Bruno Costes

2.4k total citations
40 papers, 1.9k citations indexed

About

Bruno Costes is a scholar working on Pulmonary and Respiratory Medicine, Molecular Biology and Genetics. According to data from OpenAlex, Bruno Costes has authored 40 papers receiving a total of 1.9k indexed citations (citations by other indexed papers that have themselves been cited), including 23 papers in Pulmonary and Respiratory Medicine, 11 papers in Molecular Biology and 9 papers in Genetics. Recurrent topics in Bruno Costes's work include Cystic Fibrosis Research Advances (22 papers), Neonatal Respiratory Health Research (13 papers) and Tracheal and airway disorders (7 papers). Bruno Costes is often cited by papers focused on Cystic Fibrosis Research Advances (22 papers), Neonatal Respiratory Health Research (13 papers) and Tracheal and airway disorders (7 papers). Bruno Costes collaborates with scholars based in France, United States and Italy. Bruno Costes's co-authors include Michel Goossens, Pascale Fanen, Nada Ghanem, M. Goossens, Josiane Martin, Emmanuelle Girodon, N. Ghanem, Michel Vidaud, François Plassa and Claude Besmond and has published in prestigious journals such as Journal of Clinical Investigation, The Journal of Immunology and Gastroenterology.

In The Last Decade

Bruno Costes

40 papers receiving 1.8k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Bruno Costes France 22 1.1k 512 344 214 201 40 1.9k
Emmanuelle Girodon France 22 870 0.8× 311 0.6× 282 0.8× 89 0.4× 226 1.1× 73 1.4k
Dominique Bozon France 23 1.4k 1.2× 745 1.5× 336 1.0× 295 1.4× 232 1.2× 57 2.4k
Edgar T. Ballard United States 23 388 0.3× 359 0.7× 71 0.2× 163 0.8× 169 0.8× 41 1.3k
Lori Steiner United States 22 178 0.2× 284 0.6× 153 0.4× 245 1.1× 297 1.5× 35 1.4k
Soon Keng Cheong Malaysia 18 169 0.1× 418 0.8× 223 0.6× 88 0.4× 53 0.3× 91 1.0k
T Kuriyama Japan 19 678 0.6× 452 0.9× 59 0.2× 192 0.9× 114 0.6× 59 1.4k
Véronique David France 19 155 0.1× 523 1.0× 348 1.0× 68 0.3× 406 2.0× 40 1.6k
Maryse Etienne‐Julan France 26 307 0.3× 277 0.5× 1.3k 3.8× 528 2.5× 203 1.0× 85 1.9k
Hongyan Lu China 19 274 0.2× 321 0.6× 131 0.4× 69 0.3× 49 0.2× 78 878
Simon Rinaldi United Kingdom 22 116 0.1× 292 0.6× 94 0.3× 166 0.8× 172 0.9× 61 1.6k

