Fabienne Escande

3.7k total citations
68 papers, 1.4k citations indexed

About

Fabienne Escande is a scholar working on Molecular Biology, Pulmonary and Respiratory Medicine and Oncology. According to data from OpenAlex, Fabienne Escande has authored 68 papers receiving a total of 1.4k indexed citations (citations by other indexed papers that have themselves been cited), including 30 papers in Molecular Biology, 25 papers in Pulmonary and Respiratory Medicine and 15 papers in Oncology. Recurrent topics in Fabienne Escande's work include Lung Cancer Treatments and Mutations (14 papers), Congenital limb and hand anomalies (10 papers) and Glycosylation and Glycoproteins Research (8 papers). Fabienne Escande is often cited by papers focused on Lung Cancer Treatments and Mutations (14 papers), Congenital limb and hand anomalies (10 papers) and Glycosylation and Glycoproteins Research (8 papers). Fabienne Escande collaborates with scholars based in France, United States and United Kingdom. Fabienne Escande's co-authors include Nicole Porchet, Jean‐Pierre Aubert, Marie‐Pierre Buisine, Surinder K. Batra, Sylvie Manouvrier‐Hanu, Nicolas Moniaux, Florence Petit, Muriel Holder‐Espinasse, Anne Laine and Anne‐Sophie Jourdain and has published in prestigious journals such as Nature Communications, Journal of Clinical Oncology and Scientific Reports.

In The Last Decade

Fabienne Escande

62 papers receiving 1.4k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Fabienne Escande France	22	713	356	267	196	187	68	1.4k
Kevin Ebata United States	14	992 1.4×	337 0.9×	292 1.1×	179 0.9×	236 1.3×	24	1.8k
Francesca Diomedi‐Camassei Italy	21	628 0.9×	265 0.7×	147 0.6×	143 0.7×	138 0.7×	106	1.6k
Marc‐Antoine Belaud‐Rotureau France	24	665 0.9×	606 1.7×	502 1.9×	280 1.4×	164 0.9×	65	1.7k
Yingqi Teng United States	8	882 1.2×	268 0.8×	161 0.6×	304 1.6×	96 0.5×	14	1.6k
Todd Seeley United States	12	685 1.0×	202 0.6×	207 0.8×	413 2.1×	166 0.9×	16	1.3k
José M. Larios United States	14	676 0.9×	486 1.4×	319 1.2×	220 1.1×	315 1.7×	22	1.6k
Gloria Ravegnini Italy	22	427 0.6×	333 0.9×	194 0.7×	269 1.4×	68 0.4×	87	1.4k
Kiyotaka Nagahama Japan	24	467 0.7×	304 0.9×	177 0.7×	119 0.6×	117 0.6×	83	1.4k
Tatsuro Tajiri Japan	22	638 0.9×	293 0.8×	358 1.3×	317 1.6×	114 0.6×	140	1.6k
R. Scott Pearsall United States	25	1.4k 1.9×	376 1.1×	300 1.1×	180 0.9×	339 1.8×	62	2.4k

Countries citing papers authored by Fabienne Escande

Since Specialization

Citations

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

Fields of papers citing papers by Fabienne Escande

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Fabienne Escande

This figure shows the co-authorship network connecting the top 25 collaborators of Fabienne Escande. A scholar is included among the top collaborators of Fabienne Escande 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 Fabienne Escande. Fabienne Escande 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

Maurage, Claude‐Alain, et al.. (2025). High-grade gliomas and Lynch syndrome: A retrospective descriptive study with a literature review. Neuro-Oncology Practice. 13(1). 139–148.

Lebrun, Laetitia, Olivier De Witte, Fabienne Escande, et al.. (2025). Diagnostic impact of DNA methylation classification in adult and pediatric CNS tumors. Scientific Reports. 15(1). 2857–2857. 3 indexed citations

Vanlerberghe, Clémence, Frédéric Frénois, Emilie Ait‐Yahya, et al.. (2024). Functional characterization vs in silico prediction for TBX5 missense and splice variants in Holt-Oram syndrome. Genetics in Medicine. 26(12). 101267–101267.

