Ee Von Moo

513 total citations
13 papers, 340 citations indexed

About

Ee Von Moo is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Surgery. According to data from OpenAlex, Ee Von Moo has authored 13 papers receiving a total of 340 indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Molecular Biology, 8 papers in Cellular and Molecular Neuroscience and 2 papers in Surgery. Recurrent topics in Ee Von Moo's work include Receptor Mechanisms and Signaling (13 papers), Neuropeptides and Animal Physiology (8 papers) and Protein Kinase Regulation and GTPase Signaling (4 papers). Ee Von Moo is often cited by papers focused on Receptor Mechanisms and Signaling (13 papers), Neuropeptides and Animal Physiology (8 papers) and Protein Kinase Regulation and GTPase Signaling (4 papers). Ee Von Moo collaborates with scholars based in Denmark, United States and Japan. Ee Von Moo's co-authors include Hans Bräuner‐Osborne, Thor C. Møller, Jeffrey R. van Senten, Arthur Christopoulos, Céline Valant, Patrick M. Sexton, Dahlia A. Goldfeld, Kirill A. Martemyanov, Yinglong Miao and J. Andrew McCammon and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Biological Chemistry and FEBS Letters.

In The Last Decade

Ee Von Moo

13 papers receiving 335 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Ee Von Moo Denmark	8	283	145	65	34	29	13	340
William Gowen-MacDonald United States	5	343 1.2×	232 1.6×	61 0.9×	33 1.0×	26 0.9×	6	381
Ravi Kumar Verma Singapore	15	401 1.4×	195 1.3×	50 0.8×	32 0.9×	18 0.6×	27	506
Nicole A. Perry United States	12	379 1.3×	211 1.5×	81 1.2×	33 1.0×	30 1.0×	19	413
Rory Sleno Canada	11	424 1.5×	247 1.7×	28 0.4×	52 1.5×	32 1.1×	14	490
Yanting Yin United States	8	348 1.2×	196 1.4×	38 0.6×	34 1.0×	17 0.6×	11	379
Lama Yamani Canada	5	292 1.0×	136 0.9×	23 0.4×	30 0.9×	42 1.4×	8	365
Yangxia Tan China	7	286 1.0×	127 0.9×	27 0.4×	46 1.4×	13 0.4×	10	343
Haibei Hu United States	9	323 1.1×	76 0.5×	31 0.5×	22 0.6×	20 0.7×	10	418
Laerte Oliveira Brazil	14	469 1.7×	184 1.3×	54 0.8×	44 1.3×	15 0.5×	28	546
Wanjing Guo China	4	345 1.2×	189 1.3×	44 0.7×	66 1.9×	18 0.6×	6	429

Countries citing papers authored by Ee Von Moo

Since Specialization

Citations

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

Fields of papers citing papers by Ee Von Moo

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Ee Von Moo. 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 Ee Von Moo. The network helps show where Ee Von Moo may publish in the future.

Co-authorship network of co-authors of Ee Von Moo

This figure shows the co-authorship network connecting the top 25 collaborators of Ee Von Moo. A scholar is included among the top collaborators of Ee Von Moo 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 Ee Von Moo. Ee Von Moo is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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13 of 13 papers shown

Moo, Ee Von, Thor C. Møller, Flemming Brandt Sørensen, Asuka Inoue, & Hans Bräuner‐Osborne. (2025). Arrestin‐independent internalization of the GLP ‐1 receptor is facilitated by a GRK , clathrin, and caveolae‐dependent mechanism. FEBS Journal. 292(7). 1675–1695. 5 indexed citations

Stępniewski, Tomasz Maciej, Christian M. Madsen, Asuka Inoue, et al.. (2023). Migration mediated by the oxysterol receptor GPR183 depends on arrestin coupling but not receptor internalization. Science Signaling. 16(779). eabl4283–eabl4283. 4 indexed citations

Masuho, Ikuo, Ryoji Kise, Pablo Gaínza, et al.. (2023). Rules and mechanisms governing G protein coupling selectivity of GPCRs. Cell Reports. 42(10). 113173–113173. 32 indexed citations

Møller, Thor C., et al.. (2023). Characterization of the real-time internalization of nine GPCRs reveals distinct dependence on arrestins and G proteins. Biochimica et Biophysica Acta (BBA) - Molecular Cell Research. 1871(1). 119584–119584. 9 indexed citations

Moo, Ee Von, et al.. (2023). Endocytic proteins mediating GPR15 receptor internalization provide insight into the underlying mechanisms. FEBS Letters. 597(11). 1528–1540. 1 indexed citations

Senten, Jeffrey R. van, et al.. (2022). Use of CRISPR/Cas9-edited HEK293 cells reveals that both conventional and novel protein kinase C isozymes are involved in mGlu5a receptor internalization. Journal of Biological Chemistry. 298(10). 102466–102466. 7 indexed citations

Moo, Ee Von, et al.. (2022). Delineation of the GPR15 receptor‐mediated Gα protein signalling profile in recombinant mammalian cells. Basic & Clinical Pharmacology & Toxicology. 131(2). 104–113. 7 indexed citations

Moo, Ee Von, Jeffrey R. van Senten, Hans Bräuner‐Osborne, & Thor C. Møller. (2021). Arrestin-Dependent and -Independent Internalization of G Protein–Coupled Receptors: Methods, Mechanisms, and Implications on Cell Signaling. Molecular Pharmacology. 99(4). 242–255. 71 indexed citations

Moo, Ee Von, Kasper Harpsøe, Alexander S. Hauser, et al.. (2021). Ligand-directed bias of G protein signaling at the dopamine D2 receptor. Cell chemical biology. 29(2). 226–238.e4. 22 indexed citations

10.

Bartoszek, Adrian, Ee Von Moo, Agata Binienda, et al.. (2019). Free Fatty Acid Receptors as new potential therapeutic target in inflammatory bowel diseases. Pharmacological Research. 152. 104604–104604. 49 indexed citations

11.

Korczynska, Magdalena, Mary J. Clark, Céline Valant, et al.. (2018). Structure-based discovery of selective positive allosteric modulators of antagonists for the M ₂ muscarinic acetylcholine receptor. Proceedings of the National Academy of Sciences. 115(10). E2419–E2428. 54 indexed citations

12.

Moo, Ee Von, Patrick M. Sexton, Arthur Christopoulos, & Céline Valant. (2018). Utility of an “Allosteric Site-Impaired” M2 Muscarinic Acetylcholine Receptor as a Novel Construct for Validating Mechanisms of Action of Synthetic and Putative Endogenous Allosteric Modulators. Molecular Pharmacology. 94(5). 1298–1309. 4 indexed citations

13.

Miao, Yinglong, Dahlia A. Goldfeld, Ee Von Moo, et al.. (2016). Accelerated structure-based design of chemically diverse allosteric modulators of a muscarinic G protein-coupled receptor. Proceedings of the National Academy of Sciences. 113(38). E5675–84. 75 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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