D-Index & Metrics Best Publications

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 D-index 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. Citations Publications World Ranking National Ranking
Biology and Biochemistry D-index 58 Citations 11,776 138 World Ranking 8868 National Ranking 313

Overview

What is she best known for?

The fields of study she is best known for:

  • Gene
  • Internal medicine
  • Enzyme

Her scientific interests lie mostly in Mitochondrial DNA, Mitochondrion, Endocrinology, Internal medicine and Cell biology. Her Mitochondrial DNA research entails a greater understanding of Genetics. Her Mitochondrion research incorporates themes from Proteasome, Adenosine triphosphate and Creatine kinase.

Her Adiponectin, Adipocyte and Glucagon study in the realm of Internal medicine interacts with subjects such as Lipoatrophy and Ketogenesis. Mitochondrial fission is closely connected to mitochondrial fusion in her research, which is encompassed under the umbrella topic of Cell biology. Her research in Multiple mitochondrial DNA deletions focuses on subjects like Leukodystrophy, which are connected to Respiratory chain.

Her most cited work include:

  • Mitochondrial DNA Deletions in Progressive External Ophthalmoplegia and Kearns-Sayre Syndrome (828 citations)
  • Mitochondrial fusion in human cells is efficient, requires the inner membrane potential, and is mediated by mitofusins. (519 citations)
  • Membrane topology and mitochondrial targeting of mitofusins, ubiquitous mammalian homologs of the transmembrane GTPase Fzo (438 citations)

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

Her primary areas of investigation include Mitochondrial DNA, Internal medicine, Molecular biology, Mitochondrion and Genetics. Her Mitochondrial DNA study combines topics in areas such as Mutation and Point mutation. She interconnects Gastroenterology, Endocrinology, Surgery and Cardiology in the investigation of issues within Internal medicine.

Her Molecular biology research includes elements of Multiple mitochondrial DNA deletions, Cytochrome b, Gene, Cytochrome c oxidase and Respiratory chain. In her study, Glycolysis is inextricably linked to Oxidative phosphorylation, which falls within the broad field of Mitochondrion. In general Cell biology study, her work on ATP–ADP translocase, Mitochondrial membrane transport protein and Inner mitochondrial membrane often relates to the realm of Progenitor cell, thereby connecting several areas of interest.

She most often published in these fields:

  • Mitochondrial DNA (40.37%)
  • Internal medicine (27.95%)
  • Molecular biology (31.06%)

What were the highlights of her more recent work (between 2012-2020)?

  • Cell biology (26.71%)
  • Mitochondrial DNA (40.37%)
  • Mitochondrial disease (23.60%)

In recent papers she was focusing on the following fields of study:

Her primary areas of study are Cell biology, Mitochondrial DNA, Mitochondrial disease, Internal medicine and Mitochondrion. Her Cell biology study integrates concerns from other disciplines, such as Glycolysis, Cell, Oxidative phosphorylation and Cell culture. Anne Lombès usually deals with Mitochondrial DNA and limits it to topics linked to Mutation and Phenotype.

Her studies examine the connections between Mitochondrial disease and genetics, as well as such issues in Exercise intolerance, with regards to Metabolic myopathy, Gene mutation, Masseter muscle and Endocrinology. Her study looks at the relationship between Internal medicine and topics such as Respiratory chain, which overlap with Muscle biopsy, Cristae formation, Mitochondrial Encephalomyopathies, Cytochrome c oxidase and MICOS complex. Her Mitochondrion study combines topics from a wide range of disciplines, such as Molecular biology and Protein subunit.

Between 2012 and 2020, her most popular works were:

  • Human iPSC-Derived Neural Progenitors Are an Effective Drug Discovery Model for Neurological mtDNA Disorders (67 citations)
  • Human iPSC-Derived Neural Progenitors Are an Effective Drug Discovery Model for Neurological mtDNA Disorders (67 citations)
  • Human iPSC-Derived Neural Progenitors Are an Effective Drug Discovery Model for Neurological mtDNA Disorders (67 citations)

In her most recent research, the most cited papers focused on:

  • Gene
  • Internal medicine
  • Enzyme

Her main research concerns Cell biology, Mitochondrion, Mitochondrial disease, Molecular biology and Mitochondrial DNA. Her research in Cell biology intersects with topics in Cell culture, Cell and Cell growth. Her study on Mitochondrial disease is covered under Genetics.

Her research integrates issues of Mutation, Heteroplasmy, Kearns–Sayre syndrome and Proteases in her study of Molecular biology. The concepts of her Mutation study are interwoven with issues in Phenotype, RNA and Induced pluripotent stem cell. Her studies deal with areas such as HeLa, Small hairpin RNA and Transfection as well as Mitochondrial DNA.

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

Mitochondrial DNA Deletions in Progressive External Ophthalmoplegia and Kearns-Sayre Syndrome

Carlos T. Moraes;Salvatore Dimauro;Massimo Zeviani;Anne Lombes.
The New England Journal of Medicine (1989)

1157 Citations

Mitochondrial fusion in human cells is efficient, requires the inner membrane potential, and is mediated by mitofusins.

Frédéric Legros;Anne Lombès;Paule Frachon;Manuel Rojo.
Molecular Biology of the Cell (2002)

806 Citations

Membrane topology and mitochondrial targeting of mitofusins, ubiquitous mammalian homologs of the transmembrane GTPase Fzo

Manuel Rojo;Frédéric Legros;Danielle Chateau;Anne Lombès.
Journal of Cell Science (2002)

678 Citations

Mitochondrial neurogastrointestinal encephalomyopathy (MNGIE): Clinical, biochemical, and genetic features of an autosomal recessive mitochondrial disorder

Michio Hirano;G. Silvestri;D. M. Blake;A. Lombes.
Neurology (1994)

475 Citations

Organization and dynamics of human mitochondrial DNA

Frédéric Legros;Florence Malka;Paule Frachon;Anne Lombès.
Journal of Cell Science (2004)

475 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

Zidovudine-induced mitochondrial disorder with massive liver steatosis, myopathy, lactic acidosis, and mitochondrial DNA depletion

Patrick Chariot;Irène Drogou;Isabelle de Lacroix-Szmania;Marie-Christine Eliezer-Vanerot.
Journal of Hepatology (1999)

349 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

Dysfunction of mitochondrial complex I and the proteasome: interactions between two biochemical deficits in a cellular model of Parkinson's disease.

Günter U. Höglinger;Géraldine Carrard;Patrick P. Michel;Fadia Medja.
Journal of Neurochemistry (2003)

324 Citations

Annonacin, a lipophilic inhibitor of mitochondrial complex I, induces nigral and striatal neurodegeneration in rats: possible relevance for atypical parkinsonism in Guadeloupe.

Pierre Champy;Günter U. Höglinger;Jean Feger;Christophe Gleye.
Journal of Neurochemistry (2003)

248 Citations

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