| Loss-of-function mutations in MGME1 impair mtDNA replication and cause multisystemic mitochondrial disease C Kornblum, TJ Nicholls, TB Haack, S Schöler, V Peeva, K Danhauser, ... Nature genetics 45 (2), 214-219, 2013 | 271 | 2013 |
| Linear mitochondrial DNA is rapidly degraded by components of the replication machinery V Peeva, D Blei, G Trombly, S Corsi, MJ Szukszto, P Rebelo-Guiomar, ... Nature communications 9 (1), 1727, 2018 | 210 | 2018 |
| Mitofusin 2 mutations affect mitochondrial function by mitochondrial DNA depletion S Vielhaber, G Debska-Vielhaber, V Peeva, S Schoeler, AP Kudin, I Minin, ... Acta neuropathologica 125, 245-256, 2013 | 102 | 2013 |
| Mosaic deficiency in mitochondrial oxidative metabolism promotes cardiac arrhythmia during aging OR Baris, S Ederer, JFG Neuhaus, JC von Kleist-Retzow, CM Wunderlich, ... Cell metabolism 21 (5), 667-677, 2015 | 98 | 2015 |
| Linear mtDNA fragments and unusual mtDNA rearrangements associated with pathological deficiency of MGME1 exonuclease TJ Nicholls, G Zsurka, V Peeva, S Schöler, RJ Szczesny, D Cysewski, ... Human molecular genetics 23 (23), 6147-6162, 2014 | 92 | 2014 |
| Mutant desmin substantially perturbs mitochondrial morphology, function and maintenance in skeletal muscle tissue L Winter, I Wittig, V Peeva, B Eggers, J Heidler, F Chevessier, RA Kley, ... Acta neuropathologica 132, 453-473, 2016 | 74 | 2016 |
| Is there still any role for oxidative stress in mitochondrial DNA-dependent aging? G Zsurka, V Peeva, A Kotlyar, WS Kunz Genes 9 (4), 175, 2018 | 67 | 2018 |
| Neuropathological signs of inflammation correlate with mitochondrial DNA deletions in mesial temporal lobe epilepsy E Volmering, P Niehusmann, V Peeva, A Grote, G Zsurka, J Altmüller, ... Acta neuropathologica 132, 277-288, 2016 | 51 | 2016 |
| Distinct patterns of mitochondrial genome diversity in bonobos (Pan paniscus) and humans G Zsurka, T Kudina, V Peeva, K Hallmann, CE Elger, K Khrapko, WS Kunz BMC evolutionary biology 10, 1-11, 2010 | 32 | 2010 |
| Impairment of mitochondrial oxidative phosphorylation in skin fibroblasts of SALS and FALS patients is rescued by in vitro treatment with ROS scavengers G Debska-Vielhaber, I Miller, V Peeva, W Zuschratter, J Walczak, ... Experimental neurology 339, 113620, 2021 | 22 | 2021 |
| Desmin knock-out cardiomyopathy: a heart on the verge of metabolic crisis B Elsnicova, D Hornikova, V Tibenska, D Kolar, T Tlapakova, B Schmid, ... International journal of molecular sciences 23 (19), 12020, 2022 | 21 | 2022 |
| Birth asphyxia as the most frequent perinatal complication V Peeva, O Golubnitschaja Predictive diagnostics and personalized treatment: dream or reality, 499-507, 2009 | 18 | 2009 |
| Distinct segregation of the pathogenic m. 5667G> A mitochondrial tRNAAsn mutation in extraocular and skeletal muscle in chronic progressive external ophthalmoplegia E Schlapakow, V Peeva, G Zsurka, M Jeub, B Wabbels, C Kornblum, ... Neuromuscular Disorders 29 (5), 358-367, 2019 | 11 | 2019 |
| Chromium-picolinate therapy in diabetes care: molecular and subcellular profiling revealed a necessity for individual outcome prediction, personalised treatment algorithms … K Yeghiazaryan, V Peeva, A Shenoy, H H Schild, O Golubnitschaja Infectious Disorders-Drug Targets (Formerly Current Drug Targets-Infectious …, 2011 | 11 | 2011 |
| Potential targets for early diagnosis and neuroprotection in asphyxiated newborns K Yeghiazaryan, V Peeva, O Golubnitschaja, M Morelli, ... Predictive diagnostics and personalized treatment: dream or reality, 509-526, 2009 | 11 | 2009 |
| Heart failure after pressure overload in autosomal-dominant desminopathies: Lessons from heterozygous DES-p.R349P knock-in mice F Stöckigt, L Eichhorn, T Beiert, V Knappe, T Radecke, M Steinmetz, ... PLoS One 15 (3), e0228913, 2020 | 8 | 2020 |
| A preliminary characterization of a novel bacteriocin-like substance from Enterococcus durum M-3 V Peeva, P Ivanova, N Harizanova, S Dimov Biotechnology & Biotechnological Equipment 20 (3), 120-127, 2006 | 6 | 2006 |
| The fate of oxidative strand breaks in mitochondrial DNA G Trombly, AM Said, AP Kudin, V Peeva, J Altmüller, K Becker, K Köhrer, ... Antioxidants 12 (5), 1087, 2023 | 4 | 2023 |
| Novel pathogenic sequence variation m. 5789T> C causes NARP syndrome and promotes formation of deletions of the mitochondrial genome M Hippen, G Zsurka, V Peeva, J Machts, K Schwiecker, ... Neurology: Genetics 8 (2), e660, 2021 | 4 | 2021 |
| From Planning Stage Towards FAIR Data: A Practical Metadatasheet For Biomedical Scientists L Seep, S Grein, I Splichalova, D Ran, M Mikhael, S Hildebrand, ... Scientific data 11 (1), 524, 2024 | 1 | 2024 |
Wolfram S KunzProfessor of Neurochemistry, University BonnEmail verificata su ukb.uni-bonn.de