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المؤلفون: Stefania Riva, Marco Villa, Vittoria Trezzi, Valentina Riva, Sara Mascheretti, Diego Forni, Alessandra Mozzi, Roberto Giorda, Rachele Cagliani, Manuela Sironi
المصدر: Neuropsychologia. 130:52-58
مصطلحات موضوعية: Adult, Male, Candidate gene, Genotype, Offspring, Cognitive Neuroscience, media_common.quotation_subject, Individuality, Experimental and Cognitive Psychology, Neuropsychological Tests, Polymorphism, Single Nucleotide, 050105 experimental psychology, Dyslexia, 03 medical and health sciences, Behavioral Neuroscience, 0302 clinical medicine, DCDC2, Pleiotropy, Reading (process), Humans, Genetic Predisposition to Disease, 0501 psychology and cognitive sciences, Child, Nuclear family, Genetic Association Studies, media_common, Genetics, 05 social sciences, Haplotype, Genetic Variation, Haplotypes, Reading, Trait, Female, Psychology, Microtubule-Associated Proteins, 030217 neurology & neurosurgery
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6c5f4822515d7a27d63c20b9c1ade78cTest
https://doi.org/10.1016/j.neuropsychologia.2018.05.021Test -
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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: 993مصطلحات 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 -
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المؤلفون: Roberto Giorda, Vittoria Trezzi, Cecilia Marino, Diego Forni, Sara Mascheretti, Massimo Molteni, Marco Villa
المصدر: Journal of Human Genetics. 62:949-955
مصطلحات موضوعية: Male, 0301 basic medicine, Adolescent, Nerve Tissue Proteins, Biology, Dyslexia, 03 medical and health sciences, 0302 clinical medicine, Risk Factors, Polymorphism (computer science), DCDC2, Genetic variation, Genetics, medicine, Humans, Genetic Predisposition to Disease, Regulatory Elements, Transcriptional, Allele, Child, Gene, Genetic Association Studies, Genetics (clinical), Haplotype, medicine.disease, Phenotype, Introns, 030104 developmental biology, Haplotypes, Italy, Female, Microtubule-Associated Proteins, 030217 neurology & neurosurgery
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3b31310626c6ae74bb57cc4125ae238dTest
https://doi.org/10.1038/jhg.2017.80Test -
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المؤلفون: Andrea Nordio, Cecilia Marino, Roberto Giorda, Filippo Arrigoni, Sara Mascheretti, Marco Villa, Denis Peruzzo, Vittoria Trezzi
المصدر: European Neuropsychopharmacology. 29:S923-S924
مصطلحات موضوعية: Pharmacology, medicine.medical_specialty, Visual perception, Dyslexia, Audiology, medicine.disease, Lingual gyrus, Psychiatry and Mental health, Superior temporal gyrus, Visual cortex, medicine.anatomical_structure, Neurology, DCDC2, Parvocellular cell, medicine, Pharmacology (medical), Neurology (clinical), Psychology, Insula, Biological Psychiatry
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_________::f7c30b966ba59830b18512efc73c1978Test
https://doi.org/10.1016/j.euroneuro.2017.08.255Test -
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المصدر: Human Genetics. 134:749-760
مصطلحات موضوعية: Male, Candidate gene, Nerve Tissue Proteins, Biology, Receptors, N-Methyl-D-Aspartate, Dyslexia, DCDC2, Missing heritability problem, Genetics, medicine, Humans, Family, Allele, Genetics (clinical), Phosphoric Diester Hydrolases, Genetic Diseases, Inborn, Nuclear Proteins, Epistasis, Genetic, Heritability, medicine.disease, DNA-Binding Proteins, Cytoskeletal Proteins, Phenotype, Multiple comparisons problem, Trait, Female, Transcription Factors
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cc76beb9d3dbf2c4afdde5832927907fTest
https://doi.org/10.1007/s00439-015-1555-4Test -
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المؤلفون: Cecilia Marino, Roberto Giorda, Andrea Facoetti, Monica Consonni, Pasquale Anthony Della Rosa, Maria Luisa Lorusso, Jeffrey R. Gruen, Andrea Falini, Daniela Perani, Massimo Molteni, Paola Scifo, Sara Mascheretti
المساهمون: Marino, C, Scifo, P, Della Rosa, Pa, Mascheretti, S, Facoetti, A, Lorusso, Ml, Giorda, R, Consonni, M, Falini, Andrea, Molteni, M, Gruen, Jr, Perani, DANIELA FELICITA L.
