Magner, Martin
Charles University · General University Hospital in Prague
2 papers on CoChatORCID 0000-0002-5883-9509
Most cited papers
- Verified
Deleterious, protein-altering variants in the transcriptional coregulator ZMYM3 in 27 individuals with a neurodevelopmental delay phenotype
Hiatt, S. M., Trajkova, S., Sebastiano, M. R., Partridge, E. C., Abidi, F. E., Anderson, A., Ansar, M., Antonarakis, S. E., Azadi, A., Bachmann-Gagescu, R., et al. (2023) · The American Journal of Human Genetics
Genetics and Neurodevelopmental DisordersGenomics and Rare Diseases
Cited by 21
- Verified
Psychiatric disturbances in five patients with MELAS syndrome
Magner, M., Honzik, T., Tesarova, M., Dvorakova, V., Hansikova, H., Raboch, J., & Zeman, J. (2014) · Psychiatria Polska
Mitochondrial Function and PathologyMetabolism and Genetic Disorders
Cited by 11
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