
For publications, please use the
Publications Search here

Learning Disabilities Research Group
Department of Psychiatry
Section of Developmental Psychiatry
University of Cambridge
Douglas House, 18b Trumpington
Road, CAMBRIDGE, CB2 8AH
United Kingdom
Enquiries & Reception:
+44 (0)1223 746124
+44 (0)1223 746100
FAX: +44 (0)1223
746122
Email: Sue Hampton-Matthews
The Health Foundation, Chair in Learning Disabilities,
Learning Disabilities Research Group, Section of Developmental Psychiatry
Department of Psychiatry, University of Cambridge
+44 1223 746112
Two main areas of research interest include: first, investigating the relationship between particular genetic syndromes and associated psychiatric and behavioural disorders (e.g. Prader-Willi Syndrome and over-eating, and Down’s Syndrome and Alzheimer’s disease) and, secondly, clinico-legal studies, including studies investigating the capacity of people with learning disabilities to make particular decisions.
Consultant Clinical & Forensic Psychologist (Lead Academic Psychologist in Learning Disability)/Affiliated Lecturer
+44 1223 746117
Beebe Trust Research Fellow and Senior Lecturer, Behavioural Genetics Group, Psychological Medicine, Cardiff University, Henry Wellcome Building, Heath Park, Cardiff, CF14 4XN
In my research I model the genetic and epigenetic contribution to behaviour and mental disease. I have a particular focus on the role played by imprinted genes in brain functioning and as part of the LDRG I am dissecting the molecular contribution to neuropsychiatric illness seen in PWS.
Current studies in this programme of work are aimed at examining how the imprinted snoRNA mbii-52 in modifies serotonin receptor 2C functioning, and what consequences this has for the serotonin system and serotonergic related behaviours. It is hoped this work may lead to the identification of more specific pharmacological treatments for the mood disorder and obsessive/compulsive aspects of the PWS phenotype. Additionally, we are attempting to model the role played by Ube3a in the development of psychosis in the maternal-uniparental disomy and imprinting centre mutation genetic sub-types of PWS.Beebe Trust Research Fellowship (2003-2008)
Dorothy Hodgkin Postgraduate Studentship with GSK (2005-2008)
University Lecturer in Developmental Psychiatry (Learning Disability)
+44 1223 746 121
My long research and clinical interests are in the neuropsychiatric aspects of developmental and acquired brain damage and epilepsy. Current research projects are focused on epilepsy and on autistic spectrum disorders. In the field of epilepsy, I am investigating the nature of epilepsy as it presents to locality-based psychiatric learning disability services and investigating the effects of different treatment approaches. I am also researching the relationship between psychopathological disturbances in people with epilepsy and brain pathology assessed along several axis. In people with autism I am using electrophysiological and functional imaging approaches to investigate language and the way in which differences in semantic processes can be manipulated by external factors. I am also involved in research using physical and neurocognitive methods to examine manifestations of weak central coherence in people with autism.
Various aspects of Prader-Willi Syndrome (PWS), especially cognition and behaviour and how this relates to the genetic abnormalities. Current projects concerns psychiatric illness in PWS (with Sarita Soni and Tony Holland), IQ, emotion, recognition, childrens play interests and some aspects of executive function. A further project concerns the transition from the early phenotype of PWS (0-2 years approx.) and the later phenotype.