Robert L. Chow

3.3k total citations
42 papers, 2.6k citations indexed

About

Robert L. Chow is a scholar working on Molecular Biology, Genetics and Cellular and Molecular Neuroscience. According to data from OpenAlex, Robert L. Chow has authored 42 papers receiving a total of 2.6k indexed citations (citations by other indexed papers that have themselves been cited), including 37 papers in Molecular Biology, 10 papers in Genetics and 9 papers in Cellular and Molecular Neuroscience. Recurrent topics in Robert L. Chow's work include Retinal Development and Disorders (15 papers), Developmental Biology and Gene Regulation (11 papers) and Connexins and lens biology (7 papers). Robert L. Chow is often cited by papers focused on Retinal Development and Disorders (15 papers), Developmental Biology and Gene Regulation (11 papers) and Connexins and lens biology (7 papers). Robert L. Chow collaborates with scholars based in Canada, United States and Hong Kong. Robert L. Chow's co-authors include Richard A. Lang, Curtis R. Altmann, Ali Hemmati‐Brivanlou, Yijie Gao, J. O. Thomas, Nicholas Cowan, Nicholas J. Cowan, Roderick R. McInnes, David G. Birch and David Moscatelli and has published in prestigious journals such as Cell, Proceedings of the National Academy of Sciences and Nucleic Acids Research.

In The Last Decade

Robert L. Chow

42 papers receiving 2.6k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Robert L. Chow Canada 20 2.3k 537 456 433 320 42 2.6k
Nozomu Takata Japan 15 2.9k 1.3× 397 0.7× 220 0.5× 849 2.0× 237 0.7× 35 3.5k
Kunio Yasuda Japan 35 3.8k 1.7× 685 1.3× 1.1k 2.4× 528 1.2× 303 0.9× 78 4.5k
Milan Jamrich United States 42 4.4k 1.9× 792 1.5× 1.3k 2.8× 721 1.7× 261 0.8× 87 5.3k
Jennifer P. Macke United States 17 3.0k 1.3× 546 1.0× 461 1.0× 789 1.8× 109 0.3× 22 3.6k
Masako Kawada Japan 14 3.8k 1.6× 391 0.7× 359 0.8× 1.1k 2.6× 237 0.7× 21 4.6k
C. L. Cepko United States 14 1.9k 0.8× 329 0.6× 561 1.2× 820 1.9× 132 0.4× 16 2.6k
Elizabeth E. Capowski United States 25 2.6k 1.1× 122 0.2× 281 0.6× 1.1k 2.5× 260 0.8× 36 2.9k
Philip J. Gage United States 31 2.4k 1.1× 227 0.4× 1.0k 2.3× 318 0.7× 529 1.7× 52 3.7k
Makoto Mochii Japan 28 1.7k 0.7× 500 0.9× 432 0.9× 360 0.8× 122 0.4× 65 2.3k
Robert M. Grainger United States 30 2.1k 0.9× 341 0.6× 663 1.5× 320 0.7× 172 0.5× 66 2.4k

Countries citing papers authored by Robert L. Chow

Since Specialization
Citations

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

Fields of papers citing papers by Robert L. Chow

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Robert L. Chow. 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 Robert L. Chow. The network helps show where Robert L. Chow may publish in the future.

