Joaquı́n Del Rı́o

3.0k total citations
55 papers, 2.5k citations indexed

About

Joaquı́n Del Rı́o is a scholar working on Cellular and Molecular Neuroscience, Molecular Biology and Behavioral Neuroscience. According to data from OpenAlex, Joaquı́n Del Rı́o has authored 55 papers receiving a total of 2.5k indexed citations (citations by other indexed papers that have themselves been cited), including 39 papers in Cellular and Molecular Neuroscience, 15 papers in Molecular Biology and 12 papers in Behavioral Neuroscience. Recurrent topics in Joaquı́n Del Rı́o's work include Neuroscience and Neuropharmacology Research (23 papers), Neurotransmitter Receptor Influence on Behavior (19 papers) and Receptor Mechanisms and Signaling (13 papers). Joaquı́n Del Rı́o is often cited by papers focused on Neuroscience and Neuropharmacology Research (23 papers), Neurotransmitter Receptor Influence on Behavior (19 papers) and Receptor Mechanisms and Signaling (13 papers). Joaquı́n Del Rı́o collaborates with scholars based in Spain, Germany and France. Joaquı́n Del Rı́o's co-authors include Berta Lasheras, R.M. Tordera, Marı́a J. Ramı́rez, Diana Frechilla, Bárbara Aisa, Javier Garzón, N. Elizalde, Rebeca Martínez-Turrillas, Norberto Aguirre and Ana Garcı́a-Osta and has published in prestigious journals such as Scientific Reports, Biological Psychiatry and Brain Research.

In The Last Decade

Joaquı́n Del Rı́o

55 papers receiving 2.4k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Joaquı́n Del Rı́o Spain	28	1.1k	876	625	455	424	55	2.5k
Paola Casolini Italy	24	1.0k 0.9×	1.3k 1.5×	915 1.5×	456 1.0×	394 0.9×	45	2.7k
Krzysztof Wędzony Poland	35	1.6k 1.4×	735 0.8×	552 0.9×	828 1.8×	481 1.1×	94	2.8k
Wayne Rowe Canada	27	1.2k 1.1×	951 1.1×	521 0.8×	789 1.7×	243 0.6×	44	2.7k
Sabine Chourbaji Germany	26	820 0.7×	1.1k 1.2×	613 1.0×	379 0.8×	545 1.3×	45	2.4k
R.M. Tordera Spain	30	909 0.8×	1.4k 1.6×	843 1.3×	631 1.4×	894 2.1×	51	3.0k
Monique Vallée France	28	925 0.8×	1.6k 1.8×	1.1k 1.7×	513 1.1×	320 0.8×	56	3.2k
Katerina Antoniou Greece	27	1.0k 0.9×	1.1k 1.3×	685 1.1×	310 0.7×	549 1.3×	65	2.6k
Nitsan Kozlovsky Israel	29	701 0.6×	1.2k 1.3×	541 0.9×	742 1.6×	433 1.0×	47	2.7k
Lisa E. Kalynchuk Canada	28	1.1k 0.9×	1.4k 1.6×	680 1.1×	533 1.2×	983 2.3×	87	3.2k
Lynn G. Kirby United States	24	1.8k 1.6×	838 1.0×	635 1.0×	853 1.9×	350 0.8×	44	3.0k

Countries citing papers authored by Joaquı́n Del Rı́o

Since Specialization

Citations

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

Fields of papers citing papers by Joaquı́n Del Rı́o

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Joaquı́n Del Rı́o. 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 Joaquı́n Del Rı́o. The network helps show where Joaquı́n Del Rı́o may publish in the future.

Co-authorship network of co-authors of Joaquı́n Del Rı́o

This figure shows the co-authorship network connecting the top 25 collaborators of Joaquı́n Del Rı́o. A scholar is included among the top collaborators of Joaquı́n Del Rı́o 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 Joaquı́n Del Rı́o. Joaquı́n Del Rı́o 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

Rı́o, Joaquı́n Del, et al.. (2023). Variations in cochlea shape reveal different evolutionary adaptations in primates and rodents. Scientific Reports. 13(1). 2235–2235. 3 indexed citations

Rı́o, Joaquı́n Del, et al.. (2023). The shape of water: adaptations of cochlea morphology in seals and otters. Zoological Journal of the Linnean Society. 199(1). 45–59. 1 indexed citations

Harro, Jaanus, Tanel Kaart, Denis Matrov, et al.. (2014). Revealing the cerebral regions and networks mediating vulnerability to depression: Oxidative metabolism mapping of rat brain. Behavioural Brain Research. 267. 83–94. 23 indexed citations

Garcia‐García, Álvaro L., N. Elizalde, Marı́a J. Ramı́rez, et al.. (2012). Regulation of serotonin (5-HT) function by a VGLUT1 dependent glutamate pathway. Neuropharmacology. 70. 190–199. 6 indexed citations

