CLPB Mutations Cause 3-Methylglutaconic Aciduria, Progressive Brain Atrophy, Intellectual Disability, Congenital Neutropenia, Cataracts, Movement DisorderSaskia B. Wortmann, Ron A. Wevers, Tim M. Strom et al.|The American Journal of Human Genetics|2015Cited by 135
The mitochondrial outer-membrane location of the EXD2 exonuclease contradicts its direct role in nuclear DNA repairFenna Hensen, Johannes N. Spelbrink|Scientific Reports|2018Cited by 22
A Combined Mass Spectrometry and Data Integration Approach to Predict the Mitochondrial Poly(A) RNA Interacting ProteomeSelma L. van Esveld, Johannes N. Spelbrink|Frontiers in Cell and Developmental Biology|2019Cited by 4
Uncharacterized protein C17orf80 – a novel interactor of human mitochondrial nucleoidsAlisa Potter, Johannes N. Spelbrink|Journal of Cell Science|2023Cited by 3
Let’s make it clear: Systematic exploration of mitochondrial DNA- and RNA-protein complexes by complexome profilingAlisa Potter, Johannes N. Spelbrink|bioRxiv (Cold Spring Harbor Laboratory)|2023Cited by 2