المؤلفون: Gunter Schumann, Lai Jiang, Celia M. T. Greenwood, Guillaume Huguet, David J. Porteous, Antonio Ciampi, Martineau Jean-Louis, Antoine Main, Sébastien Jacquemont, Claudine Passo, Maude Auger, Catherine Schramm

المصدر: Genetic Epidemiology. 44:825-840

مصطلحات موضوعية: Adolescent, DNA Copy Number Variations, Epidemiology, Chromosomes, Human, Pair 22, Concordance, Intelligence, Bayesian probability, Computational biology, Biology, Genome, Genomic databases, Cohort Studies, 03 medical and health sciences, Annotation, mental disorders, Humans, Copy-number variation, Child, Genetics (clinical), Prior information, 030304 developmental biology, Intelligence Tests, Principal Component Analysis, 0303 health sciences, Models, Genetic, 030305 genetics & heredity, Bayes Theorem, Sample Size, Mutation (genetic algorithm), Linear Models, Chromosomes, Human, Pair 16

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::780390db577832039cf15031e7403638
https://doi.org/10.1002/gepi.22344

المؤلفون: Ian J. Deary, Elise Douard, Thomas Renne, Gunter Schumann, Thomas Bourgeron, W. David Hill, Sarah Lippé, Tomáš Paus, Frédérique Tihy, Khadije Jizi, Sarah E. Harris, Myriam Poirier, Nadine Younis, Catherine Schramm, Zdenka Pausova, Zohra Saci, Charles-Olivier Martin, Sébastien Jacquemont, Petra Tamer, Pauline Monin, Sherif Karama, Paul Redmond, Laura Almasy, Gail Davies, Jade England, Maude Auger, Celia M. T. Greenwood, Guillaume Huguet, David J. Porteous, Antoine Main, Géraldine Mathonnet, David C. Glahn, Sabrina Nowak, Emmanuelle Lemyre, Inga Sophia Knoth, Martineau Jean-Louis, Aurélie Labbe, Catalina Maftei

المساهمون: Université de Montréal (UdeM), CHU Sainte Justine [Montréal], Jewish General Hospital, HEC Montréal (HEC Montréal), Génétique humaine et fonctions cognitives - Human Genetics and Cognitive Functions (GHFC (UMR_3571 / U-Pasteur_1)), Institut Pasteur [Paris]-Université Paris Diderot - Paris 7 (UPD7)-Centre National de la Recherche Scientifique (CNRS), Université de Rouen Normandie (UNIROUEN), Normandie Université (NU), University of Edinburgh, King‘s College London, Gènes, Synapses et Cognition (CNRS - UMR3571 ), Institut Pasteur [Paris]-Centre National de la Recherche Scientifique (CNRS), The Hospital for sick children [Toronto] (SickKids), University of Toronto, McGill University = Université McGill [Montréal, Canada], Douglas Mental Health University Institute [Montréal], Children’s Hospital of Philadelphia (CHOP ), Boston Children's Hospital, Harvard Medical School [Boston] (HMS), Hartford Hospital, This research was enabled by support provided by Calcul Quebec and Compute Canada. SJ is a recipient of a Canada Research Chair in neurodevelopmental disorders, and a chair from the Jeanne et Jean Louis Levesque Foundation. CS is supported by an Institute for Data Valorization (IVADO) fellowship. PT is supported by a Canadian Institute of Health Research (CIHR) Scholarship Program. GH is supported by the Sainte-Justine Foundation, the Merit Scholarship Program for foreign students, and the Network of Applied Genetic Medicine fellowships. TB is a recipient of a chair of the Bettencourt-Schueler foundation. This work is supported by a grant from the Brain Canada Multi-Investigator initiative and CIHR grant 159734 (SJ, CMTG, TP). The Canadian Institutes of Health Research and the Heart and Stroke Foundation of Canada fund the Saguenay Youth Study (SYS). SYS was funded by the Canadian Institutes of Health Research (TP, ZP) and the Heart and Stroke Foundation of Canada (ZP). Funding for the project was provided by the Wellcome Trust. This work was also supported by an NIH award U01 MH119690 granted to LA, SJ, and DG and U01 MH119739., Institut Pasteur [Paris] (IP)-Université Paris Diderot - Paris 7 (UPD7)-Centre National de la Recherche Scientifique (CNRS), Institut Pasteur [Paris] (IP)-Centre National de la Recherche Scientifique (CNRS)

