يعرض 1 - 4 نتائج من 4 نتيجة بحث عن '"genomic disorders"', وقت الاستعلام: 0.72s تنقيح النتائج
  1. 1

    المساهمون: Other departments, Interdisciplinary Centre Psychopathology and Emotion regulation (ICPE), Life Course Epidemiology (LCE), Clinical Neuropsychology

    المصدر: British journal of psychiatry, 203(2), 112-119. Royal College of Psychiatrists
    British Journal of Psychiatry, 203, pp. 112-119
    British Journal of Psychiatry, 203, 112-119
    The British Journal of Psychiatry, 203(2), 112-119. Cambridge University Press
    BRITISH JOURNAL OF PSYCHIATRY
    British Journal of Psychiatry, 203(2), 112-119. Royal College of Psychiatrists
    Groenman, A P, Oosterlaan, J, Rommelse, N, Franke, B, Greven, C U, Hoekstra, P J, Hartman, C A, Luman, M, Roeyers, H, Oades, R D, Sergeant, J A, Buitelaar, J K & Faraone, S V 2013, ' Stimulant treatment for attention-deficit hyperactivity disorder and risk of developing substance use disorder. ', British Journal of Psychiatry, vol. 203, no. 2, pp. 112-119 . https://doi.org/10.1192/bjp.bp.112.124784Test

    وصف الملف: application/pdf

    الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c8973dbd7eb42d0b25663f3fef7c5749Test
    https://duepublico.uni-due.de/servlets/DocumentServlet?id=33900

  2. 2

    المصدر: Journal of Child Psychology and Psychiatry and Allied Disciplines, 51, 915-23
    Sobanski, E, Banaschewski, T, Asherson, P, Buitelaar, J, Chen, W, Franke, B, Holtmann, M, Krumm, B, Sergeant, J, Sonuga-Barke, E, Stringaris, A, Taylor, E, Anney, R, Ebstein, R P, Gill, M, Miranda, A, Mulas, F, Oades, R D, Roeyers, H, Rothenberger, A, Steinhausen, H-C & Faraone, S V 2010, ' Emotional lability in children and adolescents with attention deficit/hyperactivity disorder (ADHD): clinical correlates and familial prevalence ', Journal of Child Psychology & Psychiatry, vol. 51, no. 8, pp. 915-23 . https://doi.org/10.1111/j.1469-7610.2010.02217.xTest
    Journal of Child Psychology and Psychiatry and Allied Disciplines, 51, 8, pp. 915-23

    وصف الملف: application/pdf

  3. 3

    المساهمون: University of Zurich, Clinical Neuropsychology, Artificial intelligence, Social AI

    المصدر: American Journal of Medical Genetics. Part B : Neuropsychiatric Genetics, 147B, 8, pp. 1481-7
    Zhou, K, Chen, W, Buitelaar, J K, Banaschewski, T, Oades, R D, Franke, B, Sonuga-Barke, E, Ebstein, R, Eisenberg, J, Gill, M, Manor, I, Miranda, A, Mulas, F, Roeyers, H, Rothenberger, A, Sergeant, J A, Steinhausen, H C, Lasky-Su, J, Taylor, E, Brookes, K J, Xu, X, Neale, B, Rijsdijk, F, Thompson, M, Asherson, P & Faraone, S V 2008, ' Genetic heterogeneity in ADHD: DAT1 gene only affects probands without CD ', American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, vol. 147B, no. 8, pp. 1481-1487 . https://doi.org/10.1002/ajmg.b.30644Test
    American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, 147B(8), 1481-1487. Wiley-Liss Inc.
    American Journal of Medical Genetics. Part B : Neuropsychiatric Genetics, 147B, 1481-7

