Sangdon Han

1.0k total citations · 1 hit paper
15 papers, 708 citations indexed

About

Sangdon Han is a scholar working on Endocrinology, Diabetes and Metabolism, Molecular Biology and Cellular and Molecular Neuroscience. According to data from OpenAlex, Sangdon Han has authored 15 papers receiving a total of 708 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Endocrinology, Diabetes and Metabolism, 6 papers in Molecular Biology and 4 papers in Cellular and Molecular Neuroscience. Recurrent topics in Sangdon Han's work include Pituitary Gland Disorders and Treatments (4 papers), Receptor Mechanisms and Signaling (3 papers) and Neuroendocrine Tumor Research Advances (2 papers). Sangdon Han is often cited by papers focused on Pituitary Gland Disorders and Treatments (4 papers), Receptor Mechanisms and Signaling (3 papers) and Neuroendocrine Tumor Research Advances (2 papers). Sangdon Han collaborates with scholars based in United States, Denmark and Germany. Sangdon Han's co-authors include Robert M. Jones, Kaare V. Grunddal, Stefan Offermanns, M. Hauge, Steen Seier Poulsen, Maja S. Engelstoft, Mark K. Nøhr, Andreas Gille, Anna Sofie Husted and Kristoffer L. Egerod and has published in prestigious journals such as Cancer Research, Endocrinology and Journal of Medicinal Chemistry.

In The Last Decade

Sangdon Han

14 papers receiving 698 citations

Hit Papers

GPR41/FFAR3 and GPR43/FFAR2 as Cosensors for Short-Chain ... 2013 2026 2017 2021 2013 100 200 300 400

Peers

Sangdon Han
Sangdon Han
Citations per year, relative to Sangdon Han Sangdon Han (= 1×) peers Marta Sobczak

Countries citing papers authored by Sangdon Han

Since Specialization
Citations

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

Fields of papers citing papers by Sangdon Han

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Sangdon Han. 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 Sangdon Han. The network helps show where Sangdon Han may publish in the future.

Co-authorship network of co-authors of Sangdon Han

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

All Works

15 of 15 papers shown
1.
Kim, Nam Hee, et al.. (2024). Abstract LB426: Evidence for a role of GPR35 in IDO1-mediated tumor immune escape by regulating Hippo-YAP pathway. Cancer Research. 84(7_Supplement). LB426–LB426.
2.
Han, Sangdon, Ana Karin Kusnetzow, Greg J. Reinhart, et al.. (2024). Discovery of CRN04894: A Novel Potent Selective MC2R Antagonist. ACS Medicinal Chemistry Letters. 15(4). 478–485. 5 indexed citations
3.
Kim, Sun Hee, Sangdon Han, Elizabeth Rico-Bautista, et al.. (2022). Discovery of 4-(3-aminopyrrolidinyl)-3-aryl-5-(benzimidazol-2-yl)-pyridines as potent and selective SST5 agonists for the treatment of congenital hyperinsulinism. Bioorganic & Medicinal Chemistry Letters. 71. 128807–128807. 2 indexed citations
4.
Markison, Stacy, Sangdon Han, Mi Chen, et al.. (2022). Discovery of Paltusotine (CRN00808), a Potent, Selective, and Orally Bioavailable Non-peptide SST2 Agonist. ACS Medicinal Chemistry Letters. 14(1). 66–74. 15 indexed citations
5.
Fowler, Melissa, Ana Karin Kusnetzow, Sangdon Han, et al.. (2021). Effects of CRN04894, a Nonpeptide Orally Bioavailable ACTH Antagonist, on Corticosterone in Rodent Models of ACTH Excess. Journal of the Endocrine Society. 5(Supplement_1). A167–A167. 4 indexed citations
6.
Han, Sangdon, Ana Karin Kusnetzow, Julie Nguyen, et al.. (2020). Discovery of nonpeptide 3,4-dihydroquinazoline-4-carboxamides as potent and selective sst2 agonists. Bioorganic & Medicinal Chemistry Letters. 30(17). 127391–127391. 5 indexed citations
7.
Kusnetzow, Ana Karin, Sangdon Han, Melissa Fowler, et al.. (2020). MON-176 Discovery and Identification of Late Stage Selective Nonpeptide ACTH Antagonists for the Treatment of Cushing’s Disease, Ectopic ACTH Secreting Tumors, and Congenital Adrenal Hyperplasia. Journal of the Endocrine Society. 4(Supplement_1). 4 indexed citations
8.
Kusnetzow, Ana Karin, Melissa Fowler, Greg J. Reinhart, et al.. (2019). SAT-364 Nonpeptide Orally-Bioavailable ACTH Antagonists: Suppression of ACTH-Induced Corticosterone Secretion and Adrenal Hypertrophy in Rats. Journal of the Endocrine Society. 3(Supplement_1). 4 indexed citations
9.
Gaidarov, Ibragim, Todd L. Anthony, Joel Gatlin, et al.. (2018). Embelin and its derivatives unravel the signaling, proinflammatory and antiatherogenic properties of GPR84 receptor. Pharmacological Research. 131. 185–198. 49 indexed citations
10.
Han, Sangdon, Lars Thoresen, Jae‐Kyu Jung, et al.. (2017). Discovery of APD371: Identification of a Highly Potent and Selective CB2Agonist for the Treatment of Chronic Pain. ACS Medicinal Chemistry Letters. 8(12). 1309–1313. 33 indexed citations
11.
Buzard, Daniel J., Thomas O. Schrader, Xiuwen Zhu, et al.. (2014). Design and synthesis of new tricyclic indoles as potent modulators of the S1P1 receptor. Bioorganic & Medicinal Chemistry Letters. 25(3). 659–663. 13 indexed citations
12.
Han, Sangdon, Jayant Thatte, Daniel J. Buzard, & Robert M. Jones. (2013). Therapeutic Utility of Cannabinoid Receptor Type 2 (CB2) Selective Agonists. Journal of Medicinal Chemistry. 56(21). 8224–8256. 115 indexed citations
13.
Nøhr, Mark K., M. Hauge, Andreas Gille, et al.. (2013). GPR41/FFAR3 and GPR43/FFAR2 as Cosensors for Short-Chain Fatty Acids in Enteroendocrine Cells vs FFAR3 in Enteric Neurons and FFAR2 in Enteric Leukocytes. Endocrinology. 154(10). 3552–3564. 448 indexed citations breakdown →
14.
Buzard, Daniel J., Juerg Lehmann, Sangdon Han, & Robert M. Jones. (2012). GPR119 Agonists 2009–2011. Pharmaceutical Patent Analyst. 1(3). 285–299. 8 indexed citations
15.
Semple, Graeme, Thuy-Anh Tran, Sangdon Han, et al.. (2009). Pyrimidine-based antagonists of h-MCH-R1 derived from ATC0175: In vitro profiling and in vivo evaluation. Bioorganic & Medicinal Chemistry Letters. 19(21). 6166–6171. 3 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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