José Padilla

733 total citations
40 papers, 411 citations indexed

About

José Padilla is a scholar working on Hematology, Genetics and Molecular Biology. According to data from OpenAlex, José Padilla has authored 40 papers receiving a total of 411 indexed citations (citations by other indexed papers that have themselves been cited), including 26 papers in Hematology, 10 papers in Genetics and 9 papers in Molecular Biology. Recurrent topics in José Padilla's work include Blood Coagulation and Thrombosis Mechanisms (15 papers), Platelet Disorders and Treatments (7 papers) and Coagulation, Bradykinin, Polyphosphates, and Angioedema (6 papers). José Padilla is often cited by papers focused on Blood Coagulation and Thrombosis Mechanisms (15 papers), Platelet Disorders and Treatments (7 papers) and Coagulation, Bradykinin, Polyphosphates, and Angioedema (6 papers). José Padilla collaborates with scholars based in Spain, United Kingdom and France. José Padilla's co-authors include Vicente Vicente, Javier Corral, María Eugenia de la Morena‐Barrio, Antonia Miñano, Ana Isabel Antón, Marı́a Luisa Lozano, Belén de la Morena‐Barrio, José Navarro‐Fernández, Irene Martínez‐Martínez and Sonia Águila and has published in prestigious journals such as Blood, PLoS ONE and Scientific Reports.

In The Last Decade

José Padilla

38 papers receiving 410 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
José Padilla Spain	15	238	101	69	60	59	40	411
ML Rand Canada	13	314 1.3×	78 0.8×	58 0.8×	75 1.3×	25 0.4×	20	615
Shigenori Kanazawa Japan	11	132 0.6×	157 1.6×	28 0.4×	25 0.4×	12 0.2×	23	419
Margherita Scapin Italy	12	227 1.0×	210 2.1×	28 0.4×	212 3.5×	17 0.3×	18	535
Kevin Dietrich Canada	7	56 0.2×	179 1.8×	51 0.7×	17 0.3×	31 0.5×	14	435
M. Sata Japan	10	149 0.6×	86 0.9×	84 1.2×	13 0.2×	13 0.2×	11	393
Fumiaki Urase Japan	9	153 0.6×	158 1.6×	11 0.2×	94 1.6×	14 0.2×	22	439
Zeki Üstüner Türkiye	11	65 0.3×	115 1.1×	58 0.8×	15 0.3×	13 0.2×	24	562
Masayuki Shiba Japan	11	125 0.5×	66 0.7×	17 0.2×	42 0.7×	25 0.4×	40	376
Keiko Wanaka Japan	14	226 0.9×	140 1.4×	77 1.1×	111 1.9×	14 0.2×	55	583
Kjell Sverre Galdal Norway	11	218 0.9×	97 1.0×	48 0.7×	59 1.0×	10 0.2×	14	462

Countries citing papers authored by José Padilla

Since Specialization

Citations

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

Fields of papers citing papers by José Padilla

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of José Padilla

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

All Works

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20 of 20 papers shown

Bravo‐Pérez, Carlos, José Padilla, María Eugenia de la Morena‐Barrio, et al.. (2024). The whole is greater than the sum of its parts: Long‐read sequencing for solving clinical problems in haematology. Journal of Cellular and Molecular Medicine. 28(3). e17961–e17961. 2 indexed citations

Garrido, Pedro, José Padilla, Bruno Ramos‐Molina, et al.. (2024). Landscape of antisense genes in the human genome and identification of new human hepatic antisense RNAs by long-read sequencing. BMC Genomics. 25(1). 1148–1148.

Morena‐Barrio, Belén de la, Christoph Male, Nuria Fernández‐Mosteirín, et al.. (2023). Targeted long-read sequencing identifies and characterizes structural variants in cases of inherited platelet disorders. Journal of Thrombosis and Haemostasis. 22(3). 851–859. 6 indexed citations

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

Padilla, José, María Eugenia de la Morena‐Barrio, Belén de la Morena‐Barrio, et al.. (2023). Usefulness and Limitations of Multiple Ligation-Dependent Probe Amplification in Antithrombin Deficiency. International Journal of Molecular Sciences. 24(5). 5023–5023. 3 indexed citations

