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1دورية أكاديمية
المؤلفون: Amaia Carrión-Castillo, Cedric Boeckx
المصدر: Scientific Reports, Vol 14, Iss 1, Pp 1-14 (2024)
وصف الملف: electronic resource
Relation: https://doaj.org/toc/2045-2322
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المؤلفون: Merel Postema, Amaia Carrion Castillo, Fabrice Crivello, Dick Schijven, Simon E. Fisher, Marc Joliot, Antonietta Pepe, B Mazoyer, Xiangzhen Kong, Clyde Francks
المصدر: Cerebral Cortex
Cerebral Cortex, 31, 4151-4168
Cerebral Cortex (New York, NY)
Cerebral Cortex, 31, 9, pp. 4151-4168مصطلحات موضوعية: Neuroinformatics, Adult, Male, Sociodemographic Factors, Databases, Factual, Genotype, Health Status, Cognitive Neuroscience, Population, Biology, Polymorphism, Single Nucleotide, Functional Laterality, Lateralization of brain function, handedness, Cellular and Molecular Neuroscience, medicine, lateralization, Humans, Brain asymmetry, genetics, AcademicSubjects/MED00385, Gray Matter, education, Aged, Genetic association, brain torque, Aged, 80 and over, education.field_of_study, Human Connectome Project, AcademicSubjects/SCI01870, Skew, Brain, Cognition, Genomics, Human brain, Middle Aged, Magnetic Resonance Imaging, White Matter, Phenotype, medicine.anatomical_structure, Evolutionary biology, brain asymmetry, Original Article, AcademicSubjects/MED00310, Female
وصف الملف: application/vnd.openxmlformats-officedocument.wordprocessingml.document; application/vnd.openxmlformats-officedocument.spreadsheetml.sheet; application/pdf
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e25759ec86607af281173924dd3e2ea6
https://hdl.handle.net/21.11116/0000-0009-045F-921.11116/0000-0008-4B98-921.11116/0000-0008-4B99-821.11116/0000-0006-DD10-F21.11116/0000-0008-4B9A-7 -
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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
وصف الملف: application/pdf
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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
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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: M. Arfan Ikram, Lukas Pirpamer, Daniel E. Vosberg, Edith Hofer, David Ames, Sandra van der Auwera-Palitschka, Zdenka Pausova, Xueqiu Jian, Henry Brodaty, André M. M. Sousa, Linda Ding, Tavia E. Evans, William S. Kremen, Jean Shin, Steven Tilley, Fabrice Crivello, Christophe Tzourio, Karen A. Mather, Peter R. Schofield, Joanna M. Wardlaw, Joshua C. Bis, Tomáš Paus, Bernard Mazoyer, Myriam Fornage, Thomas H. Mosley, Natalie Terzikhan, Nathan A. Gillespie, Hans J. Grabe, Michelle Luciano, Mathew A. Harris, Nenad Sestan, Wei Wen, Sherif Karama, Reinhold Schmidt, Shaojie Ma, Katharina Wittfeld, Lindsay B. Lewis, Arno Villringer, Hieab H.H. Adams, Sudha Seshadri, Neda Jahanshad, Jiyang Jiang, Sophie Maingault, Yasaman Saba, Qiong Yang, Frauke Beyer, Stéphanie Debette, Nicola J. Armstrong, Markus Scholz, Carol E. Franz, Margaret J. Wright, Shuo Li, Rebecca F. Gottesman, Aniket Mishra, Perminder S. Sachdev, Yash Patel, John B.J. Kwok, Anbupalam Thalamuthu, Helena Schmidt, Amaia Carrion-Castillo, Robin Bülow, Mark E. Bastin, Markus Loeffler, Ian E. Deary, Stefan Frenzel, Julian N. Trollor, Gennady V. Roshchupkin, A. Veronica Witte
المساهمون: Epidemiology, Medical Informatics, Radiology & Nuclear Medicine, Neurology, the ENIGMA Consortium, for the neuroCHARGE Working Group, the neuroCHARGE Working Group
المصدر: Cerebral Cortex, 30(7), 4121-4139. Oxford University Press
Cerebral cortex 30(7), 4121-4139 (2020). doi:10.1093/cercor/bhaa035
Cerebral Cortex
2020, ' Global and regional development of the human cerebral cortex : Molecular architecture and occupational aptitudes ', Cerebral Cortex . https://doi.org/10.1093/cercor/bhaa035
Cereb Cortexمصطلحات موضوعية: rho GTP-Binding Proteins, Male, Aptitude, Genome-wide association study, brain development, cortical surface area, 0302 clinical medicine, Form perception, Intracranial volume, genetics [RNA-Binding Proteins], genetics [Form Perception], Visual Cortex, media_common, Cerebral Cortex, Aged, 80 and over, 0303 health sciences, Principal Component Analysis, Career Choice, Microfilament Proteins, genomeide association study, RNA-Binding Proteins, Gene Expression Regulation, Developmental, Cognition, growth & development [Visual Cortex], Middle Aged, medicine.anatomical_structure, VINTAGE, Cerebral cortex, growth & development [Cerebral Cortex], Original Article, Female, Adult, endocrine system, Adolescent, Cognitive Neuroscience, media_common.quotation_subject, tau Proteins, Biology, occupational aptitude, 03 medical and health sciences, Cellular and Molecular Neuroscience, Young Adult, Regional development, medicine, Humans, ddc:610, 030304 developmental biology, Genetic association, Aged, physiology [Aptitude], genome-wide association study, 9. Industry and infrastructure, cortical thickness, Brain Cortical Thickness, Form Perception, genetics [tau Proteins], genetics [rho GTP-Binding Proteins], genetics [Microfilament Proteins], Transcriptome, Neuroscience, 030217 neurology & neurosurgery, Genome-Wide Association Study
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URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1d226f09a8b9d01d3a3ad18d33554ba1
https://pure.eur.nl/en/publications/72d5930b-a0bc-44d8-8d56-fd3f2f98dfc8 -
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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, Clyde Francks, Amaia Carrion-Castillo, Fabrice Crivello, Xiangzhen Kong, Antonietta Pepe, Nathalie Tzourio-Mazoyer, Bernard Mazoyer
المصدر: Cortex, 124, 137-153
Cortex, 124, pp. 137-153
Cortexمصطلحات موضوعية: Neuroinformatics, Autism Spectrum Disorder, Cognitive Neuroscience, Planum temporale, Intelligence, Population, Proteinase Inhibitory Proteins, Secretory, Experimental and Cognitive Psychology, Genome-wide association study, Biology, 050105 experimental psychology, Functional Laterality, 03 medical and health sciences, 0302 clinical medicine, medicine, Brain asymmetry, Humans, Attention deficit hyperactivity disorder, 0501 psychology and cognitive sciences, education, Genetic association, education.field_of_study, 05 social sciences, Dyslexia, Heritability, medicine.disease, Magnetic Resonance Imaging, Temporal Lobe, Neuropsychology and Physiological Psychology, Proto-Oncogene Proteins c-bcl-2, Autism spectrum disorder, Autism, Psychology, Nucleoside-Phosphate Kinase, 030217 neurology & neurosurgery, Genome-Wide Association Study, Clinical psychology
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
وصف الملف: application/pdf
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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
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