Researchers from the University of Melbourne and Murdoch Children's Research Institute (MCRI) have developed a blood test capable of rapidly diagnosing rare genetic diseases in babies and children, ...

Learn how gene editing is transforming sickle cell disease treatment and why expanding access to younger children matters.

The era of genetic medicines has ushered in novel and exciting ways of treating genetic diseases, one of which includes bringing to reality the promise of a one-time treatment by addressing the root ...

A new, rapid testing method will greatly help the diagnosis of rare diseases in babies and children, according to research presented to the annual conference of the European Society of Human Genetics.

Researchers have identify a set of biomarkers that could someday make it easy to spot the disease in a patient's blood sample. Parkinson's disease is best known for its effects on the central nervous ...

Add Yahoo as a preferred source to see more of our stories on Google. In a major leap for genetic diagnostics, scientists from the University of Melbourne and the Murdoch Children's Research Institute ...

In a global breakthrough published in Nature Genetics, researchers have successfully mapped the cells and genes that regulate ...

Noncancerous blood disorders are conditions that affect blood cells, such as red blood cells, white blood cells, and platelets. Blood disorders may cause symptoms and complications, but most are ...

This article is authored by Venkataswamy Eswarachari, associate vice president and senior director, Lab Operations, MedGenome ...