Corral, Javier, Antonia Miñano, José Padilla, et al.. (2023). Factor XI in Carriers of Antiphospholipid Antibodies: Elevated Levels Associated with Symptomatic Thrombotic Cases, While Low Levels Linked to Asymptomatic Cases. International Journal of Molecular Sciences. 24(22). 16270–16270. 1 indexed citations

Padilla, José, et al.. (2023). Top of the Basilar Syndrome: A Case Report of a Healthy Young Woman and Literature Review. Cureus. 15(9). e44663–e44663. 1 indexed citations

Palma‐Barqueros, Verónica, José María Bastida, Carlo Zaninetti, et al.. (2023). Platelet transcriptome analysis in patients with germline RUNX1 mutations. Journal of Thrombosis and Haemostasis. 21(5). 1352–1365. 7 indexed citations

Bravo‐Pérez, Carlos, Joseph E. Chambers, José A. Martínez‐Menárguez, et al.. (2022). Full-length antithrombin frameshift variant with aberrant C-terminus causes endoplasmic reticulum retention with a dominant-negative effect. JCI Insight. 7(19). 7 indexed citations

10.

Palma‐Barqueros, Verónica, Nuria Revilla, Carlo Zaninetti, et al.. (2022). Src-related thrombocytopenia: a fine line between a megakaryocyte dysfunction and an immune-mediated disease. Blood Advances. 6(17). 5244–5255. 7 indexed citations

11.

Morena‐Barrio, María Eugenia de la, Pierre Suchon, E. Jacobsen, et al.. (2022). Two SERPINC1 variants affecting N-glycosylation of Asn224 cause severe thrombophilia not detected by functional assays. Blood. 140(2). 140–151. 17 indexed citations

12.

Palma‐Barqueros, Verónica, Loredana Bury, Shinji Kunishima, et al.. (2021). Expanding the genetic spectrum of TUBB1-related thrombocytopenia. Blood Advances. 5(24). 5453–5467. 17 indexed citations

13.

Bauduer, Frédéric, María Eugenia de la Morena‐Barrio, Salam Salloum‐Asfar, et al.. (2020). When genetic and surname analyses meet historical sources: The C56R mutation associated with factor XI deficiency as a marker of human migration during the Spanish Reconquista. Medical Hypotheses. 141. 109709–109709.

14.

Morena‐Barrio, María Eugenia de la, Pilar Llamas, Ewa Wypasek, et al.. (2017). High levels of latent antithrombin in plasma from patients with antithrombin deficiency. Thrombosis and Haemostasis. 117(5). 880–888. 21 indexed citations

15.

Navarro‐Fernández, José, María Eugenia de la Morena‐Barrio, José Padilla, et al.. (2016). Antithrombin Dublin (p.Val30Glu): a relatively common variant with moderate thrombosis risk of causing transient antithrombin deficiency. Thrombosis and Haemostasis. 116(7). 146–154. 24 indexed citations

16.

Gónzález‐Conejero, Rocío, José Padilla, Juan Luis Garcı́a, et al.. (2016). Uniparental disomy causes deficiencies of vitamin K‐dependent proteins. Journal of Thrombosis and Haemostasis. 14(12). 2410–2418. 5 indexed citations

17.

Morena‐Barrio, María Eugenia de la, José Padilla, Antonia Miñano, et al.. (2016). Identification of Regulatory Mutations in SERPINC1 Affecting Vitamin D Response Elements Associated with Antithrombin Deficiency. PLoS ONE. 11(3). e0152159–e0152159. 14 indexed citations

18.

Morena‐Barrio, María Eugenia de la, Irene Martínez‐Martínez, Antonia Miñano, et al.. (2015). A new method to quantify β-antithrombin glycoform in plasma reveals increased levels during the acute stroke event. Thrombosis Research. 136(3). 634–641. 7 indexed citations

19.

Antón, Ana Isabel, José Padilla, Francisco Velasco, et al.. (2014). Functional and molecular characterization of inherited platelet disorders in the Iberian Peninsula: results from a collaborative study. Orphanet Journal of Rare Diseases. 9(1). 213–213. 28 indexed citations

20.

Antón, Ana Isabel, José Padilla, Virginia Pérez-Andreu, et al.. (2013). Novel Associations of VKORC1 Variants with Higher Acenocoumarol Requirements. PLoS ONE. 8(5). e64469–e64469. 15 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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