Background: Duplications of 15q11.2-q13.1 (Dup15q syndrome) are highly penetrant for autism spectrum disorder (ASD). A distinct electrophysiological (EEG) pattern characterized by excessive activity in the beta band has been noted in clinical reports. We asked whether EEG power in the beta band, as well as in other frequency bands, distinguished children with Dup15q syndrome from those with non-syndromic ASD and then examined the clinical correlates of this electrophysiological biomarker in Dup15q syndrome. Methods: In the first study, we recorded spontaneous EEG from children with Dup15q syndrome (n = 11), age-and-IQ-matched children with ASD (n = 10) and age-matched typically developing (TD) children (n = 9) and computed rela...
Autism Spectrum Disorders (ASD) are a collection of neurodevelopmental disorders with features of im...
In this presentation we describe research from the Swinburne Babylab investigating possible electrop...
Background: Angelman syndrome (AS) is a rare neurodevelopmental disorder caused by the absence of fu...
Background: Duplications of 15q11.2-q13.1 (Dup15q syndrome) are highly penetrant for autism spectrum...
Background: Duplications of 15q11.2-q13.1 (Dup15q syndrome) are highly penetrant for autism spectrum...
BackgroundDuplications of 15q11.2-q13.1 (Dup15q syndrome) are highly penetrant for autism spectrum d...
Neurodevelopmental disorders (NDDs) show considerable heterogeneity, both in terms of genetic under...
BackgroundSleep disturbances in autism spectrum disorder (ASD) represent a common and vexing comorbi...
<p>Qualitative analysis of spontaneous electroencephalogram (EEG) recordings from participants with ...
BackgroundDuplications of 15q11.2-q13.1 (Dup15q syndrome), including the paternally imprinted gene U...
Mechanism-based biomarkers are needed to guide clinical trials for neurodevelopmental disorders by i...
Abstract Background Sleep disturbances in autism spectrum disorder (ASD) represent a common and vexi...
Copy number variations (CNVs) at the 16p11.2 chromosomal region are associated with myriad clinical ...
BACKGROUND:Angelman syndrome (AS) is a severe neurodevelopmental disorder caused by either disruptio...
Our objective was to define the EEG features during sleep of children with neurodevelopmental disord...
Autism Spectrum Disorders (ASD) are a collection of neurodevelopmental disorders with features of im...
In this presentation we describe research from the Swinburne Babylab investigating possible electrop...
Background: Angelman syndrome (AS) is a rare neurodevelopmental disorder caused by the absence of fu...
Background: Duplications of 15q11.2-q13.1 (Dup15q syndrome) are highly penetrant for autism spectrum...
Background: Duplications of 15q11.2-q13.1 (Dup15q syndrome) are highly penetrant for autism spectrum...
BackgroundDuplications of 15q11.2-q13.1 (Dup15q syndrome) are highly penetrant for autism spectrum d...
Neurodevelopmental disorders (NDDs) show considerable heterogeneity, both in terms of genetic under...
BackgroundSleep disturbances in autism spectrum disorder (ASD) represent a common and vexing comorbi...
<p>Qualitative analysis of spontaneous electroencephalogram (EEG) recordings from participants with ...
BackgroundDuplications of 15q11.2-q13.1 (Dup15q syndrome), including the paternally imprinted gene U...
Mechanism-based biomarkers are needed to guide clinical trials for neurodevelopmental disorders by i...
Abstract Background Sleep disturbances in autism spectrum disorder (ASD) represent a common and vexi...
Copy number variations (CNVs) at the 16p11.2 chromosomal region are associated with myriad clinical ...
BACKGROUND:Angelman syndrome (AS) is a severe neurodevelopmental disorder caused by either disruptio...
Our objective was to define the EEG features during sleep of children with neurodevelopmental disord...
Autism Spectrum Disorders (ASD) are a collection of neurodevelopmental disorders with features of im...
In this presentation we describe research from the Swinburne Babylab investigating possible electrop...
Background: Angelman syndrome (AS) is a rare neurodevelopmental disorder caused by the absence of fu...