T.E. Salt

8.5k total citations · 1 hit paper
125 papers, 6.8k citations indexed

About

T.E. Salt is a scholar working on Cellular and Molecular Neuroscience, Molecular Biology and Cognitive Neuroscience. According to data from OpenAlex, T.E. Salt has authored 125 papers receiving a total of 6.8k indexed citations (citations by other indexed papers that have themselves been cited), including 96 papers in Cellular and Molecular Neuroscience, 52 papers in Molecular Biology and 33 papers in Cognitive Neuroscience. Recurrent topics in T.E. Salt's work include Neuroscience and Neuropharmacology Research (77 papers), Photoreceptor and optogenetics research (32 papers) and Retinal Development and Disorders (27 papers). T.E. Salt is often cited by papers focused on Neuroscience and Neuropharmacology Research (77 papers), Photoreceptor and optogenetics research (32 papers) and Retinal Development and Disorders (27 papers). T.E. Salt collaborates with scholars based in United Kingdom, Mexico and United States. T.E. Salt's co-authors include R.G. Hill, S.A. Eaton, K. E. Binns, J.P. Turner, M. Francesca Cordeiro, Stephen E. Moss, Adam M. Sillito, Richard Morris, Robin R. Ali and R.H. Douglas and has published in prestigious journals such as Nature, Science and Proceedings of the National Academy of Sciences.

In The Last Decade

T.E. Salt

124 papers receiving 6.6k citations

Hit Papers

Retinal repair by transplantation of photoreceptor precur... 2006 2026 2012 2019 2006 250 500 750

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
T.E. Salt United Kingdom 44 3.9k 3.5k 1.3k 1.2k 1.1k 125 6.8k
Wing‐Ho Yung Hong Kong 47 3.1k 0.8× 2.0k 0.6× 1.0k 0.8× 784 0.7× 765 0.7× 180 7.3k
Nicholas C. Brecha United States 66 8.6k 2.2× 7.1k 2.0× 1.2k 0.9× 894 0.8× 1.1k 1.1× 197 12.0k
Luciano Domenici Italy 40 2.6k 0.7× 2.0k 0.6× 921 0.7× 366 0.3× 959 0.9× 104 5.3k
Vittorio Porciatti United States 49 2.9k 0.7× 5.5k 1.6× 1.5k 1.2× 4.0k 3.4× 342 0.3× 226 9.1k
Dan Goldowitz United States 47 2.9k 0.7× 4.0k 1.2× 754 0.6× 199 0.2× 507 0.5× 201 7.4k
Fan Gao United States 38 2.5k 0.6× 4.5k 1.3× 1.0k 0.8× 182 0.2× 1.2k 1.1× 123 7.8k
Charles K. Meshul United States 39 2.7k 0.7× 1.5k 0.4× 516 0.4× 423 0.4× 546 0.5× 130 4.9k
Giorgio Carmignoto Italy 52 9.4k 2.4× 4.8k 1.4× 2.9k 2.3× 427 0.4× 1.9k 1.7× 90 13.3k
David R. Copenhagen United States 45 4.8k 1.2× 4.2k 1.2× 1.2k 1.0× 245 0.2× 271 0.3× 93 6.3k
David V. Pow Australia 47 3.5k 0.9× 2.9k 0.8× 376 0.3× 409 0.4× 525 0.5× 119 5.7k

Countries citing papers authored by T.E. Salt

Since Specialization
Citations

This map shows the geographic impact of T.E. Salt'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 T.E. Salt with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites T.E. Salt more than expected).

Fields of papers citing papers by T.E. Salt

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by T.E. Salt. 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 T.E. Salt. The network helps show where T.E. Salt may publish in the future.

