María Josep Coll

1.5k total citations
37 papers, 1.1k citations indexed

About

María Josep Coll is a scholar working on Physiology, Molecular Biology and Organic Chemistry. According to data from OpenAlex, María Josep Coll has authored 37 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 30 papers in Physiology, 13 papers in Molecular Biology and 12 papers in Organic Chemistry. Recurrent topics in María Josep Coll's work include Lysosomal Storage Disorders Research (30 papers), Carbohydrate Chemistry and Synthesis (12 papers) and Trypanosoma species research and implications (11 papers). María Josep Coll is often cited by papers focused on Lysosomal Storage Disorders Research (30 papers), Carbohydrate Chemistry and Synthesis (12 papers) and Trypanosoma species research and implications (11 papers). María Josep Coll collaborates with scholars based in Spain, Greece and France. María Josep Coll's co-authors include Amparo Chabás, Laura Gort, Daniel Grinberg, Lluı̈sa Vilageliu, M. Pineda, Judit Macías‐Vidal, Antònia Ribes, M. T. Vanier, C. Iturriaga and Oriol Bachs and has published in prestigious journals such as Journal of Biological Chemistry, Journal of Lipid Research and Journal of the Neurological Sciences.

In The Last Decade

María Josep Coll

37 papers receiving 1.0k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
María Josep Coll Spain 19 703 370 228 218 180 37 1.1k
Müge Güçsavaş‐Çalıkoğlu United States 7 797 1.1× 232 0.6× 415 1.8× 142 0.7× 277 1.5× 10 1.1k
Ana Cristina Puga United States 17 1.1k 1.5× 379 1.0× 422 1.9× 322 1.5× 200 1.1× 45 1.3k
I Maire France 17 785 1.1× 341 0.9× 279 1.2× 228 1.0× 287 1.6× 85 1.2k
Agnieszka Jurecka Poland 21 649 0.9× 405 1.1× 446 2.0× 94 0.4× 293 1.6× 63 1.2k
Vũ Chí Dũng Vietnam 18 729 1.0× 298 0.8× 319 1.4× 236 1.1× 222 1.2× 38 1.1k
Jan Lukáš Germany 19 904 1.3× 435 1.2× 326 1.4× 323 1.5× 131 0.7× 56 1.3k
Jakub Sikora Czechia 20 487 0.7× 507 1.4× 182 0.8× 137 0.6× 150 0.8× 48 1.1k
Laura Gort Spain 24 758 1.1× 629 1.7× 221 1.0× 275 1.3× 226 1.3× 67 1.3k
Clare Beesley United Kingdom 17 607 0.9× 288 0.8× 262 1.1× 240 1.1× 241 1.3× 29 980
Giulia Polo Italy 17 589 0.8× 248 0.7× 200 0.9× 165 0.8× 132 0.7× 29 871

Countries citing papers authored by María Josep Coll

Since Specialization
Citations

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

Fields of papers citing papers by María Josep Coll

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by María Josep Coll. 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 María Josep Coll. The network helps show where María Josep Coll may publish in the future.

