Belén Hurlé

956 total citations
19 papers, 728 citations indexed

About

Belén Hurlé is a scholar working on Molecular Biology, Sensory Systems and Genetics. According to data from OpenAlex, Belén Hurlé has authored 19 papers receiving a total of 728 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Molecular Biology, 5 papers in Sensory Systems and 5 papers in Genetics. Recurrent topics in Belén Hurlé's work include Hearing, Cochlea, Tinnitus, Genetics (5 papers), BRCA gene mutations in cancer (2 papers) and Genetics, Bioinformatics, and Biomedical Research (2 papers). Belén Hurlé is often cited by papers focused on Hearing, Cochlea, Tinnitus, Genetics (5 papers), BRCA gene mutations in cancer (2 papers) and Genetics, Bioinformatics, and Biomedical Research (2 papers). Belén Hurlé collaborates with scholars based in United States, Spain and Portugal. Belén Hurlé's co-authors include Eric D. Green, David M. Ornitz, Willie J. Swanson, Warren W. Kretzschmar, Aida M. Andrés, Andrew G. Clark, Inna Hughes, Carlos D. Bustamante, Jennifer L. Cannons and Sofı́a Ramos and has published in prestigious journals such as Journal of Biological Chemistry, FEBS Letters and Genome Research.

In The Last Decade

Belén Hurlé

19 papers receiving 723 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Belén Hurlé United States 12 261 170 120 113 75 19 728
Timothy Erickson United States 17 454 1.7× 234 1.4× 217 1.8× 208 1.8× 23 0.3× 26 1.1k
Stéphane Dréano France 12 159 0.6× 157 0.9× 60 0.5× 74 0.7× 53 0.7× 27 528
A Eisenberg United States 11 765 2.9× 513 3.0× 79 0.7× 91 0.8× 32 0.4× 23 1.6k
Richard Guyon France 12 329 1.3× 402 2.4× 50 0.4× 63 0.6× 50 0.7× 19 725
Carsten M. Pusch Germany 25 818 3.1× 374 2.2× 63 0.5× 243 2.2× 54 0.7× 76 1.7k
Yashoda Sharma United States 10 267 1.0× 159 0.9× 140 1.2× 53 0.5× 24 0.3× 17 735
R. Leiser Germany 24 489 1.9× 330 1.9× 277 2.3× 41 0.4× 50 0.7× 64 1.7k
Masaaki Hazama Japan 12 350 1.3× 68 0.4× 194 1.6× 59 0.5× 61 0.8× 21 848
Sofie Thys Belgium 17 313 1.2× 54 0.3× 69 0.6× 109 1.0× 27 0.4× 33 768
Becky Hoxter United States 12 290 1.1× 56 0.3× 36 0.3× 144 1.3× 34 0.5× 14 736

