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News

Stay up to date and read about our most recent milestones towards achieving CENTOGENE’s mission: To enable the cure of 100 rare diseases in 10 years.

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Bio€quity Europe 2018 Conference

CENTOGENE, the worldwide leader in using genetic knowledge to rationalize treatment decisions for rare hereditary diseases and enable patients,…

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CENTOGENE announces the appointment of a new Supervisory Board Member

CENTOGENE, the worldwide leader in elucidating rare disease genetics for patients, clinicians and pharmaceutical partners, today announced the…

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Solutions for early diagnosis at the 2nd Rare Disease Conference

CENTOGENE highlights solutions for early diagnosis of rare hereditary disorders at the 2nd Annual Recent Advances in Rare Disease Conference.

CENTOGE…

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Lyso-Gb1 for monitoring response to therapy for patients with Gaucher disease

CENTOGENE, the worldwide leader in elucidating rare disease genetics for patients, clinicians and pharmaceutical partners, announced the publication…

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CENTOGENE expands Executive Team, appoints Dr. Dirk Ehlers Chief Operating Officer

CENTOGENE, the worldwide leader in elucidating rare disease genetics for patients, clinicians and pharmaceutical partners, today announced the…

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CENTOGENE to present at the Cowen and Company 38th Annual Health Care Conference

CENTOGENE´s Chief Financial Officer, Richard Stoffelen, is scheduled to present at the upcoming Cowen and Company 38th Annual Health Care Conference…

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"50+new genes" initiative - "Un-Rare" rare diseases

There are more than 7,000 identified rare diseases where about 80% are hereditary. About 30 million Americans are living with a rare disease today;…

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New findings in hypomyelinating leukodystrophy

We mark Rare Disease Day 2018 with continued commitment to reduce time to diagnosis of rare diseases.

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Prof. Arndt Rolfs joins newly formed “Global Commission to End the Diagnostic Odyssey”

Prof. Arndt Rolfs has joined newly formed “The Global Commission to End the Diagnostic Odyssey for Children”, a dedicated group of technology…

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Rare Disease Report: CentoMD® provides a virtual encyclopedia of genetic information

One of the website for rare disease community - Rare Disease Report has shared exciting news about CentoMD® mutation database milestone - one billion…

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Here you can find forms, brochures, flyer and information sheets for download (PDF) about the broad genetic testing product and service portfolio of CENTOGENE.

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