Jean‐Pierre Salles

6.6k total citations · 1 hit paper
129 papers, 4.4k citations indexed

About

Jean‐Pierre Salles is a scholar working on Molecular Biology, Endocrinology, Diabetes and Metabolism and Genetics. According to data from OpenAlex, Jean‐Pierre Salles has authored 129 papers receiving a total of 4.4k indexed citations (citations by other indexed papers that have themselves been cited), including 60 papers in Molecular Biology, 31 papers in Endocrinology, Diabetes and Metabolism and 27 papers in Genetics. Recurrent topics in Jean‐Pierre Salles's work include Genetic Syndromes and Imprinting (18 papers), Growth Hormone and Insulin-like Growth Factors (15 papers) and Protein Tyrosine Phosphatases (15 papers). Jean‐Pierre Salles is often cited by papers focused on Genetic Syndromes and Imprinting (18 papers), Growth Hormone and Insulin-like Growth Factors (15 papers) and Protein Tyrosine Phosphatases (15 papers). Jean‐Pierre Salles collaborates with scholars based in France, United States and Netherlands. Jean‐Pierre Salles's co-authors include Bertrand Perret, Armelle Yart, Patrick Raynal, Alexandra Montagner, Marie Dance, Isabelle Gennero, M. Tauber, Michel Record, Safouane M. Hamdi and Karine Laulagnier 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

Jean‐Pierre Salles

126 papers receiving 4.3k citations

Hit Papers

align trajectories sort by overperformance

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Mast cell- and dendritic cell-derived exosomes display a specific lipid composition and an unusual membrane organization

2004 514 citations Karine Laulagnier, Safouane M. Hamdi et al. profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Jean‐Pierre Salles France	34	2.6k	672	594	576	408	129	4.4k
Hua Pan United States	37	2.7k 1.1×	546 0.8×	459 0.8×	670 1.2×	383 0.9×	160	4.7k
Je‐Yoel Cho South Korea	40	3.1k 1.2×	642 1.0×	467 0.8×	959 1.7×	461 1.1×	165	5.5k
Toshiyuki Yamada Japan	31	2.2k 0.8×	673 1.0×	435 0.7×	378 0.7×	401 1.0×	138	4.6k
Rainer M. Bohle Germany	46	2.5k 1.0×	988 1.5×	376 0.6×	815 1.4×	891 2.2×	221	6.5k
Jung‐Eun Kim South Korea	35	2.4k 0.9×	363 0.5×	430 0.7×	646 1.1×	333 0.8×	121	4.4k
Douglas J. Taatjes United States	46	2.4k 0.9×	840 1.3×	300 0.5×	464 0.8×	524 1.3×	181	5.8k
Ludger Fink Germany	44	2.6k 1.0×	1.1k 1.6×	489 0.8×	692 1.2×	543 1.3×	115	6.5k
Isao Kitajima Japan	42	2.1k 0.8×	1.2k 1.8×	289 0.5×	561 1.0×	660 1.6×	182	5.7k
Masato Tamura Japan	32	1.9k 0.7×	259 0.4×	272 0.5×	500 0.9×	538 1.3×	205	4.0k
Rosario Caltabiano Italy	38	2.1k 0.8×	470 0.7×	252 0.4×	1.3k 2.3×	540 1.3×	283	5.2k

Countries citing papers authored by Jean‐Pierre Salles

Since Specialization

Citations

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

Fields of papers citing papers by Jean‐Pierre Salles

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Jean‐Pierre Salles. 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 Jean‐Pierre Salles. The network helps show where Jean‐Pierre Salles may publish in the future.

Co-authorship network of co-authors of Jean‐Pierre Salles

This figure shows the co-authorship network connecting the top 25 collaborators of Jean‐Pierre Salles. A scholar is included among the top collaborators of Jean‐Pierre Salles 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 Jean‐Pierre Salles. Jean‐Pierre Salles 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

Rannou, François, Christelle Nguyen, Camille Daste, et al.. (2025). Safety and immunogenicity of PPV-06, an active anti-IL-6 immunotherapy targeting low-grade inflammation against knee osteoarthritis: a randomized, double-blind, placebo-controlled, clinical phase 1 study. Nature Communications. 16(1). 9767–9767.

Linglart, Agnès, Iva Gueorguieva, Jérôme Harambat, et al.. (2025). Health-related quality of life in French pediatric patients with X-linked hypophosphatemia: real-world data from the International XLH Registry. JBMR Plus. 9(10). ziaf142–ziaf142.

