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Institute of Genomic Medicine, Fortis Gurugram
Personalized Care. Powered by Your DNA.

The Institute of Genomic Medicine at Fortis Hospital, Gurugram, is at the forefront of precision healthcare — offering cutting-edge genetic testing, counseling, and tailored treatment plans to help you make informed health decisions. Our advanced genomic capabilities are transforming the way we detect, treat, and prevent diseases.

 

Our Vision

To integrate genomics into routine clinical care and empower individuals with personalized health solutions based on their unique genetic makeup.

 

Why Genomic Medicine?

Genomic medicine is a game-changer in modern healthcare. It helps us:

  • Identify genetic predispositions to various diseases, including cancers, heart conditions, neurological disorders, and more.
  • Predict treatment responses and guide targeted therapies.
  • Prevent hereditary conditions through early screening and intervention.
  • Provide reproductive guidance through prenatal and carrier screening.

 

Our Services

We offer a comprehensive range of genomic services, including:

  • Whole Genome & Exome Sequencing
    In-depth analysis for diagnosing rare and undiagnosed conditions.
  • Hereditary Cancer Screening
    Assessing inherited risk for breast, ovarian, colorectal, and other cancers.
  • Pharmacogenomics
    Personalized drug response testing to optimize treatment efficacy.
  • Prenatal & Newborn Screening
    Early detection of genetic disorders in infants and during pregnancy.
  • CardioGenomics & NeuroGenomics
    Specialized genetic testing for cardiovascular and neurological conditions.
  • Genetic Counseling
    Expert guidance to help patients and families understand test results and options.
  • Cancer directed genomic testing for hematology and oncology

 

Who Should Consider Genetic Testing?

  • Individuals with a family history of genetic disorders
  • Couples planning a pregnancy
  • Patients with early-onset or unexplained conditions
  • Those undergoing targeted cancer therapies
  • Anyone interested in understanding their genetic health risks

 

 

Why Choose Us

  • State-of-the-art genomic lab infrastructure
  • Multidisciplinary team of clinical geneticists, molecular biologists, counselors, and specialists
  • Clinically actionable insights integrated into your care plan
  • Ethical, empathetic, and confidential approach
  • Seamless coordination with your treating physician

Our Team of Experts

  • Dr. Shrinidhi Nathany
    CONSULTANT MOLECULAR HEMATOLOGY & ONCOLOGY
    Medical Genetics
  • Dr. Rahul Bhargava
    PRINCIPAL DIRECTOR HEMATO-ONCOLOGY
    Oncology
  • Dr. Vikas Dua
    PRINCIPAL DIRECTOR & HEAD - PEDIATRIC HEMATOLOGY, HEMATO ONCOLOGY & BONE MARROW TRANSPLANT
    Haematology
  • Dr. Nitesh Rohatgi
    SENIOR DIRECTOR MEDICAL ONCOLOGY
    Oncology
  • Dr. Ankur BAHL
    SENIOR DIRECTOR MEDICAL ONCOLOGY
    Oncology
  • Dr. Vinayak Agarwal
    SENIOR DIRECTOR & HEAD OF NON-INVASIVE CARDIOLOGY
    Cardiac Sciences
  • Dr. Praveen Gupta
    PRINCIPAL DIRECTOR NEUROLOGY
    Neurology

FAQs

  • What is genomic medicine?
    Genomic medicine is an advanced field of healthcare that uses your genetic information (DNA) to diagnose diseases, predict risk, guide treatment, and prevent future health issues. It enables truly personalized care.
  • Who should consider genetic testing?
    You may benefit from genetic testing if you: Have a family history of genetic or hereditary diseases Are diagnosed with early-onset or rare conditions Are undergoing cancer treatment Are planning a pregnancy or are pregnant Want to know your genetic risk for certain health conditions
  • What types of tests are offered at the Institute?
    We offer a wide range of genomic tests, including: Whole genome and exome sequencing Hereditary cancer screening Pharmacogenomic testing (how your body responds to medications) Prenatal and newborn genetic screening Cardiac and neurological genetic tests
  • How is the genetic test done?
    Most genetic tests require a simple blood or saliva sample. The sample is analyzed in our advanced genomics lab, and results are typically available within 2 to 4 weeks depending on the test type.
  • Will the results tell me if I have a disease?
    Not always. Some tests can confirm a diagnosis, while others assess your risk of developing a condition in the future. Our experts explain your results in detail and help you understand what they mean for your health.
  • Is genetic counseling available?
    Yes. We offer pre-test and post-test genetic counseling to help you make informed decisions. Our counselors explain the benefits, limitations, and implications of testing for you and your family.
  • Will my genetic information be kept confidential?
    Absolutely. We follow strict privacy and confidentiality guidelines. Your data is securely stored and only shared with your consent for your clinical care.
  • Does insurance cover genetic testing?
    Coverage for genetic testing varies by insurer and test type. Our team can help you understand your options and guide you through the process.
  • How do I book an appointment?
    You can call us at [Insert Phone Number] or email [Insert Email Address] to schedule a consultation or test. Online booking options may also be available through the Fortis website.
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