Although Kay Parkinson is officially retired, she volunteers at the Rare Disease Nurse Network where she is the Founder and […]
When a child is born, they typically undergo routine screening to check that they are healthy. In most countries, this […]
In the latest episode of the Genetics Unzipped podcast, the team explore the life and work of D’Arcy Wentworth Thompson […]
Below, we have summarised some of the latest news and research across the genomics space – enjoy! Top stories from […]
A world-first scientific study has shown that whole-genome sequencing (WGS) improves diagnosis of rare diseases and shortens diagnostic journeys for […]
Alexis Stutzman (Founder, BIG) and Markia Smith (President BIG) are both PhD candidates at UNC Chapel Hill. Not only are […]
In a recent genome-wide meta-analysis, researchers identified six sequence variants that confer risk of vertigo. The inner ear and vertigo […]
Mahsa Shabani is an Assistant Professor in Privacy Law at the Faculty of Law and Criminology, Ghent University in Belgium. […]
Michael Friend is the co-founder and CEO of the Minority Coalition for Precision Medicine, which aims to eradicate health disparities […]
Karen Massel is a Postdoctoral Research Fellow at the Centre for Crop Science at the University of Queensland, Australia. Massel’s […]
