Ignacio Blanco

23.2k total citations
149 papers, 3.4k citations indexed

About

Ignacio Blanco is a scholar working on Pathology and Forensic Medicine, Molecular Biology and Genetics. According to data from OpenAlex, Ignacio Blanco has authored 149 papers receiving a total of 3.4k indexed citations (citations by other indexed papers that have themselves been cited), including 50 papers in Pathology and Forensic Medicine, 46 papers in Molecular Biology and 32 papers in Genetics. Recurrent topics in Ignacio Blanco's work include Genetic factors in colorectal cancer (46 papers), Neurofibromatosis and Schwannoma Cases (28 papers) and Cancer Genomics and Diagnostics (27 papers). Ignacio Blanco is often cited by papers focused on Genetic factors in colorectal cancer (46 papers), Neurofibromatosis and Schwannoma Cases (28 papers) and Cancer Genomics and Diagnostics (27 papers). Ignacio Blanco collaborates with scholars based in Spain, United States and Italy. Ignacio Blanco's co-authors include Gabriel Capellá, Conxi Lázaro, Cristian Ochoa, Enric C. Sumalla, Sara González, Marta Pineda, Joan Brunet, Vı́ctor Moreno, Eduard Serra and Elisabet Guinó and has published in prestigious journals such as Proceedings of the National Academy of Sciences, The Lancet and Journal of Clinical Oncology.

In The Last Decade

Ignacio Blanco

139 papers receiving 3.3k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Ignacio Blanco Spain	30	1.1k	935	911	751	666	149	3.4k
Monica Miozzo Italy	40	1.9k 1.8×	479 0.5×	883 1.0×	1.2k 1.7×	708 1.1×	158	5.0k
Marilyn M. Li United States	26	997 0.9×	479 0.5×	589 0.6×	733 1.0×	1.0k 1.5×	105	3.2k
Frederick G. Behm United States	43	2.1k 2.0×	1.1k 1.2×	1.5k 1.6×	379 0.5×	313 0.5×	98	7.6k
Yves Benoît Belgium	34	1.2k 1.1×	226 0.2×	694 0.8×	288 0.4×	595 0.9×	139	4.1k
Donna A. Wall United States	38	1.0k 0.9×	257 0.3×	1.1k 1.2×	349 0.5×	221 0.3×	153	5.8k
Alexandros A. Drosos Greece	35	489 0.5×	808 0.9×	286 0.3×	299 0.4×	227 0.3×	127	4.2k
Margaret L. MacMillan United States	40	936 0.9×	246 0.3×	1.5k 1.6×	482 0.6×	145 0.2×	195	6.3k
Gregory A. Hale United States	40	671 0.6×	707 0.8×	1.5k 1.6×	387 0.5×	74 0.1×	133	5.3k
Elizabeth A. Beierle United States	31	1.1k 1.0×	181 0.2×	774 0.8×	442 0.6×	398 0.6×	187	3.2k
Mascha Binder Germany	28	729 0.7×	374 0.4×	866 1.0×	133 0.2×	193 0.3×	136	2.9k

Countries citing papers authored by Ignacio Blanco

Since Specialization

Citations

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

Fields of papers citing papers by Ignacio Blanco

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Ignacio Blanco

This figure shows the co-authorship network connecting the top 25 collaborators of Ignacio Blanco. A scholar is included among the top collaborators of Ignacio Blanco 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 Ignacio Blanco. Ignacio Blanco 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

Pauta, Montse, et al.. (2025). Prenatal FBXL4‐Associated Mitochondrial DNA Depletion Syndrome‐13: A New Case and Review of the Literature. Prenatal Diagnosis. 45(6). 829–834. 1 indexed citations

Alemany, Andrea, Pere Millat-Martínez, Dan Ouchi, et al.. (2024). Prognostic performance of early immune and endothelial activation markers in mild-to-moderate COVID-19 outpatients: a nested case-control study. Frontiers in Immunology. 15. 1501872–1501872.

Fernández‐Rodríguez, Juana, Ignacio Blanco, Claudia Valverde, et al.. (2024). Triple Combination of MEK, BET, and CDK Inhibitors Significantly Reduces Human Malignant Peripheral Nerve Sheath Tumors in Mouse Models. Clinical Cancer Research. 31(5). 907–920. 3 indexed citations

López‐Gallardo, Ester, Sonia Emperador, David Pacheu‐Grau, et al.. (2022). Toxic and nutritional factors trigger Leber hereditary optic neuropathy due to a mitochondrial tRNA mutation. Clinical Genetics. 102(4). 339–344. 2 indexed citations

