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You searched for: Author/Creator Sinner, Moritz F.

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1. A genetic variant alters the secondary structure of the lncRNA H19 and is associated with dilated cardiomyopathy. (15th October 2021)

2. Analysis for Genetic Modifiers of Disease Severity in Patients With Long-QT Syndrome Type 2. (June 2015)

4. Atrial Fibrillation Risk Assessment after Embolic Stroke of Undetermined Source. Issue 3 (2nd December 2022)

7. Common and Rare Coding Genetic Variation Underlying the Electrocardiographic PR Interval. (May 2018)

8. Common Coding Variants in SCN10A Are Associated With the Nav1.8 Late Current and Cardiac Conduction. (May 2018)

9. Common Genetic Variants and Response to Atrial Fibrillation Ablation. (April 2015)

10. Diminished PRRX1 Expression Is Associated With Increased Risk of Atrial Fibrillation and Shortening of the Cardiac Action Potential. (October 2017)