Esperanza Such

2.9k total citations
61 papers, 988 citations indexed

About

Esperanza Such is a scholar working on Hematology, Molecular Biology and Genetics. According to data from OpenAlex, Esperanza Such has authored 61 papers receiving a total of 988 indexed citations (citations by other indexed papers that have themselves been cited), including 45 papers in Hematology, 22 papers in Molecular Biology and 19 papers in Genetics. Recurrent topics in Esperanza Such's work include Acute Myeloid Leukemia Research (42 papers), Myeloproliferative Neoplasms: Diagnosis and Treatment (14 papers) and Acute Lymphoblastic Leukemia research (13 papers). Esperanza Such is often cited by papers focused on Acute Myeloid Leukemia Research (42 papers), Myeloproliferative Neoplasms: Diagnosis and Treatment (14 papers) and Acute Lymphoblastic Leukemia research (13 papers). Esperanza Such collaborates with scholars based in Spain, United Kingdom and Italy. Esperanza Such's co-authors include José Cervera, Miguel Á. Sanz, Guillermo Sanz, Eva Barragán, Ana Valencia, Pascual Bolufer, Federico Moscardó, Benet Nomdedeu, Mariam Ibáñez and Elisa Luño and has published in prestigious journals such as SHILAP Revista de lepidopterología, Blood and PLoS ONE.

In The Last Decade

Esperanza Such

56 papers receiving 972 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Esperanza Such Spain 17 611 508 273 140 113 61 988
Chi‐Fei Huang Taiwan 12 898 1.5× 635 1.3× 404 1.5× 141 1.0× 200 1.8× 14 1.2k
Carla Mazzone Italy 15 576 0.9× 479 0.9× 219 0.8× 191 1.4× 73 0.6× 47 951
Paola Panetta Italy 14 573 0.9× 440 0.9× 162 0.6× 234 1.7× 78 0.7× 27 858
Yu Jing China 15 443 0.7× 301 0.6× 127 0.5× 102 0.7× 135 1.2× 74 667
F. Messa Italy 8 453 0.7× 366 0.7× 208 0.8× 217 1.6× 111 1.0× 15 724
Naomi Park United Kingdom 7 353 0.6× 373 0.7× 228 0.8× 50 0.4× 184 1.6× 11 761
Amer M. Zeidan United States 7 493 0.8× 378 0.7× 126 0.5× 95 0.7× 94 0.8× 21 729
Marie Sébert France 13 313 0.5× 281 0.6× 116 0.4× 62 0.4× 41 0.4× 47 593
Muhammad Shurafa United States 12 420 0.7× 271 0.5× 262 1.0× 91 0.7× 37 0.3× 29 912

