Autism-associated 16p11.2 microdeletion impairs prefrontal functional connectivity in mouse and human

Autor: Alice Bertero 1, 2, Adam Liska 1, Marco Pagani, 1, Roberta Parolisi 3, Maria Esteban Masferrer 4, Marta Gritti 5, Matteo Pedrazzoli 5, Alberto Galbusera 1, Alessia Sarica 6, Antonio Cerasa 6, 7 Mario Buffelli 8, Raffaella Tonini 5, Annalisa Buffo 3, Cornelius Gross 4, Massimo Pasqualetti 1, Alessandro Gozzi 1

Publikováno v: Brain (Online) 141 (2018): 2055–2065. doi:10.1093/brain/awy111
info:cnr-pdr/source/autori:Alice Bertero 1,2*, Adam Liska 1*, Marco Pagani,1,* Roberta Parolisi 3, Maria Esteban Masferrer 4, Marta Gritti 5, Matteo Pedrazzoli 5, Alberto Galbusera 1, Alessia Sarica 6, Antonio Cerasa 6,7 Mario Buffelli 8, Raffaella Tonini 5, Annalisa Buffo 3, Cornelius Gross 4, Massimo Pasqualetti 1,2 and Alessandro Gozzi 1/titolo:Autism-associated 16p11.2 microdeletion impairs prefrontal functional connectivity in mouse and human/doi:10.1093%2Fbrain%2Fawy111/rivista:Brain (Online)/anno:2018/pagina_da:2055/pagina_a:2065/intervallo_pagine:2055–2065/volume:141

Human genetic studies are rapidly identifying variants that increase risk for neurodevelopmental disorders. However, it remains unclear how specific mutations impact brain function and contribute to neuropsychiatric risk. Chromosome 16p11.2 deletion

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dd5c554f4a97edcdfebdc97449f254d7
https://pubmed.ncbi.nlm.nih.gov/29722793

Deletion of Autism Risk Gene Shank3 Disrupts Prefrontal Connectivity.

Autor: Pagani, Marco, Bertero, Alice, Liska, Adam, Galbusera, Alberto, Sabbioni, Mara, Barsotti, Noemi, Colenbier, Nigel, Marinazzo, Daniele, Scattoni, Maria Luisa, Pasqualetti, Massimo, Gozzi, Alessandro

Publikováno v: Journal of Neuroscience; 7/3/2019, Vol. 39 Issue 27, p5299-5310, 12p