Lebrun, Laetitia, Claude Van Campenhout, Valentina Lolli, et al.. (2023). Clinicopathological and molecular characterization of a case classified by DNA‑methylation profiling as “CNS embryonal tumor with BRD4–LEUTX fusion”. Acta Neuropathologica Communications. 11(1). 46–46. 7 indexed citations

Duhamel, Marie, Maxence Wisztorski, Soulaimane Aboulouard, et al.. (2022). Spatial analysis of the glioblastoma proteome reveals specific molecular signatures and markers of survival. Nature Communications. 13(1). 6665–6665. 36 indexed citations

Kammerer‐Jacquet, Solène‐Florence, Frédéric Dugay, Brigitte Laguerre, et al.. (2022). Comprehensive study of nine novel cases of TFEB‐amplified renal cell carcinoma: an aggressive tumour with frequent PDL1 expression. Histopathology. 81(2). 228–238. 16 indexed citations

Haro, Endika, Florence Petit, Fabienne Escande, et al.. (2021). Identification of limb-specific Lmx1b auto-regulatory modules with Nail-patella syndrome pathogenicity. Nature Communications. 12(1). 5533–5533. 15 indexed citations

Blons, Hélène, Jean‐Philippe Merlio, D. Debieuvre, et al.. (2020). PTEN, ATM, IDH1 mutations and MAPK pathway activation as modulators of PFS and OS in patients treated by first line EGFR TKI, an ancillary study of the French Cooperative Thoracic Intergroup (IFCT) Biomarkers France project. Lung Cancer. 151. 69–75. 7 indexed citations

Beau‐Faller, Michèle, Erwan Pencreach, Charlotte Leduc, et al.. (2019). Independent prognostic value of ultra-sensitive quantification of tumor pre-treatment T790M subclones in EGFR mutated non-small cell lung cancer (NSCLC) treated by first/second generation TKI, depends on variant allele frequency (VAF): Results of the French cooperative thoracic intergroup (IFCT) biomarkers France project. Lung Cancer. 140. 19–26. 13 indexed citations

10.

Leduc, Charlotte, Erwan Pencreach, J.P. Merlio, et al.. (2017). Ultrasensitive detection of EGFR T790M mutation by droplet digital PCR (ddPCR) in TKI naïve non-small cell lung cancer (NSCLC) harboring EGFR mutation: Results of the nationwide program Biomarkers France of the French Cooperative Thoracic Intergroup (IFCT). Annals of Oncology. 28. v22–v23.

11.

Italiano, Antoîne, Gaëlle Pierron, Nathalie Auger, et al.. (2016). Clinical effect of molecular methods in sarcoma diagnosis (GENSARC): a prospective, multicentre, observational study. The Lancet Oncology. 17(4). 532–538. 118 indexed citations

12.

Petit, Florence, Joris Andrieux, Geneviève Baujat, et al.. (2013). Split hand/foot malformation with long‐bone deficiency and BHLHA9 duplication: report of 13 new families. Clinical Genetics. 85(5). 464–469. 17 indexed citations

13.

Escande, Fabienne, B. Bouchindhomme, M.C. Copin, et al.. (2013). Faisabilité de la recherche de mutations EGFR et KRAS sur des prélèvements obtenus par EBUS-PTBA. Revue des Maladies Respiratoires. 30(5). 351–356. 7 indexed citations

14.

Crépin, Michel, Sophie Lejeune, Fabienne Escande, et al.. (2011). Evidence of constitutional MLH1 epimutation associated to transgenerational inheritance of cancer susceptibility. Human Mutation. 33(1). 180–188. 47 indexed citations

15.

Garçon, Guillaume, Fabienne Escande, Imane Abbas, et al.. (2009). Role of air pollution Particulate Matter (PM2.5) in the occurrence of loss of heterozygosity in multiple critical regions of 3p chromosome in human epithelial lung cells (L132). Toxicology Letters. 187(3). 172–179. 30 indexed citations

16.

Holder‐Espinasse, Muriel, B. Herbaux, Didier Lacombe, et al.. (2008). Génétique et orthopédie : gènes impliqués dans les malformations congénitales des membres. 92(1). 83–94. 1 indexed citations

17.

Bahi‐Buisson, Nadia, Emmanuel Roze, Carlo Dionisi‐Vici, et al.. (2008). Neurological aspects of hyperinsulinism–hyperammonaemia syndrome. Developmental Medicine & Child Neurology. 50(12). 945–949. 78 indexed citations

18.

Holder‐Espinasse, Muriel, Dominique Martin‐Coignard, Fabienne Escande, & Sylvie Manouvrier‐Hanu. (2007). A new mutation in TP63 is associated with age-related pathology. European Journal of Human Genetics. 15(11). 1115–1120. 19 indexed citations

19.

Crépin, Michel, Fabienne Escande, Catherine Bauters, et al.. (2006). Evaluation of denaturing high performance liquid chromatography for the mutational analysis of the MEN1 gene. Journal of Molecular Endocrinology. 36(2). 369–376. 14 indexed citations

20.

Escande, Fabienne, L. Lemaître, Nicolas Moniaux, et al.. (2002). Genomic organization of MUC4 mucin gene. European Journal of Biochemistry. 269(15). 3637–3644. 32 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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