M. Troncoso

1.6k total citations
28 papers, 497 citations indexed

About

M. Troncoso is a scholar working on Molecular Biology, Physiology and Epidemiology. According to data from OpenAlex, M. Troncoso has authored 28 papers receiving a total of 497 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Molecular Biology, 6 papers in Physiology and 5 papers in Epidemiology. Recurrent topics in M. Troncoso's work include Biochemical and Molecular Research (4 papers), Lysosomal Storage Disorders Research (4 papers) and Autism Spectrum Disorder Research (4 papers). M. Troncoso is often cited by papers focused on Biochemical and Molecular Research (4 papers), Lysosomal Storage Disorders Research (4 papers) and Autism Spectrum Disorder Research (4 papers). M. Troncoso collaborates with scholars based in Chile, United States and Argentina. M. Troncoso's co-authors include Odile Boespflug‐Tanguy, Diana Rodriguez, Enrico Bertini, Eva Neumaier‐Probst, Georg F. Hoffmann, Esther M. Maier, Stefan Kölker, Johannes Zschocke, Chris Mühlhausen and Inga Harting and has published in prestigious journals such as SHILAP Revista de lepidopterología, Brain and Neurology.

In The Last Decade

M. Troncoso

27 papers receiving 492 citations

Peers

M. Troncoso

PHYSI

EPIDE

Deborah L. Renaud United States

Ewa Jamroz Poland

Patrick Verloo Belgium

Rabab Debs France

Mahesh Kamate India

Mika H. Martikainen Finland

Marc D’Hooghe Belgium

Auli Nuutila Finland

M. Tardieu France

Bai Jin Zeng United States

Deborah L. Renaud United States

M. Troncoso

233 ×0.7

88 ×0.8

41 ×0.6

53 ×0.8

PHYSI

33 ×0.8

EPIDE

Citations per year, relative to M. Troncoso M. Troncoso (= 1×) peers Deborah L. Renaud

Countries citing papers authored by M. Troncoso

Since Specialization

Citations

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

Fields of papers citing papers by M. Troncoso

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

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

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

All Works

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20 of 20 papers shown

Estay, Juan, Luisa Pinto, Gregory P. De Pascale, et al.. (2023). Active thrust tectonics along the western slope of the Central Andes southernmost Pampean flat-slab segment (∼33°S, Chile): The Cariño Botado fault system. Geomorphology. 437. 108801–108801. 3 indexed citations

Cárdenas‐Rebollo, José Miguel, et al.. (2023). Genotype and Phenotype Characterization of Patients with Mucopolysaccharidosis IV-A in Chile. Molecular Syndromology. 14(5). 416–427. 1 indexed citations

Castro, Pedro, Francisco Javier López‐González, Rocío Sánchez‐Carpintero, et al.. (2023). Exploring the Spectrum of RHOBTB2 Variants Associated with Developmental Encephalopathy 64: A Case Series and Literature Review. Movement Disorders Clinical Practice. 10(11). 1671–1679. 3 indexed citations

Miyake, Noriko, M. Troncoso, Nobuhiko Okamoto, et al.. (2021). A homozygous ABHD16A variant causes a complex hereditary spastic paraplegia with developmental delay, absent speech, and characteristic face. Clinical Genetics. 101(3). 359–363. 5 indexed citations

Yáñez, Carolina, et al.. (2021). Uso terapéutico de robótica en niños con Trastorno del Espectro Autista. Andes pediatrica. 92(5). 747–753. 2 indexed citations

Troncoso, M., et al.. (2021). Estudio genético de acuerdo a características fenotípicas de niños y adolescentes con discapacidad intelectual de etiología indeterminada. Andes pediatrica. 92(6). 879–887. 1 indexed citations

Troncoso, M., et al.. (2021). Super‐refractory status epilepticus related to COVID‐19 in a paediatric patient with PRRT2 mutation. Epileptic Disorders. 23(6). 951–953. 4 indexed citations

Yáñez, Carolina, et al.. (2021). Estimación de la prevalencia de trastorno del Espectro Autista en población urbana chilena. Andes pediatrica. 92(4). 519–525. 14 indexed citations

Troncoso, M., et al.. (2021). Hypomyelination and Congenital Cataract: Identification of a Novel likely pathogenic c.414+1G>A in FAM126A gene Variant. SHILAP Revista de lepidopterología. 9(5). e04171–e04171. 1 indexed citations

10.

Troncoso, M., Nobuhiko Okamoto, Kohei Hamanaka, et al.. (2020). A novel ITPA variant causes epileptic encephalopathy with multiple-organ dysfunction. Journal of Human Genetics. 65(9). 751–757. 11 indexed citations

11.

Guelbert, Norberto, et al.. (2020). Position of Experts Regarding Follow-Up of Patients with Neuronal Ceroid Lipofuscinosis-2 Disease in Latin America. SHILAP Revista de lepidopterología. 8. 1 indexed citations

12.

Román-Urrestarazu, Andrés, Carolina Yáñez, Carrie Allison, et al.. (2020). Autism screening and conditional cash transfers in Chile: Using the Quantitative Checklist (Q-CHAT) for early autism detection in a low resource setting. Autism. 25(4). 932–945. 16 indexed citations

13.

Lourenço, Charles Marques, André Luiz Santos Pessoa, M. Troncoso, et al.. (2020). Revealing the clinical phenotype of atypical neuronal ceroid lipofuscinosis type 2 disease: Insights from the largest cohort in the world. Journal of Paediatrics and Child Health. 57(4). 519–525. 15 indexed citations

14.

Gu, Shen, Chun‐An Chen, Jill A. Rosenfeld, et al.. (2019). Truncating variants in UBAP1 associated with childhood‐onset nonsyndromic hereditary spastic paraplegia. Human Mutation. 41(3). 632–640. 15 indexed citations

15.

Nguyen, Khue Vu, et al.. (2017). Lesch-Nyhan disease in two families from Chiloé Island with mutations in the HPRT1 gene. Nucleosides Nucleotides & Nucleic Acids. 36(7). 452–462. 2 indexed citations

16.

Hernández, Alejandro, et al.. (2015). Clinical and genetic characterization of patients with myotonic dystrophy type 1 (DM1) at San Borja Arriarán Hospital. Journal of the Neurological Sciences. 357. e426–e426. 1 indexed citations

17.

Xin, Winnie, Katherine B. Sims, Norberto Guelbert, et al.. (2012). Neuronal ceroid lipofuscinosis type CLN2: A new rationale for the construction of phenotypic subgroups based on a survey of 25 cases in South America. Gene. 516(1). 114–121. 34 indexed citations

18.

Harting, Inga, Eva Neumaier‐Probst, Angelika Seitz, et al.. (2009). Dynamic changes of striatal and extrastriatal abnormalities in glutaric aciduria type I. Brain. 132(7). 1764–1782. 121 indexed citations

19.

Fogli, Anne, Raphael Schiffmann, Enrico Bertini, et al.. (2004). The effect of genotype on the natural history of eIF2B-related leukodystrophies. Neurology. 62(9). 1509–1517. 117 indexed citations

20.

Rodriguez, Diana, Enrico Bertini, Marianna Bugiani, et al.. (2001). Infantile Alexander Disease: Spectrum of GFAP Mutations and Genotype-Phenotype Correlation. The American Journal of Human Genetics. 69(5). 1134–1140. 105 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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