D-Index & Metrics Best Publications

Dominique Chretien

Grenoble Alpes University
France

D-Index & Metrics D-index (Discipline H-index) only includes papers and citation values for an examined discipline in contrast to General H-index which accounts for publications across all disciplines.

Discipline name Citations Publications World Ranking National Ranking

Genetics D-index 57 Citations 12,931 100 World Ranking 2605 National Ranking 128

Overview

What is he best known for?

The fields of study Dominique Chretien is best known for:

Gene
Enzyme
Biochemistry

His Geometry study frequently involves adjacent topics like Curvature and Growth rate. Curvature and Geometry are two areas of study in which Dominique Chretien engages in interdisciplinary research. He integrates Cell biology with Biophysics in his study. He performs integrative study on Biophysics and Biochemistry in his works. His Biochemistry study frequently links to adjacent areas such as GTP'. His research on GTP' often connects related areas such as Guanosine triphosphate. He integrates Guanosine triphosphate with Hydrolysis in his study. In his research, Dominique Chretien undertakes multidisciplinary study on Hydrolysis and Enzyme. Dominique Chretien combines Enzyme and Cell biology in his research.

His most cited work include:

Structure of growing microtubule ends: two-dimensional sheets close into tubes at variable rates. (401 citations)
Structural changes accompanying GTP hydrolysis in microtubules: information from a slowly hydrolyzable analogue guanylyl-(alpha,beta)-methylene-diphosphonate. (226 citations)
Lattice defects in microtubules: protofilament numbers vary within individual microtubules (210 citations)

What are the main themes of his work throughout his whole career to date

Respiratory chain and Mitochondrial respiratory chain are the focus of his Mitochondrion studies. His Biochemistry study frequently draws connections between adjacent fields such as Oxidative phosphorylation. He integrates many fields, such as Oxidative phosphorylation and Mitochondrion, in his works. He conducted interdisciplinary study in his works that combined Cell biology and Biophysics. In his works, he conducts interdisciplinary research on Biophysics and Biochemistry. He integrates many fields, such as Microtubule and Tubulin, in his works. Dominique Chretien integrates Tubulin with Microtubule in his study. In his articles, Dominique Chretien combines various disciplines, including Gene and Mitochondrial disease. He undertakes multidisciplinary studies into Mitochondrial disease and Mitochondrial DNA in his work.

Dominique Chretien most often published in these fields:

Biochemistry (56.25%)
Cell biology (43.75%)
Microtubule (37.50%)

This overview was generated by a machine learning system which analysed the scientist’s body of work. If you have any feedback, you can contact us here.

Best Publications

Biochemical and molecular investigations in respiratory chain deficiencies

P. Rustin;D. Chretien;T. Bourgeron;B. Gérard.
Clinica Chimica Acta (1994)

1387 Citations

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

Agnès Rötig;Pascale de Lonlay;Dominique Chretien;Françoise Foury.
Nature Genetics (1997)

1121 Citations

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

Thomas Bourgeron;Pierre Rustin;Dominique Chretien;Mark Birch-Machin.
Nature Genetics (1995)

854 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.
Nature Genetics (2007)

584 Citations

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

Agnés Rötig;Eeva-Liisa Appelkvist;Vanna Geromel;Dominique Chretien.
The Lancet (2000)

402 Citations

CABC1 Gene Mutations Cause Ubiquinone Deficiency with Cerebellar Ataxia and Seizures

Julie Mollet;Agnès Delahodde;Valérie Serre;Dominique Chretien.
American Journal of Human Genetics (2008)

366 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.
Nature Genetics (2001)

346 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.
Journal of Clinical Investigation (2007)

316 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.
American Journal of Human Genetics (2001)

289 Citations

Nuclear Outsourcing of RNA Interference Components to Human Mitochondria

Simonetta Bandiera;Silvia Rüberg;Muriel Girard;Nicolas Cagnard.
PLOS ONE (2011)

263 Citations

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