Concepció Marı́n

9.7k total citations
81 papers, 2.7k citations indexed

About

Concepció Marı́n is a scholar working on Cellular and Molecular Neuroscience, Neurology and Sensory Systems. According to data from OpenAlex, Concepció Marı́n has authored 81 papers receiving a total of 2.7k indexed citations (citations by other indexed papers that have themselves been cited), including 46 papers in Cellular and Molecular Neuroscience, 45 papers in Neurology and 17 papers in Sensory Systems. Recurrent topics in Concepció Marı́n's work include Parkinson's Disease Mechanisms and Treatments (42 papers), Neurological disorders and treatments (36 papers) and Neuroscience and Neuropharmacology Research (25 papers). Concepció Marı́n is often cited by papers focused on Parkinson's Disease Mechanisms and Treatments (42 papers), Neurological disorders and treatments (36 papers) and Neuroscience and Neuropharmacology Research (25 papers). Concepció Marı́n collaborates with scholars based in Spain, United States and France. Concepció Marı́n's co-authors include José Á. Obeso, María Rodríguez‐Oroz, Manuel Rodrı́guez, Javier Blesa, Beatriz Benítez‐Temiño, Joaquim Mullol, Esther Aguilar, M. Bonastre, Isam Alobid and Eduardo Tolosa and has published in prestigious journals such as The Plant Cell, Neurology and Trends in Neurosciences.

In The Last Decade

Concepció Marı́n

78 papers receiving 2.6k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Concepció Marı́n Spain 25 1.5k 1.2k 502 376 297 81 2.7k
Laura Silveira‐Moriyama United Kingdom 27 2.5k 1.7× 796 0.7× 524 1.0× 304 0.8× 242 0.8× 79 3.4k
Philipp Mahlknecht Austria 30 2.1k 1.4× 685 0.6× 194 0.4× 200 0.5× 145 0.5× 66 2.7k
James F. Morley United States 24 1.1k 0.7× 542 0.4× 391 0.8× 953 2.5× 203 0.7× 53 3.0k
Filip Bergquist Sweden 26 730 0.5× 694 0.6× 177 0.4× 596 1.6× 161 0.5× 65 2.4k
Gordon Reid Romania 24 375 0.2× 1.1k 0.9× 890 1.8× 543 1.4× 167 0.6× 35 2.1k
Nolwen L. Rey United States 19 1.5k 1.0× 638 0.5× 322 0.6× 516 1.4× 68 0.2× 29 2.3k
Zacharias Kohl Germany 29 1.0k 0.7× 1.1k 0.9× 86 0.2× 726 1.9× 266 0.9× 72 2.7k
J. M. Henderson Australia 25 1.5k 1.0× 1.1k 0.9× 91 0.2× 259 0.7× 53 0.2× 45 2.2k
Lisa Klingelhoefer Germany 20 902 0.6× 242 0.2× 155 0.3× 170 0.5× 146 0.5× 57 1.4k
Monty Silverdale United Kingdom 29 1.6k 1.0× 569 0.5× 68 0.1× 227 0.6× 98 0.3× 79 2.3k

