Andrés Moret

553 total citations
16 papers, 207 citations indexed

About

Andrés Moret is a scholar working on Hematology, Genetics and Immunology. According to data from OpenAlex, Andrés Moret has authored 16 papers receiving a total of 207 indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Hematology, 8 papers in Genetics and 4 papers in Immunology. Recurrent topics in Andrés Moret's work include Hemophilia Treatment and Research (10 papers), Coagulation, Bradykinin, Polyphosphates, and Angioedema (7 papers) and Platelet Disorders and Treatments (7 papers). Andrés Moret is often cited by papers focused on Hemophilia Treatment and Research (10 papers), Coagulation, Bradykinin, Polyphosphates, and Angioedema (7 papers) and Platelet Disorders and Treatments (7 papers). Andrés Moret collaborates with scholars based in Spain, Mexico and Bulgaria. Andrés Moret's co-authors include José A. Aznar, Ana Rosa Cid, Pilar Casaña, Saturnino Haya, Francisco España, V. Vila, Rafael Botella‐Estrada, Eduardo Nagore, C. Guillén and Dolores Planelles and has published in prestigious journals such as British Journal of Dermatology, Vox Sanguinis and Haemophilia.

In The Last Decade

Andrés Moret

16 papers receiving 203 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Andrés Moret Spain 9 176 44 23 20 15 16 207
Elisa Civaschi Italy 4 156 0.9× 37 0.8× 15 0.7× 14 0.7× 14 0.9× 4 177
Agustín Rodríguez‐Alén Spain 7 84 0.5× 19 0.4× 18 0.8× 15 0.8× 11 0.7× 8 126
Judith M.M. van Eeuwijk Germany 3 71 0.4× 22 0.5× 19 0.8× 35 1.8× 13 0.9× 4 114
Tiphaine Oudot‐Mellakh France 6 101 0.6× 26 0.6× 34 1.5× 17 0.8× 8 0.5× 8 182
Fabrizia Favale France 4 82 0.5× 43 1.0× 43 1.9× 8 0.4× 8 0.5× 8 127
Daniela Bartoletti Italy 6 65 0.4× 38 0.9× 26 1.1× 13 0.7× 20 1.3× 10 111
Denisa Urban Canada 3 67 0.4× 16 0.4× 22 1.0× 28 1.4× 10 0.7× 3 108
Tabita Maia Portugal 6 61 0.3× 62 1.4× 29 1.3× 15 0.8× 11 0.7× 13 159
Giuseppe Auteri Italy 7 87 0.5× 63 1.4× 52 2.3× 22 1.1× 7 0.5× 22 143
Simone Gangarossa Italy 7 90 0.5× 40 0.9× 27 1.2× 22 1.1× 7 0.5× 11 171

Countries citing papers authored by Andrés Moret

Since Specialization
Citations

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

Fields of papers citing papers by Andrés Moret

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Andrés Moret

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

All Works

16 of 16 papers shown
1.
Moret, Andrés, Javier Marco, Alessandro Liquori, et al.. (2020). Factor XIII deficiency in two Spanish families with a novel variant in gene F13A1 detected by next-generation sequencing; symptoms and clinical management. Journal of Thrombosis and Thrombolysis. 50(3). 686–688. 4 indexed citations
2.
Moret, Andrés, Mariam Ibáñez, Ana Rosa Cid, et al.. (2019). Next generation sequencing in bleeding disorders: two novel variants in the F5 gene (Valencia-1 and Valencia-2) associated with mild factor V deficiency. Journal of Thrombosis and Thrombolysis. 48(4). 674–678. 1 indexed citations
3.
Mingot‐Castellano, María Eva, et al.. (2019). Involvement of antifactor VIII autoantibodies specificity in the outcome of inhibitor eradication therapies in acquired hemophilia a patients. Blood Coagulation & Fibrinolysis. 30(3). 127–132. 1 indexed citations
4.
Sempere, Amparo, Inés Gómez‐Seguí, Elena Román, et al.. (2018). Guía práctica de tratamiento urgente de la microangiopatía trombótica. Medicina Clínica. 151(3). 123.e1–123.e9. 4 indexed citations
5.
Sempere, Amparo, Inés Gómez‐Seguí, Elena Román, et al.. (2018). Practice guidelines for the emergency treatment of thrombotic microangiopathy. Medicina Clínica (English Edition). 151(3). 123.e1–123.e9. 3 indexed citations
6.
Aznar, José A., et al.. (2014). Inhibitor development after switching of FVIII concentrate in multitransfused patients with severe haemophilia A. Haemophilia. 20(5). 624–629. 8 indexed citations
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Aznar, José A., Víctor Jiménez‐Yuste, R.M. Álvarez Pérez, et al.. (2012). Is on‐demand treatment effective in patients with severe haemophilia?. Haemophilia. 18(5). 738–742. 14 indexed citations
11.
Grancha, Salvador, Ana M. Ortiz, Concepción Marañón, et al.. (2012). Kinetics of the interaction between anti‐FVIII antibodies and FVIII from therapeutic concentrates, with and without von Willebrand factor, assessed by surface plasmon resonance. Haemophilia. 18(6). 982–989. 4 indexed citations
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Casaña, Pilar, et al.. (2008). Novel missense mutation c.2685G>C (p.Q895H) in VWF gene associated with very low levels of VWF mRNA. Annals of Hematology. 88(3). 245–247. 1 indexed citations
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Haya, Saturnino, et al.. (2007). Inhibitors in haemophilia A: current management and open issues. Haemophilia. 13(s5). 52–60. 28 indexed citations
16.
Planelles, Dolores, et al.. (2005). HLA class II polymorphisms in Spanish melanoma patients: homozygosity for HLA-DQA1 locus can be a potential melanoma risk factor. British Journal of Dermatology. 154(2). 261–266. 20 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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