المؤلفون: Colin N. A. Palmer, Lindsay Burch, Alex S. F. Doney, Kaixin Zhou, Michael K. Hansen, Louise A. Donnelly, C. A. Goddard, Andrew D. Morris, Jeffrey Brady

المصدر: The Journal of Clinical Endocrinology & Metabolism. 94:2587-2593

مصطلحات موضوعية: Adult, medicine.medical_specialty, Candidate gene, Endocrinology, Diabetes and Metabolism, Clinical Biochemistry, Osteoclasts, Single-nucleotide polymorphism, Context (language use), Type 2 diabetes, Biology, Polymorphism, Single Nucleotide, Biochemistry, Linkage Disequilibrium, Cohort Studies, Exon, Endocrinology, Meta-Analysis as Topic, Polymorphism (computer science), Internal medicine, medicine, Humans, PPAR delta, Child, Growth Disorders, Genetics, Biochemistry (medical), Haplotype, Exons, medicine.disease, Body Height, Case-Control Studies, Child, Preschool, Peroxisome proliferator-activated receptor delta, Genome-Wide Association Study

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8b1c61cd6a45141b1782ad708aae8457Test
https://doi.org/10.1210/jc.2009-0392Test

المؤلفون: Nanda Rommelse, Aribert Rothenberger, Jessica Lasky-Su, Aisling Mulligan, Edmund J.S. Sonuga-Barke, Isabel Gabriëls, Richard P. Ebstein, Lamprini Psychogiou, Philip Asherson, Henrik Uebel, Hans-Christoph Steinhausen, Barbara Franke, Margaret Thompson, Fernando Mulas, Rafaela Marco, Iris Manor, Herbert Roeyers, Eric Taylor, Wai Chen, Stephen V. Faraone, Tobias Banaschewski, Michael Gill, Robert D. Oades, Jan K. Buitelaar, Kaixin Zhou, Hanna Christiansen, Ueli C Müller, Jacques Eisenberg, Joseph A. Sergeant, Cathelijne J. M. Buschgens, Ana Miranda

المساهمون: University of Zurich, Oades, R D, Clinical Neuropsychology

المصدر: Journal of Neural Transmission, 115, 2, pp. 163-75
Christiansen, H, Chen, W, Oades, R D, Asherson, P, Taylor, E, Lasky-Su, J, Zhou, K, Banaschewski, T, Buschgens, C J M, Franke, B, Gabriëls, I, Manor, I, Marco, R, Müller, U, Mulligan, A, Psychogiou, L, Rommelse, N N J, Uebel, H, Rothenberger, A, Sergeant, J A, Sonuga-Barke, E J S, Steinhausen, H C, Thompson, M & Faraone, S V 2008, ' Cotransmission of conduct problems with attention-deficit/hyperactivity disorder: familial evidence for a distinct disorder ', Journal of Neural Transmission, vol. 115, no. 2, pp. 163-175 . https://doi.org/10.1007/s00702-007-0837-yTest
Journal of Neural Transmission, 115, 163-75
Journal of Neural Transmission, 115(2), 163-175. Springer Verlag

مصطلحات موضوعية: Male, Neurology, Psychometrics, Genetics and epigenetic pathways of disease [NCMLS 6], Medizin, Comorbidity, Neuroinformatics [DCN 3], Severity of Illness Index, 2738 Psychiatry and Mental Health, 0302 clinical medicine, Perception and Action [DCN 1], Child, Age Factors, 10058 Department of Child and Adolescent Psychiatry, Psychiatry and Mental health, 2728 Neurology (clinical), Conduct disorder, Female, Psychology, 2803 Biological Psychiatry, Functional Neurogenomics [DCN 2], Clinical psychology, Conduct Disorder, medicine.medical_specialty, Adolescent, 610 Medicine & health, Mental health [NCEBP 9], behavioral disciplines and activities, Genomic disorders and inherited multi-system disorders [IGMD 3], 03 medical and health sciences, Cognitive neurosciences [UMCN 3.2], Severity of illness, 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, Psychiatry, Biological Psychiatry, Family Health, Reproducibility of Results, medicine.disease, 030227 psychiatry, Hyperkinetic disorder, Genetic defects of metabolism [UMCN 5.1], Attention Deficit Disorder with Hyperactivity, Relative risk, 2808 Neurology, Multivariate Analysis, Neurology (clinical), 030217 neurology & neurosurgery

