Continuing our Life-Long Commitment to Rare Disease Patients Around the World
As our global community continues to navigate the impact of COVID-19, CENTOGENE remains fully open and operational, underlining our continued commitment to patients globally.

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Transforming Global Genetic Data into Medical Decisions

We are a global leader in rare disease diagnosis and research by transforming real-world clinical and genetic data into actionable information for patients, physicians, and pharmaceutical companies

CENTOGENE - Revolutionising Genetic Solutions

Explore how CENTOGENE is revolutionizing genetic solutions for patients worldwide

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Coronavirus Testing With CENTOGENE

Coronavirus Testing With CENTOGENE

Enabling you to get back to normal with our range of SARS-CoV-2 testing solutions for individuals and businesses

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Improved Travel With Coronavirus Testing

The Latest Insights Into COVID-19

Keeping you up to date with the most recent news and scientific developments amid the Coronavirus pandemic

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Our goal: providing precise medical diagnosis of inherited diseases at the earliest possible moment; transforming medical expertise and analytical information into actionable results for physicians, patients, and pharmaceutical partners.

Our commitment: life-long support for our patients and partners - driven by the continuous improvement of our diagnostic quality and therapeutic options for individual patients.


Cómo los biomarcadores transforman el Diagnóstico Genético

Únase con nosotros el próximo 20 de abril, donde hablaremos sobre la enfermedad de Fabry y…

How Biomarkers Transform Genetic Diagnostics

Join us on April 15th as we share insights into Fabry Disease and a biomarker success…

A Dispute on Rare Disease Diagnostic Offerings

CENTOGENE was amongst the first providers of diagnostic Whole Genome Sequencing (WGS) and…

An Unusual Kind of Repeat Expansion Disorder

Repeat expansions are the cause of Huntington’s disease and several forms of ataxia. The…

Diagnostic Relevance of Intronic Variants

Proper splicing of mRNA requires certain DNA sequence motifs. Since these motifs are very…

Exemplifying the Strengths of Genome Sequencing

Certain genetic variants are easily missed by Exome Sequencing (ES), but readily detected…

Utilization of CentoMD® in Scientific Settings

The interpretation of newly observed genetic variants that are suspected to cause disease…

Turning Rare Disease Networks into Knowledge

CENTOGENE’s well-recognized expertise in Gaucher disease (GD) has helped to establish a…

Genetic Cause of Impaired Neurodevelopment

Development of the nervous system is a complex process, with NEUROG1 being one out of many…

Exemplifying the High Value of CentoMD®

Rare disease research usually focuses on pathogenic genetic variants. The lack of a…

Company Newsletter

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CAMBRIDGE, Mass. and ROSTOCK, Germany and BERLIN, April 14, 2021 (GLOBE NEWSWIRE) – Centogene N.V. (Nasdaq: CNTG), a commercial-stage company focused on rare...

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CAMBRIDGE, Mass. and ROSTOCK, Germany, and BERLIN, April 8, 2021 (GLOBE NEWSWIRE) – Centogene N.V. (Nasdaq: CNTG), a commercial-stage company focused on rare...

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CAMBRIDGE, Mass. and ROSTOCK, Germany and BERLIN, March 9, 2021 (GLOBE NEWSWIRE)

  • Rostock International Parkinson's Disease (ROPAD) Study aims to characterize...
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CAMBRIDGE, Mass., USA und ROSTOCK & BERLIN, Deutschland, 04. März 2021

  • Ab nächster Woche bis zu den Pfingstferien bietet CENTOGENE den etwa 30.000 Schülern...
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CAMBRIDGE, Mass., USA und ROSTOCK & BERLIN, Deutschland, 22. Februar 2021

  • Epidemiologische Studie verfolgt das Ziel, das spezifische...
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Virtuelle Konferenz und -Filmfestival 2021 am 28. Februar 2021

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Virtual Conference and Filmfestival on February 28, 2021

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CAMBRIDGE, Mass., USA und ROSTOCK & BERLIN, Deutschland, 16. Februar 2021

  • Im Zuge der aufgetretenen SARS-CoV-2 Mutationen aus Großbritannien und Südafrika hat...
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