M.T. García‐Silva

861 total citations
16 papers, 515 citations indexed

About

M.T. García‐Silva is a scholar working on Molecular Biology, Clinical Biochemistry and Organic Chemistry. According to data from OpenAlex, M.T. García‐Silva has authored 16 papers receiving a total of 515 indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Molecular Biology, 12 papers in Clinical Biochemistry and 2 papers in Organic Chemistry. Recurrent topics in M.T. García‐Silva's work include Metabolism and Genetic Disorders (12 papers), Mitochondrial Function and Pathology (9 papers) and Glycosylation and Glycoproteins Research (3 papers). M.T. García‐Silva is often cited by papers focused on Metabolism and Genetic Disorders (12 papers), Mitochondrial Function and Pathology (9 papers) and Glycosylation and Glycoproteins Research (3 papers). M.T. García‐Silva collaborates with scholars based in Spain, Belgium and United Kingdom. M.T. García‐Silva's co-authors include Joaquı́n Arenas, Yolanda Campos, Paz Briones, Miguel A. Martı́n, Javier Manzanares, Ron A. Wevers, Stephanie Grünewald, Karin Huijben, Éva Morava and Suzan Wopereis and has published in prestigious journals such as American Journal of Clinical Nutrition, Neurology and Clinical Chemistry.

In The Last Decade

M.T. García‐Silva

15 papers receiving 498 citations

Peers

M.T. García‐Silva

PHYSI

GENET

Johann Penzien Germany

María Teresa García‐Silva Spain

Teresa Pàmpols Spain

Nastassja Himmelreich Germany

Elena Martín‐Hernández Spain

Annette S. Feigenbaum Canada

M. DiRocco Italy

Jack J. Huizenga Canada

Paula M. Strasberg Canada

Véronique Rüfenacht Switzerland

Johann Penzien Germany

M.T. García‐Silva

268 ×0.7

184 ×1.1

76 ×0.9

PHYSI

14 ×0.2

72 ×1.2

GENET

Citations per year, relative to M.T. García‐Silva M.T. García‐Silva (= 1×) peers Johann Penzien

Countries citing papers authored by M.T. García‐Silva

Since Specialization

Citations

This map shows the geographic impact of M.T. García‐Silva'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.T. García‐Silva with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites M.T. García‐Silva more than expected).

Fields of papers citing papers by M.T. García‐Silva

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by M.T. García‐Silva. 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.T. García‐Silva. The network helps show where M.T. García‐Silva may publish in the future.

Co-authorship network of co-authors of M.T. García‐Silva

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

All Works

Sort: Min cites: Since: Top N: Style:

16 of 16 papers shown

Bellusci, Marcello, Pilar Quijada‐Fraile, Elena Martín‐Hernández, et al.. (2017). Carnitine palmitoyltransferase 1A deficiency: abnormal muscle biopsy findings in a child presenting with Reye's syndrome. Journal of Inherited Metabolic Disease. 40(5). 751–752. 4 indexed citations

Fiuza‐Luces, Carmen, Alejandro Santos‐Lozano, M.T. García‐Silva, et al.. (2016). Assessment of resting energy expenditure in pediatric mitochondrial diseases with indirect calorimetry. Clinical Nutrition. 35(6). 1484–1489. 3 indexed citations

Martı́n, Miguel A., M.T. García‐Silva, Giulia Barcia, et al.. (2016). The homozygous R504C mutation in MTO1 gene is responsible for ONCE syndrome. Clinical Genetics. 91(1). 46–53. 9 indexed citations

Baldellou, A, M.T. García‐Silva, Àngels García‐Cazorla, et al.. (2011). Estudio epidemiológico de las enfermedades metabólicas con homocistinuria en España. Anales de Pediatría. 76(3). 133–139. 2 indexed citations

Arredondo, Juan, M. Esther Gallardo, Pablo García‐Pavía, et al.. (2011). Mitochondrial tRNA valine as a recurrent target for mutations involved in mitochondrial cardiomyopathies. Mitochondrion. 12(2). 357–362. 13 indexed citations

Blázquez, Alberto, M.T. García‐Silva, Toni Gabaldón, et al.. (2009). Pathogenic mutations in the 5′ untranslated region of BCS1L mRNA in mitochondrial complex III deficiency. Mitochondrion. 9(5). 299–305. 26 indexed citations

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

Martín‐Hernández, Elena, M.T. García‐Silva, Julia Vara, et al.. (2005). Renal pathology in children with mitochondrial diseases. Pediatric Nephrology. 20(9). 1299–1305. 80 indexed citations

García‐Silva, M.T., Gert Matthijs, Els Schollen, et al.. (2004). Congenital disorder of glycosylation (CDG) type Ie. A new patient. Journal of Inherited Metabolic Disease. 27(5). 591–600. 38 indexed citations

10.

Wopereis, Suzan, Stephanie Grünewald, Éva Morava, et al.. (2003). Apolipoprotein C-III Isofocusing in the Diagnosis of Genetic Defects in O-Glycan Biosynthesis. Clinical Chemistry. 49(11). 1839–1845. 108 indexed citations

11.

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

12.

Martínez, Manuela, et al.. (2000). Therapeutic effects of docosahexaenoic acid ethyl ester in patients with generalized peroxisomal disorders. American Journal of Clinical Nutrition. 71(1). 376S–385S. 76 indexed citations

13.

Martı́n, Miguel A., Yolanda Campos, M.T. García‐Silva, et al.. (1999). Slow segregation and rapid shift to homoplasmy coexist in a family with the T8993>G mutation. Journal of Inherited Metabolic Disease. 22(8). 939–940. 2 indexed citations

14.

Martínez, Maria Carmen, et al.. (1999). [Treatment of generalized peroxisomal disorders with docosahexaenoic acid ethyl ether].. PubMed. 28 Suppl 1. S59–64. 6 indexed citations

15.

Martı́nez, G, Antònia Ribes, P. Briones, et al.. (1998). Medium‐chain acyl‐CoA dehydrogenase deficiency in Spain. Journal of Inherited Metabolic Disease. 21(6). 693–694.

16.

García‐Silva, M.T., Antònia Ribes, Yolanda Campos, Barbara Garavaglia, & Joaquı́n Arenas. (1997). Syndrome of encephalopathy, petechiae, and ethylmalonic aciduria. Pediatric Neurology. 17(2). 165–170. 42 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.

Explore authors with similar magnitude of impact