Kwok‐Tung Lu

3.2k total citations · 1 hit paper
46 papers, 2.7k citations indexed

About

Kwok‐Tung Lu is a scholar working on Cellular and Molecular Neuroscience, Molecular Biology and Cognitive Neuroscience. According to data from OpenAlex, Kwok‐Tung Lu has authored 46 papers receiving a total of 2.7k indexed citations (citations by other indexed papers that have themselves been cited), including 24 papers in Cellular and Molecular Neuroscience, 17 papers in Molecular Biology and 13 papers in Cognitive Neuroscience. Recurrent topics in Kwok‐Tung Lu's work include Neuroscience and Neuropharmacology Research (16 papers), Memory and Neural Mechanisms (11 papers) and Traumatic Brain Injury and Neurovascular Disturbances (9 papers). Kwok‐Tung Lu is often cited by papers focused on Neuroscience and Neuropharmacology Research (16 papers), Memory and Neural Mechanisms (11 papers) and Traumatic Brain Injury and Neurovascular Disturbances (9 papers). Kwok‐Tung Lu collaborates with scholars based in Taiwan, Russia and United States. Kwok‐Tung Lu's co-authors include Yi-Ling Yang, Kerry J. Ressler, David Walker, Michael Davis, Po‐Wu Gean, Po-Kuan Chao, Michael Davis, David L. Walker, Wen‐Chang Chang and Shiu-Hwa Yeh and has published in prestigious journals such as Neuron, Journal of Neuroscience and PLoS ONE.

In The Last Decade

Kwok‐Tung Lu

46 papers receiving 2.6k citations

Hit Papers

Facilitation of Condition... 2002 2026 2010 2018 2002 200 400 600

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Kwok‐Tung Lu Taiwan 25 1.2k 998 737 548 365 46 2.7k
Edward G. Meloni United States 26 1.5k 1.2× 651 0.7× 887 1.2× 491 0.9× 223 0.6× 37 2.7k
Susana Aznar Denmark 28 1.4k 1.2× 535 0.5× 696 0.9× 349 0.6× 324 0.9× 80 2.8k
Raymond Mongeau France 27 1.5k 1.2× 596 0.6× 858 1.2× 598 1.1× 170 0.5× 59 2.8k
Machiko Matsumoto Japan 32 1.1k 0.9× 593 0.6× 507 0.7× 408 0.7× 448 1.2× 82 2.3k
Roberto Frussa‐Filho Brazil 39 2.3k 1.9× 1.6k 1.6× 984 1.3× 586 1.1× 272 0.7× 158 4.3k
Yaghoub Fathollahi Iran 30 1.5k 1.2× 787 0.8× 489 0.7× 349 0.6× 264 0.7× 150 2.4k
Lung Yu Taiwan 29 1.1k 0.9× 468 0.5× 505 0.7× 457 0.8× 351 1.0× 85 2.5k
Anita C. Hansson Germany 33 2.6k 2.2× 1.0k 1.0× 1.3k 1.8× 702 1.3× 297 0.8× 83 4.3k
Douglas B. Matthews United States 32 2.0k 1.6× 961 1.0× 563 0.8× 586 1.1× 580 1.6× 47 2.9k
Leslie L. Devaud United States 31 2.3k 1.9× 498 0.5× 833 1.1× 793 1.4× 508 1.4× 65 3.2k

Countries citing papers authored by Kwok‐Tung Lu

Since Specialization
Citations

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

Fields of papers citing papers by Kwok‐Tung Lu

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Kwok‐Tung Lu. 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 Kwok‐Tung Lu. The network helps show where Kwok‐Tung Lu may publish in the future.

