Philip D. Kiser

3.9k total citations
87 papers, 2.9k citations indexed

About

Philip D. Kiser is a scholar working on Molecular Biology, Ophthalmology and Cellular and Molecular Neuroscience. According to data from OpenAlex, Philip D. Kiser has authored 87 papers receiving a total of 2.9k indexed citations (citations by other indexed papers that have themselves been cited), including 82 papers in Molecular Biology, 25 papers in Ophthalmology and 22 papers in Cellular and Molecular Neuroscience. Recurrent topics in Philip D. Kiser's work include Retinal Development and Disorders (46 papers), Retinal Diseases and Treatments (25 papers) and Retinoids in leukemia and cellular processes (23 papers). Philip D. Kiser is often cited by papers focused on Retinal Development and Disorders (46 papers), Retinal Diseases and Treatments (25 papers) and Retinoids in leukemia and cellular processes (23 papers). Philip D. Kiser collaborates with scholars based in United States, Poland and Canada. Philip D. Kiser's co-authors include Krzysztof Palczewski, Marcin Golczak, Johannes von Lintig, Xuewu Sui, Akiko Maeda, David T. Lodowski, Mark R. Chance, Zhiqian Dong, Wuxian Shi and Elliot H. Choi and has published in prestigious journals such as Chemical Reviews, Proceedings of the National Academy of Sciences and Journal of the American Chemical Society.

In The Last Decade

Philip D. Kiser

82 papers receiving 2.9k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Philip D. Kiser United States 31 2.4k 732 622 578 250 87 2.9k
Marcin Golczak United States 47 5.5k 2.2× 2.0k 2.7× 1.4k 2.3× 1.5k 2.6× 456 1.8× 118 6.6k
Yasuhiro Itagaki Japan 26 1.8k 0.7× 1.2k 1.7× 242 0.4× 320 0.6× 96 0.4× 65 3.0k
Vladimir Kuksa United States 19 1.7k 0.7× 542 0.7× 156 0.3× 661 1.1× 139 0.6× 31 1.9k
J. Samuel Zigler United States 39 3.3k 1.3× 632 0.9× 59 0.1× 257 0.4× 648 2.6× 118 4.4k
Konstantin Petrukhin United States 28 2.4k 1.0× 1.1k 1.6× 122 0.2× 431 0.7× 292 1.2× 58 3.5k
David T. Lodowski United States 25 2.5k 1.0× 107 0.1× 92 0.1× 1.8k 3.0× 164 0.7× 41 3.3k
Arthur S. Polans United States 28 2.3k 0.9× 430 0.6× 58 0.1× 1.1k 1.9× 318 1.3× 48 3.1k
Sidney Futterman United States 25 1.7k 0.7× 349 0.5× 276 0.4× 435 0.8× 262 1.0× 50 2.3k
E.A. Dratz United States 25 1.3k 0.5× 266 0.4× 472 0.8× 490 0.8× 110 0.4× 44 2.0k
Hitoshi Shichi United States 28 2.2k 0.9× 325 0.4× 35 0.1× 1.1k 1.9× 264 1.1× 149 3.4k

Countries citing papers authored by Philip D. Kiser

Since Specialization
Citations

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

Fields of papers citing papers by Philip D. Kiser

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Philip D. Kiser. 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 Philip D. Kiser. The network helps show where Philip D. Kiser may publish in the future.

