Josefa Sabrià

1.1k total citations
35 papers, 866 citations indexed

About

Josefa Sabrià is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Biochemistry. According to data from OpenAlex, Josefa Sabrià has authored 35 papers receiving a total of 866 indexed citations (citations by other indexed papers that have themselves been cited), including 23 papers in Molecular Biology, 18 papers in Cellular and Molecular Neuroscience and 6 papers in Biochemistry. Recurrent topics in Josefa Sabrià's work include Neuroscience and Neuropharmacology Research (16 papers), Amino Acid Enzymes and Metabolism (6 papers) and Mast cells and histamine (6 papers). Josefa Sabrià is often cited by papers focused on Neuroscience and Neuropharmacology Research (16 papers), Amino Acid Enzymes and Metabolism (6 papers) and Mast cells and histamine (6 papers). Josefa Sabrià collaborates with scholars based in Spain, United States and Sweden. Josefa Sabrià's co-authors include Anna Bassols, José Rodrı́guez-Álvarez, Jesús Osada, Cristina Costa, J. Tibau, P.D. Eckersall, Nahuai Badiola, Noemí Robles, Cristina Malagelada and Joan X. Comella and has published in prestigious journals such as PLoS ONE, Stroke and Biochemical and Biophysical Research Communications.

In The Last Decade

Josefa Sabrià

35 papers receiving 848 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Josefa Sabrià Spain 15 445 232 120 119 104 35 866
Judith Fischer Germany 19 521 1.2× 268 1.2× 168 1.4× 66 0.6× 71 0.7× 34 1.3k
Aída Marino Spain 20 439 1.0× 159 0.7× 113 0.9× 64 0.5× 40 0.4× 74 989
Tatsuo Nakahara Japan 26 859 1.9× 395 1.7× 124 1.0× 77 0.6× 48 0.5× 119 2.1k
Eun Jin Yang South Korea 21 499 1.1× 108 0.5× 215 1.8× 84 0.7× 49 0.5× 47 1.4k
Simonetta Simonetti Italy 16 909 2.0× 262 1.1× 192 1.6× 90 0.8× 47 0.5× 36 2.0k
Sunita Sharma United States 17 574 1.3× 102 0.4× 176 1.5× 50 0.4× 61 0.6× 58 1.2k
Huan Cai United States 18 599 1.3× 180 0.8× 279 2.3× 56 0.5× 115 1.1× 26 1.3k
Antonia Alonso Spain 17 305 0.7× 180 0.8× 166 1.4× 54 0.5× 74 0.7× 43 1.0k
Tatsuya Ingi Japan 11 803 1.8× 243 1.0× 87 0.7× 163 1.4× 53 0.5× 11 1.1k
Torsten Lowin Germany 19 244 0.5× 145 0.6× 106 0.9× 39 0.3× 56 0.5× 43 1.0k

