Richard K. Hite

3.7k total citations
45 papers, 2.5k citations indexed

About

Richard K. Hite is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Physiology. According to data from OpenAlex, Richard K. Hite has authored 45 papers receiving a total of 2.5k indexed citations (citations by other indexed papers that have themselves been cited), including 38 papers in Molecular Biology, 10 papers in Cellular and Molecular Neuroscience and 8 papers in Physiology. Recurrent topics in Richard K. Hite's work include Ion channel regulation and function (14 papers), Lipid Membrane Structure and Behavior (12 papers) and Calcium signaling and nucleotide metabolism (8 papers). Richard K. Hite is often cited by papers focused on Ion channel regulation and function (14 papers), Lipid Membrane Structure and Behavior (12 papers) and Calcium signaling and nucleotide metabolism (8 papers). Richard K. Hite collaborates with scholars based in United States, France and Germany. Richard K. Hite's co-authors include Roderick MacKinnon, Thomas Walz, Xiao Tao, Navid Paknejad, Zongli Li, Peng Yuan, SeCheol Oh, X. Sunney Xie, Jong‐Bong Lee and Samir M. Hamdan and has published in prestigious journals such as Nature, Science and Cell.

In The Last Decade

Richard K. Hite

43 papers receiving 2.5k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Richard K. Hite United States 27 1.9k 464 280 218 215 45 2.5k
Tomohiro Nishizawa Japan 35 2.6k 1.3× 792 1.7× 153 0.5× 236 1.1× 98 0.5× 108 4.0k
Alessio Accardi United States 31 2.9k 1.5× 1.1k 2.3× 585 2.1× 360 1.7× 200 0.9× 58 3.4k
Shigetoshi Oiki Japan 31 2.0k 1.0× 640 1.4× 353 1.3× 122 0.6× 66 0.3× 106 2.8k
Clemens Möller Germany 20 1.2k 0.6× 273 0.6× 160 0.6× 119 0.5× 310 1.4× 41 2.8k
Xiaojing Pan China 30 2.7k 1.4× 710 1.5× 613 2.2× 461 2.1× 98 0.5× 83 3.9k
Ravshan Z. Sabirov Japan 32 2.1k 1.1× 744 1.6× 335 1.2× 139 0.6× 231 1.1× 79 3.1k
Thomas Vorherr Switzerland 33 2.9k 1.5× 451 1.0× 251 0.9× 571 2.6× 102 0.5× 71 3.6k
Stephen G. Brohawn United States 21 1.8k 0.9× 603 1.3× 226 0.8× 257 1.2× 179 0.8× 36 2.5k
Xiangshu Jin United States 24 2.0k 1.0× 397 0.9× 72 0.3× 564 2.6× 418 1.9× 29 2.9k
Cristina Paulino Netherlands 18 1.1k 0.6× 302 0.7× 150 0.5× 125 0.6× 130 0.6× 30 1.4k

Countries citing papers authored by Richard K. Hite

Since Specialization
Citations

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

Fields of papers citing papers by Richard K. Hite

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Richard K. Hite. 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 Richard K. Hite. The network helps show where Richard K. Hite may publish in the future.

