Derek D. Norman

2.0k total citations
51 papers, 1.6k citations indexed

About

Derek D. Norman is a scholar working on Molecular Biology, Cell Biology and Epidemiology. According to data from OpenAlex, Derek D. Norman has authored 51 papers receiving a total of 1.6k indexed citations (citations by other indexed papers that have themselves been cited), including 33 papers in Molecular Biology, 12 papers in Cell Biology and 10 papers in Epidemiology. Recurrent topics in Derek D. Norman's work include Sphingolipid Metabolism and Signaling (26 papers), Endoplasmic Reticulum Stress and Disease (9 papers) and Research on Leishmaniasis Studies (4 papers). Derek D. Norman is often cited by papers focused on Sphingolipid Metabolism and Signaling (26 papers), Endoplasmic Reticulum Stress and Disease (9 papers) and Research on Leishmaniasis Studies (4 papers). Derek D. Norman collaborates with scholars based in United States, Hungary and Japan. Derek D. Norman's co-authors include Gábor Tigyi, Gábor Tigyi, Sue Çhin Lee, Abby L. Parrill, Duane D. Miller, Daniel L. Baker, Alan Lichtenstein, Michael L. Tuck, James R. Sowers and Renukadevi Patil and has published in prestigious journals such as Journal of the American Chemical Society, Journal of Biological Chemistry and Blood.

In The Last Decade

Derek D. Norman

50 papers receiving 1.6k citations

Author Peers

Peers are selected by citation overlap in the author's most active subfields. citations · hero ref

Author Last Decade Papers Cites
Derek D. Norman 762 307 244 201 185 51 1.6k
William T. Gunning 1.1k 1.5× 186 0.6× 406 1.7× 258 1.3× 127 0.7× 105 2.5k
Yoshiharu Takayama 1.1k 1.5× 210 0.7× 164 0.7× 177 0.9× 103 0.6× 43 2.9k
Karen M. Lounsbury 1.9k 2.4× 298 1.0× 312 1.3× 204 1.0× 101 0.5× 56 2.8k
Takayuki Okamoto 1.1k 1.4× 121 0.4× 111 0.5× 212 1.1× 112 0.6× 67 2.1k
Sabina Janciauskiene 594 0.8× 403 1.3× 78 0.3× 375 1.9× 144 0.8× 75 1.8k
Huajun Wang 1.1k 1.5× 99 0.3× 119 0.5× 186 0.9× 164 0.9× 66 2.3k
I‐Ling Lin 673 0.9× 143 0.5× 112 0.5× 170 0.8× 212 1.1× 56 1.4k
A S Harris 731 1.0× 402 1.3× 292 1.2× 109 0.5× 103 0.6× 44 2.1k
Vikas Kumar 1.4k 1.8× 310 1.0× 95 0.4× 313 1.6× 167 0.9× 70 2.7k
Valentina Pucino 919 1.2× 203 0.7× 65 0.3× 307 1.5× 219 1.2× 40 2.5k

Countries citing papers authored by Derek D. Norman

Since Specialization
Citations

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

Fields of papers citing papers by Derek D. Norman

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Derek D. Norman. 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 Derek D. Norman. The network helps show where Derek D. Norman may publish in the future.

