Dominique Chrétien - Concepedia

Author

Dominique Chrétien

Inserm ORCID

Also Known As

D Chretien, D Chrétien, D. Chretien, D. Chrétien, Dominique CHRETIEN, Dominique Chretien, Dominique Chrétien

121

Publications

12.2K

Citations

H-Index

146

Concepts

All Affiliations

Inserm Hôpital Necker-Enfants Malades Hôpital des Enfants Université Paris Cité Délégation Paris 5

About

Dominique Chrétien is an author at Inserm specializing in medicine, mitochondrial function, and genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	43	67	8K
2	Natural Sciences	11	11	2.8K
3	Health Sciences	9	9	484
4	Engineering	3	3	206
5	Public Health	2	2	99

Dominique Chrétien

Publications

9.9K

Citations

H-Index

Page 1

	Year	Citations
Aconitase and mitochondrial iron–sulphur protein deficiency in Friedreich ataxia Agnès Rötig, Pascale de Lonlay, Dominique Chrétien, Nature Genetics Mitochondrial FunctionBiochemistryIron MetabolismDegenerative DiseaseFriedreich Ataxia	1997	987
Mutation of a nuclear succinate dehydrogenase gene results in mitochondrial respiratory chain deficiency Thomas Bourgeron, Pierre Rustin, Dominique Chrétien, Nature Genetics Mitochondrial FunctionBiochemistryNatural SciencesGeneticsMitochondrial Structure	1995	723
Mutation of RRM2B, encoding p53-controlled ribonucleotide reductase (p53R2), causes severe mitochondrial DNA depletion Alice Bourdon, Limor Minai, Valérie Serre, Nature Genetics Genome InstabilityMitochondrial FunctionP53-controlled Ribonucleotide ReductaseGeneticsNatural Sciences	2007	517
Mitochondria are physiologically maintained at close to 50 °C Dominique Chrétien, Paule Bénit, Hyung‐Ho Ha, PLoS Biology Molecular BiologyMitochondrial BiologyRedox BiologyOxidative StressMitochondrial Biogenesis	2018	419
Quinone-responsive multiple respiratory-chain dysfunction due to widespread coenzyme Q10 deficiency Agnès Rötig, Eeva‐Liisa Appelkvist, Vanna Géromel, The Lancet Inflammatory Lung DiseasePhysiologyMolecular BiologyMedicineOxidative Stress	2000	357
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, Nature Genetics Liver FailureMitophagyProtein Quality ControlBiochemistryMitochondrial Function	2001	313
Nuclear Outsourcing of RNA Interference Components to Human Mitochondria Simonetta Bandiera, Silvia Rüberg, M Girard, PLoS ONE GeneticsMolecular BiologyNuclear OutsourcingEpigeneticsTranscriptional Regulation	2011	290
CABC1 Gene Mutations Cause Ubiquinone Deficiency with Cerebellar Ataxia and Seizures Julie Mollet, Agnès Delahodde, Valérie Serre, The American Journal of Human Genetics Neurodegenerative DiseasesMolecular NeuroscienceMendelian DisorderGenetic DisorderGenetics	2008	290
Large-Scale Deletion and Point Mutations of the Nuclear NDUFV1 and NDUFS1 Genes in Mitochondrial Complex I Deficiency Paule Bénit, Dominique Chrétien, N. Kadhom, The American Journal of Human Genetics Point MutationsMitochondrial FunctionMitochondrial BiogenesisMitochondrial DynamicGenetics	2001	260
Prenyldiphosphate synthase, subunit 1 (PDSS1) and OH-benzoate polyprenyltransferase (COQ2) mutations in ubiquinone deficiency and oxidative phosphorylation disorders Julie Mollet, Irina Giurgea, Dimitri Schlemmer, Journal of Clinical Investigation	2007	252

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