المصدر: Molecular Psychiatry
Molecular Psychiatry, Nature Publishing Group, 2021, ⟨10.1038/s41380-020-00985-z⟩
Mol Psychiatry
Huguet, G, Schramm, C, Douard, E, Tamer, P, Main, A, Monin, P, England, J, Jizi, K, Renné, T, Poirier, M, Nowak, S, Martin, C-O, Younis, N, Knoth, I S, Jean-louis, M, Saci, Z, Auger, M, Tihy, F, Mathonnet, G, Maftei, C, Léveillé, F, Porteous, D J, Davies, G, Redmond, P, Harris, S, Hill, W D, Lemyre, E, Schumann, G, Bourgeron, T, Pausova, Z, Paus, T, Karama, S, Lippe, S, Deary, I, Almasy, L, Labbe, A, Glahn, D C, M.T Greenwood, C & Jacquemont, S 2021, ' Genome wide analysis of gene dosage in 24,092 individuals estimates that 10,000 genes modulate cognitive ability ', Molecular Psychiatry . https://doi.org/10.1038/s41380-020-00985-z
Molecular Psychiatry, 2021, ⟨10.1038/s41380-020-00985-z⟩

مصطلحات موضوعية: 0301 basic medicine, DNA Copy Number Variations, Gene Dosage, Biology, Gene dosage, Genome, Article, 03 medical and health sciences, Cellular and Molecular Neuroscience, Cognition, 0302 clinical medicine, medicine, Humans, genetics, Copy-number variation, Molecular Biology, Gene, Intelligence Tests, Genetics, Intelligence quotient, [SCCO.NEUR]Cognitive science/Neuroscience, Inheritance (genetic algorithm), medicine.disease, Psychiatry and Mental health, psychiatric disorders, 030104 developmental biology, Autism, Haploinsufficiency, 030217 neurology & neurosurgery

وصف الملف: application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7dfdd3942cf01a09e7cfcd1239f7fd9d
https://hal-pasteur.archives-ouvertes.fr/pasteur-03325369

المؤلفون: Guillaume Huguet, Catherine Schramm, Elise Douard, Tamer Petra, Antoine Main, Pauline Monin, Jade England, Khadije Jizi, Thomas Renne, Myriam Poirier, Sabrina Nowak, Charles-Olivier Martin, Nadine Younis, Inga Sophia Knoth, Martineau Jean-Louis, Zohra Saci, Maude Auger, Frédérique Tihy, Géraldine Mathonnet, Catalina Maftei, France Léveillé, David Porteous, Gail Davies, Paul Redmond, Sarah E. Harris, W. David Hill, Emmanuelle Lemyre, Gunter Schumann, Thomas Bourgeron, Zdenka Pausova, Tomas Paus, Sherif Karama, Sarah Lippe, Ian J. Deary, Laura Almasy, Aurélie Labbe, David Glahn, Celia M.T. Greenwood, Sébastien Jacquemont

مصطلحات موضوعية: Genetics, Regulation of gene expression, 0303 health sciences, Inheritance (genetic algorithm), Biology, medicine.disease, Gene dosage, Genome, 03 medical and health sciences, 0302 clinical medicine, medicine, Autism, Copy-number variation, Haploinsufficiency, Gene, 030217 neurology & neurosurgery, 030304 developmental biology

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::9d6fa59e2d59de11e995f6b60e232585
https://doi.org/10.1101/2020.04.03.024554

المؤلفون: Guillaume Huguet, Catherine Schramm, Gunter Schumann, Sébastien Jacquemont, Celia M. T. Greenwood, Ian J. Deary, Thomas Bourgeron, Aurélie Labbe, Antoine Main, Sherif Karama, Zdenka Pausova, Tomáš Paus, Patricia J. Conrod

المصدر: Biological Psychiatry. 85:S104

مصطلحات موضوعية: Cognition, Computational biology, Biology, Genome, Biological Psychiatry

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::f16fde5406e556a880aee652f438857e
https://doi.org/10.1016/j.biopsych.2019.03.265

المؤلفون: Jean Louis Martineau

المساهمون: Antoine Main, Jean Louis Martineau, Sebastien Jacquemont

مصطلحات موضوعية: CNV, SNP ARRAY, ILLUMINA SNP ARRAY, FINAL REPORT, AFFIMETRIX, AXIOME, OMNI, HUMAN EXOM, MPI4PY

Relation: https://doi.org/10.5281/zenodo.3497399; https://doi.org/10.5281/zenodo.3497400; oai:zenodo.org:3497400

الاتاحة: https://doi.org/10.5281/zenodo.3497400