J.-F. Pellissier

662 total citations
25 papers, 484 citations indexed

About

J.-F. Pellissier is a scholar working on Molecular Biology, Clinical Biochemistry and Neurology. According to data from OpenAlex, J.-F. Pellissier has authored 25 papers receiving a total of 484 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Molecular Biology, 7 papers in Clinical Biochemistry and 5 papers in Neurology. Recurrent topics in J.-F. Pellissier's work include Mitochondrial Function and Pathology (8 papers), ATP Synthase and ATPases Research (7 papers) and Metabolism and Genetic Disorders (7 papers). J.-F. Pellissier is often cited by papers focused on Mitochondrial Function and Pathology (8 papers), ATP Synthase and ATPases Research (7 papers) and Metabolism and Genetic Disorders (7 papers). J.-F. Pellissier collaborates with scholars based in France, United States and Netherlands. J.-F. Pellissier's co-authors include Dominique Figarella‐Branger, B. Chabrol, Véronique Paquis‐Flucklinger, Konstantina Fragaki, Cécile Rouzier, Sylvie Bannwarth, Jean Pouget, Annabelle Chaussenot, Vincent Procaccio and Arnaud Chevrollier and has published in prestigious journals such as Brain, Neurology and Biochemical and Biophysical Research Communications.

In The Last Decade

J.-F. Pellissier

25 papers receiving 471 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
J.-F. Pellissier France 10 255 129 119 114 80 25 484
Geetha Anand United Kingdom 13 303 1.2× 58 0.4× 98 0.8× 77 0.7× 34 0.4× 34 565
S Vlaho Germany 10 200 0.8× 91 0.7× 90 0.8× 103 0.9× 30 0.4× 24 513
Hiroyuki Yahikozawa Japan 15 184 0.7× 105 0.8× 181 1.5× 16 0.1× 62 0.8× 37 571
Sheng Yao China 12 253 1.0× 184 1.4× 118 1.0× 56 0.5× 13 0.2× 33 434
Tingjun Dai China 13 194 0.8× 78 0.6× 75 0.6× 82 0.7× 152 1.9× 39 427
Christian Pröpper Germany 9 328 1.3× 44 0.3× 28 0.2× 31 0.3× 33 0.4× 12 442
Rune Sörnäs Sweden 7 90 0.4× 40 0.3× 46 0.4× 33 0.3× 43 0.5× 12 282
Marios Kaliakatsos United Kingdom 12 83 0.3× 64 0.5× 75 0.6× 28 0.2× 17 0.2× 31 411
Anisa B. Threlkeld United States 10 319 1.3× 47 0.4× 31 0.3× 222 1.9× 14 0.2× 14 580
J.A.P. Hiel Netherlands 10 204 0.8× 84 0.7× 29 0.2× 21 0.2× 35 0.4× 13 350

Countries citing papers authored by J.-F. Pellissier

Since Specialization
Citations

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

Fields of papers citing papers by J.-F. Pellissier

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by J.-F. Pellissier. 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 J.-F. Pellissier. The network helps show where J.-F. Pellissier may publish in the future.

