Daniels, Matthew J.
Justus-Liebig-Universität Gießen · University of Oxford · Universities of Giessen and Marburg Lung Center · Oxford University Hospitals NHS Trust · The University of Osaka
2 papers on CoChatORCID 0000-0002-9250-6214
Most cited papers
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Whole-genome sequencing of patients with rare diseases in a national health system
Turro, E., Astle, W. J., Megy, K., Gräf, S., Greene, D., Shamardina, O., Allen, H. L., Sanchis-Juan, A., Frontini, M., Thys, C., et al. (2020) · Nature
Genomics and Rare DiseasesGenetic Associations and Epidemiology
Cited by 554
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Dysregulated mitophagy and mitochondrial organization in optic atrophy due to OPA1 mutations
Liao, C., Ashley, N., Diot, A., Morten, K., Phadwal, K., Williams, A., Fearnley, I., Rosser, L., Lowndes, J., Fratter, C., et al. (2017) · Neurology
Autophagy in Disease and TherapyMitochondrial Function and Pathology
Cited by 97
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