M. Pineda

788 total citations
26 papers, 533 citations indexed

About

M. Pineda is a scholar working on Molecular Biology, Clinical Biochemistry and Physiology. According to data from OpenAlex, M. Pineda has authored 26 papers receiving a total of 533 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Molecular Biology, 10 papers in Clinical Biochemistry and 6 papers in Physiology. Recurrent topics in M. Pineda's work include Metabolism and Genetic Disorders (10 papers), Mitochondrial Function and Pathology (5 papers) and Genetics and Neurodevelopmental Disorders (5 papers). M. Pineda is often cited by papers focused on Metabolism and Genetic Disorders (10 papers), Mitochondrial Function and Pathology (5 papers) and Genetics and Neurodevelopmental Disorders (5 papers). M. Pineda collaborates with scholars based in Spain, Switzerland and France. M. Pineda's co-authors include Rafael Artuch, Eugènia Monrós, Catrina Colomé, Aída Ormazábal, Àngels García‐Cazorla, Blaise C. Martin, P. Briones, M.T. García‐Silva, Josep M. Campistol and Belén Pérez‐Dueñas and has published in prestigious journals such as Neurology, Archives of Disease in Childhood and Developmental Medicine & Child Neurology.

In The Last Decade

M. Pineda

26 papers receiving 517 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
M. Pineda Spain 13 285 127 118 111 67 26 533
Léna Damaj France 11 186 0.7× 108 0.9× 109 0.9× 78 0.7× 71 1.1× 19 479
Mar O’Callaghan Spain 12 273 1.0× 86 0.7× 98 0.8× 80 0.7× 125 1.9× 26 489
Venkateswaran Ramesh United Kingdom 13 427 1.5× 126 1.0× 146 1.2× 251 2.3× 38 0.6× 20 846
Johann Penzien Germany 14 268 0.9× 184 1.4× 72 0.6× 106 1.0× 76 1.1× 17 627
Lucia Abela Switzerland 13 259 0.9× 113 0.9× 83 0.7× 43 0.4× 28 0.4× 22 438
Maria Stella Vari Italy 13 202 0.7× 92 0.7× 126 1.1× 56 0.5× 32 0.5× 31 453
R. Kálmánchey Hungary 10 206 0.7× 105 0.8× 80 0.7× 49 0.4× 25 0.4× 27 422
Lisa Flint United States 8 199 0.7× 141 1.1× 151 1.3× 96 0.9× 99 1.5× 9 514
Naomi Kanazawa Japan 17 244 0.9× 100 0.8× 50 0.4× 138 1.2× 80 1.2× 55 781
Shinjiro Akaboshi Japan 16 317 1.1× 132 1.0× 68 0.6× 45 0.4× 237 3.5× 27 592