Co-authorship network of co-authors of Derek D. Norman

This figure shows the co-authorship network connecting the top 25 collaborators of Derek D. Norman. A scholar is included among the top collaborators of Derek D. Norman 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 Derek D. Norman. Derek D. Norman 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.
Lin, Kuan‐Hung, Sue Çhin Lee, Derek D. Norman, et al.. (2023). E2F7 drives autotaxin/Enpp2 transcription via chromosome looping: Repression by p53 in murine but not in human carcinomas. The FASEB Journal. 37(7). e23058–e23058. 2 indexed citations
2.
3.
Scheich, Bálint, Sándor Paku, Zoltán Pós, et al.. (2023). A dual role of lysophosphatidic acid type 2 receptor (LPAR2) in nonsteroidal anti-inflammatory drug-induced mouse enteropathy. Acta Pharmacologica Sinica. 45(2). 339–353. 3 indexed citations
4.
Norman, Derek D., et al.. (2023). Emerging roles of lysophosphatidic acid receptor subtype 5 (LPAR5) in inflammatory diseases and cancer. Pharmacology & Therapeutics. 245. 108414–108414. 13 indexed citations
5.
Lee, Sue Çhin, Derek D. Norman, Kuan‐Hung Lin, et al.. (2022). Prometastatic Effect of ATX Derived from Alveolar Type II Pneumocytes and B16-F10 Melanoma Cells. Cancers. 14(6). 1586–1586. 4 indexed citations
6.
Banerjee, Souvik, Sue-Chin Lee, Derek D. Norman, & Gábor Tigyi. (2022). Designing Dual Inhibitors of Autotaxin-LPAR GPCR Axis. Molecules. 27(17). 5487–5487. 12 indexed citations
7.
Tigyi, Gábor, Kuan‐Hung Lin, Junming Yue, et al.. (2021). Anti-cancer strategies targeting the autotaxin-lysophosphatidic acid receptor axis: is there a path forward?. Cancer and Metastasis Reviews. 40(1). 3–5. 13 indexed citations
8.
Lee, Sue Çhin, Derek D. Norman, Louisa Balázs, et al.. (2020). Regulation of Tumor Immunity by Lysophosphatidic Acid. Cancers. 12(5). 1202–1202. 39 indexed citations
9.
Morstein, Johannes, Derek D. Norman, Prashant Donthamsetti, et al.. (2020). Optical Control of Lysophosphatidic Acid Signaling. Journal of the American Chemical Society. 142(24). 10612–10616. 37 indexed citations
10.
Lee, Sue Çhin, Kuan‐Hung Lin, Andrea Balogh, et al.. (2020). Dysregulation of lysophospholipid signaling by p53 in malignant cells and the tumor microenvironment. Cellular Signalling. 78. 109850–109850. 7 indexed citations
11.
Banerjee, Souvik, Derek D. Norman, Shanshan Deng, et al.. (2020). Molecular modelling guided design, synthesis and QSAR analysis of new small molecule non-lipid autotaxin inhibitors. Bioorganic Chemistry. 103. 104188–104188. 6 indexed citations
12.
Morstein, Johannes, Rose Z. Hill, A. Novák, et al.. (2019). Optical control of sphingosine-1-phosphate formation and function. Nature Chemical Biology. 15(6). 623–631. 68 indexed citations
13.
Kuo, Bryan, Erzsébet Szabó, Sue Çhin Lee, et al.. (2018). The LPA2 receptor agonist Radioprotectin-1 spares Lgr5-positive intestinal stem cells from radiation injury in murine enteroids. Cellular Signalling. 51. 23–33. 19 indexed citations
14.
Tigyi, Gábor, Junming Yue, Derek D. Norman, et al.. (2018). Regulation of tumor cell – Microenvironment interaction by the autotaxin-lysophosphatidic acid receptor axis. Advances in Biological Regulation. 71. 183–193. 51 indexed citations
15.
Norman, Derek D., et al.. (2016). Discovery and synthetic optimization of a novel scaffold for hydrophobic tunnel-targeted autotaxin inhibition. Bioorganic & Medicinal Chemistry. 24(19). 4660–4674. 7 indexed citations
16.
Patil, Renukadevi, Erzsébet Szabó, James I. Fells, et al.. (2015). Combined Mitigation of the Gastrointestinal and Hematopoietic Acute Radiation Syndromes by an LPA2 Receptor-Specific Nonlipid Agonist. Chemistry & Biology. 22(2). 206–216. 34 indexed citations
17.
Balogh, Andrea, Yoshibumi Shimizu, Sue Çhin Lee, et al.. (2015). The autotaxin–LPA 2 GPCR axis is modulated by γ-irradiation and facilitates DNA damage repair. Cellular Signalling. 27(9). 1751–1762. 44 indexed citations
18.
Lee, Sue-Chin, Yuko Fujiwara, Jianxiong Liu, et al.. (2014). Autotaxin and LPA1 and LPA5 Receptors Exert Disparate Functions in Tumor Cells versus the Host Tissue Microenvironment in Melanoma Invasion and Metastasis. Molecular Cancer Research. 13(1). 174–185. 72 indexed citations
19.
Patil, Renukadevi, James I. Fells, Erzsébet Szabó, et al.. (2014). Design and Synthesis of Sulfamoyl Benzoic Acid Analogues with Subnanomolar Agonist Activity Specific to the LPA2 Receptor. Journal of Medicinal Chemistry. 57(16). 7136–7140. 13 indexed citations
20.
Morales‐Lázaro, Sara L., Itzel Llorente, Ricardo González‐Ramírez, et al.. (2014). Structural Determinants of the Transient Receptor Potential 1 (TRPV1) Channel Activation by Phospholipid Analogs. Journal of Biological Chemistry. 289(35). 24079–24090. 32 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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