PTEN mutations have previously been associated with difficulties related to autism spectrum disorder/conditions (ASD/C), but relatively little is known about other behavioural, developmental, and psychological characteristics/experiences for those with germline PTEN mutations. This thesis seeks to explore existing literature on such variables through a literature review and meta-analysis, followed by an empirical study exploring behavioural/psychological variables and their potential inter-relationships. Literature review A systematic search found 25 papers reporting on behavioural and psychological variables associated with PTEN mutations. Frequently reported characteristics included: ASD-related behaviours, intellectual disability, and de...
Background An emerging literature on behavioural phenotypes has highlighted apparent associations be...
AbstractBehavioural phenotype research is of benefit to a large number of children with genetic synd...
Behavioural phenotype research is of benefit to a large number of children with genetic syndromes an...
PTEN mutations have previously been associated with difficulties related to autism spectrum disorder...
Germline heterozygous PTEN mutations have been associated with high prevalence of autism spectrum di...
Germline mutations in PTEN, the gene that encodes phosphatase and tensin homolog, have been identifi...
Objective: The tumour suppressor gene PTEN is involved in neurogenesis and neuromodulation across t...
Behavioural correlates of specific genetic conditions are increasingly researched. Such research is ...
Thesis abstract:The current thesis aimed to explore the psychological and behavioural profile of spe...
Background: Pitt-Hopkins syndrome (PTHS) is a genetic neurodevelopmental disorder associated with in...
PTEN is a tumor suppressor associated with an inherited cancer syndrome and an important regulator o...
BackgroundPTEN is a well-established risk gene for autism spectrum disorder (ASD). Yet, little is kn...
Autism Spectrum Disorder (ASD) is amongst the most familial of psychiatric disorders. Twin and famil...
Abstract Background The limited behavioural phenotype literature on Phelan–McDermid syndrome (PMS) i...
Background: Potocki-Lupski syndrome (PTLS) is caused by a duplication within 17p11.2. A deletion wit...
Background An emerging literature on behavioural phenotypes has highlighted apparent associations be...
AbstractBehavioural phenotype research is of benefit to a large number of children with genetic synd...
Behavioural phenotype research is of benefit to a large number of children with genetic syndromes an...
PTEN mutations have previously been associated with difficulties related to autism spectrum disorder...
Germline heterozygous PTEN mutations have been associated with high prevalence of autism spectrum di...
Germline mutations in PTEN, the gene that encodes phosphatase and tensin homolog, have been identifi...
Objective: The tumour suppressor gene PTEN is involved in neurogenesis and neuromodulation across t...
Behavioural correlates of specific genetic conditions are increasingly researched. Such research is ...
Thesis abstract:The current thesis aimed to explore the psychological and behavioural profile of spe...
Background: Pitt-Hopkins syndrome (PTHS) is a genetic neurodevelopmental disorder associated with in...
PTEN is a tumor suppressor associated with an inherited cancer syndrome and an important regulator o...
BackgroundPTEN is a well-established risk gene for autism spectrum disorder (ASD). Yet, little is kn...
Autism Spectrum Disorder (ASD) is amongst the most familial of psychiatric disorders. Twin and famil...
Abstract Background The limited behavioural phenotype literature on Phelan–McDermid syndrome (PMS) i...
Background: Potocki-Lupski syndrome (PTLS) is caused by a duplication within 17p11.2. A deletion wit...
Background An emerging literature on behavioural phenotypes has highlighted apparent associations be...
AbstractBehavioural phenotype research is of benefit to a large number of children with genetic synd...
Behavioural phenotype research is of benefit to a large number of children with genetic syndromes an...