Joël Lunardi

8.5k citations

127 papers · 5.8k indexed · h-index 44

Molecular Biology top 1%
Cardiology and Cardiovascular Medicine top 1%
Cell Biology top 2%
Genetics top 5%
Genetics top 2%

Co-authors: Nicole Monnier Pierre V. Vignais Thierry Rabilloud Jean‐Paul Issartel Sylvie Luche P.V. Vignais Manfred Heller Ruedi Aebersold
Topics: Mitochondrial Function and Pathology (33 papers)ATP Synthase and ATPases Research (30 papers)Ion channel regulation and function (30 papers)
Cited by: Molecular Biology Cardiology and Cardiovascular Medicine Genetics
Journals: Proceedings of the National Academy of Sciences Journal of Biological Chemistry Circulation
Partner nations: France United States Germany

In The Last Decade

Joël Lunardi

126 papers receiving 5.6k citations

Peers

Countries citing papers authored by Joël Lunardi

Since Specialization

Citations

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

Fields of papers citing papers by Joël Lunardi

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Joël Lunardi

This figure shows the co-authorship network connecting the top 25 collaborators of Joël Lunardi. A scholar is included among the top collaborators of Joël Lunardi 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 Joël Lunardi. Joël Lunardi 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	An Integrated Diagnosis Strategy for Congenital Myopathies 2013 ·PLoS ONE ·Johann Böhm,Nasim Vasli,Edoardo Malfatti,Stéphanie Le Gras,Claire Feger,Bernard Jost,Nicole Monnier,Julie Brocard,Hatice Karasoy,Marion Gérard,Maggie C. Walter,Peter Reilich,Valérie Biancalana,Christine Kretz,Nadia Messaddeq,Isabelle Marty,Joël Lunardi,Norma B. Romero,Jocelyn Laporte	43
2	MLPA and sequence analysis of DPY19L2 reveals point mutations causing globozoospermia 2012 ·Human Reproduction ·Charles Coutton,Raoudha Zouari,(unknown),Mariem Ben Khelifa,Ghaya Merdassi,Chahnez Triki,Denise Escalier,Laëtitia Hesters,Valérie Mitchell,Rachel Lévy,Nathalie Sermondade,Florence Boitrelle,François Vialard,Véronique Satre,Sylviane Hennebicq,Pierre‐Simon Jouk,Christophe Arnoult,Joël Lunardi,Pierre F. Ray	52
3	Congenital myopathy-causing tropomyosin mutations induce thin filament dysfunction via distinct physiological mechanisms 2012 ·Human Molecular Genetics ·Julien Ochala,David S. Gokhin,I. Pénisson-Besnier,Susana Quijano-Roy,(unknown),Joël Lunardi,Norma B. Romero,Velia M. Fowler	36
4	Recessive RYR1 mutations cause unusual congenital myopathy with prominent nuclear internalization and large areas of myofibrillar disorganization 2010 ·Neuropathology and Applied Neurobiology ·Jorge A. Bevilacqua,Nicole Monnier,Marc Bitoun,B. Eymard,Ana Ferreiro,Soledad Monges,(unknown),(unknown),A. Laquérrière,Kristl G. Claeys,Isabelle Marty,Michel Fardeau,Pascale Guicheney,Joël Lunardi,Norma B. Romero	75
5	short report: Bleeding disorders in Lowe syndrome patients: evidence for a link between OCRL mutations and primary haemostasis disorders 2010 ·British Journal of Haematology ·Dominique Lasne,Geneviève Baujat,Tristan Mirault,Joël Lunardi,Françoise Grelac,(unknown),Rémi Salomon,Christilla Bachelot‐Loza	14
6	Incidence and Risk Factors of Arrhythmic Events in Catecholaminergic Polymorphic Ventricular Tachycardia 2009 ·Circulation ·Meiso Hayashi,Isabelle Denjoy,Fabrice Extramiana,Alice Maltret,(unknown),Jean‐Marc Lupoglazoff,Didier Klug,Miyuki Hayashi,Seiji Takatsuki,E Villain,J Kamblock,A. Messali,Pascale Guicheney,Joël Lunardi,Antoine Leenhardt	314
7	Triadin Deletion Induces Impaired Skeletal Muscle Function 2009 ·Journal of Biological Chemistry ·Sarah Oddoux,Julie Brocard,Annie Schweitzer,Péter Szentesi,Benoı̂t Giannesini,Jacques Brocard,Julien Fauré,(unknown),David Bendahan,Joël Lunardi,László Csernoch,Isabelle Marty	71
8	Development and implementation of standardized respiratory chain spectrophotometric assays for clinical diagnosis 2009 ·Mitochondrion ·Fadia Medja,Stéphane Allouche,Paule Frachon,Claude Jardel,Monique Malgat,(unknown),Abdelhamid Slama,Joël Lunardi,Jean‐Pierre Mazat,Anne Lombès	169