Co-authorship network of co-authors of María Josep Coll

This figure shows the co-authorship network connecting the top 25 collaborators of María Josep Coll. A scholar is included among the top collaborators of María Josep Coll 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 María Josep Coll. María Josep Coll 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.
Sisinni, Luisa, Mercédes Pineda, María Josep Coll, et al.. (2018). Haematopoietic stem cell transplantation for mucopolysaccharidosis type VII: A case report. Pediatric Transplantation. 22(7). e13278–e13278. 16 indexed citations
2.
Pineda, M., et al.. (2016). Clinical Evolution After Enzyme Replacement Therapy in Twins with the Severe Form of Maroteaux–Lamy Syndrome. JIMD Reports. 30. 7–14. 2 indexed citations
3.
Vanier, Marie T., Paul Gissen, Peter Bauer, et al.. (2016). Diagnostic tests for Niemann-Pick disease type C (NP-C): A critical review. Molecular Genetics and Metabolism. 118(4). 244–254. 88 indexed citations
4.
Matalonga, Leslie, Ángela Arias, Frederic Tort, et al.. (2015). Effect of Readthrough Treatment in Fibroblasts of Patients Affected by Lysosomal Diseases Caused by Premature Termination Codons. Neurotherapeutics. 12(4). 874–886. 18 indexed citations
5.
Couce, María L., Judit Macías‐Vidal, Daisy Castiñeiras, et al.. (2014). The early detection of Salla disease through second-tier tests in newborn screening: How to face incidental findings. European Journal of Medical Genetics. 57(9). 527–531. 4 indexed citations
6.
Tort, Frederic, María Teresa García‐Silva, Aleix Navarro‐Sastre, et al.. (2013). Exome sequencing identifies a new mutation in SERAC1 in a patient with 3-methylglutaconic aciduria. Molecular Genetics and Metabolism. 110(1-2). 73–77. 25 indexed citations
7.
Rodríguez‐Pascau, Laura, Claudio Toma, Judit Macías‐Vidal, et al.. (2012). Characterisation of two deletions involving NPC1 and flanking genes in Niemann–Pick Type C disease patients. Molecular Genetics and Metabolism. 107(4). 716–720. 14 indexed citations
8.
Rodríguez‐Pascau, Laura, María Josep Coll, Josefina Casas, Lluı̈sa Vilageliu, & Daniel Grinberg. (2011). Generation of a Human Neuronal Stable Cell Model for Niemann-Pick C Disease by RNA Interference. JIMD Reports. 4. 29–37. 7 indexed citations
9.
Aragón, Ana Martı́nez de, et al.. (2010). Enfermedad de Niemann-Pick tipo C: desde una colestasis neonatal hacia un deterioro neurológico. Variabilidad fenotípica. Anales de Pediatría. 73(5). 257–263. 3 indexed citations
10.
Pineda, M., Mar O’Callaghan, Marina Vilaseca, et al.. (2009). Clinical experience with miglustat therapy in pediatric patients with Niemann–Pick disease type C: A case series. Molecular Genetics and Metabolism. 99(4). 358–366. 93 indexed citations
11.
Macías‐Vidal, Judit, et al.. (2009). Nonsense-mediated mRNA decay process in nine alleles of Niemann-Pick type C patients from Spain. Molecular Genetics and Metabolism. 97(1). 60–64. 21 indexed citations
12.
Gort, Laura, María Josep Coll, & Amparo Chabás. (2007). Glycogen storage disease type II in Spanish patients: High frequency of c.1076-1G>C mutation. Molecular Genetics and Metabolism. 92(1-2). 183–187. 41 indexed citations
13.
Garrido, Elena, Amparo Chabás, María Josep Coll, et al.. (2007). Identification of the molecular defects in Spanish and Argentinian mucopolysaccharidosis VI (Maroteaux–Lamy syndrome) patients, including 9 novel mutations. Molecular Genetics and Metabolism. 92(1-2). 122–130. 29 indexed citations
14.
Santamaría, Raül, Amparo Chabás, María Josep Coll, et al.. (2006). Twenty-one novel mutations in the GLB1 gene identified in a large group of GM1-gangliosidosis and Morquio B patients: possible common origin for the prevalent p.R59H mutation among gypsies. Human Mutation. 27(10). 1060–1060. 52 indexed citations
15.
Coll, María Josep, et al.. (2001). Allelic heterogeneity in Spanish patients with Sanfilippo disease type B. Identification of eight new mutations.. Journal of Inherited Metabolic Disease. 24(1). 83–84. 14 indexed citations
16.
Gort, Laura, Amparo Chabás, & María Josep Coll. (1998). Analysis of five mutations in 20 mucopolysaccharidosis type I patients: High prevalence of the W402X mutation. Human Mutation. 11(4). 332–333. 21 indexed citations
17.
Gort, Laura, Amparo Chabás, & María Josep Coll. (1998). Hunter disease in the Spanish population: Molecular analysis in 31 families. Journal of Inherited Metabolic Disease. 21(6). 655–661. 34 indexed citations
18.
Busquets, C., María Josep Coll, E. Christensen, et al.. (1998). Feasibility of molecular prenatal diagnosis of glutaric aciduria type I in chorionic villi. Journal of Inherited Metabolic Disease. 21(3). 243–246. 5 indexed citations
19.
Pintos‐Morell, Guillem, et al.. (1995). Molybdenum cofactor deficiency associated with Dandy‐Walker malformation. Journal of Inherited Metabolic Disease. 18(1). 86–87. 8 indexed citations
20.
Pujol, María Jesús, et al.. (1988). New synthesis of cyclic AMP‐dependent protein kinases during liver regeneration. Cell Biochemistry and Function. 6(3). 203–208. 1 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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