Corinne Bareil

2.2k total citations
26 papers, 823 citations indexed

About

Corinne Bareil is a scholar working on Molecular Biology, Ophthalmology and Pulmonary and Respiratory Medicine. According to data from OpenAlex, Corinne Bareil has authored 26 papers receiving a total of 823 indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Molecular Biology, 7 papers in Ophthalmology and 6 papers in Pulmonary and Respiratory Medicine. Recurrent topics in Corinne Bareil's work include Retinal Development and Disorders (9 papers), Retinal Diseases and Treatments (5 papers) and Cystic Fibrosis Research Advances (5 papers). Corinne Bareil is often cited by papers focused on Retinal Development and Disorders (9 papers), Retinal Diseases and Treatments (5 papers) and Cystic Fibrosis Research Advances (5 papers). Corinne Bareil collaborates with scholars based in France, Lebanon and Denmark. Corinne Bareil's co-authors include Mireille Claustres, Jacques Demaille, Bernard Arnaud, Valérie Delague, Anne Bergougnoux, Patrick Chalbos, Andrew Kramar, Nicolas Salvetat, Caroline Mollévi and Maguy Del Rio and has published in prestigious journals such as Journal of Clinical Oncology, Annals of Neurology and Journal of Virology.

In The Last Decade

Corinne Bareil

25 papers receiving 811 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Corinne Bareil France 16 527 159 135 102 102 26 823
Susana Galli United States 14 357 0.7× 90 0.6× 104 0.8× 331 3.2× 94 0.9× 29 862
Nicole Vincent Jordan United States 9 460 0.9× 78 0.5× 44 0.3× 154 1.5× 73 0.7× 10 906
Diego Ottaviani United Kingdom 15 570 1.1× 97 0.6× 59 0.4× 179 1.8× 115 1.1× 35 935
Hanan E. Shamseldin Saudi Arabia 24 981 1.9× 77 0.5× 62 0.5× 82 0.8× 590 5.8× 55 1.5k
Metka Ravnik‐Glavač Slovenia 21 1.0k 1.9× 63 0.4× 163 1.2× 136 1.3× 110 1.1× 50 1.5k
Wojciech Wiszniewski United States 18 509 1.0× 343 2.2× 39 0.3× 24 0.2× 320 3.1× 42 1.1k
Michael T. Massengill United States 10 413 0.8× 67 0.4× 43 0.3× 246 2.4× 41 0.4× 19 659
M. Isabel Chiu United States 12 903 1.7× 107 0.7× 64 0.5× 237 2.3× 50 0.5× 22 1.3k
Cole Ferguson United States 17 616 1.2× 143 0.9× 72 0.5× 228 2.2× 365 3.6× 28 1.3k
Sigve Nakken Norway 14 354 0.7× 64 0.4× 80 0.6× 115 1.1× 89 0.9× 40 640

