Anna Marcé‐Grau

1.2k total citations
19 papers, 284 citations indexed

About

Anna Marcé‐Grau is a scholar working on Molecular Biology, Neurology and Rheumatology. According to data from OpenAlex, Anna Marcé‐Grau has authored 19 papers receiving a total of 284 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Molecular Biology, 7 papers in Neurology and 5 papers in Rheumatology. Recurrent topics in Anna Marcé‐Grau's work include Neurological disorders and treatments (5 papers), Glycogen Storage Diseases and Myoclonus (4 papers) and Genetic Neurodegenerative Diseases (3 papers). Anna Marcé‐Grau is often cited by papers focused on Neurological disorders and treatments (5 papers), Glycogen Storage Diseases and Myoclonus (4 papers) and Genetic Neurodegenerative Diseases (3 papers). Anna Marcé‐Grau collaborates with scholars based in Spain, United Kingdom and Netherlands. Anna Marcé‐Grau's co-authors include Belén Pérez‐Dueñas, Laura Martí‐Sánchez, Juan Darío Ortigoza‐Escobar, Alfons Macaya, Miquel Raspall‐Chaure, Ester Cuenca-León, Jesús Giraldo, L. Monge Galindo, James A. R. Dalton and Javier López Pisón and has published in prestigious journals such as PLoS ONE, International Journal of Molecular Sciences and Epilepsia.

In The Last Decade

Anna Marcé‐Grau

16 papers receiving 281 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Anna Marcé‐Grau Spain 10 139 77 63 52 48 19 284
Celeste Panteghini Italy 13 133 1.0× 118 1.5× 79 1.3× 65 1.3× 42 0.9× 25 329
Bianca M. L. Stelten Netherlands 11 76 0.5× 79 1.0× 47 0.7× 27 0.5× 32 0.7× 16 293
Mónica Cozar Spain 12 113 0.8× 89 1.2× 37 0.6× 25 0.5× 41 0.9× 24 369
Isabel Fineza Portugal 11 225 1.6× 29 0.4× 98 1.6× 89 1.7× 26 0.5× 25 341
Carlos E. Speck‐Martins Brazil 11 137 1.0× 27 0.4× 63 1.0× 66 1.3× 58 1.2× 23 314
Elly F. Ippel Netherlands 9 139 1.0× 49 0.6× 96 1.5× 15 0.3× 58 1.2× 10 254
Akihiko Miyauchi Japan 11 189 1.4× 43 0.6× 45 0.7× 85 1.6× 96 2.0× 24 326
Milena Janković Serbia 12 106 0.8× 152 2.0× 91 1.4× 17 0.3× 29 0.6× 37 337
Violeta Mihaylova Bulgaria 12 172 1.2× 210 2.7× 76 1.2× 15 0.3× 34 0.7× 22 424
Esther Nibbeling Netherlands 10 191 1.4× 73 0.9× 116 1.8× 12 0.2× 107 2.2× 15 408

Countries citing papers authored by Anna Marcé‐Grau

Since Specialization
Citations

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

Fields of papers citing papers by Anna Marcé‐Grau

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Anna Marcé‐Grau. 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 Anna Marcé‐Grau. The network helps show where Anna Marcé‐Grau may publish in the future.

