Sveriges mest populära poddar

The Genetics Podcast

Vetenskap Naturvetenskap

EP 16 Policy Development and Patient Engagement for Rare Disease with Alistair Kent

1 tim 8 min•6 september 2019

This week on our podcast, we speak to Alastair Kent, a world leader in policy development and patient engagement for rare disease. In this episode, we discuss how research is changing in rare conditions and what part DNA sequencing and data sharing are playing in this.

Fler avsnitt av The Genetics Podcast

EP 233: Unlocking early detection in liver disease with data and genetics with Tim Jobson of Predictive Health Intelligence

2 apr.•33 min

EP 232: How ethics and law shape reproductive technology and AI in medicine with Glenn Cohen of Harvard Law School

26 mars•24 min

EP 231: From polygenic scores to AI-driven medicine with Andrea Ganna of the Institute for Molecular Medicine Finland

19 mars•36 min

EP 230: From short reads to long reads in clinical genomics with Anna Lindstrand of Karolinska Institute

12 mars•40 min

EP 229: Turning personal tragedy into a movement for preventive genetics with Matthew Goldstein of jscreen

5 mars•40 min

EP 228: What genomes reveal about Epstein–Barr virus and human disease with Ryan Dhindsa and Caleb Lareau

26 feb.•46 min

EP 227: Discovering a new neurodevelopmental syndrome in the non-coding genome with Nicky Whiffin of the University of Oxford

19 feb.•43 min

EP 226: Scaling AAV gene therapy: Engineering delivery, safety, and cost with David Dismuke of Forge Biologics and Steven Gray of UT Southwestern

12 feb.•39 min

EP 225: Lessons from 20 years of building ocular gene therapies with Daniel Chung of Beacon Therapeutics

5 feb.•37 min

EP 224: Genomic newborn screening in Australia: From pilot studies to population-scale programs with Zornitza Stark of the University of Melbourne

29 jan.•44 min

The Genetics Podcast med Sano Genetics finns tillgänglig på flera plattformar. Informationen på denna sida kommer från offentliga podd-flöden.