Vinod Scaria
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vinodscaria.bsky.social
Vinod Scaria
@vinodscaria.bsky.social
Scientist, Former Doctor , Technology Enthusiast .
#RareDisease #Oncology #PopulationGenomics #Genomics4All
https://vinodscaria.genomes.in
February 2, 2026 at 3:07 PM
February 2, 2026 at 3:19 AM
It was a pleasure speaking on Decoding Molecular Pathology at the Dr M. Krishnan Nair International Clinical Oncology Symposium (MKN ICOS) on Lung Cancer organised by Regional Cancer Centre, Thiruvananthapuram
January 30, 2026 at 3:17 PM
Imagine doing everything “right.” You eat reasonably well, you stay active, you don’t smoke. And yet, your cholesterol stays stubbornly high—sometimes very high. For many people, this isn’t about willpower or lifestyle. It’s about genetics.

geknowmics.karkinos.in/2026/01/22/t...
January 22, 2026 at 4:04 PM
Wellness DNA tests have become incredibly popular. With a simple saliva sample, you can receive reports that claim to reveal everything from your ideal diet to your fitness “type,” vitamin needs, and even some health risks.

geknowmics.karkinos.in/2026/01/20/w...
January 20, 2026 at 11:59 AM
Today, something remarkable is happening in hospitals and clinics around the world: doctors can read nearly all of a person’s genetic instruction manual in days or sometimes even hours.

geknowmics.karkinos.in/2026/01/19/t...
January 19, 2026 at 7:26 PM
What Is Carrier Screening and Who Should Consider It?
A carrier is usually healthy and has no symptoms, but can still pass a non-working gene copy to their child. Read more at geknowmics.karkinos.in/2026/01/16/w...
January 16, 2026 at 3:13 PM
How Whole Genome Sequencing Could Change Preventive Healthcare for Everyone share.google/rBpwg9HXywlm...
January 16, 2026 at 2:15 AM
What is a “Variant of Uncertain Significance (VUS)”—and What Should You Do About It? – Geknowmics share.google/e2trmPJ2Jqyj...
January 14, 2026 at 3:13 PM
Pharmacogenomics is the study of how your genes affect the way your body responds to medicines. In simple terms, it helps explain why the same drug can work well for one person, cause side effects in another, and do very little for someone else.

geknowmics.karkinos.in/2026/01/13/w...
January 13, 2026 at 4:47 PM
Whole genome sequencing now costs less than a smartphone, reads 3B letters, and flags disease risk years early. Surprise: your DNA is stable—medicine isn’t.
January 11, 2026 at 7:10 AM
Whole Genome Sequencing benefits everyone.
It uncovers genetic risks, predicts treatment responses, and enables evidence-based prevention. More than a test, it is a once-in-a-lifetime resource that can guide truly personalized care across your entire lifespan.
January 1, 2026 at 2:51 AM
December 23, 2025 at 6:29 PM
It was a pleasure speaking on #Pharmacogenomics at the #PrecisionMedicine symposium at AIG Hospitals, Hyderabad

#genomics #wholegenomesequencing #precisionmedicine
October 24, 2025 at 5:48 PM
Memories from the session in September on Converging Genetics - What , Why and When of #WholeGenomeSequencing at Galle Medical College organised by Galle Medical Association.
Thanks Dr. Lahiru Prabodha for the invitation and the memorable event.
October 21, 2025 at 5:42 PM
Preparedness is not about predicting the future, but being ready for it in every form.
October 20, 2025 at 7:29 PM
October 18, 2025 at 9:14 AM
Reposted by Vinod Scaria
Read the latest Editorial published in TCRT
@tcrtcancer.bsky.social - The Bharat Cancer Genome Atlas: Charting India's Unique Cancer Landscape for Precision Oncology
journals.sagepub.com/doi/10.1177/...

@vinodscaria.bsky.social @karkinoshealth.bsky.social

#CancerGenomics #PrecisionOncology
Sage Journals: Discover world-class research
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journals.sagepub.com
September 22, 2025 at 11:39 AM
Yesterday, I had the pleasure of taking a workshop on Clinical Genomics and Genetic Variant Interpretation, empowering clinicians and residents with the latest genomics insights.
It is indeed exciting times for genomics in healthcare #GenomicsInMedicine #midtermPHOCON2025
August 1, 2025 at 9:25 PM
A Healthier Start: Making A Case for Genomic Newborn Screening in India
sciencechronicle.in/2025/07/14/a...
Making A Case for Genomic Newborn Screening in India
Almost 1 in 250 children born each year in India has a treatable genetic disease. Genetic screening at birth is nonexistent in public healthcare system
sciencechronicle.in
July 14, 2025 at 1:29 PM
July 12, 2025 at 4:42 AM
Chemotherapy is a double edged sword and while effective against a number of cancers, and often the first line of therapy in many, can cause significant genetic mutations in healthy cells, and sometimes increased risk of new cancers over a long time.
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July 8, 2025 at 6:53 PM
Whole-genome sequencing of 2,762 Indians has unravelled the layers of ancestry, high intermixing with Neanderthals and Denisovans. This along with high endogamy in India could potentially result in harmful mutations in some groups.

share.google/EzZEcHF47IdT...
June 28, 2025 at 10:08 AM
💔 New research from the All of Us Program reveals that 1.2% of South Asians carry key cardiomyopathy gene variants and this is almost 50% more than the frequency in people with European or African ancestry and more than double the frequency in people with East Asian ancestry
May 30, 2025 at 7:11 PM
It is time for Genomics in Chronic Kidney Disease
April 5, 2025 at 4:10 PM