    مصطلحات موضوعية: Proband, Male, Linkage disequilibrium, Genetics and epigenetic pathways of disease [NCMLS 6], 2804 Cellular and Molecular Neuroscience, Medizin, Comorbidity, Neuroinformatics [DCN 3], Linkage Disequilibrium, 2738 Psychiatry and Mental Health, 0302 clinical medicine, Gene Frequency, Perception and Action [DCN 1], Genetics(clinical), Child, Genetics (clinical), Genetics, Incidence, 10058 Department of Child and Adolescent Psychiatry, Europe, Psychiatry and Mental health, Conduct disorder, Female, Functional Neurogenomics [DCN 2], Conduct Disorder, Genetic Markers, 2716 Genetics (clinical), Genotype, Single-nucleotide polymorphism, 610 Medicine & health, Biology, Mental health [NCEBP 9], Polymorphism, Single Nucleotide, behavioral disciplines and activities, Genomic disorders and inherited multi-system disorders [IGMD 3], 03 medical and health sciences, Genetic Heterogeneity, Cellular and Molecular Neuroscience, Cognitive neurosciences [UMCN 3.2], SDG 3 - Good Health and Well-being, mental disorders, medicine, Attention deficit hyperactivity disorder, Humans, ddc:610, Medizinische Fakultät » Universitätsklinikum Essen » LVR-Klinikum Essen » Klinik für Psychiatrie, Psychosomatik und Psychotherapie des Kindes- und Jugendalters, Allele, Alleles, Dopamine Plasma Membrane Transport Proteins, Chi-Square Distribution, Genetic heterogeneity, medicine.disease, Twin study, 030227 psychiatry, Genetic defects of metabolism [UMCN 5.1], Haplotypes, Attention Deficit Disorder with Hyperactivity, 030217 neurology & neurosurgery

    وصف الملف: Zhou_AMJGP_2008_2V.pdf - application/pdf; application/pdf

    الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7349b633ff7345730ece9156425077c9Test
    https://duepublico.uni-due.de/servlets/DocumentServlet?id=25807

  4. 4

    المساهمون: University of Zurich, Asherson, P, Artificial intelligence, Clinical Neuropsychology, Network Institute, Artificial Intelligence (section level)

    المصدر: American Journal of Medical Genetics. Part B : Neuropsychiatric Genetics, 147B, 8, pp. 1564-7
    Xu, X, Hawi, Z, Brookes, K J, Anney, R, Bellgrove, M, Franke, B, Barry, E, Chen, W, Kuntsi, J, Banaschewski, T, Buitelaar, J, Ebstein, R, Fitzgerald, M, Miranda, A, Oades, R D, Roeyers, H, Rothenberger, A, Sergeant, J A, Sonuga-Barke, E, Steinhausen, H C, Faraone, S V, Gill, M & Asherson, P 2008, ' Replication of a rare protective allele in the noradrenaline transporter gene and ADHD ', American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, vol. 147B, no. 8, pp. 1564-1567 . https://doi.org/10.1002/ajmg.b.30872Test
    American Journal of Medical Genetics. Part B : Neuropsychiatric Genetics, 147B, 1564-7
    American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, 147B(8), 1564-1567. Wiley-Liss Inc.

    مصطلحات موضوعية: Parents, Candidate gene, Genetics and epigenetic pathways of disease [NCMLS 6], 2804 Cellular and Molecular Neuroscience, Medizin, Neuroinformatics [DCN 3], 2738 Psychiatry and Mental Health, 0302 clinical medicine, Gene Frequency, Odds Ratio, Perception and Action [DCN 1], Multicenter Studies as Topic, Genetics(clinical), Child, Genetics (clinical), Genetics, 10058 Department of Child and Adolescent Psychiatry, Psychiatry and Mental health, Child, Preschool, Functional Neurogenomics [DCN 2], Genetic Markers, Heterozygote, 2716 Genetics (clinical), Adolescent, Genotype, Mothers, Single-nucleotide polymorphism, 610 Medicine & health, Biology, Polymorphism, Single Nucleotide, Mental health [NCEBP 9], Article, Genomic disorders and inherited multi-system disorders [IGMD 3], 03 medical and health sciences, Cellular and Molecular Neuroscience, SDG 3 - Good Health and Well-being, Cognitive neurosciences [UMCN 3.2], mental disorders, medicine, Humans, Attention deficit hyperactivity disorder, SNP, ddc:61, Genetic Predisposition to Disease, ddc:610, Medizinische Fakultät » Universitätsklinikum Essen » LVR-Klinikum Essen » Klinik für Psychiatrie, Psychosomatik und Psychotherapie des Kindes- und Jugendalters, Allele, Allele frequency, Alleles, Genetic association, Chi-Square Distribution, Norepinephrine Plasma Membrane Transport Proteins, Siblings, Odds ratio, medicine.disease, Introns, 030227 psychiatry, Genetic defects of metabolism [UMCN 5.1], Attention Deficit Disorder with Hyperactivity, Case-Control Studies, 030217 neurology & neurosurgery

    وصف الملف: application/pdf; xu_AMJGP_2008V.pdf - application/pdf

    الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::eda872f753bceabd3b388ef2053b1e80Test
    https://duepublico.uni-due.de/servlets/DocumentServlet?id=25934