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المؤلفون: Nicholas J. Timpson, Anneli Kolk, Margit Nõukas, Anu Reigo, Helene Alavere, Andres Metspalu, Ben Cole, Sébastien Jacquemont, Liis Leitsalu, Aurélien Macé, Zoltán Kutalik, Nathan Pankratz, Anne-Maud Ferreira, Katrin Männik, Anne M. Maillard, Tom R. Gaunt, Erika Salvi, Matt McGue, Hashem A. Shihab, Evelin Mihailov, William G. Iacono, Alexandre Reymond, Reedik Mägi, Anna L. Guyatt, Alexander Teumer, Daniele Cusi, Jacques S. Beckmann
المصدر: JAMA
Scopus-Elsevier
JAMA (Chicago, Ill.) (Chic. Ill.) 313 (2015): 2044–2054. doi:10.1001/jama.2015.4845
info:cnr-pdr/source/autori:Maennik, Katrin; Maegi, Reedik; Mace, Aurelien; Guyatt, Anna L.; Shihab, Hashem A.; Maillard, Anne M.; Alavere, Helene; Kolk, Anneli; Reigo, Anu; Mihailov, Evelin; Leitsalu, Liis; Ferreira, Anne-Maud; Noukas, Margit; Teumer, Alexander; Salvi, Erika; Cusi, Daniele; McGue, Matt; Iacono, William G.; Gaunt, Tomr.; Beckmann, Jacques S.; Jacquemont, Sebastien; Kutalik, Zoltan; Pankratz, Nathan; Timpson, Nicholas; Metspalu, Andres; Reymond, Alexandre/titolo:Copy Number Variations and Cognitive Phenotypes in Unselected Populations/doi:10.1001%2Fjama.2015.4845/rivista:JAMA (Chicago, Ill.) (Chic. Ill.)/anno:2015/pagina_da:2044/pagina_a:2054/intervallo_pagine:2044–2054/volume:313
Journal of the American Medical Association, vol. 313, no. 20, pp. 2044-2054مصطلحات موضوعية: Male, Heterozygote, DNA Copy Number Variations, Population, Genome-wide association study, Disease, Adolescent, Adult, Cognition, Educational Status, Epilepsy/genetics, Estonia, Female, Genome-Wide Association Study, Great Britain, Humans, Intellectual Disability/genetics, Italy, Mental Disorders/genetics, Obesity/genetics, Phenotype, United States, Article, 03 medical and health sciences, 0302 clinical medicine, Intellectual Disability, Intellectual disability, medicine, Copy-number variation, education, 030304 developmental biology, 0303 health sciences, education.field_of_study, business.industry, Mental Disorders, General Medicine, Odds ratio, medicine.disease, Educational attainment, 3. Good health, Cohort, business, 030217 neurology & neurosurgery, Demography
وصف الملف: application/pdf
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b91e51cd3171b68f1daee4221fa7160cTest
https://europepmc.org/articles/PMC4684269Test/ -
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المؤلفون: Jacques S. Beckmann, Martine Doco-Fenzy, Mandy Barker, Alexandre Reymond, Borja Rodriguez-Herreros, Raphael Bernier, Katrin Männik, Andres Metspalu, Loyse Hippolyte, Marion Gérard, Anne M. Maillard, Bogdan Draganski, Anu Reigo, Laurent Mottron, Laurence Schneider, Philippe Conus, Cédric Le Caignec, Sandra Martin-Brevet, Carina Ferrari, Anneli Kolk, Aurélie Pain, Robin P. Goin-Kochel, Nouchine Hadjikhani, Boris Keren, Ellen Hanson, Cyril Mignot, Franck Ramus, Lee Anne Green Snyder, Sébastien Jacquemont, Aurélien Macé, Albert David, Bertrand Isidor
المساهمون: 16p11.2 European Consortium, Simons Variation in Individuals Project Consortium, 16p11.2 European Consortium, Simons Variation in Individuals Project Consortium
المصدر: Biological psychiatry, vol. 80, no. 2, pp. 129-139
Biological Psychiatry
Biological psychiatryمصطلحات موضوعية: Adult, Male, 0301 basic medicine, Heterozygote, Adolescent, DNA Copy Number Variations, Intelligence, Chromosome Disorders, Locus (genetics), ASD, Executive Function, Young Adult, 03 medical and health sciences, 0302 clinical medicine, Memory, Intellectual Disability, Chromosome Duplication, mental disorders, medicine, Humans, Cognitive Dysfunction, Copy-number variation, Autistic Disorder, Child, Biological Psychiatry, Inhibition, Language, Genetics, Working memory, Copy number variation, Neuropsychology, Cognition, Middle Aged, medicine.disease, 16p11.2, Pedigree, Autistic Disorder/diagnostic imaging, Autistic Disorder/genetics, Autistic Disorder/physiopathology, Child, Preschool, Chromosome Deletion, Chromosome Disorders/diagnostic imaging, Chromosome Disorders/genetics, Chromosome Disorders/physiopathology, Chromosome Duplication/genetics, Chromosomes, Human, Pair 16/genetics, Cognitive Dysfunction/diagnostic imaging, Cognitive Dysfunction/genetics, Cognitive Dysfunction/physiopathology, DNA Copy Number Variations/genetics, Executive Function/physiology, Female, Intellectual Disability/diagnostic imaging, Intellectual Disability/genetics, Intellectual Disability/physiopathology, Intelligence/genetics, Memory/physiology, Motor Skills/physiology, 030104 developmental biology, Motor Skills, Autism spectrum disorder, Autism, Verbal memory, Psychology, Chromosomes, Human, Pair 16, 030217 neurology & neurosurgery
وصف الملف: application/pdf
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::178ed1b8601c25473c2a6e5fb24bcc3cTest