المؤلفون: Pauline C Ng, Alexandre Reymond, Helene Alavere, Andres Metspalu, Margit Nõukas, Sébastien Jacquemont, Anu Reigo, Katrin Männik, Liis Leitsalu, Anne M. Maillard, Anneli Kolk

المصدر: Personalized medicine. 13(4)

مصطلحات موضوعية: 0301 basic medicine, Pharmacology, medicine.medical_specialty, education.field_of_study, business.industry, media_common.quotation_subject, Population, General Medicine, 030105 genetics & heredity, Biobank, Preference, 03 medical and health sciences, Carrier status, Molecular Medicine, Medicine, Genomic information, Copy-number variation, Worry, business, Return of results, Psychiatry, education, media_common

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b931db6c4823330cd0cbb9dd992014a1Test
https://pubmed.ncbi.nlm.nih.gov/29749813Test

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. 2044-2054

مصطلحات 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/

المؤلفون: Ben Cole, Alexandre Reymond, Anna L. Guyatt, Helene Alavere, Anu Reigo, Zoltán Kutalik, Evelin Mihailov, Anne M. Maillard, Reedik Mägi, Hashem A. Shihab, Katrin Männik, Jacques S. Beckmann, Alexander Teumer, Sébastien Jacquemont, Andres Metspalu, Liis Leitsalu, Erika Salvi, Matt McGue, Tom R. Gaunt, Aurélien Macé, Nathan Pankratz, Anneli Kolk, Anne-Maud Ferreira, Margit Nõukas, Daniele Cusi, William G. Iacono, Nicholas J. Timpson

المصدر: Obstetrical & Gynecological Survey. 70:559-560

مصطلحات موضوعية: medicine.medical_specialty, education.field_of_study, business.industry, Public health, Population, Obstetrics and Gynecology, General Medicine, Disease, Odds ratio, medicine.disease, Educational attainment, Intellectual disability, Cohort, Medicine, Copy-number variation, business, education, Demography

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_________::90bc4a01f98dfc0a489e41ba04f4e845Test
https://doi.org/10.1097/01.ogx.0000471594.65931.90Test

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 psychiatry

مصطلحات 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