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المؤلفون: Zhiqiang Sha, Clyde Francks, Fabrice Crivello, Bernard Mazoyer, Dick Schijven, Amaia Carrion-Castillo, Simon E. Fisher, Marc Joliot
المصدر: Nature Human Behaviour
Nature Human Behaviour, 5, pp. 1226-1236
Nature Human Behaviour, 5, 1226-1236مصطلحات موضوعية: Neuroinformatics, Genetics of the nervous system, Social Psychology, Experimental and Cognitive Psychology, Biology, Genome-wide association studies, Article, Functional Laterality, 03 medical and health sciences, Behavioral Neuroscience, 0302 clinical medicine, Magnetic resonance imaging, medicine, Image Processing, Computer-Assisted, Brain asymmetry, Humans, Association (psychology), 030304 developmental biology, Cerebral Cortex, 0303 health sciences, Mechanism (biology), Cognition, Human brain, medicine.disease, Genetic architecture, medicine.anatomical_structure, Schizophrenia, Behavioural genetics, Autism, Psychiatric disorders, Neuroscience, 030217 neurology & neurosurgery, Genome-Wide Association Study
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المصدر: Scientific Reports, Vol 9, Iss 1, Pp 1-11 (2019)
Scientific Reportsمصطلحات موضوعية: Male, 0301 basic medicine, Season of birth, General Population Cohort, Breastfeeding, lcsh:Medicine, Biology, Left handedness, 050105 experimental psychology, Functional Laterality, Article, 03 medical and health sciences, 0302 clinical medicine, Genotype, Humans, Psychology, 0501 psychology and cognitive sciences, Association (psychology), lcsh:Science, Multidisciplinary, Geography, 05 social sciences, lcsh:R, Hand, Biobank, United Kingdom, Early life, 030104 developmental biology, Scale (social sciences), Population study, Female, Multiple birth, lcsh:Q, Psychomotor Performance, 030217 neurology & neurosurgery, Demography
وصف الملف: application/pdf; application/vnd.openxmlformats-officedocument.wordprocessingml.document
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c53c6e829ce05462a7cd8abbd50a58f9
http://link.springer.com/article /10.1038/s41598-018-37423-8 -
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المصدر: Scientific Reports
SCIENTIFIC REPORTS
Scientific Reports, 10, 1, pp. 1-11
Scientific Reports, Vol 10, Iss 1, Pp 1-11 (2020)
Scientific Reports, 10, 1-11مصطلحات موضوعية: 0301 basic medicine, Male, lcsh:Medicine, LEFT-RIGHT ASYMMETRY, PROTEIN, Penetrance, CILIUM, 0302 clinical medicine, Medicine and Health Sciences, TOOL, DNA sequencing, lcsh:Science, Primary ciliary dyskinesia, LATERALITY, Genetics, Multidisciplinary, Cilium, DEFECTS, Middle Aged, Situs Inversus, Female, Neuroinformatics, Adult, animal structures, Adolescent, HANDEDNESS, Genes, Recessive, Biology, Article, 03 medical and health sciences, medicine, otorhinolaryngologic diseases, Humans, Genetic variation, Cilia, Gene, IDENTIFICATION, MUTATIONS, Kartagener Syndrome, lcsh:R, Membrane Proteins, medicine.disease, Pathogenicity, respiratory tract diseases, Situs inversus, 030104 developmental biology, Etiology, lcsh:Q, Carrier Proteins, 030217 neurology & neurosurgery, PATHOGENICITY
وصف الملف: application/pdf; application/vnd.openxmlformats-officedocument.wordprocessingml.document
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المؤلفون: Simon E. Fisher, Bernard Mazoyer, Ingrid E. Scheffer, Else Eising, Arianna Vino, Angela T Morgan, Edythe A. Strand, Richard Webster, Melanie Bahlo, Lawrence D. Shriberg, Michael S. Hildebrand, Amaia Carrion-Castillo, Clyde Francks, Thomas S. Scerri, Kathy J. Jakielski, Alan Ma