Co-authorship network of co-authors of Philip D. Kiser

This figure shows the co-authorship network connecting the top 25 collaborators of Philip D. Kiser. A scholar is included among the top collaborators of Philip D. Kiser 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 Philip D. Kiser. Philip D. Kiser 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.
Santos, Daniel J. V. A. dos, et al.. (2025). The molecular mechanisms of visual chromophore release from cellular retinaldehyde-binding protein. Structure. 33(8). 1436–1445.e2.
2.
Palczewska, Grażyna, Samuel W. Du, Jianye Zhang, et al.. (2025). Retinol tracing within murine neural retina reveals cell type–specific retinol transport and distribution. Journal of Clinical Investigation. 136(3).
3.
Palczewski, Krzysztof, et al.. (2025). Rationally Designed, Short-Acting RPE65 Inhibitors for Visual Cycle-Associated Retinopathies. Journal of Medicinal Chemistry. 68(16). 17638–17652.
4.
Salom, David, W. Clay Smith, Bruce A. Knutson, et al.. (2024). Mechanisms of amphibian arrestin 1 self-association and dynamic distribution in retinal photoreceptors. Journal of Biological Chemistry. 300(12). 107966–107966. 1 indexed citations
5.
Salom, David, Philip D. Kiser, & Krzysztof Palczewski. (2024). Insights into the Activation and Self-Association of Arrestin-1. Biochemistry. 64(2). 364–376.
6.
Salom, David, John D. Hong, Aleksander Tworak, et al.. (2023). Structural basis for the allosteric modulation of rhodopsin by nanobody binding to its extracellular domain. Nature Communications. 14(1). 5209–5209. 11 indexed citations
7.
Hong, John D., David Salom, Michał Andrzej Kochman, et al.. (2022). Chromophore hydrolysis and release from photoactivated rhodopsin in native membranes. Proceedings of the National Academy of Sciences. 119(45). e2213911119–e2213911119. 15 indexed citations
8.
Choi, Elliot H., Susie Suh, Henri Leinonen, et al.. (2021). An inducible Cre mouse for studying roles of the RPE in retinal physiology and disease. JCI Insight. 6(9). 18 indexed citations
9.
Sander, Christopher L., B.T. Eger, Hui‐Woog Choe, et al.. (2021). Structural evidence for visual arrestin priming via complexation of phosphoinositols. Structure. 30(2). 263–277.e5. 17 indexed citations
10.
Sander, Christopher L., Avery E. Sears, Antônio F. M. Pinto, et al.. (2021). Nano-scale resolution of native retinal rod disk membranes reveals differences in lipid composition. The Journal of Cell Biology. 220(8). 26 indexed citations
11.
Gazda, Małgorzata Anna, Matthew B. Toomey, Pedro M. Araújo, et al.. (2020). Genetic Basis of De Novo Appearance of Carotenoid Ornamentation in Bare Parts of Canaries. Molecular Biology and Evolution. 37(5). 1317–1328. 32 indexed citations
12.
Zhang, Jianye, Nimesh Khadka, Erik R. Farquhar, et al.. (2020). Structural basis for carotenoid cleavage by an archaeal carotenoid dioxygenase. Proceedings of the National Academy of Sciences. 117(33). 19914–19925. 20 indexed citations
13.
Suh, Susie, Elliot H. Choi, Henri Leinonen, et al.. (2020). Publisher Correction: Restoration of visual function in adult mice with an inherited retinal disease via adenine base editing. Nature Biomedical Engineering. 4(11). 1119–1119. 4 indexed citations
14.
Palczewski, Krzysztof & Philip D. Kiser. (2020). Shedding new light on the generation of the visual chromophore. Proceedings of the National Academy of Sciences. 117(33). 19629–19638. 62 indexed citations
15.
Bandara, Sepalika, Vipul M. Parmar, Srinivasagan Ramkumar, et al.. (2020). The human mitochondrial enzyme BCO2 exhibits catalytic activity toward carotenoids and apocarotenoids. Journal of Biological Chemistry. 295(46). 15553–15565. 31 indexed citations
16.
Kolesnikov, Alexander V., Philip D. Kiser, Krzysztof Palczewski, & Vladimir J. Kefalov. (2020). Function of mammalian M-cones depends on the level of CRALBP in Müller cells. The Journal of General Physiology. 153(1). 15 indexed citations
17.
Suh, Susie, Elliot H. Choi, Henri Leinonen, et al.. (2020). Restoration of visual function in adult mice with an inherited retinal disease via adenine base editing. Nature Biomedical Engineering. 5(2). 169–178. 116 indexed citations
18.
Petersen‐Jones, Simon M., Laurence M. Occelli, Paige A. Winkler, et al.. (2019). New large animal model for RDH5-associated retinopathies. Investigative Ophthalmology & Visual Science. 60(9). 458–458. 2 indexed citations
19.
Kiser, Philip D., Jianye Zhang, Juan M Angueyra, et al.. (2018). Retinoid isomerase inhibitors impair but do not block mammalian cone photoreceptor function. The Journal of General Physiology. 150(4). 571–590. 25 indexed citations
20.
Choi, Elliot H., et al.. (2018). Structural biology of 11-cis-retinaldehyde production in the classical visual cycle. Biochemical Journal. 475(20). 3171–3188. 19 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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