Co-authorship network of co-authors of T.E. Salt

This figure shows the co-authorship network connecting the top 25 collaborators of T.E. Salt. A scholar is included among the top collaborators of T.E. Salt 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 T.E. Salt. T.E. Salt 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.
2.
Luthert, Philip J., et al.. (2016). P2X7R modulation of visually evoked synaptic responses in the retina. Purinergic Signalling. 12(4). 611–625. 10 indexed citations
3.
Luthert, Philip J., et al.. (2014). Light-Evoked Retinal Ganglion Cell Synaptic Responses and Microglial Morphology are Modulated by P2X7 Receptor Activation and Bacterial Lipopolysaccharide (LPS). Investigative Ophthalmology & Visual Science. 55(13). 2384–2384. 1 indexed citations
4.
Guo, Li, et al.. (2014). Dendritic Changes in Rat Visual Pathway Associated with Experimental Ocular Hypertension. Current Eye Research. 39(9). 953–963. 17 indexed citations
5.
Jones, Helen, Ian Max Andolina, Bashir Ahmed, et al.. (2012). Differential Feedback Modulation of Center and Surround Mechanisms in Parvocellular Cells in the Visual Thalamus. Journal of Neuroscience. 32(45). 15946–15951. 32 indexed citations
6.
Guo, Li, et al.. (2010). Dendritic Changes in the Retinal Ganglion Cells in a Rat Model of Experimental Glaucoma. Investigative Ophthalmology & Visual Science. 51(13). 5217–5217. 1 indexed citations
7.
Duggan, James, et al.. (2010). Neuroprotection in glaucoma – Is there a future role?. Experimental Eye Research. 91(5). 554–566. 122 indexed citations
8.
Guo, Li, et al.. (2008). Dendritic Pathology in the Superior Colliculus in a Rat Model of Experimental Glaucoma. Investigative Ophthalmology & Visual Science. 49(13). 5199–5199. 37 indexed citations
9.
Cordeiro, M. Francesca, Li Guo, Alexander H. Maass, et al.. (2006). Beta Amyloid and Retinal Ganglion Cell Apoptosis: Implications and Applications to Glaucoma. Investigative Ophthalmology & Visual Science. 47(13). 2698–2698. 2 indexed citations
10.
Salt, T.E., Annelie Maaß, Li Guo, et al.. (2005). Retinal Ganglion Cell Apoptosis and Loss Assessed in vivo Using the ERG. Investigative Ophthalmology & Visual Science. 46(13). 3754–3754. 1 indexed citations
11.
Cirone, Jennifer, et al.. (2002). Distribution of metabotropic glutamate receptors in the superior colliculus of the adult rat, ferret and cat. Neuroscience. 109(4). 779–786. 19 indexed citations
12.
Q., Kim, et al.. (2002). Glial‐Neuronal Transfer of Arginine andS‐Nitrosothiols in Nitric Oxide Transmission. Annals of the New York Academy of Sciences. 962(1). 81–92. 16 indexed citations
13.
Binns, K. E., J.P. Turner, & T.E. Salt. (1999). Visual experience alters the molecular profile of NMDA‐receptor‐mediated sensory transmission. European Journal of Neuroscience. 11(3). 1101–1104. 7 indexed citations
14.
Turner, J.P. & T.E. Salt. (1999). Group III metabotropic glutamate receptors control corticothalamic synaptic transmission in the rat thalamus in vitro. The Journal of Physiology. 519(2). 481–491. 52 indexed citations
17.
Salt, T.E.. (1986). Mediation of thalamic sensory input by both NMDA receptors and non-NMDA receptors. Nature. 322(6076). 263–265. 162 indexed citations
18.
Sillito, Adam M., T.E. Salt, & John A. Kemp. (1984). GABAergic neuronal processes in the dorsolateral geniculate nucleus (dLGN) and putative interactions with somatostatin (SSt). Neuropharmacology. 23(7). 875–876. 3 indexed citations
19.
Salt, T.E. & R.G. Hill. (1981). Excitatory amino acids as transmitter candidates of vibrissae afferent fibres to the rat trigeminal nucleus caudalis. Neuroscience Letters. 22(2). 183–187. 26 indexed citations
20.
Salt, T.E. & R.G. Hill. (1980). The effects of microiontophoretically applied capsaicin and substance P on single neurones in the rat and cat brain. Neuroscience Letters. 20(3). 329–334. 20 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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