Olga Campos

569 total citations
18 papers, 270 citations indexed

About

Olga Campos is a scholar working on Genetics, Molecular Biology and Cancer Research. According to data from OpenAlex, Olga Campos has authored 18 papers receiving a total of 270 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Genetics, 7 papers in Molecular Biology and 7 papers in Cancer Research. Recurrent topics in Olga Campos's work include Cancer Genomics and Diagnostics (7 papers), BRCA gene mutations in cancer (5 papers) and Genetic factors in colorectal cancer (5 papers). Olga Campos is often cited by papers focused on Cancer Genomics and Diagnostics (7 papers), BRCA gene mutations in cancer (5 papers) and Genetic factors in colorectal cancer (5 papers). Olga Campos collaborates with scholars based in Spain, United States and Brazil. Olga Campos's co-authors include Gabriel Capellá, Conxi Lázaro, Sara González, Marta Pineda, Joan Brunet, Jesús Del Valle, Ignacio Blanco, Lídia Feliubadaló, Adriana López‐Doriga and Ester Castellsagué and has published in prestigious journals such as SHILAP Revista de lepidopterología, British Journal of Cancer and Clinical Chemistry.

In The Last Decade

Olga Campos

16 papers receiving 270 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Olga Campos Spain	9	138	129	100	96	67	18	270
Stavroula Droufakou United Kingdom	6	149 1.1×	51 0.4×	81 0.8×	87 0.9×	83 1.2×	9	265
Cassandra Gulden United States	5	66 0.5×	117 0.9×	158 1.6×	148 1.5×	114 1.7×	7	280
Ramūnas Janavičius Lithuania	9	133 1.0×	200 1.6×	68 0.7×	72 0.8×	73 1.1×	13	295
Baptiste Brault France	4	133 1.0×	183 1.4×	71 0.7×	116 1.2×	62 0.9×	5	271
Angélina Legros France	5	147 1.1×	189 1.5×	73 0.7×	124 1.3×	62 0.9×	9	285
H. Sobol France	7	111 0.8×	161 1.2×	73 0.7×	86 0.9×	58 0.9×	14	268
Ester Castellsagué Spain	6	88 0.6×	90 0.7×	124 1.2×	99 1.0×	73 1.1×	7	220
Adrià López‐Fernández Spain	7	112 0.8×	116 0.9×	53 0.5×	47 0.5×	33 0.5×	18	199
Emily Hallberg United States	2	165 1.2×	306 2.4×	118 1.2×	165 1.7×	104 1.6×	3	398
Bryce A. Seifert United States	7	90 0.7×	140 1.1×	67 0.7×	82 0.9×	40 0.6×	15	229

Countries citing papers authored by Olga Campos

Since Specialization

Citations

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

Fields of papers citing papers by Olga Campos

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Olga Campos

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

All Works

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18 of 18 papers shown

Rofes, Paula, Àlex Teulé, Lídia Feliubadaló, et al.. (2022). Mosaicism in PTEN—new case and comment on the literature. European Journal of Human Genetics. 30(6). 641–644. 4 indexed citations

Rofes, Paula, Jesús Del Valle, Lídia Feliubadaló, et al.. (2021). BARD1 Pathogenic Variants Are Associated with Triple-Negative Breast Cancer in a Spanish Hereditary Breast and Ovarian Cancer Cohort. Genes. 12(2). 150–150. 12 indexed citations

Valle, Jesús Del, Lídia Feliubadaló, Marta Pineda, et al.. (2020). Screening of CNVs using NGS data improves mutation detection yield and decreases costs in genetic testing for hereditary cancer. Journal of Medical Genetics. 59(1). 75–78. 6 indexed citations

Campos, Olga, et al.. (2020). Epidemiological aspects of 306 emergency cases of small animals seen at a veterinary school hospital. SHILAP Revista de lepidopterología. 14(4). 252–258.

Valle, Jesús Del, Paula Rofes, Adriana López‐Doriga, et al.. (2020). Exploring the Role of Mutations in Fanconi Anemia Genes in Hereditary Cancer Patients. Cancers. 12(4). 829–829. 51 indexed citations

Campos, Olga, et al.. (2019). Medical therapy using omeprazole in 12 hydrocephalic dogs: clinical, diagnostic, and therapeutic findings. Pesquisa Veterinária Brasileira. 39(10). 823–829. 2 indexed citations

Castillejo, Adela, Matilde Navarro, Jesús Del Valle, et al.. (2018). Primary constitutional MLH1 epimutations: a focal epigenetic event. British Journal of Cancer. 119(8). 978–987. 19 indexed citations

Stradella, Agostina, Jesús Del Valle, Paula Rofes, et al.. (2018). Does multilocus inherited neoplasia alleles syndrome have severe clinical expression?. Journal of Medical Genetics. 56(8). 521–525. 11 indexed citations

Quiles, Francisco, Mireia Menéndez, Eva Tornero, et al.. (2016). Investigating the effect of 28 BRCA1 and BRCA2 mutations on their related transcribed mRNA. Breast Cancer Research and Treatment. 155(2). 253–260. 6 indexed citations

10.

Costa, Mariana Pinto da, et al.. (2016). Using Google Translate^© in the hospital: A case report. Technology and Health Care. 24(6). 965–968. 10 indexed citations

11.

Lara, Francisco J., et al.. (2015). Sufre, luego importa: Reflexiones éticas sobre los animales. Dialnet (Universidad de la Rioja).

12.

López‐Doriga, Adriana, Lídia Feliubadaló, Mireia Menéndez, et al.. (2013). ICO Amplicon NGS Data Analysis: A Web Tool for Variant Detection in Common High-Risk Hereditary Cancer Genes Analyzed by Amplicon GS Junior Next-Generation Sequencing. Human Mutation. 35(3). 271–277. 2 indexed citations

13.

Feliubadaló, Lídia, Adriana López‐Doriga, Ester Castellsagué, et al.. (2012). Next-generation sequencing meets genetic diagnostics: development of a comprehensive workflow for the analysis of BRCA1 and BRCA2 genes. European Journal of Human Genetics. 21(8). 864–870. 82 indexed citations

14.

Pineda, Marta, Pilar Mur, Maria D. Iniesta, et al.. (2012). MLH1 methylation screening is effective in identifying epimutation carriers. European Journal of Human Genetics. 20(12). 1256–1264. 28 indexed citations

15.

Valle, Jesús Del, Olga Campos, Àngela Velasco, et al.. (2011). Identification of a new complex rearrangement affecting exon 20 of BRCA1. Breast Cancer Research and Treatment. 130(1). 341–344. 2 indexed citations

16.

Castellsagué, Ester, Sara González, Marga Nadal, et al.. (2008). Detection of APC Gene Deletions Using Quantitative Multiplex PCR of Short Fluorescent Fragments. Clinical Chemistry. 54(7). 1132–1140. 22 indexed citations

17.

Campos, Olga, et al.. (2007). Automatic Surveillance System for Large Gas Fields With MultifrequencyMeasurements. Proceedings of SPE Annual Technical Conference and Exhibition. 1 indexed citations

18.

González, Sara, Ignacio Blanco, Olga Campos, et al.. (2005). Founder mutation in familial adenomatous polyposis (FAP) in the Balearic Islands. Cancer Genetics and Cytogenetics. 158(1). 70–74. 12 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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