Valérie Benoît

2.7k total citations
43 papers, 1.5k citations indexed

About

Valérie Benoît is a scholar working on Molecular Biology, Genetics and Cancer Research. According to data from OpenAlex, Valérie Benoît has authored 43 papers receiving a total of 1.5k indexed citations (citations by other indexed papers that have themselves been cited), including 27 papers in Molecular Biology, 19 papers in Genetics and 12 papers in Cancer Research. Recurrent topics in Valérie Benoît's work include NF-κB Signaling Pathways (11 papers), Genomic variations and chromosomal abnormalities (8 papers) and Genetics and Neurodevelopmental Disorders (8 papers). Valérie Benoît is often cited by papers focused on NF-κB Signaling Pathways (11 papers), Genomic variations and chromosomal abnormalities (8 papers) and Genetics and Neurodevelopmental Disorders (8 papers). Valérie Benoît collaborates with scholars based in Belgium, United Kingdom and France. Valérie Benoît's co-authors include Vincent Bours, Marie‐Paule Merville, Isabelle Maystadt, Damien Lederer, Sylvie Delhalle, Anne‐Cecile Hellin, Christine Verellen‐Dumoulin, Bernard Grisart, Mohamed Bentires‐Alj and Valérie Deregowski and has published in prestigious journals such as Journal of Biological Chemistry, SHILAP Revista de lepidopterología and Cancer Research.

In The Last Decade

Valérie Benoît

42 papers receiving 1.5k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Valérie Benoît Belgium 22 834 564 304 212 176 43 1.5k
Yi‐Fen Lee United States 26 1.0k 1.3× 410 0.7× 328 1.1× 165 0.8× 163 0.9× 48 1.7k
Man‐Wook Hur South Korea 26 1.4k 1.7× 204 0.4× 292 1.0× 281 1.3× 184 1.0× 77 2.0k
David K. Bol United States 17 681 0.8× 199 0.4× 197 0.6× 257 1.2× 159 0.9× 25 1.3k
Esther Castaño Spain 20 856 1.0× 142 0.3× 376 1.2× 401 1.9× 157 0.9× 49 1.6k
Clint L. Miller United States 24 1.3k 1.6× 247 0.4× 285 0.9× 142 0.7× 660 3.8× 62 2.1k
Felicity Newell Australia 16 795 1.0× 243 0.4× 145 0.5× 213 1.0× 120 0.7× 29 1.3k
Chang Jae Kim South Korea 25 1.1k 1.3× 152 0.3× 239 0.8× 352 1.7× 103 0.6× 62 1.6k
Azriel Schmidt United States 21 777 0.9× 326 0.6× 117 0.4× 315 1.5× 112 0.6× 33 1.4k
Qianghua Xia United States 18 921 1.1× 210 0.4× 337 1.1× 581 2.7× 288 1.6× 39 1.7k
Per Antonson Sweden 22 783 0.9× 424 0.8× 166 0.5× 229 1.1× 329 1.9× 39 1.5k

