BACKGROUND: Behavioural phenotypes associated with genetic syndromes have been extensively investigated in order to generate rich descriptions of phenomenology, determine the degree of specificity of behaviours for a particular syndrome, and examine potential interactions between genetic predispositions for behaviour and environmental influences. However, relationships between different aspects of behavioural phenotypes have been less frequently researched and although recent interest in potential cognitive phenotypes or endophenotypes has increased, these are frequently studied independently of the behavioural phenotypes. METHOD: Taking Prader-Willi syndrome (PWS) as an example, we discuss evidence suggesting specific relationships between...
ABSTRACT. Objective. To determine whether pheno-typic differences exist among individuals with Prade...
Prader-Willi syndrome (PWS) is a complex multisystemic condition caused by a lack of paternal expres...
In both Prader-Willi syndrome (PWS) and 22q11 deletion syndrome [velo-cardio-facial syndrome (VCFS)]...
BACKGROUND: Behavioural phenotypes associated with genetic syndromes have been extensively investiga...
Hypothesis: A specific pathway can be identified between genetic characteristics and behaviour prof...
Prader-Willi syndrome (PWS) is a rare neurodevelopmental genetic disorder associated with a characte...
Funder: Foundation for Prader-Willi Research; doi: http://dx.doi.org/10.13039/100002889Abstract: Pra...
We present a mini-review of cognition in Prader-Willi syndrome. Studies cited include findings on ge...
BACKGROUND: Individuals with Prader-Willi syndrome (PWS) have been shown to demonstrate a particular...
Background Repetitive questions and temper outbursts form part of the behavioural phenotype of Prade...
The phenotypes of human imprinted neurogenetic disorders can be hypothesized as extreme alterations ...
Prader–Willi syndrome (PWS) is a neurodevelopmental disorder with aspects of psychiatric illness cau...
The purpose of this paper is to present an overview of the psychological characteristics associated ...
Prader-Willi syndrome (PWS) is characterized by temper tantrums, impulsivity, mood fluctuations, dif...
Objective: Paternal deletion and maternal uniparental disomy are the principal genetic subtypes asso...
ABSTRACT. Objective. To determine whether pheno-typic differences exist among individuals with Prade...
Prader-Willi syndrome (PWS) is a complex multisystemic condition caused by a lack of paternal expres...
In both Prader-Willi syndrome (PWS) and 22q11 deletion syndrome [velo-cardio-facial syndrome (VCFS)]...
BACKGROUND: Behavioural phenotypes associated with genetic syndromes have been extensively investiga...
Hypothesis: A specific pathway can be identified between genetic characteristics and behaviour prof...
Prader-Willi syndrome (PWS) is a rare neurodevelopmental genetic disorder associated with a characte...
Funder: Foundation for Prader-Willi Research; doi: http://dx.doi.org/10.13039/100002889Abstract: Pra...
We present a mini-review of cognition in Prader-Willi syndrome. Studies cited include findings on ge...
BACKGROUND: Individuals with Prader-Willi syndrome (PWS) have been shown to demonstrate a particular...
Background Repetitive questions and temper outbursts form part of the behavioural phenotype of Prade...
The phenotypes of human imprinted neurogenetic disorders can be hypothesized as extreme alterations ...
Prader–Willi syndrome (PWS) is a neurodevelopmental disorder with aspects of psychiatric illness cau...
The purpose of this paper is to present an overview of the psychological characteristics associated ...
Prader-Willi syndrome (PWS) is characterized by temper tantrums, impulsivity, mood fluctuations, dif...
Objective: Paternal deletion and maternal uniparental disomy are the principal genetic subtypes asso...
ABSTRACT. Objective. To determine whether pheno-typic differences exist among individuals with Prade...
Prader-Willi syndrome (PWS) is a complex multisystemic condition caused by a lack of paternal expres...
In both Prader-Willi syndrome (PWS) and 22q11 deletion syndrome [velo-cardio-facial syndrome (VCFS)]...