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المؤلفون: Julia Horjus, Tineke van Mourik-Banda, Marco A. P. Heerings, Marina Hakobjan, Ward De Witte, Dorothea J. Heersema, Anne J. Jansen, Eva M. M. Strijbis, Brigit A. de Jong, Astrid E. J. Slettenaar, Esther M. P. E. Zeinstra, Erwin L. J. Hoogervorst, Barbara Franke, Wiebe Kruijer, Peter J. Jongen, Leo J. Visser, Geert Poelmans
المساهمون: Neurology, Amsterdam Neuroscience - Neuroinfection & -inflammation, APH - Quality of Care
المصدر: International Journal of Molecular Sciences; Volume 23; Issue 19; Pages: 11461
International Journal of Molecular Sciences, 23, 19
International Journal of Molecular Sciences, 23(19):11461. MDPI AG
International Journal of Molecular Sciences, 23
Horjus, J, van Mourik-Banda, T, Heerings, M A P, Hakobjan, M, de Witte, W, Heersema, D J, Jansen, A J, Strijbis, E M M, de Jong, B A, Slettenaar, A E J, Zeinstra, E M P E, Hoogervorst, E L J, Franke, B, Kruijer, W, Jongen, P J, Visser, L J & Poelmans, G 2022, ' Whole Exome Sequencing in Multi-Incident Families Identifies Novel Candidate Genes for Multiple Sclerosis ', International Journal of Molecular Sciences, vol. 23, no. 19, 11461 . https://doi.org/10.3390/ijms231911461
International Journal of Molecular Sciences, 23(19):11461. Multidisciplinary Digital Publishing Institute (MDPI)مصطلحات موضوعية: Neurodevelopmental disorders Donders Center for Medical Neuroscience [Radboudumc 7], Multiple Sclerosis, Organic Chemistry, Intracellular Signaling Peptides and Proteins, General Medicine, Catalysis, Computer Science Applications, whole exome sequencing, Pedigree, Inorganic Chemistry, All institutes and research themes of the Radboud University Medical Center, multiple sclerosis (MS), Exome Sequencing, Humans, genetics, Family, Genetic Predisposition to Disease, Physical and Theoretical Chemistry, Molecular Biology, Spectroscopy, Genome-Wide Association Study
وصف الملف: application/pdf
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المؤلفون: Manuel Mattheisen, Jakob Grove, Thomas D. Als, Joanna Martin, Georgios Voloudakis, Sandra Meier, Ditte Demontis, Jaroslav Bendl, Raymond Walters, Caitlin E. Carey, Anders Rosengren, Nora I. Strom, Mads Engel Hauberg, Biao Zeng, Gabriel Hoffman, Wen Zhang, Jonas Bybjerg-Grauholm, Marie Bækvad-Hansen, Esben Agerbo, Bru Cormand, Merete Nordentoft, Thomas Werge, Ole Mors, David M. Hougaard, Joseph D. Buxbaum, Stephen V. Faraone, Barbara Franke, Søren Dalsgaard, Preben B. Mortensen, Elise B. Robinson, Panos Roussos, Benjamin M. Neale, Mark J. Daly, Anders D. Børglum
المصدر: Nat Genet
Nature Genetics, 54, 1470-1478
Mattheisen, M, Grove, J, Als, T D, Martin, J, Voloudakis, G, Meier, S, Demontis, D, Bendl, J, Walters, R, Carey, C E, Rosengren, A, Strom, N I, Hauberg, M E, Zeng, B, Hoffman, G, Zhang, W, Bybjerg-Grauholm, J, Bækvad-Hansen, M, Agerbo, E, Cormand, B, Nordentoft, M, Werge, T, Mors, O, Hougaard, D M, Buxbaum, J D, Faraone, S V, Franke, B, Dalsgaard, S, Mortensen, P B, Robinson, E B, Roussos, P, Neale, B M, Daly, M J & Børglum, A D 2022, ' Identification of shared and differentiating genetic architecture for autism spectrum disorder, attention-deficit hyperactivity disorder and case subgroups ', Nature Genetics, vol. 54, no. 10, pp. 1470-1478 . https://doi.org/10.1038/s41588-022-01171-3
