| The mitochondrial genome: structure, transcription, translation and replication JW Taanman Biochimica et Biophysica Acta (BBA)-Bioenergetics 1410 (2), 103-123, 1999 | 2045 | 1999 |
| Mitofusin 1 and mitofusin 2 are ubiquitinated in a PINK1/parkin-dependent manner upon induction of mitophagy ME Gegg, JM Cooper, KY Chau, M Rojo, AHV Schapira, JW Taanman Human molecular genetics 19 (24), 4861-4870, 2010 | 1046 | 2010 |
| Biochemical abnormalities and excitotoxicity in Huntington's disease brain SJ Tabrizi, MWJ Cleeter, J Xuereb, JW Taanman, JM Cooper, ... Annals of Neurology: Official Journal of the American Neurological …, 1999 | 558 | 1999 |
| Parkinson's disease induced pluripotent stem cells with triplication of the α-synuclein locus MJ Devine, M Ryten, P Vodicka, AJ Thomson, T Burdon, H Houlden, ... Nature communications 2 (1), 440, 2011 | 538 | 2011 |
| A mutant mitochondrial respiratory chain assembly protein causes complex III deficiency in patients with tubulopathy, encephalopathy and liver failure P De Lonlay, I Valnot, A Barrientos, M Gorbatyuk, A Tzagoloff, ... Nature genetics 29 (1), 57-60, 2001 | 384 | 2001 |
| Mitochondrial DNA transmission of the mitochondrial defect in Parkinson's disease M Gu, JM Cooper, JW Taanman, AHV Schapira Annals of Neurology: Official Journal of the American Neurological …, 1998 | 369 | 1998 |
| A mutation in the human heme A:farnesyltransferase gene (COX10 ) causes cytochrome c oxidase deficiency I Valnot, JC von Kleist-Retzow, A Barrientos, M Gorbatyuk, JW Taanman, ... Human molecular genetics 9 (8), 1245-1249, 2000 | 359 | 2000 |
| Cytochrome c Oxidase subunit I microdeletion in a patient with motor neuron disease GP Comi, A Bordoni, S Salani, L Franceschina, M Sciacco, A Prelle, ... Annals of neurology 43 (1), 110-116, 1998 | 317 | 1998 |
| Assembly of cytochrome‐c oxidase in cultured human cells LGJ Nijtmans, JW Taanman, AO Muijsers, D Speijer, C Van den Bogert European journal of biochemistry 254 (2), 389-394, 1998 | 310 | 1998 |
| Mitochondria in the etiology and pathogenesis of Parkinson's disease AHV Schapira, M Gu, JW Taanman, SJ Tabrizi, T Seaton, M Cleeter, ... Annals of neurology 44 (S1 1), S89-S98, 1998 | 288 | 1998 |
| Expression of mutant α-synuclein causes increased susceptibility to dopamine toxicity SJ Tabrizi, M Orth, JM Wilkinson, JW Taanman, TT Warner, JM Cooper, ... Human molecular genetics 9 (18), 2683-2689, 2000 | 253 | 2000 |
| Silencing of PINK1 expression affects mitochondrial DNA and oxidative phosphorylation in dopaminergic cells ME Gegg, JM Cooper, AHV Schapira, JW Taanman Plos one 4 (3), e4756, 2009 | 238 | 2009 |
| Dominant inheritance of premature ovarian failure associated with mutant mitochondrial DNA polymerase gamma AT Pagnamenta, JW Taanman, CJ Wilson, NE Anderson, R Marotta, ... Human Reproduction 21 (10), 2467-2473, 2006 | 182 | 2006 |
| Cytochrome c oxidase subassemblies in fibroblast cultures from patients carrying mutations in COX10, SCO1, or SURF1 SL Williams, I Valnot, P Rustin, JW Taanman Journal of Biological Chemistry 279 (9), 7462-7469, 2004 | 181 | 2004 |
| Status epilepticus in children with Alpers’ disease caused by POLG1 mutations: EEG and MRI features NI Wolf, S Rahman, B Schmitt, JW Taanman, AJ Duncan, I Harting, ... Epilepsia 50 (6), 1596-1607, 2009 | 168 | 2009 |
| A missense mutation of cytochrome oxidase subunit II causes defective assembly and myopathy S Rahman, JW Taanman, JM Cooper, I Nelson, I Hargreaves, B Meunier, ... The American Journal of Human Genetics 65 (4), 1030-1039, 1999 | 167 | 1999 |
| [9] Mammalian cytochrome-c oxidase: Characterization of enzyme and immunological detection of subunits in tissue extracts and whole cells RA Capaldi, MF Marusich, JW Taanman Methods in Enzymology 260, 117-132, 1995 | 165 | 1995 |
| A novel frameshift mutation of the mtDNA COIII gene leads to impaired assembly of cytochrome c oxidase in a patient affected by Leigh-like syndrome V Tiranti, P Corona, M Greco, JW Taanman, F Carrara, E Lamantea, ... Human molecular genetics 9 (18), 2733-2742, 2000 | 153 | 2000 |
| NDUFA4 mutations underlie dysfunction of a cytochrome c oxidase subunit linked to human neurological disease RDS Pitceathly, S Rahman, Y Wedatilake, JM Polke, S Cirak, AR Foley, ... Cell reports 3 (6), 1795-1805, 2013 | 141 | 2013 |
| Expression of mtDNA and nDNA encoded respiratory chain proteins in chemically and genetically-derived Rho0 human fibroblasts: a comparison of subunit proteins in normal … MF Marusich, BH Robinson, JW Taanman, SJ Kim, R Schillace, JL Smith, ... Biochimica et Biophysica Acta (BBA)-Molecular Basis of Disease 1362 (2-3 …, 1997 | 134 | 1997 |
