Junliang Hao
About
Junliang Hao is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Organic Chemistry.
According to data from OpenAlex, Junliang Hao has authored 34 papers receiving a total of 853 indexed citations (citations by other indexed papers that have themselves been cited), including 17 papers in Molecular Biology, 11 papers in Cellular and Molecular Neuroscience and 10 papers in Organic Chemistry. Recurrent topics in Junliang Hao's work include Receptor Mechanisms and Signaling (11 papers), Marine Toxins and Detection Methods (9 papers) and Neuroscience and Neuropharmacology Research (8 papers). Junliang Hao is often cited by papers focused on Receptor Mechanisms and Signaling (11 papers), Marine Toxins and Detection Methods (9 papers) and Neuroscience and Neuropharmacology Research (8 papers). Junliang Hao collaborates with scholars based in United States, United Kingdom and China. Junliang Hao's co-authors include Craig J. Forsyth, Josep Aiguadé, Scott A. Snyder, Paraselli Bheema Rao, David Y.‐K. Chen, Gerasimos Rassias, Mali V. Reddy, Xianhai Huang, K. C. Nicolaou and Fumiyoshi Matsuura and has published in prestigious journals such as Journal of the American Chemical Society, Angewandte Chemie International Edition and The FASEB Journal.
In The Last Decade
Junliang Hao
28 papers receiving 840 citations
Peers
Junliang Hao
Shuji Yamashita Japan
Hemaka A. Rajapakse United States
Juan Murga Spain
Laurent Ferrié France
Tatsuyoshi Tanaka Japan
Noriaki Uesaka United States
Hisae Kakoi Japan
Bruce N. Rogers United States
Eric D. Moher United States
Takahiko Taniguchi Japan
Citations per year, relative to Junliang Hao Junliang Hao (= 1×)
peers
Shuji Yamashita
Countries citing papers authored by Junliang Hao
Since
Specialization
Citations
This map shows the geographic impact of Junliang Hao'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 Junliang Hao with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Junliang Hao more than expected).
Fields of papers citing papers by Junliang Hao
Since
Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences
This network shows the impact of papers produced by Junliang Hao. 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 Junliang Hao. The network helps show where Junliang Hao may publish in the future.
Co-authorship network of co-authors of Junliang Hao
This figure shows the co-authorship network connecting the top 25 collaborators of Junliang Hao. A scholar is included among the top collaborators of Junliang Hao 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 Junliang Hao. Junliang Hao is excluded from the visualization to improve readability, since they are connected to all nodes in the network.
All Works
1.
Zhang, Lanlan, Qiyan Feng, Junliang Hao, et al.. (2025). Neuroanatomical basis of 5-HT1A receptor agonism in disruption of maternal behavior in rats. Behavioural Brain Research. 486. 115554–115554.
2.
Fan, Bin, Junliang Hao, Yuan Yao, et al.. (2025). Changes in Microbial Community Diversity and the Formation Mechanism of Flavor Metabolites in Industrial-Scale Spontaneous Fermentation of Cabernet Sauvignon Wines. Foods. 14(2). 235–235.
3.
Hao, Junliang, Xin Gu, Lanlan Zhang, et al.. (2025). Maternal depression and offspring neurodevelopmental impairments in wild rodents induced by ecologically relevant prenatal stress. Molecular Psychiatry. 31(3). 1443–1454.
4.
Castner, Stacy A., Linli Zhang, Charles R. Yang, et al.. (2023). Effects of DPTQ, a novel positive allosteric modulator of the dopamine D1 receptor, on spontaneous eye blink rate and spatial working memory in the nonhuman primate. Psychopharmacology. 240(5). 1033–1048.
5.
Richardson, Jeffery, Kevin P. Cole, Amy C. DeBaillie, et al.. (2020). Development of a Scalable Synthesis of Mevidalen (LY3154207), an Orally Available Positive Allosteric Modulator of the Human Dopamine D1 Receptor. Organic Process Research & Development. 24(11). 2549–2564.
6.
Svensson, Kjell, Junliang Hao, & Robert F. Bruns. (2019). Positive allosteric modulators of the dopamine D1 receptor: A new mechanism for the treatment of neuropsychiatric disorders. Advances in pharmacology. 86. 273–305.
7.
