It has been recently suggested to approach schizophrenia as a neurodevelopmental disorder with psychosis as a late, potentially preventable stage of the illness. While efforts have been conducted to improve our knowledge on distal and proximal risk factors, the researches conducted leave many unanswered questions concerning: 1) the interaction between genes and environment and 2) the role played by specific neurodevelopmental phases. Therefore, we decided to concentrate our research efforts on two specific populations. The 22q11.2 deletion syndrome population can contribute in providing an answer to the first pending question, while the child and adolescent population can help us to provide an answer to the second pending question. This the...
The 22q11.2 deletion syndrome (22q11DS) is associated with a 20-25% risk of schizophrenia. In a coho...
Objective: Genetic syndromes related to psychosis have become increasingly important for exploring t...
OBJECTIVE Chromosome 22q11.2 deletion syndrome is a neurogenetic disorder associated with high rates...
The purpose of this article is to provide an overview of current insights into the neurodevelopmenta...
Phenomenology has been the reference point that investigators have used in their efforts to understa...
Rare copy number variants contribute significantly to the risk for schizophrenia, with the 22q11.2 l...
22q11.2 Deletion syndrome (22q11DS) is the most common known recurrent copy-number variant disorder....
Gregory Costain1,2, Anne S Bassett1–41Clinical Genetics Research Program, Centre for Addic...
International audienceCurrent research suggests that alterations in neurodevelopmental processes, in...
It is increasingly acknowledged that psychotic disorders have a developmental nature, which might ha...
22q11.2 Deletion Syndrome (22q11DS) is the most common genetic microdeletion syndrome affect-ing hum...
Both early (i.e., pre- and perinatal periods) and late (i.e., adolescent period) neurodevelopmental ...
The past two decades have witnessed an accelerated effort to understand the nature of schizophrenia ...
22q11.2 deletion syndrome is characterised by a well defined microdeletion that is associated with a...
It is now well recognized that as well as having a characteristic facial dysmorphology and a range o...
The 22q11.2 deletion syndrome (22q11DS) is associated with a 20-25% risk of schizophrenia. In a coho...
Objective: Genetic syndromes related to psychosis have become increasingly important for exploring t...
OBJECTIVE Chromosome 22q11.2 deletion syndrome is a neurogenetic disorder associated with high rates...
The purpose of this article is to provide an overview of current insights into the neurodevelopmenta...
Phenomenology has been the reference point that investigators have used in their efforts to understa...
Rare copy number variants contribute significantly to the risk for schizophrenia, with the 22q11.2 l...
22q11.2 Deletion syndrome (22q11DS) is the most common known recurrent copy-number variant disorder....
Gregory Costain1,2, Anne S Bassett1–41Clinical Genetics Research Program, Centre for Addic...
International audienceCurrent research suggests that alterations in neurodevelopmental processes, in...
It is increasingly acknowledged that psychotic disorders have a developmental nature, which might ha...
22q11.2 Deletion Syndrome (22q11DS) is the most common genetic microdeletion syndrome affect-ing hum...
Both early (i.e., pre- and perinatal periods) and late (i.e., adolescent period) neurodevelopmental ...
The past two decades have witnessed an accelerated effort to understand the nature of schizophrenia ...
22q11.2 deletion syndrome is characterised by a well defined microdeletion that is associated with a...
It is now well recognized that as well as having a characteristic facial dysmorphology and a range o...
The 22q11.2 deletion syndrome (22q11DS) is associated with a 20-25% risk of schizophrenia. In a coho...
Objective: Genetic syndromes related to psychosis have become increasingly important for exploring t...
OBJECTIVE Chromosome 22q11.2 deletion syndrome is a neurogenetic disorder associated with high rates...