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

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:57

مصطلحات 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

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

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