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Gillian Bates is a Professor of Molecular Neuroscience and Co-Director of the Huntington’s Disease Centre at University College London. Her research focuses on understanding the molecular basis of Huntington’s disease and validating therapeutic targets for clinical development. After completing her postdoctoral work in Hans Lehrach’s lab as part of an international collaboration that cloned the Huntington’s disease gene, she established her own lab at King's College London (KCL), developing a mouse model of Huntington’s disease in 1996. In 2016, she moved to University College London to establish the Huntington’s Disease Centre alongside Professor Sarah Tabrizi. Bates was elected to the Academy of Medical Sciences in 1999, to the European Molecular Biology Organization (EMBO) in 2002, and to the Royal Society in 2007. Her academic career includes significant positions such as Vice Dean (Research) at University College London and Head of the Division of Genetics and Molecular Medicine at KCL.
University College London, Institute of Neurology • United Kingdom
Leading research on Huntington's disease.
University College London, Faculty of Brain Sciences • United Kingdom
Oversaw research agendas within the Faculty.
King's College London, Division of Genetics and Molecular Medicine • United Kingdom
Managed the division focused on genetics and molecular medicine.
King's College London, Medical Molecular Genetics • United Kingdom
Taught and researched in the field of medical molecular genetics.
United Medical Dental Schools, Medical Molecular Genetics • United Kingdom
Educated students while conducting research.
Imperial Cancer Research Fund, Genome Analysis • United Kingdom
Conducted postdoctoral research in genome analysis.
St Mary's Hospital Medical School, Biochemistry Molecular Biology • United Kingdom
Assisted in research projects.
Queen Elizabeth Hospital Sick Children, Cytogenetics • United Kingdom
Worked on clinical cytogenetic analyses.