Joël Lunardi

8.5k total citations
127 papers, 5.8k citations indexed

About

Joël Lunardi is a scholar working on Molecular Biology, Cardiology and Cardiovascular Medicine and Cell Biology. According to data from OpenAlex, Joël Lunardi has authored 127 papers receiving a total of 5.8k indexed citations (citations by other indexed papers that have themselves been cited), including 106 papers in Molecular Biology, 32 papers in Cardiology and Cardiovascular Medicine and 18 papers in Cell Biology. Recurrent topics in Joël Lunardi's work include Mitochondrial Function and Pathology (33 papers), ATP Synthase and ATPases Research (30 papers) and Ion channel regulation and function (30 papers). Joël Lunardi is often cited by papers focused on Mitochondrial Function and Pathology (33 papers), ATP Synthase and ATPases Research (30 papers) and Ion channel regulation and function (30 papers). Joël Lunardi collaborates with scholars based in France, United States and Germany. Joël Lunardi's co-authors include Nicole Monnier, Pierre V. Vignais, Thierry Rabilloud, Jean‐Paul Issartel, Sylvie Luche, P.V. Vignais, Ruedi Aebersold, Manfred Heller, Alain Dupuis and Jean‐Marc Strub and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Biological Chemistry and Circulation.

In The Last Decade

Joël Lunardi

126 papers receiving 5.6k citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
Joël Lunardi France	44	4.3k	1.3k	652	531	518	127	5.8k
Alain Doucet France	46	4.8k 1.1×	364 0.3×	302 0.5×	397 0.7×	127 0.2×	160	6.9k
Zu-Xi Yu United States	24	3.2k 0.7×	522 0.4×	439 0.7×	242 0.5×	298 0.6×	26	5.5k
Y. James Kang United States	40	3.1k 0.7×	1.5k 1.1×	239 0.4×	225 0.4×	131 0.3×	130	6.8k
Belinda Willard United States	46	3.3k 0.8×	422 0.3×	546 0.8×	431 0.8×	82 0.2×	189	6.3k
Kıvanç Birsoy United States	37	6.7k 1.6×	283 0.2×	544 0.8×	611 1.2×	401 0.8×	73	9.9k
M Chiariello Italy	43	4.5k 1.0×	1.6k 1.2×	1.4k 2.2×	291 0.5×	273 0.5×	215	8.6k
Lei Wei United States	41	4.3k 1.0×	1.1k 0.8×	877 1.3×	300 0.6×	288 0.6×	103	6.4k
Jacques H. Veerkamp Netherlands	44	4.0k 0.9×	316 0.2×	1.5k 2.2×	423 0.8×	93 0.2×	124	6.6k
Andreas Stahl United States	45	3.0k 0.7×	291 0.2×	650 1.0×	274 0.5×	119 0.2×	82	6.1k
Amalia Bosìa Italy	45	2.0k 0.5×	486 0.4×	211 0.3×	216 0.4×	282 0.5×	146	5.4k

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

Böhm, Johann, Nasim Vasli, Edoardo Malfatti, et al.. (2013). An Integrated Diagnosis Strategy for Congenital Myopathies. PLoS ONE. 8(6). e67527–e67527. 43 indexed citations

Coutton, Charles, Raoudha Zouari, Mariem Ben Khelifa, et al.. (2012). MLPA and sequence analysis of DPY19L2 reveals point mutations causing globozoospermia. Human Reproduction. 27(8). 2549–2558. 52 indexed citations

Ochala, Julien, David S. Gokhin, I. Pénisson-Besnier, et al.. (2012). Congenital myopathy-causing tropomyosin mutations induce thin filament dysfunction via distinct physiological mechanisms. Human Molecular Genetics. 21(20). 4473–4485. 36 indexed citations

Bevilacqua, Jorge A., Nicole Monnier, Marc Bitoun, et al.. (2010). Recessive RYR1 mutations cause unusual congenital myopathy with prominent nuclear internalization and large areas of myofibrillar disorganization. Neuropathology and Applied Neurobiology. 37(3). 271–284. 75 indexed citations

