STAY TOGETHER AND HEALTHY
ACCREDITED LABORATORY
All analyses are performed in our own accredited laboratory.
THE WIDEST RANGE OF TESTS AND ANALYSES
Extensive portfolio of tests and analyses offered.
CONTRACTS WITH ALL HEALTH INSURANCE COMPANIES
Tests recommended by a physician are covered by public health insurance.
COMPREHENSIVE SERVICES IN ONE PLACE
Consultation with a clinical geneticist for selected analyses.
AVAILABLE TO EVERYONE, FROM ANYWHERE
You can take the DNA sample yourself from the comfort of your own home.
ACCREDITED OUTPATIENT CLINIC
We are accredited for medical education in the field of genetics.
MOST DEMANDED TESTS
Predictive genetics can use DNA analysis to detect innate predispositions to inherited diseases. By identifying the hereditary cause of a health risk, appropriate prevention can be initiated in time to minimize potential health complications. Genetics is the most advanced yet easily accessible tool in health care.
WHY GHC GENETICS IS THE BEST CHOICE
We are one of the few facilities in the Czech Republic that perform complex genetic analyses in their own accredited laboratory. We don't send DNA samples to any third party, they're perfectly safe with us. If a positive result is detected, it is essential to consult a doctor or geneticist who will explain the results of the analysis in detail and help to set up appropriate measures.
80+ TESTS
Our portfolio of analyses consists of more than 80 tests in various areas that are available to anyone. Each test can be taken at your own discretion or on the advice of your physician.
6,300 CONSULTATIONS
Each year, our doctors provide thousands of genetic consultations and advisory opinions. Whether to help you choose the right test for you or to provide information and recommendations specifically for you.
1,400 PHYSICIANS
We cooperate with major teaching hospitals and physicians across the Czech Republic, through which we provide the general public with the opportunity to use genetic tests and analyses for diagnosis and prevention.
OVER 15 YEARS OF EXPERIENCE
The GHC Genetics laboratory has been performing molecular genetic analyses since 2007. At that time, it was one of the first on the market to make genetic testing available to the general public. It is equipped with state-of-the-art equipment, uses the latest technology and has established a highly professional environment with its own medical team. Thanks to this, we are able to provide comprehensive services of the highest quality in one place, ensuring maximum comfort for our clients. We are constantly educating ourselves and following new developments in the industry, continuously upgrading our laboratory equipment, expanding our portfolio of services and, last but not least, listening to the needs of our clients.
What is predictive genetics?
It is a relatively young, but rapidly developing medical field, which was created on the basis of the decoding of the human genome in 2003, as part of the Human Genome Project. Predictive genetics combines genetics with preventive medicine, where the analysis of DNA samples can reveal the predispositions for a number of civilisational diseases and inherited diseases. This allows the necessary preventive measures to be set up and the onset of disease to be prevented in time. In addition, the body's ability to metabolize certain harmful substances or drugs, food intolerances and gene mutations that increase the risk of cardiovascular or cancer diseases, and many others can be detected. Having a predisposition or a predisposition to a disease does not mean that you have the disease or that you are certain to develop it in the future. The development of a disease is influenced by many factors. In addition to the genetic code, there are also external factors, including lifestyle and environment, dietary habits, stress and others. Therefore, an integral part of a predictive genetic analysis is a consultation with a physician and a personalized set of recommendations on what measures to take in case of a positive result and how to effectively prevent the risks of developing the disease.
HOW DOES THE WHOLE PROCESS WORK?
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Sample collection
A sample of your DNA is most often obtained through an oral swab or blood collection.3
Analysis
Our team of experienced experts will use the latest methods and technologies to analyse the sample.4
Result
After the test has been evaluated, you will receive a detailed and easy-to-understand laboratory report, or a consultation with a clinical geneticist will be recommended.News from the world of GHC Genetics
Thanks to GHC Genetics, the ‘Plešouni’ are now adorning the corridors of the paediatric oncology ward in Motol
On Friday 28 August at 12.00, the grand opening of the newly refurbished corridor at the Department of Paediatric Haematology and Oncology (Motol and Homolka University Hospital, Motol site, 5th floor) took place. The new design of the space was created as part of the Plešouni project, conceived by the artist Eliška Soffer Podzimek, and will now bring a world full of colour, imagination and joy to young patients and their loved ones. The event took place with the significant support of GHC Genetics, which has been providing long-term financial backing for the entire Plešouni project.
01. 09. 2026
The latest issue of GHC Genetics magazine (3/2026) has been published
Dear readers,
The latest issue of GHC Genetics magazine offers a look at the diverse fields of modern medicine in which genetics is finding ever-wider application. In an interview with our colleague Tereza Lackner, we take a look behind the scenes at healthcare reporting and communication with health insurers. Although this is an area that often remains hidden from patients, its proper functioning is an essential part of the day-to-day running of a healthcare facility. The specialist section of the magazine focuses on the genetic links in addiction medicine and the issue of co-occurring disorders, where current findings in the fields of genomics and epigenetics are opening up new possibilities for personalised care. There is also a case report by Dr Kristýna Kroupová focusing on Stickler syndrome, which highlights the importance of interdisciplinary collaboration and the benefits of modern genetic diagnostics in identifying rare hereditary diseases. We also present an article on polycystic kidney disease, which emphasises that clinical diagnosis alone may not be sufficient and that molecular genetic testing plays a crucial role in determining the prognosis and in the care of other family members. We hope you find this issue inspiring.
26. 08. 2026
Two scholarly articles from the journal *Pohybové ústrojí* featuring Dr. Veronika Krulišová
In the latest issue of the journal "Pohybové ústrojí" (Vol. 32, 2025, No. 1 | Publication date: February 28, 2026), MUDr. Veronika Krulišová, Ph.D., along with other authors, published two scientific papers related to osteogenesis imperfecta:
17. 07. 2026
GHC Genetics is among the TOP 10 genetic laboratories in Europe
Award by HealthcareTech OUTLOOK
GHC Genetics is among the top 10 ranked genetic laboratories in Europe in 2023. The ranking is announced annually by the prestigious international magazine HealthcareTech OUTLOOK.
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