How can we, humans, look at our relationship to nature differently? In season three of Going Wild, on top of stories about animals, we invite you to journey through the entire ecological web — from the tiniest of life forms to apex predators — alongside the scientists, activists and adventurers who study it. Wildlife biologist and host Dr. Rae Wynn-Grant has been studying wild animals in their natural habitats all over the world for years. Our award-winning podcast takes you inside the hidde ...
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EP 135: Integration of newborn sequencing programs into healthcare systems with Dr. Ingrid Holm
MP3•Thuis aflevering
Manage episode 418536804 series 2631947
Inhoud geleverd door Sano Genetics. Alle podcastinhoud, inclusief afleveringen, afbeeldingen en podcastbeschrijvingen, wordt rechtstreeks geüpload en geleverd door Sano Genetics of hun podcastplatformpartner. Als u denkt dat iemand uw auteursrechtelijk beschermde werk zonder uw toestemming gebruikt, kunt u het hier beschreven proces https://nl.player.fm/legal volgen.
0:00 Introduction
1:30 Ingrid’s initial interests in genetics, paediatrics, and newborn screening
2:45 How the original BabySeq project, a pioneering newborn sequencing program got started, how it’s going, and the launch of BabySeq2
8:45 Lessons from BabySeq1 and goals for BabySeq2
10:30 Potential societal and long-term considerations for those involved in newborn sequencing programs
15:00 The range of genes tested in newborns and potential implications for family members
20:00 Ingrid’s predictions for the field of paediatrics and the medical school curriculum
24:00 Thoughts on Sudden Infant Death Syndrome (SIDS) and ethical considerations for parents wanting to have another child
30:30 Projections for BabySeq2, as well as barriers and facilitators to universal newborn screening
35:45 Addressing affordability of newborn genetic programs and commentary on healthcare economics
38:50 Predictions for how paediatric care will change if healthcare systems widely adopt newborn sequencing
42:15 A promising study targeting the FUS mutation for childhood ALS
43:30 Closing remarks
Please consider rating and reviewing us on your chosen podcast listening platform!
183 afleveringen
MP3•Thuis aflevering
Manage episode 418536804 series 2631947
Inhoud geleverd door Sano Genetics. Alle podcastinhoud, inclusief afleveringen, afbeeldingen en podcastbeschrijvingen, wordt rechtstreeks geüpload en geleverd door Sano Genetics of hun podcastplatformpartner. Als u denkt dat iemand uw auteursrechtelijk beschermde werk zonder uw toestemming gebruikt, kunt u het hier beschreven proces https://nl.player.fm/legal volgen.
0:00 Introduction
1:30 Ingrid’s initial interests in genetics, paediatrics, and newborn screening
2:45 How the original BabySeq project, a pioneering newborn sequencing program got started, how it’s going, and the launch of BabySeq2
8:45 Lessons from BabySeq1 and goals for BabySeq2
10:30 Potential societal and long-term considerations for those involved in newborn sequencing programs
15:00 The range of genes tested in newborns and potential implications for family members
20:00 Ingrid’s predictions for the field of paediatrics and the medical school curriculum
24:00 Thoughts on Sudden Infant Death Syndrome (SIDS) and ethical considerations for parents wanting to have another child
30:30 Projections for BabySeq2, as well as barriers and facilitators to universal newborn screening
35:45 Addressing affordability of newborn genetic programs and commentary on healthcare economics
38:50 Predictions for how paediatric care will change if healthcare systems widely adopt newborn sequencing
42:15 A promising study targeting the FUS mutation for childhood ALS
43:30 Closing remarks
Please consider rating and reviewing us on your chosen podcast listening platform!
183 afleveringen
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