Mercè Pineda

2.9k total citations
54 papers, 2.0k citations indexed

About

Mercè Pineda is a scholar working on Molecular Biology, Physiology and Genetics. According to data from OpenAlex, Mercè Pineda has authored 54 papers receiving a total of 2.0k indexed citations (citations by other indexed papers that have themselves been cited), including 24 papers in Molecular Biology, 15 papers in Physiology and 13 papers in Genetics. Recurrent topics in Mercè Pineda's work include Lysosomal Storage Disorders Research (14 papers), Genetics and Neurodevelopmental Disorders (13 papers) and Metabolism and Genetic Disorders (11 papers). Mercè Pineda is often cited by papers focused on Lysosomal Storage Disorders Research (14 papers), Genetics and Neurodevelopmental Disorders (13 papers) and Metabolism and Genetic Disorders (11 papers). Mercè Pineda collaborates with scholars based in Spain, United States and France. Mercè Pineda's co-authors include Rafael Artuch, Marc C. Patterson, Paz Briones, Marie T. Vanier, Eugen Mengel, Plácido Navas, Mark Walterfang, José A. Sánchez‐Alcázar, Barbara Schwierin and Audrey Muller and has published in prestigious journals such as SHILAP Revista de lepidopterología, Scientific Reports and International Journal of Molecular Sciences.

In The Last Decade

Mercè Pineda

54 papers receiving 2.0k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Mercè Pineda Spain 26 995 642 407 234 220 54 2.0k
M. Pineda Spain 22 618 0.6× 660 1.0× 398 1.0× 201 0.9× 299 1.4× 51 1.7k
Mercédes Pineda Spain 18 499 0.5× 368 0.6× 278 0.7× 161 0.7× 94 0.4× 29 1.0k
Rose‐Mary Boustany United States 25 960 1.0× 1.2k 1.9× 181 0.4× 110 0.5× 89 0.4× 52 2.0k
Roser Pons Greece 21 644 0.6× 261 0.4× 273 0.7× 826 3.5× 155 0.7× 58 1.6k
Giovanna Zorzi Italy 30 898 0.9× 206 0.3× 213 0.5× 436 1.9× 222 1.0× 101 2.5k
Xinhua Bao China 24 1.1k 1.1× 152 0.2× 864 2.1× 276 1.2× 388 1.8× 130 2.0k
Andreea Nissenkorn Israel 25 729 0.7× 83 0.1× 314 0.8× 228 1.0× 281 1.3× 59 1.5k
Yu-ichi Goto Japan 21 1.6k 1.6× 312 0.5× 276 0.7× 576 2.5× 52 0.2× 39 2.1k
Andrea Whitney United Kingdom 15 340 0.3× 982 1.5× 231 0.6× 691 3.0× 488 2.2× 19 1.6k
Andrea Dardis Italy 30 719 0.7× 1.8k 2.8× 232 0.6× 112 0.5× 199 0.9× 98 2.6k

