Dominique Chretien

Overview

Best Publications

• Biochemical and molecular investigations in respiratory chain deficiencies

  P. Rustin;D. Chretien;T. Bourgeron;B. Gérard

  1448
  Citations

• Aconitase and mitochondrial iron-sulphur protein deficiency in Friedreich ataxia.

  Agnès Rötig;Pascale de Lonlay;Dominique Chretien;Françoise Foury

  1168
  Citations

• Mutation of a nuclear succinate dehydrogenase gene results in mitochondrial respiratory chain deficiency

  Thomas Bourgeron;Pierre Rustin;Dominique Chretien;Mark Birch-Machin

  883
  Citations

• Mutation of RRM2B, encoding p53-controlled ribonucleotide reductase (p53R2), causes severe mitochondrial DNA depletion.

  Alice Bourdon;Limor Minai;Valérie Serre;Valérie Serre;Jean-Philippe Jais

  608
  Citations

• Mitochondria are physiologically maintained at close to 50 °C.

  Dominique Chretien;Paule Benit;Paule Benit;Hyung-Ho Ha;Susanne Keipert

  450
  Citations

• Quinone-responsive multiple respiratory-chain dysfunction due to widespread coenzyme Q10 deficiency

  Agnés Rötig;Eeva-Liisa Appelkvist;Vanna Geromel;Dominique Chretien

  421
  Citations

• CABC1 Gene Mutations Cause Ubiquinone Deficiency with Cerebellar Ataxia and Seizures

  Julie Mollet;Agnès Delahodde;Valérie Serre;Dominique Chretien

  388
  Citations

• A mutant mitochondrial respiratory chain assembly protein causes complex III deficiency in patients with tubulopathy, encephalopathy and liver failure

  Pascale De Lonlay;Isabelle Valnot;Antoni Barrientos;Marina Gorbatyuk

  368
  Citations

• Prenyldiphosphate synthase, subunit 1 (PDSS1) and OH-benzoate polyprenyltransferase (COQ2) mutations in ubiquinone deficiency and oxidative phosphorylation disorders

  Julie Mollet;Irina Giurgea;Dimitri Schlemmer;Gustav Dallner

  336
  Citations

• Nuclear Outsourcing of RNA Interference Components to Human Mitochondria

  Simonetta Bandiera;Silvia Rüberg;Muriel Girard;Nicolas Cagnard

  309
  Citations

• Large-Scale Deletion and Point Mutations of the Nuclear NDUFV1 and NDUFS1 Genes in Mitochondrial Complex I Deficiency

  Paule Bénit;Dominique Chretien;Nohman Kadhom;Pascale de Lonlay-Debeney

  302
  Citations

• Compound heterozygous mutations in the flavoprotein gene of the respiratory chain complex II in a patient with Leigh syndrome.

  Béatrice Parfait;Dominique Chretien;Agnès Rötig;Cécile Marsac

  251
  Citations

• Spectrum of mitochondrial DNA rearrangements in the Pearson marrow-pancreas syndrome

  Agnès Rötig;Thomas Bourgeron;Dominique Chretien;Pierre Rustin

  245
  Citations

• Clinical aspects of mitochondrial disorders.

  A. Munnich;P. Rustin;A. Rötig;D. Chretien

  230
  Citations

• Coenzyme Q10 and idebenone in the therapy of respiratory chain diseases: rationale and comparative benefits

  Vanna Geromel;Niklas Darin;Dominique Chrétien;Paule Bénit

  225
  Citations

• Mitochondrial DNA depletion is a prevalent cause of multiple respiratory chain deficiency in childhood.

  Emmanuelle Sarzi;Alice Bourdon;Dominique Chrétien;Mohamed Zarhrate

  222
  Citations

• Mutant NDUFS3 subunit of mitochondrial complex I causes Leigh syndrome

  P Bénit;A Slama;F Cartault;I Giurgea

  221
  Citations

• Mutation of the fumarase gene in two siblings with progressive encephalopathy and fumarase deficiency.

  T Bourgeron;D Chretien;J Poggi-Bach;S Doonan

  216
  Citations

• Multiple OXPHOS deficiency in the liver, kidney, heart, and skeletal muscle of patients with methylmalonic aciduria and propionic aciduria.

  Yves de Keyzer;Vassili Valayannopoulos;Jean-François Benoist;Frédéric Batteux

  209
  Citations

• Clinical presentation of mitochondrial disorders in childhood.

  A. Munnich;A. Rötig;D. Chretien;V. Cormier

  208
  Citations