Merçè Pineda

741 total citations
19 papers, 562 citations indexed

About

Merçè Pineda is a scholar working on Clinical Biochemistry, Molecular Biology and Rheumatology. According to data from OpenAlex, Merçè Pineda has authored 19 papers receiving a total of 562 indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Clinical Biochemistry, 10 papers in Molecular Biology and 7 papers in Rheumatology. Recurrent topics in Merçè Pineda's work include Metabolism and Genetic Disorders (13 papers), Folate and B Vitamins Research (7 papers) and Amino Acid Enzymes and Metabolism (5 papers). Merçè Pineda is often cited by papers focused on Metabolism and Genetic Disorders (13 papers), Folate and B Vitamins Research (7 papers) and Amino Acid Enzymes and Metabolism (5 papers). Merçè Pineda collaborates with scholars based in Spain, Denmark and Austria. Merçè Pineda's co-authors include Rafael Artuch, Paz Briones, Aída Ormazábal, María Antònia Vilaseca, Jaume Campistol, Julio Montoya, Marina Vilaseca, Esther Cardo, Catrina Colomé and Lourdes Ibáñez and has published in prestigious journals such as PEDIATRICS, Annals of Neurology and Clinica Chimica Acta.

In The Last Decade

Merçè Pineda

19 papers receiving 548 citations

Peers

Merçè Pineda

RHEUM

PPCH

BIOCH

Elena Martín‐Hernández Spain

Apolline Imbard France

J. M. Saudubray France

Patrik Feyh Germany

María Teresa García‐Silva Spain

Komudi Siriwardena Canada

Hélène Ogier France

Cynthia S. Gubbels United States

C Clow Canada

Annette S. Feigenbaum Canada

Elena Martín‐Hernández Spain

Merçè Pineda

408 ×1.4

331 ×1.1

88 ×0.5

RHEUM

69 ×0.8

PPCH

52 ×0.7

BIOCH

Citations per year, relative to Merçè Pineda Merçè Pineda (= 1×) peers Elena Martín‐Hernández

Countries citing papers authored by Merçè Pineda

Since Specialization

Citations

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

Fields of papers citing papers by Merçè Pineda

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Merçè Pineda

This figure shows the co-authorship network connecting the top 25 collaborators of Merçè Pineda. A scholar is included among the top collaborators of Merçè 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 Merçè Pineda. Merçè Pineda is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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19 of 19 papers shown

Vallejo‐Torres, Laura, Iván Castilla‐Rodríguez, María L. Couce, et al.. (2015). Cost-Effectiveness Analysis of a National Newborn Screening Program for Biotinidase Deficiency. PEDIATRICS. 136(2). e424–e432. 15 indexed citations

Couce, María L., Celia Pérez‐Cerdá, Àngels García Cazorla, et al.. (2011). Hallazgos clínicos y genéticos en pacientes con deficiencia de biotinidasa detectados en el cribado neonatal o selectivo de sordera o de enfermedades metabólicas hereditarias. Medicina Clínica. 137(11). 500–503. 5 indexed citations

Ormazábal, Aída, Belén Pérez‐Dueñas, Cristina Sierra, et al.. (2011). Folate analysis for the differential diagnosis of profound cerebrospinal fluid folate deficiency. Clinical Biochemistry. 44(8-9). 719–721. 12 indexed citations

Tondo, Mireia, Ignacio Málaga, Mar O’Callaghan, et al.. (2011). Biochemical parameters to assess choroid plexus dysfunction in Kearns–Sayre syndrome patients. Mitochondrion. 11(6). 867–870. 5 indexed citations

Iqbal, Furhan, Chike Bellarmine Item, María Antònia Vilaseca, et al.. (2010). The identification of novel mutations in the biotinidase gene using denaturing high pressure liquid chromatography (dHPLC). Molecular Genetics and Metabolism. 100(1). 42–45. 17 indexed citations

Grandis, Elisa De, Mercedes Serrano, Belén Pérez‐Dueñas, et al.. (2010). Cerebrospinal fluid alterations of the serotonin product, 5‐hydroxyindolacetic acid, in neurological disorders. Journal of Inherited Metabolic Disease. 33(6). 803–809. 28 indexed citations

Quintana, Ester, Merçè Pineda, Aida Font, et al.. (2010). Dihydrolipoamide dehydrogenase (DLD) deficiency in a Spanish patient with myopathic presentation due to a new mutation in the interface domain. Journal of Inherited Metabolic Disease. 33(S3). 315–319. 28 indexed citations

Tondo, Mireia, Nilo Lambruschini, L. Gómez‐López, et al.. (2010). The monitoring of trace elements in blood samples from patients with inborn errors of metabolism. Journal of Inherited Metabolic Disease. 33(S3). 43–49. 2 indexed citations

Campistol, Jaume, Belén Pérez‐Dueñas, Pilar Póo, et al.. (2009). Seizures Versus Dystonia in Encephalopathic Crisis of Glutaric Aciduria Type I. Pediatric Neurology. 40(6). 426–431. 8 indexed citations

10.

Ormazábal, Aída, Àngels García‐Cazorla, Belén Pérez‐Dueñas, et al.. (2006). Determination of 5-methyltetrahydrofolate in cerebrospinal fluid of paediatric patients: Reference values for a paediatric population. Clinica Chimica Acta. 371(1-2). 159–162. 39 indexed citations

11.

Ormazábal, Aída, Àngels García Cazorla, Belén Pérez‐Dueñas, et al.. (2006). Utilidad del análisis del líquido cefalorraquídeo para el estudio de las deficiencias del metabolismo de neurotransmisores y pterinas y del transporte de glucosa y folato a través de la barrera hematoencefálica. Medicina Clínica. 127(3). 81–85. 6 indexed citations

12.

Møller, Lisbeth Birk, Anne Romstad, Aída Ormazábal, et al.. (2005). Pre- and postnatal diagnosis of tyrosine hydroxylase deficiency. Prenatal Diagnosis. 25(8). 671–675. 13 indexed citations

13.

Pineda, Merçè, Aída Ormazábal, Ester López‐Gallardo, et al.. (2005). Cerebral folate deficiency and leukoencephalopathy caused by a mitochondrial DNA deletion. Annals of Neurology. 59(2). 394–398. 119 indexed citations

14.

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

15.

Pineda, Merçè, et al.. (2000). Mutation analysis of 16S rRNA in patients with Rett syndrome. Pediatric Neurology. 23(1). 85–87. 4 indexed citations

16.

Vilaseca, Marina, Eugènia Monrós, Rafael Artuch, et al.. (2000). Anti-Epileptic drug treatment in children: Hyperhomocysteinaemia, B-Vitamins and the 677C→T Mutation of the Methylenetetrahydrofolate Reductase Gene. European Journal of Paediatric Neurology. 4(6). 269–277. 51 indexed citations

17.

Merinero, B., Ernst Christensen, Josep Lluís Gelpí, et al.. (2000). Glutaryl-CoA Dehydrogenase Deficiency in Spain: Evidence of Two Groups of Patients, Genetically, and Biochemically Distinct. Pediatric Research. 48(3). 315–322. 102 indexed citations

18.

Cardo, Esther, et al.. (1999). Evaluation of hyperhomocysteinaemia in children with stroke. European Journal of Paediatric Neurology. 3(3). 113–117. 33 indexed citations

19.

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

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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