H C Guan

1.3k total citations
11 papers, 1.1k citations indexed

About

H C Guan is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Organic Chemistry. According to data from OpenAlex, H C Guan has authored 11 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Molecular Biology, 5 papers in Cellular and Molecular Neuroscience and 4 papers in Organic Chemistry. Recurrent topics in H C Guan's work include Receptor Mechanisms and Signaling (4 papers), Neurotransmitter Receptor Influence on Behavior (3 papers) and Cyclopropane Reaction Mechanisms (3 papers). H C Guan is often cited by papers focused on Receptor Mechanisms and Signaling (4 papers), Neurotransmitter Receptor Influence on Behavior (3 papers) and Cyclopropane Reaction Mechanisms (3 papers). H C Guan collaborates with scholars based in Canada, United States and Austria. H C Guan's co-authors include Philip Seeman, Hyman B. Niznik, H H Van Tol, Carla Ulpian, Gillian L. Booth, Gavin P. Reynolds, K. A. Jellinger, Shuzo Watanabe, Wallace W. Tourtellotte and Catherine Bergeron and has published in prestigious journals such as Proceedings of the National Academy of Sciences, FEBS Letters and Endocrinology.

In The Last Decade

H C Guan

10 papers receiving 1.1k citations

Peers

Countries citing papers authored by H C Guan

Since Specialization

Citations

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

Fields of papers citing papers by H C Guan

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by H C Guan. 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 H C Guan. The network helps show where H C Guan may publish in the future.

Co-authorship network of co-authors of H C Guan

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

All Works

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11 of 11 papers shown

#	Work	Indexed citations
1	Peripheral Serotonin Controls Dietary Fat Absorption and Chylomicron Secretion via 5-HT4 Receptor in Males 2024 ·Endocrinology ·(unknown), (unknown), (unknown), H C Guan, (unknown), Huaqing Wang, Waliul I. Khan, Khosrow Adeli	0
2	Promoter‐independent regulation of cell‐specific dopamine receptor expression 1998 ·FEBS Letters ·(unknown), Albert H.C. Wong, Oscar Schoots, H C Guan, Hubert H.M. Van Tol	7
3	Dopamine D4 receptor repeat: analysis of different native and mutant forms of the human and rat genes. 1994 ·Molecular Pharmacology ·Vida Asghari, Oscar Schoots, (unknown), Koichi Ohara, Vera Jovanović, H C Guan, James R. Bunzow, Artūras Petronis, H H Van Tol	157
4	Serotonin receptor cDNA cloned from Lymnaea stagnalis. 1993 ·Proceedings of the National Academy of Sciences ·Kim S. Sugamori, Roger K. Sunahara, H C Guan, Andrew GM Bulloch, Cornelis P. Tensen, Philip Seeman, Hyman B. Niznik, H H Van Tol	127
5	(.+-.)-3-Allyl-7-halo-8-hydroxy-1-phenyl-2,3,4,5-tetrahydro-1H-3-benzazepines as selective high affinity D1 dopamine receptor antagonists: synthesis and structure-activity relationship 1992 ·Journal of Medicinal Chemistry ·(unknown), M. A. Tran, Hyman B. Niznik, H C Guan, Philip Seeman, John L. Neumeyer	17
6	ChemInform Abstract: (.+‐.)‐3‐Allyl‐7‐halo‐8‐hydroxy‐1‐phenyl‐2,3,4,5‐tetrahydro‐1H‐3‐ benzazepines as Selective High Affinity D1 Dopamine Receptor Antagonists: Synthesis and Structure‐Activity Relationship. 1992 ·ChemInform ·(unknown), (unknown), Hyman B. Niznik, H C Guan, P Seeman, John L. Neumeyer	1
7	(.+-.)-3-Allyl-6-bromo-7,8-dihydroxy-1-phenyl-2,3,4,5-tetrahydro-1H-3-benzazepine, a new high affinity D1 dopamine receptor ligand: synthesis and structure-activity relationship 1991 ·Journal of Medicinal Chemistry ·John L. Neumeyer, (unknown), Hyman B. Niznik, H C Guan, Philip Seeman	18
8	Endogenous dopamine lowers the dopamine D₂ receptor density as measured by [³H]raclopride: Implications for positron emission tomography of the human brain 1989 ·Synapse ·Philip Seeman, H C Guan, Hyman B. Niznik	251
9	Link between D1 and D2 dopamine receptors is reduced in schizophrenia and Huntington diseased brain. 1989 ·Proceedings of the National Academy of Sciences ·Philip Seeman, Hyman B. Niznik, H C Guan, Gillian L. Booth, Carla Ulpian	162
10	Human brain dopamine receptors in children and aging adults 1987 ·Synapse ·Philip Seeman, Natalie Bzowej, H C Guan, Catherine Bergeron, Lawrence E. Becker, Gavin P. Reynolds, Edward D. Bird, Peter Riederer, K. A. Jellinger, Shuzo Watanabe, Wallace W. Tourtellotte	337
11	Dopamine D1 and D2 receptors are sensitive to the cationic form of apomorphine. 1987 ·Molecular Pharmacology ·Philip Seeman, H C Guan	3

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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