Caroline Bénech

512 total citations
14 papers, 278 citations indexed

About

Caroline Bénech is a scholar working on Genetics, Physiology and Hematology. According to data from OpenAlex, Caroline Bénech has authored 14 papers receiving a total of 278 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Genetics, 7 papers in Physiology and 6 papers in Hematology. Recurrent topics in Caroline Bénech's work include Erythrocyte Function and Pathophysiology (6 papers), Blood groups and transfusion (6 papers) and Genomic variations and chromosomal abnormalities (4 papers). Caroline Bénech is often cited by papers focused on Erythrocyte Function and Pathophysiology (6 papers), Blood groups and transfusion (6 papers) and Genomic variations and chromosomal abnormalities (4 papers). Caroline Bénech collaborates with scholars based in France, Thailand and Belgium. Caroline Bénech's co-authors include Claude Férec, Jian‐Min Chen, Sylvia Redon, Marie‐Pierre Audrézet, I. Quéré, Yannick Le Meur, Émilie Cornec-Le Gall, Cédric Le Maréchal, Gaëlle Friocourt and B Cavelier and has published in prestigious journals such as PLoS ONE, Human Mutation and Transfusion.

In The Last Decade

Caroline Bénech

12 papers receiving 267 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Caroline Bénech France 8 196 132 72 62 41 14 278
Brian Gibbs United States 5 98 0.5× 123 0.9× 98 1.4× 101 1.6× 33 0.8× 8 254
Unnur Thorsteindottir United Kingdom 2 207 1.1× 221 1.7× 24 0.3× 20 0.3× 22 0.5× 2 336
Amy J. Lambert United States 10 52 0.3× 87 0.7× 42 0.6× 62 1.0× 8 0.2× 15 219
Yaser Heshmati Sweden 9 36 0.2× 103 0.8× 38 0.5× 30 0.5× 20 0.5× 15 201
E. Munro United Kingdom 9 131 0.7× 259 2.0× 22 0.3× 20 0.3× 35 0.9× 12 346
C R Müller Germany 12 70 0.4× 262 2.0× 40 0.6× 45 0.7× 13 0.3× 17 387
A. Saad Tunisia 9 130 0.7× 97 0.7× 13 0.2× 13 0.2× 42 1.0× 24 255
Stefano Petrocchi Italy 8 129 0.7× 84 0.6× 8 0.1× 15 0.2× 16 0.4× 15 236
Houda Hamdi‐Rozé France 10 71 0.4× 107 0.8× 72 1.0× 6 0.1× 27 0.7× 14 228
Oumar Samassékou Canada 9 28 0.1× 131 1.0× 18 0.3× 129 2.1× 30 0.7× 22 241

Countries citing papers authored by Caroline Bénech

Since Specialization
Citations

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

Fields of papers citing papers by Caroline Bénech

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Caroline Bénech

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

All Works

14 of 14 papers shown
1.
2.
Uguen, Kévin, Sylvia Redon, Karen Rouault, et al.. (2024). An unusual diagnosis of alpha‐mannosidosis with ocular anomalies: Behind the scenes of a hidden copy number variation. American Journal of Medical Genetics Part A. 194(5). e63532–e63532.
3.
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Bénech, Caroline, et al.. (2023). Anti-D alloimmunization by Asia type DEL red blood cell units in a D-negative Thai patient. Transfusion and Apheresis Science. 62(6). 103837–103837. 4 indexed citations
5.
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Nuchnoi, Pornlada, Caroline Bénech, Pawinee Kupatawintu, et al.. (2023). Serologically D-negative blood donors in Thailand: molecular variants and diagnostic strategy.. PubMed. 21(3). 209–217. 7 indexed citations
7.
Masson, Emmanuelle, Pascal Hammel, Caroline Bénech, et al.. (2013). Characterization of two deletions of the CTRC locus. Molecular Genetics and Metabolism. 109(3). 296–300. 8 indexed citations
8.
Redon, Sylvia, Caroline Bénech, Séverine Audebert‐Bellanger, et al.. (2013). A small de novo 16q24.1 duplication in a woman with severe clinical features. European Journal of Medical Genetics. 56(4). 211–215. 16 indexed citations
9.
Audrézet, Marie‐Pierre, Émilie Cornec-Le Gall, Jian‐Min Chen, et al.. (2012). Autosomal dominant polycystic kidney disease: Comprehensive mutation analysis of PKD1 and PKD2 in 700 unrelated patients. Human Mutation. 33(8). 1239–1250. 122 indexed citations
10.
Redon, Sylvia, Edouard Hirchaud, Daniel Barón, et al.. (2011). High-Throughput Analysis of Promoter Occupancy Reveals New Targets for Arx, a Gene Mutated in Mental Retardation and Interneuronopathies. PLoS ONE. 6(9). e25181–e25181. 29 indexed citations
11.
Fichou, Yann, Cédric Le Maréchal, Caroline Bénech, et al.. (2011). Variant screening of the RHD gene in a large cohort of subjects with D phenotype ambiguity: report of 17 novel rare alleles. Transfusion. 52(4). 759–764. 22 indexed citations
12.
Chen, Jian‐Min, Nadia Chuzhanova, Caroline Bénech, et al.. (2010). Complete ascertainment of intragenic copy number mutations (CNMs) in the CFTR gene and its implications for CNM formation at other autosomal loci. Human Mutation. 31(4). 421–428. 23 indexed citations
13.
Basinko, Audrey, Aurore Perrin, Fréderic Morel, et al.. (2010). Balanced transmission of a paternal complex chromosomal rearrangement involving chromosomes 2, 3, and 18. American Journal of Medical Genetics Part A. 152A(10). 2646–2650. 8 indexed citations
14.
Maréchal, Cédric Le, Caroline Bénech, B Cavelier, et al.. (2007). Identification of 12 novel RHD alleles in western France by denaturing high‐performance liquid chromatography analysis. Transfusion. 47(5). 858–863. 36 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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2026