Stephen B. Long

7.6k total citations · 4 hit papers
32 papers, 6.0k citations indexed

About

Stephen B. Long is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Sensory Systems. According to data from OpenAlex, Stephen B. Long has authored 32 papers receiving a total of 6.0k indexed citations (citations by other indexed papers that have themselves been cited), including 28 papers in Molecular Biology, 12 papers in Cellular and Molecular Neuroscience and 7 papers in Sensory Systems. Recurrent topics in Stephen B. Long's work include Ion channel regulation and function (12 papers), Ion Channels and Receptors (7 papers) and Neuroscience and Neuropharmacology Research (6 papers). Stephen B. Long is often cited by papers focused on Ion channel regulation and function (12 papers), Ion Channels and Receptors (7 papers) and Neuroscience and Neuropharmacology Research (6 papers). Stephen B. Long collaborates with scholars based in United States, United Kingdom and Italy. Stephen B. Long's co-authors include Roderick MacKinnon, Ernest B. Campbell, Xiao Tao, Leanne Pedi, Alexandria N. Miller, Xiaowei Hou, Melinda M. Diver, L.S. Beese, Patrick J. Casey and Veronica Kane Dickson and has published in prestigious journals such as Nature, Science and Cell.

In The Last Decade

Stephen B. Long

31 papers receiving 5.9k citations

Hit Papers

Crystal Structure of a Mammalian Voltage-Dependent Shaker... 2005 2026 2012 2019 2005 2007 2005 2012 500 1000 1.5k

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Stephen B. Long United States 22 5.0k 2.4k 1.6k 821 474 32 6.0k
Daniel L. Minor United States 43 5.3k 1.1× 1.9k 0.8× 1.3k 0.8× 594 0.7× 352 0.7× 88 6.2k
Ernest B. Campbell United States 16 6.1k 1.2× 2.7k 1.1× 2.0k 1.3× 499 0.6× 483 1.0× 18 7.2k
Xiao Tao China 22 3.7k 0.7× 1.6k 0.7× 1.1k 0.7× 268 0.3× 189 0.4× 50 4.6k
Donald W. Hilgemann United States 46 6.6k 1.3× 3.2k 1.4× 3.0k 1.9× 599 0.7× 799 1.7× 92 7.7k
William N. Zagotta United States 50 8.5k 1.7× 5.5k 2.3× 3.4k 2.1× 980 1.2× 258 0.5× 111 10.1k
Michael Fill United States 38 4.7k 1.0× 1.9k 0.8× 2.5k 1.5× 481 0.6× 428 0.9× 92 5.7k
Jiayun Chen China 11 4.6k 0.9× 2.2k 0.9× 1.6k 1.0× 232 0.3× 163 0.3× 25 5.1k
Filip Van Petegem Canada 38 3.6k 0.7× 1.1k 0.4× 1.9k 1.2× 229 0.3× 320 0.7× 133 4.4k
Alessio Accardi United States 31 2.9k 0.6× 1.1k 0.4× 585 0.4× 200 0.2× 360 0.8× 58 3.4k
Noriaki Ikemoto United States 48 5.0k 1.0× 1.4k 0.6× 2.8k 1.8× 309 0.4× 586 1.2× 116 5.7k

Countries citing papers authored by Stephen B. Long

Since Specialization
Citations

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

Fields of papers citing papers by Stephen B. Long

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Stephen B. Long. 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 Stephen B. Long. The network helps show where Stephen B. Long may publish in the future.

