FIMM HiLIFE Unit logo black
The Ripatti group studies genetics of common complex diseases from discovery to translation to health care. We utilize Finnish research cohorts and a global network of biobank data with longitudinal health event histories to identify genetic associations and potential causal variants modifying the risks of diseases. We also develop and test risk models to stratify individuals based on their risks for preventive actions or stratified treatment. With health care partners, we develop approaches to apply these models in routine health care.
Institute for Molecular Medicine Finland FIMM

Follow us on Twitter

@CoECDG

Finishing the day on a high note with talks on the progress in the genetics of IBD by Mark Daly and mental illness… twitter.com/i/web/status/1…

Moving from the excellent speed talks by the junior researchers at the Meilahti campus to the Personalized Medicine… twitter.com/i/web/status/1…

Continuing the seminar with exciting talks on functional genetics by Riikka Lund, Olli Pietiläinen and Helena Kilpinen @HKilpinen

@okada_yukinori contrasting selection pressure and loci associated with dietary habits twitter.com/CoECDG/status/… https://t.co/2iTUye96O0