Webinar Replay: The Power of Knowing Early - Genomic Screening for Newborns
- aneeshhiremath3
- Oct 12
- 2 min read
Updated: Oct 12
Date: Sunday, 12th October 2025 Speaker: Dr. Bani Jolly, Section Head (R&D, Genome Informatics) and Senior Scientist, Karkinos Healthcare
Every healthy beginning deserves a deeper look
Every year, thousands of babies are born appearing perfectly healthy - yet silently carry genetic conditions that may not show up until months or even years later. By the time symptoms appear, the crucial windows for early brain and body development may already have closed.
Genomic newborn screening has the power to change that story. With a single test at birth, families can uncover hidden risks early - opening doors to timely treatment, preventive care, and a healthier future.
Watch the Full Webinar Recording
(Click below to watch the session)
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In this exclusive session, Dr. Bani Jolly explains how genomics is redefining newborn health - helping clinicians and parents detect and act on genetic risks that traditional heel-prick tests might miss.
Key Takeaways from the Session
What genomic newborn screening is and why it matters
Real-life examples of conditions often missed by standard newborn screening
How early detection can protect critical developmental windows
Global progress and India’s opportunity to lead in preventive genomics
Insights from the Live Q&A with Dr. Bani
Who Should Watch
This session is valuable for:
Expecting and new parents
Pediatricians and family doctors
Genetic counselors and caregivers
Anyone passionate about proactive and preventive child healthcare
About the Expert
Dr. Bani Jolly leads the R&D and Genome Informatics division at Karkinos Healthcare and previously worked at the Council of Scientific and Industrial Research – Institute of Genomics and Integrative Biology (CSIR-IGIB).Her research focuses on genomic data interpretation, molecular diagnostics, and bringing advanced genomics closer to real-world healthcare.
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