Co-authorship network of co-authors of Kwok‐Tung Lu

This figure shows the co-authorship network connecting the top 25 collaborators of Kwok‐Tung Lu. A scholar is included among the top collaborators of Kwok‐Tung Lu 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 Kwok‐Tung Lu. Kwok‐Tung Lu 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
2.
Chan, Michael W.Y., et al.. (2018). Neonatal Dexamethasone Treatment Suppresses Hippocampal Estrogen Receptor α Expression in Adolescent Female Rats. Molecular Neurobiology. 56(3). 2224–2233. 1 indexed citations
3.
Amstislavskaya, Tamara G., et al.. (2017). Fragile X Mental Retardation-1 Knockout Zebrafish Shows Precocious Development in Social Behavior. Zebrafish. 14(5). 438–443. 21 indexed citations
4.
Lu, Kwok‐Tung, et al.. (2016). Transient receptor potential vanilloid type 4 channels mediate Na‐K‐Cl‐co‐transporter‐induced brain edema after traumatic brain injury. Journal of Neurochemistry. 140(5). 718–727. 51 indexed citations
5.
Amstislavskaya, Tamara G., et al.. (2014). Inhibition of NKCC1 Attenuated Hippocampal LTP Formation and Inhibitory Avoidance in Rat. PLoS ONE. 9(11). e106692–e106692. 7 indexed citations
6.
Hung, Kuo‐Chuan, et al.. (2012). The pre‐emptive analgesic effect of a cyclooxygenase‐2 inhibitor in a rat model of acute postoperative pain. Anaesthesia. 67(11). 1225–1231. 6 indexed citations
7.
Yang, Yi-Ling, et al.. (2012). Effect of MK-801-induced impairment of inhibitory avoidance learning in zebrafish via inactivation of extracellular signal-regulated kinase (ERK) in telencephalon. Fish Physiology and Biochemistry. 38(4). 1099–1106. 40 indexed citations
9.
Lu, Kwok‐Tung, et al.. (2012). Early Systemic Granulocyte-Colony Stimulating Factor Treatment Attenuates Neuropathic Pain after Peripheral Nerve Injury. PLoS ONE. 7(8). e43680–e43680. 27 indexed citations
10.
Yang, Yi-Ling, et al.. (2012). Stimulation of the lateral division of the dorsal telencephalon induces synaptic plasticity in the medial division of adult zebrafish. Neuroscience Letters. 512(2). 109–113. 14 indexed citations
11.
Chen, Mei‐Yu, et al.. (2011). The novel indole compound SK228 induces apoptosis and FAK/Paxillin disruption in tumor cell lines and inhibits growth of tumor graft in the nude mouse. International Journal of Cancer. 131(3). 722–732. 28 indexed citations
12.
Yang, Yi-Ling, et al.. (2011). The role of the dorsal hippocampus on the Ginkgo biloba facilitation effect of fear extinction as assessed with fear-potentiated startle. Psychopharmacology. 215(3). 403–411. 7 indexed citations
13.
Lu, Kwok‐Tung, et al.. (2008). NKCC1-mediated traumatic brain injury-induced brain edema and neuron death via Raf/MEK/MAPK cascade. Critical Care Medicine. 36(3). 917–922. 74 indexed citations
14.
Yang, Yi-Ling, et al.. (2006). Extract of Ginkgo biloba EGb761 Facilitates Extinction of Conditioned Fear Measured by Fear-Potentiated Startle. Neuropsychopharmacology. 32(2). 332–342. 12 indexed citations
15.
Lu, Kwok‐Tung, et al.. (2006). Inhibition of the Na+–K+–2Cl−-cotransporter in choroid plexus attenuates traumatic brain injury-induced brain edema and neuronal damage. European Journal of Pharmacology. 548(1-3). 99–105. 57 indexed citations
16.
Yang, Yi-Ling, Po-Kuan Chao, & Kwok‐Tung Lu. (2005). Systemic and Intra-Amygdala Administration of Glucocorticoid Agonist and Antagonist Modulate Extinction of Conditioned Fear. Neuropsychopharmacology. 31(5). 912–924. 171 indexed citations
17.
Yang, Yi-Ling, et al.. (2005). Extract of Ginkgo biloba EGb 761 facilitates fear conditioning measured by fear-potentiated startle. Neuroscience Letters. 383(1-2). 145–150. 10 indexed citations
18.
Lu, Kwok‐Tung, et al.. (1999). Involvement of mitogen-activated protein kinase in hippocampal long-term potentiation. Journal of Biomedical Science. 6(6). 409–417. 35 indexed citations
19.
Yang, Yi-Ling, et al.. (1998). Heat shock protein expression protects against death following exposure to heatstroke in rats. Neuroscience Letters. 252(1). 9–12. 41 indexed citations
20.
Lu, Kwok‐Tung & Po‐Wu Gean. (1998). Endogenous serotonin inhibits epileptiform activity in rat hippocampal CA1 neurons via 5-hydroxytryptamine1A receptor activation. Neuroscience. 86(3). 729–737. 61 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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