Haiqing Zhao

5.7k total citations · 2 hit papers
51 papers, 4.1k citations indexed

About

Haiqing Zhao is a scholar working on Cellular and Molecular Neuroscience, Sensory Systems and Molecular Biology. According to data from OpenAlex, Haiqing Zhao has authored 51 papers receiving a total of 4.1k indexed citations (citations by other indexed papers that have themselves been cited), including 28 papers in Cellular and Molecular Neuroscience, 23 papers in Sensory Systems and 17 papers in Molecular Biology. Recurrent topics in Haiqing Zhao's work include Olfactory and Sensory Function Studies (23 papers), Neurobiology and Insect Physiology Research (16 papers) and Biochemical Analysis and Sensing Techniques (15 papers). Haiqing Zhao is often cited by papers focused on Olfactory and Sensory Function Studies (23 papers), Neurobiology and Insect Physiology Research (16 papers) and Biochemical Analysis and Sensing Techniques (15 papers). Haiqing Zhao collaborates with scholars based in United States, China and United Kingdom. Haiqing Zhao's co-authors include Samer Hattar, Stuart Firestein, Katherine D. Cygnar, Johannes Reisert, Joji M. Otaki, Aaron B. Stephan, Cara M. Altimus, Mitsuhiro Hashimoto, Lidija Ivic and David M. Berson and has published in prestigious journals such as Nature, Science and Cell.

In The Last Decade

Haiqing Zhao

50 papers receiving 4.0k citations

Hit Papers

Melanopsin cells are the ... 2008 2026 2014 2020 2008 2018 200 400 600

Author Peers

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

Author Last Decade Papers Cites
Haiqing Zhao 1.7k 1.5k 1.2k 1.2k 882 51 4.1k
Fuqiang Xu 2.1k 1.2× 1.3k 0.8× 571 0.5× 1.3k 1.1× 762 0.9× 178 5.1k
Stephen D. Liberles 2.1k 1.2× 1.6k 1.0× 1.4k 1.1× 2.2k 1.8× 1.8k 2.0× 54 6.5k
Hyosang Lee 1.6k 0.9× 1.2k 0.8× 632 0.5× 2.2k 1.8× 465 0.5× 42 5.0k
Rui B. Chang 735 0.4× 839 0.5× 614 0.5× 878 0.7× 664 0.8× 35 3.0k
Darren W. Logan 1.1k 0.6× 683 0.4× 376 0.3× 1.3k 1.1× 1.1k 1.2× 53 3.4k
Catia Sternini 3.9k 2.2× 2.4k 1.6× 958 0.8× 915 0.7× 1.2k 1.3× 163 7.4k
Gary D. Housley 1.1k 0.6× 2.1k 1.4× 2.3k 1.8× 3.3k 2.7× 405 0.5× 162 6.8k
X.Z. Shawn Xu 1.1k 0.6× 1.7k 1.1× 1.8k 1.5× 875 0.7× 939 1.1× 92 5.6k
Thomas R. Scott 880 0.5× 335 0.2× 736 0.6× 1.7k 1.4× 2.1k 2.4× 152 4.4k
Hideto Kaba 1.3k 0.7× 413 0.3× 494 0.4× 1.1k 0.9× 536 0.6× 120 2.7k