Co-authorship network of co-authors of J.-F. Pellissier

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

All Works

20 of 20 papers shown
1.
Rouzier, Cécile, Sylvie Bannwarth, Annabelle Chaussenot, et al.. (2011). The MFN2 gene is responsible for mitochondrial DNA instability and optic atrophy 'plus' phenotype. Brain. 135(1). 23–34. 176 indexed citations
2.
Rouzier, Cécile, Konstantina Fragaki, Valérie Serre, et al.. (2010). The severity of phenotype linked to SUCLG1 mutations could be correlated with residual amount of SUCLG1 protein. Journal of Medical Genetics. 47(10). 670–676. 37 indexed citations
3.
Serratrice, G, Jean‐Philippe Azulay, & J.-F. Pellissier. (2009). Neuropathies héréditaires sensibles à la pression (neuropathie tomaculaire ou allantoïdienne). 32(4). 1–7. 2 indexed citations
4.
Laforêt, Pascal, A Pagès, D. Figarella-Branger, et al.. (2008). Forme adulte de la maladie de Pompe : à propos de six cas de la région du Languedoc-Roussillon. Revue Neurologique. 164(4). 336–342. 2 indexed citations
5.
6.
Bannwarth, Sylvie, Vincent Procaccio, Cécile Rouzier, et al.. (2007). Rapid identification of mitochondrial DNA (mtDNA) mutations in neuromuscular disorders by using surveyor strategy. Mitochondrion. 8(2). 136–145. 17 indexed citations
7.
Monnot, Sophie, B. Chabrol, A. Caño, et al.. (2005). Syndrome de Leigh avec déficit en cytochrome c oxydase lié à une mutation homozygote du gène SURF1. Archives de Pédiatrie. 12(5). 568–571. 4 indexed citations
8.
Figarella‐Branger, Dominique, Jean-François Pouget, Rafaëlle Bernard, et al.. (2003). Limb-girdle muscular dystrophy in a 71-year-old woman with an R27Q mutation in the CAV3 gene. Neurology. 61(4). 562–564. 17 indexed citations
9.
Serratrice, J., et al.. (2001). A Case of Polymyositis with Anti-Histidyl-t-RNA Synthetase (Jo-1) Antibody Syndrome following Extensive Vinyl Chloride Exposure. Clinical Rheumatology. 20(5). 379–382. 8 indexed citations
10.
Paul, Rachel, Claude Desnuelle, Jean Pouget, et al.. (2000). Importance of searching for associated mitochondrial DNA alterations in patients with multiple deletions. European Journal of Human Genetics. 8(5). 331–338. 6 indexed citations
11.
Granel, B., Rey J, C Bouvier, et al.. (2000). Chronic hepatitis C virus infection associated with a generalized granuloma annulare. Journal of the American Academy of Dermatology. 43(5). 918–919. 26 indexed citations
12.
Figarella‐Branger, Dominique, et al.. (2000). Immunohistochemical localization of cytokines, C5b-9 and ICAM-1 in peripheral nerve of Guillain–Barré Syndrome. Journal of the Neurological Sciences. 174(1). 16–21. 70 indexed citations
13.
Figarella‐Branger, Dominique, et al.. (2000). IMMUNOHISTOCHEMICAL LOCALIZATION OF CYTOKINES, C5B‐9 AND ICAM‐1 IN PERIPHERAL NERVE OF GUILLAIN‐BARRE SYNDROME. Journal of the Peripheral Nervous System. 5(4). 238–239. 6 indexed citations
14.
Daniel, Laurent, et al.. (1998). [General principles of macroscopic examination of kidney tumors].. PubMed. 18(2). 152–5. 1 indexed citations
15.
Daniel, Laurent, et al.. (1998). [Malignant Leydig cell tumor of the testis secreting progesterone].. PubMed. 8(6). 1047–50. 3 indexed citations
16.
Daniel, Laurent, et al.. (1997). Sarcomes aortiques avec embolies périphériques: à propos de deux cas. La Revue de Médecine Interne. 18(10). 799–805. 19 indexed citations
17.
Reynier, Pascal, J.-F. Pellissier, Jean‐Robert Harlé, & Yves Malthièry. (1994). Multiple Deletions of the Mitochondrial DNA in Polymyalgia Rheumatica. Biochemical and Biophysical Research Communications. 205(1). 375–380. 10 indexed citations
18.
Bouillot, P., J.-F. Pellissier, B Devictor, et al.. (1994). Quantitative imaging of estrogen and progesterone receptors, estrogen-regulated protein, and growth fraction: immunocytochemical assays in 52 meningiomas. Journal of neurosurgery. 81(5). 765–773. 43 indexed citations
19.
Barsy, Th. de & J.-F. Pellissier. (1991). Les glycogénoses musculaires. La Revue de Médecine Interne. 12(3). 198–204. 3 indexed citations
20.
Desnuelle, Claude, J.-F. Pellissier, Th. de Barsy, & G Serratrice. (1990). [Intolerance to exercise caused by carnitine palmitoyltransferase deficiency].. PubMed. 146(3). 231–4. 3 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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