Learning and behavioral deficits associated with the absence of the fragile X mental retardation protein: what a fly and mouse model can teach us
AR Santos, AK Kanellopoulos, C Bagni - Learning & memory, 2014 - learnmem.cshlp.org
The Fragile X syndrome (FXS) is the most frequent form of inherited mental disability and is
considered a monogenic cause of autism spectrum disorder. FXS is caused by a triplet …
considered a monogenic cause of autism spectrum disorder. FXS is caused by a triplet …
Aberrant development of speech processing in young children with autism: New insights from neuroimaging biomarkers
HF Sperdin, M Schaer - Frontiers in neuroscience, 2016 - frontiersin.org
From the time of birth, a newborn is continuously exposed and naturally attracted to human
voices, and as he grows, he becomes increasingly responsive to these speech stimuli …
voices, and as he grows, he becomes increasingly responsive to these speech stimuli …
Mutations associated with neuropsychiatric conditions delineate functional brain connectivity dimensions contributing to autism and schizophrenia
Abstract 16p11. 2 and 22q11. 2 Copy Number Variants (CNVs) confer high risk for Autism
Spectrum Disorder (ASD), schizophrenia (SZ), and Attention-Deficit-Hyperactivity-Disorder …
Spectrum Disorder (ASD), schizophrenia (SZ), and Attention-Deficit-Hyperactivity-Disorder …
Deviant dynamics of EEG resting state pattern in 22q11. 2 deletion syndrome adolescents: a vulnerability marker of schizophrenia?
Previous studies have repeatedly found altered temporal characteristics of EEG microstates
in schizophrenia. The aim of the present study was to investigate whether adolescents …
in schizophrenia. The aim of the present study was to investigate whether adolescents …
[HTML][HTML] Schizophrenia patients and 22q11. 2 deletion syndrome adolescents at risk express the same deviant patterns of resting state EEG microstates: a candidate …
Schizophrenia is a complex psychiatric disorder and many of the factors contributing to its
pathogenesis are poorly understood. In addition, identifying reliable neurophysiological …
pathogenesis are poorly understood. In addition, identifying reliable neurophysiological …
Persistent gating deficit and increased sensitivity to NMDA receptor antagonism after puberty in a new mouse model of the human 22q11. 2 microdeletion syndrome: a …
M Didriksen, K Fejgin, SRO Nilsson, MR Birknow… - Journal of Psychiatry and …, 2017 - jpn.ca
Background: The hemizygous 22q11. 2 microdeletion is a common copy number variant in
humans. The deletion confers high risk for neurodevelopmental disorders, including autism …
humans. The deletion confers high risk for neurodevelopmental disorders, including autism …
Abnormal development and dysconnectivity of distinct thalamic nuclei in patients with 22q11. 2 deletion syndrome experiencing auditory hallucinations
Background Several studies in patients with schizophrenia have demonstrated an abnormal
thalamic volume and thalamocortical connectivity. Specifically, hyperconnectivity with …
thalamic volume and thalamocortical connectivity. Specifically, hyperconnectivity with …
Auditory N100 gating in patients with schizophrenia: a systematic meta-analysis
T Rosburg - Clinical Neurophysiology, 2018 - Elsevier
Objective The study sought to assess the presence of auditory N100 gating deficits in
patients with schizophrenia by meta-analysis. Methods Literature was screened for studies …
patients with schizophrenia by meta-analysis. Methods Literature was screened for studies …
Estimates of the prevalence of speech and motor speech disorders in youth with 22q11. 2 deletion syndrome
AL Baylis, LD Shriberg - American Journal of Speech-Language Pathology, 2019 - ASHA
Purpose Speech sound disorders and velopharyngeal dysfunction are frequent features of
22q11. 2 deletion syndrome (22q). We report the first estimate of the prevalence of motor …
22q11. 2 deletion syndrome (22q). We report the first estimate of the prevalence of motor …
22q11. 2 deletion syndrome is associated with impaired auditory steady-state gamma response
KM Larsen, G Pellegrino, MR Birknow… - Schizophrenia …, 2018 - academic.oup.com
Abstract Background The 22q11. 2 deletion syndrome confers a markedly increased risk for
schizophrenia. 22q11. 2 deletion carriers without manifest psychotic disorder offer the …
schizophrenia. 22q11. 2 deletion carriers without manifest psychotic disorder offer the …