Abstract Prader–Willi Syndrome (PWS) is a genetically determined neurodevelopmental
disorder associated with mild to moderate intellectual disability, growth and sex-hormone …

Abstract The Research Domain Criteria project (RDoc) proposes a new classification system
based on information from several fields in order to encourage translational perspectives …

We investigated autism spectrum disorder (ASD) symptomatology, hyperactivity and affect in
seven genetic syndromes; Angelman (AS; n= 104), Cri du Chat (CdCS; 58), Cornelia de …

With its spread of chapters covering key issues across the life cycle this text has established
itself as the foundational primer for those studying the lived experiences of people with …

Background Temper outbursts are common in P rader–W illi syndrome but rarely described
in detail. This study investigated the phenomenology of temper outbursts in terms of …

Despite behavioral differences between genetic subtypes of Prader–Willi syndrome (PWS),
no studies have been published characterizing brain structure in these subgroups. Our goal …

Syndrome specific repetitive behavior profiles have been described previously. A detailed
profile is absent for Rubinstein–Taybi syndrome (RTS). The Repetitive Behaviour …

Abstract Background Individuals with Prader–Willi syndrome (PWS) have been shown to
demonstrate a particular cognitive deficit in attention switching and high levels of preference …

The operant learning theory account of behaviors of clinical significance in people with
intellectual disability (ID) has dominated the field for nearly 50 years. However, in the last …

We report a first study of brain activity linked to task switching in individuals with Prader–Willi
syndrome (PWS). PWS individuals show a specific cognitive deficit in task switching which …