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Genome‑wide insights into severity and progression of CCTA‑defined coronary disease phenotypes in HURRICANE study

30 August 2026 (10:15 - 11:00)
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Congress Presentation Part of: Genetics, genomics, and precision cardiovascular medicine Genetics, Epigenetics, ncRNA ESC2026 Premium Access ESC Congress 2026 European Society of Cardiology

About the speaker

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Mrs Katia Pane

IRCCS SYNLAB SDN, Napoli (Italy)

7 More presentations in this session

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Genetic regulation of alternative splicing in the human heart: a splice QTL analysis
Associate Professor O. Gidlof (Lund, SE)
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Genome-wide meta-analysis of echocardiographic left ventricular size and function in over 100,000 individuals
Mr S. Rand (Copenhagen, DK)
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Genetic determinants of left ventricular diastolic function
Mr S. Rand (Copenhagen, DK)
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Trio-based whole genome sequencing identifies coding and regulatory de novo variants in sporadic young-onset atrioventricular block
Doctor K. Shimamoto (Nantes, FR)
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Long-read sequencing as an all-in-one diagnostic approach for genetic testing in cardiovascular diseases
Mr A. Tescari (Pavia, IT)
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Genetics, genomics, and precision cardiovascular medicine

The Event

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ESC Congress 2026

30 August 2026 10:15 CET
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