Irene Corrales

484 total citations
18 papers, 188 citations indexed

About

Irene Corrales is a scholar working on Hematology, Genetics and Immunology. According to data from OpenAlex, Irene Corrales has authored 18 papers receiving a total of 188 indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Hematology, 6 papers in Genetics and 4 papers in Immunology. Recurrent topics in Irene Corrales's work include Platelet Disorders and Treatments (10 papers), Blood groups and transfusion (5 papers) and Hemophilia Treatment and Research (4 papers). Irene Corrales is often cited by papers focused on Platelet Disorders and Treatments (10 papers), Blood groups and transfusion (5 papers) and Hemophilia Treatment and Research (4 papers). Irene Corrales collaborates with scholars based in Spain, Denmark and United Kingdom. Irene Corrales's co-authors include Francisco Vidal, Lorena Ramírez, Carme Altisent, R. Parra, Rafael Parra, Leonardo Juan Ramírez López, José Martínez‐González, Laia Cañes, Cristina Rodrı́guez and Antonio Rodríguez‐Sinovas and has published in prestigious journals such as PLoS ONE, Scientific Reports and International Journal of Molecular Sciences.

In The Last Decade

Irene Corrales

16 papers receiving 184 citations

Peers

Countries citing papers authored by Irene Corrales

Since Specialization

Citations

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

Fields of papers citing papers by Irene Corrales

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Irene Corrales

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

All Works

Sort: Min cites: Since: Top N: Style:

