Eduardo Calpena

982 total citations
21 papers, 272 citations indexed

About

Eduardo Calpena is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Genetics. According to data from OpenAlex, Eduardo Calpena has authored 21 papers receiving a total of 272 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Molecular Biology, 8 papers in Cellular and Molecular Neuroscience and 8 papers in Genetics. Recurrent topics in Eduardo Calpena's work include Hereditary Neurological Disorders (7 papers), Craniofacial Disorders and Treatments (7 papers) and Genetic Neurodegenerative Diseases (4 papers). Eduardo Calpena is often cited by papers focused on Hereditary Neurological Disorders (7 papers), Craniofacial Disorders and Treatments (7 papers) and Genetic Neurodegenerative Diseases (4 papers). Eduardo Calpena collaborates with scholars based in Spain, United Kingdom and United States. Eduardo Calpena's co-authors include Carmen Espinós, Francesc Palau, Vincenzo Lupo, David Pla‐Martín, Teresa Sevilla, Máximo Ibo Galindo, Rafael Sivera, Dolores Martínez‐Rubio, Paloma González‐Sánchez and Eloy Rivas and has published in prestigious journals such as Bioinformatics, PLoS ONE and Scientific Reports.

In The Last Decade

Eduardo Calpena

21 papers receiving 271 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Eduardo Calpena Spain 11 153 114 42 39 29 21 272
Hannah E. Steele United Kingdom 9 180 1.2× 77 0.7× 30 0.7× 51 1.3× 33 1.1× 14 275
Alexander P. Drew Australia 10 152 1.0× 148 1.3× 31 0.7× 45 1.2× 84 2.9× 15 303
Marie‐France Rioux Canada 6 140 0.9× 117 1.0× 38 0.9× 20 0.5× 48 1.7× 8 270
Esther Gill Germany 10 151 1.0× 62 0.5× 50 1.2× 23 0.6× 29 1.0× 13 224
Monia Hammer United States 8 111 0.7× 71 0.6× 30 0.7× 42 1.1× 43 1.5× 12 213
Manuela Pendziwiat Germany 12 204 1.3× 70 0.6× 103 2.5× 73 1.9× 18 0.6× 21 379
Claire Guissart France 12 174 1.1× 76 0.7× 73 1.7× 17 0.4× 35 1.2× 22 301
Adeline Ngoh United Kingdom 8 136 0.9× 69 0.6× 175 4.2× 15 0.4× 41 1.4× 15 367
Anna Walczak Poland 11 174 1.1× 79 0.7× 68 1.6× 50 1.3× 30 1.0× 19 271
Adam R. Fenton United States 5 183 1.2× 37 0.3× 16 0.4× 85 2.2× 16 0.6× 11 276

