Jaume Colomer

1.4k total citations
19 papers, 422 citations indexed

About

Jaume Colomer is a scholar working on Molecular Biology, Cell Biology and Cellular and Molecular Neuroscience. According to data from OpenAlex, Jaume Colomer has authored 19 papers receiving a total of 422 indexed citations (citations by other indexed papers that have themselves been cited), including 18 papers in Molecular Biology, 7 papers in Cell Biology and 5 papers in Cellular and Molecular Neuroscience. Recurrent topics in Jaume Colomer's work include Muscle Physiology and Disorders (13 papers), Mitochondrial Function and Pathology (7 papers) and Metabolism and Genetic Disorders (4 papers). Jaume Colomer is often cited by papers focused on Muscle Physiology and Disorders (13 papers), Mitochondrial Function and Pathology (7 papers) and Metabolism and Genetic Disorders (4 papers). Jaume Colomer collaborates with scholars based in Spain, United Kingdom and Germany. Jaume Colomer's co-authors include A. Nascimento, Adriana Lasa, C. Jimenez‐Mallebrera, Michel Fardeau, Keith Davison, J. Beckmann, Isabelle Richard, Louise V.B. Anderson, F.M.S. Tomé and Christoph Hübner and has published in prestigious journals such as PLoS ONE, Scientific Reports and American Journal Of Pathology.

In The Last Decade

Jaume Colomer

16 papers receiving 414 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Jaume Colomer Spain 11 356 126 102 73 62 19 422
Daniel Beltrán Valero de Bernabé United States 6 469 1.3× 85 0.7× 84 0.8× 93 1.3× 41 0.7× 6 556
Lenka Mrázová Czechia 12 181 0.5× 81 0.6× 45 0.4× 93 1.3× 56 0.9× 33 308
Ademuyiwa S. Aromolaran United States 6 458 1.3× 153 1.2× 111 1.1× 38 0.5× 63 1.0× 15 591
Simone Spinozzi United States 9 213 0.6× 39 0.3× 50 0.5× 46 0.6× 118 1.9× 12 314
Ulrike Grieben Germany 10 239 0.7× 19 0.2× 65 0.6× 48 0.7× 54 0.9× 14 348
Uwe Lenk Germany 9 372 1.0× 132 1.0× 48 0.5× 82 1.1× 47 0.8× 12 448
Hannah E. Steele United Kingdom 9 180 0.5× 51 0.4× 77 0.8× 32 0.4× 14 0.2× 14 275
Robert D. Guber United States 6 189 0.5× 71 0.6× 46 0.5× 26 0.4× 27 0.4× 8 306
Jonathan R. Davey Australia 10 337 0.9× 151 1.2× 33 0.3× 135 1.8× 47 0.8× 13 465
Karina Formoso Argentina 12 213 0.6× 62 0.5× 46 0.5× 33 0.5× 36 0.6× 18 345