9	C.P.1.05 Congenital fibre type disproportion associated with de novo mutations in TPM3 and ACTA1 genes 2007 ·Neuromuscular Disorders ·Nicole Monnier,Annick Labarre‐Vila,(unknown),Paulette Mezin,(unknown),Isabelle Marty,Joël Lunardi	1
10	C.P.1.13 A homozygous null mutation in TPM2 gene causes autosomal recessive nemaline myopathy associated with multiple pterygia 2007 ·Neuromuscular Disorders ·Pierre‐Simon Jouk,Annick Labarre‐Vila,Paulette Mezin,(unknown),Isabelle Marty,Joël Lunardi,Nicole Monnier	2
11	Two EPR-detectable [4Fe–4S] clusters, N2a and N2b, are bound to the NuoI (TYKY) subunit of NADH:ubiquinone oxidoreductase (Complex I) from Rhodobacter capsulatus 2003 ·Biochimica et Biophysica Acta (BBA) - Bioenergetics ·Mireille Chevallet,Alain Dupuis,Jean‐Paul Issartel,Joël Lunardi,(unknown),Simon P. J. Albracht	20
12	Presence of Two Different Genetic Traits in Malignant Hyperthermia Families 2002 ·Anesthesiology ·Nicole Monnier,R Krivosic-Horber,Jean‐François Payen,G. Kozak‐Ribbens,Y. Nivoche,P Adnet,H. Reyford,Joël Lunardi	127
13	Proteomics Analysis of Cellular Response to Oxidative Stress 2002 ·Journal of Biological Chemistry ·Thierry Rabilloud,Manfred Heller,Françoise Gasnier,Sylvie Luche,Catherine Rey,Ruedi Aebersold,Mohamed Benahmed,Pierre Louisot,Joël Lunardi	340
14	Detection of chemoresistance profile of cell lines K562, KB, GLC4 and HL60 through characterisation of the hmdr1, mrp and lrp transcripts. 2001 ·PubMed ·Anne‐Sophie Gauchez,Joël Lunardi,(unknown),(unknown),Daniel Fagret	4
15	Characterization of a Germline Mosaicism in Families with Lowe Syndrome, and Identification of Seven Novel Mutations in the OCRL1 Gene 1999 ·The American Journal of Human Genetics ·Véronique Satre,Nicole Monnier,(unknown),Carmen Ayuso,(unknown),Pierre‐Simon Jouk,Isidora López‐Pajares,(unknown),(unknown),Henri Plauchu,María Torres,Joël Lunardi	42
16	The nuoM arg368his mutation in NADH:ubiquinone oxidoreductase from Rhodobacter capsulatus: a model for the human nd4-11778 mtDNA mutation associated with Leber’s hereditary optic neuropathy 1998 ·Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease ·Joël Lunardi,(unknown),Alain Dupuis,Jean‐Paul Issartel	16
17	Distal genes of the nuo operon of Rhodobacter capsulatus equivalent to the mitochondrial ND subunits are all essential for the biogenesis of the respiratory NADH–ubiquinone oxidoreductase 1998 ·Molecular Microbiology ·Alain Dupuis,Élisabeth Darrouzet,Hervé Duborjal,(unknown),Mireille Chevallet,(unknown),Simon P. J. Albracht,Joël Lunardi	26
18	Immuno‐purification of a dimeric subcomplex of the respiratory NAHD‐CoQ reductase of Rhodobacter capsulatus equivalent to the FP fraction of the mitochondrial complex I 1997 ·FEBS Letters ·Hervé Duborjal,Alain Dupuis,Agnès Chapel,(unknown),Joël Lunardi,Jean‐Paul Issartel	11
19	Does pyrophosphate bind to the catalytic sites of mitochondrial F1-ATPase? 1992 ·Biochemistry ·André Peinnequin,Jean Paul Issartel,Joël Lunardi,(unknown)	15
20	Exploration of δ‐subunit interactions in beef heart mitochondrial F₁ ‐ATPase by monoclonal antibodies 1989 ·FEBS Letters ·Joël Lunardi,Alain Dupuis,Yveline Frobert,(unknown),Pierre V. Vignais	6

About Joël Lunardi

Joël Lunardi is a scholar working on Molecular Biology, Cardiology and Cardiovascular Medicine and Genetics, having authored 127 papers that have together received 5.8k indexed citations. Recurring topics across this work include Mitochondrial Function and Pathology (33 papers), ATP Synthase and ATPases Research (30 papers) and Ion channel regulation and function (30 papers). The work is most often cited by research in Molecular Biology (4.3k citations), Cardiology and Cardiovascular Medicine (1.3k citations) and Genetics (518 citations). Joël Lunardi has collaborated with scholars based in France, United States and Germany. Frequent co-authors include Nicole Monnier, Pierre V. Vignais, Thierry Rabilloud, Jean‐Paul Issartel, Sylvie Luche, P.V. Vignais, Manfred Heller, Ruedi Aebersold, Jean‐Marc Strub and Alain Dupuis. Their work appears in journals such as Proceedings of the National Academy of Sciences, Journal of Biological Chemistry and Circulation.

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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