وصف الملف: application/pdf; Christiansen_co-transmission_2008_V.pdf - application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d1fc00bdfe97fa58080fba30d541b3caTest
http://www.springerlink.com/content/g48j7657k040753k/fulltext.pdfTest

المؤلفون: Ellen A. Fliers, Margaret Thompson, Hanna Christiansen, Richard P. Ebstein, She'era Medad, Philip Asherson, Aribert Rothenberger, Keeley J. Brookes, Fernando Mulas, Stephen V. Faraone, Fruhling Rijsdijk, A. Goldfarb, Aisling Mulligan, K. Fleischman, R. Barrett, Jan K. Buitelaar, Barbara Franke, Frits Boer, Ruud B. Minderaa, Robert D. Oades, J. Eisenberg, Louise Butler, Kaixin Zhou, I. Lubetzki, Rafaela Marco, Nanda Rommelse, Eric Taylor, J. Sorohan, Leonard C. Feldman, Hans-Christoph Steinhausen, Edmund J.S. Sonuga-Barke, K. Rabin, Alexander Heise, Ana Miranda, Vaheshta Sethna, Cathelijne J. M. Buschgens, Michael Gill, Iris Manor, Raoul Arnold, Benjamin M. Neale, Wai Chen, Herbert Roeyers, Lena Johansson, D. Cambell, Tobias Banaschewski, Richard Anney, Marieke E. Altink, Joseph A. Sergeant, Ulrike Müller, Raoul Howe-Forbes, Henrik Uebel, Xiaohui Xu, Isabel Gabriëls, Lamprini Psychogiou, Anne Weeks

المساهمون: Amsterdam Neuroscience, Child Psychiatry, Amsterdam Gastroenterology Endocrinology Metabolism, Endocrinology, Clinical Neuropsychology, Artificial intelligence, University of Zurich, Asherson, P

المصدر: Molecular Psychiatry, 13(5), 514-521. Nature Publishing Group
Molecular Psychiatry, 13, 5, pp. 514-21
Molecular psychiatry, 13(5), 514-521. Nature Publishing Group
Molecular Psychiatry, 13, 514-21
Asherson, P, Zhou, K, Anney, R J, Franke, B, Buitelaar, J, Ebstein, R, Gill, M, Altink, M, Arnold, R, Boer, F C, Brookes, K, Buschgens, C, Butler, L, Cambell, D, Chen, W, Christiansen, H, Feldman, L, Fleischman, K, Fliers, E, Howe-Forbes, R, Goldfarb, A, Heise, A, Gabriels, I, Johansson, L, Lubetzki, I, Marco, R, Medad, S, Minderaa, R, Mulas, F, Müller, U, Mulligan, A, Neale, B, Rijsdijk, F, Rabin, K, Rommelse, N N J, Sethna, V, Sorohan, J, Uebel, H, Psychogiou, L, Weeks, A, Barrett, R, Xu, X, Banaschewski, T, Sonuga-Barke, E J S, 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, ' A high-density SNP linkage scan with 142 combined subtype ADHD sib pairs identifies linkage regions on chromosomes 9 and 16 ', Molecular Psychiatry, vol. 13, no. 5, pp. 514-521 . https://doi.org/10.1038/sj.mp.4002140Test

مصطلحات موضوعية: Male, Genetics and epigenetic pathways of disease [NCMLS 6], GENOMEWIDE SCAN, Medizin, 2804 Cellular and Molecular Neuroscience, CHILDREN, Comorbidity, Neuroinformatics [DCN 3], Severity of Illness Index, Developmental psychology, 2738 Psychiatry and Mental Health, 0302 clinical medicine, Perception and Action [DCN 1], HETEROGENEITY, Israel, Child, Genetics, Observer Variation, 0303 health sciences, ATTENTION-DEFICIT/HYPERACTIVITY DISORDER, PSYCHIATRIC-DISORDERS, DOPAMINE TRANSPORTER GENE, ASSOCIATION, 10058 Department of Child and Adolescent Psychiatry, Europe, Psychiatry and Mental health, Female, Psychology, Chromosomes, Human, Pair 9, linkage, Functional Neurogenomics [DCN 2], Genotype, DEFICIT HYPERACTIVITY DISORDER, 610 Medicine & health, Polymorphism, Single Nucleotide, Mental health [NCEBP 9], Genetic determinism, White People, Genomic disorders and inherited multi-system disorders [IGMD 3], 03 medical and health sciences, Cellular and Molecular Neuroscience, Cognitive neurosciences [UMCN 3.2], Genetic linkage, 1312 Molecular Biology, medicine, SNP, Attention deficit hyperactivity disorder, Humans, ADHD, Sibling, Molecular Biology, 030304 developmental biology, Linkage (software), Siblings, Chromosome, medicine.disease, Sib pairs, United States, affected sib pairs, Genetic defects of metabolism [UMCN 5.1], Attention Deficit Disorder with Hyperactivity, CONDUCT DISORDER, Lod Score, DISEQUILIBRIUM, 030217 neurology & neurosurgery, Chromosomes, Human, Pair 16