18 of 18 papers shown

#	Work	Indexed citations
1	Integrating Next‐Generation Sequencing Into Routine Molecular Diagnosis of Inherited Coagulation Factor Deficiencies: Real‐World Data From Spanish Patients 2025 ·Haemophilia ·(unknown), (unknown), Lorena Ramírez, Rafael Parra, Carmen Altisent, (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), Irene Corrales, Francisco Vidal	0
2	Key Genes of the Immune System and Predisposition to Acquired Hemophilia A: Evidence from a Spanish Cohort of 49 Patients Using Next-Generation Sequencing 2023 ·International Journal of Molecular Sciences ·José Pardos‐Gea, (unknown), (unknown), (unknown), (unknown), Manuel Rubio‐Rivas, Francesca Mitjavila, José Ramón González‐Porras, José María Bastida, José Mateo, (unknown), (unknown), Itziar Astigarraga, (unknown), Irene Corrales, Iris Garcia‐Martínez, Francisco Vidal	2
3	Gaining Insights into Inherited Bleeding Disorders of Complex Etiology in Pediatric Patients: Whole-Exome Sequencing as First-Line Investigation Tool 2023 ·Thrombosis and Haemostasis ·(unknown), (unknown), Rubén Berrueco, (unknown), (unknown), (unknown), (unknown), Lorena Ramírez, (unknown), Francisco Vidal, Irene Corrales	2
4	Multiallelic Copy Number Variation in ORM1 is Associated with Plasma Cell-Free DNA Levels as an Intermediate Phenotype for Venous Thromboembolism 2023 ·Thrombosis and Haemostasis ·(unknown), Iris Garcia‐Martínez, Sònia López, Ángel Martínez-Pérez, N. Vilalta, (unknown), (unknown), Ana Viñuela, Andrew Brown, Nikolaos I. Panousis, Alfonso Buil, Emmanouil T. Dermitzakis, Irene Corrales, Juan Carlos Souto, Francisco Vidal, José Manuel Soria	0
5	NR4A3: A Key Nuclear Receptor in Vascular Biology, Cardiovascular Remodeling, and Beyond 2021 ·International Journal of Molecular Sciences ·José Martínez‐González, Laia Cañes, Judith Alonso, (unknown), Antonio Rodríguez‐Sinovas, Irene Corrales, Cristina Rodrı́guez	28
6	Improving cord blood typing with next-generation sequencing: impact of allele-level HLA and NIMA determination on their selection for transplantation 2020 ·Bone Marrow Transplantation ·(unknown), Francisco Vidal, Irene Corrales, (unknown), (unknown), (unknown), (unknown), Sergi Querol, Francesc Rudilla	3
7	Diagnostic challenges in von Willebrand disease. Report of two cases with emphasis on multimeric and molecular analysis 2020 ·Platelets ·Ana Belén Moreno‐Castaño, (unknown), Marcos Pino, R. Parra, Carme Altisent, Francisco Vidal, Irene Corrales, (unknown), Sergi Torramadé‐Moix, Marta Palomo, Ginés Escolar, Maribel Díaz‐Ricart	1
8	Common Genetic Variants in ABO and CLEC4M Modulate the Pharmacokinetics of Recombinant FVIII in Severe Hemophilia A Patients 2020 ·Thrombosis and Haemostasis ·Iris Garcia‐Martínez, (unknown), (unknown), Rafael Parra, Carme Altisent, Lorena Ramírez, María Román, Ramiro Núñez, Juan Eduardo Megías‐Vericat, Irene Corrales, (unknown), Francisco Vidal	12
9	Update on Molecular Testing in von Willebrand Disease 2019 ·Seminars in Thrombosis and Hemostasis ·Javier Batlle, Almudena Pérez‐Rodríguez, Irene Corrales, (unknown), (unknown), (unknown), Francisco Vidal, (unknown)	10
10	Novel Double Factor PGT strategy analyzing blastocyst stage embryos in a single NGS procedure 2018 ·PLoS ONE ·Javier del Rey, Francisco Vidal, Lorena Ramírez, (unknown), Irene Corrales, Iris Garcia‐Martínez, O. Martínez-Pasarell, (unknown), (unknown), Aïda Pujol, Alberto Plaja, Itziar Salaverría, M. Oliver‐Bonet, J. Benet, J. Navarro	10
11	Advanced cell‐based modeling of the royal disease: characterization of the mutated F9mRNA 2017 ·Journal of Thrombosis and Haemostasis ·(unknown), (unknown), (unknown), Yvonne Richaud‐Patín, Senda Jiménez‐Delgado, Irene Corrales, (unknown), Sílvia Casacuberta‐Serra, Anne Weber, R. Parra, Carmen Altisent, Antonia Follenzi, Anne Dubart‐Kupperschmitt, Ángel Raya, Francisco Vidal, Jordi Barquinero	5
12	Next generation sequencing to dissect the genetic architecture of KNG1 and F11 loci using factor XI levels as an intermediate phenotype of thrombosis 2017 ·PLoS ONE ·(unknown), Giovana Gavidia‐Bovadilla, Irene Corrales, Héléna Brunel, Lorena Ramírez, Sònia López, Juan Carlos Souto, Francisco Vidal, José Manuel Soria	3
13	Combined study of ADAMTS13 and complement genes in the diagnosis of thrombotic microangiopathies using next‐generation sequencing 2017 ·Research and Practice in Thrombosis and Haemostasis ·(unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), Licínio Manco, Tabita Maia, (unknown), (unknown), Irene Corrales, Francisco Vidal, Letícia Ribeiro	17
14	The Unravelling of the Genetic Architecture of Plasminogen Deficiency and its Relation to Thrombotic Disease 2016 ·Scientific Reports ·(unknown), Pascual Marco, Irene Corrales, (unknown), Lorena Ramírez, Sònia López, Francisco Vidal, José Manuel Soria	16
15	Molecular characterization of ten F8 splicing mutations in RNA isolated from patient's leucocytes: assessment of in silico prediction tools accuracy 2015 ·Haemophilia ·(unknown), Irene Corrales, Lorena Ramírez, R. Parra, Ángel Raya, Jordi Barquinero, Francisco Vidal	11
16	High-throughput molecular diagnosis of von Willebrand disease by next generation sequencing methods 2012 ·Haematologica ·Irene Corrales, Steve Catarino, (unknown), (unknown), Carmen Altisent, R. Parra, Francisco Vidal	18
17	The study of the effect of splicing mutations in von Willebrand factor using RNA isolated from patients’ platelets and leukocytes 2011 ·Journal of Thrombosis and Haemostasis ·Irene Corrales, Leonardo Juan Ramírez López, Carme Altisent, R. Parra, Francisco Vidal	18
18	Rapid molecular diagnosis of von Willebrand disease by direct sequencing. Detection of 12 novel putative mutations in VWF gene 2009 ·Thrombosis and Haemostasis ·Irene Corrales, Lorena Ramírez, Carme Altisent, Rafael Parra, Francisco Vidal	32

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