Maarten G. Van Den Hoogenhof
Heidelberg, BW, Germany
Last Updated: 09/26/2026
Save publications for later
Sign Up
Not sure about your diagnosis?
Check Your Symptoms
Found 19 publications
Novel Truncating Variant c.1222DupC in RBM20 Causes Cardiomyopathy Consistent With Haploinsufficiency.
Journal: Circulation. Genomic and precision medicine
Published: April 30, 2026
AAV9-Mediated TNPO3 Overexpression in the Heart Rescues RBM20 Cardiomyopathy in Mice.
Journal: Circulation
Published: September 08, 2025
CAMK2D causes heart failure in mice with RBM20 cardiomyopathy.
Journal: Nature cardiovascular research
Published: May 23, 2025
Striated muscle-specific base editing enables correction of mutations causing dilated cardiomyopathy.
Journal: Nature communications
Published: December 13, 2022
Deep phenotyping of two preclinical mouse models and a cohort of RBM20 mutation carriers reveals no sex-dependent disease severity in RBM20 cardiomyopathy.
Journal: American journal of physiology. Heart and circulatory physiology
Published: November 11, 2022
Editorial: RNA Biology in Cardiovascular Disease.
Journal: Frontiers in genetics
Published: September 13, 2021
CaMKIIδ Splice Variants in the Healthy and Diseased Heart.
Journal: Frontiers in cell and developmental biology
Published: December 21, 2020
New Insights in RBM20 Cardiomyopathy.
Journal: Current heart failure reports
Published: August 14, 2020
Young@Heart: empowering the next generation of cardiovascular researchers.
Journal: Netherlands heart journal : monthly journal of the Netherlands Society of Cardiology and the Netherlands Heart Foundation
Published: August 12, 2020
Physiological and unappreciated roles of CaMKII in the heart.
Journal: Basic research in cardiology
Published: March 28, 2018
Last Updated: 09/26/2026