Genomics of Common Disease
Our main research aim is to support and advance scientific understanding of the heritable molecular mechanisms and environmental factors that control human susceptibility to complex common diseases, in particular, Type 2 Diabetes, obesity and linked illnesses, including cancer.
The methods we use range from innovative big data “omics” analysis to testing specific gene variants in vitro and in vivo. Our results will lay the foundation for precision and personalised medicine, leading to improved medical treatment for patients and targeted lifestyle or pharmaceutical preventative strategies for high-risk individuals
Study options and Genotyping facility
Study options
We run a yearly 12-month MSc in Human Molecular Genetics which includes a 6-month hands-on research project. This MSc provides practical training in human molecular genetics, genomics and precision medicine, using advanced molecular and bioinformatic techniques.
In addition, we run an annual short course providing an introduction to the statistical analysis of genome-wide association.
Genotyping Facility
The Genotyping Facility is linked to the NIHR Imperial BRC Institute for Translational Medicine and Therapeutics (ITMAT) and provides cutting-edge genotyping capability to internal and external clients.
Our capabilities range from low-throughput single sample SNPs to high throughput Illumina and Fluidigm assays. It also offers state of art Next Generation Sequencing. Find out more about the services we offer.
Key researchers
Dr Toby Andrew
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Dr Toby Andrew
Lecturer in Human Genomics
Professor Philippe Froguel
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Professor Philippe Froguel
Chair in Genomic Medicine
Dr Marika Kaakinen
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Dr Marika Kaakinen
Research Associate in Statistical Multiomics Modelling
Dr Inga Prokopenko
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Dr Inga Prokopenko
Senior Lecturer in Human Genomics
Dr Filippo Tamanini
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Dr Filippo Tamanini
Teaching Fellow in Human Molecular Genetics