Caroline Raynal

1.2k total citations
37 papers, 638 citations indexed

About

Caroline Raynal is a scholar working on Pulmonary and Respiratory Medicine, Genetics and Molecular Biology. According to data from OpenAlex, Caroline Raynal has authored 37 papers receiving a total of 638 indexed citations (citations by other indexed papers that have themselves been cited), including 23 papers in Pulmonary and Respiratory Medicine, 8 papers in Genetics and 7 papers in Molecular Biology. Recurrent topics in Caroline Raynal's work include Cystic Fibrosis Research Advances (23 papers), Tracheal and airway disorders (13 papers) and Neonatal Respiratory Health Research (11 papers). Caroline Raynal is often cited by papers focused on Cystic Fibrosis Research Advances (23 papers), Tracheal and airway disorders (13 papers) and Neonatal Respiratory Health Research (11 papers). Caroline Raynal collaborates with scholars based in France, United States and Switzerland. Caroline Raynal's co-authors include Alexandre Evrard, Mireille Claustres, Anne Bergougnoux, Jean‐Paul Brouillet, Serge Lumbroso, Frédéric Hollande, Dominique Joubert, Benjamin Lallemant, Magali Taulan‐Cadars and Cédric Mercier and has published in prestigious journals such as Journal of Clinical Oncology, Molecular Cancer and BMC Cancer.

