Valérie Benoît

2.7k citations

43 papers · 1.5k indexed · h-index 22

Co-authors: Vincent Bours Marie‐Paule Merville Isabelle Maystadt Damien Lederer Sylvie Delhalle Anne‐Cecile Hellin Christine Verellen‐Dumoulin Bernard Grisart
Topics: NF-κB Signaling Pathways (11 papers)Genomic variations and chromosomal abnormalities (8 papers)Genetics and Neurodevelopmental Disorders (8 papers)
Cited by: Cancer Research Genetics Molecular Biology
Journals: Journal of Biological ChemistrySHILAP Revista de lepidopterologíaCancer Research
Partner nations: Belgium United Kingdom France

In The Last Decade

Valérie Benoît

42 papers receiving 1.5k citations

Peers

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

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20 of 20 papers shown

#	Work	Indexed citations
1	Case Report: Inactivating PTH/PTHrP Signaling Disorder Type 1 Presenting With PTH Resistance 2022 ·Frontiers in Endocrinology ·Tanguy Demaret,René Wintjens,(unknown),(unknown),(unknown),C Ide,(unknown),(unknown),Valérie Benoît,Isabelle Maystadt	5
2	Frequency of Participation in External Quality Assessment Programs Focused on Rare Diseases: Belgian Guidelines for Human Genetics Centers 2021 ·JMIR Medical Informatics ·(unknown),(unknown),Vinciane Dideberg,Kathleen Claes,Sofie Symoens,Wim Coucke,Valérie Benoît,(unknown),Martine De Rycke,Sara Seneca,Lut Van Laer,Wim Wuyts,Anniek Corveleyn,(unknown),(unknown),Françoise Wilkin,Marie Ravoet,(unknown),(unknown),(unknown)	0
3	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 2021 ·European Journal of Medical Genetics ·Jean‐Marc Biard,(unknown),Philippe Clapuyt,Catherine Barréa,Valérie Benoît,Paméla Baldin,Pierre Bernard,(unknown),Yves Sznajer	9
4	Two novel GJA1 variants in oculodentodigital dysplasia 2019 ·Molecular Genetics & Genomic Medicine ·Nikolai Paul Pace,Valérie Benoît,(unknown),(unknown),(unknown),Pascale Hilbert,Isabella Borg	6
5	Simultaneous sequencing of 37 genes identified causative mutations in the majority of children with renal tubulopathies 2018 ·Kidney International ·Emma Ashton,Anne Debost‐Legrand,Valérie Benoît,(unknown),Annabelle Vénisse,Maria‐Christina Zennaro,Xavier Jeunemaı̂tre,Daniela Iancu,William G. van’t Hoff,Stephen B. Walsh,Nathalie Godefroid,Annelies Rotthier,Elena Del Favero,Olivier Devuyst,Franz Schaefer,Lucy Jenkins,Robert Kleta,Karin Dahan,Rosa Vargas‐Poussou,Detlef Böckenhauer	67
6	Case report: An infantile lethal form of Albright hereditary osteodystrophy due to a GNAS mutation 2018 ·Clinical Case Reports ·(unknown),Valérie Benoît,Damien Lederer,(unknown),(unknown),(unknown),(unknown),Catherine Wanty,Isabelle Maystadt	5
7	Expanding the phenotypic spectrum associated with OPHN1 mutations: Report of 17 individuals with intellectual disability but no cerebellar hypoplasia 2018 ·European Journal of Medical Genetics ·Stéphanie Moortgat,Damien Lederer,Marie Deprez,Marga Buzatu,Philippe Clapuyt,(unknown),Valérie Benoît,Sandrine Mary,Agnès Guichet,(unknown),Estelle Colin,Dominique Bonneau,Isabelle Maystadt	8
8	Novel PAX3 mutations causing Waardenburg syndrome type 1 in Tunisian patients 2017 ·International Journal of Pediatric Otorhinolaryngology ·(unknown),(unknown),Faouzi Mâazoul,Lilia Kraoua,(unknown),Inès Ouertani,(unknown),Valérie Benoît,G. Besbes,Ridha Mrad	3
9	Two novel EIF2S3 mutations associated with syndromic intellectual disability with severe microcephaly, growth retardation, and epilepsy 2016 ·American Journal of Medical Genetics Part A ·Stéphanie Moortgat,Julie Désir,Valérie Benoît,(unknown),Hélène Pendeville,Marie‐Cécile Nassogne,Damien Lederer,Isabelle Maystadt	41