Nature Genetics, 54, 10, pp. 1470-1478مصطلحات موضوعية: RISK, Neurodevelopmental disorders Donders Center for Medical Neuroscience [Radboudumc 7], Genètica humana, HERITABILITY, Autism Spectrum Disorder, LD SCORE REGRESSION, PSYCHIATRIC-DISORDERS, LOCI, Brain, CHILDREN, Autism spectrum disorders, Trastorns de l'espectre autista, Phenotype, Human genetics, Attention Deficit Disorder with Hyperactivity, Genetics, ADHD, Humans, Trastorns per dèficit d'atenció amb hiperactivitat en els adults, Attention deficit disorder with hyperactivity in adults, Genetic Predisposition to Disease, DEFICIT/HYPERACTIVITY DISORDER, GENOME-WIDE ASSOCIATION, METAANALYSIS
وصف الملف: application/pdf
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المؤلفون: Ting Li, Barbara Franke, Nina Roth Mota, Alejandro Arias-Vasquez
المصدر: American Journal of Medical Genetics. Part B : Neuropsychiatric Genetics, 186, 242-250
American Journal of Medical Genetics
American Journal of Medical Genetics Part B: Neuropsychiatric Genetics
American Journal of Medical Genetics. Part B : Neuropsychiatric Genetics, 186, 4, pp. 242-250مصطلحات موضوعية: Adult, Male, Mediation (statistics), Population sample, Population, Adult population, behavioral disciplines and activities, Life Change Events, 03 medical and health sciences, Cellular and Molecular Neuroscience, Cognition, 0302 clinical medicine, Environmental risk, mental disorders, Humans, Medicine, Genetic Predisposition to Disease, Longitudinal Studies, Adhd symptoms, mediation analysis, education, ADHD scores, Genetic Association Studies, Genetics (clinical), 030304 developmental biology, ADHD‐polygenic risk scores (ADHD‐PRSs), 0303 health sciences, education.field_of_study, Neurodevelopmental disorders Donders Center for Medical Neuroscience [Radboudumc 7], business.industry, Life events, Chromosome Mapping, Original Articles, Healthy Volunteers, childhood trauma (CT), Psychiatry and Mental health, Phenotype, Attention Deficit Disorder with Hyperactivity, stressful life events (SLEs), Female, Original Article, Polygenic risk score, business, Stress, Psychological, 030217 neurology & neurosurgery, Clinical psychology
وصف الملف: application/pdf
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المؤلفون: Ben Maassen, Simon E. Fisher, Sara Busquets Estruch, Amaia Carrion-Castillo, Clyde Francks, Barbara Franke
المصدر: Addi. Archivo Digital para la Docencia y la Investigación
instname
Human Genetics, 140, 1183-1200
Human Genetics, 140, 8, pp. 1183-1200
HUMAN GENETICS, 140(8), 1183-1200. SPRINGER
Human Geneticsمصطلحات موضوعية: Male, Genetic Linkage, Inheritance Patterns, Neurons/metabolism, Gene Expression, Genome-wide association study, Semaphorins, Dyslexia, 0302 clinical medicine, Cell Movement, Genetics (clinical), Original Investigation, Genes, Dominant, Neurons, Genetics, 0303 health sciences, Semaphorins/deficiency, Single Nucleotide, Pedigree, Phenotype, Pair 7, Female, Chromosomes, Human, Pair 7, Human, Neuroinformatics, Neuroimaging, Locus (genetics), Biology, Polymorphism, Single Nucleotide, Chromosomes, 03 medical and health sciences, Genetic linkage, medicine, Humans, Family, Dominant, Genetic Predisposition to Disease, Polymorphism, Gene, 030304 developmental biology, Whole genome sequencing, Phenocopy, Neurodevelopmental disorders Donders Center for Medical Neuroscience [Radboudumc 7], Base Sequence, Whole Genome Sequencing, Dyslexia/diagnostic imaging, medicine.disease, Introns, Human genetics, Genes, Haplotypes, Genetic Loci, Lod Score, 030217 neurology & neurosurgery, Genome-Wide Association Study
وصف الملف: application/pdf; application/vnd.openxmlformats-officedocument.spreadsheetml.sheet
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المؤلفون: S.E.E.C. Bauduin, Alessandro Serretti, Geert Poelmans, Brenda W.J.H. Penninx, David A. Collier, Nina Roth Mota, Hilde de Kluiver, Celso Arango, Nic J.A. van der Wee, Barbara Franke, José Luis Ayuso-Mateos, Cornelius J. H. M. Klemann, Emma Laing, Ward De Witte, Janita Bralten, Chiara Fabbri, Martien J H Kas