Countries citing papers authored by Belén Hurlé

Since Specialization
Citations

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

Fields of papers citing papers by Belén Hurlé

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Belén Hurlé

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

All Works

19 of 19 papers shown
2.
Hurlé, Belén, Toby Citrin, Jean Jenkins, et al.. (2013). What does it mean to be genomically literate?: National Human Genome Research Institute Meeting Report. Genetics in Medicine. 15(8). 658–663. 91 indexed citations
3.
Seixas, Susana, Aida M. Andrés, Warren W. Kretzschmar, et al.. (2013). Reproduction and Immunity-Driven Natural Selection in the Human WFDC Locus. Molecular Biology and Evolution. 30(4). 938–950. 14 indexed citations
4.
Hurlé, Belén, Aida M. Andrés, Warren W. Kretzschmar, et al.. (2013). Sequence Diversity of Pan troglodytes Subspecies and the Impact of WFDC6 Selective Constraints in Reproductive Immunity. Genome Biology and Evolution. 5(12). 2512–2523. 1 indexed citations
5.
Hurlé, Belén, Tomàs Marquès‐Bonet, Francesca Antonacci, et al.. (2011). Lineage-specific evolution of the vertebrate Otopetringene family revealed by comparative genomic analyses. BMC Evolutionary Biology. 11(1). 23–23. 16 indexed citations
6.
Hurlé, Belén, et al.. (2011). Differing Evolutionary Histories of WFDC8 (Short-Term Balancing) in Europeans and SPINT4 (Incomplete Selective Sweep) in Africans. Molecular Biology and Evolution. 28(10). 2811–2822. 6 indexed citations
7.
Andrés, Aida M., Megan Y. Dennis, Warren W. Kretzschmar, et al.. (2010). Balancing Selection Maintains a Form of ERAP2 that Undergoes Nonsense-Mediated Decay and Affects Antigen Presentation. PLoS Genetics. 6(10). e1001157–e1001157. 186 indexed citations
8.
Hughes, Inna, Jonathan Binkley, Belén Hurlé, et al.. (2008). Identification of the Otopetrin Domain, a conserved domain in vertebrate otopetrins and invertebrate otopetrin-like family members. BMC Evolutionary Biology. 8(1). 41–41. 31 indexed citations
9.
Hurlé, Belén, et al.. (2007). Comparative sequence analyses reveal rapid and divergent evolutionary changes of theWFDClocus in the primate lineage. Genome Research. 17(3). 276–286. 58 indexed citations
10.
Hughes, Inna, Brian Blasiole, David Huss, et al.. (2004). Otopetrin 1 is required for otolith formation in the zebrafish Danio rerio. Developmental Biology. 276(2). 391–402. 98 indexed citations
11.
Pompéia, Celine, Belén Hurlé, Inna A. Belyantseva, et al.. (2004). Gene Expression Profile of the Mouse Organ of Corti at the Onset of Hearing. Genomics. 83(6). 1000–1011. 14 indexed citations
12.
Hurlé, Belén. (2003). Non-syndromic vestibular disorder with otoconial agenesis in tilted/mergulhador mice caused by mutations in otopetrin 1. Human Molecular Genetics. 12(7). 777–789. 105 indexed citations
13.
Hurlé, Belén, Keara Lane, Jane P. Kenney‐Hunt, et al.. (2001). Physical Mapping of the Mouse Tilted Locus Identifies an Association between Human Deafness Loci DFNA6/14 and Vestibular System Development. Genomics. 77(3). 189–199. 15 indexed citations
14.
Tarantino, Lisa M., Leonard Feiner, Alireza Alavi, et al.. (2000). A High-Resolution Radiation Hybrid Map of the Proximal Portion of Mouse Chromosome 5. Genomics. 66(1). 55–64. 7 indexed citations
15.
Hurlé, Belén, et al.. (1999). High-resolution mapping of tlt, a mouse mutant lacking otoconia. Mammalian Genome. 10(6). 544–548. 11 indexed citations
16.
Hurlé, Belén, Fernando Segade, René Rodrı́guez, Sofı́a Ramos, & Pedro S. Lazo. (1998). The Mouse Tumor Necrosis Factor Receptor 2 Gene: Genomic Structure and Characterization of the Two Transcripts. Genomics. 52(1). 79–89. 9 indexed citations
17.
Segade, Fernando, Belén Hurlé, Estefanı́a Claudio, Sofı́a Ramos, & Pedro S. Lazo. (1996). Identification of an Additional Member of the Cytochrome c Oxidase Subunit VIIa Family of Proteins. Journal of Biological Chemistry. 271(21). 12343–12349. 22 indexed citations
18.
Segade, Fernando, Belén Hurlé, Estefanı́a Claudio, Sofı́a Ramos, & Pedro S. Lazo. (1996). Molecular cloning of a mouse homologue for the Drosophila splicing regulator Tra2. FEBS Letters. 387(2-3). 152–156. 29 indexed citations
19.
Segade, Fernando, Estefanı́a Claudio, Belén Hurlé, Sofı́a Ramos, & Pedro S. Lazo. (1995). Differential regulation of the murine ribosomal protein L26 gene in macrophage activation. Life Sciences. 58(4). 277–285. 11 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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