Countries citing papers authored by Concepció Marı́n

Since Specialization
Citations

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

Fields of papers citing papers by Concepció Marı́n

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Concepció Marı́n

This figure shows the co-authorship network connecting the top 25 collaborators of Concepció Marı́n. A scholar is included among the top collaborators of Concepció Marı́n 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 Concepció Marı́n. Concepció Marı́n 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.
Marı́n, Concepció, et al.. (2024). Type 2 and Non-type 2 Inflammation in the Upper Airways: Cellular and Molecular Alterations in Olfactory Neuroepithelium Cell Populations. Current Allergy and Asthma Reports. 24(4). 211–219.
2.
Marı́n, Concepció, M. Bonastre, Mireya Fuentes, & Joaquim Mullol. (2020). Lack of correlation between dyskinesia and pallidal serotonin transporter expression-induced by L-Dopa and Pramipexole in hemiparkinsonian rats. Pharmacology Biochemistry and Behavior. 197. 173012–173012. 1 indexed citations
3.
Jiménez‐Urbieta, Haritz, Belén Gago, Ana Quiroga‐Varela, et al.. (2020). Motor impulsivity and delay intolerance are elicited in a dose-dependent manner with a dopaminergic agonist in parkinsonian rats. Psychopharmacology. 237(8). 2419–2431. 5 indexed citations
4.
Marı́n, Concepció, Cristóbal Langdon, Isam Alobid, & Joaquim Mullol. (2020). Olfactory Dysfunction in Traumatic Brain Injury: the Role of Neurogenesis. Current Allergy and Asthma Reports. 20(10). 55–55. 17 indexed citations
5.
Marı́n, Concepció, M. Bonastre, Mireya Fuentes, & Joaquim Mullol. (2020). Globus pallidus, but not entopeduncular nucleus, 6-OHDA-induced lesion attenuates L-Dopa-induced dyskinesia in the rat model of Parkinson's disease. Pharmacology Biochemistry and Behavior. 197. 173013–173013. 1 indexed citations
6.
Langdon, Cristóbal, Isam Alobid, Llorenç Quintó, et al.. (2019). Self-perception of olfactory dysfunction is associated with history of Traumatic Brain Injury: post-hoc analysis from the OLFACAT survey. Rhinology Journal. 57(6). 460–468. 4 indexed citations
7.
Gago, Belén, Ana Quiroga‐Varela, Carlos Juri, et al.. (2015). Monoaminergic PET imaging and histopathological correlation in unilateral and bilateral 6-hydroxydopamine lesioned rat models of Parkinson's disease: A longitudinal in-vivo study. Neurobiology of Disease. 77. 165–172. 17 indexed citations
8.
Marı́n, Concepció, M. Bonastre, Guadalupe Mengod, Roser Cortés, & María Rodríguez‐Oroz. (2015). From unilateral to bilateral parkinsonism: Effects of lateralization on dyskinesias and associated molecular mechanisms. Neuropharmacology. 97. 365–375. 12 indexed citations
9.
Roé-Vellvé, Núria, Carles Falcón, A. Cot, et al.. (2014). Quantification of rat brain SPECT with123I-ioflupane: evaluation of different reconstruction methods and image degradation compensations using Monte Carlo simulation. Physics in Medicine and Biology. 59(16). 4567–4582. 2 indexed citations
10.
Marı́n, Concepció, M. Bonastre, Guadalupe Mengod, et al.. (2013). Subthalamic 6-OHDA-induced lesion attenuates levodopa-induced dyskinesias in the rat model of Parkinson's disease. Experimental Neurology. 250. 304–312. 9 indexed citations
11.
Mullol, Joaquim, Isam Alobid, Franklin Mariño‐Sánchez, et al.. (2012). Furthering the understanding of olfaction, prevalence of loss of smell and risk factors: a population-based survey (OLFACAT study). BMJ Open. 2(6). e001256–e001256. 161 indexed citations
12.
Marı́n, Concepció & Esther Aguilar. (2011). In vivo 6-OHDA-induced neurodegeneration and nigral autophagic markers expression. Neurochemistry International. 58(4). 521–526. 29 indexed citations
13.
Marı́n, Concepció, Esther Aguilar, María Rodríguez‐Oroz, Gerd D. Bartoszyk, & José Á. Obeso. (2009). Local administration of sarizotan into the subthalamic nucleus attenuates levodopa-induced dyskinesias in 6-OHDA-lesioned rats. Psychopharmacology. 204(2). 241–250. 48 indexed citations
14.
Aguilar, Esther, et al.. (2007). Differential nigral expression of bcl-2 protein family in the pure and common forms of Dementia with Lewy bodies: relevance for dopaminergic neuronal vulnerability. Journal of Neural Transmission. 114(11). 1469–1477. 4 indexed citations
15.
Marı́n, Concepció, Esther Aguilar, M. Bonastre, Eduardo Tolosa, & José Á. Obeso. (2005). Early administration of entacapone prevents levodopa-induced motor fluctuations in hemiparkinsonian rats. Experimental Neurology. 192(1). 184–193. 33 indexed citations
16.
Marı́n, Concepció, M. Bonastre, Miquel Vila, et al.. (2001). LY293558, an AMPA glutamate receptor antagonist, prevents and reverses levodopa‐induced motor alterations in Parkinsonian rats. Synapse. 42(1). 40–47. 44 indexed citations
17.
Vila, Miquel, Concepció Marı́n, Merle Ruberg, et al.. (1999). Systemic Administration of NMDA and AMPA Receptor Antagonists Reverses the Neurochemical Changes Induced by Nigrostriatal Denervation in Basal Ganglia. Journal of Neurochemistry. 73(1). 344–352. 44 indexed citations
18.
Barone, Paolo, et al.. (1990). Dopamine D1 receptor modulation of pilocarpine-induced convulsions. Neuroscience. 34(1). 209–217. 39 indexed citations
19.
Parashos, Sotirios A., et al.. (1990). Effect of chronic D-1 and/or D-2 dopamine antagonist treatment on SKF 38393-induced non-stereotyped grooming. Psychopharmacology. 102(3). 411–413. 14 indexed citations
20.
Parashos, Sotirios A., Concepció Marı́n, & Thomas N. Chase. (1989). Synergy between a selective D1 antagonist and a selective D2 antagonist in the induction of catalepsy. Neuroscience Letters. 105(1-2). 169–173. 26 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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