Jahanshahi, Ali, Erwan Le Maître, Yasin Temel, et al.. (2011). Altered expression of neuronal tryptophan hydroxylase-2 mRNA in the dorsal and median raphe nuclei of three genetically modified mouse models relevant to depression and anxiety. Journal of Chemical Neuroanatomy. 41(4). 227–233. 12 indexed citations

Solas, Maite, Bárbara Aisa, Carmen Mugueta, et al.. (2010). Interactions Between Age, Stress and Insulin on Cognition: Implications for Alzheimer's Disease. Neuropsychopharmacology. 35(8). 1664–1673. 100 indexed citations

Garcia‐García, Álvaro L., N. Elizalde, Denis Matrov, et al.. (2009). Increased Vulnerability to Depressive-Like Behavior of Mice with Decreased Expression of VGLUT1. Biological Psychiatry. 66(3). 275–282. 105 indexed citations

Viñuela, Alicia Celemín, et al.. (2009). Electromyographic study of activity of the masseter and anterior temporalis muscles in patients with temporomandibular joint (TMJ) dysfuction: Comparison with the clinical dysfunction index. Medicina oral, patología oral y cirugía bucal. 15(1). e14–e19. 22 indexed citations

Aisa, Bárbara, N. Elizalde, R.M. Tordera, et al.. (2009). Effects of neonatal stress on markers of synaptic plasticity in the hippocampus: Implications for spatial memory. Hippocampus. 19(12). 1222–1231. 149 indexed citations

10.

Salazar‐Colocho, Pablo, José L. Lanciego, Joaquı́n Del Rı́o, & Diana Frechilla. (2008). Ischemia induces cell proliferation and neurogenesis in the gerbil hippocampus in response to neuronal death. Neuroscience Research. 61(1). 27–37. 41 indexed citations

11.

Salazar‐Colocho, Pablo, Joaquı́n Del Rı́o, & Diana Frechilla. (2008). Neuroprotective effects of serotonin 5-HT1A receptor activation against ischemic cell damage in gerbil hippocampus: Involvement of NMDA receptor NR1 subunit and BDNF. Brain Research. 1199. 159–166. 34 indexed citations

12.

Salazar‐Colocho, Pablo, Joaquı́n Del Rı́o, & Diana Frechilla. (2008). Involvement of the vascular wall in regenerative processes after CA1 ischemic neuronal death. International Journal of Developmental Neuroscience. 26(6). 541–550. 5 indexed citations

13.

Martínez-Turrillas, Rebeca, et al.. (2006). Differential effects of 3,4-methylenedioxymethamphetamine (MDMA, “ecstasy”) on BDNF mRNA expression in rat frontal cortex and hippocampus. Neuroscience Letters. 402(1-2). 126–130. 35 indexed citations

14.

Martínez-Turrillas, Rebeca, Joaquı́n Del Rı́o, & Diana Frechilla. (2006). Neuronal proteins involved in synaptic targeting of AMPA receptors in rat hippocampus by antidepressant drugs. Biochemical and Biophysical Research Communications. 353(3). 750–755. 27 indexed citations

15.

Schiapparelli, Lucio, Joaquı́n Del Rı́o, & Diana Frechilla. (2005). Serotonin 5‐HT_1Areceptor blockade enhances Ca²⁺/calmodulin‐dependent protein kinase II function and membrane expression of AMPA receptor subunits in the rat hippocampus: implications for memory formation. Journal of Neurochemistry. 94(4). 884–895. 41 indexed citations

16.

Garcı́a-Osta, Ana, Joaquı́n Del Rı́o, & Diana Frechilla. (2004). Increased CRE-binding activity and tryptophan hydroxylase mRNA expression induced by 3,4-methylenedioxymethamphetamine (MDMA, “ecstasy”) in the rat frontal cortex but not in the hippocampus. Molecular Brain Research. 126(2). 181–187. 21 indexed citations

17.

Pérez‐Silanes, Silvia, Thierry Langer, Salvatore Guccione, et al.. (2002). Synthesis and Molecular Modeling of New 1-Aryl-3-[4-arylpiperazin-1-yl]-1-propane Derivatives with High Affinity at the Serotonin Transporter and at 5-HT_1A Receptors. Journal of Medicinal Chemistry. 45(19). 4128–4139. 39 indexed citations

18.

Ballaz, Santiago, A Barber, Ana Fortuño, et al.. (1997). Pharmacological evaluation of IQM‐95,333, a highly selective CCK_Areceptor antagonist with anxiolytic‐like activity in animal models. British Journal of Pharmacology. 121(4). 759–767. 34 indexed citations

19.

Romero, Gonzalo, et al.. (1994). Effect of prenatal exposure to antidepressants on 5-HT-stimulated phosphoinositide hydrolysis and 5-HT2 receptors in rat brain. General Pharmacology The Vascular System. 25(5). 851–856. 16 indexed citations

20.

Fernández-Tomé, Paz, et al.. (1980). Increased dopamine receptor binding in the striatum of rats after long-term isolation. European Journal of Pharmacology. 65(4). 463–464. 55 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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