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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
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 | Index Medicus | Abridged Index Medicus
Journal Article
2010, 2nd ed., ISBN 9780195398441, xxiii, 676
With contributions from leaders in the field from around the world, this new edition of Human Genome Epidemiology is a fully updated look at the ways in which... 
Genetic disorders | Methodology | Epidemiology | Genomics | Medical genetics
Book
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 | Index Medicus
Journal Article
Journal Article
Nature Neuroscience, ISSN 1097-6256, 09/2013, Volume 16, Issue 9, pp. 1228 - 1237
Journal Article
by Debette, S and Kamatani, Y and Metso, T.M and Kloss, M and Chauhan, G and Engelter, S.T and Pezzini, S and Thijs, V and Markus, H.S and Dichgans, M and Wolf, C and Dittrich, R and Touze, E and Southerland, A.M and Samson, Y and Abboud, S and Bejot, Y and Caso, V and Bersano, A and Gschwendtner, A and Sessa, M and Cole, J and Lamy, C and Medeiros, E and Beretta, S and Bonati, L.H and Grau, A.J and Michel, P and Majersik, J.J and Sharma, P and Kalashnikova, L and Nazarova, M and Dobrynina, L and Bartels, E and Guillon, B and Herik, E.G. van den and Fernandez-Cadenas, I and Jood, K and Nalls, M.A and Leeuw, H.F. de and Jern, C and Cheng, Y.C and Werner, I and Metso, A.J and Lichy, C and Lyrer, P.A and Brandt, T and Boncoraglio, G.B and Wichmann, H.E and Gieger, C and Johnson, A.D and Bottcher, T and Castellano, M and Arveiler, D and Ikram, M.A and Breteler, M.M and Padovani, A and Meschia, J.F and Kuhlenbaumer, G and Rolfs, A and Worrall, B.B and Ringelstein, E.B and Zelenika, D and Tatlisumak, T and Lathrop, M and Leys, D and Amouyel, P and Dallongeville, J and CADISP Grp and Int Stroke Genetics Consortium and International Stroke Genetics Consortium and CADISP Group and the CADISP group and Institutionen för neurovetenskap och fysiologi, sektionen för klinisk neurovetenskap och rehabilitering and Sahlgrenska akademin and Göteborgs universitet and Gothenburg University and Sahlgrenska Academy and Institute of Neuroscience and Physiology, Department of Clinical Neuroscience and Rehabilitation
Nature Genetics, ISSN 1061-4036, 2015, Volume 47, Issue 1, pp. 78 - 83
Cervical artery dissection (CeAD), a mural hematoma in a carotid or vertebral artery, is a major cause of ischemic stroke in young adults although relatively... 
YOUNG-ADULTS | VASCULAR RISK-FACTORS | IDENTIFIES 3 | MYOCARDIAL-INFARCTION | ABDOMINAL AORTIC-ANEURYSM | GENETICS & HEREDITY | INTRACRANIAL ANEURYSM | LOCI | ISCHEMIC-STROKE | HUMAN ENDOTHELIAL-CELLS | GENOME-WIDE ASSOCIATION | Myocardial Infarction - epidemiology | Follow-Up Studies | Humans | Middle Aged | Brain Ischemia - genetics | Microfilament Proteins - physiology | Male | Vertebral Artery Dissection - genetics | Adult | Female | Hypertension - epidemiology | Odds Ratio | Microfilament Proteins - genetics | Hypercholesterolemia - epidemiology | Migraine Disorders - epidemiology | Brain Ischemia - epidemiology | Genetic Predisposition to Disease | Genome-Wide Association Study | Risk Factors | Genetic Pleiotropy | Vertebral Artery Dissection - epidemiology | Carotid Artery, Internal, Dissection - epidemiology | Carotid Artery, Internal, Dissection - genetics | Obesity - epidemiology | Alleles | Polymorphism, Single Nucleotide | Finland - epidemiology | Genetic aspects | Research | Genetic susceptibility | Genomics | Risk factors | Hematoma | Studies | Stroke | Genealogy | Genomes | Genetic testing | Dissection | Chromosomes | Deoxyribonucleic acid--DNA | Meta-analysis | Index Medicus | Bioengineering | Brain Ischemia | Neurons and Cognition | Neurobiology | Computer Vision and Pattern Recognition | Medical Imaging | Life Sciences | Carotid Artery, Internal, Dissection | Image Processing | Imaging | Computer Science | Hypertension | Obesity | Vertebral Artery Dissection | Signal and Image processing | Myocardial Infarction | Hypercholesterolemia | Microfilament Proteins | Migraine Disorders | Finland | Engineering Sciences | Medicinska grundvetenskaper | Basic Medicine
Journal Article