المؤلفون: Roger Tavendale, Colin N. A. Palmer, Ewan R. Pearson, Kaixin Zhou, Tanja Dujic

المصدر: Diabetes Care. 39:1896-1901

مصطلحات موضوعية: Adult, Male, 0301 basic medicine, medicine.medical_specialty, Serotonin uptake, Genotype, Gastrointestinal Diseases, Endocrinology, Diabetes and Metabolism, 030209 endocrinology & metabolism, Article, Intestinal absorption, 03 medical and health sciences, 0302 clinical medicine, Internal medicine, Diabetes mellitus, Internal Medicine, medicine, Humans, Hypoglycemic Agents, Alleles, Serotonin transporter, Aged, Serotonin Plasma Membrane Transport Proteins, Advanced and Specialized Nursing, Polymorphism, Genetic, biology, business.industry, Odds ratio, Middle Aged, medicine.disease, Metformin, 3. Good health, 030104 developmental biology, Endocrinology, Diabetes Mellitus, Type 2, biology.protein, Female, Serotonin, business, Octamer Transcription Factor-1, medicine.drug

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3a7bbd70935d75cc2165f29d3b5a1d79Test
https://doi.org/10.2337/dc16-0706Test

المؤلفون: Adem Y, Dawed, Kaixin, Zhou, Nienke, van Leeuwen, Anubha, Mahajan, Neil, Robertson, Robert, Koivula, Petra J M, Elders, Simone P, Rauh, Angus G, Jones, Reinhard W, Holl, Julia C, Stingl, Paul W, Franks, Mark I, McCarthy, Leen M, 't Hart, Ewan R, Pearson, B, Whitcher

المصدر: Diabetes care. 42(6)

مصطلحات موضوعية: Male, Gastrointestinal Diseases, Organic Cation Transporter 1, Middle Aged, Polymorphism, Single Nucleotide, Metformin, Drug Hypersensitivity, Diabetes Mellitus, Type 2, Risk Factors, Equilibrative Nucleoside Transport Proteins, Humans, Hypoglycemic Agents, Female, Alleles, Genetic Association Studies, Aged

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=pmid________::9bfcc332cb10cf2afc42716968aae24dTest
https://pubmed.ncbi.nlm.nih.gov/30885951Test

المؤلفون: Tanja, Dujic, Kaixin, Zhou, Louise A, Donnelly, Graham, Leese, Colin N A, Palmer, Ewan R, Pearson

المصدر: Diabetes, Obesity & Metabolism

مصطلحات موضوعية: Male, Heterozygote, Drug Resistance, Polymorphism, Single Nucleotide, Severity of Illness Index, Cohort Studies, Gene Frequency, Humans, Longitudinal Studies, Alleles, Genetic Association Studies, Cytochrome P-450 CYP2C9, NADPH-Ferrihemoprotein Reductase, pharmacogenetics, Glycated Hemoglobin, Brief Report, Hypoglycemia, Sulfonylurea Compounds, Amino Acid Substitution, Diabetes Mellitus, Type 2, Scotland, sulphonylureas, Case-Control Studies, Drug Therapy, Combination, Female, Brief Reports, type 2 diabetes, hypoglycaemia

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=pmid________::01f7410460868bc93ea543d6b2eaba9bTest
https://pubmed.ncbi.nlm.nih.gov/28656666Test

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: Stephen V. Faraone, Robert D. Oades, Kaixin Zhou, Aisling Mulligan, Jan K. Buitelaar, Michael Gill, Ziarih Hawi, Edmund J.S. Sonuga-Barke, Margaret Thompson, Tobias Banaschewski, Richard P. Ebstein, Richard Anney, Philip Asherson, Joseph A. Sergeant, Herbert Roeyers, Xaiohui Xu, Barbara Franke, Nanda Rommelse, E. Taylor, Keeley J. Brookes, Fernando Mulas, Iris Manor, Carlos Pinto, Ana Miranda, Sita H. Vermeulen, Hans-Christoph Steinhausen, Aribert Rothenberger, Karen Sheehan

المساهمون: University of Zurich

المصدر: American Journal of Medical Genetics. Part B : Neuropsychiatric Genetics, 147B, 1495-500
American Journal of Medical Genetics. Part B : Neuropsychiatric Genetics, 147B, 8, pp. 1495-500

مصطلحات موضوعية: Parents, Candidate gene, Genetics and epigenetic pathways of disease [NCMLS 6], 2804 Cellular and Molecular Neuroscience, Medizin, Neuroinformatics [DCN 3], Linkage Disequilibrium, 2738 Psychiatry and Mental Health, 0302 clinical medicine, Risk Factors, Perception and Action [DCN 1], Genetics(clinical), Genetics (clinical), 0303 health sciences, TPH2, 10058 Department of Child and Adolescent Psychiatry, Psychiatry and Mental health, Data Interpretation, Statistical, Functional Neurogenomics [DCN 2], Clinical psychology, Genetic Markers, 2716 Genetics (clinical), Single-nucleotide polymorphism, 610 Medicine & health, Mental health [NCEBP 9], Polymorphism, Single Nucleotide, Genetic determinism, Genomic disorders and inherited multi-system disorders [IGMD 3], Molecular epidemiology [NCEBP 1], 03 medical and health sciences, Cellular and Molecular Neuroscience, Cognitive neurosciences [UMCN 3.2], Translational research [ONCOL 3], medicine, Attention deficit hyperactivity disorder, Humans, Family, Genetic Predisposition to Disease, ddc:610, Medizinische Fakultät » Universitätsklinikum Essen » LVR-Klinikum Essen » Klinik für Psychiatrie, Psychosomatik und Psychotherapie des Kindes- und Jugendalters, Allele, Alleles, 030304 developmental biology, Chi-Square Distribution, Endocrinology and reproduction [UMCN 5.2], business.industry, medicine.disease, Genetic defects of metabolism [UMCN 5.1], Multicenter study, Attention Deficit Disorder with Hyperactivity, Etiology, business, 030217 neurology & neurosurgery

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

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e31eda18cf25addb851090c483d73151Test
https://pubmed.ncbi.nlm.nih.gov/18163388Test

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: Xiaohui Xu, Aribert Rothenberger, Barbara Franke, Herbert Roeyers, Ana Miranda, Richard Anney, Jacques Eisenberg, Wai Chen, Stephen V. Faraone, Tobias Banaschewski, Jan K. Buitelaar, Joseph Sergeant, Michael Gill, Keeley J. Brookes, Eric Taylor, Robert D. Oades, Kaixin Zhou, Hans-Christoph Steinhausen, Edmund J.S. Sonuga-Barke, Richard P. Ebstein, Philip Asherson

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

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: Dujic, Tanja^1,2, Kaixin Zhou², Tavendale, Roger², Palmer, Colin N. A.², Pearson, Ewan R.² e.z.pearson@dundee.ac.uk, Zhou, Kaixin³ (AUTHOR)

المصدر: Diabetes Care. Nov2016, Vol. 39 Issue 11, p1896-1901. 6p. 3 Charts, 1 Graph.

مصطلحات موضوعية: *SEROTONIN transporters, *GENETIC polymorphisms, *GASTROINTESTINAL diseases, *METFORMIN, *GENOTYPES, *ALLELES, *HYPOGLYCEMIC agents, *MEMBRANE proteins, *TYPE 2 diabetes, *PROTEINS, *RESEARCH funding