المؤلفون: Roberto Giorda, Vittoria Trezzi, Ginette Dionne, Bei Feng, Andrea Facoetti, Chiara Andreola, Valentina Riva, Sara Mascheretti, Cecilia Marino, Simone Gori, Marco Villa

المساهمون: IRCCS E. Medea, LAVAL UNIVERSITY QUEBEC CAN, Partenaires IRSTEA, Institut national de recherche en sciences et technologies pour l'environnement et l'agriculture (IRSTEA)-Institut national de recherche en sciences et technologies pour l'environnement et l'agriculture (IRSTEA), Laboratoire de psychologie du développement et de l'éducation de l'enfant (LaPsyDÉ - UMR 8240), Centre National de la Recherche Scientifique (CNRS)-Université de Paris (UP), University of Bergamo, Departments of Psychology and Psychiatry, University of Toronto, Toronto, Centre for Addiction and Mental Health [Toronto] (CAMH), University of Padua

المصدر: Brain Sciences, Vol 10, Iss 993, p 993 (2020)
Brain Sciences
Brain Sciences, MDPI, 2020, 10, ⟨10.3390/brainsci10120993⟩
Brain Sciences; Volume 10; Issue 12; Pages: 993

مصطلحات موضوعية: Settore M-PSI/01 - Psicologia Generale, Mediation (statistics), Candidate gene, media_common.quotation_subject, Article, lcsh:RC321-571, 03 medical and health sciences, 0302 clinical medicine, DCDC2, Reading (process), medicine, Candidate genes, Developmental dyslexia, Endophenotypes, Mediation, Multisensory temporal processing, mediation, Rapid automatized naming, lcsh:Neurosciences. Biological psychiatry. Neuropsychiatry, 030304 developmental biology, media_common, 0303 health sciences, biology, General Neuroscience, [SCCO.NEUR]Cognitive science/Neuroscience, Dyslexia, multisensory temporal processing, medicine.disease, developmental dyslexia, endophenotypes, Endophenotype, [SCCO.PSYC]Cognitive science/Psychology, biology.protein, GRIN2B, Psychology, candidate genes, Neuroscience, 030217 neurology & neurosurgery

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3d56b7944dd3dbc8557b64a291072a73Test
https://www.mdpi.com/2076-3425/10/12/993Test

المؤلفون: Cecilia Marino, Vickie Plourde, Frank Vitaro, Roberto Giorda, Ginette Dionne, Sara Mascheretti, Vittoria Trezzi, Mara Brendgen, Michel Boivin

المساهمون: Université de Montréal. Faculté des arts et des sciences. École de psychoéducation

المصدر: Journal of child psychology and psychiatry. 2017. Vol. 58, № 1. P. 75-82

مصطلحات موضوعية: 0301 basic medicine, Gene-by-gene interaction, Male, Adolescent, Developmental dyslexia, Gene-by-environment interaction, синдром дефицита внимания, Comorbidity, Impulsivity, Polymorphism, Single Nucleotide, Developmental psychology, дислексия, Dyslexia, 03 medical and health sciences, 0302 clinical medicine, DCDC2, Risk Factors, Developmental and Educational Psychology, medicine, Attention deficit hyperactivity disorder, ADHD, Humans, Gene–environment interaction, Child, Genetic association, Pleiotropy, плейотропия, Epistasis, Genetic, Genetic Pleiotropy, Transmission disequilibrium test, Heritability, medicine.disease, 3. Good health, Association study, Psychiatry and Mental health, гиперактивность, 030104 developmental biology, Italy, Attention Deficit Disorder with Hyperactivity, Pediatrics, Perinatology and Child Health, Female, Gene-Environment Interaction, medicine.symptom, Psychology, Microtubule-Associated Proteins, 030217 neurology & neurosurgery

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f3cf14855f9e9f3856265e472d6046e3Test
https://openrepository.ru/article?id=799490Test

المؤلفون: Cecilia Marino, Sara Mascheretti, Roberto Giorda, Haiying Meng, Natalie Cope, Marianna Rusconi, Jeffrey R. Gruen, Massimo Molteni

مصطلحات موضوعية: media_common.quotation_subject, Biology, Quantitative trait locus, Neuropsychological Tests, Polymorphism, Single Nucleotide, Article, Dyslexia, DCDC2, Genetic linkage, Reading (process), Genetics, medicine, Humans, Genetic Predisposition to Disease, Gene, Nuclear family, Biological Psychiatry, Genetics (clinical), media_common, Transmission disequilibrium test, medicine.disease, Psychiatry and Mental health, Phenotype, Microtubule-Associated Proteins

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::18403843a6f338eb6c0d1a4047d15330Test
https://europepmc.org/articles/PMC3232293Test/

المؤلفون: Sara Mascheretti, Roberto Giorda, Claudio Lazazzera, Cecilia Marino, Catia Rigoletto, Massimo Molteni, Francesca Cattaneo, Marianna Rusconi, Jeffrey R. Gruen, Valentina Riva

مصطلحات موضوعية: Proband, Genetic Markers, Male, Linkage disequilibrium, Genotype, Genome-wide association study, Biology, Neuropsychological Tests, Article, Linkage Disequilibrium, Nuclear Family, Cohort Studies, Dyslexia, Pleiotropy, DCDC2, Genetics, medicine, Humans, Genetic Predisposition to Disease, Language Development Disorders, Child, Nuclear family, Genetics (clinical), Ecology, Evolution, Behavior and Systematics, Learning Disabilities, Genetic Pleiotropy, Transmission disequilibrium test, medicine.disease, Phenotype, Child, Preschool, Female, Mathematics, Genome-Wide Association Study

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::58299ff450dd3bb0648efefef8b2f9f9Test
https://europepmc.org/articles/PMC3939676Test/

المؤلفون: Maria Nobile, Laura Vanzin, Roberto Giorda, Cecilia Marino, Giorgia Menozzi, Massimo Molteni, Alessandra Citterio, Maria Luisa Lorusso, Andrea Facoetti

مصطلحات موضوعية: Genetic Markers, Male, Linkage disequilibrium, Genotype, Intelligence, Short-term memory, Nerve Tissue Proteins, Single-nucleotide polymorphism, Neuropsychological Tests, Biology, Linkage Disequilibrium, Dyslexia, Behavioral Neuroscience, DCDC2, Genetics, Humans, Child, Association (psychology), Genetic association, Intelligence Tests, Haplotype, Nuclear Proteins, DNA, Phenotype, Cytoskeletal Proteins, Memory, Short-Term, Haplotypes, Reading, Neurology, Female, Psychomotor Performance

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ef0eef0cf1512ec115530c34173a8ebfTest
http://hdl.handle.net/11577/1773598Test