Countries citing papers authored by Jaume Colomer

Since Specialization
Citations

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

Fields of papers citing papers by Jaume Colomer

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Jaume Colomer

This figure shows the co-authorship network connecting the top 25 collaborators of Jaume Colomer. A scholar is included among the top collaborators of Jaume Colomer 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 Jaume Colomer. Jaume Colomer 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
1.
Milev, Miroslav P., Daniela Stanga, Anne Schänzer, et al.. (2019). Characterization of three TRAPPC11 variants suggests a critical role for the extreme carboxy terminus of the protein. Scientific Reports. 9(1). 14036–14036. 9 indexed citations
2.
Benito, Daniel Natera‐de, C. Ortez, A. Nascimento, et al.. (2017). Clinical and genetic characterization of collagen VI-related myopathies: difficulties in phenotypic characterization in the first years of life. Neuromuscular Disorders. 27. S105–S105.
3.
Benito, Daniel Natera‐de, A. Nascimento, Angela Abicht, et al.. (2016). KLHL40-related nemaline myopathy with a sustained, positive response to treatment with acetylcholinesterase inhibitors. Journal of Neurology. 263(3). 517–523. 25 indexed citations
4.
Ortez, C., Cristina Jou, Josep M. Campistol, et al.. (2016). Exercise intolerance and myalgia: First clinical sign of a primary alpha-sarcoglycanopathy. Neuromuscular Disorders. 26. S92–S92.
5.
Paco, Sonia, Cristina Jou, Montse Puigdelloses, et al.. (2015). Transcriptome Analysis of Ullrich Congenital Muscular Dystrophy Fibroblasts Reveals a Disease Extracellular Matrix Signature and Key Molecular Regulators. PLoS ONE. 10(12). e0145107–e0145107. 21 indexed citations
6.
Paco, Sonia, Susana G. Kalko, Cristina Jou, et al.. (2013). Gene Expression Profiling Identifies Molecular Pathways Associated with Collagen VI Deficiency and Provides Novel Therapeutic Targets. PLoS ONE. 8(10). e77430–e77430. 12 indexed citations
7.
Juan‐Mateu, Jonàs, Lidia González‐Quereda, Maria José Rodríguez, et al.. (2013). Interplay between DMD Point Mutations and Splicing Signals in Dystrophinopathy Phenotypes. PLoS ONE. 8(3). e59916–e59916. 39 indexed citations
8.
Nascimento, A., Cristina Jou, C. Ortez, et al.. (2013). P.15.11 Megaconial congenital muscular dystrophy in two children with mutations in the CHKB Gene. Neuromuscular Disorders. 23(9-10). 822–822. 1 indexed citations
9.
Jimenez‐Mallebrera, C., Xavier Palomer, Valeria De Nigris, et al.. (2012). PGC-1α Induces Mitochondrial and Myokine Transcriptional Programs and Lipid Droplet and Glycogen Accumulation in Cultured Human Skeletal Muscle Cells. PLoS ONE. 7(1). e29985–e29985. 48 indexed citations
10.
Paco, Sonia, Isidró Ferrer, Cristina Jou, et al.. (2012). Muscle Fiber Atrophy and Regeneration Coexist in Collagen VI-Deficient Human Muscle: Role of Calpain-3 and Nuclear Factor-κB Signaling. Journal of Neuropathology & Experimental Neurology. 71(10). 894–906. 21 indexed citations
11.
Raymond, Frédéric, Sylviane Métairon, Martin Kussmann, et al.. (2010). Comparative gene expression profiling between human cultured myotubes and skeletal muscle tissue. BMC Genomics. 11(1). 125–125. 25 indexed citations
12.
13.
Briones, Paz, Marta Vilaseca, M.T. García‐Silva, et al.. (2001). Congenital disorders of glycosylation (CDG) may be underdiagnosed when mimicking mitochondrial disease. European Journal of Paediatric Neurology. 5(3). 127–131. 39 indexed citations
14.
Lasa, Adriana, Fédérica Piccolo, Marc Jeanpierre, et al.. (1998). Severe limb girdle muscular dystrophy in Spanish gypsies: further evidence for a founder mutation in the γ-sarcoglycan gene. European Journal of Human Genetics. 6(4). 396–399. 15 indexed citations
15.
Artuch, Rafael, María Antònia Vilaseca, Jaume Colomer, et al.. (1998). Multiple Endocrine Involvement in Two Pediatric Patients with Kearns-Sayre Syndrome. Hormone Research in Paediatrics. 50(2). 99–104. 36 indexed citations
16.
Anderson, Louise V.B., Keith Davison, Jennifer A. Moss, et al.. (1998). Characterization of Monoclonal Antibodies to Calpain 3 and Protein Expression in Muscle from Patients with Limb-Girdle Muscular Dystrophy Type 2A. American Journal Of Pathology. 153(4). 1169–1179. 122 indexed citations
17.
Artuch, Rafael, Manuel Pineda, Marta Vilaseca, et al.. (1998). [Respiratory chain and pyruvate metabolism deficiencies in pediatric patients: evaluation of biochemical tests for selective screening].. PubMed. 26(149). 38–42. 4 indexed citations
18.
Lasa, Adriana, P. Gallano, Jaume Colomer, & Montserrat Baiget. (1995). A novel insertional mutation of a single base in exon 12 of the dystrophin gene. Clinical Genetics. 48(3). 128–130. 2 indexed citations
19.
Colomer, Jaume, P. Gallano, Eduardo F. Tizzano, M. Baiget, & L. V. B. Nicholson. (1994). Severe mental retardation in a young boy with an in-frame deletion in the dystrophin gene. European Journal of Pediatrics. 153(7). 492–494. 3 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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