Francisco Vidal

1.7k total citations
60 papers, 985 citations indexed

About

Francisco Vidal is a scholar working on Hematology, Molecular Biology and Immunology. According to data from OpenAlex, Francisco Vidal has authored 60 papers receiving a total of 985 indexed citations (citations by other indexed papers that have themselves been cited), including 30 papers in Hematology, 22 papers in Molecular Biology and 15 papers in Immunology. Recurrent topics in Francisco Vidal's work include Hemophilia Treatment and Research (15 papers), Platelet Disorders and Treatments (12 papers) and Cancer-related gene regulation (10 papers). Francisco Vidal is often cited by papers focused on Hemophilia Treatment and Research (15 papers), Platelet Disorders and Treatments (12 papers) and Cancer-related gene regulation (10 papers). Francisco Vidal collaborates with scholars based in Spain, United States and United Kingdom. Francisco Vidal's co-authors include José Martínez‐González, Lina Badimón, Carme Altisent, L. Puig, Irene Corrales, Hiroshi Kondoh, Matilde E. Lleonart, Santiago Ramón y Cajal, Lorena Ramírez and Andrea Feliciano and has published in prestigious journals such as PLoS ONE, Clinical Infectious Diseases and Scientific Reports.

In The Last Decade

Francisco Vidal

57 papers receiving 967 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Francisco Vidal Spain	19	440	287	179	177	109	60	985
Michael Bernimoulin Switzerland	13	336 0.8×	156 0.5×	180 1.0×	133 0.8×	74 0.7×	17	714
Anja Vales Austria	20	433 1.0×	282 1.0×	338 1.9×	115 0.6×	50 0.5×	30	1.0k
James H. Finigan United States	17	307 0.7×	189 0.7×	149 0.8×	79 0.4×	76 0.7×	25	974
George Grigoriadis Australia	19	276 0.6×	284 1.0×	305 1.7×	151 0.9×	61 0.6×	62	978
Shogo Kasuda Japan	12	202 0.5×	171 0.6×	69 0.4×	72 0.4×	86 0.8×	54	582
Jeannig Berrou France	13	386 0.9×	271 0.9×	204 1.1×	60 0.3×	48 0.4×	26	910
Kohei Hosokawa Japan	17	177 0.4×	341 1.2×	311 1.7×	104 0.6×	43 0.4×	80	903
Zhimin Zhai China	16	217 0.5×	393 1.4×	287 1.6×	48 0.3×	75 0.7×	49	910
Bregt Roerdinkholder‐Stoelwinder Netherlands	12	379 0.9×	363 1.3×	135 0.8×	89 0.5×	76 0.7×	15	1.4k
Mohamed Hatmi France	18	315 0.7×	330 1.1×	52 0.3×	148 0.8×	132 1.2×	39	978

Countries citing papers authored by Francisco Vidal

Since Specialization

Citations

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

Fields of papers citing papers by Francisco Vidal

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Francisco Vidal

This figure shows the co-authorship network connecting the top 25 collaborators of Francisco Vidal. A scholar is included among the top collaborators of Francisco Vidal 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 Francisco Vidal. Francisco Vidal 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:

20 of 20 papers shown

Morena‐Barrio, Belén de la, José Padilla, Carlos Bravo‐Pérez, et al.. (2023). Impact of genetic structural variants in factor XI deficiency: identification, accurate characterization, and inferred mechanism by long-read sequencing. Journal of Thrombosis and Haemostasis. 21(7). 1779–1788. 1 indexed citations

Pardos‐Gea, José, Manuel Rubio‐Rivas, Francesca Mitjavila, et al.. (2023). Key Genes of the Immune System and Predisposition to Acquired Hemophilia A: Evidence from a Spanish Cohort of 49 Patients Using Next-Generation Sequencing. International Journal of Molecular Sciences. 24(22). 16372–16372. 2 indexed citations

Berrueco, Rubén, et al.. (2023). Gaining Insights into Inherited Bleeding Disorders of Complex Etiology in Pediatric Patients: Whole-Exome Sequencing as First-Line Investigation Tool. Thrombosis and Haemostasis. 124(7). 628–640. 2 indexed citations

Garcia‐Martínez, Iris, Sònia López, Ángel Martínez-Pérez, et al.. (2023). Multiallelic Copy Number Variation in ORM1 is Associated with Plasma Cell-Free DNA Levels as an Intermediate Phenotype for Venous Thromboembolism. Thrombosis and Haemostasis. 123(4). 438–452.

