Adrià Closa

538 total citations
9 papers, 278 citations indexed

About

Adrià Closa is a scholar working on Molecular Biology, Pathology and Forensic Medicine and Cancer Research. According to data from OpenAlex, Adrià Closa has authored 9 papers receiving a total of 278 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Molecular Biology, 3 papers in Pathology and Forensic Medicine and 3 papers in Cancer Research. Recurrent topics in Adrià Closa's work include Genetic factors in colorectal cancer (3 papers), RNA Research and Splicing (3 papers) and RNA modifications and cancer (2 papers). Adrià Closa is often cited by papers focused on Genetic factors in colorectal cancer (3 papers), RNA Research and Splicing (3 papers) and RNA modifications and cancer (2 papers). Adrià Closa collaborates with scholars based in Spain, Australia and Netherlands. Adrià Closa's co-authors include Vı́ctor Moreno, Rebeca Sanz‐Pamplona, Adriana López‐Doriga, David Cordero, Elisabet Guinó, Ramón Salazar, Lucas B. Carey, Xavier Solé, Laia Paré and Juana Díez and has published in prestigious journals such as Nature Communications, Scientific Reports and Clinical Cancer Research.

In The Last Decade

Adrià Closa

9 papers receiving 276 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Adrià Closa Spain 6 200 128 47 47 36 9 278
Melike Çağlayan United States 15 445 2.2× 92 0.7× 30 0.6× 79 1.7× 36 1.0× 35 485
Raymond Che United States 8 275 1.4× 70 0.5× 17 0.4× 55 1.2× 48 1.3× 8 315
Gergana Bounova Netherlands 7 307 1.5× 95 0.7× 46 1.0× 80 1.7× 32 0.9× 7 390
Yizhi Xiao China 9 202 1.0× 99 0.8× 28 0.6× 69 1.5× 19 0.5× 16 264
Erin E. Henninger United States 5 213 1.1× 167 1.3× 143 3.0× 63 1.3× 34 0.9× 5 333
Andreana Holowatyj United States 7 414 2.1× 78 0.6× 17 0.4× 59 1.3× 19 0.5× 8 452
Laia Richart Spain 8 220 1.1× 51 0.4× 15 0.3× 48 1.0× 26 0.7× 12 262
Elena Tosti United States 10 183 0.9× 50 0.4× 42 0.9× 101 2.1× 15 0.4× 13 261
Liangru Fei China 11 292 1.5× 103 0.8× 27 0.6× 70 1.5× 13 0.4× 13 353

Countries citing papers authored by Adrià Closa

Since Specialization
Citations

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

Fields of papers citing papers by Adrià Closa

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Adrià Closa

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

All Works

9 of 9 papers shown
1.
Moratalla-Navarro, Ferrán, Anna Díez-Villanueva, Adrià Closa, et al.. (2023). Identification of a Twelve-microRNA Signature with Prognostic Value in Stage II Microsatellite Stable Colon Cancer. Cancers. 15(13). 3301–3301. 3 indexed citations
2.
Closa, Adrià, Antonio C. Fuentes-Fayos, Katharina E. Hayer, et al.. (2022). A convergent malignant phenotype in B-cell acute lymphoblastic leukemia involving the splicing factor SRRM1. NAR Cancer. 4(4). zcac041–zcac041. 5 indexed citations
3.
Jiménez‐Vacas, Juan M., Enrique Gómez‐Gómez, Antonio C. Fuentes-Fayos, et al.. (2022). Tumor suppressor role of RBM22 in prostate cancer acting as a dual-factor regulating alternative splicing and transcription of key oncogenic genes. Translational research. 253. 68–79. 4 indexed citations
4.
Tavella, Teresa, et al.. (2019). Extensive post-transcriptional buffering of gene expression in the response to severe oxidative stress in baker’s yeast. Scientific Reports. 9(1). 11005–11005. 45 indexed citations
5.
López‐Doriga, Adriana, Laura Valle, M. Henar Alonso, et al.. (2018). Telomere length alterations in microsatellite stable colorectal cancer and association with the immune response. Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. 1864(9). 2992–3000. 6 indexed citations
6.
Moreno, Vı́ctor, M. Henar Alonso, Adrià Closa, et al.. (2018). Colon-specific eQTL analysis to inform on functional SNPs. British Journal of Cancer. 119(8). 971–977. 16 indexed citations
7.
Sanz‐Pamplona, Rebeca, Adriana López‐Doriga, Laia Paré, et al.. (2015). Exome Sequencing Reveals AMER1 as a Frequently Mutated Gene in Colorectal Cancer. Clinical Cancer Research. 21(20). 4709–4718. 44 indexed citations
8.
Bu, Pengcheng, Kai‐Yuan Chen, Nikolai Rakhilin, et al.. (2015). miR-1269 promotes metastasis and forms a positive feedback loop with TGF-β. Nature Communications. 6(1). 6879–6879. 102 indexed citations
9.
Closa, Adrià, David Cordero, Rebeca Sanz‐Pamplona, et al.. (2014). Identification of candidate susceptibility genes for colorectal cancer through eQTL analysis. Carcinogenesis. 35(9). 2039–2046. 53 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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