Richard I. Dorsky

4.6k total citations
53 papers, 3.6k citations indexed

About

Richard I. Dorsky is a scholar working on Molecular Biology, Cell Biology and Developmental Neuroscience. According to data from OpenAlex, Richard I. Dorsky has authored 53 papers receiving a total of 3.6k indexed citations (citations by other indexed papers that have themselves been cited), including 42 papers in Molecular Biology, 22 papers in Cell Biology and 17 papers in Developmental Neuroscience. Recurrent topics in Richard I. Dorsky's work include Developmental Biology and Gene Regulation (24 papers), Zebrafish Biomedical Research Applications (19 papers) and Neurogenesis and neuroplasticity mechanisms (17 papers). Richard I. Dorsky is often cited by papers focused on Developmental Biology and Gene Regulation (24 papers), Zebrafish Biomedical Research Applications (19 papers) and Neurogenesis and neuroplasticity mechanisms (17 papers). Richard I. Dorsky collaborates with scholars based in United States, Germany and Switzerland. Richard I. Dorsky's co-authors include Randall T. Moon, David W. Raible, William A. Harris, David Rapaport, Laird C. Sheldahl, Wesley Chang, Yuanyuan Xie, Jennifer Bonner, Motoyuki Itoh and Shami Kanekar and has published in prestigious journals such as Nature, Neuron and Genes & Development.

In The Last Decade

Richard I. Dorsky

53 papers receiving 3.5k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Richard I. Dorsky United States 31 2.8k 1.2k 670 538 464 53 3.6k
Jimann Shin United States 22 1.5k 0.5× 1.1k 0.9× 386 0.6× 757 1.4× 258 0.6× 31 2.6k
Mengqing Xiang United States 39 3.7k 1.3× 762 0.6× 1.4k 2.0× 712 1.3× 334 0.7× 99 4.9k
Monica L. Vetter United States 33 3.2k 1.1× 609 0.5× 1.1k 1.6× 462 0.9× 380 0.8× 72 4.5k
Xavier Morin France 26 3.0k 1.1× 1.6k 1.3× 1.0k 1.5× 538 1.0× 536 1.2× 39 4.7k
Tamar Sapir Israel 30 1.6k 0.6× 1.3k 1.0× 840 1.3× 931 1.7× 450 1.0× 58 3.0k
Chi‐Bin Chien United States 26 2.6k 0.9× 1.8k 1.5× 1.4k 2.1× 470 0.9× 359 0.8× 39 4.1k
Corinne Houart United Kingdom 33 3.2k 1.1× 935 0.8× 758 1.1× 508 0.9× 568 1.2× 61 4.0k
Luis C. Fuentealba United States 19 2.2k 0.8× 513 0.4× 644 1.0× 1.1k 2.0× 373 0.8× 22 3.3k
Rivka A. Rachel United States 27 2.6k 0.9× 960 0.8× 755 1.1× 237 0.4× 605 1.3× 38 3.3k
Jeremy S. Dasen United States 31 3.2k 1.1× 761 0.6× 884 1.3× 628 1.2× 964 2.1× 49 4.8k

Countries citing papers authored by Richard I. Dorsky

Since Specialization
Citations

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

Fields of papers citing papers by Richard I. Dorsky

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Richard I. Dorsky. 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 Richard I. Dorsky. The network helps show where Richard I. Dorsky may publish in the future.

