NCGM Global

01/03/2026

Your kidneys work silently — regular screening helps protect them.
This Kidney Cancer Awareness Month, choose early detection and stay one step ahead.

28/02/2026

Rare Disease Day is a day to celebrate the remarkable individuals, families, caregivers, and healthcare professionals who tirelessly advocate for those impacted by rare conditions.

25/02/2026

Your pregnancy deserves clarity, confidence, and care.
Because every pregnancy is precious, early and accurate screening makes all the difference.

21/02/2026

Early detection can make all the difference.

Introducing NeuOnco & NeuOncoPlus – Comprehensive Cancer Screening Packages designed for proactive health monitoring and early risk detection. Because when it comes to cancer, timely screening saves lives.

18/02/2026

Your baby’s first test could protect their entire future.

Newborn Screening helps detect silent genetic and metabolic disorders early — when treatment makes the biggest difference. Because when it comes to your baby’s health, early action matters.

To consult our team of expert doctors and genetic counselors, Call us on +91 6357244307.

15/02/2026

Early detection is key to fighting childhood cancer. Know the symptoms, raise awareness, and help save lives. Every second counts.

17/01/2026

We are looking for a Junior Genetic Counselor to join our personalized genomics team.
Apply now to be part of a team advancing individualized healthcare through genomics.

17/01/2026

Every pregnancy begins with a decision—to be informed.
From the 10th week onwards, access trusted insights about your baby’s health and development with expert genetic guidance.

16/01/2026

Early detection through regular screening can save lives.
Stay informed, choose timely screening, and take control of your cervical health.

15/01/2026

Your future can change with one informed choice—awareness.
Knowing the signs, understanding risks, and choosing the right test can lead to early detection and better outcomes.

10/12/2025

Neuberg Center for Genomic Medicine participated in the 10th Annual Conference of the Society for the Indian Academy of Medical Genetics (IAMG) 2025. We extend our sincere thanks to the organisers for providing such a valuable platform to engage with experts and specialists from across the field.
Dr Sheetal Sharda, Director- Genomics Development and Implementation, delivered an oral presentation titled “Molecular cytogenetic characterization and genotype–phenotype analysis in 20 patients with copy number variants involving chromosome 8.”
Dr Ashka Prajapati, Consultant Clinical Geneticist, presented a poster on “Evaluating reasons for discordance between manual and automated variant classification in NGS-based testing for inherited disorders: a single-centre pilot study of 50 discordant variants,” which was well received.
Here are a few glimpses from the event.

27/11/2025