Co-authorship network of co-authors of Stephen B. Long

This figure shows the co-authorship network connecting the top 25 collaborators of Stephen B. Long. A scholar is included among the top collaborators of Stephen B. Long 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 Stephen B. Long. Stephen B. Long 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.
2.
Wang, Chongyuan, et al.. (2020). Structures reveal gatekeeping of the mitochondrial Ca2+ uniporter by MICU1-MICU2. eLife. 9. 50 indexed citations
3.
Wang, Chongyuan, Rozbeh Baradaran, & Stephen B. Long. (2020). Structure and Reconstitution of an MCU–EMRE Mitochondrial Ca2+ Uniporter Complex. Journal of Molecular Biology. 432(20). 5632–5648. 13 indexed citations
4.
Hou, Xiaowei, et al.. (2019). Structures Reveal Opening of the Store-Operated Calcium Channel ORAI. Biophysical Journal. 116(3). 302a–302a. 1 indexed citations
5.
Baradaran, Rozbeh, et al.. (2018). Cryo-EM structures of fungal and metazoan mitochondrial calcium uniporters. Nature. 559(7715). 580–584. 126 indexed citations
6.
Diver, Melinda M., Leanne Pedi, Akiko Koide, Shohei Koide, & Stephen B. Long. (2018). Atomic structure of the eukaryotic intramembrane RAS methyltransferase ICMT. Nature. 553(7689). 526–529. 31 indexed citations
7.
Hou, Xiaowei, et al.. (2018). Structures reveal opening of the store-operated calcium channel Orai. eLife. 7. 67 indexed citations
8.
Long, Stephen B., et al.. (2018). An allosteric mechanism of inactivation in the calcium-dependent chloride channel BEST1. The Journal of General Physiology. 150(11). 1484–1497. 18 indexed citations
9.
Hou, Xiaowei & Stephen B. Long. (2015). Functional Reconstitution and Structural Flexibility of the CRAC Channel Orai. Biophysical Journal. 108(2). 178a–178a. 2 indexed citations
10.
Diver, Melinda M. & Stephen B. Long. (2014). Mutational Analysis of the Integral Membrane Methyltransferase Isoprenylcysteine Carboxyl Methyltransferase (ICMT) Reveals Potential Substrate Binding Sites. Journal of Biological Chemistry. 289(38). 26007–26020. 8 indexed citations
11.
Dickson, Veronica Kane, Leanne Pedi, & Stephen B. Long. (2014). Structure and insights into the function of a Ca2+-activated Cl− channel. Nature. 516(7530). 213–218. 166 indexed citations
12.
Okada, Tomoyo, Surajit Sinha, Gaia Schiavon, et al.. (2014). The Rho GTPase Rnd1 suppresses mammary tumorigenesis and EMT by restraining Ras-MAPK signalling. Nature Cell Biology. 17(1). 81–94. 92 indexed citations
13.
Miller, Alexandria N. & Stephen B. Long. (2012). Crystal Structure of the Human Two–Pore Domain Potassium Channel K2P1. Science. 335(6067). 432–436. 254 indexed citations
14.
Hou, Xiaowei, Leanne Pedi, Melinda M. Diver, & Stephen B. Long. (2012). Crystal Structure of the Calcium Release–Activated Calcium Channel Orai. Science. 338(6112). 1308–1313. 442 indexed citations breakdown →
15.
Li, Wei, Li‐Ru You, Jonathan M. Cooper, et al.. (2010). Merlin/NF2 Suppresses Tumorigenesis by Inhibiting the E3 Ubiquitin Ligase CRL4DCAF1 in the Nucleus. Cell. 140(4). 477–490. 254 indexed citations
16.
Long, Stephen B., et al.. (2008). Crystal structure of an RNA aptamer bound to thrombin. RNA. 14(12). 2504–2512. 126 indexed citations
17.
Long, Stephen B., Xiao Tao, Ernest B. Campbell, & Roderick MacKinnon. (2007). Atomic structure of a voltage-dependent K+ channel in a lipid membrane-like environment. Nature. 450(7168). 376–382. 1172 indexed citations breakdown →
18.
Long, Stephen B., Ernest B. Campbell, & Roderick MacKinnon. (2005). Crystal Structure of a Mammalian Voltage-Dependent Shaker Family K + Channel. Science. 309(5736). 897–903. 1748 indexed citations breakdown →
19.
Long, Stephen B., Patrick J. Casey, & L.S. Beese. (2002). Reaction path of protein farnesyltransferase at atomic resolution. Nature. 419(6907). 645–650. 138 indexed citations
20.
Long, Stephen B., et al.. (2001). The crystal structure of human protein farnesyltransferase reveals the basis for inhibition by CaaX tetrapeptides and their mimetics. Proceedings of the National Academy of Sciences. 98(23). 12948–12953. 83 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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