نتائج البحث - "Kaixin Zhou"

101

Genome-wide association scan of attention deficit hyperactivity disorder

المساهمون: Clinical Neuropsychology, University of Zurich

المصدر: American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, 147B(8), 1337-1344. Wiley-Liss Inc.
Neale, B, Lasky-Su, J, Anney, R J, Franke, B, Zhou, K, Maller, J B, Vasquez, A A, Asherson, P, Chen, W, Banaschewski, T, Buitelaar, J, Ebstein, R, Gill, M, Miranda, A, Oades, R D, Roeyers, H, Rothenberger, A, Sergeant, J A, Steinhausen, H C, Sonuga-Barke, E J S, Mulas, F, Taylor, E, Laird, N, Lange, C, Daly, M J & Faraone, S V 2008, ' Genome-wide association scan of attention deficit hyperactivity disorder ', American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, vol. 147B, no. 8, pp. 1337-1344 . https://doi.org/10.1002/ajmg.b.30866Test
American Journal of Medical Genetics. Part B : Neuropsychiatric Genetics, 147B, 8, pp. 1337-44
American Journal of Medical Genetics. Part B : Neuropsychiatric Genetics, 147B, 1337-44

مصطلحات موضوعية: Candidate gene, Linkage disequilibrium, Genetics and epigenetic pathways of disease [NCMLS 6], Medizin, 2804 Cellular and Molecular Neuroscience, Genome-wide association study, Neuroinformatics [DCN 3], Linkage Disequilibrium, 2738 Psychiatry and Mental Health, 0302 clinical medicine, Perception and Action [DCN 1], Genetics(clinical), Child, Genetics (clinical), Genetics, 0303 health sciences, Homozygote, 10058 Department of Child and Adolescent Psychiatry, SNP genotyping, Psychiatry and Mental health, Child, Preschool, Data Interpretation, Statistical, Functional Neurogenomics [DCN 2], Algorithms, 2716 Genetics (clinical), Adolescent, Single-nucleotide polymorphism, 610 Medicine & health, Biology, Mental health [NCEBP 9], Polymorphism, Single Nucleotide, Genetic determinism, Article, Genomic disorders and inherited multi-system disorders [IGMD 3], 03 medical and health sciences, Cellular and Molecular Neuroscience, Cognitive neurosciences [UMCN 3.2], SDG 3 - Good Health and Well-being, medicine, SNP, Attention deficit hyperactivity disorder, Humans, ddc:610, Medizinische Fakultät » Universitätsklinikum Essen » LVR-Klinikum Essen » Klinik für Psychiatrie, Psychosomatik und Psychotherapie des Kindes- und Jugendalters, Alleles, 030304 developmental biology, Genome, Human, medicine.disease, Genetic defects of metabolism [UMCN 5.1], Attention Deficit Disorder with Hyperactivity, Case-Control Studies, 030217 neurology & neurosurgery, Genome-Wide Association Study

وصف الملف: application/pdf; Neale_genome-wide_V.pdf - application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a16f71fd41a06e37c3857770b62fbceeTest
https://research.vu.nl/en/publications/be23fc27-f9ed-4651-9e00-e3172b538bb4Test

102

Association of ADHD with genetic variants in the 5'-region of the dopamine transporter gene: evidence for allelic heterogeneity

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

المصدر: American Journal of Medical Genetics. Part B : Neuropsychiatric Genetics, 147B, 8, pp. 1519-23
Brookes, K J, Xu, X, Anney, R J, Franke, B, Zhou, K, Chen, X, Banaschewski, T, Buitelaar, J, Ebstein, J, Eisenberg, M, Gill, A, Miranda, A, Oades, R D, Roeyers, H, Rothenberger, A, Sergeant, J A, Steinhausen, H C, Faraone, S V, Asherson, P & Sonuga-Barke, E J S 2008, ' Association of ADHD with genetic variants in the 5prime-region of the dopamine transporter gene: Evidence for allelic heterogenity ', American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, vol. 147B, no. 8, pp. 1519-1523 . https://doi.org/10.1002/ajmg.b.30782Test
American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, 147B(8), 1519-1523. Wiley-Liss Inc.
American Journal of Medical Genetics. Part B : Neuropsychiatric Genetics, 147B, 1519-23

