Gwendoline Soler

760 total citations
14 papers, 415 citations indexed

About

Gwendoline Soler is a scholar working on Molecular Biology, Hematology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Gwendoline Soler has authored 14 papers receiving a total of 415 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Molecular Biology, 6 papers in Hematology and 3 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Gwendoline Soler's work include Acute Myeloid Leukemia Research (5 papers), Prenatal Screening and Diagnostics (3 papers) and Genomic variations and chromosomal abnormalities (3 papers). Gwendoline Soler is often cited by papers focused on Acute Myeloid Leukemia Research (5 papers), Prenatal Screening and Diagnostics (3 papers) and Genomic variations and chromosomal abnormalities (3 papers). Gwendoline Soler collaborates with scholars based in France, Spain and Germany. Gwendoline Soler's co-authors include Moying Tang, Pedro P. Medina, Ana Suárez‐Gauthier, Fernando López‐Ríos, Montse Sánchez‐Céspedes, Esther Conde, R. Corre, Laura Mesturoux, Marc‐Antoine Belaud‐Rotureau and Alexandra Lespagnol and has published in prestigious journals such as Journal of Clinical Oncology, Blood and The Journal of Pathology.

In The Last Decade

Gwendoline Soler

13 papers receiving 404 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Gwendoline Soler France	11	200	170	150	96	72	14	415
Caroline Weipert United States	11	107 0.5×	60 0.4×	101 0.7×	124 1.3×	58 0.8×	40	296
Sebastian Uhrig Germany	7	65 0.3×	162 1.0×	115 0.8×	101 1.1×	35 0.5×	17	360
P Autzen United Kingdom	7	115 0.6×	250 1.5×	213 1.4×	89 0.9×	18 0.3×	10	399
Stephen J Chanock United States	6	44 0.2×	153 0.9×	159 1.1×	100 1.0×	125 1.7×	7	434
Marie Pierre Gaub France	8	202 1.0×	180 1.1×	124 0.8×	118 1.2×	16 0.2×	11	430
Qingyi Wei United States	11	44 0.2×	383 2.3×	132 0.9×	149 1.6×	30 0.4×	29	548
Hari A. Deshpande United States	10	90 0.5×	120 0.7×	136 0.9×	39 0.4×	32 0.4×	46	363
Paulina Lange United States	10	43 0.2×	73 0.4×	179 1.2×	88 0.9×	147 2.0×	15	417
Francis Wright United States	10	49 0.2×	162 1.0×	168 1.1×	110 1.1×	41 0.6×	21	437
Byung Woog Kang South Korea	10	193 1.0×	66 0.4×	241 1.6×	44 0.5×	38 0.5×	21	406

Countries citing papers authored by Gwendoline Soler

Since Specialization

Citations

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

Fields of papers citing papers by Gwendoline Soler

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Gwendoline Soler

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

All Works

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14 of 14 papers shown

Soler, Gwendoline, et al.. (2023). Optical Genome Mapping in Routine Cytogenetic Diagnosis of Acute Leukemia. Cancers. 15(7). 2131–2131. 13 indexed citations

Goumy, Carole, Gwendoline Soler, Éléonore Eymard-Pierre, et al.. (2023). Optical genome mapping for prenatal diagnosis: A prospective study. Clinica Chimica Acta. 551. 117594–117594. 12 indexed citations

Goumy, Carole, Éléonore Eymard-Pierre, Gwendoline Soler, et al.. (2023). Feasibility of Optical Genome Mapping from Placental and Umbilical Cord Sampled after Spontaneous or Therapeutic Pregnancy Termination. Diagnostics. 13(23). 3576–3576. 1 indexed citations

Cabillic, Florian, Audrey Gros, Frédéric Dugay, et al.. (2014). Parallel FISH and Immunohistochemical Studies of ALK Status in 3244 Non–Small-Cell Lung Cancers Reveal Major Discordances. Journal of Thoracic Oncology. 9(3). 295–306. 118 indexed citations

Soler, Gwendoline, Sophie Kaltenbach, Sophie Dobbelstein, et al.. (2013). Identification of GSX2 and AF10 as NUP98 partner genes in myeloid malignancies. Blood Cancer Journal. 3(7). e124–e124. 15 indexed citations

Toutain, Jérôme, et al.. (2012). Proportion of Parents Agreeing to Delay Fetal Karyotyping until the Third Trimester of Pregnancy in Cases with an Indication. Fetal Diagnosis and Therapy. 31(2). 115–121. 1 indexed citations

Quelen, Cathy, Éric Lippert, Stéphanie Struski, et al.. (2011). Identification of a transforming MYB-GATA1 fusion gene in acute basophilic leukemia: a new entity in male infants. Blood. 117(21). 5719–5722. 29 indexed citations

Kaltenbach, Sophie, Gwendoline Soler, Carole Barin, et al.. (2010). NUP98-MLL fusion in human acute myeloblastic leukemia. Blood. 116(13). 2332–2335. 24 indexed citations

Malan, Valérie, Gwendoline Soler, Christine Coubes, et al.. (2009). Array-based comparative genomic hybridization identifies a high frequency of copy number variations in patients with syndromic overgrowth. European Journal of Human Genetics. 18(2). 227–232. 12 indexed citations

10.

Soler, Gwendoline, Isabelle Radford, Claus Meyer, et al.. (2008). MLL insertion with MLL-MLLT3 gene fusion in acute leukemia: case report and review of the literature. Cancer Genetics and Cytogenetics. 183(1). 53–59. 5 indexed citations

11.

Suárez‐Gauthier, Ana, Fernando López‐Ríos, Pedro P. Medina, et al.. (2007). Expression signatures in lung cancer reveal a profile for EGFR ‐mutant tumours and identify selective PIK3CA overexpression by gene amplification. The Journal of Pathology. 214(3). 347–356. 86 indexed citations

12.

Bergeron, Julie, Emmanuelle Clappier, Isabelle Radford, et al.. (2007). Prognostic and oncogenic relevance of TLX1/HOX11 expression level in T-ALLs. Blood. 110(7). 2324–2330. 38 indexed citations

13.

Saffroy, Raphaël, Philippe Riou, Gwendoline Soler, et al.. (2002). Analysis of alterations of WFDC1, a new putative tumour suppressor gene, in hepatocellular carcinoma. European Journal of Human Genetics. 10(4). 239–244. 19 indexed citations

14.

Grau, Juan J., J. Fuster, Xavier Filella, et al.. (1998). Randomized trial of adjuvant chemotherapy with mitomycin plus ftorafur versus mitomycin alone in resected locally advanced gastric cancer.. Journal of Clinical Oncology. 16(3). 1036–1039. 42 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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