Leicester Institute of Genetics and Genome Sciences

Members of the Institute and their Research Interests


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Electrophoresis of DNA and a cell in mitosis. Wellcome Trust image library


Department of Biochemistry



Professor Felix Beck
Genetic Regulation of Mammalian Development, in particular homeobox genes.


Professor Ian Eperon
The molecular mechanisms of splice site selection.


Professor Catrin Pritchard
Mammalian Raf kinases and their role in ERK activation and tumour development.






Department of Biology


Dr Richard Gornall
Plant taxonomy, population genetics & evolution.


Professor Paul Hart  
(Head of Department)
Competition and adaptive radiation in group living animals.


Professor Pat Heslop-Harrison
The cell nucleus: its spatial and dynamic organisation or architecture.


Dr Paul Jarvis
Import of nucleus-encoded proteins into chloroplasts; and strategies used by plant hosts in controlling the activity of DNA-type transposable elements.


Dr Trude Schwarzacher

Function of meiotic and recombination specific genes, gene expression and promoter studies.


Professor David Twell
Cell and molecular biology of plant reproductive development.






Department of Cancer Studies and Molecular Medicine (Leicester Royal Infirmary)


Professor Rosemary Walker
Research focuses on understanding biological aspects of human breast and breast cancer and relating this to the clinical situation.



Dr Margaret Barrow
Clinical studies - patient awareness.



Dr Marcus Cooke
The role of genotoxicology in the pathogenesis of disease is the central theme in my research programme, focussed primarily upon free radical mechanisms of cellular damage, particular oxidative DNA damage and repair.



Dr G Don Jones
Radiotherapy and chemotherapy, used either singly or in combination, are two of the principal modalities of cancer treatment. For radiation and many chemotherapeutic drugs, genomic DNA is the primary cellular target for the damaging effects of these agents; indeed it is the DNA damage induced which is thought to be responsible for the killing of the cancer cells.



Dr Howard Pringle
The main emphasis of my current research is to investigate the molecular and cellular mechanisms that influence early stages of cancer and effect the progression of this disease. To achieve this I interact with two research groups, one studying skin cancer and the other investigating breast cancer. 


Dr Jacqueline Shaw
Collaboration with Prof. R.A. Walker and Dr. J.L. Jones (Pathology). Application of molecular approaches to microdissected tumour tissue with analysis of mutator and suppressor pathways. Analysis of oestrogen receptors a and b and variants in breast cancers and surrounds. Analysis of tumour specific alterations in plasma DNA from breast cancer patients. Analysis of the invasion-promoting function of the myofibroblast: role of a5b1 integrin.





The Department of Cardiovascular Science


Dr Nelson Chong
Coronary Heart Disease, Circadian Timing and Cardiovascular Function.


Dr Karl E. Herbert

Research interests are, molecular and cellular mechanisms of cardiovascular ageing and oxidative DNA damage and repair in humans, mitochondria and cellular oxidative stress.


Professor Nilesh Samani
Molecular genetic basis of complex cardiovascular traits, particularly hypertension and coronary heart disease.





Department of Cell Physiology & Pharmacology


Dr Steve Ennion
Purinergic signalling in the cardiovascular system.





Department of Genetics


Professor Peter Williams (Head of Department)
Molecular and cell biological analysis of host pathogen interactions, especially with regard to the human diarrhoeal organisms Escherichia coli, Campylobacter jejuni and Salmonella spp.


Professor Sir Alec J. Jeffreys FRS
Direct analysis of the dynamics of heritable mutation in humans, and of the molecular basis and consequences of human meiotic recombination.


Professor Rhona H. Borts

The roles of mismatch repair proteins in meiotic recombination, heteroduplex processing and chromosome segregation and the control of crossing over in general.


Professor Anthony J. Brookes
Exploring DNA sequence variation in humans by technology development, bioinformatics, and genotyping, to understand common disease aetiology, drug responses, genome structure/function, and population genetics.


Professor Annette Cashmore
Genetics of fungal pathogenicity - iron uptake and metabolism in the human pathogen Candida albicans.


Professor Yuri Dubrova
The genetic risks of ionizing radiation and chemical mutagens: germline mutation induction and radiation-induced genomic instability in irradiated human families and laboratory mice.


Professor Mark Jobling
Y chromosomal, autosomal and X-chromosomal haplotypes and the histories of human populations. Mutation processes, including ectopic recombination and gene conversion.


Professor Julian Ketley
Gene regulation and host pathogen interactions by Campylobacter jejuni. Research areas include the characterisation of chemotaxis signal transduction pathways, lipooligosaccharidebiosynthesis and iron regulation.