Hao, Junliang & Qi Chen. (2019). Insights into the Structural Aspects of the mGlu Receptor Orthosteric Binding Site. Current Topics in Medicinal Chemistry. 19(26). 2421–2446.
8.
Zhou, Xin, et al.. (2019). Enterohepatic circulation of glucuronide metabolites of drugs in dog. Pharmacology Research & Perspectives. 7(4). e00502–e00502.
9.
Meltzer, Herbert Y., Lakshmi Rajagopal, Francesco Matrisciano, et al.. (2018). The allosteric dopamine D1 receptor potentiator, DETQ, ameliorates subchronic phencyclidine-induced object recognition memory deficits and enhances cortical acetylcholine efflux in male humanized D1 receptor knock-in mice. Behavioural Brain Research. 361. 139–150.
10.
Wang, Xushan, Beverly A. Heinz, Yuewei Qian, et al.. (2018). Intracellular Binding Site for a Positive Allosteric Modulator of the Dopamine D1 Receptor. Molecular Pharmacology. 94(4). 1232–1245.
11.
Hao, Junliang & Qi Chen. (2018). On the origin of the 2-aminobicyclo[3.1.0]hexane-2,6-dicarboxylate scaffold’s unique group II selectivity for the mGlu receptors. Bioorganic & Medicinal Chemistry Letters. 29(2). 297–301.
12.
Chen, Qi, Joseph D. Ho, S. Atwell, et al.. (2018). Determination of L-AP4-bound human mGlu8 receptor amino terminal domain structure and the molecular basis for L-AP4’s group III mGlu receptor functional potency and selectivity. Bioorganic & Medicinal Chemistry Letters. 28(4). 612–617.
13.
Zhou, Xin, Yu‐Hua Hui, Michael A. Mohutsky, et al.. (2018). In Vitro and In Vivo Correlation of Hepatic Fraction of Metabolism by P450 in Dogs. Journal of Pharmaceutical Sciences. 108(2). 1017–1026.
14.
Falcone, Julie F., Stephen N. Mitchell, Jason Katner, et al.. (2016). Neurochemical Profile of a Novel Allosteric Potentiator of the Dopamine D1 Receptor. The FASEB Journal. 30(S1).
15.
Hao, Junliang & Hui Xiong. (2014). SAR Studies on mGlu<sub>5</sub> Receptor Positive Allosteric Modulators (2003- 2013). Current Topics in Medicinal Chemistry. 14(15). 1789–1841.
16.
Nicolaou, K. C., Junliang Hao, Mali V. Reddy, et al.. (2004). Chemistry and Biology of Diazonamide A: Second Total Synthesis and Biological Investigations. Journal of the American Chemical Society. 126(40). 12897–12906.
17.
Nicolaou, K. C., Paraselli Bheema Rao, Junliang Hao, et al.. (2003). The Second Total Synthesis of Diazonamide A. Angewandte Chemie International Edition. 42(15). 1753–1758.
18.
Hao, Junliang & Craig J. Forsyth. (2002). Application of the double intramolecular hetero-Michael addition (DIHMA) approach in spiroketal synthesis: total synthesis of (±)-(4S*,6S*)-4-hydroxy-1,7-dioxaspiro[5.5]undecane, a Dacus oleae olive fly pheromone. Tetrahedron Letters. 43(1). 1–2.
19.
Forsyth, Craig J., Junliang Hao, & Josep Aiguadé. (2001). Synthesis of the (+)-C26–C40 Domain of the Azaspiracids by a Novel Double Intramolecular Hetero-Michael Addition Strategy This work was supported by the United States National Institute of Environmental Health Sciences (NIEHS; grant number ES10615), NIH, and by Bristol-Myers Squibb (CJF). Its contents are solely the responsibility of the authors and do not necessarily represent the official views of the NIEHS, NIH, or BMS. We thank Dr. A. B. Dounay and Dr. G. Florence for critical reading of the manuscript.. Angewandte Chemie International Edition. 40(19). 3663–3663.
20.
Hao, Junliang, Josep Aiguadé, & Craig J. Forsyth. (2001). Remarkably chemoselective indium-mediated coupling en route to the C21–C40 acyclic portion of the azaspiracids. Tetrahedron Letters. 42(5). 821–824.
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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