Chloé Arfeuille

569 total citations
11 papers, 46 citations indexed

About

Chloé Arfeuille is a scholar working on Pediatrics, Perinatology and Child Health, Public Health, Environmental and Occupational Health and Hematology. According to data from OpenAlex, Chloé Arfeuille has authored 11 papers receiving a total of 46 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Pediatrics, Perinatology and Child Health, 5 papers in Public Health, Environmental and Occupational Health and 5 papers in Hematology. Recurrent topics in Chloé Arfeuille's work include Acute Lymphoblastic Leukemia research (5 papers), Acute Myeloid Leukemia Research (4 papers) and Childhood Cancer Survivors' Quality of Life (4 papers). Chloé Arfeuille is often cited by papers focused on Acute Lymphoblastic Leukemia research (5 papers), Acute Myeloid Leukemia Research (4 papers) and Childhood Cancer Survivors' Quality of Life (4 papers). Chloé Arfeuille collaborates with scholars based in France, United Kingdom and Belgium. Chloé Arfeuille's co-authors include Hélène Cavé, André Baruchel, Nathalie Grardel, Pauline Arnaud, Geneviève Plat, Christine Chomienne, Yves Bertrand, C Turleau, Cathérine Boileau and Dominique Bonnet and has published in prestigious journals such as Blood, Leukemia and Haematologica.

In The Last Decade

Chloé Arfeuille

9 papers receiving 46 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Chloé Arfeuille France 5 21 16 14 14 13 11 46
Anne Lutun France 3 26 1.2× 12 0.8× 8 0.6× 19 1.4× 14 1.1× 4 60
Maria C. Putti Italy 5 26 1.2× 26 1.6× 11 0.8× 28 2.0× 7 0.5× 5 64
Caroline Barbieri Blunck Brazil 6 35 1.7× 22 1.4× 21 1.5× 44 3.1× 7 0.5× 10 76
Catherine Devoldère France 3 31 1.5× 13 0.8× 9 0.6× 27 1.9× 14 1.1× 7 68
Frédéric Millot France 3 18 0.9× 12 0.8× 4 0.3× 7 0.5× 8 0.6× 9 38
Salvatore Gattillo Italy 4 51 2.4× 15 0.9× 6 0.4× 15 1.1× 4 0.3× 5 58
Eileen Stonerock United States 4 13 0.6× 21 1.3× 7 0.5× 18 1.3× 7 0.5× 6 55
Katharina L. Gössling Germany 4 6 0.3× 21 1.3× 14 1.0× 7 0.5× 5 0.4× 5 41
Paola Bonaccorso Italy 3 14 0.7× 18 1.1× 3 0.2× 12 0.9× 4 0.3× 11 33
Željko Antić Netherlands 5 23 1.1× 20 1.3× 16 1.1× 32 2.3× 3 0.2× 8 45

Countries citing papers authored by Chloé Arfeuille

Since Specialization
Citations

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

Fields of papers citing papers by Chloé Arfeuille

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Chloé Arfeuille

This figure shows the co-authorship network connecting the top 25 collaborators of Chloé Arfeuille. A scholar is included among the top collaborators of Chloé Arfeuille 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 Chloé Arfeuille. Chloé Arfeuille is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

11 of 11 papers shown
1.
Strullu, Marion, Chloé Arfeuille, Aurélie Caye‐Eude, et al.. (2025). Two distinct fetal‐type signatures characterize juvenile myelomonocytic leukemia. HemaSphere. 9(3). e70104–e70104.
2.
Caye‐Eude, Aurélie, et al.. (2023). Partitioning for Easy Multiplexing. Journal of Molecular Diagnostics. 25(8). 592–601.
3.
Kiciński, Michal, Chloé Arfeuille, Nathalie Grardel, et al.. (2023). The prognostic value of IKZF1plus in B‐cell progenitor acute lymphoblastic leukemia: Results from the EORTC 58951 trial. Pediatric Blood & Cancer. 70(6). e30313–e30313. 7 indexed citations
4.
Simand, Célestine, Céline Keime, Aurélie Caye, et al.. (2021). Ikaros deficiency is associated with aggressive BCR-ABL1 B-cell precursor acute lymphoblastic leukemia independent of the lineage and developmental origin. Haematologica. 107(1). 316–320. 1 indexed citations
5.
Arfeuille, Chloé, Stefan Suciu, Nicolas Sirvent, et al.. (2020). Pediatric randomized trial EORTC CLG 58951: Outcome for adolescent population with acute lymphoblastic leukemia. Hematological Oncology. 38(5). 763–772. 8 indexed citations
6.
Caye, Aurélie, Kevin Rouault‐Pierre, Marion Strullu, et al.. (2020). Correction: Despite mutation acquisition in hematopoietic stem cells, JMML-propagating cells are not always restricted to this compartment. Leukemia. 34(7). 1973–1973. 1 indexed citations
7.
Caye, Aurélie, Kevin Rouault‐Pierre, Marion Strullu, et al.. (2019). Despite mutation acquisition in hematopoietic stem cells, JMML-propagating cells are not always restricted to this compartment. Leukemia. 34(6). 1658–1668. 12 indexed citations
8.
Arfeuille, Chloé & Hélène Cavé. (2019). Relevant subtypes in childhood ALL. HemaSphere. 3(S2). 174–177. 1 indexed citations
9.
Meyer, Claus, Bruno A. Lopes, Aurélie Caye‐Eude, et al.. (2018). MLL-USP2: An Underestimated New Entity of MLL-Rearranged Leukemia Identified By NGS Analysis. Blood. 132(Supplement 1). 3920–3920. 2 indexed citations
10.
Arfeuille, Chloé, Pascale Sonigo, Michel Vekemans, et al.. (2017). Large Duplications Can Be Benign Copy Number Variants: A Case of a 3.6-Mb Xq21.33 Duplication. Cytogenetic and Genome Research. 151(3). 115–118. 7 indexed citations
11.
Gloan, Laurianne Le, Albert David, Nadine Hanna, et al.. (2015). Neonatal Marfan Syndrome: Report of a Case with an Inherited Splicing Mutation outside the Neonatal Domain. Molecular Syndromology. 6(6). 281–286. 7 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 Anne Lutun Breakdown of academic impact, for papers by Maria C. Putti Breakdown of academic impact, for papers by Caroline Barbieri Blunck Breakdown of academic impact, for papers by Catherine Devoldère Breakdown of academic impact, for papers by Frédéric Millot Breakdown of academic impact, for papers by Salvatore Gattillo Breakdown of academic impact, for papers by Eileen Stonerock Breakdown of academic impact, for papers by Katharina L. Gössling Breakdown of academic impact, for papers by Paola Bonaccorso Breakdown of academic impact, for papers by Željko Antić
Rankless by CCL
2026