المصدر: Cortex (Testo stamp.) 57 (2014): 227–243. doi:10.1016/j.cortex.2014.04.016
info:cnr-pdr/source/autori:Marino, Cecilia; Scifo, Paola; Della Rosa, Pasquale A.; Mascheretti, Sara; Facoetti, Andrea; Lorusso, Maria L.; Giorda, Roberto; Consonni, Monica; Falini, Andrea; Molteni, Massimo; Gruen, Jeffrey R.; Perani, Daniela/titolo:The DCDC2%2Fintron 2 deletion and white matter disorganization: Focus on developmental dyslexia/doi:10.1016%2Fj.cortex.2014.04.016/rivista:Cortex (Testo stamp.)/anno:2014/pagina_da:227/pagina_a:243/intervallo_pagine:227–243/volume:57مصطلحات موضوعية: Adult, Male, DCDC2, medicine.medical_specialty, Genu of the corpus callosum, Adolescent, Developmental dyslexia, Cognitive Neuroscience, Splenium, Experimental and Cognitive Psychology, Audiology, Corpus callosum, Neuronal migration, behavioral disciplines and activities, Article, Lateralization of brain function, Dyslexia, White matter, Young Adult, mental disorders, Fractional anisotropy, medicine, Humans, Inferior longitudinal fasciculus, READ1, Diffusion tensor imaging, medicine.disease, White Matter, Introns, Neuropsychology and Physiological Psychology, medicine.anatomical_structure, Reading, Female, Nerve Net, Psychology, Microtubule-Associated Proteins, Neuroscience
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4402cf8cf8e524346742eeae9855a349Test
https://doi.org/10.1016/j.cortex.2014.04.016Test -
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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 -
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المؤلفون: Roberto Giorda, Nello Salandi, Alessandra Citterio, Massimo Molteni, Valentina Crespi, Silvana Beri, Cecilia Marino, Maria Luisa Lorusso, Marco Battaglia, Laura Vanzin, Maria Nobile
المصدر: European Journal of Human Genetics. 13:491-499
مصطلحات موضوعية: Male, Candidate gene, Adolescent, Genotype, Nerve Tissue Proteins, Single-nucleotide polymorphism, Biology, Polymorphism, Single Nucleotide, Genetic determinism, Nuclear Family, Dyslexia, DCDC2, Genetics, medicine, Humans, Genetic Predisposition to Disease, Child, Nuclear family, Genetics (clinical), Chromosomes, Human, Pair 15, Genetic heterogeneity, Nuclear Proteins, medicine.disease, Cytoskeletal Proteins, Phenotype, Female
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9b0dbf9bbe5887cf3789b0f18c586855Test
https://doi.org/10.1038/sj.ejhg.5201356Test -
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المؤلفون: Marco Battaglia, Maria Nobile, Laura Riva, Roberto Giorda, Laura Vanzin, Maria Luisa Lorusso, C Baschirotto, Massimo Molteni, Cecilia Marino
المصدر: Scopus-Elsevier
CIÊNCIAVITAEمصطلحات موضوعية: Genetic Markers, Adolescent, Genetic Linkage, Population, behavioral disciplines and activities, Biological theories of dyslexia, Linkage Disequilibrium, Dyslexia, Communication disorder, mental disorders, Genetics, medicine, Humans, Language disorder, Child, education, Genetics (clinical), Language, Chromosomes, Human, Pair 15, education.field_of_study, Neuropsychology, medicine.disease, Haplotypes, Italy, Psychology, Letter to JMG, Spoken language, Cognitive psychology, Surface dyslexia
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::63358f006025035782a66f96faccb08aTest
https://doi.org/10.1136/jmg.2003.010603Test -
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المؤلفون: Roberto Giorda, Sara Mascheretti, Maria Rosaria Cellino, Cecilia Marino, Silvana Beri, Valentina Riva, Lara Francesca Emilia Lanzoni
المصدر: Journal of human genetics. 59(4)
مصطلحات موضوعية: Proband, medicine.medical_specialty, Adolescent, Nerve Tissue Proteins, Biology, Quantitative trait locus, Language Development, Polymorphism, Single Nucleotide, Developmental psychology, Cohort Studies, Dyslexia, Cognition, Genetics, medicine, Humans, Receptors, Immunologic, Child, Nuclear family, Genetics (clinical), Genetic Association Studies, Language, Genetic Pleiotropy, Transmission disequilibrium test, Mathematical Concepts, medicine.disease, Developmental disorder, Phenotype, Genetic epidemiology, Reading, Trait, Medical genetics
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::826442afb179b0f9300a481d7078872dTest
https://pubmed.ncbi.nlm.nih.gov/24430574Test
