Welcome to the Centre for Personalised Medicine podcast, where we explore the promises and pitfalls of personalised medicine and ask questions about the ethical and societal challenges it creates. The Centre for Personalised Medicine is a partnership between the University of Oxford’s Wellcome Centre for Human Genetics and St Anne’s College, Oxford. It is a communication, engagement and research vehicle for students, academics, clinicians, the public and policy makers to explore the benefits ...
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Series 2 Episode 8 - Navigating a genetic diagnosis
16:58
16:58
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16:58
What might it be like to navigate a genetic diagnosis and share it with family members? We talk to Julie Young from the CanGene CanVar patient reference panel about her experience.Kirjoittanut Rachel Horton, Gabrielle Samuel, Julie Young
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Series 2 Episode 7 - Why research regulation falls short in genomic medicine
20:49
20:49
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20:49
As a society, we tend to focus a lot on risk and try to control it through regulation - but how well does that work for ensuring ethical practice in genomics? We talk to Dr Kate Lyle about her research on this topic.Kirjoittanut Rachel Horton, Gabrielle Samuel, Kate Lyle
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Series 2 Episode 6 - Diversifying genomics
18:14
18:14
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18:14
What are the ethical challenges with diversifying genomic data? We talk to Faranak Hardcastle about her work exploring this.Kirjoittanut Rachel Horton, Gabrielle Samuel, Faranak Hardcastle
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Series 2 Episode 5 - Who's 'the patient' in genomic medicine?
18:09
18:09
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18:09
We live our lives alongside others, and our decisions have consequences for those close to us - what does this mean for how we define 'the patient' in genomic medicine? Susie Weller talks to us about this issue.Kirjoittanut Rachel Horton, Gabrielle Samuel, Susie Weller
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Series 2 Episode 4 - Newborn genome screening
19:02
19:02
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19:02
What sort of findings might we get from newborn genome screening? What might this mean for the NHS? Rachel Horton talks to Gabby Samuel and Lisa Ballard.Kirjoittanut Rachel Horton, Gabrielle Samuel, Lisa Ballard
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Series 2 Episode 3 - Sharing genetic results within families
26:36
26:36
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26:36
Who does a genetic result belong to? What might help people to share genetic information with their relatives? We talk to Lisa Ballard and Anneke Lucassen.Kirjoittanut Rachel Horton, Gabrielle Samuel, Lisa Ballard, Anneke Lucassen
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Series 2 Episode 2 - Why context matters in genetic testing
14:46
14:46
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14:46
How can the same genetic finding can mean different things in different people? What does this mean for 'personalising' genetic results? Anneke Lucassen talks to us about this issue.Kirjoittanut Rachel Horton, Gabrielle Samuel, Anneke Lucassen
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Series 2 Episode 1 - The environmental cost of personalised medicine
14:39
14:39
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14:39
How does personalised medicine impact on the environment? What does this mean for how we should collect and store data? Gabrielle Samuel talks to us about these issues. A transcript of this episode is available at https://media.podcasts.ox.ac.uk/medsci/cpm/2022-06-15-medsci-cpm-s2-ep-1.pdfKirjoittanut Rachel Horton, Gabrielle Samuel, Susie Weller
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Series 1 Episode 2 - Meet the Advisory Board: Dame Mary Archer
32:05
32:05
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32:05
In the second episode of the Meet the Advisory Board Series we talked to Dame Mary Archer about personalised medicine in practice, her academic career and her plethora of other roles she has held and is holding at the moment. This interview was created by the Centre for Personalised Medicine (CPM), a partnership between University of Oxford’s Wellc…
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Series 1 Episode 1 - Meet the Advisory Board: Dr Magdalena Skipper
40:19
40:19
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40:19
In the first episode of the Meet the Advisory Board Series we talked to Dr Magdalena Skipper to find out about her remarkable career in academia, science publishing and her views on personalised medicine. This interview was created by the Centre for Personalised Medicine (CPM), a partnership between University of Oxford’s Wellcome Centre for Human …
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