L. Černá

Tissue-specific cytochrome c oxidase assembly defects due to mutations in SCO2 and SURF1.

K. Vesela, M. Tesařová, J. Zeman, 2005, The Biochemical journal.

Segregation pattern and biochemical effect of the G3460A mtDNA mutation in 27 members of LHON family

V. Kaplanová, J. Zeman, J. Houštěk, 2004, Journal of the Neurological Sciences.

Clinical Heterogeneity, Tissue Distribution, and Intergenerational Segregation of mtDNA Mutation A3243G

M. Tesařová, J. Zeman, J. Houštěk, 2004, Toxicology mechanisms and methods.

Multigene Panel Germline Testing of 1333 Czech Patients with Ovarian Cancer

L. Forétova, M. Zikan, S. Kmoch, 2020, Cancers.

Biogenesis of eukaryotic cytochrome c oxidase.

M. Tesařová, J. Zeman, H. Hansíková, 2006, Physiological research.

Accurate Microbiome Sequencing with Synthetic Long Read Sequencing

I. Wu, F. Garcia-Pichel, Michael A. Balamotis, 2020, bioRxiv.

Novel mutations in a boy with dihydrolipoamide dehydrogenase deficiency.

J. Zeman, S. Kmoch, H. Hansíková, 2001, Medical science monitor : international medical journal of experimental and clinical research.

DICER1 Syndrome.

H. Nosková, J. Šoukalová, O. Slabý, 2019, Klinicka onkologie : casopis Ceske a Slovenske onkologicke spolecnosti.

ENIGMA CHEK2gether Project: A Comprehensive Study Identifies Functionally Impaired CHEK2 Germline Missense Variants Associated with Increased Breast Cancer Risk

James M. Hodge, E. Burnside, Y. Kamatani, 2023, Clinical cancer research : an official journal of the American Association for Cancer Research.

DICER1 Syndrome.

H. Nosková, J. Šoukalová, O. Slabý, 2019, Klinicka onkologie : casopis Ceske a Slovenske onkologicke spolecnosti.