M. Pineda

2.7k total citations
51 papers, 1.7k citations indexed

About

M. Pineda is a scholar working on Molecular Biology, Physiology and Genetics. According to data from OpenAlex, M. Pineda has authored 51 papers receiving a total of 1.7k indexed citations (citations by other indexed papers that have themselves been cited), including 20 papers in Molecular Biology, 15 papers in Physiology and 10 papers in Genetics. Recurrent topics in M. Pineda's work include Lysosomal Storage Disorders Research (14 papers), Genetics and Neurodevelopmental Disorders (10 papers) and Metabolism and Genetic Disorders (8 papers). M. Pineda is often cited by papers focused on Lysosomal Storage Disorders Research (14 papers), Genetics and Neurodevelopmental Disorders (10 papers) and Metabolism and Genetic Disorders (8 papers). M. Pineda collaborates with scholars based in Spain, France and United States. M. Pineda's co-authors include Isidró Ferrer, Rafael Artuch, C. Iturriaga, María Josep Coll, M. T. Vanier, David Ravine, Helen Leonard, Ami Bebbington, Alison Anderson and Alan K. Percy and has published in prestigious journals such as Neurology, Human Molecular Genetics and Acta Neuropathologica.

In The Last Decade

M. Pineda

51 papers receiving 1.7k 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 22 660 618 398 299 253 51 1.7k
Mercè Pineda Spain 26 642 1.0× 995 1.6× 407 1.0× 220 0.7× 208 0.8× 54 2.0k
Mercédes Pineda Spain 18 368 0.6× 499 0.8× 278 0.7× 94 0.3× 84 0.3× 29 1.0k
Teresa Temudo Portugal 16 137 0.2× 299 0.5× 413 1.0× 291 1.0× 263 1.0× 51 1.0k
Karen Weissbecker United States 16 54 0.1× 337 0.5× 253 0.6× 221 0.7× 96 0.4× 31 957
Xinhua Bao China 24 152 0.2× 1.1k 1.7× 864 2.2× 388 1.3× 341 1.3× 130 2.0k
Mercedes Serrano Spain 24 159 0.2× 611 1.0× 308 0.8× 79 0.3× 58 0.2× 80 1.4k
Laura Bannach Jardim Brazil 28 536 0.8× 1.5k 2.4× 169 0.4× 78 0.3× 36 0.1× 144 2.6k
Justyna Paprocka Poland 15 127 0.2× 341 0.6× 231 0.6× 139 0.5× 86 0.3× 82 892
Maria Luiza Saraiva Pereira Brazil 24 325 0.5× 977 1.6× 148 0.4× 68 0.2× 37 0.1× 126 1.7k
Mahim Jain United States 17 282 0.4× 481 0.8× 337 0.8× 69 0.2× 232 0.9× 36 1.3k

