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Interview with Alastair Greystoke, Senior Lecturer & Honorary Consultant, Newcastle Hospitals Trust

Alastair Greystoke joined Newcastle University and the Northern Centre for Cancer Care, in Newcastle upon Tyne, UK, in 2014 after […]

Interview with CRUK: Promises and pitfalls of precision medicine clinical trials

Ahead of our virtual panel discussion on the promises and pitfalls of precision medicine trials: now and in the future […]

Interview with Derek Burke, Regional Manager at WekaIO

Derek Burke has sixteen years’ experience in scale-out computing, introducing new technologies across Europe. He has previously held the VP […]

Interview with Jeanette Mostert, Radboud University Medical Center

Jeanette Mostert (PhD) is science dissemination manager at the department of genetics of the Radboud University Hospital Medical Center in […]

Interview with Seven Bridges: Bill Moss, CEO and Brandi Davis- Dusenbery, CSO tell us what the future holds for Big Data

Data is more than just a hot topic; everyone is focusing on how they can better gather, handle and manipulate […]

Opinion: Genomics education should be introduced earlier in the curriculum. An interview with Lisa Mullan

We caught up with Lisa Mullan (creator of Dinky Amigos, lovable characters that aim to teach a young audience about […]

“Our geneticist could only find three published articles about the GRIN1 gene at the time” – Interview with Jillian Hastings Ward, Chair of the Participant Panel at Genomics England

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.

Interview with Dr Luigi Grassi, Informatics Scientist, AstraZeneca

I’m Luigi Grassi and I’m an Informatics Scientist at AstraZeneca. I’m responsible for designing and performing bioinformatical analyses of the […]

Providing Information And Support to Families Affected by Rare Genetic Diseases – Interview with Arti Patel, Unique

Arti Patel is an Information Officer at Unique, where she acts as the first point of contact on the helpline […]

“Usually, you’re relatively alone in your rare disease community” – Interview with Shelley Simmonds, Patient Advocate for rare diseases

Shelley Simmonds is a patient advocate whose son has Duchenne muscular dystrophy. Duchenne causes muscle weakening and wasting and is […]