- The JDRF/WT Diabetes and Inflammation Laboratory, including John Todd and Linda Wicker: diabetes inflammation, genome informatics, statistical and non-Mendelian genetics.
- Fiona Karet: renal genetics (acid base homeostasis).
- Eamonn Maher: Cancer genetics, genomic imprinting, autosomal recessive disease.
- David Rubinsztein: Autophagy and neurodegeneration and the biological effects of triplet repeat diseases.
- Lucy Raymond: Genetics of Learning Disability (GOLD) Study – applying genomic methods to X-linked learning disability.
- Dr Evan Reid: studies on axonal degenerative disorders
- Dr Richard Sandford: Renal genetics (autosomal dominant polycystic kidney disease ) and genetics of autoimmune liver disease. PBC Genetics Study – study to determine the genetic cause of Primary Biliary Cirrhosis, PSC Genetics Study – study to determine the genetic cause of Primary Sclerosing Cholangitis.
- Dr Marc Tischkowitz: Cancer genetics
- Dr Geoff Woods: autosomal recessive primary microcephaly; Mendelian disorders of painlessness.
Research is carried out in the home Department of Medical Genetics located on level 6 of the Addenbrooke’s Treatment Centre (Professor Eamonn Maher, Dr Richard Sandford and Dr Marc Tischkowitz groups) and also in the Cambridge Institute for Medical Research (Professor John Todd and Professor Linda Wicker (JDRF/WT Laboratory), Professor Fiona Karet, Dr Lucy Raymond, Dr Evan Reid, Professor David Rubinsztein and Professor Geoff Woods groups).
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