Frédérique Béna

4.1k total citations
34 papers, 819 citations indexed

About

Frédérique Béna is a scholar working on Genetics, Molecular Biology and Plant Science. According to data from OpenAlex, Frédérique Béna has authored 34 papers receiving a total of 819 indexed citations (citations by other indexed papers that have themselves been cited), including 21 papers in Genetics, 18 papers in Molecular Biology and 7 papers in Plant Science. Recurrent topics in Frédérique Béna's work include Genomic variations and chromosomal abnormalities (14 papers), Genetics and Neurodevelopmental Disorders (8 papers) and Prenatal Screening and Diagnostics (6 papers). Frédérique Béna is often cited by papers focused on Genomic variations and chromosomal abnormalities (14 papers), Genetics and Neurodevelopmental Disorders (8 papers) and Prenatal Screening and Diagnostics (6 papers). Frédérique Béna collaborates with scholars based in Switzerland, France and United States. Frédérique Béna's co-authors include Stefania Gimelli, Stylianos E. Antonarakis, Sophie Dahoun, Michel Guipponi, Audrey Letourneau, M. Reza Sailani, Federico Santoni, Anis Féki, Maria Teresa Divizia and Youssef Hibaoui and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Biological Chemistry and Nature Communications.

In The Last Decade

Frédérique Béna

34 papers receiving 780 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Frédérique Béna Switzerland 15 440 366 131 113 94 34 819
Shila Mekhoubad United States 5 1.2k 2.7× 356 1.0× 147 1.1× 80 0.7× 71 0.8× 5 1.3k
Robert Wallerstein United States 17 410 0.9× 399 1.1× 180 1.4× 45 0.4× 48 0.5× 66 924
Sylvie Jaillard France 16 435 1.0× 397 1.1× 148 1.1× 123 1.1× 44 0.5× 54 802
Dilek Aktaş Türkiye 17 423 1.0× 455 1.2× 104 0.8× 60 0.5× 70 0.7× 68 873
Stefania Gimelli Switzerland 21 787 1.8× 900 2.5× 228 1.7× 113 1.0× 225 2.4× 64 1.6k
Jesper Graakjær Denmark 20 615 1.4× 212 0.6× 151 1.2× 43 0.4× 153 1.6× 32 1.3k
Mark V. Sauer United States 17 990 2.3× 212 0.6× 147 1.1× 360 3.2× 30 0.3× 28 1.3k
Christian W. Ehrenfels United States 9 392 0.9× 166 0.5× 70 0.5× 170 1.5× 42 0.4× 9 731
Brigitte Benzacken France 20 462 1.1× 737 2.0× 426 3.3× 294 2.6× 156 1.7× 61 1.3k
Sandra Chantot‐Bastaraud France 24 759 1.7× 939 2.6× 404 3.1× 142 1.3× 152 1.6× 67 1.4k