Soria, José Manuel, Sergi Mojal, Ángel Martínez-Pérez, et al.. (2022). A validated clinical-genetic score for assessing the risk of thrombosis in patients with COVID-19 receiving thromboprophylaxis. Haematologica. 107(9). 2244–2248. 1 indexed citations

Rey, Javier del, Iris Garcia‐Martínez, Francisco Vidal, et al.. (2022). Seminal Microbiota of Idiopathic Infertile Patients and Its Relationship With Sperm DNA Integrity. Frontiers in Cell and Developmental Biology. 10. 937157–937157. 28 indexed citations

Fornaguera, Cristina, Sejin Oh, Steven H.Y. Fan, et al.. (2021). Preclinical Assessment of a Gene-Editing Approach in a Mouse Model of Mitochondrial Neurogastrointestinal Encephalomyopathy. Human Gene Therapy. 32(19-20). 1210–1223. 13 indexed citations

Vidal, Francisco, et al.. (2020). Improving cord blood typing with next-generation sequencing: impact of allele-level HLA and NIMA determination on their selection for transplantation. Bone Marrow Transplantation. 55(8). 1623–1631. 3 indexed citations

Herrero, María José, et al.. (2019). HLA‐A, ‐B, ‐C, ‐DRB1, and ‐DQB1 allele and haplotype frequencies: An analysis of umbilical cord blood units at the Barcelona Cord Blood Bank. HLA. 94(4). 347–359. 18 indexed citations

10.

Vidal, Francisco, Juan Miguel Gómez‐Zumaquero, A. Balas, et al.. (2018). Analysis of the Spanish CCR5-∆32 inventory of cord blood units: lower cell counts in homozygous donors. Bone Marrow Transplantation. 53(6). 741–748. 4 indexed citations

11.

Sánchez‐Raya, Judith, et al.. (2018). Patients with bleeding of unknown cause and joint hypermobility: Clinical assessment and genetic screening. Annals of Physical and Rehabilitation Medicine. 61. e389–e390. 2 indexed citations

12.

Ferrando‐Martínez, Sara, Santiago Jiménez de Ory, Miguel Genebat, et al.. (2017). Thymic Function Failure Is Associated With Human Immunodeficiency Virus Disease Progression. Clinical Infectious Diseases. 64(9). 1191–1197. 28 indexed citations

13.

Richaud‐Patín, Yvonne, Senda Jiménez‐Delgado, Irene Corrales, et al.. (2017). Advanced cell‐based modeling of the royal disease: characterization of the mutated F9mRNA. Journal of Thrombosis and Haemostasis. 15(11). 2188–2197. 5 indexed citations

14.

Ferrán, Beatriz, Íngrid Martí-Pàmies, Judith Alonso, et al.. (2016). The nuclear receptor NOR-1 regulates the small muscle protein, X-linked (SMPX) and myotube differentiation. Scientific Reports. 6(1). 25944–25944. 15 indexed citations

15.

Feliciano, Andrea, Josep Castellví, Ana Artero‐Castro, et al.. (2013). miR-125b Acts as a Tumor Suppressor in Breast Tumorigenesis via Its Novel Direct Targets ENPEP, CK2-α, CCNJ, and MEGF9. PLoS ONE. 8(10). e76247–e76247. 132 indexed citations

16.

Corrales, Irene, Leonardo Juan Ramírez López, Carme Altisent, R. Parra, & Francisco Vidal. (2011). The study of the effect of splicing mutations in von Willebrand factor using RNA isolated from patients’ platelets and leukocytes. Journal of Thrombosis and Haemostasis. 9(4). 679–688. 18 indexed citations

17.

Eixarch, Herena, Carmen Espejo, María José Mansilla, et al.. (2009). Tolerance Induction in Experimental Autoimmune Encephalomyelitis Using Non-myeloablative Hematopoietic Gene Therapy With Autoantigen. Molecular Therapy. 17(5). 897–905. 22 indexed citations

18.

Julià, Antonio, et al.. (2004). Lack of association between the corticotropin‐releasing hormone locus and rheumatoid arthritis. Arthritis & Rheumatism. 50(8). 2706–2708. 2 indexed citations

19.

Martínez‐González, José, et al.. (2000). Small oxidative changes in atherogenic LDL concentrations irreversibly regulate adhesiveness of human endothelial cells: effect of the lazaroid U74500A. Atherosclerosis. 149(2). 295–302. 18 indexed citations

20.

Vidal, Francisco, et al.. (1998). Atherogenic concentrations of native low‐density lipoproteins down‐regulate nitric‐oxide‐synthase mRNA and protein levels in endothelial cells. European Journal of Biochemistry. 252(3). 378–384. 72 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.

Explore authors with similar magnitude of impact