Countries citing papers authored by Josefa Sabrià

Since Specialization
Citations

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

Fields of papers citing papers by Josefa Sabrià

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Josefa Sabrià

This figure shows the co-authorship network connecting the top 25 collaborators of Josefa Sabrià. A scholar is included among the top collaborators of Josefa Sabrià 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 Josefa Sabrià. Josefa Sabrià 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.
González-Sepúlveda, Marta, Miquel Vila, Jesús Giraldo, et al.. (2022). Spontaneous changes in brain striatal dopamine synthesis and storage dynamics ex vivo reveal end-product feedback-inhibition of tyrosine hydroxylase. Neuropharmacology. 212. 109058–109058. 6 indexed citations
2.
Arroyo, Laura, et al.. (2020). Neurobiology of environmental enrichment in pigs: hanges in monoaminergic neurotransmitters in several brain areas and in the hippocampal proteome. Journal of Proteomics. 229. 103943–103943. 14 indexed citations
3.
Sabrià, Josefa, et al.. (2014). Agonist and Antagonist Effects of Aripiprazole on D2-Like Receptors Controlling Rat Brain Dopamine Synthesis Depend on the Dopaminergic Tone. The International Journal of Neuropsychopharmacology. 18(4). pyu046–pyu046. 23 indexed citations
4.
Gallego, Xavier, Jéssica Ruiz‐Medina, Olga Valverde, et al.. (2012). Transgenic over expression of nicotinic receptor alpha 5, alpha 3, and beta 4 subunit genes reduces ethanol intake in mice. Alcohol. 46(3). 205–215. 26 indexed citations
5.
Badiola, Nahuai, Clara Penas, Alfredo J. Miñano‐Molina, et al.. (2011). Induction of ER stress in response to oxygen-glucose deprivation of cortical cultures involves the activation of the PERK and IRE-1 pathways and of caspase-12. Cell Death and Disease. 2(4). e149–e149. 135 indexed citations
6.
Gallego, Xavier, Susanna Molas, Alejandro Amador‐Arjona, et al.. (2011). Overexpression of the CHRNA5/A3/B4 genomic cluster in mice increases the sensitivity to nicotine and modifies its reinforcing effects. Amino Acids. 43(2). 897–909. 30 indexed citations
7.
Badiola, Nahuai, Cristina Malagelada, Núria Llecha, et al.. (2009). Activation of caspase-8 by tumour necrosis factor receptor 1 is necessary for caspase-3 activation and apoptosis in oxygen–glucose deprived cultured cortical cells. Neurobiology of Disease. 35(3). 438–447. 41 indexed citations
8.
Robles, Noemí & Josefa Sabrià. (2008). Effects of moderate chronic ethanol consumption on hippocampal nicotinic receptors and associative learning. Neurobiology of Learning and Memory. 89(4). 497–503. 26 indexed citations
9.
Robles, Noemí & Josefa Sabrià. (2006). Ethanol Consumption Produces Changes in Behavior and on Hippocampal α7 and α4β2 Nicotinic Receptors. Journal of Molecular Neuroscience. 30(1-2). 119–120. 4 indexed citations
10.
Malagelada, Cristina, et al.. (2005). Contribution of caspase-mediated apoptosis to the cell death caused by oxygen–glucose deprivation in cortical cell cultures. Neurobiology of Disease. 20(1). 27–37. 43 indexed citations
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Toledo, Alessandra Choqueta de, et al.. (1991). A comparative study of histamine and K+ effects on (Ca2+Mg2+)-ATPase activity in synaptosomes. Biochemical Pharmacology. 41(12). 1981–1986. 2 indexed citations
14.
Sabrià, Josefa, et al.. (1990). Separation and quantification of histamine and Nτ‐methylhistamine in brain extracts. Biomedical Chromatography. 4(6). 245–248. 3 indexed citations
15.
Sabrià, Josefa, et al.. (1989). Synaptosomal (Ca2+-Mg2+)-ATPase activity modulation by cyclic AMP. Biochemical Pharmacology. 38(19). 3219–3222. 1 indexed citations
16.
Sabrià, Josefa, et al.. (1988). Histamine stimulated synaptosomal Ca2+ uptake through activation of calcium channels. Biochemical and Biophysical Research Communications. 153(3). 1136–1143. 7 indexed citations
17.
Toledo, Alessandra Choqueta de, et al.. (1988). Properties and Ontogenic Development of Membrane‐Bound Histidine Decarboxylase from Rat Brain. Journal of Neurochemistry. 51(5). 1400–1406. 6 indexed citations
18.
Ferrer, Isidró, Alessandra Choqueta de Toledo, Josefa Sabrià, et al.. (1987). Subcellular localization of brain mast cell histamine in developing rat. Neurochemistry International. 11(4). 451–461. 4 indexed citations
19.
Sabrià, Josefa, et al.. (1987). Effects of altered thyroid function on histamine levels and mast cell number in neonatal rat brain.. Journal of Pharmacology and Experimental Therapeutics. 240(2). 612–616. 13 indexed citations
20.
Blanco, Isabel, et al.. (1978). Effect of experimental hyper-and hypothyroidism on neonatal rat brain histamine levels. Inflammation Research. 8(4). 384–384. 1 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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