Co-authorship network of co-authors of Anna Marcé‐Grau

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

All Works

19 of 19 papers shown
1.
Marcé‐Grau, Anna, et al.. (2025). Approach to Myoclonus Dystonia Syndrome: A European Reference Network Survey. Movement Disorders Clinical Practice. 12(7). 957–968.
2.
Español‐Martín, Gemma, David Gómez‐Andrés, Anna Marcé‐Grau, et al.. (2024). Natural history of SGCE‐associated myoclonus dystonia in children and adolescents. Developmental Medicine & Child Neurology. 67(6). 740–749. 1 indexed citations
3.
Álvarez, Ramiro, et al.. (2022). Early recognition of SGCE‐myoclonus–dystonia in children. Developmental Medicine & Child Neurology. 65(2). 207–214. 4 indexed citations
4.
Marcé‐Grau, Anna, et al.. (2022). Genetic diagnosis of basal ganglia disease in childhood. Developmental Medicine & Child Neurology. 64(6). 743–752.
5.
Marcé‐Grau, Anna, et al.. (2021). Muscarinic acetylcholine receptor M1 mutations causing neurodevelopmental disorder and epilepsy. Human Mutation. 42(10). 1215–1220. 4 indexed citations
6.
Urbizu, Aintzane, Melanie E. Garrett, Karen Soldano, et al.. (2021). Rare functional genetic variants in COL7A1, COL6A5, COL1A2 and COL5A2 frequently occur in Chiari Malformation Type 1. PLoS ONE. 16(5). e0251289–e0251289. 13 indexed citations
7.
Raspall‐Chaure, Miquel, et al.. (2021). Early-onset eyelid stereotypies are a frequent and distinctive feature in Dravet syndrome. Seizure. 92. 155–157. 3 indexed citations
8.
Marcé‐Grau, Anna, et al.. (2021). ε-Sarcoglycan: Unraveling the Myoclonus-Dystonia Gene. Molecular Neurobiology. 58(8). 3938–3952. 8 indexed citations
9.
Lupo, Vincenzo, Anna Marcé‐Grau, Jorge Hernández‐Vara, et al.. (2020). Impaired proteasome activity and neurodegeneration with brain iron accumulation in FBXO7 defect. Annals of Clinical and Translational Neurology. 7(8). 1436–1442. 20 indexed citations
10.
Martí‐Sánchez, Laura, Sonia Emperador, Ángel Sánchez‐Montáñez, et al.. (2019). Mutations in the mitochondrial complex I assembly factor NDUFAF6 cause isolated bilateral striatal necrosis and progressive dystonia in childhood. Molecular Genetics and Metabolism. 126(3). 250–258. 17 indexed citations
11.
Vilas, Dolores, Anna Marcé‐Grau, Alfons Macaya, Josep Valls‐Solé, & Eduard Tolosa. (2019). Galloping tongue syndrome in a PRRT2 mutation carrier. Neurology Genetics. 5(6). e377–e377. 4 indexed citations
12.
Marcé‐Grau, Anna, et al.. (2019). Genetic defects of thiamine transport and metabolism: A review of clinical phenotypes, genetics, and functional studies. Journal of Inherited Metabolic Disease. 42(4). 581–597. 81 indexed citations
13.
Santana-Codina, Naiara, Anna Marcé‐Grau, Laia Muixí, et al.. (2019). GRP94 Is Involved in the Lipid Phenotype of Brain Metastatic Cells. International Journal of Molecular Sciences. 20(16). 3883–3883. 13 indexed citations
14.
Santana-Codina, Naiara, Laia Muixí, Rebeca Sanz‐Pamplona, et al.. (2019). GRP94 promotes brain metastasis by engaging pro-survival autophagy. Neuro-Oncology. 22(5). 652–664. 28 indexed citations
15.
Gomis‐Pérez, Carolina, Janire Urrutia, Anna Marcé‐Grau, et al.. (2018). Homomeric Kv7.2 current suppression is a common feature in KCNQ2 epileptic encephalopathy. Epilepsia. 60(1). 139–148. 22 indexed citations
16.
Macaya, Alfons, Oliver Drechsel, Anna Marcé‐Grau, et al.. (2017). WES in nonprogressive congenital ataxia: Diagnostic yield and identification of novel loci. European Journal of Paediatric Neurology. 21. e219–e220.
17.
Marcé‐Grau, Anna, James A. R. Dalton, Javier López Pisón, et al.. (2016). GNAO1 encephalopathy: further delineation of a severe neurodevelopmental syndrome affecting females. Orphanet Journal of Rare Diseases. 11(1). 38–38. 31 indexed citations
18.
Bahamonde, María Isabel, Selma A. Serra, Oliver Drechsel, et al.. (2015). A Single Amino Acid Deletion (ΔF1502) in the S6 Segment of CaV2.1 Domain III Associated with Congenital Ataxia Increases Channel Activity and Promotes Ca2+ Influx. PLoS ONE. 10(12). e0146035–e0146035. 19 indexed citations
19.
Vila‐Pueyo, Marta, Roser Pons, Miquel Raspall‐Chaure, et al.. (2014). Clinical and genetic analysis in alternating hemiplegia of childhood: Ten new patients from Southern Europe. Journal of the Neurological Sciences. 344(1-2). 37–42. 16 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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