Countries citing papers authored by Haiqing Zhao

Since Specialization
Citations

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

Fields of papers citing papers by Haiqing Zhao

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Haiqing Zhao

This figure shows the co-authorship network connecting the top 25 collaborators of Haiqing Zhao. A scholar is included among the top collaborators of Haiqing Zhao 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 Haiqing Zhao. Haiqing Zhao 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.
Boehm, Erica, Corinne Beier, William T. Keenan, et al.. (2022). Satellite glia modulate sympathetic neuron survival, activity, and autonomic function. eLife. 11. 24 indexed citations
2.
Thomsen, Michael B, et al.. (2022). Diversity of satellite glia in sympathetic and sensory ganglia. Cell Reports. 38(5). 110328–110328. 50 indexed citations
3.
Fernandez, Diego C., Jun Ma, Phan Q. Duy, et al.. (2020). Retinal innervation tunes circuits that drive nonphotic entrainment to food. Nature. 581(7807). 194–198. 32 indexed citations
4.
Reisert, Johannes, et al.. (2017). Cilia- and Flagella-Associated Protein 69 Regulates Olfactory Transduction Kinetics in Mice. Journal of Neuroscience. 37(23). 5699–5710. 26 indexed citations
5.
Gigante, Crystal M., Michele Dibattista, Xiaobin Zheng, et al.. (2017). Lamin B1 is required for mature neuron-specific gene expression during olfactory sensory neuron differentiation. Nature Communications. 8(1). 15098–15098. 24 indexed citations
6.
Keenan, William T., et al.. (2017). Eye-Drops for Activation of DREADDs. Frontiers in Neural Circuits. 11. 93–93. 13 indexed citations
7.
María, Alicia, Haiqing Zhao, & Steven Bassnett. (2017). Expression of potassium-dependent sodium-calcium exchanger in the murine lens. Experimental Eye Research. 167. 18–24. 5 indexed citations
8.
Zhao, Haiqing, et al.. (2016). Simultaneous Loss of NCKX4 and CNG Channel Desensitization Impairs Olfactory Sensitivity. Journal of Neuroscience. 37(1). 110–119. 8 indexed citations
9.
Chen, Dawei, Zhenquan Yang, Yujun Huang, et al.. (2014). The effect of Lactobacillus rhamnosus hsryfm 1301 on the intestinal microbiota of a hyperlipidemic rat model. BMC Complementary and Alternative Medicine. 14(1). 386–386. 69 indexed citations
10.
Parry, David, James A. Poulter, Clare V. Logan, et al.. (2013). Identification of Mutations in SLC24A4, Encoding a Potassium-Dependent Sodium/Calcium Exchanger, as a Cause of Amelogenesis Imperfecta. The American Journal of Human Genetics. 92(2). 307–312. 94 indexed citations
11.
Cygnar, Katherine D., et al.. (2012). Phosphorylation of Adenylyl Cyclase III at Serine1076Does Not Attenuate Olfactory Response in Mice. Journal of Neuroscience. 32(42). 14557–14562. 15 indexed citations
12.
LeGates, Tara A., Cara M. Altimus, Hui Wang, et al.. (2012). Aberrant light directly impairs mood and learning through melanopsin-expressing neurons. Nature. 491(7425). 594–598. 399 indexed citations
13.
Stephan, Aaron B., Steven Tobochnik, Michele Dibattista, et al.. (2011). The Na+/Ca2+ exchanger NCKX4 governs termination and adaptation of the mammalian olfactory response. Nature Neuroscience. 15(1). 131–137. 91 indexed citations
14.
Güler, Ali D., Jennifer L. Ecker, Gurprit S. Lall, et al.. (2008). Melanopsin cells are the principal conduits for rod–cone input to non-image-forming vision. Nature. 453(7191). 102–105. 641 indexed citations breakdown →
15.
Song, Yijun, Katherine D. Cygnar, Botir T. Sagdullaev, et al.. (2008). Olfactory CNG Channel Desensitization by Ca2+/CaM via the B1b Subunit Affects Response Termination but Not Sensitivity to Recurring Stimulation. Neuron. 58(3). 374–386. 70 indexed citations
16.
Zhao, Haiqing, et al.. (2001). X Inactivation of the OCNC1 Channel Gene Reveals a Role for Activity-Dependent Competition in the Olfactory System. Cell. 104(5). 651–660. 161 indexed citations
17.
Zhao, Haiqing & Stuart Firestein. (1999). Vertebrate odorant receptors. Cellular and Molecular Life Sciences. 56(7-8). 647–659. 25 indexed citations
18.
Zhao, Haiqing, Joji M. Otaki, & Stuart Firestein. (1996). Adenovirus-mediated gene transfer in olfactory neuronsin vivo. Journal of Neurobiology. 30(4). 521–530. 39 indexed citations
19.
Zhao, Haiqing, Stuart Firestein, & Charles A. Greer. (1994). NADPH-diaphorase localization in the olfactory system. Neuroreport. 6(1). 149–152. 23 indexed citations
20.
Bergson, Clare, Haiqing Zhao, Kiyofumi Saijoh, Ronald S. Duman, & Eric J. Nestler. (1993). Ezrin and Osteonectin, Two Proteins Associated with Cell Shape and Growth, Are Enriched in the Locus Coeruleus. Molecular and Cellular Neuroscience. 4(1). 64–73. 9 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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