Professor Richard Cotton
- Professor Richard Cotton
AM BAgSc PhD DSc (Melb)
Senior Principal Research Fellow
Group Leader, Genomic Disorders Research Centre
Contact Details
Email: | |
Phone: | +61 (0)3 9288 2980 |
Fax: | +61 (0)3 9288 2989 |
Richard Cotton initiated the Mutation Research Centre, now renamed the Genomic Disorders Research Centre, in January, 1996 (www.genomic.unimelb.edu.au). He has always been interested in the biochemical genetics of human disease and has recently focused on mutation. Amongst his more notable scientific achievements are the conception, planning and execution of the fundamental experiment, which proved that when two immunoglobulin producing cells were fused, the immunoglobulin of both parental cells were produced in the hybrid. This laid the experimental and theoretical foundation for the widely used monoclonal antibody technique. He also conceived the widely used tetrohydrobiopterin (BH4) load test to identify the serious variants of PKU, but BH4 is currently being trialled in heart disease. He is particularly interested in improving mutation detection technologies to make them cheaper and simpler, so that they can be more widely applied, and holds several patents in the area. A recent development has been a method to detect DNA damaging compounds.
Prof Cotton has written two books entitled "Mutation Detection", initiated the journal entitled "Human Mutation", and in 1991 initiated bi-yearly international workshops on Mutation Detection and in 1998, bi-yearly HUGO Mutation Detection Courses. In 1996 he has also started a worldwide initiative (The HUGO Mutation Detection Database Initiative, recently formed into the Human Genome Variation Society (HGVS); www.hgvs.org) to capture and distribute lists of mutations.
In June 2005, he was admitted as a Member of the Order of Australia for service to science through genetic research, particularly through the development of technologies to detect gene mutations that underlie birth defects or cause disease and through efforts to document findings. In June 2006, he convened a Meeting, co-sponsored by WHO, which initiated the Human Variome Project (www.humanvariomeproject.org). This project aims to collect worldwide genetic variation and its associated phenotype. He is Treasurer of the Human Genome Organisation (HUGO) and the author of over 200 scientific papers and three patents.
Research Interests
- Human Variome Project
- Mutation documentation & databases
- Genetics
- Mutation Detection
- DNA sequencing
Laboratory Techniques
- Mutation Detection
- Denaturing High Performance Liquid Chromatography (dHPLC)
- Chemical Cleavage of Mismatch (CCM)
Additional Information
Research
Date | Initiatives | Link |
1973 | Genetics for Monoclonal Antibody Technique | |
1984 | Murdoch Institute Co-Founder | |
1986 - 2002 | 3 Mutation Detection Methods Patents (Chemical and Enzyme Cleavage) | |
1991 | Mutation Detection Workshop Series (International) | |
Journal – Human Mutation | ||
1994 | HUGO Mutation Database Initiative / Human Genome Variation Society | |
1996 | Genomic Disorders Research Centre | |
Mutation Detection Workshop Series (Australia) | ||
1997 | Book – Mutation Detection, Oxford University Press | |
HGVS Meetings – associated with the American Society of Human Genetics | ||
1998 | HGVS Meetings – associated with HUGO / HGM | |
HUGO Mutation Detection Course Series | ||
2002 | DNA Damage and Novel Mutation Detection Method | |
2003 | Genvartec Pty Ltd, Co-founder | |
2005 | Queens Birthday Honours – Member of the Order of Australia | |
2006 | Convenor and Initiator – The Human Variome Project |
Boards
Date | Organisation | Link |
1983 - 1995 | Murdoch Institute | |
1996 - present | Genomic Disorders Research Centre | |
1997 - 2002 | HUGO (London) | |
1998 - 2000 | Australian Club (Melbourne) | |
2002 – present | Trust for Nature (Melbourne) | |
2003 - present | Genvartec Pty Ltd |
Publications & Articles
Please see PubMed.
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