Countries citing papers authored by Valérie Benoît

Since Specialization
Citations

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

Fields of papers citing papers by Valérie Benoît

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Valérie Benoît

This figure shows the co-authorship network connecting the top 25 collaborators of Valérie Benoît. A scholar is included among the top collaborators of Valérie Benoît 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 Valérie Benoît. Valérie Benoît 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.
Demaret, Tanguy, et al.. (2022). Case Report: Inactivating PTH/PTHrP Signaling Disorder Type 1 Presenting With PTH Resistance. Frontiers in Endocrinology. 13. 928284–928284. 5 indexed citations
2.
Dideberg, Vinciane, Kathleen Claes, Sofie Symoens, et al.. (2021). Frequency of Participation in External Quality Assessment Programs Focused on Rare Diseases: Belgian Guidelines for Human Genetics Centers. JMIR Medical Informatics. 9(7). e27980–e27980.
3.
Biard, Jean‐Marc, Philippe Clapuyt, Catherine Barréa, et al.. (2021). Antenatal diagnosis of CHARGE syndrome: Prenatal ultrasound findings and crucial role of fetal dysmorphic signs. About a series of 10 cases and review of literature. European Journal of Medical Genetics. 64(4). 104189–104189. 9 indexed citations
4.
Pace, Nikolai Paul, et al.. (2019). Two novel GJA1 variants in oculodentodigital dysplasia. Molecular Genetics & Genomic Medicine. 7(9). e882–e882. 6 indexed citations
5.
Ashton, Emma, Anne Debost‐Legrand, Valérie Benoît, et al.. (2018). Simultaneous sequencing of 37 genes identified causative mutations in the majority of children with renal tubulopathies. Kidney International. 93(4). 961–967. 67 indexed citations
6.
Benoît, Valérie, et al.. (2018). Case report: An infantile lethal form of Albright hereditary osteodystrophy due to a GNAS mutation. Clinical Case Reports. 6(10). 1933–1940. 5 indexed citations
7.
Moortgat, Stéphanie, Damien Lederer, Marie Deprez, et al.. (2018). Expanding the phenotypic spectrum associated with OPHN1 mutations: Report of 17 individuals with intellectual disability but no cerebellar hypoplasia. European Journal of Medical Genetics. 61(8). 442–450. 8 indexed citations
8.
Mâazoul, Faouzi, Lilia Kraoua, Inès Ouertani, et al.. (2017). Novel PAX3 mutations causing Waardenburg syndrome type 1 in Tunisian patients. International Journal of Pediatric Otorhinolaryngology. 103. 14–19. 3 indexed citations
9.
Moortgat, Stéphanie, Julie Désir, Valérie Benoît, et al.. (2016). Two novel EIF2S3 mutations associated with syndromic intellectual disability with severe microcephaly, growth retardation, and epilepsy. American Journal of Medical Genetics Part A. 170(11). 2927–2933. 41 indexed citations
10.
Parker, Michael, Alan Fryer, Deborah Shears, et al.. (2015). De novo, heterozygous, loss‐of‐function mutations in SYNGAP1 cause a syndromic form of intellectual disability. American Journal of Medical Genetics Part A. 167(10). 2231–2237. 79 indexed citations
11.
Mignot, Cyril, Agnès Guët, Caroline Nava, et al.. (2015). DYRK1A mutations in two unrelated patients. European Journal of Medical Genetics. 58(3). 168–174. 24 indexed citations
12.
Banka, Siddharth, Damien Lederer, Valérie Benoît, et al.. (2014). Novel KDM6A (UTX) mutations and a clinical and molecular review of the X‐linked Kabuki syndrome (KS2). Clinical Genetics. 87(3). 252–258. 91 indexed citations
13.
Lederer, Damien, Debbie Shears, Valérie Benoît, Christine Verellen‐Dumoulin, & Isabelle Maystadt. (2014). A three generation X‐linked family with Kabuki syndrome phenotype and a frameshift mutation in KDM6A. American Journal of Medical Genetics Part A. 164(5). 1289–1292. 32 indexed citations
14.
Leval, Xavier de, Jean‐Michel Dogné, David Waltregny, et al.. (2006). Evaluation of Original Dual Thromboxane A2 Modulators as Antiangiogenic Agents. Journal of Pharmacology and Experimental Therapeutics. 318(3). 1057–1067. 14 indexed citations
15.
Lechanteur, Chantal, Nathalie Jacobs, Roland Greimers, et al.. (2005). Low daunomycin concentrations protect colorectal cancer cells from hypoxia-induced apoptosis. Oncogene. 24(10). 1788–1793. 4 indexed citations
16.
Benoît, Valérie, Biserka Relić, Xavier de Leval, et al.. (2004). Regulation of HER-2 oncogene expression by cyclooxygenase-2 and prostaglandin E2. Oncogene. 23(8). 1631–1635. 62 indexed citations
17.
Relić, Biserka, Valérie Benoît, Nathalie Franchimont, et al.. (2004). 15-Deoxy-Δ12,14-prostaglandin J2 Inhibits Bay 11-7085-induced Sustained Extracellular Signal-regulated Kinase Phosphorylation and Apoptosis in Human Articular Chondrocytes and Synovial Fibroblasts. Journal of Biological Chemistry. 279(21). 22399–22403. 40 indexed citations
18.
Leval, Xavier de, Valérie Benoît, J. Delarge, et al.. (2003). Pharmacological evaluation of the novel thromboxane modulator BM-567 (II/II). Effects of BM-567 on osteogenic sarcoma-cell-induced platelet aggregation. Prostaglandins Leukotrienes and Essential Fatty Acids. 68(1). 55–59. 36 indexed citations
19.
Deregowski, Valérie, Sylvie Delhalle, Valérie Benoît, Vincent Bours, & Marie‐Paule Merville. (2002). Identification of cytokine-induced nuclear factor-kappaB target genes in ovarian and breast cancer cells. Biochemical Pharmacology. 64(5-6). 873–881. 27 indexed citations
20.
Delhalle, Sylvie, Valérie Deregowski, Valérie Benoît, Marie‐Paule Merville, & Vincent Bours. (2002). NF-κB-dependent MnSOD expression protects adenocarcinoma cells from TNF-α-induced apoptosis. Oncogene. 21(24). 3917–3924. 103 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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