Matthew S. Creamer

545 total citations
14 papers, 302 citations indexed

About

Matthew S. Creamer is a scholar working on Cellular and Molecular Neuroscience, Cognitive Neuroscience and Molecular Biology. According to data from OpenAlex, Matthew S. Creamer has authored 14 papers receiving a total of 302 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Cellular and Molecular Neuroscience, 6 papers in Cognitive Neuroscience and 4 papers in Molecular Biology. Recurrent topics in Matthew S. Creamer's work include Neurobiology and Insect Physiology Research (6 papers), Neural dynamics and brain function (5 papers) and Photoreceptor and optogenetics research (3 papers). Matthew S. Creamer is often cited by papers focused on Neurobiology and Insect Physiology Research (6 papers), Neural dynamics and brain function (5 papers) and Photoreceptor and optogenetics research (3 papers). Matthew S. Creamer collaborates with scholars based in United States, Australia and Belgium. Matthew S. Creamer's co-authors include Damon A. Clark, Omer Mano, Kevin M. Collins, Jessica E. Tanis, Michael R. Koelle, Robert W. Fernandez, Jacob A. Zavatone-Veth, Joseph Pottackal, Daniel D. Von Hoff and Ryosuke Tanaka and has published in prestigious journals such as Nature Communications, Neuron and Nature Neuroscience.

In The Last Decade

Matthew S. Creamer

14 papers receiving 296 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Matthew S. Creamer United States 10 166 100 71 65 64 14 302
Ugur Dag United States 9 161 1.0× 114 1.1× 59 0.8× 38 0.6× 32 0.5× 13 305
Altar Sorkaç United States 6 203 1.2× 116 1.2× 65 0.9× 16 0.2× 54 0.8× 9 346
Hsuan-Wen Lin Taiwan 6 270 1.6× 82 0.8× 28 0.4× 25 0.4× 74 1.2× 9 323
Adriane G. Otopalik United States 7 226 1.4× 57 0.6× 17 0.2× 133 2.0× 57 0.9× 10 311
Yongjun Qian United States 4 234 1.4× 99 1.0× 25 0.4× 42 0.6× 61 1.0× 8 339
Szi-chieh Yu Germany 7 109 0.7× 63 0.6× 34 0.5× 34 0.5× 15 0.2× 8 191
Seol Hee Im United States 9 306 1.8× 82 0.8× 51 0.7× 24 0.4× 35 0.5× 12 431
Claire McKellar United States 10 260 1.6× 92 0.9× 17 0.2× 52 0.8× 99 1.5× 11 383
Kohei Shimono Japan 7 170 1.0× 130 1.3× 26 0.4× 28 0.4× 20 0.3× 8 299
Mochi Liu United States 6 118 0.7× 55 0.6× 144 2.0× 103 1.6× 14 0.2× 8 324

Countries citing papers authored by Matthew S. Creamer

Since Specialization
Citations

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

Fields of papers citing papers by Matthew S. Creamer

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Matthew S. Creamer. 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 Matthew S. Creamer. The network helps show where Matthew S. Creamer may publish in the future.

Co-authorship network of co-authors of Matthew S. Creamer

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

All Works

14 of 14 papers shown
1.
Mano, Omer, et al.. (2023). Long-timescale anti-directional rotation in Drosophila optomotor behavior. eLife. 12. 3 indexed citations
2.
Creamer, Matthew S., Kevin S. Chen, Andrew M. Leifer, & Jonathan W. Pillow. (2022). Correcting motion induced fluorescence artifacts in two-channel neural imaging. PLoS Computational Biology. 18(9). e1010421–e1010421. 1 indexed citations
4.
Mano, Omer, et al.. (2021). Predicting individual neuron responses with anatomically constrained task optimization. Current Biology. 31(18). 4062–4075.e4. 9 indexed citations
5.
Mano, Omer, et al.. (2019). Using slow frame rate imaging to extract fast receptive fields. Nature Communications. 10(1). 4979–4979. 8 indexed citations
6.
Creamer, Matthew S., Omer Mano, Ryosuke Tanaka, & Damon A. Clark. (2019). A flexible geometry for panoramic visual and optogenetic stimulation during behavior and physiology. Journal of Neuroscience Methods. 323. 48–55. 17 indexed citations
7.
Creamer, Matthew S., et al.. (2019). Dynamic nonlinearities enable direction opponency in Drosophila elementary motion detectors. Nature Neuroscience. 22(8). 1318–1326. 21 indexed citations
8.
Tarnogorska, Dorota, Matthew S. Creamer, Omer Mano, et al.. (2018). DrosophilaSidekick is required in developing photoreceptors to enable visual motion detection. Development. 145(3). 17 indexed citations
9.
Creamer, Matthew S., Omer Mano, & Damon A. Clark. (2018). Visual Control of Walking Speed in Drosophila. Neuron. 100(6). 1460–1473.e6. 44 indexed citations
10.
Schaefer, Andrew W., et al.. (2016). Local Arp2/3-dependent actin assembly modulates applied traction force during apCAM adhesion site maturation. Molecular Biology of the Cell. 28(1). 98–110. 6 indexed citations
12.
Creamer, Matthew S., et al.. (2016). Direct Measurement of Correlation Responses in Drosophila Elementary Motion Detectors Reveals Fast Timescale Tuning. Neuron. 92(1). 227–239. 46 indexed citations
13.
Stites, Edward C., Meraj Aziz, Matthew S. Creamer, et al.. (2015). Use of Mechanistic Models to Integrate and Analyze Multiple Proteomic Datasets. Biophysical Journal. 108(7). 1819–1829. 18 indexed citations
14.
Creamer, Matthew S., Edward C. Stites, Meraj Aziz, et al.. (2012). Specification, annotation, visualization and simulation of a large rule-based model for ERBB receptor signaling. BMC Systems Biology. 6(1). 107–107. 27 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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