A mutation in a previously unexamined Notch ligand, JAG2, is found to cause a rare form of muscular dystrophy (MD) […]
Stephen Scherer is a Canadian scientist who founded Canada’s first human genome centre, the Centre for Applied Genomics (TCAG) at […]
Dame Kay Davies is a human geneticist and Professor of Genetics at the University of Oxford. Davies has spent her […]
Another month, another genomics week in brief – full of all the latest genomics news and research from the past […]
In the latest genomics week in brief, we have summarised all of the most recent and exciting genomics news and […]
The advancements in base editing, a new genome editing approach, have generated a lot of excitement amongst scientists in recent […]
Sano Genetics, Zetta Genomics and Genomics England have partnered to develop a novel system to allow rare disease patients and […]
“Nothing about me without me!” is the rallying cry for patient involvement in research. In the latest episode of Genetics […]
Shelley Simmonds is a patient advocate whose son has Duchenne muscular dystrophy. Duchenne causes muscle weakening and wasting and is […]