Kamenický, Peter, Karine Briot, Volha V. Zhukouskaya, et al.. (2023). Adult height improved over decades in patients with X-linked hypophosphatemia: a cohort study. European Journal of Endocrinology. 189(4). 469–475. 4 indexed citations

Bacchetta, Justine, Thomas Édouard, Gilles Laverny, et al.. (2022). Vitamin D and calcium intakes in general pediatric populations: A French expert consensus paper. Archives de Pédiatrie. 29(4). 312–325. 41 indexed citations

Collet, Corinne, Isabelle Gennero, Sanaa Eddiry, et al.. (2022). Diagnostic yield of bone fragility gene panel sequencing in children and young adults referred for idiopathic primary osteoporosis at a single regional reference centre. Bone Reports. 16. 101176–101176. 11 indexed citations

Linglart, Agnès, Aurélie Portefaix, Aurélia Bertholet‐Thomas, et al.. (2022). X-linked hypophosphatemia, obesity and arterial hypertension: data from the XLH21 study. Pediatric Nephrology. 38(3). 697–704. 6 indexed citations

Eddiry, Sanaa, Gwénaëlle Diene, Catherine Molinas, et al.. (2021). SNORD116 and growth hormone therapy impact IGFBP7 in Prader–Willi syndrome. Genetics in Medicine. 23(9). 1664–1672. 12 indexed citations

Laurencin‐Dalicieux, Sara, Delphine Farlay, Hélène Follet, et al.. (2020). Expression of the type 1 lysophosphatidic acid receptor in osteoblastic cell lineage controls both bone mineralization and osteocyte specification. Biochimica et Biophysica Acta (BBA) - Molecular and Cell Biology of Lipids. 1865(8). 158715–158715. 15 indexed citations

Capri, Yline, Catherine Pienkowski, Benoît Lepage, et al.. (2019). Gonadal Function of Female Patients with Noonan Syndrome. 92. 1 indexed citations

10.

Dulac, Yves, C. Baunin, Isabelle Gennero, et al.. (2017). Rachitisme carentiel sévère du nourrisson : de nouveau d’actualité. Archives de Pédiatrie. 24(8). 737–742. 5 indexed citations

11.

Pourpoint, Frédérique, Cristina Coelho Diogo, Christel Gervais, et al.. (2011). High-resolution solid state NMR experiments for the characterization of calcium phosphate biomaterials and biominerals. Journal of materials research/Pratt's guide to venture capital sources. 26(18). 2355–2368. 23 indexed citations

12.

Feigerlová, Eva, Gwénaëlle Diene, Isabelle Oliver, et al.. (2010). Elevated Insulin-Like Growth Factor-I Values in Children with Prader-Willi Syndrome Compared with Growth Hormone (GH) Deficiency Children over Two Years of GH Treatment. The Journal of Clinical Endocrinology & Metabolism. 95(10). 4600–4608. 29 indexed citations

13.

Touvier, Thierry, F. Conte-Auriol, Olivier Briand, et al.. (2009). LEPROT and LEPROTL1 cooperatively decrease hepatic growth hormone action in mice. Journal of Clinical Investigation. 119(12). 3830–3838. 39 indexed citations

14.

Moulin, Pierre, Frédéric Vaysse, Éric Bieth, et al.. (2008). Hypophosphatasia may lead to bone fragility: don’t miss it. European Journal of Pediatrics. 168(7). 783–788. 30 indexed citations

15.

Gennero, Isabelle, Thomas Édouard, Mona M. Rashad, et al.. (2007). Identification of a Novel Mutation in the Human Growth Hormone Receptor Gene (GHR) in a Patient with Laron Syndrome. Journal of Pediatric Endocrinology and Metabolism. 20(7). 825–31. 9 indexed citations

16.

Gayral, Stéphanie, Paul Déléris, Karine Laulagnier, et al.. (2006). Selective Activation of Nuclear Phospholipase D-1 by G Protein–Coupled Receptor Agonists in Vascular Smooth Muscle Cells. Circulation Research. 99(2). 132–139. 17 indexed citations

17.

Mottier, L., G. Virkel, Hugo Solana, et al.. (2004). Triclabendazole biotransformation and comparative diffusion of the parent drug and its oxidized metabolites into Fasciola hepatica . Xenobiotica. 34(11-12). 1043–1057. 45 indexed citations

18.

Dubouix, Anne, Isabelle Gennero, Jacques Pourrat, et al.. (2000). Polymorphism of the 5′ Untranslated Region of NHE1 Gene Associated with Type-I Diabetes. PubMed. 3(3). 141–144. 4 indexed citations

19.

Gennero, Isabelle, Marie Simon, Frédérique Gaits‐Iacovoni, et al.. (2000). Effect of Sphingosine‐1‐phosphate and Analogues of Lysophosphatidic Acid on Mesangial Cell Proliferation. Annals of the New York Academy of Sciences. 905(1). 340–343. 6 indexed citations

20.

Salles, Jean‐Pierre, J. C. Netelenbos, & M C Slootweg. (1996). Growth hormone induces tyrosine phosphorylation of annexin I in rat osteosarcoma cells.. Endocrinology. 137(10). 4358–4362. 13 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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