News

Scientists identify four distinct autism subtypes with unique genetic and clinical traits, reshaping personalized diagnosis ...
A new study has traced the genetic roots of several rare and complex disorders to mutations in a single critical gene: IKBKG, ...
Bedford has Schwartz-Jampel syndrome. It's a rare genetic disorder with just 150 cases reported across the world, his parents ...
Sparked by mysterious symptoms in a young girl, the discovery reveals the power of global collaboration and digital-age data ...
Scientists have corrected gene mutations in mice causing an ultra-rare disease by editing DNA directly in the brain with a single injection, a feat with profound implications for patients with ...
Mutations in the HNF1A gene impair insulin secretion by disrupting hundreds of genes in β‑cells and causing RNA splicing ...
A team from UC San Diego, John Hopkins and UC Berkeley Universities found a way to edit a single gene in a mosquito that ...
Ocugen says it is on track to reshape the market for gene therapies against eye disorders over the next three years, by ...
A new study reveals four distinct autism subtypes, each with unique traits and genetic patterns—reshaping how we understand, ...
August 01, 2025 - The increasing prevalence of chronic and genetic diseases is a major factor driving revenue growth in the gene expression analysis ...
Neurodegenerative disorders, including Alzheimer's disease, Parkinson's disease, and Amyotrophic Lateral Sclerosis, constitute a primary global health ...
Meet 12 biotech companies with promising genetic disease therapies that successfully closed funding rounds recently.