In The Last Decade

Caroline Raynal

35 papers receiving 628 citations

Peers

Countries citing papers authored by Caroline Raynal

Since Specialization

Citations

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

Fields of papers citing papers by Caroline Raynal

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Caroline Raynal

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

#	Work	Indexed citations
1	P075 Discrepancy between in vitro CFTR functional analysis and clinical response to elexacaftor/tezacaftor/ivacaftor (ETI) in a homozygous S364P (c.1090T>C) patient with cystic fibrosis 2023 ·Journal of Cystic Fibrosis ·Anne Sevin, (unknown), Caroline Raynal, Anne Bergougnoux, (unknown), R. Chiron	0
2	Penetrance is a critical parameter for assessing the disease liability of CFTR variants 2020 ·Journal of Cystic Fibrosis ·(unknown), M.‐P. Audrézet, Caroline Raynal, Isabelle Sermet‐Gaudelus, Thierry Bienvenu, Claude Férec, Anne Bergougnoux, (unknown), Virginie Scotet, À. Munck, Emmanuelle Girodon	11
3	Exon identity influences splicing induced by exonic variants and in silico prediction efficacy 2020 ·Journal of Cystic Fibrosis ·Natacha Martin, Anne Bergougnoux, (unknown), B. Chevalier, (unknown), David Baux, Bruno Costes, Pascale Fanen, Caroline Raynal, Isabelle Sermet‐Gaudelus, Emmanuelle Girodon, Magali Taulan‐Cadars, Alexandre Hinzpeter	6
4	Variant classifications, databases and genotype-phenotype correlations 2020 ·Archives de Pédiatrie ·Caroline Raynal, Harriet Corvol	10
5	Pitfalls in the interpretation of CFTR variants in the context of incidental findings 2019 ·Human Mutation ·(unknown), Anne Bergougnoux, Caroline Raynal, Marie‐Pierre Audrézet, Souphatta Sasorith, Claude Férec, Thierry Bienvenu, Emmanuelle Girodon	7
6	A Broad Test Based on Fluorescent-Multiplex PCR for Noninvasive Prenatal Diagnosis of Cystic Fibrosis 2018 ·Fetal Diagnosis and Therapy ·Claire Guissart, Frédéric Tran Mau‐Them, (unknown), (unknown), (unknown), Victoria L. Pritchard, Cécile Rouzier, (unknown), (unknown), Jacques Puechberty, Éric Bieth, Philippe Khau Van Kien, (unknown), Caroline Raynal, Anne Girardet, Mireille Claustres, M. Kœnig, Marie‐Claire Vincent	9
7	Isolated Nonvisualization of the Fetal Gallbladder Should Be Considered for the Prenatal Diagnosis of Cystic Fibrosis 2018 ·Fetal Diagnosis and Therapy ·Anne Bergougnoux, Jean‐Marie Jouannic, (unknown), Thierry Bienvenu, (unknown), Caroline Raynal, Emmanuelle Girodon	12
8	Functional characterization and phenotypic spectrum of three recurrent disease-causing deep intronic variants of the CFTR gene 2018 ·Journal of Cystic Fibrosis ·Anne Bergougnoux, (unknown), (unknown), (unknown), (unknown), (unknown), M. Kœnig, Claude Férec, Mireille Claustres, G. Lalau, Thierry Bienvenu, Marie‐Pierre Audrézet, A. Pagin, (unknown), Caroline Raynal, Magali Taulan‐Cadars	32
9	Recommandations pour la prise en charge et le suivi des nourrissons pour lesquels un diagnostic de mucoviscidose n’a pu être conclu après dépistage néonatal 2017 ·Archives de Pédiatrie ·Isabelle Sermet‐Gaudelus, J. Brouard, M.‐P. Audrézet, (unknown), Laurence Weiss, Nathalie Wizla, (unknown), (unknown), Muriel Le Bourgeois, (unknown), (unknown), Thao Nguyen‐Khoa, Caroline Raynal, M. Roussey, Emmanuelle Girodon	2
10	Guidelines for the clinical management and follow-up of infants with inconclusive cystic fibrosis diagnosis through newborn screening 2017 ·Archives de Pédiatrie ·Isabelle Sermet‐Gaudelus, J. Brouard, M.‐P. Audrézet, (unknown), Laurence Weiss, Nathalie Wizla, (unknown), (unknown), Muriel Le Bourgeois, (unknown), (unknown), Thao Nguyen‐Khoa, Caroline Raynal, M. Roussey, Emmanuelle Girodon	21
11	Non-invasive prenatal diagnosis (NIPD) of cystic fibrosis: an optimized protocol using MEMO fluorescent PCR to detect the p.Phe508del mutation 2016 ·Journal of Cystic Fibrosis ·Claire Guissart, (unknown), Caroline Raynal, Anne Girardet, Frédéric Tran Mau‐Them, (unknown), Cécile Rouzier, (unknown), (unknown), Jacques Puechberty, Éric Bieth, (unknown), Philippe Khau Van Kien, (unknown), Victoria L. Pritchard, M. Kœnig, Mireille Claustres, (unknown)	12
12	A false positive newborn screening result due to a complex allele carrying two frequent CF-causing variants 2016 ·Journal of Cystic Fibrosis ·Anne Bergougnoux, (unknown), Cécile Rouzier, (unknown), (unknown), Lise Larrieu, M. Kœnig, Mireille Claustres, Caroline Raynal	12
13	Small-scale high-throughput sequencing–based identification of new therapeutic tools in cystic fibrosis 2015 ·Genetics in Medicine ·(unknown), (unknown), Caroline Raynal, (unknown), Emmanuelle Beyne, Marie‐Pierre Audrézet, Claude Férec, Thierry Bienvenu, (unknown), Sylvie Tuffery‐Giraud, Marie des Georges, Mireille Claustres, Magali Taulan‐Cadars	25
14	The improvement of the best practice guidelines for preimplantation genetic diagnosis of cystic fibrosis: toward an international consensus 2015 ·European Journal of Human Genetics ·Anne Girardet, (unknown), Stéphanie Plaza, (unknown), Martine De Rycke, Marie des Georges, Francesco Fiorentino, G. Harton, (unknown), J. Navarro, Caroline Raynal, Pamela Renwick, (unknown), Martin Schwarz, Sioban SenGupta, Maria Tzetis, Anne‐Françoise Roux, Mireille Claustres	24
15	A Classification Model Relative to Splicing for Variants of Unknown Clinical Significance: Application to theCFTRGene 2013 ·Human Mutation ·Caroline Raynal, David Baux, (unknown), Corinne Bareil, Magali Taulan‐Cadars, Anne‐Françoise Roux, Mireille Claustres, Sylvie Tuffery‐Giraud, Marie des Georges	23
16	Pregnane × Receptor (PXR) expression in colorectal cancer cells restricts irinotecan chemosensitivity through enhanced SN-38 glucuronidation 2010 ·Molecular Cancer ·Caroline Raynal, Jean‐Marc Pascussi, (unknown), Cyril Breuker, (unknown), Benjamin Lallemant, Sylvain Poujol, Caroline Bonnans, Dominique Joubert, Frédéric Hollande, Serge Lumbroso, Jean‐Paul Brouillet, Alexandre Evrard	85
17	High-Resolution Melting Analysis of Sequence Variations in the Cytidine Deaminase Gene (CDA) in Patients With Cancer Treated With Gemcitabine 2010 ·Therapeutic Drug Monitoring ·Caroline Raynal, Joseph Ciccolini, Cédric Mercier, Jean-Christophe Boyer, Anne Polge, Benjamin Lallemant, Kévin Mouzat, Serge Lumbroso, Jean‐Paul Brouillet, Alexandre Evrard	14
18	Reference gene selection for head and neck squamous cell carcinoma gene expression studies 2009 ·BMC Molecular Biology ·Benjamin Lallemant, Alexandre Evrard, Christophe Combescure, H Chapuis, Guillaume Chambon, Caroline Raynal, (unknown), Omar Sabra, Dominique Joubert, Frédéric Hollande, Jean‐Gabriel Lallemant, Serge Lumbroso, Jean‐Paul Brouillet	45
19	Clinical relevance of nine transcriptional molecular markers for the diagnosis of head and neck squamous cell carcinoma in tissue and saliva rinse 2009 ·BMC Cancer ·Benjamin Lallemant, Alexandre Evrard, Christophe Combescure, H Chapuis, Guillaume Chambon, Caroline Raynal, (unknown), Omar Sabra, Dominique Joubert, Frédéric Hollande, Jean‐Gabriel Lallemant, Serge Lumbroso, Jean‐Paul Brouillet	45
20	Toxic death case in a patient undergoing gemcitabine-based chemotherapy in relation with cytidine deaminase downregulation 2007 ·Pharmacogenetics and Genomics ·Cédric Mercier, Caroline Raynal, Laëtitia Dahan, (unknown), Alexandre Evrard, Charlotte Dupuis, Aurore Blesius, Muriel Duluc, (unknown), Sarah Giacometti, Sébastien Salas, G. Milano, Roger Favre, Jean‐François Seitz, Joseph Ciccolini	43

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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