Laura E. Chavez-Noriega

2.3k total citations
22 papers, 1.9k citations indexed

About

Laura E. Chavez-Noriega is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Pharmacology. According to data from OpenAlex, Laura E. Chavez-Noriega has authored 22 papers receiving a total of 1.9k indexed citations (citations by other indexed papers that have themselves been cited), including 20 papers in Molecular Biology, 15 papers in Cellular and Molecular Neuroscience and 6 papers in Pharmacology. Recurrent topics in Laura E. Chavez-Noriega's work include Nicotinic Acetylcholine Receptors Study (15 papers), Neuroscience and Neuropharmacology Research (15 papers) and Receptor Mechanisms and Signaling (12 papers). Laura E. Chavez-Noriega is often cited by papers focused on Nicotinic Acetylcholine Receptors Study (15 papers), Neuroscience and Neuropharmacology Research (15 papers) and Receptor Mechanisms and Signaling (12 papers). Laura E. Chavez-Noriega collaborates with scholars based in United States, France and United Kingdom. Laura E. Chavez-Noriega's co-authors include Arturo Urrutia, Edwin C. Johnson, Kathryn Elliott, James H. Crona, Mark Washburn, R. Adron Harris, J. V. Halliwell, T.V.P. Bliss, Michael M. Harpold and Tomohiro Yamakura and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Biological Chemistry and Brain Research.

In The Last Decade

Laura E. Chavez-Noriega

22 papers receiving 1.9k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Laura E. Chavez-Noriega United States	20	1.5k	1.0k	268	265	122	22	1.9k
Mark Washburn United States	16	1.5k 1.0×	1.3k 1.3×	221 0.8×	291 1.1×	72 0.6×	18	2.1k
William Marszalec United States	24	957 0.6×	976 0.9×	167 0.6×	199 0.8×	75 0.6×	56	1.5k
Christopher M. de Fiebre United States	22	1.1k 0.7×	755 0.7×	255 1.0×	126 0.5×	77 0.6×	37	1.5k
Peter Curzon United States	28	1.3k 0.9×	855 0.8×	321 1.2×	288 1.1×	43 0.4×	41	1.9k
William E. Hoffmann United States	22	1.1k 0.7×	1.1k 1.1×	369 1.4×	584 2.2×	41 0.3×	44	2.2k
Katumi Sumikawa United States	26	1.5k 1.0×	1.2k 1.1×	217 0.8×	302 1.1×	69 0.6×	65	1.9k
Arturo Urrutia United States	11	1.2k 0.8×	664 0.6×	149 0.6×	59 0.2×	88 0.7×	12	1.3k
C. Reavill United Kingdom	23	1.0k 0.7×	1.2k 1.2×	166 0.6×	147 0.6×	32 0.3×	48	1.7k
Manolo Mugnaini Italy	19	881 0.6×	996 1.0×	119 0.4×	164 0.6×	22 0.2×	28	1.4k
Alexis Evrard France	15	1.0k 0.7×	1.1k 1.1×	114 0.4×	222 0.8×	31 0.3×	21	1.6k

Countries citing papers authored by Laura E. Chavez-Noriega

Since Specialization

Citations

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

Fields of papers citing papers by Laura E. Chavez-Noriega

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Laura E. Chavez-Noriega. 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 Laura E. Chavez-Noriega. The network helps show where Laura E. Chavez-Noriega may publish in the future.

Co-authorship network of co-authors of Laura E. Chavez-Noriega

This figure shows the co-authorship network connecting the top 25 collaborators of Laura E. Chavez-Noriega. A scholar is included among the top collaborators of Laura E. Chavez-Noriega 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 Laura E. Chavez-Noriega. Laura E. Chavez-Noriega 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

Chavez-Noriega, Laura E., Michael J. Marino, Hervé Schaffhauser, Una C. Campbell, & P. Jeffrey Conn. (2005). Novel Potential Therapeutics for Schizophrenia: Focus on the Modulation of Metabotropic Glutamate Receptor Function. Current Neuropharmacology. 3(1). 9–34. 18 indexed citations

Williams, Mark E., Bill Burton, Arturo Urrutia, et al.. (2004). Ric-3 Promotes Functional Expression of the Nicotinic Acetylcholine Receptor α7 Subunit in Mammalian Cells. Journal of Biological Chemistry. 280(2). 1257–1263. 134 indexed citations

Schaffhauser, Hervé, Blake A. Rowe, Laura E. Chavez-Noriega, et al.. (2003). Pharmacological Characterization and Identification of Amino Acids Involved in the Positive Modulation of Metabotropic Glutamate Receptor Subtype 2. Molecular Pharmacology. 64(4). 798–810. 137 indexed citations

Chavez-Noriega, Laura E., Hervé Schaffhauser, & Una C. Campbell. (2002). Metabotropic Glutamate Receptors: Potential Drug Targets for the Treatment of Schizophrenia. PubMed. 1(3). 261–281. 74 indexed citations

Zuo, Yi, Gary L. Aistrup, William Marszalec, et al.. (2001). Dual Action of n-Alcohols on Neuronal Nicotinic Acetylcholine Receptors. Molecular Pharmacology. 60(4). 700–711. 59 indexed citations

