For my undergraduate research project, I studied a rare neurological disease known as Landau-Kleffner Syndrome. It was then that I […]
October is Breast Cancer Awareness month and on Friday (23rd October) charities are encouraging individuals to wear pink to raise […]
Don’t worry! We are back again for the second week bringing you the latest genomics updates over the past week. […]
In the latest episode of the Genetics Society’s ‘Genetics Unzipped’ podcast, Geneticist Dr Kat Arney takes a look at the […]
In this episode of the Genetics Unzipped podcast, supported by the UK Medical Research Council, Kat Arney and stay-at-home roving […]
Ahead of our virtual panel discussion on the promises and pitfalls of precision medicine trials: now and in the future […]
Jillian Hastings Ward is Chair of the Participant Panel at Genomics England. The Panel acts as an advisory body to the Genomics England board to ensure that the data collected by the 100,000 Genomes Project is being used for the best interests of the participants.
Arti Patel is an Information Officer at Unique, where she acts as the first point of contact on the helpline […]
Shelley Simmonds is a patient advocate whose son has Duchenne muscular dystrophy. Duchenne causes muscle weakening and wasting and is […]
Rory Collins, Principal Investigator and Chief Executive of UK Biobank leads this landmark project. We talk to him about some of the research outcomes from UK Biobank, and why he’s excited to be speaking at the Festival of Genomics this January.
