Carriers of the rare 22q11.2 microdeletion present with a high percentage of positive and negative symptoms and a high genetic risk for schizophrenia. Visual processing impairments have been characterized in schizophrenia, but less so in 22q11.2 Deletion Syndrome (DS). Here, we focus on visual processing using high-density EEG and source imaging in 22q11.2DS participants (N = 25) and healthy controls (N = 26) with an illusory contour discrimination task. Significant differences between groups emerged at early and late stages of visual processing. In 22q11.2DS, we first observed reduced amplitudes over occipital channels and reduced source activations within dorsal and ventral visual stream areas during the P1 (100-125 ms) and within ventral...
The 22q11.2 deletion (22q11DS) is a common chromosomal microdeletion and a potent risk factor for ps...
The 22q11.2 deletion syndrome (22q11DS) is a widely recognized genetic model allowing the study of n...
22q11.2 Deletion Syndrome (22q11DS) is the most common genetic microdeletion syndrome affect-ing hum...
Carriers of the rare 22q11.2 microdeletion present with a high percentage of positive and negative s...
Carriers of the rare 22q11.2 microdeletion present with a high percentage of positive and negative s...
In order to investigate the electroencephalographic (EEG) biomarkers of visual processing of illusor...
The clinical picture associated with 22q11.2 deletion syndrome (22q11DS) includes mild mental retard...
Patients with 22q11.2 deletion syndrome (22q11.2DS) represent a population at high risk for developi...
22q11.2 deletion syndrome (22q11DS) is a neurogenetic disorder that causes a high risk of developing...
The 22q11.2 deletion is one of the most common copy number variants in humans. Carriers of the delet...
22q11.2 deletion syndrome (22q11DS) represents a homogeneous model of schizophrenia particularly sui...
22q11.2 deletion syndrome (22q11DS) is a recurrent genetic mutation that is highly penetrant for psy...
The 22q11.2 deletion (22q11DS) is a common chromosomal microdeletion and a potent risk factor for ps...
The 22q11.2 deletion (22q11DS) is a common chromosomal microdeletion and a potent risk factor for ps...
Adults with 22q11.2 Deletion syndrome (22q11DS) have increased prevalence of schizophrenia features....
The 22q11.2 deletion (22q11DS) is a common chromosomal microdeletion and a potent risk factor for ps...
The 22q11.2 deletion syndrome (22q11DS) is a widely recognized genetic model allowing the study of n...
22q11.2 Deletion Syndrome (22q11DS) is the most common genetic microdeletion syndrome affect-ing hum...
Carriers of the rare 22q11.2 microdeletion present with a high percentage of positive and negative s...
Carriers of the rare 22q11.2 microdeletion present with a high percentage of positive and negative s...
In order to investigate the electroencephalographic (EEG) biomarkers of visual processing of illusor...
The clinical picture associated with 22q11.2 deletion syndrome (22q11DS) includes mild mental retard...
Patients with 22q11.2 deletion syndrome (22q11.2DS) represent a population at high risk for developi...
22q11.2 deletion syndrome (22q11DS) is a neurogenetic disorder that causes a high risk of developing...
The 22q11.2 deletion is one of the most common copy number variants in humans. Carriers of the delet...
22q11.2 deletion syndrome (22q11DS) represents a homogeneous model of schizophrenia particularly sui...
22q11.2 deletion syndrome (22q11DS) is a recurrent genetic mutation that is highly penetrant for psy...
The 22q11.2 deletion (22q11DS) is a common chromosomal microdeletion and a potent risk factor for ps...
The 22q11.2 deletion (22q11DS) is a common chromosomal microdeletion and a potent risk factor for ps...
Adults with 22q11.2 Deletion syndrome (22q11DS) have increased prevalence of schizophrenia features....
The 22q11.2 deletion (22q11DS) is a common chromosomal microdeletion and a potent risk factor for ps...
The 22q11.2 deletion syndrome (22q11DS) is a widely recognized genetic model allowing the study of n...
22q11.2 Deletion Syndrome (22q11DS) is the most common genetic microdeletion syndrome affect-ing hum...