Cathérine Costa

1.1k total citations
32 papers, 749 citations indexed

About

Cathérine Costa is a scholar working on Pulmonary and Respiratory Medicine, Molecular Biology and Epidemiology. According to data from OpenAlex, Cathérine Costa has authored 32 papers receiving a total of 749 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Pulmonary and Respiratory Medicine, 9 papers in Molecular Biology and 7 papers in Epidemiology. Recurrent topics in Cathérine Costa's work include Cystic Fibrosis Research Advances (10 papers), Neonatal Respiratory Health Research (4 papers) and Hemophilia Treatment and Research (4 papers). Cathérine Costa is often cited by papers focused on Cystic Fibrosis Research Advances (10 papers), Neonatal Respiratory Health Research (4 papers) and Hemophilia Treatment and Research (4 papers). Cathérine Costa collaborates with scholars based in France, Italy and United States. Cathérine Costa's co-authors include Stéphane Bretagne, Christophe Desterke, Françoise Botterel, Jean‐Marc Costa, Catherine Cordonnier, Michel Goossens, Michel Vidaud, Dominique Vidaud, Emmanuelle Bart–Delabesse and Martine Olivi and has published in prestigious journals such as Blood, Journal of Clinical Microbiology and Clinical Chemistry.

In The Last Decade

Cathérine Costa

31 papers receiving 719 citations

Peers

Cathérine Costa

EPIDE

PRM

HEMAT

Yuji Tanaka Japan

Vincent Sinickas Australia

Heike Kotarsky Sweden

Julio E. Figueroa United States

L. K. Bhutani India

Fabio Fuligni Italy

Annalisa Pianta United States

I Montfort Mexico

Michael E. Miller United States

Karin van Leeuwen Netherlands

Yuji Tanaka Japan

Cathérine Costa

305 ×1.1

283 ×1.1

EPIDE

121 ×0.7

42 ×0.3

PRM

134 ×1.4

HEMAT

Citations per year, relative to Cathérine Costa Cathérine Costa (= 1×) peers Yuji Tanaka

Countries citing papers authored by Cathérine Costa

Since Specialization

Citations

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

Fields of papers citing papers by Cathérine Costa

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Cathérine Costa

This figure shows the co-authorship network connecting the top 25 collaborators of Cathérine Costa. A scholar is included among the top collaborators of Cathérine Costa 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 Cathérine Costa. Cathérine Costa 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

Seck, Moussa, Blaise Félix Faye, Macoura Gadji, et al.. (2017). Bleeding risk assessment in hemophilia A carriers from Dakar, Senegal. Blood Coagulation & Fibrinolysis. 28(8). 642–645. 7 indexed citations

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

Repessé, Yohann, Ivan Peyron, Jordan D. Dimitrov, et al.. (2013). Development of inhibitory antibodies to therapeutic factor VIII in severe hemophilia A is associated with microsatellite polymorphisms in the HMOX1 promoter. Haematologica. 98(10). 1650–1655. 27 indexed citations

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

Boutron, Audrey, Anna Marabotti, Angelo Facchiano, et al.. (2012). Mutation spectrum in the French cohort of galactosemic patients and structural simulation of 27 novel missense variations. Molecular Genetics and Metabolism. 107(3). 438–447. 20 indexed citations

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

Becdelièvre, Alix de, Cathérine Costa, Jean‐Marie Jouannic, et al.. (2010). Comprehensive description of CFTR genotypes and ultrasound patterns in 694 cases of fetal bowel anomalies: a revised strategy. Human Genetics. 129(4). 387–396. 14 indexed citations

René, Céline, Damien Paulet, Emmanuelle Girodon, et al.. (2010). p.Ser1235Arg should no longer be considered as a cystic fibrosis mutation: results from a large collaborative study. European Journal of Human Genetics. 19(1). 36–42. 5 indexed citations

Hinzpeter, Alexandre, Elvira Sondo, Cathérine Costa, et al.. (2010). Alternative Splicing at a NAGNAG Acceptor Site as a Novel Phenotype Modifier. PLoS Genetics. 6(10). e1001153–e1001153. 51 indexed citations

10.

Costa, Cathérine, V. Prulière‐Escabasse, Lisa Golmard, et al.. (2009). A new cryptic CFTR exon in mild CF. Journal of Cystic Fibrosis. 8. S2–S2. 1 indexed citations

11.

Ratbi, Ilham, Emmanuelle Génin, Marie Legendre, et al.. (2008). Cystic fibrosis carrier frequency and estimated prevalence of the disease in Morocco. Journal of Cystic Fibrosis. 7(5). 440–443. 15 indexed citations

12.

Davit–Spraul, Anne, Cathérine Costa, Mokhtar Zater, et al.. (2008). Hereditary fructose intolerance: Frequency and spectrum mutations of the aldolase B gene in a large patients cohort from France—Identification of eight new mutations. Molecular Genetics and Metabolism. 94(4). 443–447. 18 indexed citations

13.

Ratbi, Ilham, Marie Legendre, Florence Niel, et al.. (2007). Detection of cystic fibrosis transmembrane conductance regulator (CFTR) gene rearrangements enriches the mutation spectrum in congenital bilateral absence of the vas deferens and impacts on genetic counselling. Human Reproduction. 22(5). 1285–1291. 50 indexed citations

14.

Repessé, Yohann, M. Slaoui, Philippe Gautier, et al.. (2007). Factor VIII (FVIII) gene mutations in 120 patients with hemophilia A: detection of 26 novel mutations and correlation with FVIII inhibitor development. Journal of Thrombosis and Haemostasis. 5(7). 1469–1476. 42 indexed citations

15.

Niel, Florence, Marie Legendre, Thierry Bienvenu, et al.. (2006). A new largeCFTRrearrangement illustrates the importance of searching for complex alleles. Human Mutation. 27(7). 716–717. 27 indexed citations

16.

Richardet, Jean‐Philippe, et al.. (2006). Combined polymorphisms of tumour necrosis factor alpha and interleukin-10 genes in patients with alcoholic hepatitis. European Journal of Gastroenterology & Hepatology. 18(6). 673–679. 13 indexed citations

17.

Costa, Cathérine, et al.. (2005). Génétique de la mucoviscidose. MTP. Médecine thérapeutique pédiatrie. 8(3). 126–134. 1 indexed citations

18.

Costa, Cathérine, et al.. (2003). A One-Step Real-Time PCR Assay for Rapid Prenatal Diagnosis of Sickle Cell Disease and Detection of Maternal Contamination. Molecular Diagnosis. 7(1). 45–48. 7 indexed citations

19.

Costa, Cathérine, Dominique Vidaud, Martine Olivi, et al.. (2001). Development of two real-time quantitative TaqMan PCR assays to detect circulating Aspergillus fumigatus DNA in serum. Journal of Microbiological Methods. 44(3). 263–269. 80 indexed citations

20.

Costa, Cathérine. (1996). "My George Eliot": Deutera Dickinson/Mutter Eliot. The Emily Dickinson journal. 5(2). 59–65. 1 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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