Clinical insights, updates, and learning from Genetico
A curated collection of videos, articles, and clinical updates from Genetico's work in rare and genetic diseases. Built for clinicians, researchers, and healthcare teams.
28:34Arjun Gupta sat down with Amar Ujala Limited's startup show, 𝐿𝑒𝑡'𝑠 𝑆𝑡𝑎𝑟𝑡, to talk through it. Sincere thanks to the 𝐀𝐦𝐚𝐫 𝐔𝐣𝐚𝐥𝐚 team for the conversation and for putting rare disease innovation in front of a wider audience.
InnovationAmar UjalaInterview
Global Rare Disease Summit · Geneva
EVENT
Keynote and Q&A on policy frameworks, technology stack, and cross-institutional data sharing for LMICs.
RESEARCH
Panel discussion on rare disease burden, registry development, and AI-assisted clinical tools across five Indian states.
ISHG Annual Conference
Clinical
Fragmented records and inconsistent capture slow rare disease diagnosis. Structured genomic workflows are helping referral centers move from suspicion to actionable reports faster.
Policy
India's national rare disease framework created momentum. The next challenge is turning policy intent into registries that clinicians, researchers, and public health teams can actually use.
Research
AI tools can accelerate variant triage, but clinical teams still need transparency, override paths, and workflow fit. Here is a practical framing for adoption in diagnostic labs.
Get the latest clinical insights, research updates, and product developments in genetic and rare disease diagnosis.