Professor Charalambos P. Kyriacou
The molecular basis of circadian, tidal, and seasonal behavioural rhythms in insects, annelids and mammals; also the molecular basis of sexual/aggressive behaviour in Drosophila.


Dr Peter Meacock
Analysis of gene function, regulation and evolution in yeast; the genetics of B-vitamin metabolism


Dr Richard Badge
The role of L1 retrotransposons (mobile sequences that constitute 17% of human DNA) in genetic diversity, genetic disease, and genome evolution of humans and primates.


Dr Julian Barwell
Understanding how treatment may itself alter the cell's ability to recognise and repair further DNA damage in different groups of patients, including those who carry mutations that predispose to breast cancer.


Dr Christopher D. Bayliss
Mechanistic basis for generation of mutations in tandem DNA repeat tracts of bacterial pathogens and their contributions to virulence, host adaptation and population structure.


Dr Raymond Dalgleish
The identification and analysis of genes involved in the bone mineral density and osteoporosis in man; research strategies iclude the use of other model organisms.


Dr Flaviano Giorgini
Molecular analysis of genetic modifiers of toxicity using yeast and mammalian models of Huntingdon's disease; genetic analysis of toxicity in yest models of neurodegenerative disorders.


Dr Colin R.A. Hewitt
Real time, single cell analysis of iron metabolism and regulation by Salmonella in vitro infection.


Dr Edward J. Hollox
The evolution and genetic variation of human antimicrobal genes, and the relationship of this variation with susceptibility to infectious and inflammatory disease.


Dr Celia May
Using the major pseudoautosomal region and other targets within the human genome to understand patterns of DNA diversity.


Dr Peter A. Meacock
Yeast molecular genetics; analysis of gene function, regulation and evolution in Saccharomyces cerevisiae and related species; biosynthesis and metabolism of the B-vitamins thiamin and pyridoxine.


Dr Julie Morrissey
Molecular analysis of the pathogenesis of Staphylococcus aureus: Areas of study include the mechanisms and regulation of the adaptive stress response and biofilm formation.


Dr Ezio Rosato
Molecular neurobiology of complex behaviours in Drosophila, especially circadian rhythms. Molecular investigation of diel vertical migration in Arctic and Antarctic Krill.


Dr Nicola J. Royle
The investigation of telomere molecular dynamics in normal and immortal cells, including cells that use the ALT (Alternative Lengthening of Telomeres) pathway.


Dr Raffael Schaffrath
Yeast as a eukaryotic model to analyse a tRNA modification pathway that controls cell proliferation and cell death by a tRNAse killer toxin.


Dr Nuala Sheehan
Reader in Statistical Genetics. Research interests are applied statistics motivated by complex problems in genetics.


Dr Chris Talbot
The identification of genetic causes of brain diseases like Alzheimer's disease and the development of new therapies. A developing interest is in genomic structural variation.


Dr Fred Tata
Scaffold proteins provide specificity to kinase-based signal transduction, and mediate attachment of signalling complexes to cellular motor proteins; analysis of cellullar phenotypes; targeted gene knockdown by RNAi.


Dr Eran Tauber  
Genes, brain and behaviour; identifying molecular mechanisms of behaviour using Drosophila as a model system; research combines molecular genetics, bioinformatics and population biology.


Dr Martin Tobin   (Joint with Health Sciences)
MRC Clinician Scientist Fellow. Research into Investigation of the genetic determinants of common complex diseases and traits.





Department of Health Sciences : Epidemiology & Public Health



Professor Paul Burton
Statistical methods for the analysis of genetic and environmental determinants of common complex diseases.


Professor John Thompson
My research involves developing and applying new statistical methods to problems in genetics and epidemiology.





Infection Immunity & Inflammation


Professor Wilhelm Schwaeble
Professor Wilhelm Schwaeble started his scientific career in the Institute of Immunology in Munich, Germany, where he worked on the molecular characterisation of complement factor H, a regulatory component of the complement system. This project was jointly supported by Professor Elisabeth Weiss (Munich) and Professors Manfred Dierich and Thomas Schulz (Innsbruck).





Faculty of Law


Professor Jean McHale
Health care law and issues of ownership of human material and health care privacy.





Institute of Lung Health (Leicester Royal Infirmary)


Dr Andy Wardlaw
Mechanisms of eosinophil trafficking and activation in asthma, T-cell homing to the lung in health and inflammatory lung disease.





MRC Toxicology Unit


Dr Tim Gant
Toxicogenomics.


Dr Andrew Smith
Genetic Susceptibility and Resistance to Toxic Chemicals.

UPDATED: 11th May 2009
MAINTAINER : E.A.Le-Butt
This document has been approved by the head of department or section.