Marta Llop

416 total citations
22 papers, 206 citations indexed

About

Marta Llop is a scholar working on Hematology, Molecular Biology and Public Health, Environmental and Occupational Health. According to data from OpenAlex, Marta Llop has authored 22 papers receiving a total of 206 indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Hematology, 11 papers in Molecular Biology and 8 papers in Public Health, Environmental and Occupational Health. Recurrent topics in Marta Llop's work include Acute Myeloid Leukemia Research (15 papers), Acute Lymphoblastic Leukemia research (8 papers) and Cancer Genomics and Diagnostics (6 papers). Marta Llop is often cited by papers focused on Acute Myeloid Leukemia Research (15 papers), Acute Lymphoblastic Leukemia research (8 papers) and Cancer Genomics and Diagnostics (6 papers). Marta Llop collaborates with scholars based in Spain, United Kingdom and Russia. Marta Llop's co-authors include Eva Barragán, Miguel Á. Sanz, José Cervera, Esperanza Such, Sarai Palanca, Inés Gómez‐Seguí, Maria López‐Pavía, Pascual Bolufer, Pau Montesinos and Mariam Ibáñez and has published in prestigious journals such as PLoS ONE, International Journal of Molecular Sciences and British Journal of Cancer.

In The Last Decade

Marta Llop

19 papers receiving 199 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Marta Llop Spain 9 131 79 77 37 35 22 206
Freek Manders Netherlands 8 122 0.9× 36 0.5× 114 1.5× 44 1.2× 18 0.5× 14 202
Sue Naim United States 5 233 1.8× 134 1.7× 37 0.5× 43 1.2× 29 0.8× 8 299
T. Peretz Israel 4 122 0.9× 78 1.0× 76 1.0× 67 1.8× 36 1.0× 8 223
E. L. Woodward Sweden 8 113 0.9× 42 0.5× 33 0.4× 50 1.4× 42 1.2× 14 225
Nicholas Hickson United Kingdom 8 66 0.5× 35 0.4× 54 0.7× 39 1.1× 20 0.6× 10 185
Jolien De Bie Belgium 6 174 1.3× 111 1.4× 47 0.6× 52 1.4× 92 2.6× 12 273
Ramy Rahmé France 4 135 1.0× 201 2.5× 37 0.5× 40 1.1× 48 1.4× 12 268
Mrinal Y. Shah United States 5 334 2.5× 90 1.1× 34 0.4× 29 0.8× 14 0.4× 10 366
Mays Jawad United Kingdom 8 109 0.8× 88 1.1× 23 0.3× 35 0.9× 30 0.9× 13 187
Sally Jeffries United Kingdom 6 66 0.5× 183 2.3× 58 0.8× 25 0.7× 50 1.4× 10 235

Countries citing papers authored by Marta Llop

Since Specialization
Citations

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

Fields of papers citing papers by Marta Llop

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Marta Llop

This figure shows the co-authorship network connecting the top 25 collaborators of Marta Llop. A scholar is included among the top collaborators of Marta Llop 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 Marta Llop. Marta Llop 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.
Sargas, Claudia, Marta Llop, Rebeca Rodríguez‐Veiga, et al.. (2025). Feasible and Rapid Screening of IDH1/2 and FLT3-TKD2 Mutations by High-Resolution Melting for Patients with Acute Myeloid Leukemia. Diagnostics. 15(10). 1230–1230.
2.
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.
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.
Sargas, Claudia, Marta Llop, Laura Arnal, et al.. (2025). Identification of relevant features using SEQENS to improve supervised machine learning models predicting AML treatment outcome. BMC Medical Informatics and Decision Making. 25(1). 179–179.
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.
Gil, José Vicente, Esperanza Such, Claudia Sargas, et al.. (2023). Design and Validation of a Custom Next-Generation Sequencing Panel in Pediatric Acute Lymphoblastic Leukemia. International Journal of Molecular Sciences. 24(5). 4440–4440. 6 indexed citations
7.
Llop, Marta, Claudia Sargas, & Eva Barragán. (2022). The role of next-generation sequencing in acute myeloid leukemia. Current Opinion in Oncology. 34(6). 723–728. 9 indexed citations
8.
9.
Such, Esperanza, Alessandro Liquori, Elvira Mora, et al.. (2019). RNA Sequencing Analysis for the Identification of a <b><i>PCM1/PDGFRB</i></b> Fusion Gene Responsive to Imatinib. Acta Haematologica. 142(2). 92–97. 3 indexed citations
10.
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
11.
Pallarès, Víctor, Montserrat Hoyos, Carmen Chillón, et al.. (2018). Focal Adhesion Genes Refine the Intermediate-Risk Cytogenetic Classification of Acute Myeloid Leukemia. Cancers. 10(11). 436–436. 7 indexed citations
12.
Pallarès, Víctor, Montserrat Hoyos, Carmen Chillón, et al.. (2017). NEDD9, an independent good prognostic factor in intermediate-risk acute myeloid leukemia patients. Oncotarget. 8(44). 76003–76014. 5 indexed citations
13.
Ibáñez, Mariam, José Carbonell‐Caballero, Luz García‐Alonso, et al.. (2016). The Mutational Landscape of Acute Promyelocytic Leukemia Reveals an Interacting Network of Co-Occurrences and Recurrent Mutations. PLoS ONE. 11(2). e0148346–e0148346. 21 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.
Gómez‐Seguí, Inés, Dolors Sánchez-Izquierdo, Eva Barragán, et al.. (2014). Single-Nucleotide Polymorphism Array-Based Karyotyping of Acute Promyelocytic Leukemia. PLoS ONE. 9(6). e100245–e100245. 4 indexed citations
16.
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
17.
Luna, Irene, Esperanza Such, José Cervera, et al.. (2013). WT1 isoform expression pattern in acute myeloid leukemia. Leukemia Research. 37(12). 1744–1749. 9 indexed citations
18.
Fuster, Óscar, Marta Llop, Paloma García, et al.. (2013). Adverse prognostic value of MYBL2 overexpression and association with microRNA-30 family in acute myeloid leukemia patients. Leukemia Research. 37(12). 1690–1696. 36 indexed citations
19.
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
20.
Ibáñez, Mariam, Esperanza Such, José Cervera, et al.. (2012). Rapid Screening of ASXL1, IDH1, IDH2, and c-CBL Mutations in de Novo Acute Myeloid Leukemia by High-Resolution Melting. Journal of Molecular Diagnostics. 14(6). 594–601. 14 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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