Ana Osório

16.3k total citations
72 papers, 2.0k citations indexed

About

Ana Osório is a scholar working on Molecular Biology, Genetics and Cancer Research. According to data from OpenAlex, Ana Osório has authored 72 papers receiving a total of 2.0k indexed citations (citations by other indexed papers that have themselves been cited), including 52 papers in Molecular Biology, 52 papers in Genetics and 19 papers in Cancer Research. Recurrent topics in Ana Osório's work include BRCA gene mutations in cancer (47 papers), DNA Repair Mechanisms (29 papers) and Genomic variations and chromosomal abnormalities (22 papers). Ana Osório is often cited by papers focused on BRCA gene mutations in cancer (47 papers), DNA Repair Mechanisms (29 papers) and Genomic variations and chromosomal abnormalities (22 papers). Ana Osório collaborates with scholars based in Spain, United States and United Kingdom. Ana Osório's co-authors include Javier Benı́tez, Emiliano Honrado, Orland Dı́ez, Miguel de la Hoya, Alicia Barroso, Miguel Urioste, José Palacios, Trinidad Caldés, Beatriz Martı́nez-Delgado and Carmen Rivas and has published in prestigious journals such as Journal of Clinical Oncology, PLoS ONE and Cancer Research.

In The Last Decade

Ana Osório

71 papers receiving 2.0k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Ana Osório Spain 27 1.2k 1.2k 703 465 328 72 2.0k
Miguel de la Hoya Spain 26 1.0k 0.8× 945 0.8× 575 0.8× 488 1.0× 565 1.7× 92 1.9k
Lesley McGuffog United Kingdom 6 1.4k 1.1× 1.7k 1.5× 810 1.2× 628 1.4× 533 1.6× 6 2.4k
Barbara Wappenschmidt Germany 27 1.1k 0.9× 732 0.6× 536 0.8× 364 0.8× 233 0.7× 62 1.7k
Maaike P.G. Vreeswijk Netherlands 22 992 0.8× 649 0.6× 363 0.5× 518 1.1× 166 0.5× 50 1.7k
Oskar T. Johannsson Iceland 19 1.0k 0.8× 1.2k 1.0× 650 0.9× 594 1.3× 309 0.9× 37 2.0k
Valgarður Egilsson Iceland 24 1.0k 0.8× 975 0.8× 586 0.8× 450 1.0× 498 1.5× 45 1.9k
Zdeněk Kleibl Czechia 23 745 0.6× 557 0.5× 326 0.5× 473 1.0× 277 0.8× 77 1.4k
Bernard Peissel Italy 21 942 0.8× 948 0.8× 208 0.3× 253 0.5× 265 0.8× 63 1.7k
Rósa B. Barkardóttir Iceland 26 1.1k 0.9× 1.3k 1.1× 739 1.1× 482 1.0× 447 1.4× 50 2.2k
Francesco Schittulli Italy 24 976 0.8× 393 0.3× 728 1.0× 817 1.8× 167 0.5× 75 1.9k