المساهمون: Max Planck Institute for Psycholinguistics, Max-Planck-Gesellschaft, Mayo Clinic [Rochester], University of Melbourne, [GIN] Grenoble Institut des Neurosciences (GIN), Institut National de la Santé et de la Recherche Médicale (INSERM)-Université Grenoble Alpes [2016-2019] (UGA [2016-2019]), Hal, GIN
المصدر: Molecular Psychiatry
Molecular Psychiatry, 24, 1065-1078
Molecular Psychiatry, Nature Publishing Group, In press
Molecular Psychiatry, 24, pp. 1065-1078مصطلحات موضوعية: Neuroinformatics, 0301 basic medicine, Proband, Apraxias, [SDV.NEU.NB]Life Sciences [q-bio]/Neurons and Cognition [q-bio.NC]/Neurobiology, Gene regulatory network, [SDV.GEN.GH] Life Sciences [q-bio]/Genetics/Human genetics, Biology, Genome, Speech Disorders, Article, Language in Interaction, 03 medical and health sciences, Cellular and Molecular Neuroscience, 0302 clinical medicine, [SDV.BBM.GTP]Life Sciences [q-bio]/Biochemistry, Molecular Biology/Genomics [q-bio.GN], Genetics, medicine, Humans, Speech, Gene Regulatory Networks, Gene, Molecular Biology, Histone Acetyltransferases, Regulator gene, Homeodomain Proteins, Regulation of gene expression, [SDV.NEU.NB] Life Sciences [q-bio]/Neurons and Cognition [q-bio.NC]/Neurobiology, DNA Helicases, Intracellular Signaling Peptides and Proteins, Brain, Gene Expression Regulation, Developmental, Nuclear Proteins, RNA-Binding Proteins, FOXP2, Histone-Lysine N-Methyltransferase, medicine.disease, Psychiatry and Mental health, 030104 developmental biology, [SDV.GEN.GH]Life Sciences [q-bio]/Genetics/Human genetics, Childhood apraxia of speech, [SDV.BBM.GTP] Life Sciences [q-bio]/Biochemistry, Molecular Biology/Genomics [q-bio.GN], Carrier Proteins, 030217 neurology & neurosurgery, Mi-2 Nucleosome Remodeling and Deacetylase Complex, Transcription Factors, Neuroscience
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المؤلفون: Amaia Carrion-Castillo, Barbara Franke, Simon E. Fisher, Clyde Francks, Ben Maassen, Aryan van der Leij, Marlies Naber, Angelien Heister
المساهمون: Neurolinguistics and Language Development
المصدر: European Journal of Human Genetics, 25(4), 452-460. Nature Publishing Group
European Journal of Human Genetics
European Journal of Human Genetics, 25, 4, pp. 452-460
European Journal of Human Genetics, 25, 452-460مصطلحات موضوعية: 0301 basic medicine, Male, Neuroinformatics, DCDC2, Candidate gene, Reading disability, Population, LANGUAGE, Single-nucleotide polymorphism, Nerve Tissue Proteins, CHILDREN, Quantitative trait locus, Biology, Polymorphism, Single Nucleotide, Article, FAMILIES, Dyslexia, READING-DISABILITY, 03 medical and health sciences, 0302 clinical medicine, Child Development, Genetics, medicine, KIAA0319, Humans, Longitudinal Studies, Receptors, Immunologic, education, Child, Genetics (clinical), POPULATION, Genetic association, Netherlands, COGNITIVE TRAIT LOCI, education.field_of_study, Neurodevelopmental disorders Donders Center for Medical Neuroscience [Radboudumc 7], Nuclear Proteins, medicine.disease, Cytoskeletal Proteins, 030104 developmental biology, SUSCEPTIBILITY GENE, Female, DEVELOPMENTAL DYSLEXIA, Microtubule-Associated Proteins, 030217 neurology & neurosurgery
وصف الملف: application/pdf