Dominique Chrétien

12.3k citations

106 papers · 9.2k indexed · 3 hit papers · h-index 50

Molecular Biology top 0.5%
Clinical Biochemistry top 0.02%
Cellular and Molecular Neuroscience top 2%
Physiology top 5%
Biochemistry top 0.5%

Co-authors: Arnold Münnich Agnès Rötig Pierre Rustin Thomas Bourgeron Pascale de Lonlay Jean‐Marie Saudubray Bénédicte Gérard Paule Bénit
Topics: Mitochondrial Function and Pathology (70 papers)Metabolism and Genetic Disorders (61 papers)ATP Synthase and ATPases Research (30 papers)
Cited by: Clinical Biochemistry Molecular Biology Biochemistry
Journals: The Lancet Journal of Biological Chemistry Journal of Clinical Investigation
Partner nations: France United Kingdom Germany

In The Last Decade

Dominique Chrétien

106 papers receiving 9.0k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Biochemical and molecular investigations in respiratory chain deficiencies

1994 1.1k citations Pierre Rustin, Dominique Chrétien et al. Clinica Chimica Acta profile →
Aconitase and mitochondrial iron–sulphur protein deficiency in Friedreich ataxia

1997 786 citations Agnès Rötig, Pascale de Lonlay et al. Nature Genetics profile →
Mutation of a nuclear succinate dehydrogenase gene results in mitochondrial respiratory chain deficiency

1995 544 citations Thomas Bourgeron, Pierre Rustin et al. Nature Genetics profile →

Peers

Countries citing papers authored by Dominique Chrétien

Since Specialization

Citations

This map shows the geographic impact of Dominique Chrétien's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Dominique Chrétien with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Dominique Chrétien more than expected).

Fields of papers citing papers by Dominique Chrétien

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Dominique Chrétien. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Dominique Chrétien. The network helps show where Dominique Chrétien may publish in the future.

Co-authorship network of co-authors of Dominique Chrétien

This figure shows the co-authorship network connecting the top 25 collaborators of Dominique Chrétien. A scholar is included among the top collaborators of Dominique Chrétien based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Dominique Chrétien. Dominique Chrétien is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

