About us
Blueprint Genetics is a genetic testing company based in Helsinki, Seattle, and Dubai, with a customer base spanning over 70 countries. We provide world-class genetic diagnostics and clinical interpretation for rare inherited diseases in 14 medical specialties.

What we do

We do high quality genetics testing for a global clinical community. By combining a state-of-the-art laboratory process, the latest sequencing technology, AI empowered data-crunching tools and techniques, world-class professionals, and a holistic customer experience approach, we are leading the way in changing mainstream healthcare of tomorrow.

Our promise

We provide clinicians and their patients with comprehensive and high-quality tools and resources for diagnosis of genetic conditions. In doing so, we provide possibilities for targeted treatment and individualized care for patients.

Key facts

Based in

Helsinki

Seattle

Dubai

170+
Employees
> 3000
Clinicians in 70 countries
Founded in
2012
Quality Management
CLIA
Clinical laboratory certification by US regulatory authority
CAP
All laboratory functions accredited by College of American Pathologists
ISO 15189
Our processes and documentation comply with the most widely used standards worldwide

Founders

Tommi leads Blueprint Genetics as VP & GM of Specialty Genetics and is also a co-founder of the company. He has been running Blueprint Genetics since the beginning, growing the company into a leading clinical genetic testing provider. Over time he has held various responsibilities focused around sales and marketing, organizational development, business development and financing. Prior to Blueprint Genetics he founded a data analytics company called Whitevector and grew it to the Nordics and UK. Tommi holds a MSc (Tech) from the Helsinki University of Technology where he studied business strategy and applied mathematics.
Juha is the Executive Director of Medical & Lab Director at Blueprint Genetics. He is a co-founder of the company as well. Juha is responsible for supervising laboratory production and for designing new diagnostic tests. On a daily basis, he participates in the clinical evaluation of genetic findings and further develops the company's variant classification and interpretation practices in collaboration with a team of geneticists. Juha has an MD-PhD from the University of Turku. In 2006, Juha completed his fellowship program in clinical physiology and nuclear medicine. The following year, he became a docent. From 2007 to 2009, he joined the University of California San Francisco’s Cardiac Stem Cell Translational Development Program as a postdoctoral researcher and later as a research specialist. He also teaches at the University of Helsinki.
Samuel is the Executive Director of Strategy at Blueprint Genetics as well as a co-founder of the company. He is an expert in genome analysis technologies and has extensive experience in bioinformatics and cancer genomics research. Samuel received his PhD from the University of Helsinki and completed his postdoctoral research at Stanford University. At Stanford, he developed high-throughput sequencing technologies such as Oligonucleotide-Selective Sequencing (OS-Seq™). He is an adjunct professor in genetics at the University of Helsinki, an author of several high-impact publications, and an inventor and patent holder of DNA sequencing methods.
Tero-Pekka is the Executive Director of Medical, and also a co-founder at Blueprint Genetics. He is based in San Francisco and holds various responsibilities in the North American operations of the company. Tero-Pekka has an MD-PhD degree and is specialized in pediatrics and pediatric cardiology. He has a PhD in molecular and cellular biology as well. During his 3-year postdoctoral training at Stanford University School of Medicine, he focused on the molecular genetic mechanisms of cardiovascular disease.

News

AGTC Joins the My Retina Tracker® Program as a New Scientific Collaborator

Oct 07, 2020

The My Retina Tracker Program, a collaboration between Blueprint Genetics, Foundation Fighting Blindness and InformedDNA, is an open access, no-cost program that offers individuals with IRD living in the US easy access to high-quality genetic diagnostics and genetic counseling. AGTC joins the program as a new scientific collaborator to enhance development of  their investigational gene therapy for inherited retinal diseases (IRD).

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Last modified: 06.17.2020