GUaRDIAN is a consortium of over 100 clinicians and researchers from over 25 medical and research centers making it one of the largest clinical genomics research networks in India
What is GUaRDIAN ?
  GUaRDIAN is a collaborative research programme towards understanding the genetic basis and molecular mechanisms underlying rare genetic disorders. We use the advanced sequencing technologies, extensive bioinformatics and animal models. Our collaborators include a large number of clinicians and scientists.

Genomics for Precision Medicine in India
Our collaborative network includes pioneers in personal genome sequencing and analysis in India, and the collaborative network brings together the enormous expertise in clinical assessment, genome sequencing, analysis and interpretation. 

Focus areas of Research and Cohorts
Our network encompasses a wide variety of clinical specialties. Our large cohorts include Dermatology, Neurological disorders, Cardiovascular Diseases, Vascular Diseases, Immune Diseases, Opthalmological/Eye Diseases and Metabolic Diseases, just to name a few. We are open to include more cohorts in collaboration with clinical groups.  Please contact us for more details.

How can we help you
If you are a Clinician or Researcher, you could collaborate with the network and participate in ongoing research initiatives. Please contact us for more details
Give to GUaRDIAN
We look forward to working with organisations to advance the cause of education, genetic testing and research. 



Pulse

  • Personal genomics in clinical medicine : it is not in the future anymore Vinod Scaria and Sridhar Sivasubbu. The decade following the International human genome sequencing initiative, which drew the blueprint of the human genome, has seen tremendous advancements that has made genomics ...
    Posted Mar 13, 2016, 3:11 AM by Vinod Scaria
Showing posts 1 - 1 of 2. View more »

Events and CME Update

  • Genomics for Clinicians / Workshop on the Concept & Application of Genomics in Clinical Medicine - Mizoram 2018 IntroductionGenomic technologies have been progressing rapidly in the recent years. Many of these advances have accelerated our understanding of human disease biology with implications in better molecular characterization of ...
    Posted Jul 11, 2018, 5:21 AM by Vinod Scaria
  • AIIMS Delhi CSIR-IGIB Joint Workshop on Exome Sequence Analysis and Interpretation Who should attend ?Faculty Members with ongoing research programmes on Whole Exome Sequencing or keen at implementing Whole Exome Sequencing in Clinical CarePostgraduate or Postdoctoral Medical StudentsMBBS Students ...
    Posted Jul 10, 2018, 9:46 PM by Vinod Scaria
  • Advances in Genetic Diagnosis of Neurological Disorders / 3MGM2018 Jointly organized by  MMM-CGSR & CSIR-IGIB September 7-9, 2018 MADRAS MEDICAL MISSION, CHENNAIFacultyDr. Vishwanathan V (Chennai) | Dr. Deepak Arjundas(Chennai) | Dr. Sunil K. Narayanan (Pondicherry) Prof ...
    Posted Jun 17, 2018, 11:46 PM by Vinod Scaria
Showing posts 1 - 3 of 14. View more »

Recent Publications

Showing posts 1 - 2 of 15. View more »
In Media 
  • 5-year-old ‘butterfly’ boy at PGI for treatment By Shimona Kanwar CHANDIGARH: A five-year-old suffering from dystrophic Epidermolysis Bullosa (EB), a painful and rare genetic skin disease, is being treated in PGI. Kids with EB are ...
    Posted Apr 13, 2018, 10:38 PM by Vinod Scaria
Showing posts 1 - 1 of 9. View more »
Interpretation of a malady: how scientists zeroed in on one family's rare and crippling disease (15th April 2017)
http://www.genomes.in/