depressive | symptoms | Medicinsk genetik | Medical Genetics | general-population | birth-cohort | Psykiatri | risk | population-based cohort | twin
Journal Article
by Neale, Benjamin M and Neale, Benjamin M and Kou, Yan and Samocha, Kaitlin E and Liu, Li and Lim, Elaine and Ma'Ayan, Avi and Rossin, Elizabeth and Samocha, Kaitlin E and Kirby, Andrew and Fromer, Menachem and Sabo, Aniko and Lin, Chiao-Feng and Daly, Mark J and Stevens, Christine and Rossin, Elizabeth and Kirby, Andrew and Wang, Li-San and Makarov, Vladimir and Flannick, Jason and Polak, Paz and Fromer, Menachem and Shakir, Khalid and Yoon, Seungtai and Maguire, Jared and Fennell, Tim and Garimella, Kiran and Crawford, Emily L and Banks, Eric and Campbell, Nicholas G and Poplin, Ryan and Geller, Evan T and Valladares, Otto and Gabriel, Stacey and Schafer, Chad and De Pristo, Mark and Sunyaev, Shamil and Liu, Han and Daly, Mark J and Zhao, Tuo and Cai, Guiqing and Lihm, Jayon and Dannenfelser, Ruth and Jabado, Omar and Peralta, Zuleyma and Nagaswamy, Uma and Muzny, Donna and Reid, Jeffrey G and Newsham, Irene and Wu, Yuanqing and Lewis, Lora and Han, Yi and Voight, Benjamin F and Lim, Elaine and Rossin, Elizabeth and Kirby, Andrew and Flannick, Jason and Fromer, Menachem and Shakir, Khalid and Fennell, Tim and Garimella, Kiran and Banks, Eric and Poplin, Ryan and Gabriel, Stacey and Depristo, Mark and Wimbish, Jack R and Boone, Braden E and Levy, Shawn E and Betancur, Catalina and Sunyaev, Shamil and Boerwinkle, Eric and Buxbaum, Joseph D and Cook Jr, Edwin H and Devlin, Bernie and Gibbs, Richard A and Roeder, Kathryn and Schellenberg, Gerard D and Sutcliffe, James S and Daly, Mark J
Nature (London), ISSN 0028-0836, 05/2012, Volume 484, Issue 7397, pp. 242 - 246