Gustav Ahlberg
0000-0003-0066-2779
Laboratory for Molecular Cardiology, Copenhagen University Hospital
6 papers found
Refreshing results…
Clinical Implications of SCN10A Loss-of-Function Variants in 169 610 Exomes Representing the General Population
Genome-wide association study identifies 18 novel loci associated with left atrial volume and function
Human iPSC modelling of a familial form of atrial fibrillation reveals a gain of function of If and ICaL in patient-derived cardiomyocytes
Reappraisal of variants previously linked with sudden infant death syndrome: results from three population-based cohorts
Deep sequencing of atrial fibrillation patients with mitral valve regurgitation shows no evidence of mosaicism but reveals novel rare germline variants
Numerous Brugada syndrome-associated genetic variants have no effect on J-point elevation, syncope susceptibility, malignant cardiac arrhythmia, and all-cause mortality
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