المساهمون: Bralten J., Mota N.R., Klemann C.J.H.M., De Witte W., Laing E., Collier D.A., de Kluiver H., Bauduin S.E.E.C., Arango C., Ayuso-Mateos J.L., Fabbri C., Kas M.J., van der Wee N., Penninx B.W.J.H., Serretti A., Franke B., Poelmans G., Kas lab, Psychiatry, APH - Mental Health, Amsterdam Neuroscience - Mood, Anxiety, Psychosis, Stress & Sleep, Amsterdam Neuroscience - Complex Trait Genetics, APH - Digital Health
المصدر: Neuropsychopharmacology, 46, 1627-1634
Bralten, J, Mota, N R, Klemann, C J H M, de Witte, W, Laing, E, Collier, D A, de Kluiver, H, Bauduin, S E E C, Arango, C, Ayuso-Mateos, J L, Fabbri, C, Kas, M J, van der Wee, N, Penninx, B W J H, Serretti, A, Franke, B & Poelmans, G 2021, ' Genetic underpinnings of sociability in the general population ', Neuropsychopharmacology, vol. 46, no. 9, pp. 1627-1634 . https://doi.org/10.1038/s41386-021-01044-z
Neuropsychopharmacology, 46(9), 1627-1634. SPRINGERNATURE
Neuropsychopharmacology, 46. Nature Publishing Group
Neuropsychopharmacology, 46, 9, pp. 1627-1634
Neuropsychopharmacology, 46(9), 1627-1634. Nature Publishing Group
Neuropsychopharmacologyمصطلحات موضوعية: Adult, Bipolar Disorder, Population, Genome-wide association study, Disease, Polymorphism, Single Nucleotide, Article, 03 medical and health sciences, 0302 clinical medicine, medicine, Humans, SNP, Genetic Predisposition to Disease, Bipolar disorder, education, 030304 developmental biology, Pharmacology, 0303 health sciences, education.field_of_study, Depressive Disorder, Major, Neurodevelopmental disorders Donders Center for Medical Neuroscience [Radboudumc 7], Depression, Autism spectrum disorders, medicine.disease, Psychiatry and Mental health, Schizophrenia, Behavioural genetics, Major depressive disorder, Autism, Psychology, 030217 neurology & neurosurgery, Clinical psychology, Genome-Wide Association Study, Human
وصف الملف: application/pdf; STAMPA
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المؤلفون: Melanie A. Manning, Xiaobing Zou, Maurizio Elia, Geert Vandeweyer, Nanda Rommelse, Christopher Barnett, Karen Pierce, Arie van Haeringen, Marketa Havlovicova, Ann Nordgren, Bing Du, Eric Courchesne, Madelyn A. Gillentine, Sedlácek Z, Davide Vecchio, Lin Han, Britt-Marie Anderlid, Madeleine R. Geisheker, Jianjun Ou, Kun Xia, Paul J. Lockhart, Gijs W. E. Santen, Rachael Catford, Jill A. Rosenfeld, Bernardo Dalla Bernardina, Gerarda Cappuccio, Anna Lindstrand, Raphael Bernier, Marie Shaw, Amy B. Wilfert, R. Frank Kooy, Tianyun Wang, Donatella Greco, Corrado Romano, Hilde Peeters, Barbara Franke, Magnus Nordenskjöld, Huidan Wu, Elizabeth E. Palmer, Yoeri Sleyp, Mariëtte J.V. Hoffer, Kathryn Friend, Anke Van Dijck, Giovanni Malerba, Hui Guo, Rachel K. Earl, Arvis Sulovari, Evan E. Eichler, Bradley P. Coe, Jacob J. Michaelson, Martin B. Delatycki, Elizabeth Thompson, Brooke G. McKenna, Miroslava Hancarova, Pierandrea Muglia, Sarka Bendova, Malin Kvarnung, Renee Carroll, Elisabetta Trabetti, Giuseppe Calabrese, Jennifer Gerdts, Kendra Hoekzema, Emanuela Avola, David G. Amaral, Ingrid E. Scheffer, Jozef Gecz, Pengfei Liu, Luis A. Pérez-Jurado, Nicola Brunetti-Pierri, Honghui Li, Nathalie Van der Aa
المصدر: Nature communications, vol 11, iss 1
Nature Communications, Vol 11, Iss 1, Pp 1-1 (2020)
