Marc Corral‐Juan

503 total citations
15 papers, 336 citations indexed

About

Marc Corral‐Juan is a scholar working on Cellular and Molecular Neuroscience, Molecular Biology and Neurology. According to data from OpenAlex, Marc Corral‐Juan has authored 15 papers receiving a total of 336 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Cellular and Molecular Neuroscience, 11 papers in Molecular Biology and 3 papers in Neurology. Recurrent topics in Marc Corral‐Juan's work include Genetic Neurodegenerative Diseases (11 papers), Mitochondrial Function and Pathology (9 papers) and Neurological diseases and metabolism (3 papers). Marc Corral‐Juan is often cited by papers focused on Genetic Neurodegenerative Diseases (11 papers), Mitochondrial Function and Pathology (9 papers) and Neurological diseases and metabolism (3 papers). Marc Corral‐Juan collaborates with scholars based in Spain, United States and Portugal. Marc Corral‐Juan's co-authors include Antoni Matilla‐Dueñas, Ivelisse Sánchez, Vı́ctor Volpini, Ramiro Álvarez, Antoni Dávalos, Pilar Latorre, Lourdes Ispierto, Carmen Serrano, Dolores Vilas and Carlota Méndez‐del‐Barrio and has published in prestigious journals such as Brain, Human Molecular Genetics and Advances in experimental medicine and biology.

In The Last Decade

Marc Corral‐Juan

14 papers receiving 332 citations

Peers

Marc Corral‐Juan

CMN

NEURO

GENET

NEURO

Wai Yan Yau Australia

Nicolas Chrestian Canada

Maartje Pennings Netherlands

Hyang-Sook Kim South Korea

Isabel Banchs Spain

M. Kéfi Tunisia

Isabelle Vuillaume France

Florian Harmuth Germany

Janel O. Johnson United States

Daniele Galatolo Italy

Wai Yan Yau Australia

Marc Corral‐Juan

255 ×1.0

275 ×1.3

CMN

112 ×1.5

NEURO

56 ×0.9

GENET

50 ×1.4

NEURO

Citations per year, relative to Marc Corral‐Juan Marc Corral‐Juan (= 1×) peers Wai Yan Yau

Countries citing papers authored by Marc Corral‐Juan

Since Specialization

Citations

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

Fields of papers citing papers by Marc Corral‐Juan

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Marc Corral‐Juan. 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 Marc Corral‐Juan. The network helps show where Marc Corral‐Juan may publish in the future.

Co-authorship network of co-authors of Marc Corral‐Juan

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

All Works

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15 of 15 papers shown

Corral‐Juan, Marc, et al.. (2024). Novel genotype–phenotype correlations, differential cerebellar allele-specific methylation, and a common origin of the (ATTTC)n insertion in spinocerebellar ataxia type 37. Human Genetics. 143(3). 211–232. 4 indexed citations

Corral‐Juan, Marc, Pilar Casquero, Steven Laurie, et al.. (2022). New spinocerebellar ataxia subtype caused bySAMD9Lmutation triggering mitochondrial dysregulation (SCA49). Brain Communications. 4(2). fcac030–fcac030. 21 indexed citations

Pelayo‐Negro, Ana L., et al.. (2021). Ataxia and Action Myoclonus Related to Novel Mutations in ATP13A2 Gene. Movement Disorders Clinical Practice. 8(6). 969–971.

Delgado‐Alvarado, Manuel, et al.. (2020). A novel SGCE variant is associated with myoclonus-dystonia with phenotypic variability. Neurological Sciences. 41(12). 3779–3781. 2 indexed citations

García-Martínez, Alberto, Marc Corral‐Juan, Ángel I Pérez-Álvarez, et al.. (2019). Perrault syndrome with neurological features in a compound heterozygote for two TWNK mutations: overlap of TWNK-related recessive disorders. Journal of Translational Medicine. 17(1). 290–290. 17 indexed citations

Infante, Jon, Marc Corral‐Juan, Xavier Farré, et al.. (2019). POLR3A-related spastic ataxia: new mutations and a look into the phenotype. Journal of Neurology. 267(2). 324–330. 14 indexed citations

Nieto, Antonieta, et al.. (2019). Cognitive characterization of SCAR10 caused by a homozygous c.132dupA mutation in the ANO10 gene. Neurocase. 25(5). 195–201. 5 indexed citations

Corral‐Juan, Marc, Carmen Serrano, Alberto Rábano, et al.. (2018). Clinical, genetic and neuropathological characterization of spinocerebellar ataxia type 37. Brain. 141(7). 1981–1997. 40 indexed citations

Matilla‐Dueñas, Antoni, Marc Corral‐Juan, Agustí Rodríguez‐Palmero, et al.. (2017). Rare Neurodegenerative Diseases: Clinical and Genetic Update. Advances in experimental medicine and biology. 1031. 443–496. 30 indexed citations

10.

Martín‐Hernández, Elena, María Elena Rodríguez‐García, Ana Camacho, et al.. (2016). New ATP8A2 gene mutations associated with a novel syndrome: encephalopathy, intellectual disability, severe hypotonia, chorea and optic atrophy. Neurogenetics. 17(4). 259–263. 30 indexed citations

11.

Serrano, Carmen, Marc Corral‐Juan, Giovanni Stévanin, et al.. (2013). New Subtype of Spinocerebellar Ataxia With Altered Vertical Eye Movements Mapping to Chromosome 1p32. JAMA Neurology. 70(6). 764–764. 29 indexed citations

12.

Sánchez, Ivelisse, et al.. (2013). A novel function of Ataxin-1 in the modulation of PP2A activity is dysregulated in the spinocerebellar ataxia type 1. Human Molecular Genetics. 22(17). 3425–3437. 13 indexed citations

13.

Matilla‐Dueñas, Antoni, Marc Corral‐Juan, Vı́ctor Volpini, & Ivelisse Sánchez. (2012). The Spinocerebellar Ataxias: Clinical Aspects And Molecular Genetics. Advances in experimental medicine and biology. 724. 351–374. 47 indexed citations

14.

Martín-Trujillo, Álex, Isabel Iglesias‐Platas, Eliécer Coto, et al.. (2011). Genotype of an individual single nucleotide polymorphism regulates DNA methylation at theTRPC3alternative promoter. Epigenetics. 6(10). 1236–1241. 17 indexed citations

15.

Matilla‐Dueñas, Antoni, Ivelisse Sánchez, Marc Corral‐Juan, et al.. (2009). Cellular and Molecular Pathways Triggering Neurodegeneration in the Spinocerebellar Ataxias. The Cerebellum. 9(2). 148–166. 67 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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