Genetic Tests

Discover your genetic secrets with expertise at IntroLab.

IntroLab is at the forefront of genetic testing, providing accurate genes, chromosomes, and protein analyses. Genetic tests are crucial for detecting hereditary diseases, assessing disease risks, and guiding treatment options. They also offer insights into your genetic ancestry. Utilizing cutting-edge technology, our experienced team ensures precision and reliability in every test. Whether for risk assessment, chronic disease management, or exploring your genetic heritage, IntroLab is committed to offering top-notch services. We empower individuals with essential genetic information, aiding in informed health decisions. Trust IntroLab for comprehensive and dependable genetic testing tailored to your unique health needs.

A lab technician conducting genetic tests
Explore your genetic heritage with precision through genetic analyses at IntroLab.

Types of genetic tests

Various genetic tests are available, each tailored to specific goals and information requirements. Key types include:

  • Single gene test: Targets a specific gene linked to a disease, like the BRCA gene, for breast or ovarian cancer risk.
  • Gene panel test: Examines multiple genes simultaneously, identifying those associated with certain diseases or conditions.
  • Whole Genome Sequencing (WGS): Analyzes all 3 billion base pairs in the human genome, detecting various genetic variations linked to diseases.
  • Whole Exome Sequencing (WES): Focuses on about 1.5% of the genome, specifically the exomes (exons), protein-coding regions often associated with genetic disorders.
  • Chromosome or cytogenetic test: Studies chromosome structure and number to identify conditions like Down syndrome.
  • Mitochondrial DNA test: Investigates variations in mitochondrial DNA, crucial for diagnosing certain inherited disorders.
  • Pharmacogenomic test: Assesses how genetic makeup influences drug response, aiding in personalized treatment.
  • Thrombophilia factor test: Analyzes common genetic mutations that increase the risk of thrombophilia, a condition characterized by an elevated propensity for blood clot formation.
  • Prenatal and postnatal genetic tests: Used to detect genetic disorders in fetuses and newborns.

The choice of test depends on individual needs, health status, and medical history. Consulting with a doctor or geneticist is recommended to determine the most appropriate test for you.

Who benefits from genetic testing?

At our Belgrade laboratory, we offer genetic testing for diverse needs. These tests are ideal for identifying hereditary disease genes or understanding their personal disease risk. Essential for health insights, these tests can influence medication responses and aid in chronic disease management. They are also crucial in prenatal diagnosis and oncology. Our expert team is committed to guiding and supporting you through your genetic testing journey, no matter your specific requirements.

Understanding the process of genetic testing

The procedure typically involves collecting a blood sample, although swabs or specific tissues can also be used depending on the test. This initial step is both quick and straightforward. DNA is isolated from the sample following collection, and a series of specialized tests are performed to identify genetic variations or mutations. These tests employ advanced technologies like next-generation sequencing for accuracy and detail. After the analysis, results are carefully interpreted, considering medical history and other relevant information. A comprehensive report is then prepared and sent to the consulting physician, who will discuss the findings and advise on subsequent steps.

Genetic test results timeline

The turnaround time for genetic test results typically ranges from 2 to 4 weeks. This allows for a thorough analysis of your sample, ensuring the highest accuracy in the results.

Revolutionizing preventive medicine with genetic testing

Genetic testing is a game-changer in preventive healthcare, offering tailored care based on individual genetic profiles. By pinpointing gene mutations linked to increased risks of diseases such as heart disease, cancer, and diabetes, we enable proactive health management. This approach not only elevates the standard of healthcare but also plays a crucial role in enhancing disease prevention and improving patients’ quality of life. These tests lay the groundwork for customized preventive health strategies, adapting care to each person’s unique genetic blueprint

Genetic testin- A cornerstone of personalized medicine

Genetic testing is vital in shaping personalized medicine, a healthcare model that tailors treatment to each person’s unique genetic makeup. By analyzing DNA, these tests reveal specific genetic variations that influence individual responses to medications and therapies. With this precise information, healthcare providers can customize treatments, significantly enhancing their effectiveness and safety and elevating the standard of patient care. Genetic analyses have thus become crucial in modern medicine, enabling more focused and efficient healthcare strategies.

Genetics and mental health

Emerging studies consistently underscore the significant role of genetics in a range of mental health conditions. By examining gene variations and mutations, genetic testing provides valuable insights into an individual’s predisposition to these disorders, facilitating the selection of the most appropriate and effective treatments.

The role of nutrigenomics in genetic tests

Understanding and managing mental disorders like depression, schizophrenia, and bipolar disorder is significantly enhanced by recognizing the crucial role of genetics. Through detailed gene analysis, it’s possible to identify specific genetic markers that may increase susceptibility to these conditions. This critical information not only aids in assessing individual risk but also plays a pivotal role in customizing treatment approaches. Medical professionals can more accurately determine the most beneficial treatment strategies by utilizing genetic insights, thereby reducing potential side effects and optimizing treatment outcomes.

Pharmacogenomics and genetic testing

Pharmacogenomics is a vital component of personalized medicine, examining the influence of a patient’s genetic makeup on their response to medications. By conducting genetic testing, it’s possible to uncover gene variations that can affect treatment effectiveness and safety. Armed with this information, healthcare professionals can tailor therapies to align with the genetic profile of each patient. This personalized approach not only boosts the efficacy of treatments but also minimizes the risk of adverse reactions. Therefore, these tests are instrumental in ensuring each patient receives the safest and most effective medication, significantly advancing the quality of healthcare provided.

Why choose IntroLab for genetic tests?

IntroLab stands out with its advanced technology and expert interpretation of genetic testing results. Our team, anchored by a leading geneticist, prioritizes a tailored approach to each patient, ensuring the highest standards of privacy and confidentiality. We’re dedicated to delivering superior genetic analysis services. Our mission is to provide patients with detailed, accurate, and easily understandable genetic profiles. Catering to a range of needs, from early disease detection and personalized medicine to reproductive, mental health, nutrigenomics, and pharmacogenomics, IntroLab is committed to offering dependable genetic testing that enhances your understanding of health and supports sound healthcare decisions. Contact us for more information and discover why IntroLab is the esteemed choice for genetic testing.



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