المؤلفون: Barbara Franke, Catharina A. Hartman, Hilde M. Geurts, Jan K. Buitelaar, Nanda Rommelse

المساهمون: Donders Institute for Brain, Cognition and Behaviour, Radboud university [Nijmegen], Karakter Child and Adolescent Psychiatry University Centre [Nijmegen], Department of Human Genetics, Radboud University Medical Center [Nijmegen], Department of Psychonomics, University of Amsterdam [Amsterdam] (UvA), Dr Leo Kannerhuis, Amsterdam Clinic, Department of Psychiatry, University Medical Center Groningen, University of Groningen [Groningen], Brein en Cognitie (Psychologie, FMG)

المصدر: European Child and Adolescent Psychiatry
European Child and Adolescent Psychiatry, Springer Verlag (Germany), 2010, 19 (3), pp.281-295. ⟨10.1007/s00787-010-0092-x⟩
European Child & Adolescent Psychiatry, 19(3), 281-295. D. Steinkopff-Verlag
European Child & Adolescent Psychiatry
European Child & Adolescent Psychiatry, 19, 3, pp. 281-95
European Child & Adolescent Psychiatry, 19, 281-95

مصطلحات موضوعية: Candidate gene, Genome-wide association study, Comorbidity, Review, Personality Assessment, Social Environment, Attention-deficit/ hyperactivity disorder, Autism spectrum disorder, Molecular genetics, Shared heritability, 0302 clinical medicine, ddc:150, GENETIC INFLUENCES, Developmental and Educational Psychology, Perception and Action [DCN 1], Psychology, Child, Mental Health [NCEBP 9], Psychological Disorders, Mental Health Treatment and Prevention, PSYCHIATRIC-DISORDERS, 05 social sciences, General Medicine, 3. Good health, Psychiatry and Mental health, Phenotype, psychische Störungen, Behandlung und Prävention, Functional Neurogenomics [DCN 2], 050104 developmental & child psychology, Genetic Markers, medicine.medical_specialty, SUSCEPTIBILITY LOCI, Adolescent, DEFICIT HYPERACTIVITY DISORDER, Polymorphism, Single Nucleotide, Risk Assessment, behavioral disciplines and activities, Genomic disorders and inherited multi-system disorders [IGMD 3], MONOAMINE-OXIDASE-A, 03 medical and health sciences, mental disorders, medicine, Pervasive developmental disorder, Attention deficit hyperactivity disorder, Humans, 0501 psychology and cognitive sciences, Genetic Predisposition to Disease, Pediatrics, Perinatology, and Child Health, GENOME-WIDE ASSOCIATION, Autistic Disorder, Psychiatry, LINKAGE ANALYSIS, PERVASIVE DEVELOPMENTAL DISORDERS, SIB-PAIRS, medicine.disease, Twin study, Actigraphy, Developmental disorder, PREFERENTIAL TRANSMISSION, Attention-deficit/hyperactivity disorder, Psychologie, Attention Deficit Disorder with Hyperactivity, Pediatrics, Perinatology and Child Health, Autism, 030217 neurology & neurosurgery, Genome-Wide Association Study

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5143f4132b256d10f22a3d9dfa3dcf7bTest
https://hdl.handle.net/11245/1.345238Test

المؤلفون: Altink, M.E., Slaats-Willemse, D.I.E., Rommelse, N.N.J., Buschgens, C.J.M., Fliers, E.A., Arias Vasquez, A., Xu, X., Franke, B., Sergeant, J.A., Faraone, S.V., Buitelaar, J.K.

المصدر: European Child & Adolescent Psychiatry, 18, 8, pp. 465-75

مصطلحات موضوعية: 110 012 Social cognition of verbal communication, 150 000 MR Techniques in Brain Function, DCN 1: Perception and Action, DCN 2: Functional Neurogenomics, IGMD 3: Genomic disorders and inherited multi-system disorders, NCEBP 9: Mental health, NCMLS 6: Genetics and epigenetic pathways of disease, psy

العلاقة: http://hdl.handle.net/2066/80806Test

الإتاحة: http://hdl.handle.net/2066/80806Test