Nature Communicationsمصطلحات موضوعية: Male, CCCTC-Binding Factor, Scale (ratio), Science, DNA Mutational Analysis, MEDLINE, General Physics and Astronomy, Computational biology, Heterogeneous-Nuclear Ribonucleoprotein U, Biology, General Biochemistry, Genetics and Molecular Biology, KCNQ3 Potassium Channel, Cohort Studies, Basic Helix-Loop-Helix Transcription Factors, Humans, SPARK Consortium, Genetic Predisposition to Disease, Author Correction, lcsh:Science, Genetic Association Studies, Multidisciplinary, Neurodevelopmental disorders, High-Throughput Nucleotide Sequencing, RNA-Binding Proteins, General Chemistry, Autism spectrum disorders, DNA-Binding Proteins, Repressor Proteins, Case-Control Studies, Mutation, Next-generation sequencing, Female, lcsh:Q, Transcription Factors
وصف الملف: application/pdf
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::20f56b0a3b8f4b8f1d7101badc16ecf8
https://escholarship.org/uc/item/5450h9c4 -
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المؤلفون: Marieke Klein, Monique van der Voet, Charlotte W. Ockeloen, Annette Schenck, Marlies Schimmel-Naber, Nicole de Leeuw, Barbara Franke, Benjamin Harich
المصدر: Journal of Child Psychology and Psychiatry, and Allied Disciplines
Journal of Child Psychology and Psychiatry and Allied Disciplines, 61, 5, pp. 545-555
Journal of Child Psychology and Psychiatry
Journal of Child Psychology and Psychiatry and Allied Disciplines, 61, 545-555مصطلحات موضوعية: Male, Disease, Comorbidity, TDRP, 0302 clinical medicine, Developmental and Educational Psychology, biology, 05 social sciences, Nuclear Proteins, Phenotype, 3. Good health, Pedigree, Psychiatry and Mental health, Drosophila melanogaster, Child, Preschool, Female, Original Article, Psychology, Rare cancers Radboud Institute for Health Sciences [Radboudumc 9], 050104 developmental & child psychology, medicine.medical_specialty, Single-nucleotide polymorphism, Locus (genetics), Nerve Tissue Proteins, Polymorphism, Single Nucleotide, Healthcare improvement science Radboud Institute for Health Sciences [Radboudumc 18], Evolution, Molecular, 03 medical and health sciences, psychiatric comorbidities, mental disorders, medicine, SNP, Animals, Humans, ADHD, 0501 psychology and cognitive sciences, Genetic Predisposition to Disease, Psychiatry, Gene, Genetic association, Family Health, Neurodevelopmental disorders Donders Center for Medical Neuroscience [Radboudumc 7], F-Box Proteins, Original Articles, FBXO25, biology.organism_classification, Disease Models, Animal, Attention Deficit Disorder with Hyperactivity, Pediatrics, Perinatology and Child Health, 030217 neurology & neurosurgery
وصف الملف: application/pdf
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المؤلفون: Henrik Larsson, Paul Lichtenstein, Laura Ghirardi, Christine M. Freitag, Barbara Franke, Philip Asherson, Isabell Brikell, Ralf Kuja-Halkola
المصدر: Molecular Psychiatry, 23, 257-262
Ghirardi, L, Brikell, I, Kuja-Halkola, R, Freitag, C M, Franke, B, Asherson, P, Lichtenstein, P & Larsson, H 2017, ' The familial co-aggregation of ASD and ADHD : a register-based cohort study ', Molecular Psychiatry . https://doi.org/10.1038/mp.2017.17
Molecular Psychiatry
Molecular Psychiatry, 23, 2, pp. 257-262مصطلحات موضوعية: Male, genetic structures, Autism Spectrum Disorder, Cohort Studies, 0302 clinical medicine, Risk Factors, Intellectual disability, Odds Ratio, Twins, Dizygotic, Registries, Child, 05 social sciences, Middle Aged, Psychiatry and Mental health, Schizophrenia, Child, Preschool, Female, Original Article, Psychology, 050104 developmental & child psychology, Cohort study, Clinical psychology, Adult, medicine.medical_specialty, Adolescent, behavioral disciplines and activities, 03 medical and