Vinod Scaria (@vinodscaria) 's Twitter Profile
Vinod Scaria

@vinodscaria

Scientist | Former Doctor | Passionate about Genomics in Clinical Medicine #Genomics4Everyone | Occassional #MysteryDisease tracker
| Views are personal

ID: 131401138

linkhttp://vinodscaria.genomes.in calendar_today10-04-2010 04:36:59

6,6K Tweet

11,11K Followers

3,3K Following

R. Prasad (@rprasad12) 's Twitter Profile Photo

If seven Indian universities were among the 17 that belonged to the red flag category initially, as per current data based on 1,500 most-publishing universities, the number of Indian universities in the red flag category has swelled to 32 sciencechronicle.in/2025/06/12/a-r…

Vinod Scaria (@vinodscaria) 's Twitter Profile Photo

Some Indian universities are gaming publication metrics and the numbers have grown over years. R. Prasad writes in #ScienceChronicle sciencechronicle.in/2025/06/12/a-r…

Vinod Scaria (@vinodscaria) 's Twitter Profile Photo

▶️ Still testing only some patients with cancer for inherited genetic variants ? 🔍 1 in 10 cancer patients has a heritable mutation. Yet most never get tested. Is it time to change ?

▶️ Still testing only some patients with cancer for inherited genetic variants ?
🔍 1 in 10 cancer patients has a heritable mutation.
Yet most never get tested.
Is it time to change ?
Vinod Scaria (@vinodscaria) 's Twitter Profile Photo

Eligible residents of #Singapore will be able to access subsidized genetic testing for #familialhypercholesterolemia (FH), a genetic condition causing high #cholesterol levels, as part of a national initiative launching June 30.

Eligible residents of #Singapore will be able to access subsidized genetic testing for #familialhypercholesterolemia (FH), a genetic condition causing high #cholesterol levels, as part of a national initiative launching June 30.
Vinod Scaria (@vinodscaria) 's Twitter Profile Photo

A study showed Whole Genome Sequencing has superior diagnostic power for #RareDisease . It found causative variants in 43% of cases, with over 1/5th attributed to technically challenging variants which are often missed by standard genetic tests. cell.com/hgg-advances/f…

A study showed Whole Genome Sequencing has superior diagnostic power for #RareDisease . It found causative variants in 43% of cases, with over 1/5th attributed to technically challenging variants which are often missed by standard genetic tests. cell.com/hgg-advances/f…
Vinod Scaria (@vinodscaria) 's Twitter Profile Photo

Some news are more heartening than others. In a first, Princess Máxima Center for pediatric oncology will perform Whole Genome Sequencing of every newly admitted child before the start of their treatment.

Some news are more heartening than others.
In a first, Princess Máxima Center for pediatric oncology will perform Whole Genome Sequencing of every newly admitted child before the start of their treatment.
Vinod Scaria (@vinodscaria) 's Twitter Profile Photo

Every newborn baby in England will have their #wholegenomesequence to assess their risk of hundreds of diseases, under NHS plans for the next 10 years. bbc.com/news/articles/…

Every newborn baby in England will have their #wholegenomesequence  to assess their risk of hundreds of diseases, under NHS plans for the next 10 years. 
bbc.com/news/articles/…