Nathan Alexander

2.1k total citations
54 papers, 1.7k citations indexed

About

Nathan Alexander is a scholar working on Molecular Biology, Biophysics and Materials Chemistry. According to data from OpenAlex, Nathan Alexander has authored 54 papers receiving a total of 1.7k indexed citations (citations by other indexed papers that have themselves been cited), including 25 papers in Molecular Biology, 13 papers in Biophysics and 10 papers in Materials Chemistry. Recurrent topics in Nathan Alexander's work include Protein Structure and Dynamics (9 papers), Electron Spin Resonance Studies (9 papers) and Enzyme Structure and Function (7 papers). Nathan Alexander is often cited by papers focused on Protein Structure and Dynamics (9 papers), Electron Spin Resonance Studies (9 papers) and Enzyme Structure and Function (7 papers). Nathan Alexander collaborates with scholars based in United States, Germany and Poland. Nathan Alexander's co-authors include Jens Meiler, Nils Woetzel, Hassane S. Mchaourab, Mert Karakaş, Krzysztof Palczewski, Ali İ. Kaya, Heidi E. Hamm, Anita M. Preininger, Bradford A. Woodworth and James W. Schroeder and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Biological Chemistry and Nature Medicine.

In The Last Decade

Nathan Alexander

53 papers receiving 1.7k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Nathan Alexander United States 23 936 272 246 231 181 54 1.7k
Alice Soragni United States 18 1.3k 1.4× 112 0.4× 400 1.6× 166 0.7× 124 0.7× 32 3.4k
Petra Weber Germany 23 816 0.9× 282 1.0× 95 0.4× 50 0.2× 30 0.2× 104 1.6k
Peter M. Haggie United States 27 1.7k 1.8× 227 0.8× 279 1.1× 104 0.5× 105 0.6× 46 2.8k
Lajos Trón Hungary 26 873 0.9× 236 0.9× 191 0.8× 51 0.2× 29 0.2× 131 2.4k
Timo Liimatainen Finland 26 546 0.6× 97 0.4× 55 0.2× 108 0.5× 118 0.7× 88 1.8k
И. В. Решетов Russia 23 294 0.3× 155 0.6× 64 0.3× 107 0.5× 170 0.9× 200 2.1k
Rainer Müller Germany 21 933 1.0× 34 0.1× 155 0.6× 154 0.7× 25 0.1× 50 1.8k
Philipp Niethammer United States 20 1.6k 1.7× 103 0.4× 273 1.1× 192 0.8× 101 0.6× 34 3.0k
Monica Monici Italy 22 495 0.5× 249 0.9× 73 0.3× 137 0.6× 34 0.2× 87 2.1k
Yuki Shinohara Japan 21 478 0.5× 52 0.2× 118 0.5× 125 0.5× 50 0.3× 108 1.9k

Countries citing papers authored by Nathan Alexander

Since Specialization
Citations

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

Fields of papers citing papers by Nathan Alexander

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Nathan Alexander

This figure shows the co-authorship network connecting the top 25 collaborators of Nathan Alexander. A scholar is included among the top collaborators of Nathan Alexander 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 Nathan Alexander. Nathan Alexander 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.
Alexander, Nathan, et al.. (2024). A passive, blade-mounted ultrasonic bat deterrent for wind turbines. Applied Acoustics. 229. 110392–110392.
2.
Fleming, Jonathan A.E., et al.. (2022). Measured Acoustic Characteristics of Low Tip Speed eVTOL Rotors in Hover. 1–15. 3 indexed citations
3.
Xu, Han, et al.. (2020). PAR4 activation involves extracellular loop 3 and transmembrane residue Thr153. Blood. 136(19). 2217–2228. 21 indexed citations
4.
Katayama, Kota, Sahil Gulati, Joseph T. Ortega, et al.. (2019). Specificity of the chromophore-binding site in human cone opsins. Journal of Biological Chemistry. 294(15). 6082–6093. 9 indexed citations
5.
Palczewska, Grażyna, Patrycjusz Stremplewski, Susie Suh, et al.. (2018). Two-photon imaging of the mammalian retina with ultrafast pulsing laser. JCI Insight. 3(17). 23 indexed citations
6.
Hofmann, Lukas, Nathan Alexander, Wenyu Sun, et al.. (2017). Hydrogen/Deuterium Exchange Mass Spectrometry of Human Green Opsin Reveals a Conserved Pro-Pro Motif in Extracellular Loop 2 of Monostable Visual G Protein-Coupled Receptors. Biochemistry. 56(17). 2338–2348. 7 indexed citations
7.
Alexander, Nathan, Grażyna Palczewska, Patrycjusz Stremplewski, et al.. (2016). Image registration and averaging of low laser power two-photon fluorescence images of mouse retina. Biomedical Optics Express. 7(7). 2671–2671. 17 indexed citations
8.
Leman, Julia Koehler, et al.. (2015). A survey of conformational and energetic changes in G protein signaling. SHILAP Revista de lepidopterología. 2(4). 630–648. 1 indexed citations
9.
10.
Glegg, Stewart, William J. Devenport, & Nathan Alexander. (2014). Broadband rotor noise predictions using a time domain approach. Journal of Sound and Vibration. 335. 115–124. 38 indexed citations
11.
Palczewska, Grażyna, Zhiqian Dong, Marcin Golczak, et al.. (2014). Noninvasive two-photon microscopy imaging of mouse retina and retinal pigment epithelium through the pupil of the eye. Nature Medicine. 20(7). 785–789. 84 indexed citations
12.
Weiner, Brian E., Nils Woetzel, Mert Karakaş, Nathan Alexander, & Jens Meiler. (2013). BCL::MP-Fold: Folding Membrane Proteins through Assembly of Transmembrane Helices. Structure. 21(7). 1107–1117. 28 indexed citations
13.
Alexander, Nathan & James W. Schroeder. (2013). Pediatric Obstructive Sleep Apnea Syndrome. Pediatric Clinics of North America. 60(4). 827–840. 37 indexed citations
14.
Alexander, Nathan, Anita M. Preininger, Ali İ. Kaya, et al.. (2013). Energetic analysis of the rhodopsin–G-protein complex links the α5 helix to GDP release. Nature Structural & Molecular Biology. 21(1). 56–63. 59 indexed citations
15.
Pysh, Leonard D., et al.. (2012). Four alleles of AtCESA3 form an allelic series with respect to root phenotype in Arabidopsis thaliana. Physiologia Plantarum. 144(4). 369–381. 17 indexed citations
16.
Alexander, Nathan, et al.. (2011). ROSETTAEPR: An Integrated Tool for Protein Structure Determination From Sparse EPR Data. Biophysical Journal. 100(3). 216a–216a. 4 indexed citations
17.
Alexander, Nathan, Nils Woetzel, & Jens Meiler. (2011). Bcl::Cluster: A method for clustering biological molecules coupled with visualization in the Pymol Molecular Graphics System. PubMed. 2011. 13–18. 145 indexed citations
18.
Alexander, Nathan, et al.. (2010). Rosettaepr: Developing Protein Structure Prediction Methods using Sparse SDSL-EPR Data. Biophysical Journal. 98(3). 461a–462a. 1 indexed citations
19.
Alexander, Nathan, et al.. (2010). RosettaEPR: An integrated tool for protein structure determination from sparse EPR data. Journal of Structural Biology. 173(3). 506–514. 96 indexed citations
20.
Alexander, Nathan, et al.. (2008). De Novo High-Resolution Protein Structure Determination from Sparse Spin-Labeling EPR Data. Structure. 16(2). 181–195. 109 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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