Sergi Beltrán

22.4k total citations
51 papers, 1.2k citations indexed

About

Sergi Beltrán is a scholar working on Molecular Biology, Genetics and Cancer Research. According to data from OpenAlex, Sergi Beltrán has authored 51 papers receiving a total of 1.2k indexed citations (citations by other indexed papers that have themselves been cited), including 31 papers in Molecular Biology, 22 papers in Genetics and 8 papers in Cancer Research. Recurrent topics in Sergi Beltrán's work include Genomics and Rare Diseases (12 papers), Cancer Genomics and Diagnostics (7 papers) and Genetic factors in colorectal cancer (6 papers). Sergi Beltrán is often cited by papers focused on Genomics and Rare Diseases (12 papers), Cancer Genomics and Diagnostics (7 papers) and Genetic factors in colorectal cancer (6 papers). Sergi Beltrán collaborates with scholars based in Spain, Germany and United Kingdom. Sergi Beltrán's co-authors include Josep V. Planas, Marta Gut, Berta Fusté, Montserrat Corominas, António Figueras, Pablo Balseiro, Raúl Tonda, Beatriz Novoa, Conchi Estarás and Marian A. Martínez‐Balbás and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nature Communications and Blood.

In The Last Decade

Sergi Beltrán

47 papers receiving 1.2k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Sergi Beltrán Spain 20 513 354 244 121 118 51 1.2k
Nathan D. Meeker United States 13 560 1.1× 232 0.7× 478 2.0× 63 0.5× 96 0.8× 25 1.3k
Anirban Chakraborty United States 24 1.5k 2.9× 169 0.5× 347 1.4× 155 1.3× 83 0.7× 47 2.0k
Alessandro Coppe Italy 18 604 1.2× 154 0.4× 191 0.8× 297 2.5× 131 1.1× 29 1.1k
Mamiko Yajima United States 19 651 1.3× 149 0.4× 253 1.0× 97 0.8× 67 0.6× 45 1.2k
Jérôme Briolay France 17 800 1.6× 375 1.1× 262 1.1× 44 0.4× 261 2.2× 30 1.7k
Reade B. Roberts United States 18 378 0.7× 767 2.2× 61 0.3× 63 0.5× 129 1.1× 32 1.4k
Britta Meyer Germany 22 1.1k 2.1× 309 0.9× 125 0.5× 198 1.6× 313 2.7× 55 1.9k
Sven Klages Germany 18 707 1.4× 418 1.2× 175 0.7× 44 0.4× 261 2.2× 23 1.5k
Domitille Chalopin France 13 656 1.3× 336 0.9× 110 0.5× 63 0.5× 80 0.7× 22 1.1k
Daji Luo China 20 691 1.3× 330 0.9× 238 1.0× 171 1.4× 54 0.5× 54 1.4k

