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The "Neglected Middle": Redefining HCM Genetics with Intermediate Effect Variants

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Content provided by Jason Gillikin and Hypertrophic Cardiomyopathy Medical Society. All podcast content including episodes, graphics, and podcast descriptions are uploaded and provided directly by Jason Gillikin and Hypertrophic Cardiomyopathy Medical Society 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.

In this episode of In the Thick of It, genetic counselor Matthew Thomas sits down with Dr. Roddy Walsh and Dr. Juan Pablo Ochoa to discuss their groundbreaking research on the genetic architecture of Hypertrophic Cardiomyopathy (HCM). The conversation centers on "Intermediate Effect Variants" (IEVs)—genetic markers that fall between rare, high-impact Mendelian mutations and common, low-impact polygenic risk factors. By utilizing a massive dataset of over 20,000 patients and robust ancestry-matched controls, the researchers demonstrate how these variants contribute to disease severity, age of onset, and wall thickness. This episode explores the practical implications for clinical genetic testing, the necessity of diverse genomic data, and how these findings are shifting the field toward a more quantitative and comprehensive understanding of HCM risk.

References: https://www.ahajournals.org/doi/10.1161/CIRCULATIONAHA.125.074529

  continue reading

32 episodes

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Manage episode 525542227 series 3488208
Content provided by Jason Gillikin and Hypertrophic Cardiomyopathy Medical Society. All podcast content including episodes, graphics, and podcast descriptions are uploaded and provided directly by Jason Gillikin and Hypertrophic Cardiomyopathy Medical Society 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.

In this episode of In the Thick of It, genetic counselor Matthew Thomas sits down with Dr. Roddy Walsh and Dr. Juan Pablo Ochoa to discuss their groundbreaking research on the genetic architecture of Hypertrophic Cardiomyopathy (HCM). The conversation centers on "Intermediate Effect Variants" (IEVs)—genetic markers that fall between rare, high-impact Mendelian mutations and common, low-impact polygenic risk factors. By utilizing a massive dataset of over 20,000 patients and robust ancestry-matched controls, the researchers demonstrate how these variants contribute to disease severity, age of onset, and wall thickness. This episode explores the practical implications for clinical genetic testing, the necessity of diverse genomic data, and how these findings are shifting the field toward a more quantitative and comprehensive understanding of HCM risk.

References: https://www.ahajournals.org/doi/10.1161/CIRCULATIONAHA.125.074529

  continue reading

32 episodes

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