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.. (2024). "Treatment for Anxiety and Future Treatments in Rett Syndrome". Biomedical Journal of Scientific & Technical Research. 54(5). 1 indexed citations
2.
Bachiller, Alejandro, Joan Francesc Alonso, Anna López‐Sala, et al.. (2021). Cognitive stimulation has potential for brain activation in individuals with Rett syndrome. Journal of Intellectual Disability Research. 66(3). 213–224. 8 indexed citations
3.
Pineda, M., Parvaneh Karimzadeh, Miriam Kolníková, et al.. (2019). Evaluation of different suspicion indices in identifying patients with Niemann-Pick disease Type C in clinical practice: a post hoc analysis of a retrospective chart review. Orphanet Journal of Rare Diseases. 14(1). 161–161. 6 indexed citations
4.
Ulate-Campos, Adriana, Carmen Fons, Jaume Campistol, et al.. (2014). Hemiplejía alternante de la infancia: estudio del gen ATP1A3 en 16 pacientes. Medicina Clínica. 143(1). 25–28. 2 indexed citations
5.
Plana, Jaume Campistol, et al.. (2011). Benign Afebrile Convulsions in the Course of Mild Acute Gastroenteritis. Pediatric Emergency Care. 27(11). 1062–1064. 16 indexed citations
6.
Bebbington, Ami, Alan K. Percy, John Christodoulou, et al.. (2009). Updating the profile of C-terminal MECP2 deletions in Rett syndrome. Journal of Medical Genetics. 47(4). 242–248. 54 indexed citations
7.
Pineda, M., et al.. (2008). Vanishing White Matter Disease Associated with Progressive Macrocephaly. Neuropediatrics. 39(1). 29–32. 7 indexed citations
8.
Pérez‐Dueñas, Belén, Àngels García‐Cazorla, M. Pineda, et al.. (2008). Long-term evolution of eight Spanish patients with CDG type Ia: Typical and atypical manifestations. European Journal of Paediatric Neurology. 13(5). 444–451. 36 indexed citations
9.
Ramaekers, V., J.M. Sequeira, Rafael Artuch, et al.. (2007). Folate Receptor Autoantibodies and Spinal Fluid 5-Methyltetrahydrofolate Deficiency in Rett Syndrome. Neuropediatrics. 38(4). 179–183. 49 indexed citations
10.
Iturriaga, C., et al.. (2005). Identification of 25 new mutations in 40 unrelated Spanish Niemann‐Pick type C patients: genotype‐phenotype correlations. Clinical Genetics. 68(3). 245–254. 68 indexed citations
11.
Ormazábal, Aída, et al.. (2005). Cerebrospinal Fluid Concentrations of Folate, Biogenic Amines and Pterins in Rett Syndrome: Treatment with Folinic Acid. Neuropediatrics. 36(6). 380–385. 30 indexed citations
12.
Montero, Raquel, Rafael Artuch, P. Briones, et al.. (2005). Muscle coenzyme Q10 concentrations in patients with probable and definite diagnosis of respiratory chain disorders. BioFactors. 25(1-4). 109–115. 30 indexed citations
13.
Pineda, M., et al.. (2004). Primera crisis convulsiva afebril. Conducta en urgencias y evolución en un año. 60(6). 424–429. 1 indexed citations
14.
Alvarez, Vincent, et al.. (2003). Hemiparálisis velopalatina idiopática. Anales de Pediatría. 59(6). 595–598. 1 indexed citations
15.
Armstrong, Judith, M. Pineda, Esther Geán, et al.. (2002). Prenatal Diagnosis in Rett Syndrome. Fetal Diagnosis and Therapy. 17(4). 200–204. 2 indexed citations
16.
Koning, Tom J. de, J. Jaeken, M. Pineda, et al.. (2000). Hypomyelination and Reversible White Matter Attenuation in 3-Phosphoglycerate Dehydrogenase Deficiency. Neuropediatrics. 31(6). 287–292. 54 indexed citations
17.
Pàmpols, Teresa, M. Pineda, M. Girós, et al.. (1999). Neuronopathic juvenile glucosylceramidosis due to sap -C deficiency: clinical course, neuropathology and brain lipid composition in this Gaucher disease variant. Acta Neuropathologica. 97(1). 91–97. 38 indexed citations
18.
Artuch, Rafael, Marta Vilaseca, & M. Pineda. (1998). Biochemical monitoring of the treatment in paediatric patients with mitochondrial disease. Journal of Inherited Metabolic Disease. 21(8). 837–845. 17 indexed citations
19.
Ferrer, Isidró, et al.. (1992). Abnormal local-circuit neurons in epilepsia partialis continua associated with focal cortical dysplasia. Acta Neuropathologica. 83(6). 647–652. 118 indexed citations
20.
Ferrer, Isidró, et al.. (1988). FOCAL DENDRITIC SWELLINGS IN PURKINJE CELLS IN MUCOPOLYSACCHARIDOSES TYPES I, II AND III. A GOLGI AND ULTRASTRUCTURAL STUDY. Neuropathology and Applied Neurobiology. 14(4). 315–323. 26 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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