María Rey

2.2k total citations
33 papers, 1.6k citations indexed

About

María Rey is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Neurology. According to data from OpenAlex, María Rey has authored 33 papers receiving a total of 1.6k indexed citations (citations by other indexed papers that have themselves been cited), including 20 papers in Molecular Biology, 12 papers in Cellular and Molecular Neuroscience and 12 papers in Neurology. Recurrent topics in María Rey's work include Parkinson's Disease Mechanisms and Treatments (9 papers), Genetic Neurodegenerative Diseases (9 papers) and CRISPR and Genetic Engineering (8 papers). María Rey is often cited by papers focused on Parkinson's Disease Mechanisms and Treatments (9 papers), Genetic Neurodegenerative Diseases (9 papers) and CRISPR and Genetic Engineering (8 papers). María Rey collaborates with scholars based in Spain, Switzerland and France. María Rey's co-authors include Isidró Ferrer, Merçé Boada, Eduardo Tolosa, Francesc Valldeoriola, Carles Gaig, Ellen Gelpí, Yaroslau Compta, Isabel de la Torre Díez, Nicole Déglon and Judith Navarro‐Otano and has published in prestigious journals such as Nature Neuroscience, PLoS ONE and Nutrients.

In The Last Decade

María Rey

33 papers receiving 1.6k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
María Rey Spain 19 717 620 585 464 339 33 1.6k
Dominique Langui France 20 1.0k 1.4× 680 1.1× 335 0.6× 316 0.7× 453 1.3× 37 1.8k
Martin C. Herzig Switzerland 13 1.0k 1.4× 475 0.8× 445 0.8× 370 0.8× 279 0.8× 17 1.4k
Kunié Ando Belgium 25 1.1k 1.5× 869 1.4× 187 0.3× 394 0.8× 512 1.5× 57 1.8k
Janusz Frackowiak United States 21 888 1.2× 462 0.7× 254 0.4× 322 0.7× 164 0.5× 43 1.3k
Laura Ghezzi Italy 22 727 1.0× 697 1.1× 276 0.5× 464 1.0× 133 0.4× 57 1.9k
Valérie Drouet France 13 651 0.9× 631 1.0× 232 0.4× 285 0.6× 463 1.4× 16 1.4k
Renzo Mancuso Spain 25 956 1.3× 1.1k 1.7× 651 1.1× 1.4k 3.0× 537 1.6× 50 3.0k
Felix L. Yeh United States 10 626 0.9× 406 0.7× 667 1.1× 760 1.6× 507 1.5× 24 1.9k
Anthony DelleDonne United States 17 790 1.1× 406 0.7× 1.0k 1.8× 581 1.3× 446 1.3× 21 1.9k
S Hirai Japan 28 1.3k 1.8× 914 1.5× 688 1.2× 407 0.9× 463 1.4× 64 2.3k

