In 2011 the Netherlands Heart Foundation allocated funding (CVON, Cardiovasculair Onderzoek Nederland) to stimulate collaboration between clinical and preclinical researchers on specific areas of research. One of those areas involves genetic heart diseases, which are frequently caused by pathogenic variants in genes that encode sarcomere proteins. In 2014, the DOSIS (Determinants of susceptibility in inherited cardiomyopathy: towards novel therapeutic approaches) consortium was initiated, focusing their research on secondary disease hits involved in the onset and progression of cardiomyopathies. Here we highlight several recent observations from our consortium and collaborators which may ultimately be relevant for clinical practice.

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Keywords Cardiomyopathies, Gene variants, Patient cohorts
Persistent URL dx.doi.org/10.1007/s12471-020-01456-4, hdl.handle.net/1765/129521
Journal Netherlands Heart Journal
Citation
de Boer, R.A, Nijenkamp, L.L.A.M, Silljé, H.H.W. (H. H.W.), Eijgenraam, T.R. (T. R.), Parbhudayal, R, van Driel, B. (B.), … van der Velden, J. (2020). Strength of patient cohorts and biobanks for cardiomyopathy research. Netherlands Heart Journal (Vol. 28, pp. 50–56). doi:10.1007/s12471-020-01456-4