Chantal Calis

Nonsense mutations in CABC1/ADCK3 cause progressive cerebellar ataxia and atrophy.

H. Smeets, B. J. van den Bosch, M. Tijssen, 2010, Mitochondrion.

Defective complex I assembly due to C20orf7 mutations as a new cause of Leigh syndrome

I. D. de Coo, H. Smeets, B. J. van den Bosch, 2009, Journal of Medical Genetics.

Identification of differential protein interactors of lamin A and progerin

T. Misteli, Jeroen A. A. Demmers, Y. Pinto, 2010, Nucleus.

Whole Exome Sequencing Is the Preferred Strategy to Identify the Genetic Defect in Patients With a Probable or Possible Mitochondrial Cause

H. Smeets, R. Kamps, B. de Koning, 2018, Front. Genet..

Post-natal myogenic and adipogenic developmental

T. Misteli, Y. Pinto, B. J. van den Bosch, 2011, Nucleus.