Tiina Tyni

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

Exome Sequencing Identifies Mitochondrial Alanyl-tRNA Synthetase Mutations in Infantile Mitochondrial Cardiomyopathy

Alexandra Götz, Henna Tyynismaa, Liliya Euro et al. · The American Journal of Human Genetics · 2011 · 252 citations · Full text

Cardiomyopathy, Mendelian Disorder, Mitochondrial Function +6

Genetic Basis of Severe Childhood-Onset Cardiomyopathies

Catalina Vasilescu, Tiina Ojala, Virginia Brilhante et al. · Journal of the American College of Cardiology · 2018 · 156 citations

Cardiomyopathy, Heart Failure, Genetics +5

Riboflavin-Responsive and -Non-responsive Mutations in FAD Synthase Cause Multiple Acyl-CoA Dehydrogenase and Combined Respiratory-Chain Deficiency

Rikke Katrine Jentoft Olsen, Eliška Koňaříková, Teresa Anna Giancaspero et al. · The American Journal of Human Genetics · 2016 · 146 citations · Full text

Pregnancy complications are frequent in long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency

Tiina Tyni, Eeva Ekholm, Helena Pihko · American Journal of Obstetrics and Gynecology · 1998 · 141 citations

Infertility, Genetics, Reproductive Health +12