وصف الملف: application/pdf; Asherson_high-density_V.pdf - application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b1574a04069cbaa82059cea00e8cc1f5Test
https://research.rug.nl/en/publications/4aef69cd-5123-4377-b028-a3e1923e1373Test

المؤلفون: Richard P. Ebstein, Philip Asherson, Keeley Joane Brookes, Wai Chen, Xiaohui Xu, Jessica Lasky-Su, Margaret Thompson, Barbara Franke, Stephen V. Faraone, Hans-Christoph Steinhausen, Joseph A. Sergeant, Tobias Banaschewski, Fruhling Rijsdijk, Jan K. Buitelaar, Ana Miranda, Robert D. Oades, Kaixin Zhou, Michael Gill, Jacques Eisenberg, Edmund J.S. Sonuga-Barke, Fernando Mulas, Benjamin M. Neale, Iris Manor, Eric Taylor, Herbert Roeyers, Aribert Rothenberger

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=25807Test

المؤلفون: Herbert Roeyers, Colm O'Dushlaine, Edmund J.S. Sonuga-Barke, Richard P. Ebstein, Ana Miranda, Aribert Rothenberger, Philip Asherson, Jessica Lasky-Su, Tobias Banaschewski, Stephen V. Faraone, Wai Chen, Fernando Mulas, Aisling Mulligan, Joseph A. Sergeant, Jan K. Buitelaar, Barbara Franke, Elaine Kenny, Benjamin M. Neale, Robert D. Oades, Kaixin Zhou, H. C. Steinhausen, Richard Anney, Michael Gill, Hanna Christiansen, Alejandro Arias-Vásquez

المساهمون: University of Zurich

المصدر: American Journal of Medical Genetics. Part B : Neuropsychiatric Genetics, 147B, 8, pp. 1369-78
American Journal of Medical Genetics. Part B : Neuropsychiatric Genetics, 147B, 1369-78

مصطلحات موضوعية: Genetics and epigenetic pathways of disease [NCMLS 6], 2804 Cellular and Molecular Neuroscience, Medizin, Poison control, Comorbidity, Neuroinformatics [DCN 3], Linkage Disequilibrium, Cohort Studies, 2738 Psychiatry and Mental Health, 0302 clinical medicine, Perception and Action [DCN 1], Genetics(clinical), Child, Genetics (clinical), Oligonucleotide Array Sequence Analysis, 0303 health sciences, Antisocial Personality Disorder, 10058 Department of Child and Adolescent Psychiatry, 3. Good health, Pedigree, Europe, Psychiatry and Mental health, Conduct disorder, Attention Deficit and Disruptive Behavior Disorders, ADHD -- conduct disorder -- genome wide association study -- genetic association information network, medicine.symptom, Psychology, Functional Neurogenomics [DCN 2], Anxiety disorder, Algorithms, Clinical psychology, Conduct Disorder, Genetic Markers, 2716 Genetics (clinical), Quantitative Trait Loci, Context (language use), 610 Medicine & health, Child Behavior Disorders, Impulsivity, Polymorphism, Single Nucleotide, Mental health [NCEBP 9], behavioral disciplines and activities, Genomic disorders and inherited multi-system disorders [IGMD 3], 03 medical and health sciences, Cellular and Molecular Neuroscience, Cognitive neurosciences [UMCN 3.2], mental disorders, medicine, Pervasive developmental disorder, Humans, ddc:610, Medizinische Fakultät » Universitätsklinikum Essen » LVR-Klinikum Essen » Klinik für Psychiatrie, Psychosomatik und Psychotherapie des Kindes- und Jugendalters, 030304 developmental biology, Psychiatric Status Rating Scales, Genome, Human, Antisocial personality disorder, medicine.disease, Genetic defects of metabolism [UMCN 5.1], Attention Deficit Disorder with Hyperactivity, 030217 neurology & neurosurgery, Genome-Wide Association Study