#	Work	Indexed citations
1	The class 3 PI3K coordinates autophagy and mitochondrial lipid catabolism by controlling nuclear receptor PPARα 2019 ·Nature Communications ·(unknown),Ivan Nemazanyy,(unknown),M Girard,Esther Barth,Nicolas Cagnard,Alexandra Montagner,Dominique Chrétien,Elena I. Rugarli,Hervé Guillou,Mario Pende,Ganna Panasyuk	82
2	Evolutionarily conserved susceptibility of the mitochondrial respiratory chain to SDHI pesticides and its consequence on the impact of SDHIs on human cultured cells 2019 ·PLoS ONE ·Paule Bénit,(unknown),Dominique Chrétien,Sylvie Bortoli,Laurence Huc,Manuel Schiff,Anne‐Paule Gimenez‐Roqueplo,Judith Favier,Pierre Gressèns,Malgorzata Rak,Pierre Rustin	48
3	Mitochondria are physiologically maintained at close to 50 °C 2018 ·PLoS Biology ·Dominique Chrétien,Paule Bénit,Hyung‐Ho Ha,Susanne Keipert,Riyad El‐Khoury,Young‐Tae Chang,Martin Jastroch,Howard T. Jacobs,Pierre Rustin,Malgorzata Rak	320
4	Unusual clinical expression and long survival of a pseudouridylate synthase (PUS1) mutation into adulthood 2014 ·European Journal of Human Genetics ·Metodi D. Metodiev,Zahra Assouline,P. Landrieu,Dominique Chrétien,Brigitte Bader‐Meunier,Corinne Guitton,Arnold Münnich,Agnès Rötig	19
5	Multiple OXPHOS Deficiency in the Liver, Kidney, Heart, and Skeletal Muscle of Patients With Methylmalonic Aciduria and Propionic Aciduria 2009 ·Pediatric Research ·Yves de Keyzer,Vassili Valayannopoulos,Jean‐François Benoist,Frédéric Batteux,Florence Lacaille,Laurence Hubert,Dominique Chrétien,(unknown),Patrick Niaudet,Guy Touati,Arnold Münnich,Pascale de Lonlay	121
6	CABC1 Gene Mutations Cause Ubiquinone Deficiency with Cerebellar Ataxia and Seizures 2008 ·The American Journal of Human Genetics ·(unknown),Agnès Delahodde,Valérie Serre,Dominique Chrétien,Dimitri Schlemmer,Anne Lombès,Nathalie Boddaert,Isabelle Desguerre,Pascale de Lonlay,Hélène Ogier de Baulny,Arnold Münnich,Agnès Rötig	215
7	Mutation of RRM2B, encoding p53-controlled ribonucleotide reductase (p53R2), causes severe mitochondrial DNA depletion 2007 ·Nature Genetics ·(unknown),Limor Minai,Valérie Serre,Jean-Philippe Jaı̈s,Emmanuelle Sarzi,Sophie Aubert,Dominique Chrétien,Pascale de Lonlay,Véronique Paquis‐Flucklinger,Hirofumi Arakawa,Yusuke Nakamura,Arnold Münnich,Agnès Rötig	428
8	A novel recurrent mitochondrial DNA mutation in ND3 gene is associated with isolated complex I deficiency causing Leigh syndrome and dystonia 2006 ·American Journal of Medical Genetics Part A ·Emmanuelle Sarzi,Michael D. Brown,Sophie Lebon,Dominique Chrétien,Arnold Münnich,Agnès Rötig,Vincent Procaccio	86
9	Respiratory chain deficiency presenting as congenital nephrotic syndrome 2005 ·Pediatric Nephrology ·Alice Goldenberg,(unknown),(unknown),Valérie Cormier‐Daire,Marie‐France Gagnadoux,Dominique Chrétien,(unknown),Vanna Géromel,Agnès Rötig,Pierre Rustin,Arnold Münnich,(unknown),Corinne Antignac,Marie-Claire Gübler,Patrick Niaudet,Pascale de Lonlay,E. Bérard	29
10	Mitochondrial activities in human cultured skin fibroblasts contaminated by Mycoplasma hyorhinis 2003 ·BMC Biochemistry ·Niklas Darín,(unknown),Jean-Jacques Brière,Dominique Chrétien,Cécile Bébéar,Agnès Rötig,Arnold Münnich,Pierre Rustin	11
11	Mutations in BCS1, a mitochondrial respiratory chain assembly gene, are responsible for complex III deficiency in patients with tubulopathy, encephalopathy and liver failure. 2001 ·UCL Discovery (University College London) ·Pascale de Lonlay,Isabelle Valnot,(unknown),Marina S. Gorbatyuk,Alexander Tzagoloff,Jan‐Willem Taanman,Dominique Chrétien,N. Kadhom,Anne Lombès,(unknown),Patrick Niaudet,Arnold Münnich,Pierre Rustin,Agnès Rötig	3
12	Frataxin gene expansion causes aconitase and mitochondrial iron-sulphur protein deficiency in Friedreich ataxia 1998 ·European Journal of Human Genetics ·Agnès Rötig,Pascale de Lonlay,Dominique Chrétien,Françoise Foury,M. Koenig,Daniel Sidi,A Munnich,Pierre Rustin	2
13	Inborn errors of the Krebs cycle: a group of unusual mitochondrial diseases in human 1997 ·Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease ·Pierre Rustin,Thomas Bourgeron,Béatrice Parfait,Dominique Chrétien,Arnold Münnich,Agnès Rötig	104
14	Craniofacial anomalies and malformations in respiratory chain deficiency 1996 ·American Journal of Medical Genetics ·Valérie Cormier‐Daire,Pierre Rustin,Agnès Rötig,Dominique Chrétien,M. Le Merrer,Dominique C. Belli,(unknown),Philippe Hubert,C. Ricour,Arnold Münnich	43
15	Mutation of a nuclear succinate dehydrogenase gene results in mitochondrial respiratory chain deficiencybreakdown → 1995 ·Nature Genetics ·Thomas Bourgeron,Pierre Rustin,Dominique Chrétien,Mark A. Birch‐Machin,Marie Bourgeois,E. Viégas-Pèquignot,Arnold Münnich,Agnès Rötig	544
16	Spectrum of mitochondrial DNA rearrangements in the Pearson marrow-pancreas syndrome 1995 ·Human Molecular Genetics ·Agnès Rötig,Thomas Bourgeron,Dominique Chrétien,Pierre Rustin,Arnold Münnich	145
17	Mutation of the fumarase gene in two siblings with progressive encephalopathy and fumarase deficiency. 1994 ·Journal of Clinical Investigation ·Thomas Bourgeron,Dominique Chrétien,(unknown),Shawn Doonan,Daniel Rabier,(unknown),Arnold Münnich,Agnès Rötig,P. Landrieu,Pierre Rustin	114
18	Reference charts for respiratory chain activities in human tissues 1994 ·Clinica Chimica Acta ·Dominique Chrétien,Pierre Rustin,Thomas Bourgeron,Agnès Rötig,Jean Marie Saudubray,Arnold Münnich	120
19	Valproate-induced hepatic failure in a case of cytochromec oxidase deficiency 1994 ·European Journal of Pediatrics ·B. Chabrol,Julien Mancini,Dominique Chrétien,Pierre Rustin,Arnold Münnich,N Pinsard	39
20	Lipid changes in jojoba explants in relation to callus or shoot development. 1990 ·Plant Physiology and Biochemistry ·Dominique Chrétien,(unknown),(unknown),(unknown),(unknown),Catherine Cantrel,J.P. Dubacq	2

About Dominique Chrétien

Dominique Chrétien is a scholar working on Clinical Biochemistry, Molecular Biology and Biochemistry, having authored 106 papers that have together received 9.2k indexed citations. Recurring topics across this work include Mitochondrial Function and Pathology (70 papers), Metabolism and Genetic Disorders (61 papers) and ATP Synthase and ATPases Research (30 papers). The work is most often cited by research in Clinical Biochemistry (3.7k citations), Molecular Biology (7.5k citations) and Biochemistry (660 citations). Dominique Chrétien has collaborated with scholars based in France, United Kingdom and Germany. Frequent co-authors include Arnold Münnich, Agnès Rötig, Pierre Rustin, Thomas Bourgeron, Pascale de Lonlay, Jean‐Marie Saudubray, Bénédicte Gérard, Paule Bénit, Daniel Sidi and Valérie Cormier‐Daire. Their work appears in journals such as The Lancet, Journal of Biological Chemistry and Journal of Clinical Investigation.

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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