I. Boesten

Differences in Strength and Timing of the mtDNA Bottleneck between Zebrafish Germline and Non-germline Cells.

H. Smeets, B. J. van den Bosch, E. Raz, 2016, Cell reports.

Novel pathogenic SLC25A46 splice‐site mutation causes an optic atrophy spectrum disorder

I. D. de Coo, H. Smeets, D. Hellebrekers, 2017, Clinical genetics.

Replication Errors Made During Oogenesis Lead to Detectable De Novo mtDNA Mutations in Zebrafish Oocytes with a Low mtDNA Copy Number

H. Smeets, R. Kamps, M. Adriaens, 2016, Genetics.

Exome sequencing reveals a novel Moroccan founder mutation in SLC19A3 as a new cause of early-childhood fatal Leigh syndrome.

H. Smeets, R. Kamps, B. J. van den Bosch, 2013, Brain : a journal of neurology.

Genetic defects in mtDNA-encoded protein translation cause pediatric, mitochondrial cardiomyopathy with early-onset brain disease

H. Smeets, R. Kamps, B. J. van den Bosch, 2018, European Journal of Human Genetics.

Pathogenic CWF19L1 variants as a novel cause of autosomal recessive cerebellar ataxia and atrophy

H. Smeets, R. Kamps, D. Hellebrekers, 2015, European Journal of Human Genetics.