| Series 3 Episode 1 - What is personalised medicine? |
The CPM team discuss what we mean when we talk about personalised medicine. |
Rachel Horton, Anneke Lucassen, Susie Weller, Ali Kay, Sarah Briggs, Sally Sansom |
24 January, 2025 |
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| Extra - 2023-24: the year in review |
We discuss the highlights for the CPM in 2023-24, and look forward to the next year. |
Rachel Horton, Anneke Lucassen, Susie Weller, Padraig Dixon |
15 November, 2024 |
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| Series 2 Episode 8 - Navigating a genetic diagnosis |
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. |
Rachel Horton, Gabrielle Samuel, Julie Young |
12 June, 2023 |
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| Series 2 Episode 7 - Why research regulation falls short in genomic medicine |
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. |
Rachel Horton, Gabrielle Samuel, Kate Lyle |
2 May, 2023 |
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| Series 2 Episode 6 - Diversifying genomics |
What are the ethical challenges with diversifying genomic data? We talk to Faranak Hardcastle about her work exploring this. |
Rachel Horton, Gabrielle Samuel, Faranak Hardcastle |
7 March, 2023 |
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| Series 2 Episode 5 - Who's 'the patient' in genomic medicine? |
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. |
Rachel Horton, Gabrielle Samuel, Susie Weller |
25 January, 2023 |
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| Series 2 Episode 4 - Newborn genome screening |
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. |
Rachel Horton, Gabrielle Samuel, Lisa Ballard |
20 October, 2022 |
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| Series 2 Episode 3 - Sharing genetic results within families |
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. |
Rachel Horton, Gabrielle Samuel, Lisa Ballard, Anneke Lucassen |
16 August, 2022 |
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| Series 2 Episode 2 - Why context matters in genetic testing |
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. |
Rachel Horton, Gabrielle Samuel, Anneke Lucassen |
18 July, 2022 |
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| Series 2 Episode 1 - The environmental cost of personalised medicine |
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. |
Rachel Horton, Gabrielle Samuel, Susie Weller |
16 June, 2022 |
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