Co-authorship network of co-authors of Richard I. Dorsky

This figure shows the co-authorship network connecting the top 25 collaborators of Richard I. Dorsky. A scholar is included among the top collaborators of Richard I. Dorsky 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 Richard I. Dorsky. Richard I. Dorsky 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.
Veit, Florian, et al.. (2020). Bsx Is Essential for Differentiation of Multiple Neuromodulatory Cell Populations in the Secondary Prosencephalon. Frontiers in Neuroscience. 14. 525–525. 12 indexed citations
3.
Xie, Yuanyuan, Dan Kaufmann, Matthew J. Moulton, et al.. (2017). Lef1-dependent hypothalamic neurogenesis inhibits anxiety. PLoS Biology. 15(8). e2002257–e2002257. 21 indexed citations
4.
Eisenhoffer, George T., Gloria Slattum, Oscar E. Ruiz, et al.. (2016). A toolbox to study epidermal cell types in zebrafish. Journal of Cell Science. 130(1). 269–277. 38 indexed citations
5.
Poulain, Fabienne E., et al.. (2015). Wnt/ß-catenin signaling is required for radial glial neurogenesis following spinal cord injury. Developmental Biology. 403(1). 15–21. 80 indexed citations
6.
Dorsky, Richard I., et al.. (2014). Spinal Cord Transection in the Larval Zebrafish. Journal of Visualized Experiments. 14 indexed citations
7.
Dorsky, Richard I., et al.. (2014). Radial glial progenitors repair the zebrafish spinal cord following transection. Experimental Neurology. 256. 81–92. 54 indexed citations
8.
Wang, Xu, Daniel Kopinke, Hideo Otsuna, et al.. (2012). Wnt Signaling Regulates Postembryonic Hypothalamic Progenitor Differentiation. Developmental Cell. 23(3). 624–636. 70 indexed citations
9.
Fuhrmann, Sabine, et al.. (2012). Extraocular ectoderm triggers dorsal retinal fate during optic vesicle evagination in zebrafish. Developmental Biology. 371(1). 57–65. 10 indexed citations
10.
Wang, Xu, Ji Eun Lee, & Richard I. Dorsky. (2009). Identification of Wnt-Responsive Cells in the Zebrafish Hypothalamus. Zebrafish. 6(1). 49–58. 32 indexed citations
11.
Topczewska, Jolanta M., et al.. (2008). Hh and Wnt signaling regulate formation of olig2+ neurons in the zebrafish cerebellum. Developmental Biology. 318(1). 162–171. 45 indexed citations
12.
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
13.
Dorsky, Richard I., et al.. (2005). Expression pattern of zebrafish tcf7 suggests unexplored domains of Wnt/β‐catenin activity. Developmental Dynamics. 233(1). 233–239. 29 indexed citations
14.
Lewis, Jessica L., Jennifer Bonner, Melinda S. Modrell, et al.. (2004). Reiterated Wnt signaling during zebrafish neural crest development. Development. 131(6). 1299–1308. 208 indexed citations
15.
Dorsky, Richard I., Motoyuki Itoh, Randall T. Moon, & Ajay Chitnis. (2003). Twotcf3genes cooperate to pattern the zebrafish brain. Development. 130(9). 1937–1947. 125 indexed citations
16.
Dorsky, Richard I., Chris J. Cretekos, David J. Grunwald, et al.. (1999). Maternal and embryonic expression of zebrafish lef1. Mechanisms of Development. 86(1-2). 147–150. 49 indexed citations
17.
Rapaport, David & Richard I. Dorsky. (1998). Inductive competence, its significance in retinal cell fate determination and a role for Delta–Notch signaling. Seminars in Cell and Developmental Biology. 9(3). 241–247. 30 indexed citations
18.
Kanekar, Shami, Muriel Perron, Richard I. Dorsky, et al.. (1997). Xath5 Participates in a Network of bHLH Genes in the Developing Xenopus Retina. Neuron. 19(5). 981–994. 216 indexed citations
19.
Dorsky, Richard I., Wesley Chang, David Rapaport, & William A. Harris. (1997). Regulation of neuronal diversity in the Xenopus retina by Delta signalling. Nature. 385(6611). 67–70. 231 indexed citations
20.
Ferreiro, Beatriz, Paul Skoglund, Adina Bailey, Richard I. Dorsky, & William A. Harris. (1993). XASH1, a Xenopus homolog of achaete-scute: a proneural gene in anterior regions of the vertebrate CNS. Mechanisms of Development. 40(1-2). 25–36. 78 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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