I work as a Senior Geneticist in the Clinical Interpretation team at Blueprint Genetics. My main responsibilities are to analyse and interpret the NGS data and to write clinical reports together with the clinicians.
I joined Blueprint Genetics on June 2015. I have a Master’s degree in human genetics (University of Helsinki, 2003) and a PhD in cancer genetics (University of Helsinki, 2009). After the PhD, Icontinued as a postdoctoral researcher in the same field and applied next-generation sequencing technologiesin cancer research. My long-time dream has been to work in the field of genetic diagnostics, which is becoming as a part of the mainstream healthcare. At BpG, I’m able to help patients with rare diseases by providing them high-quality genetic diagnostics. I really enjoy working in the fast-paced environment with other enthusiastic people and take every patient case I open as a challenge.
We are changing diagnostics by providing accessible and actionable genetic knowledge in all medical specialties. Our mission is to support healthcare professionals around the world in providing the best care for patients and families with rare inherited diseases. We do that by delivering answers using fast, affordable, and comprehensive genetic diagnostics.
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