Countries citing papers authored by Esperanza Such

Since Specialization
Citations

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

Fields of papers citing papers by Esperanza Such

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Esperanza Such

This figure shows the co-authorship network connecting the top 25 collaborators of Esperanza Such. A scholar is included among the top collaborators of Esperanza Such 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 Esperanza Such. Esperanza Such 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.
Avetisyan, Gayane, António A. Vicente, Rafael Andreu, et al.. (2025). Benchmarking standard-of-care and emerging genomic approaches to enhance diagnosis in pediatric acute lymphoblastic leukemia. British Journal of Cancer. 133(11). 1744–1754.
2.
Mora, Elvira, Rafael Hernani, José Cervera, et al.. (2025). Rapid Screening and Monitoring of UBA1 Mutations in VEXAS Syndrome. Journal of Molecular Diagnostics. 27(6). 431–437.
3.
Avetisyan, Gayane, Marion G. Valerio, Carmen Orellana, et al.. (2025). Atypical B-Cell Acute Lymphoblastic Leukemia with iAMP21 in the Context of Constitutional Ring Chromosome 21: A Case Report and Review of the Genetic Insights. International Journal of Molecular Sciences. 26(1). 357–357. 1 indexed citations
4.
Dávila, Julio, Maria López‐Pavía, Esperanza Such, et al.. (2024). Outcomes and effect of somatic mutations after erythropoiesis stimulating agents in patients with lower-risk myelodysplastic syndromes. Therapeutic Advances in Hematology. 15. 1564135917–1564135917. 3 indexed citations
5.
Gil, José Vicente, Esperanza Such, Gayane Avetisyan, et al.. (2024). Comprehensive detection of CRLF2 alterations in acute lymphoblastic leukemia: a rapid and accurate novel approach. Frontiers in Molecular Biosciences. 11. 1362081–1362081. 5 indexed citations
6.
Mallo, Mar, Heinz Tuechler, Leonor Arenillas, et al.. (2023). Regions of homozygosity confer a worse prognostic impact in myelodysplastic syndrome with normal karyotype. SHILAP Revista de lepidopterología. 4(2). 446–449. 3 indexed citations
7.
Such, Esperanza, Montserrat Arnán, Françesc Solé, et al.. (2023). Mutational Profile Enables the Identification of a High-Risk Subgroup in Myelodysplastic Syndromes with Isolated Trisomy 8. Cancers. 15(15). 3822–3822. 5 indexed citations
9.
Ribera, Jordi, Isabel Granada, Mireia Morgades, et al.. (2021). Prognostic heterogeneity of adult B‐cell precursor acute lymphoblastic leukaemia patients with t(1;19)(q23;p13)/TCF3‐PBX1 treated with measurable residual disease‐oriented protocols. British Journal of Haematology. 196(3). 670–675. 6 indexed citations
11.
Ibáñez, Mariam, José Carbonell‐Caballero, Esperanza Such, et al.. (2018). The modular network structure of the mutational landscape of Acute Myeloid Leukemia. PLoS ONE. 13(10). e0202926–e0202926. 5 indexed citations
12.
Villamón, Eva, et al.. (2018). Imiquimod inhibits growth and induces differentiation of myeloid leukemia cell lines. Cancer Cell International. 18(1). 15–15. 20 indexed citations
13.
Niveiro, Marı́a, M Tasso, Francisco López, et al.. (2017). A Rare Case of Pure Erythroid Sarcoma in a Pediatric Patient: Case Report and Literature Review. Children. 4(12). 113–113. 8 indexed citations
14.
García, Paloma, Marta Llop, Óscar Fuster, et al.. (2015). Study of the S427G polymorphism and ofMYBL2variants in patients with acute myeloid leukemia. Leukemia & lymphoma. 57(2). 429–435. 9 indexed citations
15.
Barragán, Eva, Óscar Fuster, Marta Llop, et al.. (2013). Novel Real-Time Polymerase Chain Reaction Assay for Simultaneous Detection of Recurrent Fusion Genes in Acute Myeloid Leukemia. Journal of Molecular Diagnostics. 15(5). 678–686. 7 indexed citations
16.
Luna, Irene, Esperanza Such, José Cervera, et al.. (2012). Analysis of SNP rs16754 of WT1 gene in a series of de novo acute myeloid leukemia patients. Annals of Hematology. 91(12). 1845–1853. 6 indexed citations
17.
González‐Porras, José Ramón, Esperanza Such, Benet Nomdedeu, et al.. (2011). The degree of neutropenia has a prognostic impact in low risk myelodysplastic syndrome. Leukemia Research. 36(3). 287–292. 17 indexed citations
18.
Valencia, Ana, José Cervera, Esperanza Such, et al.. (2010). A new reliable fluorescencein situhybridization method for identifying multiple specific cytogenetic abnormalities in acute myeloid leukemia. Leukemia & lymphoma. 51(4). 680–685. 1 indexed citations
19.
Valencia, Ana, José Cervera, Esperanza Such, et al.. (2010). Aberrant methylation of tumor suppressor genes in patients with refractory anemia with ring sideroblasts. Leukemia Research. 35(4). 479–483. 7 indexed citations
20.
Valencia, Ana, José Román‐Gómez, José Cervera, et al.. (2009). Wnt signaling pathway is epigenetically regulated by methylation of Wnt antagonists in acute myeloid leukemia. Leukemia. 23(9). 1658–1666. 120 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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