Bernat Gel

3.8k total citations · 1 hit paper
48 papers, 2.4k citations indexed

About

Bernat Gel is a scholar working on Molecular Biology, Neurology and Cancer Research. According to data from OpenAlex, Bernat Gel has authored 48 papers receiving a total of 2.4k indexed citations (citations by other indexed papers that have themselves been cited), including 24 papers in Molecular Biology, 15 papers in Neurology and 14 papers in Cancer Research. Recurrent topics in Bernat Gel's work include Neurofibromatosis and Schwannoma Cases (15 papers), MicroRNA in disease regulation (7 papers) and Sarcoma Diagnosis and Treatment (7 papers). Bernat Gel is often cited by papers focused on Neurofibromatosis and Schwannoma Cases (15 papers), MicroRNA in disease regulation (7 papers) and Sarcoma Diagnosis and Treatment (7 papers). Bernat Gel collaborates with scholars based in Spain, United States and United Kingdom. Bernat Gel's co-authors include Eduard Serra, Alfons Navarro, Mariano Monzó, Tania Díaz, Marcus Buschbeck, Roberto Malinverni, Miguel A. Peinado, Anna Díez-Villanueva, Rosa Artells and Antonio Martı́nez and has published in prestigious journals such as Nature Genetics, Blood and Bioinformatics.

In The Last Decade

Bernat Gel

46 papers receiving 2.4k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

karyoploteR: an R/Bioconductor package to plot customizable genomes displaying arbitrary data

2017 397 citations Bernat Gel, Eduard Serra Bioinformatics profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Bernat Gel Spain	22	1.6k	965	364	319	243	48	2.4k
Xiaole Shirley Liu United States	19	2.6k 1.7×	802 0.8×	445 1.2×	593 1.9×	249 1.0×	25	3.3k
Xingzhi Song United States	15	1.2k 0.8×	470 0.5×	388 1.1×	345 1.1×	185 0.8×	44	2.0k
Ashley Lau United States	8	2.8k 1.8×	710 0.7×	277 0.8×	299 0.9×	157 0.6×	10	3.2k
Sebastian Bender Germany	20	1.4k 0.9×	547 0.6×	368 1.0×	347 1.1×	504 2.1×	33	2.3k
Pamela Rabbitts United Kingdom	33	1.8k 1.1×	752 0.8×	644 1.8×	682 2.1×	212 0.9×	84	2.9k
Violaine Saint‐André France	9	2.5k 1.6×	438 0.5×	295 0.8×	280 0.9×	143 0.6×	11	3.0k
Tilman Borggrefe Germany	31	2.5k 1.6×	388 0.4×	255 0.7×	347 1.1×	145 0.6×	63	3.3k
Warren A. Whyte United States	6	3.3k 2.1×	537 0.6×	410 1.1×	240 0.8×	199 0.8×	7	3.7k
Göran Levan Sweden	26	1.5k 1.0×	347 0.4×	874 2.4×	416 1.3×	259 1.1×	121	2.6k
Richard N. Freiman United States	24	1.2k 0.8×	252 0.3×	483 1.3×	303 0.9×	85 0.3×	34	2.1k

Countries citing papers authored by Bernat Gel

Since Specialization

Citations

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

Fields of papers citing papers by Bernat Gel

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Bernat Gel

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

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

Carrió, Meritxell, Bernat Gel, Alberto Villanueva, et al.. (2025). New models for MPNST: establishment and comprehensive characterization of two tumor cell lines. Cancer Cell International. 25(1). 268–268.

Fernández‐Rodríguez, Juana, Ignacio Blanco, Claudia Valverde, et al.. (2024). Triple Combination of MEK, BET, and CDK Inhibitors Significantly Reduces Human Malignant Peripheral Nerve Sheath Tumors in Mouse Models. Clinical Cancer Research. 31(5). 907–920. 3 indexed citations

Valle, Jesús Del, Lídia Feliubadaló, Marta Pineda, et al.. (2024). Detection of germline CNVs from gene panel data: benchmarking the state of the art. Briefings in Bioinformatics. 26(1). 1 indexed citations

Malinverni, Roberto, David Corujo, Bernat Gel, & Marcus Buschbeck. (2023). regioneReloaded: evaluating the association of multiple genomic region sets. Bioinformatics. 39(11). 4 indexed citations

