Arnaud Lagarde

2.9k total citations
27 papers, 927 citations indexed

About

Arnaud Lagarde is a scholar working on Molecular Biology, Oncology and Pathology and Forensic Medicine. According to data from OpenAlex, Arnaud Lagarde has authored 27 papers receiving a total of 927 indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Molecular Biology, 13 papers in Oncology and 7 papers in Pathology and Forensic Medicine. Recurrent topics in Arnaud Lagarde's work include Genetic factors in colorectal cancer (7 papers), Colorectal Cancer Treatments and Studies (7 papers) and Neuroendocrine Tumor Research Advances (4 papers). Arnaud Lagarde is often cited by papers focused on Genetic factors in colorectal cancer (7 papers), Colorectal Cancer Treatments and Studies (7 papers) and Neuroendocrine Tumor Research Advances (4 papers). Arnaud Lagarde collaborates with scholars based in France, Tunisia and Luxembourg. Arnaud Lagarde's co-authors include Daniel Birnbaum, Sylviane Olschwang, José Adélaı̈de, Max Chaffanet, Luc Xerri, Norbert Vey, Nathalie Cervera, Virginie Trouplin, Véronique Gelsi‐Boyer and Thomas Prébet and has published in prestigious journals such as PLoS ONE, The Journal of Clinical Endocrinology & Metabolism and European Journal of Cancer.

In The Last Decade

Arnaud Lagarde

27 papers receiving 916 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Arnaud Lagarde France 14 506 333 243 224 164 27 927
Kenichi Chiba Japan 15 629 1.2× 312 0.9× 167 0.7× 147 0.7× 273 1.7× 49 1.1k
Idoya Lahortiga Spain 20 672 1.3× 595 1.8× 226 0.9× 260 1.2× 136 0.8× 40 1.3k
Xinyan Lu United States 20 280 0.6× 375 1.1× 292 1.2× 313 1.4× 118 0.7× 58 969
Teresa Flores Spain 19 539 1.1× 255 0.8× 492 2.0× 285 1.3× 177 1.1× 25 1.3k
Rüediger Liersch Germany 18 438 0.9× 182 0.5× 332 1.4× 84 0.4× 216 1.3× 33 942
Natalia González-Paz United States 8 835 1.7× 763 2.3× 343 1.4× 264 1.2× 76 0.5× 10 1.2k
María José Larráyoz Spain 19 405 0.8× 417 1.3× 148 0.6× 268 1.2× 87 0.5× 34 801
Konstantinos Kaloulis Switzerland 2 492 1.0× 257 0.8× 219 0.9× 122 0.5× 117 0.7× 2 884
Nicolas Goardon France 16 470 0.9× 249 0.7× 160 0.7× 91 0.4× 223 1.4× 29 905
Cristina Panaroni United States 14 377 0.7× 248 0.7× 231 1.0× 129 0.6× 102 0.6× 31 908

