| Premature ageing in mice expressing defective mitochondrial DNA polymerase A Trifunovic, A Wredenberg, M Falkenberg, JN Spelbrink, AT Rovio, ... Nature 429 (6990), 417-423, 2004 | 3053 | 2004 |
| Muscle Biopsy E-Book: A Practical Approach V Dubowitz, A Oldfors, CA Sewry Elsevier Health Sciences, 2013 | 2515* | 2013 |
| Mitochondrial transcription factor A is necessary for mtDNA maintance and embryogenesis in mice NG Larsson, J Wang, H Wilhelmsson, A Oldfors, P Rustin, M Lewandoski, ... Nature genetics 18 (3), 231-236, 1998 | 1783 | 1998 |
| Parkinsonism, premature menopause, and mitochondrial DNA polymerase γ mutations: clinical and molecular genetic study P Luoma, A Melberg, JO Rinne, JA Kaukonen, NN Nupponen, ... The Lancet 364 (9437), 875-882, 2004 | 650 | 2004 |
| Impaired insulin secretion and β-cell loss in tissue-specific knockout mice with mitochondrial diabetes JP Silva, M Köhler, C Graff, A Oldfors, MA Magnuson, PO Berggren, ... Nature genetics 26 (3), 336-340, 2000 | 510 | 2000 |
| Dilated cardiomyopathy and atrioventricular conduction blocks induced by heart-specific inactivation of mitochondrial DNA gene expression J Wang, H Wilhelmsson, C Graff, H Li, A Oldfors, P Rustin, JC Brüning, ... Nature genetics 21 (1), 133-137, 1999 | 490 | 1999 |
| The incidence of mitochondrial encephalomyopathies in childhood: clinical features and morphological, biochemical, and DNA abnormalities N Darin, A Oldfors, AR Moslemi, E Holme, M Tulinius Annals of neurology 49 (3), 377-383, 2001 | 443 | 2001 |
| Mutations in amphiphysin 2 (BIN1) disrupt interaction with dynamin 2 and cause autosomal recessive centronuclear myopathy AS Nicot, A Toussaint, V Tosch, C Kretz, C Wallgren-Pettersson, ... Nature genetics 39 (9), 1134-1139, 2007 | 413 | 2007 |
| Progressive increase of the mutated mitochondrial DNA fraction in Kearns-Sayre syndrome N Larsson, E Holme, B Kristiansson, A Oldfors, M Tulinius Pediatric research 28 (2), 131-136, 1990 | 378 | 1990 |
| ETFDH mutations as a major cause of riboflavin-responsive multiple acyl-CoA dehydrogenation deficiency RKJ Olsen, SE Olpin, BS Andresen, ZH Miedzybrodzka, M Pourfarzam, ... Brain 130 (8), 2045-2054, 2007 | 346 | 2007 |
| Increased mitochondrial mass in mitochondrial myopathy mice A Wredenberg, R Wibom, H Wilhelmsson, C Graff, HH Wiener, SJ Burden, ... Proceedings of the National Academy of Sciences 99 (23), 15066-15071, 2002 | 322 | 2002 |
| Cardiomyopathy in children with mitochondrial disease: clinical course and cardiological findings D Holmgren, H Wahlander, BO Eriksson, A Oldfors, E Holme, M Tulinius European heart journal 24 (3), 280-288, 2003 | 282 | 2003 |
| Rett syndrome: 3-D confocal microscopy of cortical pyramidal dendrites and afferents PV Belichenko, A Oldfors, B Hagberg, A Dahlström Neuroreport 5 (12), 1509-1513, 1994 | 276 | 1994 |
| Low levels of mitochondrial transcription factor A in mitochondrial DNA depletion NG Larsson, A Oldfors, E Holme, DA Clayton Biochemical and biophysical research communications 200 (3), 1374-1381, 1994 | 253 | 1994 |
| Ageing muscle: clonal expansions of mitochondrial DNA point mutations and deletions cause focal impairment of mitochondrial function G Fayet, M Jansson, D Sternberg, AR Moslemi, P Blondy, A Lombès, ... Neuromuscular Disorders 12 (5), 484-493, 2002 | 235 | 2002 |
| Segregation and manifestations of the mtDNA tRNA (Lys) A--> G (8344) mutation of myoclonus epilepsy and ragged-red fibers (MERRF) syndrome. NG Larsson, MH Tulinius, E Holme, A Oldfors, O Andersen, J Wahlström, ... American journal of human genetics 51 (6), 1201, 1992 | 215 | 1992 |
| Myosinopathies: pathology and mechanisms H Tajsharghi, A Oldfors Acta neuropathologica 125, 3-18, 2013 | 203 | 2013 |
| Leber's hereditary optic neuropathy and complex I deficiency in muscle NG Larsson, O Andersen, E Holme, A Oldfors, J Wahlström Annals of Neurology: Official Journal of the American Neurological …, 1991 | 191 | 1991 |
| Autosomal dominant myopathy: missense mutation (Glu-706→ Lys) in the myosin heavy chain IIa gene T Martinsson, A Oldfors, N Darin, K Berg, H Tajsharghi, M Kyllerman, ... Proceedings of the National Academy of Sciences 97 (26), 14614-14619, 2000 | 187 | 2000 |
| Hexosamine biosynthetic pathway mutations cause neuromuscular transmission defect J Senderek, JS Müller, M Dusl, TM Strom, V Guergueltcheva, I Diepolder, ... The American Journal of Human Genetics 88 (2), 162-172, 2011 | 179 | 2011 |
Maria FalkenbergProfessorVerified email at medkem.gu.se