Fernández‐Rodríguez, Juana, Yvonne Richaud‐Patín, Ernest Terribas, et al.. (2022). Modeling iPSC-derived human neurofibroma-like tumors in mice uncovers the heterogeneity of Schwann cells within plexiform neurofibromas. Cell Reports. 38(7). 110385–110385. 24 indexed citations

Rodríguez, Anna Duat, Juan Luís Becerra, Sandra Bonache, et al.. (2022). Neurofibromatosis type 1 families with first-degree relatives harbouring distinct NF1 pathogenic variants. Genetic counselling and familial diagnosis: what should be offered?. Journal of Medical Genetics. 59(10). 1017–1023. 7 indexed citations

Evans, D. Gareth, David Pang, Nicolas Champollion, et al.. (2022). ERN GENTURIS clinical practice guidelines for the diagnosis, treatment, management and surveillance of people with schwannomatosis. European Journal of Human Genetics. 30(7). 812–817. 16 indexed citations

Kilpeläinen, Athina, Dan Ouchi, Ruth Peña, et al.. (2022). Skewed Cellular Distribution and Low Activation of Functional T-Cell Responses in SARS-CoV-2 Non-Seroconvertors. Frontiers in Immunology. 13. 815041–815041. 1 indexed citations

Munera‐Campos, Mónica, et al.. (2022). Skin lesions in neurofibromatosis type 2: diagnostic and prognostic significance of cutaneous (plexiform) schwannomas. Journal of the European Academy of Dermatology and Venereology. 36(9). 1632–1640. 1 indexed citations

10.

Català, Martí, Ermengol Coma, Sergio Alonso, et al.. (2022). Transmissibility, hospitalization, and intensive care admissions due to omicron compared to delta variants of SARS-CoV-2 in Catalonia: A cohort study and ecological analysis. Frontiers in Public Health. 10. 961030–961030. 14 indexed citations

11.

Galván‐Femenía, Iván, Juan Luís Becerra, Isabel Bielsa, et al.. (2021). Revisiting the UK Genetic Severity Score for NF2: a proposal for the addition of a functional genetic component. Journal of Medical Genetics. 59(7). 678–686. 7 indexed citations

12.

Fernández‐Rodríguez, Juana, Ernest Terribas, Cleofé Romagosa, et al.. (2021). Chromosomal translocations inactivating CDKN2A support a single path for malignant peripheral nerve sheath tumor initiation. Human Genetics. 140(8). 1241–1252. 12 indexed citations

13.

Terribas, Ernest, Marco A. Fernández, Juana Fernández‐Rodríguez, et al.. (2020). KIF11 and KIF15 mitotic kinesins are potential therapeutic vulnerabilities for malignant peripheral nerve sheath tumors. Neuro-Oncology Advances. 2(Supplement_1). i62–i74. 11 indexed citations

14.

Segalés, Joaquím, Jordi Rodon, Carlos Ávila‐Nieto, et al.. (2020). Detection of SARS-CoV-2 in a cat owned by a COVID-19−affected patient in Spain. Proceedings of the National Academy of Sciences. 117(40). 24790–24793. 124 indexed citations

15.

Castellanos, Elisabeth, Bernat Gel, Andreu Alibés, et al.. (2019). Mutational spectrum by phenotype: panel‐based NGS testing of patients with clinical suspicion of RASopathy and children with multiple café‐au‐lait macules. Clinical Genetics. 97(2). 264–275. 12 indexed citations

16.

Azuara, Daniel, Francisco Rodríguez‐Moranta, Javier de, et al.. (2010). Novel Methylation Panel for the Early Detection of Colorectal Tumors in Stool DNA. Clinical Colorectal Cancer. 9(3). 168–176. 57 indexed citations

17.

Rosa-Rosa, Juan Manuel, Guillermo Pita, Miguel Urioste, et al.. (2009). Genome-wide Linkage Scan Reveals Three Putative Breast-Cancer-Susceptibility Loci. The American Journal of Human Genetics. 84(2). 115–122. 25 indexed citations

18.

Blanco, Ignacio, et al.. (2005). Cáncer colorrectal hereditario. Hispana. 2(2). 213–228. 1 indexed citations

19.

Palicio, Marta, Ignacio Blanco, Silvia Tórtola, et al.. (2000). Intron splice acceptor site polymorphism in the hMSH2 gene in sporadic and familial colorectal cancer. British Journal of Cancer. 82(3). 535–537. 12 indexed citations

20.

Blanco, Ignacio, Andrew G. Villanueva, Père Clavé, et al.. (1996). [Activity and subcellular distribution of lysosomal enzymes in acute pancreatitis induced by CDE diet in mice].. PubMed. 19(3). 146–52. 1 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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