Co-authorship network of co-authors of Robert L. Chow

This figure shows the co-authorship network connecting the top 25 collaborators of Robert L. Chow. A scholar is included among the top collaborators of Robert L. Chow 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 Robert L. Chow. Robert L. Chow 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.
Kim, Bo‐Hyun, Anna Mikhailov, Robert L. Chow, et al.. (2024). Testing the PEST hypothesis using relevant Rett mutations in MeCP2 E1 and E2 isoforms. Human Molecular Genetics. 33(21). 1833–1845. 1 indexed citations
2.
Gowen, Brent, et al.. (2023). Laser-induced microinjury of the corneal basal epithelium and imaging of resident macrophage responses in a live, whole-eye preparation. Frontiers in Immunology. 14. 1050594–1050594. 1 indexed citations
3.
Smazynski, Julian, et al.. (2023). MHCII+CD80+ thymic eosinophils increase in abundance during neonatal development in mice and their accumulation is microbiota dependent. Journal of Leukocyte Biology. 114(3). 223–236. 8 indexed citations
4.
Hamilton, Phineas T., Alex Miranda, Robert L. Chow, et al.. (2022). Cytoplasmic switch of ARS2 isoforms promotes nonsense-mediated mRNA decay and arsenic sensitivity. Nucleic Acids Research. 50(3). 1620–1638. 3 indexed citations
5.
Bromma, Kyle, Wonmo Sung, Perry L. Howard, et al.. (2019). Modulation of nanoparticle uptake, intracellular distribution, and retention with docetaxel to enhance radiotherapy. British Journal of Radiology. 93(1106). 20190742–20190742. 26 indexed citations
6.
Baudouin, Christophe, María Hidalgo‐Figueroa, Barbara Pelosi, et al.. (2019). Vsx1 and Chx10 paralogs sequentially secure V2 interneuron identity during spinal cord development. Cellular and Molecular Life Sciences. 77(20). 4117–4131. 8 indexed citations
7.
Howard, Perry L., et al.. (2018). Mapping the Pax6 3’ untranslated region microRNA regulatory landscape. BMC Genomics. 19(1). 820–820. 6 indexed citations
8.
Alford, Spencer C., et al.. (2018). Protecting Pax6 3′ UTR from MicroRNA-7 Partially Restores PAX6 in Islets from an Aniridia Mouse Model. Molecular Therapy — Nucleic Acids. 13. 144–153. 11 indexed citations
9.
Howard, Perry L., et al.. (2016). ImiRP: a computational approach to microRNA target site mutation. BMC Bioinformatics. 17(1). 190–190. 15 indexed citations
10.
Francius, Cédric, María Hidalgo‐Figueroa, Barbara Pelosi, et al.. (2016). Vsx1 Transiently Defines an Early Intermediate V2 Interneuron Precursor Compartment in the Mouse Developing Spinal Cord. Frontiers in Molecular Neuroscience. 9. 145–145. 11 indexed citations
11.
Nickerson, Philip E. B., Kara Ronellenfitch, Jamie D. Boyd, et al.. (2013). Live imaging and analysis of postnatal mouse retinal development. BMC Developmental Biology. 13(1). 24–24. 12 indexed citations
12.
Park, Han Na, C.C. Tan, Robert L. Chow, P. Michael Iuvone, & Machelle T. Pardue. (2012). Role of Vsx1 in Refractive Development. Investigative Ophthalmology & Visual Science. 53(14). 4658–4658. 1 indexed citations
13.
Nickerson, Philip E. B., et al.. (2011). Requirement for the paired‐like homeodomain transcription factor VSX1 in type 3a mouse retinal bipolar cell terminal differentiation. The Journal of Comparative Neurology. 520(1). 117–129. 17 indexed citations
14.
Trenholm, Stuart, et al.. (2011). Vsx1Regulates Terminal Differentiation of Type 7 ON Bipolar Cells. Journal of Neuroscience. 31(37). 13118–13127. 38 indexed citations
15.
Crawford, Cynthia A., Garnik Akopian, Michael W. Jakowec, et al.. (2010). Acute and long‐term response of dopamine nigrostriatal synapses to a single, low‐dose episode of 3‐nitropropionic acid‐mediated chemical hypoxia. Synapse. 65(4). 339–350. 9 indexed citations
16.
Kerschensteiner, Daniel, Haiquan Liu, Chi Cheng, et al.. (2008). Genetic Control of Circuit Function:Vsx1andIrx5Transcription Factors Regulate Contrast Adaptation in the Mouse Retina. Journal of Neuroscience. 28(10). 2342–2352. 33 indexed citations
17.
Clark, Anna M., et al.. (2007). Negative regulation of Vsx1 by its paralog Chx10/Vsx2 is conserved in the vertebrate retina. Brain Research. 1192. 99–113. 56 indexed citations
18.
Altmann, Curtis R., Robert L. Chow, Richard A. Lang, & Ali Hemmati‐Brivanlou. (1997). Lens Induction by Pax-6 inXenopus laevis. Developmental Biology. 185(1). 119–123. 142 indexed citations
19.
Chow, Robert L. & Richard P. Elinson. (1993). Local alteration of cortical actin in Xenopus eggs by the fertilizing sperm. Molecular Reproduction and Development. 35(1). 69–75. 6 indexed citations
20.
Gao, Yijie, et al.. (1992). A cytoplasmic chaperonin that catalyzes β-actin folding. Cell. 69(6). 1043–1050. 431 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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