Anders Oldfors

Research.com Recognitions

• 2023 - Research.com Biology and Biochemistry in Sweden Leader Award

Overview

Best Publications

• Premature ageing in mice expressing defective mitochondrial DNA polymerase

  Aleksandra Trifunovic;Anna Wredenberg;Maria Falkenberg;Johannes N. Spelbrink

  3061
  Citations

• Muscle Biopsy: A Practical Approach

  Victor Dubowitz;Caroline A. Sewry;Anders Oldfors;Russell J. M. Lane

  2112
  Citations

• Mitochondrial transcription factor A is necessary for mtDNA maintenance and embryogenesis in mice

  Nils-Göran Larsson;Jianming Wang;Hans Wilhelmsson;Anders Oldfors

  1781
  Citations

• Parkinsonism, premature menopause, and mitochondrial DNA polymerase gamma mutations: clinical and molecular genetic study.

  Petri Luoma;Atle Melberg;Juha O Rinne;Jyrki A Kaukonen

  642
  Citations

• Impaired insulin secretion and β-cell loss in tissue-specific knockout mice with mitochondrial diabetes

  José P. Silva;Martin Köhler;Caroline Graff;Anders Oldfors

  499
  Citations

• Dilated cardiomyopathy and atrioventricular conduction blocks induced by heart-specific inactivation of mitochondrial DNA gene expression

  Jianming Wang;H. Wilhelmsson;C. Graff;Hong Li

  477
  Citations

• The incidence of mitochondrial encephalomyopathies in childhood: clinical features and morphological, biochemical, and DNA abnormalities.

  Niklas Darin;Anders Oldfors;Ali‐Reza Moslemi;Elisabeth Holme

  432
  Citations

• Mutations in amphiphysin 2 ( BIN1 ) disrupt interaction with dynamin 2 and cause autosomal recessive centronuclear myopathy

  Anne-Sophie Nicot;Anne Toussaint;Valérie Tosch;Christine Kretz

  421
  Citations

• Progressive increase of the mutated mitochondrial DNA fraction in Kearns-Sayre syndrome.

  Nils-göran Larsson;Elisabeth Holme;Bengt Kristiansson;Anders Oldfors

  377
  Citations

• ETFDH mutations as a major cause of riboflavin-responsive multiple acyl-CoA dehydrogenation deficiency

  Rikke K J Olsen;Simon E Olpin;Brage S Andresen;Zofia H Miedzybrodzka

  341
  Citations

• Increased mitochondrial mass in mitochondrial myopathy mice.

  Anna Wredenberg;Rolf Wibom;Hans Wilhelmsson;Caroline Graff

  322
  Citations

• Rett syndrome: 3-D confocal microscopy of cortical pyramidal dendrites and afferents.

  Pavel V. Belichenko;Anders Oldfors;Bengt Hagberg;Annica Dahlström

  322
  Citations

• Cardiomyopathy in children with mitochondrial disease; clinical course and cardiological findings.

  D Holmgren;H Wåhlander;B O Eriksson;A Oldfors

  270
  Citations

• Low Levels of Mitochondrial Transcription Factor A in Mitochondrial DNA Depletion

  N.G. Larsson;A. Oldfors;E. Holme;D.A. Clayton

  259
  Citations

• Ageing muscle: clonal expansions of mitochondrial DNA point mutations and deletions cause focal impairment of mitochondrial function.

  Guillemette Fayet;Monica Jansson;Damien Sternberg;Ali Reza Moslemi

  235
  Citations

• Segregation and manifestations of the mtDNA tRNA(Lys) A-->G(8344) mutation of myoclonus epilepsy and ragged-red fibers (MERRF) syndrome.

  N G Larsson;M H Tulinius;E Holme;A Oldfors

  213
  Citations

• Myosinopathies: pathology and mechanisms.

  Homa Tajsharghi;Anders Oldfors

  212
  Citations

• A single mouse gene encodes the mitochondrial transcription factor A and a testis-specific nuclear HMG-box protein.

  Larsson Ng;Garman Jd;Oldfors A;Barsh Gs

  206
  Citations

• Leber's hereditary optic neuropathy and complex I deficiency in muscle.

  Nils-Göran Larsson;Oluf Andersen;Elisabeth Holme;Anders Oldfors

  190
  Citations

• Autosomal dominant myopathy: missense mutation (Glu-706 --> Lys) in the myosin heavy chain IIa gene.

  Tommy Martinsson;Anders Oldfors;Niklas Darin;Kerstin Berg

  184
  Citations