A. Lombès

509 total citations
8 papers, 373 citations indexed

About

A. Lombès is a scholar working on Molecular Biology, Clinical Biochemistry and Cellular and Molecular Neuroscience. According to data from OpenAlex, A. Lombès has authored 8 papers receiving a total of 373 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Molecular Biology, 5 papers in Clinical Biochemistry and 2 papers in Cellular and Molecular Neuroscience. Recurrent topics in A. Lombès's work include Mitochondrial Function and Pathology (5 papers), Metabolism and Genetic Disorders (5 papers) and RNA modifications and cancer (3 papers). A. Lombès is often cited by papers focused on Mitochondrial Function and Pathology (5 papers), Metabolism and Genetic Disorders (5 papers) and RNA modifications and cancer (3 papers). A. Lombès collaborates with scholars based in France, United Kingdom and Australia. A. Lombès's co-authors include Damien Sternberg, Pascal Laforêt, Andy J. Wills, J. P. Mottershead, Margaret Jackson, N. Quinn, Mark Kellett, Douglas E. Crompton, David Bates and Claude Jardel and has published in prestigious journals such as Brain, Neurology and Human Molecular Genetics.

In The Last Decade

A. Lombès

8 papers receiving 366 citations

Peers

Countries citing papers authored by A. Lombès

Since Specialization

Citations

This map shows the geographic impact of A. Lombès'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 A. Lombès with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites A. Lombès more than expected).

Fields of papers citing papers by A. Lombès

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by A. Lombès. 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 A. Lombès. The network helps show where A. Lombès may publish in the future.

Co-authorship network of co-authors of A. Lombès

This figure shows the co-authorship network connecting the top 25 collaborators of A. Lombès. A scholar is included among the top collaborators of A. Lombès 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 A. Lombès. A. Lombès is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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8 of 8 papers shown

#	Work	Indexed citations
1	Severe epilepsy as the major symptom of new mutations in the mitochondrial tRNA ^Phe gene 2010 ·Neurology ·Gábor Zsurka, Kevin G. Hampel, Isabelle Nelson, Claude Jardel, Sandra R. Mirandola, Robert Sassen, Cornelia Kornblum, Pascale Marcorelles, Sébastien Lavoué, A. Lombès, Wolfram S. Kunz	36
2	Clinical features and natural history of neuroferritinopathy caused by the FTL1 460InsA mutation 2006 ·Brain ·Patrick F. Chinnery, Douglas E. Crompton, D. Birchall, Margaret Jackson, Alan Coulthard, A. Lombès, N. Quinn, Andy J. Wills, Nicholas Fletcher, J. P. Mottershead, Paul R. Cooper, Mark Kellett, David Bates, John Burn	134
3	Adult‐onset chorea and mitochondrial cytopathy 2004 ·Movement Disorders ·(unknown), Karine Viala, Richard Lévy, Thierry Maisonobe, F Chochon, A. Lombès, Yves Agid	13
4	Atypical MELAS syndrome associated with a new mitochondrial tRNA glutamine point mutation 2001 ·Neurology ·Marc Bataillard, (unknown), L. Rumbach, Damien Sternberg, (unknown), Pascal Laforêt, Claude Jardel, Thierry Maisonobe, A. Lombès	65
5	Exhaustive Scanning Approach to Screen All the Mitochondrial tRNA Genes for Mutations and Its Application to the Investigation of 35 Independent Patients with Mitochondrial Disorders 1998 ·Human Molecular Genetics ·Damien Sternberg, Claude Danan, A. Lombès, Pascal Laforêt, Emmanuelle Girodon, Michel Goossens, Serge Amselem	63
6	Clinical approach to inherited metabolic diseases in the neonatal period: A 20‐year survey 1989 ·Journal of Inherited Metabolic Disease ·J. M. Saudubray, H. Ogier, Jean‐Paul Bonnefont, Arnold Münnich, A. Lombès, François Hervé, (unknown), (unknown), Norma Spécola, P Parvy, J. Bardet, Daniel Rabier, M. Coudé, C. Charpentier, J Frézal	38
7	Infantile ketoacidosis associated with decreased activity of succinyl‐CoA: 3‐ketoacid CoA‐transferase 1987 ·Journal of Inherited Metabolic Disease ·B. Middleton, R.S. Day, A. Lombès, Jean Marie Saudubray	19
8	[Apparently idiopathic primary myocardiopathies in children. The role of metabolic etiology]. 1987 ·PubMed ·A. Lombès, Françoise Hervé, (unknown), (unknown), Daniel Sidi, E Villain, J Kachaner, C. Charpentier, Marion Paturneau-Jouas, Michel Fardeau	5

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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