مصطلحات موضوعية: Linkage disequilibrium, Genetics and epigenetic pathways of disease [NCMLS 6], Medizin, 2804 Cellular and Molecular Neuroscience, Neuroinformatics [DCN 3], Linkage Disequilibrium, 2738 Psychiatry and Mental Health, 0302 clinical medicine, Gene Frequency, Risk Factors, Perception and Action [DCN 1], Genetics(clinical), Promoter Regions, Genetic, Genetics (clinical), Genetics, 0303 health sciences, 10058 Department of Child and Adolescent Psychiatry, Europe, Variable number tandem repeat, Psychiatry and Mental health, Allelic heterogeneity, Functional Neurogenomics [DCN 2], Genetic Markers, 2716 Genetics (clinical), Single-nucleotide polymorphism, 610 Medicine & health, Biology, Polymorphism, Single Nucleotide, Mental health [NCEBP 9], White People, Genomic disorders and inherited multi-system disorders [IGMD 3], Genetic Heterogeneity, 03 medical and health sciences, Cellular and Molecular Neuroscience, SDG 3 - Good Health and Well-being, Cognitive neurosciences [UMCN 3.2], Humans, ddc:610, Medizinische Fakultät » Universitätsklinikum Essen » LVR-Klinikum Essen » Klinik für Psychiatrie, Psychosomatik und Psychotherapie des Kindes- und Jugendalters, Allele, Allele frequency, Alleles, 030304 developmental biology, Dopamine Plasma Membrane Transport Proteins, Genetic heterogeneity, Haplotype, Genetic Variation, Haplotypes, Genetic defects of metabolism [UMCN 5.1], Attention Deficit Disorder with Hyperactivity, 5' Untranslated Regions, 030217 neurology & neurosurgery, Microsatellite Repeats

وصف الملف: Brookes_Association-of-ADHD_2008_V.pdf - application/pdf; application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::59814d3500f479a8842bcf3a63930faeTest
https://hdl.handle.net/2066/69953Test

103

Linkage to chromosome 1p36 for attention-deficit/hyperactivity disorder traits in school and home settings

المساهمون: Clinical Neuropsychology, Artificial intelligence, University of Zurich, Asherson, P

المصدر: Biological Psychiatry, 64, 7, pp. 571-6
Biological Psychiatry, 64(7), 571-576. Elsevier USA
Zhou, K, Asherson, P, Sham, P, Franke, B, Anney, R J, Buitelaar, J K, Ebstein, R, Gill, M, Brookes, K, Buschgens, C J M, Campbell, D, Chen, W, Christiansen, H, Fliers, E, Gabriëls, I, Johansson, L, Marco, R, Mulas, F, Müller, U, Mulligan, A, Neale, B, Rijsdijk, F, Rommelse, N N J, Uebel, H, Psychogiou, L, Xu, X, Banaschewski, T, Sonuga-Barke, E, Eisenberg, J, Manor, I, Miranda, A, Oades, R D, Roeyers, H, Rothenberger, A, Sergeant, J A, Steinhausen, H C, Taylor, E, Thompson, M & Faraone, S V 2008, ' Linkage to chromosome 1p36 for attention-deficit/ hyperactivity disorder traits in school and home settings ', Biological Psychiatry, vol. 64, no. 7, pp. 571-576 . https://doi.org/10.1016/j.biopsych.2008.02.024Test
Biological Psychiatry, 64, 571-6

مصطلحات موضوعية: Male, Adolescent, Genetics and epigenetic pathways of disease [NCMLS 6], Genetic Linkage, Medizin, 610 Medicine & health, Single-nucleotide polymorphism, Locus (genetics), Quantitative trait locus, Neuroinformatics [DCN 3], Social Environment, Mental health [NCEBP 9], Article, White People, Dyslexia, Genomic disorders and inherited multi-system disorders [IGMD 3], 03 medical and health sciences, 0302 clinical medicine, Cognitive neurosciences [UMCN 3.2], Genetic linkage, mental disorders, medicine, Perception and Action [DCN 1], Humans, Attention deficit hyperactivity disorder, ddc:610, Medizinische Fakultät » Universitätsklinikum Essen » LVR-Klinikum Essen » Klinik für Psychiatrie, Psychosomatik und Psychotherapie des Kindes- und Jugendalters, Child, Biological Psychiatry, Genetics, 0303 health sciences, Schools, 030305 genetics & heredity, 10058 Department of Child and Adolescent Psychiatry, Heritability, medicine.disease, 030227 psychiatry, Phenotype, Genetic defects of metabolism [UMCN 5.1], Attention Deficit Disorder with Hyperactivity, Chromosomes, Human, Pair 1, Child, Preschool, Trait, Female, Psychology, 2803 Biological Psychiatry, Functional Neurogenomics [DCN 2]

وصف الملف: application/pdf; Zhou_Linkage_1p36_V.pdf - application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8b1cf3653579c35357545a7c3eea7d44Test
https://doi.org/10.1016/j.biopsych.2008.02.024Test

104

Family-based association study between brain-derived neurotrophic factor gene polymorphisms and attention deficit hyperactivity disorder in UK and Taiwanese samples

المؤلفون: Jonathan Mill, Keeley J. Brookes, Philip Asherson, Chih-Ken Chen, Xiaohui Xu, Kaixin Zhou

المصدر: American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics. (1)