Countries citing papers authored by Sergi Beltrán

Since Specialization
Citations

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

Fields of papers citing papers by Sergi Beltrán

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Sergi Beltrán

This figure shows the co-authorship network connecting the top 25 collaborators of Sergi Beltrán. A scholar is included among the top collaborators of Sergi Beltrán 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 Sergi Beltrán. Sergi Beltrán 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.
Ratnaike, Thiloka, Ida Paramonov, Alexander Hoischen, et al.. (2025). Mitochondrial DNA disease discovery through evaluation of genotype and phenotype data: The Solve-RD experience. The American Journal of Human Genetics. 112(6). 1376–1387. 2 indexed citations
2.
Rigau, Maria, Mattia Bosio, Emily O’Connor, et al.. (2024). Rare disease research workflow using multilayer networks elucidates the molecular determinants of severity in Congenital Myasthenic Syndromes. Nature Communications. 15(1). 1227–1227. 12 indexed citations
3.
Hernández‐Illán, Eva, Elena Asensio, Jordi Morata, et al.. (2023). Quantification of rare somatic single nucleotide variants by droplet digital PCR using SuperSelective primers. Scientific Reports. 13(1). 18997–18997. 3 indexed citations
4.
Lagorce, David, Leslie Matalonga, Ida Paramonov, et al.. (2023). Phenotypic similarity-based approach for variant prioritization for unsolved rare disease: a preliminary methodological report. European Journal of Human Genetics. 32(2). 182–189. 5 indexed citations
5.
Musacchia, Francesco, Marianthi Karali, Annalaura Torella, et al.. (2021). VarGenius-HZD Allows Accurate Detection of Rare Homozygous or Hemizygous Deletions in Targeted Sequencing Leveraging Breadth of Coverage. Genes. 12(12). 1979–1979. 2 indexed citations
6.
Athanasiadis, Georgios, Raúl Tonda, Jordi Camps, et al.. (2021). Fine-scale population structure in five rural populations from the Spanish Eastern Pyrenees using high-coverage whole-genome sequence data. European Journal of Human Genetics. 29(10). 1557–1565. 2 indexed citations
7.
McMacken, Grace, Hanns Lochmüller, Boglárka Bánsági, et al.. (2020). Behr syndrome and hypertrophic cardiomyopathy in a family with a novel UCHL1 deletion. Journal of Neurology. 267(12). 3643–3649. 5 indexed citations
8.
Whalley, Justin P., Ivo Buchhalter, Esther Rheinbay, et al.. (2020). Framework for quality assessment of whole genome cancer sequences. Nature Communications. 11(1). 5040–5040. 4 indexed citations
9.
Martı́nez, Nerea, Sonia González de Villambrosía, Sanam Loghavi, et al.. (2020). Genetic lesions in MYC and STAT3 drive oncogenic transcription factor overexpression in plasmablastic lymphoma. Haematologica. 106(4). 1120–1128. 40 indexed citations
10.
Martı́nez, Nerea, Sonia González de Villambrosía, A. Insunza, et al.. (2020). Diagnostic value of bone marrow core biopsy patterns in lymphoplasmacytic lymphoma/Waldenström macroglobulinaemia and description of its mutational profiles by targeted NGS. Journal of Clinical Pathology. 73(9). 571–577. 8 indexed citations
11.
González‐Rincón, Julia, Sagrario Gómez, Nerea Martı́nez, et al.. (2019). Clonal dynamics monitoring during clinical evolution in chronic lymphocytic leukaemia. Scientific Reports. 9(1). 975–975. 6 indexed citations
12.
Feliubadaló, Lídia, Raúl Tonda, Jean-Rémi Trotta, et al.. (2017). Benchmarking of Whole Exome Sequencing and Ad Hoc Designed Panels for Genetic Testing of Hereditary Cancer. Scientific Reports. 7(1). 37984–37984. 31 indexed citations
13.
Álvarez‐Satta, María, et al.. (2017). Whole exome sequencing as a diagnostic tool for patients with ciliopathy-like phenotypes. PLoS ONE. 12(8). e0183081–e0183081. 10 indexed citations
14.
Clop, Alex, Abdoallah Sharaf, Anna Castelló, et al.. (2016). Identification of protein-damaging mutations in 10 swine taste receptors and 191 appetite-reward genes. BMC Genomics. 17(1). 685–685. 6 indexed citations
15.
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
16.
Metzger, Julia, Raúl Tonda, Sergi Beltrán, et al.. (2015). Runs of homozygosity reveal signatures of positive selection for reproduction traits in breed and non-breed horses. BMC Genomics. 16(1). 764–764. 107 indexed citations
17.
Palstra, Arjan P., Sergi Beltrán, Erik Burgerhout, et al.. (2013). Deep RNA Sequencing of the Skeletal Muscle Transcriptome in Swimming Fish. PLoS ONE. 8(1). e53171–e53171. 55 indexed citations
18.
Moreira, Rebeca, Pablo Balseiro, Josep V. Planas, et al.. (2012). Transcriptomics of In Vitro Immune-Stimulated Hemocytes from the Manila Clam Ruditapes philippinarum Using High-Throughput Sequencing. PLoS ONE. 7(4). e35009–e35009. 106 indexed citations
19.
Yúfera, Manuel, Silke Halm, Sergi Beltrán, et al.. (2011). Transcriptomic Characterization of the Larval Stage in Gilthead Seabream (Sparus aurata) by 454 Pyrosequencing. Marine Biotechnology. 14(4). 423–435. 38 indexed citations
20.

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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