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EP 135: Integration of newborn sequencing programs into healthcare systems with Dr. Ingrid Holm

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Manage episode 418536804 series 2631947
Content provided by Sano Genetics. All podcast content including episodes, graphics, and podcast descriptions are uploaded and provided directly by Sano Genetics or their podcast platform partner. If you believe someone is using your copyrighted work without your permission, you can follow the process outlined here https://player.fm/legal.
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!
  continue reading

167 episodes

Artwork
iconShare
 
Manage episode 418536804 series 2631947
Content provided by Sano Genetics. All podcast content including episodes, graphics, and podcast descriptions are uploaded and provided directly by Sano Genetics or their podcast platform partner. If you believe someone is using your copyrighted work without your permission, you can follow the process outlined here https://player.fm/legal.
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!
  continue reading

167 episodes

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