Yamakura, Tomohiro, Laura E. Chavez-Noriega, & R. Adron Harris. (2000). Subunit-dependent Inhibition of Human Neuronal Nicotinic Acetylcholine Receptors and Other Ligand-gated Ion Channels by Dissociative Anesthetics Ketamine and Dizocilpine. Anesthesiology. 92(4). 1144–1153. 124 indexed citations

Chavez-Noriega, Laura E., Alison Gillespie, Kenneth A. Stauderman, et al.. (2000). Characterization of the recombinant human neuronal nicotinic acetylcholine receptors α3β2 and α4β2 stably expressed in HEK293 cells. Neuropharmacology. 39(13). 2543–2560. 63 indexed citations

Cosford, Nicholas D. P., Leo Bleicher, Jean‐Michel Vernier, et al.. (2000). Recombinant human receptors and functional assays in the discovery of altinicline (SIB-1508Y), a novel acetylcholine-gated ion channel (nAChR) agonist. Pharmaceutica Acta Helvetiae. 74(2-3). 125–130. 20 indexed citations

Vernier, Jean‐Michel, Nicholas D. P. Cosford, Leo Bleicher, et al.. (1999). 4-[[2-(1-Methyl-2-pyrrolidinyl)ethyl]thio]- phenol Hydrochloride (SIB-1553A): A Novel Cognitive Enhancer with Selectivity for Neuronal Nicotinic Acetylcholine Receptors. Journal of Medicinal Chemistry. 42(10). 1684–1686. 36 indexed citations

10.

Cardoso, Rita A., et al.. (1999). Human Neuronal Nicotinic Acetylcholine Receptors Expressed in Xenopus Oocytes Predict Efficacy of Halogenated Compounds That Disobey the Meyer-Overton Rule . Anesthesiology. 91(5). 1370–1370. 40 indexed citations

11.

Lloyd, G. Kenneth, Frédérique Menzaghi, Bruno Bontempi, et al.. (1998). The potential of subtype-selective neuronal nicotinic acetylcholine receptor agonists as therapeutic agents. Life Sciences. 62(17-18). 1601–1606. 51 indexed citations

12.

Vernier, Jean‐Michel, Nicholas D. P. Cosford, Jeffrey P. Whitten, et al.. (1998). Conformationally restricted analogues of nicotine and anabasine. Bioorganic & Medicinal Chemistry Letters. 8(16). 2173–2178. 34 indexed citations

13.

Stauderman, Kenneth A., M. Akong, Gönül Veliçelebi, et al.. (1998). Characterization of Human Recombinant Neuronal Nicotinic Acetylcholine Receptor Subunit Combinations α2β4, α3β4 and α4β4 Stably Expressed in HEK293 Cells. Journal of Pharmacology and Experimental Therapeutics. 284(2). 777–789. 47 indexed citations

14.

Chavez-Noriega, Laura E., James H. Crona, Mark Washburn, et al.. (1997). Pharmacological Characterization of Recombinant Human Neuronal Nicotinic Acetylcholine Receptors hα2β2, hα2β4, hα3β2, hα3β4, hα4β2, hα4β4 and hα7 Expressed in Xenopus Oocytes. Journal of Pharmacology and Experimental Therapeutics. 280(1). 346–356. 180 indexed citations

15.

Hess, Stephen D., Lorrie P. Daggett, James H. Crona, et al.. (1996). Cloning and functional characterization of human heteromeric N-methyl-D-aspartate receptors.. Journal of Pharmacology and Experimental Therapeutics. 278(2). 808–816. 62 indexed citations

16.

Elliott, Kathryn, S.B. Ellis, Arturo Urrutia, et al.. (1996). Comparative structure of human neuronal α2–α7 and β2–β4 nicotinic acetylcholine receptor subunits and functional expression of the α2, α3, α4, α7, β2, and β4 subunits. Journal of Molecular Neuroscience. 7(3). 217–228. 89 indexed citations

17.

Chavez-Noriega, Laura E., J. V. Halliwell, & T.V.P. Bliss. (1990). A decrease in firing threshold observed after induction of the EPSP-spike (E-S) component of long-term potentiation in rat hippocampal slices. Experimental Brain Research. 79(3). 633–41. 95 indexed citations

18.

Chavez-Noriega, Laura E., et al.. (1990). Failure to reverse long-term potentiation by coupling sustained presynaptic activity and N-methyl-D-aspartate receptor blockade.. Proceedings of the National Academy of Sciences. 87(18). 7165–7169. 20 indexed citations

19.

Chavez-Noriega, Laura E., T.V.P. Bliss, & J. V. Halliwell. (1989). The EPSP-spike (E-S) component of long-term potentiation in the rat hippocampal slice is modulated by GABAergic but not cholinergic mechanisms. Neuroscience Letters. 104(1-2). 58–64. 102 indexed citations

20.

Chavez-Noriega, Laura E., et al.. (1986). Excitability changes induced in the striatal dopamine-containing terminals following frontal cortex stimulation. Brain Research. 379(2). 300–306. 13 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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