Henna Tyynismaa

FGF-21 as a biomarker for muscle-manifesting mitochondrial respiratory chain deficiencies: a diagnostic study

Anu Suomalainen, Jenni M. Elo, Kirsi H. Pietiläinen et al. · The Lancet Neurology · 2011 · 414 citations · Full text

Diagnostic Study, Fibrosis, Mitochondrial Function +3

Mutant mitochondrial helicase Twinkle causes multiple mtDNA deletions and a late-onset mitochondrial disease in mice

Henna Tyynismaa, Katja Peltola Mjøsund, Sjoerd Wanrooij et al. · Proceedings of the National Academy of Sciences · 2005 · 327 citations · Full text

Mitochondrial myopathy induces a starvation-like response

Henna Tyynismaa, Christopher J. Carroll, Nuno Raimundo et al. · Human Molecular Genetics · 2010 · 300 citations

Genetics, Pathology, Oxidative Stress +17

Mitochondrial DNA Replication Defects Disturb Cellular dNTP Pools and Remodel One-Carbon Metabolism

Joni Nikkanen, Saara Forsström, Liliya Euro et al. · Cell Metabolism · 2016 · 284 citations · Full text

Genome Instability, Mitochondrial Biogenesis, Mitochondrial Function +6

Comparison of solution-based exome capture methods for next generation sequencing

Anna-Maija Sulonen, Pekka Ellonen, Henrikki Almusa et al. · Genome biology · 2011 · 269 citations · Full text