Miguel Urioste

9.0k total citations
110 papers, 2.4k citations indexed

About

Miguel Urioste is a scholar working on Molecular Biology, Genetics and Pathology and Forensic Medicine. According to data from OpenAlex, Miguel Urioste has authored 110 papers receiving a total of 2.4k indexed citations (citations by other indexed papers that have themselves been cited), including 48 papers in Molecular Biology, 42 papers in Genetics and 35 papers in Pathology and Forensic Medicine. Recurrent topics in Miguel Urioste's work include Genetic factors in colorectal cancer (31 papers), Genomic variations and chromosomal abnormalities (19 papers) and DNA Repair Mechanisms (16 papers). Miguel Urioste is often cited by papers focused on Genetic factors in colorectal cancer (31 papers), Genomic variations and chromosomal abnormalities (19 papers) and DNA Repair Mechanisms (16 papers). Miguel Urioste collaborates with scholars based in Spain, United States and United Kingdom. Miguel Urioste's co-authors include Javier Benı́tez, Ana Osório, Eva Bermejo, Laura Valle, María Luisa Martínez‐Frías, José Perea, María Victoria Fernández, María‐Luisa Martínez‐Frías, Beatriz Martı́nez-Delgado and Amelia Villa and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Clinical Oncology and PLoS ONE.

In The Last Decade

Miguel Urioste

108 papers receiving 2.3k citations

Peers

Miguel Urioste

GENET

PFM

ONCOL

Rob B. van der Luijt Netherlands

Olivier Caron France

Michael C. Luce United States

Lone Sunde Denmark

Marion Gauthier‐Villars France

Conxi Lázaro Spain

Daynna J. Wolff United States

Jennifer Ivanovich United States

Anthony Moran United Kingdom

Victoria A. Murday United Kingdom

Rob B. van der Luijt Netherlands

Miguel Urioste

802 ×0.8

531 ×0.7

GENET

804 ×1.2

PFM

931 ×1.4

ONCOL

782 ×1.8

Citations per year, relative to Miguel Urioste Miguel Urioste (= 1×) peers Rob B. van der Luijt

Countries citing papers authored by Miguel Urioste

Since Specialization

Citations

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

Fields of papers citing papers by Miguel Urioste

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Miguel Urioste

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

Rodríguez‐Escudero, Isabel, Caroline E. Nunes‐Xavier, José I. López, et al.. (2022). Functional analysis of PTEN variants of unknown significance from PHTS patients unveils complex patterns of PTEN biological activity in disease. European Journal of Human Genetics. 31(5). 568–577. 4 indexed citations

Perea, José, Juan Luis Garcı́a, Luís A. Corchete, et al.. (2021). A clinico-pathological and molecular analysis reveals differences between solitary (early and late-onset) and synchronous rectal cancer. Scientific Reports. 11(1). 2202–2202. 10 indexed citations

Olmedillas‐López, Susana, Daniel Rueda, Juan Luis Garcı́a, et al.. (2019). Cimp-Positive Status is More Representative in Multiple Colorectal Cancers than in Unique Primary Colorectal Cancers. Scientific Reports. 9(1). 10516–10516. 20 indexed citations

Cano, Juana María, Juan Luis Garcı́a, Susana Olmedillas‐López, et al.. (2019). Clinical and Molecular Comparative Study of Colorectal Cancer Based on Age-of-Onset and Tumor Location: Two Main Criteria for Subclassifying Colorectal Cancer. International Journal of Molecular Sciences. 20(4). 968–968. 24 indexed citations

Rueda, Daniel, Yolanda Rodríguez, Juan Luis Garcı́a, et al.. (2019). Intermediate-onset colorectal cancer: A clinical and familial boundary between both early and late-onset colorectal cancer. PLoS ONE. 14(5). e0216472–e0216472. 11 indexed citations

Perea, José, Julia Arribas, Juan Luis Garcı́a, et al.. (2019). Association of Polyps with Early-Onset Colorectal Cancer and Throughout Surveillance: Novel Clinical and Molecular Implications. Cancers. 11(12). 1900–1900. 11 indexed citations

Perea, José, Juan Luis Garcı́a, Luís A. Corchete, et al.. (2018). Redefining synchronous colorectal cancers based on tumor clonality. International Journal of Cancer. 144(7). 1596–1608. 8 indexed citations

Mur, Pilar, Ann‐Sofie Jemth, Nuno Amaral, et al.. (2018). Germline variation in the oxidative DNA repair genesNUDT1andOGG1is not associated with hereditary colorectal cancer or polyposis. Human Mutation. 39(9). 1214–1225. 5 indexed citations

Perea, José, Soraia Melo, Fátima Mercadillo, et al.. (2018). Clinical and functional characterization of the CDH1 germline variant c.1679C>G in three unrelated families with hereditary diffuse gastric cancer. European Journal of Human Genetics. 26(9). 1348–1353. 6 indexed citations

10.

Sánchez, Ricardo, Daniel Rueda, Laura Gómez, et al.. (2016). Toward a Molecular Classification of Synchronous Colorectal Cancer: Clinical and Molecular Characterization. Clinical Colorectal Cancer. 16(1). 31–37. 11 indexed citations

11.

Vaclová, Tereza, Gonzalo Goméz-López, Fernando Setién, et al.. (2015). DNA repair capacity is impaired in healthy BRCA1 heterozygous mutation carriers. Breast Cancer Research and Treatment. 152(2). 271–282. 24 indexed citations

12.

Yanowsky, Kira, Alicia Barroso, Ana Osório, et al.. (2012). Mutational analysis of telomere genes in BRCA1/2-negative breast cancer families with very short telomeres. Breast Cancer Research and Treatment. 134(3). 1337–1343. 6 indexed citations

13.

Hafner, Christian, Agustí Toll, Julie Earl, et al.. (2010). Multiple oncogenic mutations and clonal relationship in spatially distinct benign human epidermal tumors. Proceedings of the National Academy of Sciences. 107(48). 20780–20785. 63 indexed citations

14.

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

15.

Perea, José, Iago Justo, José Díaz-Tasende, et al.. (2009). Surgical management of hereditary colorectal cancer: surgery based on molecular analysis and family history. Revista Española de Enfermedades Digestivas. 101(8). 536–40. 7 indexed citations

16.

Honrado, Emiliano, Ana Osório, Roger L. Milne, et al.. (2007). Immunohistochemical classification of non-BRCA1/2 tumors identifies different groups that demonstrate the heterogeneity of BRCAX families. Modern Pathology. 20(12). 1298–1306. 41 indexed citations

17.

Urioste, Miguel. (2001). Bolivia: Reform and Resistance in the Countryside (1982-2000). Americanae (AECID Library). 1 indexed citations

18.

Urioste, Miguel, et al.. (1994). Short rib‐polydactyly syndrome and pericentric inversion of chromosome 4. American Journal of Medical Genetics. 49(1). 94–97. 42 indexed citations

19.

Martínez‐Frías, María Luisa & Miguel Urioste. (1994). Segmentation anomalies of the vertebras and ribs: A developmental field defect: Epidemiologic evidence. American Journal of Medical Genetics. 49(1). 36–44. 57 indexed citations

20.

Martínez‐Frías, M. L., Jaime L. Frías, Elvira Rodríguez‐Pinilla, et al.. (1991). Value of clinical analysis in epidemiological research: The Spanish registry experience. American Journal of Medical Genetics. 41(2). 192–195. 32 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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