Countries citing papers authored by Eduardo Calpena

Since Specialization
Citations

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

Fields of papers citing papers by Eduardo Calpena

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Eduardo Calpena

This figure shows the co-authorship network connecting the top 25 collaborators of Eduardo Calpena. A scholar is included among the top collaborators of Eduardo Calpena 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 Eduardo Calpena. Eduardo Calpena 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.
Calpena, Eduardo, et al.. (2023). Review of Recurrently Mutated Genes in Craniosynostosis Supports Expansion of Diagnostic Gene Panels. Genes. 14(3). 615–615. 3 indexed citations
2.
Díaz, Francisca, Stephen R.F. Twigg, Eduardo Calpena, et al.. (2023). Case report: A third variant in the 5′ UTR of TWIST1 creates a novel upstream translation initiation site in a child with Saethre-Chotzen syndrome. Frontiers in Genetics. 13. 1089417–1089417. 3 indexed citations
3.
Calpena, Eduardo, et al.. (2022). Craniosynostosis, inner ear, and renal anomalies in a child with complete loss of SPRY1 (sprouty homolog 1) function. Journal of Medical Genetics. 60(7). 712–716. 2 indexed citations
4.
Calpena, Eduardo, Simon J. McGowan, Fiona Blanco‐Kelly, et al.. (2021). Dissection of contiguous gene effects for deletions around ERF on chromosome 19. Human Mutation. 42(7). 811–817. 2 indexed citations
5.
Calpena, Eduardo, Maud Wurmser, Simon J. McGowan, et al.. (2021). Unexpected role of SIX1 variants in craniosynostosis: expanding the phenotype of SIX1-related disorders. Journal of Medical Genetics. 59(2). 165–169. 5 indexed citations
6.
Goos, Jacqueline A.C., W. Vogel, Hana Mlčochová, et al.. (2019). A de novo substitution in BCL11B leads to loss of interaction with transcriptional complexes and craniosynostosis. Human Molecular Genetics. 28(15). 2501–2513. 22 indexed citations
7.
Koelling, Nils, Marie Bernkopf, Eduardo Calpena, et al.. (2019). amplimap: a versatile tool to process and analyze targeted NGS data. Bioinformatics. 35(24). 5349–5350. 4 indexed citations
8.
Zhou, Yan, Nils Koelling, Aimée L Fenwick, et al.. (2018). Disruption ofTWIST1translation by 5′ UTR variants in Saethre-Chotzen syndrome. Human Mutation. 39(10). 1360–1365. 13 indexed citations
9.
Calpena, Eduardo, Víctor López Del Amo, Beatriz Llamusí, et al.. (2017). The Drosophila junctophilin gene is functionally equivalent to its four mammalian counterparts and is a modifier of a Huntingtin poly-Q expansion and the Notch pathway. Disease Models & Mechanisms. 11(1). 14 indexed citations
10.
González‐Sánchez, Paloma, David Pla‐Martín, Carlos B. Rueda, et al.. (2017). CMT-linked loss-of-function mutations in GDAP1 impair store-operated Ca2+ entry-stimulated respiration. Scientific Reports. 7(1). 31 indexed citations
11.
Calpena, Eduardo, Francesc Palau, Carmen Espinós, & Máximo Ibo Galindo. (2015). Evolutionary History of the Smyd Gene Family in Metazoans: A Framework to Identify the Orthologs of Human Smyd Genes in Drosophila and Other Animal Species. PLoS ONE. 10(7). e0134106–e0134106. 16 indexed citations
12.
Sevilla, Teresa, Rafael Sivera, Dolores Martínez‐Rubio, et al.. (2015). The EGR2 gene is involved in axonal Charcot−Marie−Tooth disease. European Journal of Neurology. 22(12). 1548–1555. 22 indexed citations
13.
Calpena, Eduardo, Sufin Yap, Akhilesh Kumar, et al.. (2014). New insights into the genetics of 5-oxoprolinase deficiency and further evidence that it is a benign biochemical condition. European Journal of Pediatrics. 174(3). 407–411. 7 indexed citations
14.
Calpena, Eduardo, Dolores Martínez‐Rubio, Javier Arpa, et al.. (2014). A novel locus for a hereditary recurrent neuropathy on chromosome 21q21. Neuromuscular Disorders. 24(8). 660–665. 2 indexed citations
15.
Pla‐Martín, David, Eduardo Calpena, Vincenzo Lupo, et al.. (2014). Junctophilin-1 is a modifier gene of GDAP1-related Charcot–Marie–Tooth disease. Human Molecular Genetics. 24(1). 213–229. 38 indexed citations
16.
Curto, M.-Ángeles, Mohammad Reza Sharifmoghadam, Eduardo Calpena, et al.. (2014). Membrane Organization and Cell Fusion During Mating in Fission Yeast Requires Multipass Membrane Protein Prm1. Genetics. 196(4). 1059–1076. 21 indexed citations
17.
Lupo, Vincenzo, Eduardo Calpena, Luca Bartesaghi, et al.. (2013). Sh3tc2 deficiency affects neuregulin‐1/ErbB signaling. Glia. 61(7). 1041–1051. 36 indexed citations
18.
Tondo, Mireia, Eduardo Calpena, Paloma Sanz, et al.. (2013). Clinical, biochemical, molecular and therapeutic aspects of 2 new cases of 2-aminoadipic semialdehyde synthase deficiency. Molecular Genetics and Metabolism. 110(3). 231–236. 13 indexed citations
19.
Calpena, Eduardo, Mercedes Casado, Dolores Martínez‐Rubio, et al.. (2012). 5-Oxoprolinuria in Heterozygous Patients for 5-Oxoprolinase (OPLAH) Missense Changes. JIMD Reports. 7. 123–128. 13 indexed citations
20.
Espinós, Carmen, Eduardo Calpena, Dolores Martínez‐Rubio, & Vincenzo Lupo. (2012). Autosomal Recessive Charcot-Marie-Tooth Neuropathy. Advances in experimental medicine and biology. 724. 61–75. 4 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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