Countries citing papers authored by M. Pineda

Since Specialization
Citations

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

Fields of papers citing papers by M. Pineda

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of M. Pineda

This figure shows the co-authorship network connecting the top 25 collaborators of M. Pineda. A scholar is included among the top collaborators of M. Pineda 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 M. Pineda. M. Pineda 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.
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
2.
Ortez, C., Sofia Duarte, Aída Ormazábal, et al.. (2014). Cerebrospinal fluid synaptic proteins as useful biomarkers in tyrosine hydroxylase deficiency. Molecular Genetics and Metabolism. 114(1). 34–40. 11 indexed citations
3.
Montero, Raquel, Celia Pérez‐Cerdá, Belén Pérez, et al.. (2011). Mild Clinical and Biochemical Phenotype in Two Patients with PMM2-CDG (Congenital Disorder of Glycosylation Ia). The Cerebellum. 11(2). 557–563. 17 indexed citations
4.
Serrano, Mercedes, Aída Ormazábal, Marta Vilaseca, et al.. (2011). Assessment of plasma ammonia and glutamine concentrations in urea cycle disorders. Clinical Biochemistry. 44(8-9). 742–744. 8 indexed citations
5.
Canals, Isaac, et al.. (2010). Molecular analysis of Sanfilippo syndrome type C in Spain: seven novel HGSNAT mutations and characterization of the mutant alleles. Clinical Genetics. 80(4). 367–374. 23 indexed citations
6.
Urreizti, Roser, Almudena Pino‐Ángeles, Mónica Cozar, et al.. (2010). Molecular characterization of five patients with homocystinuria due to severe methylenetetrahydrofolate reductase deficiency. Clinical Genetics. 78(5). 441–448. 15 indexed citations
7.
Mencarelli, Maria Antonietta, Ariele Spanhol-Rosseto, Rosangela Artuso, et al.. (2009). Novel FOXG1 mutations associated with the congenital variant of Rett syndrome. Journal of Medical Genetics. 47(1). 49–53. 74 indexed citations
8.
Trenchs, Victoria, et al.. (2009). Do retinal haemorrhages occur in infants with convulsions?. Archives of Disease in Childhood. 94(11). 873–875. 12 indexed citations
9.
García‐Cazorla, Àngels, Elizabeth Quadros, M.T. García‐Silva, et al.. (2008). MITOCHONDRIAL DISEASES ASSOCIATED WITH CEREBRAL FOLATE DEFICIENCY. Neurology. 70(16). 1360–1362. 67 indexed citations
10.
García‐Cazorla, Àngels, Mercedes Serrano, Belén Pérez‐Dueñas, et al.. (2007). Secondary abnormalities of neurotransmitters in infants with neurological disorders. Developmental Medicine & Child Neurology. 49(10). 740–744. 34 indexed citations
11.
Cervera, Carlos, M. Pineda, Laura Linares, et al.. (2007). Impact of Valganciclovir Prophylaxis on the Development of Severe Late-Cytomegalovirus Disease in High-Risk Solid Organ Transplant Recipients. Transplantation Proceedings. 39(7). 2228–2230. 20 indexed citations
12.
Cervera, Carlos, Xavier Filella, Laura Linares, et al.. (2007). Th1/Th2 Cytokine Release Pattern During In Vivo Cytomegalovirus Disease in Solid Organ Transplantation. Transplantation Proceedings. 39(7). 2233–2235. 17 indexed citations
13.
Artuch, Rafael, et al.. (2004). Cerebrospinal Fluid Concentrations of Idebenone in Friedreich Ataxia Patients. Neuropediatrics. 35(2). 95–98. 13 indexed citations
14.
Artuch, Rafael, et al.. (2002). Friedreich's Ataxia: Idebenone Treatment in Early Stage Patients. Neuropediatrics. 33(4). 190–193. 94 indexed citations
15.
16.
Pineda, M., et al.. (1993). The allopurinol test in patients with Rett syndrome. Journal of Inherited Metabolic Disease. 16(3). 577–580. 1 indexed citations
17.
Pineda, M., et al.. (1993). Docosahexaenoic acid–A new therapeutic approach to peroxisomal‐disorder patients. Neurology. 43(7). 1389–1389. 49 indexed citations
18.
Pàmpols, Teresa, Antònia Ribes, M. Pineda, et al.. (1987). Medium chain dicarboxylic and hydroxydicarboxylic aciduria in a case of neonatal adrenoleukodystrophy. Journal of Inherited Metabolic Disease. 10(S2). 217–219. 4 indexed citations
19.
Casaer, Paul, Jean Aicardi, Paolo Curatolo, et al.. (1987). Flunarizine in Alternating Hemiplegia in Childhood. An International Study in 12 Children. Neuropediatrics. 18(4). 191–195. 43 indexed citations
20.
Pineda, M., et al.. (1984). Considerations sur les encephalopathies epileptiques neonatales a propos d'une observation personnelle. Revue d Electroencé phalographie et de Neurophysiologie Clinique. 14(3). 197–202. 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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