ePrints

The Newcastle University research output collection, currently available on ePrints, will shortly be moving to a new open repository platform, Figshare. To prepare for the data migration we have paused adding new content to ePrints, and will resume once the new repository is launched. During this time you will continue to have access to ePrints (but no new content will appear). We will share updates here when available.

Browsing publications by Dr Monika Olahova

Newcastle Authors	Title	Year	Full text
Dr Mahmoud Fassad Dr Monika Olahova Dr Jack Collier Charlotte Knowles Eleni Mavraki et al.	Expanding the Genetic and Phenotypic Spectrum of POLRMT-Related Mitochondrial Disease	2026
Dr Monika Olahova Dr Kyle Thompson Dr Langping He Professor Robert Taylor	Bi-allelic variants in MRPL49 cause variable clinical presentations, including sensorineural hearing loss, leukodystrophy, and ovarian insufficiency	2025
Dr Charlotte Alston Dr Monika Olahova Dr Langping He Professor Bobby McFarland Professor Robert Taylor	A recessive homozygous p.Asp92Gly SDHD mutation causes prenatal cardiomyopathy and a severe mitochondrial complex II deficiency	2015