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

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d06ff2a000ecf0eff6674dff6714f6a6Test
https://doi.org/10.1002/ajmg.b.30871Test

المؤلفون: Joseph A. Sergeant, Aisling Mulligan, Pak C. Sham, Eric Taylor, Iris Manor, Herbert Roeyers, Shaun Purcell, Ana Miranda, Benjamin M. Neale, Hans-Christoph Steinhausen, Jacques Eisenberg, Tobias Banaschewski, Fernando Mulas, Stephen V. Faraone, Richard P. Ebstein, Jan K. Buitelaar, Aribert Rothenberger, Philip Asherson, Barbara Franke, Robert D. Oades, Kaixin Zhou, Margaret Thompson, Michael Gill, Edmund J.S. Sonuga-Barke

المساهمون: Clinical Neuropsychology, University of Zurich, Neale, B M

المصدر: Genetic Epidemiology, 32, 98-107
Neale, B, Sham, P, Purcell, S, Banaschewski, T, Buitelaar, J, Franke, B, Sonuga-Barke, E J S, Ebstein, R, Eisenberg, J, Mulligan, A, Gill, M, Manor, I, Miranda, A, Mulas, F, Oades, R D, Roeyers, H, Rothenberger, A, Sergeant, J A, Steinhausen, H C, Taylor, E, Thompson, M, Chen, W, Zhou, K, Asherson, P & Faraone, S V 2008, ' Population differences in the International Multi-Centre ADHD Gene Project ', Genetic Epidemiology, vol. 32, no. 2, pp. 98-107 . https://doi.org/10.1002/gepi.20265Test
Genetic Epidemiology, 32(2), 98-107. Wiley-Liss Inc.
Genetic Epidemiology, 32, 2, pp. 98-107

مصطلحات موضوعية: Male, Linkage disequilibrium, Internationality, Genetics and epigenetic pathways of disease [NCMLS 6], Epidemiology, Medizin, Neuroinformatics [DCN 3], Linkage Disequilibrium, 0302 clinical medicine, Gene Frequency, Perception and Action [DCN 1], International HapMap Project, Israel, Child, Genetics (clinical), 0303 health sciences, education.field_of_study, Chromosome Mapping, SDG 10 - Reduced Inequalities, 10058 Department of Child and Adolescent Psychiatry, Geography, Child, Preschool, Female, Functional Neurogenomics [DCN 2], Genetic Markers, 2716 Genetics (clinical), Adolescent, Population, Sample (statistics), Single-nucleotide polymorphism, 610 Medicine & health, Mental health [NCEBP 9], Polymorphism, Single Nucleotide, White People, Genomic disorders and inherited multi-system disorders [IGMD 3], 03 medical and health sciences, Cognitive neurosciences [UMCN 3.2], SNP, Humans, ddc:610, Medizinische Fakultät » Universitätsklinikum Essen » LVR-Klinikum Essen » Klinik für Psychiatrie, Psychosomatik und Psychotherapie des Kindes- und Jugendalters, education, Gene, 030304 developmental biology, Genetic Variation, Genetics, Population, Genetic defects of metabolism [UMCN 5.1], Haplotypes, Sample size determination, Attention Deficit Disorder with Hyperactivity, 030217 neurology & neurosurgery, Demography, 2713 Epidemiology

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

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2a82f3b0caf728ab7142616d800ce2eeTest
http://hdl.handle.net/2066/71443Test

المؤلفون: Benjamin M. Neale, Barbara Franke, Jan K. Buitelaar, Stephen V. Faraone, Hans-Christoph Steinhausen, Herbert Roeyers, Alejandro Arias Vasquez, Edmund J.S. Sonuga-Barke, Richard P. Ebstein, Fernando Mulas, Joseph Sergeant, Ana Miranda, Nan M. Laird, Wai Chen, Aribert Rothenberger, Richard Anney, Jessica Lasky-Su, Julian Maller, Christoph Lange, Tobias Banaschewski, Mark J. Daly, Robert D. Oades, Kaixin Zhou, Michael Gill, Philip Asherson, Eric Taylor

