J. Colomer

2.2k total citations
42 papers, 934 citations indexed

About

J. Colomer is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Neurology. According to data from OpenAlex, J. Colomer has authored 42 papers receiving a total of 934 indexed citations (citations by other indexed papers that have themselves been cited), including 19 papers in Molecular Biology, 12 papers in Cellular and Molecular Neuroscience and 12 papers in Neurology. Recurrent topics in J. Colomer's work include Hereditary Neurological Disorders (10 papers), Neurological diseases and metabolism (8 papers) and Myasthenia Gravis and Thymoma (8 papers). J. Colomer is often cited by papers focused on Hereditary Neurological Disorders (10 papers), Neurological diseases and metabolism (8 papers) and Myasthenia Gravis and Thymoma (8 papers). J. Colomer collaborates with scholars based in Spain, United Kingdom and Australia. J. Colomer's co-authors include A. Nascimento, Jon Andoni Urtizberea, Judith Melki, Suzie Lefebvre, Elena Bussaglia, Olivier Clermont, Arnold Münnich, Corinne Cruaud, Lydie Bürglen and Eduardo F. Tizzano and has published in prestigious journals such as Nature Genetics, Brain and Neurology.

In The Last Decade

J. Colomer

38 papers receiving 909 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
J. Colomer Spain 17 479 260 214 213 160 42 934
Lucía Galán Spain 14 442 0.9× 153 0.6× 103 0.5× 285 1.3× 71 0.4× 41 789
Michela Catteruccia Italy 16 602 1.3× 233 0.9× 130 0.6× 45 0.2× 73 0.5× 32 865
Susana Quijano-Roy France 18 961 2.0× 406 1.6× 175 0.8× 79 0.4× 173 1.1× 51 1.3k
Francesca Madia Italy 18 351 0.7× 81 0.3× 290 1.4× 438 2.1× 95 0.6× 62 1.0k
Nobuyoshi Fukuhara Japan 17 693 1.4× 48 0.2× 205 1.0× 139 0.7× 91 0.6× 35 1.1k
Luca Chiveri Italy 9 291 0.6× 112 0.4× 61 0.3× 199 0.9× 41 0.3× 13 540
Robyn Labrum United Kingdom 14 488 1.0× 44 0.2× 400 1.9× 175 0.8× 41 0.3× 21 772
Elena Abati Italy 15 405 0.8× 187 0.7× 164 0.8× 157 0.7× 18 0.1× 38 725
Meriel McEntagart United Kingdom 14 273 0.6× 66 0.3× 157 0.7× 49 0.2× 41 0.3× 24 576
Ko Sahashi Japan 16 535 1.1× 31 0.1× 247 1.2× 289 1.4× 67 0.4× 42 857