10	De novo, heterozygous, loss‐of‐function mutations in SYNGAP1 cause a syndromic form of intellectual disability 2015 ·American Journal of Medical Genetics Part A ·Michael Parker,Alan Fryer,Deborah Shears,Katherine Lachlan,Shane McKee,Alex Magee,Shehla Mohammed,Pradeep Vasudevan,Soo‐Mi Park,Valérie Benoît,Damien Lederer,Isabelle Maystadt,(unknown),David Fitzpatrick	79
11	DYRK1A mutations in two unrelated patients 2015 ·European Journal of Medical Genetics ·(unknown),Cyril Mignot,Agnès Guët,(unknown),Caroline Nava,Delphine Héron,Boris Keren,Christel Depienne,Valérie Benoît,Isabelle Maystadt,Damien Lederer,Daniel Amsallem,Juliette Piard	24
12	Novel KDM6A (UTX) mutations and a clinical and molecular review of the X‐linked Kabuki syndrome (KS2) 2014 ·Clinical Genetics ·Siddharth Banka,Damien Lederer,Valérie Benoît,Emma Jenkins,Emma Howard,(unknown),Bronwyn Kerr,Shane McKee,I. Christopher Lloyd,(unknown),Helen Stewart,Susan M. White,Ravi Savarirayan,Grazia M.S. Mancini,Diane Beysen,Ronald D. Cohn,Bernard Grisart,Isabelle Maystadt,Dian Donnai	91
13	A three generation X‐linked family with Kabuki syndrome phenotype and a frameshift mutation in KDM6A 2014 ·American Journal of Medical Genetics Part A ·Damien Lederer,Debbie Shears,Valérie Benoît,Christine Verellen‐Dumoulin,Isabelle Maystadt	32
14	Evaluation of Original Dual Thromboxane A2 Modulators as Antiangiogenic Agents 2006 ·Journal of Pharmacology and Experimental Therapeutics ·Xavier de Leval,(unknown),Jean‐Michel Dogné,David Waltregny,Akeila Bellahcène,Valérie Benoît,Bernard Pirotte,Vincent Castronovo	14
15	Low daunomycin concentrations protect colorectal cancer cells from hypoxia-induced apoptosis 2005 ·Oncogene ·Chantal Lechanteur,Nathalie Jacobs,Roland Greimers,Valérie Benoît,Valérie Deregowski,Alain Chariot,Marie‐Paule Merville,Vincent Bours	4
16	Regulation of HER-2 oncogene expression by cyclooxygenase-2 and prostaglandin E2 2004 ·Oncogene ·Valérie Benoît,Biserka Relić,Xavier de Leval,Alain Chariot,Marie‐Paule Merville,Vincent Bours	62
17	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 2004 ·Journal of Biological Chemistry ·Biserka Relić,Valérie Benoît,Nathalie Franchimont,Clio Ribbens,Marie-Joëlle Kaiser,Philippe Gillet,Marie‐Paule Merville,Vincent Bours,Michel Malaise	40
18	Pharmacological evaluation of the novel thromboxane modulator BM-567 (II/II). Effects of BM-567 on osteogenic sarcoma-cell-induced platelet aggregation 2003 ·Prostaglandins Leukotrienes and Essential Fatty Acids ·Xavier de Leval,Valérie Benoît,J. Delarge,Fabien Julémont,Bernard Masereel,Bernard Pirotte,(unknown),Jean‐Louis David,Jean‐Michel Dogné	36
19	Identification of cytokine-induced nuclear factor-kappaB target genes in ovarian and breast cancer cells 2002 ·Biochemical Pharmacology ·Valérie Deregowski,Sylvie Delhalle,Valérie Benoît,Vincent Bours,Marie‐Paule Merville	27
20	NF-κB-dependent MnSOD expression protects adenocarcinoma cells from TNF-α-induced apoptosis 2002 ·Oncogene ·Sylvie Delhalle,Valérie Deregowski,Valérie Benoît,Marie‐Paule Merville,Vincent Bours	103

About Valérie Benoît

Valérie Benoît is a scholar working on Cancer Research, Genetics and Developmental Biology, having authored 43 papers that have together received 1.5k indexed citations. Recurring topics across this work include NF-κB Signaling Pathways (11 papers), Genomic variations and chromosomal abnormalities (8 papers) and Genetics and Neurodevelopmental Disorders (8 papers). The work is most often cited by research in Cancer Research (304 citations), Genetics (564 citations) and Molecular Biology (834 citations). Valérie Benoît has collaborated with scholars based in Belgium, United Kingdom and France. Frequent 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. Their work appears in journals such as Journal of Biological Chemistry, SHILAP Revista de lepidopterología and Cancer Research.

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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