Countries citing papers authored by Arnaud Lagarde

Since Specialization
Citations

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

Fields of papers citing papers by Arnaud Lagarde

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Arnaud Lagarde

This figure shows the co-authorship network connecting the top 25 collaborators of Arnaud Lagarde. A scholar is included among the top collaborators of Arnaud Lagarde 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 Arnaud Lagarde. Arnaud Lagarde 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.
Lagarde, Arnaud, Lucie Coppin, Magalie Haissaguerre, et al.. (2022). Systematic detection of mosaicism by using digital NGS reveals three new MEN1 mosaicisms. Endocrine Connections. 11(11). 12 indexed citations
2.
Chanez, Brice, Romain Appay, Arnaud Guillé, et al.. (2022). Genomic analysis of paired IDHwt glioblastomas reveals recurrent alterations of MPDZ at relapse after radiotherapy and chemotherapy. Journal of the Neurological Sciences. 436. 120207–120207. 5 indexed citations
3.
Othman, Houcemeddine, Sahar Elouej, M. Jones, et al.. (2021). Case Report: Identification of Novel Variants in ERCC4 and DDB2 Genes in Two Tunisian Patients With Atypical Xeroderma Pigmentosum Phenotype. Frontiers in Genetics. 12. 650639–650639. 3 indexed citations
4.
Ghedira, Kaïs, Yosr Hamdi, Sahar Elouej, et al.. (2020). Identification of a CDH12 potential candidate genetic variant for an autosomal dominant form of transgrediens and progrediens palmoplantar keratoderma in a Tunisian family. Journal of Human Genetics. 65(4). 397–410. 3 indexed citations
5.
Elouej, Sahar, M. Jones, Arnaud Lagarde, et al.. (2019). Identification of a ERCC5 c.2333T>C (L778P) Variant in Two Tunisian Siblings With Mild Xeroderma Pigmentosum Phenotype. Frontiers in Genetics. 10. 111–111. 11 indexed citations
6.
Cuny, Thomas, Pauline Romanet, Henry Dufour, et al.. (2019). Acromegaly in Carney complex. Pituitary. 22(5). 456–466. 14 indexed citations
7.
Laquière, A., Arnaud Lagarde, Bertrand Napoléon, et al.. (2019). Genomic profile concordance between pancreatic cyst fluid and neoplastic tissue. World Journal of Gastroenterology. 25(36). 5530–5542. 10 indexed citations
8.
Roche, Stéphane, Camille Dion, Natacha Broucqsault, et al.. (2019). Methylation hotspots evidenced by deep sequencing in patients with facioscapulohumeral dystrophy and mosaicism. Neurology Genetics. 5(6). e372–e372. 16 indexed citations
9.
Lagarde, Arnaud, Sahar Elouej, Emna Kerkeni, et al.. (2018). Clinical profile of comorbidity of rare diseases in a Tunisian patient: a case report associating incontinentia pigmenti and Noonan syndrome. BMC Pediatrics. 18(1). 286–286. 3 indexed citations
10.
Fabre, Aurélie, et al.. (2017). OISO, traitement informatisé de la prise en charge en oncogénétique clinique. Bulletin du Cancer. 104(7-8). 602–607. 1 indexed citations
11.
Nguyen, Karine, Francesca Puppo, Stéphane Roche, et al.. (2017). Molecular combing reveals complex 4q35 rearrangements in Facioscapulohumeral dystrophy. Human Mutation. 38(10). 1432–1441. 30 indexed citations
12.
Kraoua, Lilia, Arnaud Lagarde, Sylviane Olschwang, et al.. (2017). Further Evidence for the Implication of LZTR1, a Gene not Associated with the Ras-Mapk Pathway, in the Pathogenesis of Noonan Syndrome. Biology and Medicine. 9(6). 6 indexed citations
13.
Gaborit, Bénédicte, Inès Abdesselam, Monique Bernard, et al.. (2016). A Heterozygous ZMPSTE24 Mutation Associated with Severe Metabolic Syndrome, Ectopic Fat Accumulation, and Dilated Cardiomyopathy. Cells. 5(2). 21–21. 27 indexed citations
14.
Mancini, Julien, Aurélie Fabre, Arnaud Lagarde, et al.. (2014). Vascular Endothelial Growth Factor A c.*237C>T polymorphism is associated with bevacizumab efficacy and related hypertension in metastatic colorectal cancer. Digestive and Liver Disease. 47(4). 331–337. 22 indexed citations
15.
Birnbaum, David, Anthony Ferrari, Arnaud Lagarde, et al.. (2012). Expression Profiles in Stage II Colon Cancer According to APC Gene Status. Translational Oncology. 5(2). 72–76. 16 indexed citations
16.
Bertucci, François, Arnaud Lagarde, Anthony Ferrari, et al.. (2012). 8q24 Cancer Risk Allele Associated with Major Metastatic Risk in Inflammatory Breast Cancer. PLoS ONE. 7(5). e37943–e37943. 36 indexed citations
17.
Birnbaum, David, José Adélaı̈de, Émilie Mamessier, et al.. (2011). Genome profiling of pancreatic adenocarcinoma. Genes Chromosomes and Cancer. 50(6). 456–465. 100 indexed citations
18.
Gelsi‐Boyer, Véronique, Virginie Trouplin, José Adélaı̈de, et al.. (2009). Mutations of polycomb‐associated gene ASXL1 in myelodysplastic syndromes and chronic myelomonocytic leukaemia. British Journal of Haematology. 145(6). 788–800. 407 indexed citations
19.
Gonçalvès, Anthony, Séverine Esteyriès, Arnaud Lagarde, et al.. (2008). A polymorphism of EGFR extracellular domain is associated with progression free-survival in metastatic colorectal cancer patients receiving cetuximab-based treatment. BMC Cancer. 8(1). 169–169. 62 indexed citations
20.
Mourra, Najat, Guy Zeitoun, Bruno Buecher, et al.. (2007). High Frequency of Chromosome 14 Deletion in Early-Onset Colon Cancer. Diseases of the Colon & Rectum. 50(11). 1881–1886. 22 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.

Explore authors with similar magnitude of impact

Breakdown of academic impact, for papers by Kenichi Chiba Breakdown of academic impact, for papers by Idoya Lahortiga Breakdown of academic impact, for papers by Xinyan Lu Breakdown of academic impact, for papers by Teresa Flores Breakdown of academic impact, for papers by Rüediger Liersch Breakdown of academic impact, for papers by Natalia González-Paz Breakdown of academic impact, for papers by María José Larráyoz Breakdown of academic impact, for papers by Konstantinos Kaloulis Breakdown of academic impact, for papers by Nicolas Goardon Breakdown of academic impact, for papers by Cristina Panaroni
Rankless by CCL
2026