Countries citing papers authored by J. Colomer

Since Specialization
Citations

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

Fields of papers citing papers by J. Colomer

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of J. Colomer

This figure shows the co-authorship network connecting the top 25 collaborators of J. Colomer. A scholar is included among the top collaborators of J. 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 J. Colomer. J. Colomer 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.
Carrera‐García, Laura, Jordi Muchart, Juan José Lázaro, et al.. (2021). Pediatric SMA patients with complex spinal anatomy: Implementation and evaluation of a decision-tree algorithm for administration of nusinersen. European Journal of Paediatric Neurology. 31. 92–101. 10 indexed citations
2.
Benito, Daniel Natera‐de, Susana Boronat, J. Expósito, et al.. (2021). Copper Toxicity Associated With an ATP7A-Related Complex Phenotype. Pediatric Neurology. 119. 40–44. 6 indexed citations
3.
Benito, Daniel Natera‐de, C. Ortez, Cristina Jou, et al.. (2020). The Phenotype and Genotype of Congenital Myopathies Based on a Large Pediatric Cohort. Pediatric Neurology. 115. 50–65. 13 indexed citations
4.
Frongia, A., Daniel Natera‐de Benito, C. Ortez, et al.. (2019). Salbutamol tolerability and efficacy in patients with spinal muscular atrophy type II. Neuromuscular Disorders. 29(7). 517–524. 16 indexed citations
5.
Benito, Daniel Natera‐de, Nuria Muelas, A. Nascimento, et al.. (2016). Phenotypic heterogeneity in two large Roma families with a congenital myasthenic syndrome due to CHRNE 1267delG mutation. A long-term follow-up. Neuromuscular Disorders. 26(11). 789–795. 17 indexed citations
6.
O’Connor, Emily, Ana Töpf, Juliane S. Müller, et al.. (2016). Identification of mutations in theMYO9Agene in patients with congenital myasthenic syndrome. Brain. 139(8). 2143–2153. 37 indexed citations
7.
Ortez, C., et al.. (2014). Hypotonic male infant and MCT8 deficiency - a diagnosis to think about. BMC Pediatrics. 14(1). 252–252. 16 indexed citations
8.
Sevilla, Teresa, Dolores Martínez‐Rubio, Catalina Márquez-Vega, et al.. (2012). Genetics of the Charcot‐Marie‐Tooth disease in the Spanish Gypsy population: the hereditary motor and sensory neuropathy‐Russe in depth. Clinical Genetics. 83(6). 565–570. 25 indexed citations
9.
Navarro‐Sastre, Aleix, Frederic Tort, Judit García‐Villoria, et al.. (2012). Mitochondrial DNA depletion syndrome: New descriptions and the use of citrate synthase as a helpful tool to better characterise the patients. Molecular Genetics and Metabolism. 107(3). 409–415. 24 indexed citations
10.
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
11.
Chaouch, Amina, Juliane S. Müller, Velina Guergueltcheva, et al.. (2011). A retrospective clinical study of the treatment of slow-channel congenital myasthenic syndrome. Journal of Neurology. 259(3). 474–481. 50 indexed citations
12.
Cabrerizo, María, Núria Rabella, Núria Torner, et al.. (2011). Molecular identification of an enterovirus 99 strain in Spain. Archives of Virology. 157(3). 551–554. 6 indexed citations
13.
Martí, Ramón, A. Nascimento, J. Colomer, et al.. (2010). Hearing Loss in a Patient With the Myopathic Form of Mitochondrial DNA Depletion Syndrome and a Novel Mutation in the TK2 Gene. Pediatric Research. 68(2). 151–154. 12 indexed citations
14.
Majumdar, Anirban, Pilar Póo, J. Colomer, et al.. (2008). Syndrome of fixed dystonia in adolescents – Short term outcome in 4 cases. European Journal of Paediatric Neurology. 13(5). 466–472. 9 indexed citations
15.
Colomer, J., Juliane Müller, A. Nascimento, et al.. (2006). Long-term improvement of slow-channel congenital myasthenic syndrome with fluoxetine. Neuromuscular Disorders. 16(5). 329–333. 30 indexed citations
16.
Kalaydjieva, Luba, Hanns Lochmüller, Ivailo Tournev, et al.. (2004). 125th ENMC International Workshop: Neuromuscular Disorders in the Roma (Gypsy) Population, 23–25 April 2004, Naarden, The Netherlands. Neuromuscular Disorders. 15(1). 65–71. 22 indexed citations
17.
Hunter, Michael, Rafaëlle Bernard, Elizabeth Freitas, et al.. (2003). Mutation screening of the N-myc downstream-regulated gene 1 (NDRG1) in patients with Charcot-Marie-Tooth Disease. Human Mutation. 22(2). 129–135. 41 indexed citations
18.
Fusco, Carlo, Josep Valls‐Solé, C. Iturriaga, J. Colomer, & E Fernández-Álvarez. (2003). Electrophysiological approach to the study of essential tremor in children and adolescents. Developmental Medicine & Child Neurology. 45(9). 624–7. 9 indexed citations
19.
Bussaglia, Elena, Olivier Clermont, Eduardo F. Tizzano, et al.. (1995). A frame–shift deletion in the survival motor neuron gene in Spanish spinal muscular atrophy patients. Nature Genetics. 11(3). 335–337. 184 indexed citations
20.
Fernández‐Espejo, Emilio, et al.. (1985). Peripheral Neuropathy in Meningococcal Septicemia. European Neurology. 24(5). 310–313. 2 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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