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Publications by Marielle Alders
Phylogenetic and Physicochemical Analyses Enhance the Classification of Rare Nonsynonymous Single Nucleotide Variants in Type 1 and 2 Long-Qt Syndrome
Circulation: Cardiovascular Genetics
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Clinical and Molecular Genetic Risk Determinants in Adult Long QT Syndrome Type 1 and 2 Patients
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Figure 2: Phylogenetic Relationship and Identification of Single-Nucleotide Variations for 105 CSVd Variants.
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Small Effective Population Sizes and Rare Nonsynonymous Variants in Potyviruses
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Enhanced Classification of Brugada Syndrome–Associated and Long-Qt Syndrome–Associated Genetic Variants in theSCN5A-Encoded Nav1.5 Cardiac Sodium ChannelCLINICAL PERSPECTIVE
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Statin Therapy in Long QT Syndrome Type II
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Rare Single‐nucleotide Variants in Oculo‐auriculo‐vertebral Spectrum (OAVS)
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Association of a Congenital Long QT Syndrome Type 1 With Takotsubo Cardiomyopathy
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