Additional file 1: Supplementary Table 1. Primary research articles which passed the criteria for inclusion in the systematic review. Studies conducted using mouse models on the C57/Black6 background at an age over 3 months are indicated by an asterisk after the author name. Supplementary Table 2. Rodent models with auditory phenotypes described in this review. Gene names are formatted as in the cited papers, with alternate names for equivalent human genes used in SFARI gene in brackets where relevant. Supplementary Figure 1. The ascending auditory processing pathway with presumed changes in autism based on results from human studies. Excitatory (red) and inhibitory (blue) connections between structures along the pathway are illustrated alo...
Figure S1. AKT phosphorylation is reduced in VPA mice but normal in all other models examined. Relat...
Mice are increasingly used as models of human-acquired neurological or neurodevelopmental conditions...
Autism is a neurodevelopmental disorder clinically characterized by deficits in communication, lack ...
International audienceBACKGROUND: There is interest in defining mouse neurobiological phenotypes use...
This dissertation examined how the auditory system in the Fmr1 KO mouse, amodel of Fragile X Syndrom...
Abstract Background There is interest in defining mouse neurobiological phenotypes useful for studyi...
Sensory processing abnormalities are frequently associated with autism spectrum disorders, but the u...
Lay Summary: It has always been difficult to relate results from animal research to humans. We try t...
Methyl-CpG binding protein 2 (MECP2) is a gene associated with DNA methylation and has been found to...
Autism is a neurodevelopmental syndrome with markedly high heritability. The diagnostic indicators o...
Sensory processing, and auditory processing in particular, is altered in individuals with neurodevel...
Fragile X Syndrome (FXS), a neurodevelopmental disorder, is the most prevalent single-gene cause of ...
Autism Spectrum Disorder (ASD) is an invasive neurodevelopmental disorder characterized by impaired ...
Microglial cells “play a pivotal role in refining neural networks during early critical periods” (Ga...
Figure S1. Distribution of ASD factor in rodent data. A. The stacked plot shows that the genes compr...
Figure S1. AKT phosphorylation is reduced in VPA mice but normal in all other models examined. Relat...
Mice are increasingly used as models of human-acquired neurological or neurodevelopmental conditions...
Autism is a neurodevelopmental disorder clinically characterized by deficits in communication, lack ...
International audienceBACKGROUND: There is interest in defining mouse neurobiological phenotypes use...
This dissertation examined how the auditory system in the Fmr1 KO mouse, amodel of Fragile X Syndrom...
Abstract Background There is interest in defining mouse neurobiological phenotypes useful for studyi...
Sensory processing abnormalities are frequently associated with autism spectrum disorders, but the u...
Lay Summary: It has always been difficult to relate results from animal research to humans. We try t...
Methyl-CpG binding protein 2 (MECP2) is a gene associated with DNA methylation and has been found to...
Autism is a neurodevelopmental syndrome with markedly high heritability. The diagnostic indicators o...
Sensory processing, and auditory processing in particular, is altered in individuals with neurodevel...
Fragile X Syndrome (FXS), a neurodevelopmental disorder, is the most prevalent single-gene cause of ...
Autism Spectrum Disorder (ASD) is an invasive neurodevelopmental disorder characterized by impaired ...
Microglial cells “play a pivotal role in refining neural networks during early critical periods” (Ga...
Figure S1. Distribution of ASD factor in rodent data. A. The stacked plot shows that the genes compr...
Figure S1. AKT phosphorylation is reduced in VPA mice but normal in all other models examined. Relat...
Mice are increasingly used as models of human-acquired neurological or neurodevelopmental conditions...
Autism is a neurodevelopmental disorder clinically characterized by deficits in communication, lack ...