Countries citing papers authored by Corinne Bareil

Since Specialization
Citations

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

Fields of papers citing papers by Corinne Bareil

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Corinne Bareil

This figure shows the co-authorship network connecting the top 25 collaborators of Corinne Bareil. A scholar is included among the top collaborators of Corinne Bareil 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 Corinne Bareil. Corinne Bareil 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.
Bareil, Corinne & Anne Bergougnoux. (2020). CFTR gene variants, epidemiology and molecular pathology. Archives de Pédiatrie. 27. eS8–eS12. 47 indexed citations
2.
Guissart, Claire, Marie Desgeorges, Corinne Bareil, et al.. (2014). Non-invasive prenatal diagnosis of monogenic disorders: an optimized protocol using MEMO qPCR with miniSTR as internal control. Clinical Chemistry and Laboratory Medicine (CCLM). 53(2). 205–15. 13 indexed citations
3.
Raynal, Caroline, David Baux, Corinne Bareil, et al.. (2013). A Classification Model Relative to Splicing for Variants of Unknown Clinical Significance: Application to theCFTRGene. Human Mutation. 34(5). 774–784. 23 indexed citations
4.
Bareil, Corinne, Christophe Béroud, Dalil Hamroun, et al.. (2010). UMD-CFTR: A database dedicated to CF and CFTR-related disorders. Human Mutation. 31(9). 1011–1019. 22 indexed citations
5.
Barat‐Houari, Mouna, Karine Nguyen, Rafaëlle Bernard, et al.. (2009). New multiplex PCR-based protocol allowing indirect diagnosis of FSHD on single cells: can PGD be offered despite high risk of recombination?. European Journal of Human Genetics. 18(5). 533–538. 11 indexed citations
6.
Humbertclaude, Véronique, Sylvie Tuffery‐Giraud, Corinne Bareil, et al.. (2009). Banques de données de mutations : enjeux et perspectives pour les maladies génétiques orphelines. Pathologie Biologie. 58(5). 387–395.
7.
8.
Copois, Virginie, Frédéric Bibeau, Caroline Mollévi, et al.. (2006). Impact of RNA degradation on gene expression profiles: Assessment of different methods to reliably determine RNA quality. Journal of Biotechnology. 127(4). 549–559. 151 indexed citations
9.
10.
Bareil, Corinne, Christian Hamel, Valérie Delague, et al.. (2001). Segregation of a mutation in CNGB1 encoding the β-subunit of the rod cGMP-gated channel in a family with autosomal recessive retinitis pigmentosa. Human Genetics. 108(4). 328–334. 83 indexed citations
11.
Griffoin, Jean‐Michel, Corinne Bareil, Sarah Bonnet, et al.. (2000). [Molecular genetics of pigmentary retinopathies: identification of mutations in CHM, RDS, RHO, RPE65, USH2A and XLRS1 genes].. Journal Français d Ophtalmologie. 23(10). 985–95. 18 indexed citations
12.
Bareil, Corinne, Valérie Delague, Bernard Arnaud, et al.. (2000). W179R: A novel missense mutation in the peripherin/RDS gene in a family with autosomal dominant retinitis pigmentosa. Human Mutation. 15(6). 583–584. 6 indexed citations
13.
Delague, Valérie, Corinne Bareil, Sylvie Tuffery‐Giraud, et al.. (2000). Mapping of a New Locus for Autosomal Recessive Demyelinating Charcot-Marie-Tooth Disease to 19q13.1-13.3 in a Large Consanguineous Lebanese Family: Exclusion of MAG as a Candidate Gene. The American Journal of Human Genetics. 67(1). 236–243. 64 indexed citations
14.
Bareil, Corinne, Christian Hamel, Nathalie Pallarès-Ruiz, et al.. (1999). Molecular analysis of the rhodopsin gene in southern France: identification of the first duplication responsible for retinitis pigmentosa, c.998^999ins4. Ophthalmic Genetics. 20(3). 173–182. 14 indexed citations
15.
Marlhens, F., Jean‐Michel Griffoin, Corinne Bareil, et al.. (1998). Autosomal recessive retinal dystrophy associated with two novel mutations in the RPE65 gene. European Journal of Human Genetics. 6(5). 527–531. 53 indexed citations
16.
Tuffery‐Giraud, Sylvie, Corinne Bareil, Pierre Sarda, et al.. (1998). Mutation analysis of the dystrophin gene in Southern French DMD or BMD families: from Southern blot to protein truncation test. Human Genetics. 102(3). 334–342. 22 indexed citations
17.
Bareil, Corinne, Christian Hamel, Bernard Arnaud, Jacques Demaille, & Mireille Claustres. (1997). A complex allele (1064 del TC and IVS2 + 22 ins 7) in the peripherin/RDS gene in retinitis pigmentosa with macular dystrophy. Ophthalmic Genetics. 18(3). 129–138. 8 indexed citations
18.
Hamel, Christian, et al.. (1997). The Protein Truncation Test (PTT) as a Method of Detection for Choroideremia Mutations. Experimental Eye Research. 65(6). 849–854. 19 indexed citations
19.
Hamel, Christian, et al.. (1997). An exonic polymorphism (381A/G) in the choroideremia gene.. PubMed. 8(3). 223–5. 1 indexed citations
20.
Tuffery‐Giraud, Sylvie, Corinne Bareil, Jacques Demaille, & Mireille Claustres. (1996). Four Novel Dystrophin Point Mutations: Detection by Protein Truncation Test and Transcript Analysis in Lymphocytes from Duchenne Muscular Dystrophy Patients. European Journal of Human Genetics. 4(3). 143–152. 26 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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