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Europace : European Pacing, Arrhythmias, and Cardiac Electrophysiology : Journal of the Working Groups on Cardiac Pacing, Arrhythmias, and Cardiac Cellular Electrophysiology of the European Society of Cardiology|July 19, 2020
Pregnancies, ventricular arrhythmias, and substrate progression in women with arrhythmogenic right ventricular cardiomyopathy in the Nordic ARVC RegistryPyotr G Platonov, Anna I Castrini, Anneli Svensson, et al.
Nature Communications|December 22, 2022
Actin-microtubule cytoskeletal interplay mediated by MRTF-A/SRF signaling promotes dilated cardiomyopathy caused by LMNA mutationsCaroline Le Dour, Maria Chatzifrangkeskou, Coline Macquart, et al.
Scientific Reports|March 13, 2019
Relevance of Titin Missense and Non-Frameshifting Insertions/Deletions Variants in Dilated CardiomyopathyOyediran Akinrinade, Tiina Heliö, Ronald H Lekanne Deprez, et al.
Scientific Reports|October 10, 2020
Publisher Correction: Relevance of Titin Missense and Non-Frameshifting Insertions/Deletions Variants in Dilated CardiomyopathyOyediran Akinrinade, Tiina Heliö, Ronald H Lekanne Deprez, et al.
BMC Cardiovascular Disorders|March 6, 2021
Diagnostic yield of genetic testing in a heterogeneous cohort of 1376 HCM patientsJulie Hathaway, Krista Heliö, Inka Saarinen, et al.
ESC Heart Failure|November 12, 2020
Differences between familial and sporadic dilated cardiomyopathy: ESC EORP Cardiomyopathy & Myocarditis registryFolkert W Asselbergs, Arjan Sammani, Perry Elliott, et al.
Frontiers in Genetics|December 13, 2021
GRINL1A Complex Transcription Unit Containing GCOM1, MYZAP, and POLR2M Genes Associates with Fully Penetrant Recessive Dilated CardiomyopathyKrista Heliö, Mikko I Mäyränpää, Inka Saarinen, et al.
European Heart Journal|April 9, 2024
Endomyocardial biopsy: safety and prognostic utility in paediatric and adult myocarditis in the European Society of Cardiology EURObservational Research Programme Cardiomyopathy and Myocarditis Long-Term RegistryAlida L P Caforio, Juan P Kaski, Juan R Gimeno, et al.
Neurology|October 30, 2016
FGF21 is a biomarker for mitochondrial translation and mtDNA maintenance disordersJenni M Lehtonen, Saara Forsström, Emanuela Bottani, et al.
Plos One|February 3, 2021
Biallelic loss-of-function in NRAP is a cause of recessive dilated cardiomyopathyJuha W Koskenvuo, Inka Saarinen, Saija Ahonen, et al.
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