Countries citing papers authored by Mercè Pineda

Since Specialization
Citations

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

Fields of papers citing papers by Mercè Pineda

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Mercè Pineda

This figure shows the co-authorship network connecting the top 25 collaborators of Mercè Pineda. A scholar is included among the top collaborators of Mercè 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 Mercè Pineda. Mercè 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.
Fernández‐Carasa, Irene, Carles Calatayud, Meritxell Pons‐Espinal, et al.. (2023). iPSC ‐based modeling of THD recapitulates disease phenotypes and reveals neuronal malformation. EMBO Molecular Medicine. 15(3). e15847–e15847. 8 indexed citations
2.
Castellanos, Elisabeth, Bernat Gel, Andreu Alibés, et al.. (2019). Mutational spectrum by phenotype: panel‐based NGS testing of patients with clinical suspicion of RASopathy and children with multiple café‐au‐lait macules. Clinical Genetics. 97(2). 264–275. 12 indexed citations
3.
Vidal, Enrique, Silvia M. Vidal, Mauricio Sáez, et al.. (2016). Whole exome sequencing of Rett syndrome-like patients reveals the mutational diversity of the clinical phenotype. Human Genetics. 135(12). 1343–1354. 48 indexed citations
4.
Patterson, Marc C., Eugen Mengel, Marie T. Vanier, et al.. (2015). Stable or improved neurological manifestations during miglustat therapy in patients from the international disease registry for Niemann-Pick disease type C: an observational cohort study. Orphanet Journal of Rare Diseases. 10(1). 65–65. 69 indexed citations
5.
Emperador, Sonia, Mercè Pineda, Ester López‐Gallardo, et al.. (2015). Mutation loads in different tissues from six pathogenic mtDNA point mutations. Mitochondrion. 22. 17–22. 11 indexed citations
6.
Fernández‐Marmiesse, Ana, Mercè Pineda, Jesús Manuel Eirís Puñal, et al.. (2014). Assessment of a targeted resequencing assay as a support tool in the diagnosis of lysosomal storage disorders. Orphanet Journal of Rare Diseases. 9(1). 59–59. 38 indexed citations
7.
Quijada‐Fraile, Pilar, Mar O’Callaghan, Elena Martín‐Hernández, et al.. (2014). Follow-up of folinic acid supplementation for patients with cerebral folate deficiency and Kearns-Sayre syndrome. Orphanet Journal of Rare Diseases. 9(1). 217–217. 31 indexed citations
8.
Patterson, Marc C., Eugen Mengel, Frits A. Wijburg, et al.. (2013). Disease and patient characteristics in NP-C patients: findings from an international disease registry. Orphanet Journal of Rare Diseases. 8(1). 12–12. 145 indexed citations
9.
Armstrong, Judith, et al.. (2012). CDKL5 in different atypical Rett syndrome variants: Description of the first eight patients from Spain. 1(1). 27–35. 7 indexed citations
10.
Pérez-Poyato, María & Mercè Pineda. (2011). New Agents and Approaches to Treatment in Niemann-Pick Type C Disease. Current Pharmaceutical Biotechnology. 12(6). 897–901. 17 indexed citations
11.
Pineda, Mercè, Raquel Montero, Ana Mas, et al.. (2010). Coenzyme Q10‐responsive ataxia: 2‐year‐treatment follow‐up. Movement Disorders. 25(9). 1262–1268. 39 indexed citations
12.
Fyfe, Sue, Ami Bebbington, Nadia Bahi‐Buisson, et al.. (2009). InterRett, a model for international data collection in a rare genetic disorder. Research in autism spectrum disorders. 3(3). 639–659. 45 indexed citations
13.
Arias, Ángela, Carmen Fons, Judit García‐Villoria, et al.. (2007). Creatine transporter deficiency: Prevalence among patients with mental retardation and pitfalls in metabolite screening. Clinical Biochemistry. 40(16-17). 1328–1331. 51 indexed citations
14.
Artuch, Rafael, Gloria Brea‐Calvo, Paz Briones, et al.. (2006). Cerebellar ataxia with coenzyme Q10 deficiency: Diagnosis and follow-up after coenzyme Q10 supplementation. Journal of the Neurological Sciences. 246(1-2). 153–158. 74 indexed citations
15.
Ragione, Floriana Della, А. А. Тиунова, Marcella Vacca, et al.. (2006). The X-linked methyl binding protein gene Kaiso is highly expressed in brain but is not mutated in Rett syndrome patients. Gene. 373. 83–89. 9 indexed citations
16.
Santos, Cristina, Laia Rodríguez‐Revenga, Irene Madrigal, et al.. (2006). A novel mutation in JARID1C gene associated with mental retardation. European Journal of Human Genetics. 14(5). 583–586. 62 indexed citations
17.
Monrós, Eugènia, et al.. (2001). Rett syndrome in Spain: mutation analysis and clinical correlations. Brain and Development. 23. S251–S253. 66 indexed citations
18.
Klomp, Leo W. J., Tom J. de Koning, Helga E.M. Malingré, et al.. (2000). Molecular Characterization of 3-Phosphoglycerate Dehydrogenase Deficiency—a Neurometabolic Disorder Associated with Reduced L-Serine Biosynthesis. The American Journal of Human Genetics. 67(6). 1389–1399. 86 indexed citations
19.
Artuch, Rafael, Catrina Colomé, Paz Briones, et al.. (2000). Oxygen consumption measurement in lymphocytes for the diagnosis of pediatric patients with oxidative phosphorylation diseases. Clinical Biochemistry. 33(6). 481–485. 9 indexed citations
20.
Pineda, Mercè, Jaume Campistol, Marina Vilaseca, et al.. (1995). An atypical French form of pyruvate carboxylase deficiency. Brain and Development. 17(4). 276–279. 15 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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