We found 10 episodes of The Genetics Podcast with the tag “genetics”.
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EP 93: International Perspectives on Access to Genetic Testing in ALS
January 24th, 2023 | 41 mins 20 secs
als, dr patrick short, genetics, international als, precision medicine, sano genetics
In this webinar, Paul Wicks leads the discussion with Professor Ammar Al-Chalabi, Dr Patrick Short and Kristina Salmon on international perspectives on genetic testing for ALS.
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EP 92: Four Predictions for 2023
January 5th, 2023 | 13 mins 41 secs
genetics, genetics 2023, genetics predictions
From changing drug pricing legislation to AI breakthroughs, in the first episode of The Genetics Podcast for 2023, Patrick makes four predictions for the biggest stories of 2023.
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EP 91: 2022 Genetics Round-up with Dr Veera Rajagopal
December 24th, 2022 | 1 hr 29 mins
dna 2022, genetics, genetics news, precision medicine, sano
In the final episode of The Genetics Podcast for 2022, we’re joined by Dr Veera Rajagopal, who is known as the ‘GWAS storyteller’ on Twitter for his prolific threads breaking down the latest findings in genetics.
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EP 89: Baroness Nicola Blackwood on the UK's leading role in delivering 'genomic healthcare for everyone'
November 24th, 2022 | 33 mins 22 secs
baroness blackwood, genetic testing, genetics, genomics england, nicola blackwood
This week Patrick is joined by Baroness Nicola Blackwood of North Oxford. Nicola is chair of Genomics England, a diverse community of genomic clinicians and researchers providing a world-class service platform for genetic testing to patients.
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EP 88: Precision oncology: how Next Generation Sequencing (NGS) is powering care today and the treatments of the future with Christine Ward (Takeda) and Geoff Oxnard (Foundation Medicine)
November 10th, 2022 | 42 mins 30 secs
clinicalgenetics, genetics, precisionmedicine, thegeneticspodcast
In this episode, guests Christine Ward, VP and Head of Oncology and Cell Therapy Precision & Translational Medicine at Takeda and Geoff Oxnard, Thoracic Oncologist and VP of Foundation Medicine talk to Patrick about Next Generation Sequencing (NGS) in precision oncology.
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EP 86: Heidi Rehm PhD, Chief Genomics Officer at Massachusetts General Hospital on curating and collaborating genomic datasets to guide the future of diagnostic and clinical research
October 13th, 2022 | 36 mins 59 secs
clinicalgenetics, genetics, precisionmedicine, thegeneticspodcast
Patrick speaks to Heidi Rehm who is at the top of the field of genome interpretation and medical genetics.
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EP 85: Dr Jessica Kissinger on large-scale parasite genomics and the power of multi-omic data
September 29th, 2022 | 33 mins 55 secs
biology, genetics, pathogens, thegeneticspodcast
In this episode, we explore major findings in the field and Dr Kissinger's vision of large-scale interoperable datasets driving novel discoveries. Plus, Dr Kissinger shares her recent and personal experience of diagnosis with a rare disease, Ehlers-Danlos Syndrome, that puts everything into perspective.
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EP 84: Mark Kotter, CEO, and Founder of bit.bio, on creating every cell type and kickstarting a cell therapy revolution
September 1st, 2022 | 34 mins 50 secs
bitbio, drugdiscovery, genetics, thegeneticspodcast
Doctors have been transplanting organs for decades, but can we transplant reprogrammed stem cells to rejuvenate the human body?
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EP 83: Daphne Koller, Founder & CEO of Insitro - Integrating machine learning and biology at scale to reimagine drug discovery
August 11th, 2022 | 45 mins 10 secs
drugdiscovery, genetics, insitro, thegeneticspodcast
This week’s guest, Daphne Koller, is the Founder and CEO of Insitro - a company shifting the paradigm of new drug discovery using predictive models.
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EP 41 Keith McArthur, the rare disease dad who is re-writing the rules in order to find a cure for his son - Live Podcast
July 25th, 2020 | 50 mins 27 secs
genetics, grin, patients, rare disease, research
Keith McArthur is one of the parents re-writing the rules for research in rare disease. Keith is CEO of the CureGRIN foundation, a non-profit backed by the Chan-Zuckerberg Initiative. Keith and his co-founder Denise Rehner believe that patients hold the power to accelerate research and drive progress, and that a cure for GRIN Disorders is possible.