Fernández‐Rodríguez, Juana, Alberto Villanueva, Conxi Lázaro, et al.. (2023). Generation of human iPSC-derived neurofibromaspheres for in vitro and in vivo uses. STAR Protocols. 4(2). 102198–102198. 1 indexed citations

Fernández‐Rodríguez, Juana, Yvonne Richaud‐Patín, Ernest Terribas, et al.. (2022). Modeling iPSC-derived human neurofibroma-like tumors in mice uncovers the heterogeneity of Schwann cells within plexiform neurofibromas. Cell Reports. 38(7). 110385–110385. 24 indexed citations

Fernández‐Rodríguez, Juana, Ernest Terribas, Cleofé Romagosa, et al.. (2021). Chromosomal translocations inactivating CDKN2A support a single path for malignant peripheral nerve sheath tumor initiation. Human Genetics. 140(8). 1241–1252. 12 indexed citations

Valle, Jesús Del, Elisabeth Castellanos, Lídia Feliubadaló, et al.. (2021). CNVfilteR: an R/Bioconductor package to identify false positives produced by germline NGS CNV detection tools. Bioinformatics. 37(22). 4227–4229. 2 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

10.

Terribas, Ernest, Marco A. Fernández, Juana Fernández‐Rodríguez, et al.. (2020). KIF11 and KIF15 mitotic kinesins are potential therapeutic vulnerabilities for malignant peripheral nerve sheath tumors. Neuro-Oncology Advances. 2(Supplement_1). i62–i74. 11 indexed citations

11.

Valle, Jesús Del, Elisabeth Castellanos, Lídia Feliubadaló, et al.. (2020). Evaluation of CNV detection tools for NGS panel data in genetic diagnostics. European Journal of Human Genetics. 28(12). 1645–1655. 76 indexed citations

12.

Castellanos, Elisabeth, Bernat Gel, Andreu Alibés, et al.. (2019). Mutational spectrum by phenotype: panel‐based NGS testing of patients with clinical suspicion of RASopathy and children with multiple café‐au‐lait macules. Clinical Genetics. 97(2). 264–275. 12 indexed citations

13.

Torrebadell, Montserrat, Marina Díaz‐Beyá, Susana G. Kalko, et al.. (2018). A 4-gene expression prognostic signature might guide post-remission therapy in patients with intermediate-risk cytogenetic acute myeloid leukemia. Leukemia & lymphoma. 59(10). 2394–2404. 16 indexed citations

14.

Gel, Bernat & Eduard Serra. (2017). karyoploteR: an R/Bioconductor package to plot customizable genomes displaying arbitrary data. Bioinformatics. 33(19). 3088–3090. 397 indexed citations breakdown →

15.

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

16.

Rahrmann, Eric P., Adrienne L. Watson, Vincent W. Keng, et al.. (2013). Forward genetic screen for malignant peripheral nerve sheath tumor formation identifies new genes and pathways driving tumorigenesis. Nature Genetics. 45(7). 756–766. 108 indexed citations

17.

Díaz, Tania, Alfons Navarro, Gerardo Ferrer, et al.. (2011). Lestaurtinib Inhibition of the JAK/STAT Signaling Pathway in Hodgkin Lymphoma Inhibits Proliferation and Induces Apoptosis. PLoS ONE. 6(4). e18856–e18856. 62 indexed citations

18.

Campayo, Marc, Núria Viñolas, Alfons Navarro, et al.. (2011). Single Nucleotide Polymorphisms in Tobacco Metabolism and DNA Repair Genes and Prognosis in Resected Non-Small-Cell Lung Cancer. Journal of Surgical Research. 167(1). e5–e12. 6 indexed citations

19.

Pons, Aina, Benet Nomdedeu, Alfons Navarro, et al.. (2009). Hematopoiesis-related microRNA expression in myelodysplastic syndromes. Leukemia & lymphoma. 50(11). 1854–1859. 79 indexed citations

20.

Monzó, Mariano, Isabel Moreno, Alfons Navarro, et al.. (2007). Single Nucleotide Polymorphisms in Nucleotide Excision Repair Genes XPA, XPD, XPG and ERCC1 in Advanced Colorectal Cancer Patients Treated with First-Line Oxaliplatin/Fluoropyrimidine. Oncology. 72(5-6). 364–370. 50 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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