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

المؤلفون: Richard P. Ebstein, Philip Asherson, Benjamin M. Neale, Henrik Uebel, Stephen V. Faraone, Xiaohui Xu, Wai Chen, Michael Gill, Eric Taylor, Fruhling Rijsdijk, Cathelijne J. M. Buschgens, Jan K. Buitelaar, Robert D. Oades, Kaixin Zhou, Aribert Rothenberger, Ellen A. Fliers, Barbara Franke, Rafaela Marco, Desmond Campbell, Aisling Mulligan, Tobias Banaschewski, Iris Manor, Herbert Roeyers, Ana Miranda, Nanda Rommelse, Lena Johansson, Margaret Thompson, Richard Anney, Joseph A. Sergeant, Ueli C Müller, Edmund J.S. Sonuga-Barke, Hanna Christiansen, Isabel Gabriëls, Lamprini Psychogiou, Keeley J. Brookes, Fernando Mulas, Hans-Christoph Steinhausen, Pak C. Sham, Jacques Eisenberg

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

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)

مصطلحات موضوعية: Proband, Oncology, Male, Parents, medicine.medical_specialty, Adolescent, Taiwan, Single-nucleotide polymorphism, Polymorphism, Single Nucleotide, Cellular and Molecular Neuroscience, Gene Frequency, Neurotrophic factors, Internal medicine, medicine, Attention deficit hyperactivity disorder, Humans, Allele, Child, Genetics (clinical), Alleles, Genetic association, Brain-derived neurotrophic factor, business.industry, Brain-Derived Neurotrophic Factor, Haplotype, medicine.disease, United Kingdom, Psychiatry and Mental health, Amino Acid Substitution, Haplotypes, Attention Deficit Disorder with Hyperactivity, Child, Preschool, Female, business

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d8f7ebe132d5204c1806e4d6bdc0426bTest
https://pubmed.ncbi.nlm.nih.gov/17044097Test

المؤلفون: Joseph A. Sergeant, Fernando Mulas, Michael Gill, Richard P. Ebstein, Eric Taylor, Philip Asherson, Keeley Joane Brookes, Ana Miranda, Aribert Rothenberger, Herbert Roeyers, Tobias Banaschewski, Hans-Christoph Steinhausen, Robert D. Oades, Kaixin Zhou, Jacques Eisenberg, Stephen V. Faraone, Jessica Lasky-Su, Barbara Franke, Jan K. Buitelaar, Margaret Thompson, Iris Manor, Edmund J.S. Sonuga-Barke

المصدر: Biological Psychiatry, 62, 9, pp. 985-90
Biological Psychiatry, 62, 985-90

مصطلحات موضوعية: Male, Linkage disequilibrium, Genetics and epigenetic pathways of disease [NCMLS 6], Databases, Factual, Medizin, Neuroinformatics [DCN 3], Severity of Illness Index, 0302 clinical medicine, Perception and Action [DCN 1], Determinants in Health and Disease [EBP 1], Child, Promoter Regions, Genetic, Genetics, 0303 health sciences, Europe, Phenotype, Child, Preschool, Female, medicine.symptom, Psychology, Functional Neurogenomics [DCN 2], medicine.medical_specialty, Adolescent, Single-nucleotide polymorphism, Quantitative trait locus, Impulsivity, Mental health [NCEBP 9], Polymorphism, Single Nucleotide, Genomic disorders and inherited multi-system disorders [IGMD 3], 03 medical and health sciences, Quantitative Trait, Heritable, Cognitive neurosciences [UMCN 3.2], Genetic model, mental disorders, medicine, Attention deficit hyperactivity disorder, SNP, Humans, Genetic Predisposition to Disease, ddc:610, Medizinische Fakultät » Universitätsklinikum Essen » LVR-Klinikum Essen » Klinik für Psychiatrie, Psychosomatik und Psychotherapie des Kindes- und Jugendalters, Psychiatry, Biological Psychiatry, 030304 developmental biology, Family Health, Receptors, Dopamine D4, Heritability, medicine.disease, Genetic defects of metabolism [UMCN 5.1], Attention Deficit Disorder with Hyperactivity, 030217 neurology & neurosurgery

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::60acaf5351ac5aab860e846034a33b68Test
https://pubmed.ncbi.nlm.nih.gov/17560555Test