health sciences, Cellular and Molecular Neuroscience, All institutes and research themes of the Radboud University Medical Center, mental disorders, medicine, Dementia, Humans, 0501 psychology and cognitive sciences, Family, Genetic Predisposition to Disease, ddc:610, Autistic Disorder, Psychiatry, Molecular Biology, Genetic Association Studies, Sweden, Neurodevelopmental disorders Donders Center for Medical Neuroscience [Radboudumc 7], Siblings, Odds ratio, Twins, Monozygotic, medicine.disease, Twin study, Attention Deficit Disorder with Hyperactivity, Behavioral medicine, Autism, 030217 neurology & neurosurgery
وصف الملف: application/pdf; application/octet-stream
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المؤلفون: Saskia W. de Ruiter, Jeffrey C. Glennon, Jilly Naaijen, David J. Lythgoe, Jan K. Buitelaar, Steven Williams, Daniel Brandeis, Sarah Durston, Tobias Banaschewski, Marcel P. Zwiers, Barbara Franke
المساهمون: University of Zurich, Naaijen, Jilly
المصدر: BMC Psychiatry, Vol 16, Iss 1, Pp 1-10 (2016)
BMC psychiatry [E], 16, 16:361. BioMed Central
BMC Psychiatry, 16, 361-361
Naaijen, J, de Ruiter, S, Zwiers, M P, Glennon, J C, Durston, S, Lythgoe, D J, Williams, S C R, Banaschewski, T, Brandeis, D, Franke, B & Buitelaar, J K 2016, ' COMPULS : Design of a multicenter phenotypic, cognitive, genetic, and magnetic resonance imaging study in children with compulsive syndromes ', BMC Psychiatry, vol. 16, no. 1, 361, pp. 361 . https://doi.org/10.1186/s12888-016-1072-6, https://doi.org/10.1186/s12888-016-1072-6
BMC Psychiatry
BMC Psychiatry, 16, 1, pp. 361-361
BMC Psychiatry, 16 (1)مصطلحات موضوعية: Male, Obsessive-Compulsive Disorder, Autism Spectrum Disorder, Child Behavior, 2738 Psychiatry and Mental Health, Study Protocol, Cognition, 0302 clinical medicine, Surveys and Questionnaires, lcsh:Psychiatry, Longitudinal Studies, Prospective Studies, 10064 Neuroscience Center Zurich, Child, Prospective cohort study, media_common, Fronto-striatal circuit, Brain, Syndrome, 10058 Department of Child and Adolescent Psychiatry, Compulsivity, Magnetic Resonance Imaging, Europe, Multicenter Study, Psychiatry and Mental health, Phenotype, Autism spectrum disorder, 10076 Center for Integrative Human Physiology, Compulsive behavior, Compulsive Behavior, Trait, Glutamate, ADHD, ASD, OCD, Female, medicine.symptom, Psychology, Clinical psychology, medicine.medical_specialty, lcsh:RC435-571, media_common.quotation_subject, 610 Medicine & health, Neuroimaging, Impulsivity, behavioral disciplines and activities, 150 000 MR Techniques in Brain Function, 03 medical and health sciences, mental disorders, medicine, Journal Article, Humans, Genetic Predisposition to Disease, Psychiatry, Neurodevelopmental disorders Donders Center for Medical Neuroscience [Radboudumc 7], Addiction, medicine.disease, 030227 psychiatry, Attention Deficit Disorder with Hyperactivity, 030217 neurology & neurosurgery
وصف الملف: image/pdf; application/pdf; Naaijen_et_al_2016_COMPULS_design_of_a_multicenter_phenotypic,_cognitive.pdf - application/pdf; application/application/pdf
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المؤلفون: René Pool, Sabine Spijker, T. E. Galesloot, Josep Antoni Ramos-Quiroga, Barbara Franke, Jan K. Buitelaar, Marieke Klein, Catharina A. Hartman, Janita Bralten, Christel M. Middeldorp, Michel G. Nivard, Conor V. Dolan, Dina Vojinovic, Lambertus A. Kiemeney, Ilja M. Nolte, Najaf Amin, Alexander J. Groffen, V. M. Kattenberg, Alejandro Arias-Vasquez, A. den Braber, Cristina Sánchez-Mora, Iryna O. Fedko, J.J.S. Kooij, J-J Hottenga, Sita H. Vermeulen, August B. Smit, Klaasjan G. Ouwens, Dorret I. Boomsma, Martine Hoogman, C.M. van Duijn, Pieter J. Hoekstra, Harmen H.M. Draisma, Marta Ribasés, Brenda W.J.H. Penninx, P. J. van der Most