Co-authorship network of co-authors of Richard K. Hite

This figure shows the co-authorship network connecting the top 25 collaborators of Richard K. Hite. A scholar is included among the top collaborators of Richard K. Hite 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 Richard K. Hite. Richard K. Hite 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.
Kumar, Charanya, et al.. (2025). G-quadruplex–stalled eukaryotic replisome structure reveals helical inchworm DNA translocation. Science. 387(6738). eadt1978–eadt1978. 5 indexed citations
2.
Planells‐Cases, Rosa, F. Schmitt, Uwe Schulte, et al.. (2025). Endosomal chloride/proton exchangers need inhibitory TMEM9 β-subunits for regulation and prevention of disease-causing overactivity. Nature Communications. 16(1). 3117–3117.
3.
Liu, Shian, Jinan Wang, Lan Zhu, et al.. (2024). Architecture and activation of single-pass transmembrane receptor guanylyl cyclase. Nature Structural & Molecular Biology. 32(3). 469–478. 2 indexed citations
4.
Kenny, Timothy C., et al.. (2024). Structural basis of lipid head group entry to the Kennedy pathway by FLVCR1. Nature. 629(8012). 710–716. 19 indexed citations
5.
Oh, SeCheol, Fabrizio Marinelli, Wenchang Zhou, et al.. (2022). Differential ion dehydration energetics explains selectivity in the non-canonical lysosomal K+ channel TMEM175. eLife. 11. 15 indexed citations
6.
Oh, SeCheol, et al.. (2022). Structure of the Wilson disease copper transporter ATP7B. Science Advances. 8(9). eabl5508–eabl5508. 59 indexed citations
7.
Remus, Dirk, et al.. (2022). Mechanisms of loading and release of the 9-1-1 checkpoint clamp. Nature Structural & Molecular Biology. 29(4). 369–375. 26 indexed citations
8.
Devbhandari, Sujan, et al.. (2022). Multistep loading of a DNA sliding clamp onto DNA by replication factor C. eLife. 11. 23 indexed citations
9.
Jiang, Yining, et al.. (2022). Membrane-mediated protein interactions drive membrane protein organization. Nature Communications. 13(1). 7373–7373. 33 indexed citations
10.
Alegre, Kamela O., Navid Paknejad, Minfei Su, et al.. (2021). Structural basis and mechanism of activation of two different families of G proteins by the same GPCR. Nature Structural & Molecular Biology. 28(11). 936–944. 26 indexed citations
11.
Su, Minfei, Lan Zhu, Yixiao Zhang, et al.. (2020). Structural Basis of the Activation of Heterotrimeric Gs-Protein by Isoproterenol-Bound β1-Adrenergic Receptor. Molecular Cell. 80(1). 59–71.e4. 62 indexed citations
12.
Kern, David M., SeCheol Oh, Richard K. Hite, & Stephen G. Brohawn. (2019). Cryo-EM structures of the DCPIB-inhibited volume-regulated anion channel LRRC8A in lipid nanodiscs. eLife. 8. 87 indexed citations
13.
Ruan, Yi, Kevin S. Kao, S. Lefebvre, et al.. (2018). Structural titration of receptor ion channel GLIC gating by HS-AFM. Proceedings of the National Academy of Sciences. 115(41). 10333–10338. 36 indexed citations
14.
Deng, Zengqin, Navid Paknejad, Grigory Maksaev, et al.. (2018). Cryo-EM and X-ray structures of TRPV4 reveal insight into ion permeation and gating mechanisms. Nature Structural & Molecular Biology. 25(3). 252–260. 167 indexed citations
15.
Oldham, Michael L., et al.. (2016). A mechanism of viral immune evasion revealed by cryo-EM analysis of the TAP transporter. Nature. 529(7587). 537–540. 97 indexed citations
16.
Tao, Xiao, Richard K. Hite, & Roderick MacKinnon. (2016). Cryo-EM structure of the open high-conductance Ca2+-activated K+ channel. Nature. 541(7635). 46–51. 190 indexed citations
17.
Hite, Richard K., Joel A. Butterwick, & Roderick MacKinnon. (2014). Phosphatidic acid modulation of Kv channel voltage sensor function. eLife. 3. 49 indexed citations
18.
Hite, Richard K., Andreas D. Schenk, Zongli Li, Yifan Cheng, & Thomas Walz. (2010). Collecting Electron Crystallographic Data of Two-Dimensional Protein Crystals. Methods in enzymology on CD-ROM/Methods in enzymology. 481. 251–282. 11 indexed citations
19.
Hite, Richard K., Zongli Li, & Thomas Walz. (2010). Principles of membrane protein interactions with annular lipids deduced from aquaporin-0 2D crystals. The EMBO Journal. 29(10). 1652–1658. 103 indexed citations
20.
John, Corinne, Richard K. Hite, Christine S. Weirich, et al.. (2007). The Caenorhabditis elegans septin complex is nonpolar. The EMBO Journal. 26(14). 3296–3307. 112 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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