Countries citing papers authored by María Rey

Since Specialization
Citations

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

Fields of papers citing papers by María Rey

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of María Rey

This figure shows the co-authorship network connecting the top 25 collaborators of María Rey. A scholar is included among the top collaborators of María Rey 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 María Rey. María Rey 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.
Cailleret, Michel, Margot Jarrige, Sophie Lenoir, et al.. (2024). Mono- and Biallelic Inactivation of Huntingtin Gene in Patient-Specific Induced Pluripotent Stem Cells Reveal HTT Roles in Striatal Development and Neuronal Functions. Journal of Huntington s Disease. 13(1). 41–53. 3 indexed citations
2.
Rey, María, et al.. (2023). Semi-automated workflows to quantify AAV transduction in various brain areas and predict gene editing outcome for neurological disorders. Molecular Therapy — Methods & Clinical Development. 29. 254–270. 4 indexed citations
3.
Caron, Nicholas S., et al.. (2023). Limitations of Dual-Single Guide RNA CRISPR Strategies for the Treatment of Central Nervous System Genetic Disorders. Human Gene Therapy. 34(17-18). 958–974. 5 indexed citations
4.
Richetin, Kevin, Pascal Steullet, Romain Perbet, et al.. (2020). Tau accumulation in astrocytes of the dentate gyrus induces neuronal dysfunction and memory deficits in Alzheimer’s disease. Nature Neuroscience. 23(12). 1567–1579. 150 indexed citations
5.
Cheng, Shi, Catherine Pythoud, María Rey, et al.. (2018). Therapeutic efficacy of regulable GDNF expression for Huntington's and Parkinson's disease by a high-induction, background-free “GeneSwitch” vector. Experimental Neurology. 309. 79–90. 17 indexed citations
6.
Mérienne, Nicolas, Cécile Meunier, Guillaume Perriard, et al.. (2017). The Self-Inactivating KamiCas9 System for the Editing of CNS Disease Genes. Cell Reports. 20(12). 2980–2991. 90 indexed citations
7.
Cambon, Karine, Sylvain Martineau, Marie‐Claude Gaillard, et al.. (2017). Preclinical Evaluation of a Lentiviral Vector for Huntingtin Silencing. Molecular Therapy — Methods & Clinical Development. 5. 259–276. 13 indexed citations
8.
Drouet, Valérie, Marta Ruiz, Diana Zala, et al.. (2014). Allele-Specific Silencing of Mutant Huntingtin in Rodent Brain and Human Stem Cells. PLoS ONE. 9(6). e99341–e99341. 45 indexed citations
9.
Calero, Olga, María J. Bullido, Jordi Clarimón, et al.. (2012). Genetic variability of the gene cluster CALHM1–3 in sporadic Creutzfeldt-Jakob disease. Prion. 6(4). 407–412. 12 indexed citations
10.
Gaig, Carles, Francesc Valldeoriola, Ellen Gelpí, et al.. (2011). Rapidly progressive diffuse Lewy body disease. Movement Disorders. 26(7). 1316–1323. 42 indexed citations
11.
Rodriguez, Roberta Diehl, María Rey, Alexandre Gironell, et al.. (2011). “Preclinical” MSA in definite Creutzfeldt‐Jakob disease. Neuropathology. 32(2). 158–163. 17 indexed citations
12.
Lladó, Albert, Raquel Sánchez‐Valle, María Rey, et al.. (2008). Clinicopathological and genetic correlates of frontotemporal lobar degeneration and corticobasal degeneration. Journal of Neurology. 255(4). 488–494. 26 indexed citations
13.
Gaig, Carles, Mario Ezquerra, Marı́a José Martı́, et al.. (2008). Screening for the LRRK2 G2019S and codon-1441 mutations in a pathological series of parkinsonian syndromes and frontotemporal lobar degeneration. Journal of the Neurological Sciences. 270(1-2). 94–98. 31 indexed citations
14.
Molina‐Porcel, Laura, Albert Lladó, María Rey, et al.. (2008). Clinical and Pathological Heterogeneity of Neuronal Intermediate Filament Inclusion Disease. Archives of Neurology. 65(2). 272–5. 21 indexed citations
15.
Terni, Beatrice, María Rey, Susana Boluda, et al.. (2007). Mutant ubiquitin and p62 immunoreactivity in cases of combined multiple system atrophy and Alzheimer’s disease. Acta Neuropathologica. 113(4). 403–416. 35 indexed citations
16.
Compta, Yaroslau, Francesc Valldeoriola, Eduardo Tolosa, et al.. (2007). Long lasting pure freezing of gait preceding progressive supranuclear palsy: A clinicopathological study. Movement Disorders. 22(13). 1954–1958. 37 indexed citations
17.
Puig, Berta, María Rey, & Isidró Ferrer. (2005). Individual and regional variations of phospho-tau species in progressive supranuclear palsy. Acta Neuropathologica. 110(3). 261–268. 16 indexed citations
18.
Berciano, José, Francesc Valldeoriola, Isidró Ferrer, et al.. (2002). Presynaptic parkinsonism in multiple system atrophy mimicking Parkinson's disease: A clinicopathological case study. Movement Disorders. 17(4). 812–816. 32 indexed citations
19.
Rey, María, et al.. (2000). Efectos de un procedimiento de inducción de estados de ánimo sobre la autoeficacia. Anales de Psicología. 16(1). 23–31. 4 indexed citations
20.
Rey, María, Pedro L. Fernández, Pedro Jares, et al.. (1998). p21WAF1/Cip1 is associated with cyclin D1CCND1 expression and tubular differentiation but is independent of p53 overexpression in human breast carcinoma. The Journal of Pathology. 184(3). 265–271. 46 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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