المساهمون: Human genetics, APH - Mental Health, Psychiatry, Neurology, Amsterdam Neuroscience - Compulsivity, Impulsivity & Attention, APH - Health Behaviors & Chronic Diseases, APH - Digital Health, Epidemiology, Life Course Epidemiology (LCE), Interdisciplinary Centre Psychopathology and Emotion regulation (ICPE), Clinical Cognitive Neuropsychiatry Research Program (CCNP), Functional Genomics, Molecular and Cellular Neurobiology, Amsterdam Neuroscience - Cellular & Molecular Mechanisms, Amsterdam Neuroscience - Mood, Anxiety, Psychosis, Stress & Sleep, Biological Psychology, APH - Personalized Medicine, APH - Methodology, EMGO+ - Lifestyle, Overweight and Diabetes, Center for Neurogenomics and Cognitive Research, Amsterdam Neuroscience - Neurodegeneration
المصدر: Arias-Vásquez, A, Groffen, A J, Spijker, S, Ouwens, K G, Klein, M, Vojinovic, D, Galesloot, T E, Bralten, J, Hottenga, J J, van der Most, P J, Kattenberg, V M, Pool, R, Nolte, I M, Penninx, B W J H, Fedko, I O, Dolan, C V, Nivard, M G, den Braber, A, van Duijn, C M, Hoekstra, P J, Buitelaar, J K, Kiemeney, L A, Hoogman, M, Middeldorp, C M, Draisma, H H M, Vermeulen, S H, Sánchez-Mora, C, Ramos-Quiroga, J A, Ribasés, M, Hartman, C A, Kooij, J J S, Amin, N, Smit, A B, Franke, B, Boomsma, D I & The EAGLE-ADHD Consortium 2019, ' A Potential Role for the STXBP5-AS1 Gene in Adult ADHD Symptoms ', Behavior Genetics, vol. 49, no. 3, pp. 270-285 . https://doi.org/10.1007/s10519-018-09947-2
The EAGLE-ADHD Consortium 2019, ' A Potential Role for the STXBP5-AS1 Gene in Adult ADHD Symptoms ', Behavior Genetics, vol. 49, no. 3, pp. 270-285 . https://doi.org/10.1007/s10519-018-09947-2
Behavior Genetics, 49(3), 270-285. Springer US
Behavior Genetics
Behavior Genetics, 49(3), 270-285. Springer New York
Behavior Genetics, 49(3), 270-285. SPRINGER
Behavior Genetics, 49, 3, pp. 270-285
Behavior Genetics, 49(3), 270-285. Springer
Behavior Genetics, 49, 270-285مصطلحات موضوعية: Male, 0301 basic medicine, Oncology, Netherlands Twin Register (NTR), Genome-wide association study, TOMOSYN, Cohort Studies, R-SNARE Proteins, Mice, 0302 clinical medicine, Risk Factors, Epidemiology, GWAS, Prefrontal cortex, Genetics (clinical), education.field_of_study, ATTENTION-DEFICIT/HYPERACTIVITY DISORDER, ASSOCIATION, Phenotype, Urological cancers Radboud Institute for Health Sciences [Radboudumc 15], Female, RNA, Long Noncoding, medicine.symptom, SNARE COMPLEX, Adult, medicine.medical_specialty, Genotype, Population, Nerve Tissue Proteins, Single-nucleotide polymorphism, Impulsivity, BIOBANK, Polymorphism, Single Nucleotide, ADHD symptoms, DNA, Antisense, ENVIRONMENTAL-INFLUENCES, 03 medical and health sciences, All institutes and research themes of the Radboud University Medical Center, SDG 3 - Good Health and Well-being, Internal medicine, Genetics, medicine, Animals, Humans, SNP, Adults, Genetic Predisposition to Disease, AUTISM, education, Ecology, Evolution, Behavior and Systematics, DEFICIT-HYPERACTIVITY-DISORDER, Neurodevelopmental disorders Donders Center for Medical Neuroscience [Radboudumc 7], business.industry, Heritability, STXBP5-AS1 gene, Genetics, Population, HEK293 Cells, 030104 developmental biology, Attention Deficit Disorder with Hyperactivity, RNA, SCALES, business, 030217 neurology & neurosurgery, Genome-Wide Association Study
وصف الملف: application/pdf
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