Shared genetic pathways contribute to risk of hypertrophic and dilated cardiomyopathies with opposite directions of effect
2021 · Nature Genetics · 285 citations
https://doi.org/10.1038/s41588-020-00762-2
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Marjon A. van Slegtenhorst
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Marjon A. van Slegtenhorst is an academic researcher from Guy's and St Thomas' NHS Foundation Trust. The author has contributed to research in topics: Cardiomyopathy and Myosin Studies & Congenital heart defects research & Cardiovascular Function and Risk Factors. The author has an h-index of 31, co-authored 80 publications.
Papers by this author
worksLarge-scale genome-wide association analyses identify novel genetic loci and mechanisms in hypertrophic cardiomyopathy
2025 · Nature Genetics · 43 citations
https://doi.org/10.1038/s41588-025-02087-4
Spliceosome malfunction causes neurodevelopmental disorders with overlapping features
2023 · Journal of Clinical Investigation · 41 citations
https://doi.org/10.1172/jci171235
The broader phenotypic spectrum of congenital caudal abnormalities associated with mutations in the caudal type homeobox 2 gene
2021 · Clinical Genetics · 17 citations
https://doi.org/10.1111/cge.14076
Five-year prognostic significance of global longitudinal strain in individuals with a hypertrophic cardiomyopathy gene mutation without hypertrophic changes
2019 · Netherlands Heart Journal · 11 citations
https://doi.org/10.1007/s12471-019-1226-5
Desmoplakin cardiomyopathy—an inherited cardiomyopathy presenting with recurrent episodes of acute myocardial injury
2022 · Netherlands Heart Journal · 9 citations
https://doi.org/10.1007/s12471-022-01735-2
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