Hayashi, Meiso, Isabelle Denjoy, Fabrice Extramiana, et al.. (2009). Incidence and Risk Factors of Arrhythmic Events in Catecholaminergic Polymorphic Ventricular Tachycardia. Circulation. 119(18). 2426–2434. 314 indexed citations

Oddoux, Sarah, Julie Brocard, Annie Schweitzer, et al.. (2009). Triadin Deletion Induces Impaired Skeletal Muscle Function. Journal of Biological Chemistry. 284(50). 34918–34929. 71 indexed citations

Medja, Fadia, Stéphane Allouche, Paule Frachon, et al.. (2009). Development and implementation of standardized respiratory chain spectrophotometric assays for clinical diagnosis. Mitochondrion. 9(5). 331–339. 169 indexed citations

Sethi, Sidharth Kumar, Arvind Bagga, Ashima Gulati, et al.. (2008). Mutations in OCRL1 gene in Indian children with Lowe syndrome. Clinical and Experimental Nephrology. 12(5). 358–362. 8 indexed citations

Monnier, Nicole, et al.. (2007). C.P.1.05 Congenital fibre type disproportion associated with de novo mutations in TPM3 and ACTA1 genes. Neuromuscular Disorders. 17(9-10). 835–835. 1 indexed citations

10.

Jouk, Pierre‐Simon, Annick Labarre‐Vila, Paulette Mezin, et al.. (2007). C.P.1.13 A homozygous null mutation in TPM2 gene causes autosomal recessive nemaline myopathy associated with multiple pterygia. Neuromuscular Disorders. 17(9-10). 837–838. 2 indexed citations

11.

Chevallet, Mireille, et al.. (2003). 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. Biochimica et Biophysica Acta (BBA) - Bioenergetics. 1557. 51–66. 20 indexed citations

12.

Monnier, Nicole, R Krivosic-Horber, Jean‐François Payen, et al.. (2002). Presence of Two Different Genetic Traits in Malignant Hyperthermia Families. Anesthesiology. 97(5). 1067–1074. 127 indexed citations

13.

Ferreiro, Ana, Nicole Monnier, Norma B. Romero, et al.. (2002). A recessive form of central core disease, transiently presenting as multi‐minicore disease, is associated with a homozygous mutation in the ryanodine receptor type 1 gene. Annals of Neurology. 51(6). 750–759. 137 indexed citations

14.

Gauchez, Anne‐Sophie, et al.. (2001). Detection of chemoresistance profile of cell lines K562, KB, GLC4 and HL60 through characterisation of the hmdr1, mrp and lrp transcripts.. PubMed. 15(1). 101–4. 4 indexed citations

15.

Rabilloud, Thierry, et al.. (2001). The mitochondrial antioxidant defence system and its response to oxidative stress. PROTEOMICS. 1(8). 1105–1110. 87 indexed citations

16.

Rabilloud, Thierry, Jean‐Marc Strub, Sylvie Luche, Alain Van Dorsselaer, & Joël Lunardi. (2001). A comparison between Sypro Ruby and ruthenium II tris (bathophenanthroline disulfonate) as fluorescent stains for protein detection in gels. PROTEOMICS. 1(5). 699–704. 253 indexed citations

17.

Satre, Véronique, Nicole Monnier, Carmen Ayuso, et al.. (1999). Characterization of a Germline Mosaicism in Families with Lowe Syndrome, and Identification of Seven Novel Mutations in the OCRL1 Gene. The American Journal of Human Genetics. 65(1). 68–76. 42 indexed citations

18.

Rabilloud, Thierry, Thierry Blisnick, Manfred Heller, et al.. (1999). Analysis of membrane proteins by two-dimensional electrophoresis: Comparison of the proteins extracted from normal orPlasmodium falciparum - infected erythrocyte ghosts. Electrophoresis. 20(18). 3603–3610. 110 indexed citations

19.

Lunardi, Joël, et al.. (1998). 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. Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. 1407(2). 114–124. 16 indexed citations

20.

Peinnequin, André, et al.. (1992). Does pyrophosphate bind to the catalytic sites of mitochondrial F1-ATPase?. Biochemistry. 31(7). 2088–2092. 15 indexed citations

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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