| Phenotypic spectrum associated with mutations of the mitochondrial polymerase γ gene R Horvath, G Hudson, G Ferrari, N Fütterer, S Ahola, E Lamantea, ... Brain 129 (7), 1674-1684, 2006 | 452 | 2006 |
| Mitochondrial myopathy induces a starvation-like response H Tyynismaa, CJ Carroll, N Raimundo, S Ahola-Erkkilä, T Wenz, ... Human molecular genetics 19 (20), 3948-3958, 2010 | 330 | 2010 |
| Mitochondrial DNA replication defects disturb cellular dNTP pools and remodel one-carbon metabolism J Nikkanen, S Forsström, L Euro, I Paetau, RA Kohnz, L Wang, D Chilov, ... Cell metabolism 23 (4), 635-648, 2016 | 256 | 2016 |
| Ketogenic diet slows down mitochondrial myopathy progression in mice S Ahola-Erkkilä, CJ Carroll, K Peltola-Mjösund, V Tulkki, I Mattila, ... Human molecular genetics 19 (10), 1974-1984, 2010 | 218 | 2010 |
| Mitochondrial DNA polymerase gamma variants in idiopathic sporadic Parkinson disease PT Luoma, J Eerola, S Ahola, AH Hakonen, O Hellstrom, KT Kivisto, ... Neurology 69 (11), 1152-1159, 2007 | 165 | 2007 |
| Thymidine kinase 2 mutations in autosomal recessive progressive external ophthalmoplegia with multiple mitochondrial DNA deletions H Tyynismaa, R Sun, S Ahola-Erkkilä, H Almusa, R Pöyhönen, M Korpela, ... Human molecular genetics 21 (1), 66-75, 2012 | 110 | 2012 |
| Modified Atkins diet induces subacute selective ragged‐red‐fiber lysis in mitochondrial myopathy patients S Ahola, M Auranen, P Isohanni, S Niemisalo, N Urho, J Buzkova, ... EMBO Molecular Medicine 8 (11), 1234-1247, 2016 | 71 | 2016 |
| Metabolomes of mitochondrial diseases and inclusion body myositis patients: treatment targets and biomarkers J Buzkova, J Nikkanen, S Ahola, AH Hakonen, K Sevastianova, ... EMBO molecular medicine 10 (12), e9091, 2018 | 68 | 2018 |
| OMA1-mediated integrated stress response protects against ferroptosis in mitochondrial cardiomyopathy S Ahola, PR Mejías, S Hermans, S Chandragiri, P Giavalisco, H Nolte, ... Cell metabolism 34 (11), 1875-1891. e7, 2022 | 64 | 2022 |
| MtDNA mutagenesis impairs elimination of mitochondria during erythroid maturation leading to enhanced erythrocyte destruction KJ Ahlqvist, S Leoncini, A Pecorelli, SB Wortmann, S Ahola, S Forsström, ... Nature communications 6 (1), 6494, 2015 | 58 | 2015 |
| Loss of the mitochondrial i‐AAA protease YME1L leads to ocular dysfunction and spinal axonopathy HG Sprenger, G Wani, A Hesseling, T König, M Patron, T MacVicar, ... EMBO molecular medicine 11 (1), e9288, 2019 | 48 | 2019 |
| Mitochondrial EFTs defects in juvenile-onset Leigh disease, ataxia, neuropathy, and optic atrophy S Ahola, P Isohanni, L Euro, V Brilhante, A Palotie, H Pihko, T Lönnqvist, ... Neurology 83 (8), 743-751, 2014 | 44 | 2014 |
| Capsid-modified adenoviral vectors for improved muscle-directed gene therapy K Guse, M Suzuki, G Sule, TK Bertin, H Tyynismaa, S Ahola-Erkkilä, ... Human gene therapy 23 (10), 1065-1070, 2012 | 30 | 2012 |
| Mitochondrial proteolysis and metabolic control S Ahola, T Langer, T MacVicar Cold Spring Harbor Perspectives in Biology 11 (7), a033936, 2019 | 26 | 2019 |
| Ferroptosis in mitochondrial cardiomyopathy S Ahola, T Langer Trends in Cell Biology 34 (2), 150-160, 2024 | 10 | 2024 |
| The mitochondrial protease OMA1 acts as a metabolic safeguard upon nuclear DNA damage P Rivera-Mejías, ÁJ Narbona-Pérez, L Hasberg, L Kroczek, A Bahat, ... Cell Reports 42 (4), 2023 | 4 | 2023 |
| Pilot study: Modified Atkins diet trial for adult-onset mitochondrial myopathy S Ahola-Erkkilä, M Auranen, P Isohanni, N Lundbom, P Piirilä, ... Mitochondrion 6 (13), 911, 2013 | 1 | 2013 |
| Intracellular phase separation and its role in nickel sensing B Zambelli, S Ahola, T Langer Trends in Cell Biology, 2023 | | 2023 |
| Diagnosis and therapy for mitochondrial diseases S Ahola | | 2014 |
| 144 Aberrant amino acid signalling and metabolism in the Deletor mouse CJ Carroll, S Ahola, H Tyynismaa, M Oresic, A Suomalainen-Wartiovaara Mitochondrion 2 (10), 240-241, 2010 | | 2010 |
