<div><p>The 22q11.2 deletion syndrome (22q11DS) is a widely recognized genetic model allowing the study of neuroanatomical biomarkers that underlie the risk for developing schizophrenia. Recent advances in magnetic resonance image analyses enable the examination of structural connectivity integrity, scarcely used in the 22q11DS field. This framework potentially provides evidence for the disconnectivity hypothesis of schizophrenia in this high-risk population. In the present study, we quantify the whole brain white matter connections in 22q11DS using deterministic tractography. Diffusion Tensor Imaging was acquired in 30 affected patients and 30 age- and gender-matched healthy participants. The Human Connectome technique was applied to regis...
The 22q11.2 deletion syndrome (22q11DS) is a recurrent copy number variant with high penetrance for ...
The 22q11.2 deletion syndrome (22q11DS) is associated with cognitive impairments and a 41% risk of d...
22q11.2 deletion syndrome (22q11DS) is a neurogenetic disorder that causes a high risk of developing...
The 22q11.2 deletion syndrome (22q11DS) is a widely recognized genetic model allowing the study of n...
The 22q11.2 deletion syndrome (22q11DS) is a widely recognized genetic model allowing the study of n...
The 22q11.2 deletion syndrome (22q11DS) is a widely recognized genetic model allowing the study of n...
22q11.2 deletion syndrome (22q11DS) represents a homogeneous model of schizophrenia particularly sui...
At the convergence of neuroimaging, genetic polymorphism and psychiatry, this thesis highlights thro...
The clinical picture associated with 22q11.2 deletion syndrome (22q11DS) includes mild mental retard...
The clinical picture associated with 22q11.2 deletion syndrome (22q11DS) includes mild mental retard...
Schizophrenia is a devastating neurodevelopmental disorder that assaults the afflicted with visual a...
Abstract Background 22q11.2 deletion syndrome (22q11DS) is a neurodevelopmental syndrome associated ...
Background: Dysconnectivity has been consistently proposed as a major key mechanism in psychosis. In...
BACKGROUND: Hippocampal alterations are among the most replicated neuroimaging findings across the p...
Background: Chromosome 22q11.2 deletion syndrome (22q11.2DS) is a neurogenetic disorder that is asso...
The 22q11.2 deletion syndrome (22q11DS) is a recurrent copy number variant with high penetrance for ...
The 22q11.2 deletion syndrome (22q11DS) is associated with cognitive impairments and a 41% risk of d...
22q11.2 deletion syndrome (22q11DS) is a neurogenetic disorder that causes a high risk of developing...
The 22q11.2 deletion syndrome (22q11DS) is a widely recognized genetic model allowing the study of n...
The 22q11.2 deletion syndrome (22q11DS) is a widely recognized genetic model allowing the study of n...
The 22q11.2 deletion syndrome (22q11DS) is a widely recognized genetic model allowing the study of n...
22q11.2 deletion syndrome (22q11DS) represents a homogeneous model of schizophrenia particularly sui...
At the convergence of neuroimaging, genetic polymorphism and psychiatry, this thesis highlights thro...
The clinical picture associated with 22q11.2 deletion syndrome (22q11DS) includes mild mental retard...
The clinical picture associated with 22q11.2 deletion syndrome (22q11DS) includes mild mental retard...
Schizophrenia is a devastating neurodevelopmental disorder that assaults the afflicted with visual a...
Abstract Background 22q11.2 deletion syndrome (22q11DS) is a neurodevelopmental syndrome associated ...
Background: Dysconnectivity has been consistently proposed as a major key mechanism in psychosis. In...
BACKGROUND: Hippocampal alterations are among the most replicated neuroimaging findings across the p...
Background: Chromosome 22q11.2 deletion syndrome (22q11.2DS) is a neurogenetic disorder that is asso...
The 22q11.2 deletion syndrome (22q11DS) is a recurrent copy number variant with high penetrance for ...
The 22q11.2 deletion syndrome (22q11DS) is associated with cognitive impairments and a 41% risk of d...
22q11.2 deletion syndrome (22q11DS) is a neurogenetic disorder that causes a high risk of developing...