Jo M Vanoevelen (Jo Vanoevelen)

Years Active: 2018-2023
Publications (10 Years): 3

This page only lists publications with an associated author ORCID identifier.

Publications

Rachel M A Ter Bekke, Koen de Schouwer, Sergio Conti, Godelieve R F Claes, Jo M Vanoevelen, Suzanne Gommers, Apollonia T J M Helderman-van den Enden, Hans-Peter Brunner-LaRocca
Juvenile-onset multifocal atrial arrhythmias, atrial standstill and compound heterozygosity of genetic variants in TAF1A : sentinel event for evolving dilated cardiomyopathy-a case report. European heart journal. Case reports 7 (6) (2023)
Jo M Vanoevelen, Jörgen Bierau, Janine C Grashorn, Ellen Lambrichs, Erik-Jan Kamsteeg, Levinus A Bok, Ron A Wevers, Marjo S van der Knaap, Marianna Bugiani, Junmei Hu Frisk, Rita Colnaghi, Mark O'Driscoll, Debby M E I Hellebrekers, Richard Rodenburg, Carlos R Ferreira, Han G Brunner, Arthur van den Wijngaard, Ghada M H Abdel-Salam, Liya Wang, Constance T R M Stumpel
DTYMK is essential for genome integrity and neuronal survival. Acta neuropathologica 143 (2) (2021)
Rick Kamps, Radek Szklarczyk, Tom E Theunissen, Debby M E I Hellebrekers, Suzanne C E H Sallevelt, Iris B Boesten, Bart de Koning, Bianca J van den Bosch, Gajja S Salomons, Marisa Simas-Mendes, Rob Verdijk, Kees Schoonderwoerd, Irenaeus F M de Coo, Jo M Vanoevelen, Hubert J M Smeets
Genetic defects in mtDNA-encoded protein translation cause pediatric, mitochondrial cardiomyopathy with early-onset brain disease. European journal of human genetics : EJHG 26 (4) (2018)

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