Countries citing papers authored by Frédérique Béna

Since Specialization
Citations

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

Fields of papers citing papers by Frédérique Béna

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Frédérique Béna

This figure shows the co-authorship network connecting the top 25 collaborators of Frédérique Béna. A scholar is included among the top collaborators of Frédérique Béna 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 Frédérique Béna. Frédérique Béna 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.
Nikolaev, Sergey I., Federico Santoni, Marco Garieri, et al.. (2014). Extrachromosomal driver mutations in glioblastoma and low-grade glioma. Nature Communications. 5(1). 5690–5690. 52 indexed citations
2.
Béna, Frédérique, A. Mrabet, Michel Guipponi, et al.. (2013). A new locus on chromosome 22q13.31 linked to recessive genetic epilepsy with febrile seizures plus (GEFS+) in a Tunisian consanguineous family. BMC Genetics. 14(1). 93–93. 10 indexed citations
3.
Hibaoui, Youssef, Iwona Grad, Audrey Letourneau, et al.. (2013). Modelling and rescuing neurodevelopmental defect of D own syndrome using induced pluripotent stem cells from monozygotic twins discordant for trisomy 21. EMBO Molecular Medicine. 6(2). 259–277. 132 indexed citations
4.
Borel, Christelle, Eugenia Migliavacca, Audrey Letourneau, et al.. (2012). Tandem repeat sequence variation as causative Cis-eQTLs for protein-coding gene expression variation: The case of CSTB. Human Mutation. 33(8). 1302–1309. 25 indexed citations
5.
Radhakrishna, Uppala, Swapan K. Nath, Ken McElreavey, et al.. (2012). Genome-wide linkage and copy number variation analysis reveals 710 kb duplication on chromosome 1p31.3 responsible for autosomal dominant omphalocele. Journal of Medical Genetics. 49(4). 270–276. 9 indexed citations
6.
Sappino, André‐Pascal, Raphaële Buser, Stefania Gimelli, et al.. (2012). Aluminium chloride promotes anchorage‐independent growth in human mammary epithelial cells. Journal of Applied Toxicology. 32(3). 233–243. 50 indexed citations
7.
Béna, Frédérique, et al.. (2011). Developmental expression and organisation of fibrinogen genes in the zebrafish. Thrombosis and Haemostasis. 107(1). 158–166. 21 indexed citations
8.
Béna, Frédérique, Stefania Gimelli, Diderik Tirefort, et al.. (2011). Cellular diversity within embryonic stem cells: pluripotent clonal sublines show distinct differentiation potential. Journal of Cellular and Molecular Medicine. 16(3). 456–467. 12 indexed citations
9.
Wonkam, Ambroise, et al.. (2011). Initiation of a medical genetics service in sub-Saharan Africa: Experience of prenatal diagnosis in Cameroon. European Journal of Medical Genetics. 54(4). e399–e404. 36 indexed citations
10.
Makrythanasis, Periklis, Stefania Gimelli, Frédérique Béna, et al.. (2011). Homozygous deletion of a gene-free region of 4p15 in a child with multiple anomalies: Could biallelic loss of conserved, non-coding elements lead to a phenotype?. European Journal of Medical Genetics. 55(1). 63–66. 3 indexed citations
11.
Božović, Ivana Babič, Zorana Grubić, Jasenka Wagner, et al.. (2011). Down Syndrome: Parental Origin, Recombination, and Maternal Age. Genetic Testing and Molecular Biomarkers. 16(1). 70–73. 33 indexed citations
12.
Cuoco, Cristina, Patrizia Ronchetto, Stefania Gimelli, et al.. (2011). Microarray based analysis of an inherited terminal 3p26.3 deletion, containing only the CHL1 gene, from a normal father to his two affected children. Orphanet Journal of Rare Diseases. 6(1). 12–12. 42 indexed citations
13.
Wonkam, Ambroise, et al.. (2011). Initiation of prenatal genetic diagnosis of chromosomal anomalies in Cameroon. International Journal of Gynecology & Obstetrics. 116(2). 174–175. 1 indexed citations
14.
Hovatta, Outi, Marisa Jaconi, Virpi Töhönen, et al.. (2010). A Teratocarcinoma-Like Human Embryonic Stem Cell (hESC) Line and Four hESC Lines Reveal Potentially Oncogenic Genomic Changes. PLoS ONE. 5(4). e10263–e10263. 39 indexed citations
15.
Mandriota, Stefano J., Raphaële Buser, Christelle Stouder, et al.. (2010). Ataxia Telangiectasia Mutated (ATM) Inhibition Transforms Human Mammary Gland Epithelial Cells. Journal of Biological Chemistry. 285(17). 13092–13106. 17 indexed citations
16.
Béna, Frédérique, Stefania Gimelli, Eugenia Migliavacca, et al.. (2010). A recurrent 14q32.2 microdeletion mediated by expanded TGG repeats. Human Molecular Genetics. 19(10). 1967–1973. 42 indexed citations
17.
Gimelli, Stefania, Maria Teresa Divizia, Margherita Lerone, et al.. (2010). Array‐CGH analysis in a patient with WAGR syndrome and a reciprocal translocation t(2;11) inherited from the normal father with double translocation. American Journal of Medical Genetics Part A. 152A(8). 2130–2133. 3 indexed citations
18.
Martinet, Danielle, Isabel Filges, Michael A. Morris, et al.. (2008). Subtelomeric 6p deletion: Clinical and array‐CGH characterization in two patients. American Journal of Medical Genetics Part A. 146A(16). 2094–2102. 27 indexed citations
19.
Lespinasse, James, Stefania Gimelli, Frédérique Béna, et al.. (2008). Characterization of an interstitial deletion 6q13–q14.1 in a female with mild mental retardation, language delay and minor dysmorphisms. European Journal of Medical Genetics. 52(1). 49–52. 10 indexed citations
20.
Béna, Frédérique, et al.. (2007). A de novo 1.1–1.6 Mb subtelomeric deletion of chromosome 20q13.33 in a patient with learning difficulties but without obvious dysmorphic features. American Journal of Medical Genetics Part A. 143A(16). 1894–1899. 13 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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