Solenn Pruvost

667 total citations
10 papers, 213 citations indexed

About

Solenn Pruvost is a scholar working on Molecular Biology, Surgery and Epidemiology. According to data from OpenAlex, Solenn Pruvost has authored 10 papers receiving a total of 213 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Molecular Biology, 2 papers in Surgery and 2 papers in Epidemiology. Recurrent topics in Solenn Pruvost's work include Mesenchymal stem cell research (1 paper), Tissue Engineering and Regenerative Medicine (1 paper) and Mitochondrial Function and Pathology (1 paper). Solenn Pruvost is often cited by papers focused on Mesenchymal stem cell research (1 paper), Tissue Engineering and Regenerative Medicine (1 paper) and Mitochondrial Function and Pathology (1 paper). Solenn Pruvost collaborates with scholars based in Switzerland, France and Netherlands. Solenn Pruvost's co-authors include Patrick Nitschké, Christine Bôle‐Feysot, Laure‐Hélène Noël, Vincent Morinière, Saïd Lebbah, Alexandra Topa, Laurence Heidet, Karin Dahan, Emmanuelle Plaisier and Marie-Claire Gübler and has published in prestigious journals such as The EMBO Journal, Scientific Reports and Journal of the American Society of Nephrology.

In The Last Decade

Solenn Pruvost

10 papers receiving 202 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Solenn Pruvost Switzerland	7	101	67	60	45	36	10	213
Julie Brault France	9	145 1.4×	4 0.1×	39 0.7×	6 0.1×	12 0.3×	14	282
Ana Lucia A. Pires Brazil	12	95 0.9×	43 0.6×	27 0.5×	2 0.0×	3 0.1×	18	341
S Rogers United Kingdom	7	61 0.6×	20 0.3×	37 0.6×		8 0.2×	10	323
Pranav Sheth United States	10	51 0.5×	22 0.3×	16 0.3×	1 0.0×	9 0.3×	16	337
Shaoping Zhu China	6	172 1.7×	14 0.2×	7 0.1×	9 0.2×	5 0.1×	17	283
Bolong Lin China	5	166 1.6×	4 0.1×	6 0.1×	29 0.6×	11 0.3×	9	278
Katharina Baebler Switzerland	7	94 0.9×	4 0.1×	37 0.6×	10 0.2×	3 0.1×	10	188
Xiangyu Wang China	10	158 1.6×	5 0.1×	25 0.4×	24 0.5×	2 0.1×	33	291
Ravinder Atkar United Kingdom	5	22 0.2×	10 0.1×	15 0.3×	6 0.1×		12	140
Woon‐Hae Kim South Korea	11	96 1.0×	28 0.4×	39 0.7×	18 0.4×	2 0.1×	20	399

Countries citing papers authored by Solenn Pruvost

Since Specialization

Citations

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

Fields of papers citing papers by Solenn Pruvost

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Solenn Pruvost

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

All Works

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10 of 10 papers shown

Cottenet, Geoffrey, et al.. (2024). An AmpliSeq™ HD approach for specific and sensitive identification of GMO by Next Generation Sequencing. Journal of Food Composition and Analysis. 139. 107038–107038. 2 indexed citations

Duboux, Stéphane, et al.. (2023). The Pleiotropic Effects of Carbohydrate-Mediated Growth Rate Modifications in Bifidobacterium longum NCC 2705. Microorganisms. 11(3). 588–588. 4 indexed citations

Modesto, Monica, Catherine Ngom‐Bru, Anne Bruttin, et al.. (2023). Bifidobacterium longum subsp. iuvenis subsp. nov., a novel subspecies isolated from the faeces of weaning infants. INTERNATIONAL JOURNAL OF SYSTEMATIC AND EVOLUTIONARY MICROBIOLOGY. 73(10). 10 indexed citations

Mashinchian, Omid, Filippo De Franceschi, Sina Nassiri, et al.. (2022). An engineered multicellular stem cell niche for the 3D derivation of human myogenic progenitors from iPSCs. The EMBO Journal. 41(14). e110655–e110655. 7 indexed citations

Fuzo, Carlos Alessandro, Fábio da Veiga Ued, Sofia Moco, et al.. (2021). Contribution of genetic ancestry and polygenic risk score in meeting vitamin B12 needs in healthy Brazilian children and adolescents. Scientific Reports. 11(1). 11992–11992. 5 indexed citations

Raymond, Frédéric, Grégory Lefebvre, Lorane Texari, et al.. (2021). Longitudinal Human Milk miRNA Composition over the First 3 mo of Lactation in a Cohort of Healthy Mothers Delivering Term Infants. Journal of Nutrition. 152(1). 94–106. 15 indexed citations

Morinière, Vincent, Karin Dahan, Pascale Hilbert, et al.. (2014). Improving Mutation Screening in Familial Hematuric Nephropathies through Next Generation Sequencing. Journal of the American Society of Nephrology. 25(12). 2740–2751. 102 indexed citations

Duchatelet, Sabine, Solenn Pruvost, Simon J. de Veer, et al.. (2014). A NewTRPV3Missense Mutation in a Patient With Olmsted Syndrome and Erythromelalgia. JAMA Dermatology. 150(3). 303–303. 40 indexed citations

Lonlay, Pascale de, Valérie Malan, Christine Bôle‐Feysot, et al.. (2012). Maternal uniparental disomy of chromosome 2 in a patient with a DGUOK mutation associated with hepatocerebral mitochondrial DNA depletion syndrome. Molecular Genetics and Metabolism. 107(4). 700–704. 11 indexed citations

10.

Delphin, Nathalie, Sylvain Hanein, Lucas Fares‐Taie, et al.. (2011). Intellectual disability associated with retinal dystrophy in the Xp11.3 deletion syndrome: ZNF674 on trial. Guilty or innocent?. European Journal of Human Genetics. 20(3). 352–356. 17 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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