Countries citing papers authored by Bruno Costes

Since Specialization
Citations

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

Fields of papers citing papers by Bruno Costes

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Bruno Costes

This figure shows the co-authorship network connecting the top 25 collaborators of Bruno Costes. A scholar is included among the top collaborators of Bruno Costes 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 Bruno Costes. Bruno Costes 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.
Martin, Natacha, Anne Bergougnoux, B. Chevalier, et al.. (2020). Exon identity influences splicing induced by exonic variants and in silico prediction efficacy. Journal of Cystic Fibrosis. 20(3). 464–472. 6 indexed citations
2.
Pranke, Iwona, Laure Bidou, Natacha Martin, et al.. (2018). Factors influencing readthrough therapy for frequent cystic fibrosis premature termination codons. ERJ Open Research. 4(1). 80–2017. 36 indexed citations
3.
Savary, Guillaume, Fanny Lidouren, Jérôme Rambaud, et al.. (2018). Argon attenuates multiorgan failure following experimental aortic cross‐clamping. British Journal of Clinical Pharmacology. 84(6). 1170–1179. 9 indexed citations
4.
Hinzpeter, Alexandre, Isabelle Callebaut, Cécile Zordan, et al.. (2017). The importance of functional tests to assess the effect of a new CFTR variant when genotype–phenotype correlation is not possible. Clinical Case Reports. 5(5). 658–663. 4 indexed citations
5.
Delestrain, Céline, Stéphanie Simon, Xavier Decrouy, et al.. (2017). Deciphering the mechanism of Q145H SFTPC mutation unmasks a splicing defect and explains the severity of the phenotype. European Journal of Human Genetics. 25(6). 779–782. 11 indexed citations
6.
Damy, Thibaud, Bruno Costes, Albert Hagège, et al.. (2015). Prevalence and clinical phenotype of hereditary transthyretin amyloid cardiomyopathy in patients with increased left ventricular wall thickness. European Heart Journal. 37(23). 1826–1834. 161 indexed citations
7.
Becdelièvre, Alix de, Lisa Golmard, Christian Vasseur, et al.. (2013). Combined Computational-Experimental Analyses ofCFTRExon Strength Uncover Predictability of Exon-Skipping Level. Human Mutation. 34(6). 873–881. 25 indexed citations
8.
Hinzpeter, Alexandre, Alix de Becdelièvre, Éric Bieth, et al.. (2012). Alternative Splicing of In-Frame Exon Associated with Premature Termination Codons: Implications for Readthrough Therapies. Human Mutation. 34(2). 287–291. 10 indexed citations
9.
Lecerf, Laure, Bruno Costes, Kamran Moradkhani, et al.. (2012). Estimation of the difference in HbF expression due to loss of the 5'  -globin BCL11A binding region. Haematologica. 98(2). 305–308. 10 indexed citations
10.
Costa, Cathérine, V. Prulière‐Escabasse, Alix de Becdelièvre, et al.. (2011). A recurrent deep-intronic splicing CF mutation emphasizes the importance of mRNA studies in clinical practice. Journal of Cystic Fibrosis. 10(6). 479–482. 17 indexed citations
11.
Tournamille, Christophe, Bruno Costes, Philippe Gauthier, et al.. (2009). Partial C antigen in sickle cell disease patients: clinical relevance and prevention of alloimmunization. Transfusion. 50(1). 13–19. 67 indexed citations
12.
Dubern, Béatrice, Cécile Lubrano-Berthelier, Monica Mencarelli, et al.. (2008). Mutational Analysis of the Pro-opiomelanocortin Gene in French Obese Children Led to the Identification of a Novel Deleterious Heterozygous Mutation Located in the α-Melanocyte Stimulating Hormone Domain. Pediatric Research. 63(2). 211–216. 50 indexed citations
13.
14.
Galietta, Luis J. V., Patrick Pagésy, Chiara Folli, et al.. (2002). IL-4 Is a Potent Modulator of Ion Transport in the Human Bronchial Epithelium In Vitro. The Journal of Immunology. 168(2). 839–845. 121 indexed citations
15.
Cuppens, Harry, Wen‐chang Lin, Martine Jaspers, et al.. (1998). Polyvariant mutant cystic fibrosis transmembrane conductance regulator genes. The polymorphic (Tg)m locus explains the partial penetrance of the T5 polymorphism as a disease mutation.. Journal of Clinical Investigation. 101(2). 487–496. 315 indexed citations
16.
Costes, Bruno, E. Girodon, N. Ghanem, et al.. (1995). Frequent Occurrence of the CFTRIntron 8 (TG)n 5T Allele in Men withCongenital Bilateral Absence of the Vas Deferens. European Journal of Human Genetics. 3(5). 285–293. 115 indexed citations
17.
Audrézet, M.‐P., Bruno Costes, N. Ghanem, et al.. (1993). Screening for cystic fibrosis in dried blood spots of newborns. Molecular and Cellular Probes. 7(6). 497–502. 25 indexed citations
18.
Ghanem, N., et al.. (1993). Twenty-Four Novel Hemophilia B Mutations Revealed by Rapid Scanning of the Whole Factor IX Gene in a French Population Sample. European Journal of Human Genetics. 1(2). 144–155. 28 indexed citations
19.
Costes, Bruno, Emmanuelle Girodon, N. Ghanem, et al.. (1993). Psoralen-modified oligonucleotide primers improve detection of mutations by denaturing gradient gel electrophoresis and provide an alternative to GC-clamping. Human Molecular Genetics. 2(4). 393–397. 52 indexed citations
20.

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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