Countries citing papers authored by Ana Osório

Since Specialization
Citations

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

Fields of papers citing papers by Ana Osório

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Ana Osório

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

All Works

20 of 20 papers shown
1.
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
2.
Rico, Daniel, Ana Osório, Miguel Urioste, et al.. (2013). DNA copy number profiling reveals extensive genomic loss in hereditary BRCA1 and BRCA2 ovarian carcinomas. British Journal of Cancer. 108(8). 1732–1742. 11 indexed citations
3.
Tanić, Miljana, Eduardo Andrés‐León, Socorro Marıá Rodríguez-Pinilla, et al.. (2013). MicroRNA-based molecular classification of non-BRCA1/2 hereditary breast tumours. British Journal of Cancer. 109(10). 2724–2734. 18 indexed citations
4.
Infante, Mar, M. Durán, Alberto Acedo, et al.. (2013). The highly prevalent BRCA2 mutation c.2808_2811del (3036delACAA) is located in a mutational hotspot and has multiple origins. Carcinogenesis. 34(11). 2505–2511. 14 indexed citations
5.
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
6.
Osório, Ana, Daniela Endt, Fernando Fernández, et al.. (2012). Predominance of pathogenic missense variants in the RAD51C gene occurring in breast and ovarian cancer families. Human Molecular Genetics. 21(13). 2889–2898. 76 indexed citations
7.
Menéndez, Mireia, Joan Castellsagué, Eva Pros, et al.. (2011). Assessing the RNA effect of 26 DNA variants in the BRCA1 and BRCA2 genes. Breast Cancer Research and Treatment. 132(3). 979–992. 13 indexed citations
8.
Fernández‐Ramires, Ricardo, Xavier Solé, Loris De Cecco, et al.. (2009). Gene expression profiling integrated into network modelling reveals heterogeneity in the mechanisms of BRCA1 tumorigenesis. British Journal of Cancer. 101(8). 1469–1480. 12 indexed citations
9.
García, María J., María Victoria Fernández, Ana Osório, et al.. (2008). Analysis of FANCB and FANCN/PALB2 Fanconi Anemia genes in BRCA1/2-negative Spanish breast cancer families. Breast Cancer Research and Treatment. 113(3). 545–551. 68 indexed citations
10.
Melchor, Lorenzo, Emiliano Honrado, Jia Huang, et al.. (2007). Estrogen Receptor Status Could Modulate the Genomic Pattern in Familial and Sporadic Breast Cancer. Clinical Cancer Research. 13(24). 7305–7313. 28 indexed citations
11.
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
12.
Kote‐Jarai, Zsofia, Lucy Matthews, Ana Osório, et al.. (2006). Accurate Prediction of BRCA1 and BRCA2 Heterozygous Genotype Using Expression Profiling after Induced DNA Damage. Clinical Cancer Research. 12(13). 3896–3901. 29 indexed citations
13.
Honrado, Emiliano, Ana Osório, José Palacios, & Javier Benı́tez. (2006). Pathology and gene expression of hereditary breast tumors associated with BRCA1, BRCA2 and CHEK2 gene mutations. Oncogene. 25(43). 5837–5845. 74 indexed citations
14.
Melchor, Lorenzo, Sara Álvarez, Emiliano Honrado, et al.. (2005). The Accumulation of Specific Amplifications Characterizes Two Different Genomic Pathways of Evolution of Familial Breast Tumors. Clinical Cancer Research. 11(24). 8577–8584. 15 indexed citations
15.
Honrado, Emiliano, Ana Osório, Alicia Cazorla, et al.. (2005). Phenotypic characterization of BRCA1 and BRCA2 tumors based in a tissue microarray study with 37 immunohistochemical markers. Breast Cancer Research and Treatment. 90(1). 5–14. 127 indexed citations
16.
Hoya, Miguel de la, Hanne Meijers‐Heijboer, Juan Manuel Fernández, et al.. (2004). Mutant BRCA1 alleles transmission: Different approaches and different biases. International Journal of Cancer. 113(1). 166–167.
17.
Osório, Ana, Miguel de la Hoya, Raquel Rodríguez‐López, et al.. (2003). Over-representation of two specific haplotypes among chromosomes harbouring BRCA1 mutations. European Journal of Human Genetics. 11(6). 489–492. 15 indexed citations
18.
Osório, Ana, Raquel Rodríguez‐López, Orland Dı́ez, et al.. (2003). The breast cancer low‐penetrance allele 1100delC in the CHEK2 gene is not present in Spanish familial breast cancer population. International Journal of Cancer. 108(1). 54–56. 59 indexed citations
19.
Hoya, Miguel de la, Ana Osório, Alicia Tosar, et al.. (2001). Association between BRCA1 and BRCA2 mutations and cancer phenotype in Spanish breast/ovarian cancer families: Implications for genetic testing. International Journal of Cancer. 97(4). 466–471. 62 indexed citations
20.
Osório, Ana, Mercedes Robledo, Beatriz Fernández-Martínez, et al.. (1998). Molecular analysis of the BRCA2 gene in 16 breast/ovarian cancer Spanish families. Clinical Genetics. 54(2). 142–147. 7 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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