Daniel Goldman

9.8k total citations · 1 hit paper
107 papers, 7.0k citations indexed

About

Daniel Goldman is a scholar working on Molecular Biology, Cell Biology and Cellular and Molecular Neuroscience. According to data from OpenAlex, Daniel Goldman has authored 107 papers receiving a total of 7.0k indexed citations (citations by other indexed papers that have themselves been cited), including 92 papers in Molecular Biology, 29 papers in Cell Biology and 26 papers in Cellular and Molecular Neuroscience. Recurrent topics in Daniel Goldman's work include Retinal Development and Disorders (41 papers), Nicotinic Acetylcholine Receptors Study (23 papers) and Zebrafish Biomedical Research Applications (22 papers). Daniel Goldman is often cited by papers focused on Retinal Development and Disorders (41 papers), Nicotinic Acetylcholine Receptors Study (23 papers) and Zebrafish Biomedical Research Applications (22 papers). Daniel Goldman collaborates with scholars based in United States, Italy and Australia. Daniel Goldman's co-authors include Blake V. Fausett, Rajesh Ramachandran, Jin Wan, Xiao‐Feng Zhao, George Ordal, Steve Heinemann, Peter Macpherson, Curtis Powell, Julie K. Staple and Huibin Tang and has published in prestigious journals such as Science, Cell and Proceedings of the National Academy of Sciences.

In The Last Decade

Daniel Goldman

107 papers receiving 6.9k citations

Hit Papers

Müller glial cell reprogr... 2014 2026 2018 2022 2014 100 200 300 400

Author Peers

Peers are selected by citation overlap in the author's most active subfields. citations · hero ref

Author Last Decade Papers Cites
Daniel Goldman 5.7k 1.9k 1.6k 1.0k 652 107 7.0k
Roderick R. McInnes 5.4k 0.9× 2.1k 1.1× 746 0.5× 421 0.4× 893 1.4× 124 7.0k
David L. Turner 7.3k 1.3× 1.3k 0.7× 1.0k 0.6× 928 0.9× 1.3k 2.0× 37 8.6k
Ronald G. Gregg 5.4k 0.9× 2.6k 1.4× 725 0.4× 286 0.3× 1.1k 1.7× 132 7.1k
Rafael Linden 4.5k 0.8× 1.9k 1.0× 486 0.3× 503 0.5× 235 0.4× 164 6.2k
A.A. Moscona 4.9k 0.9× 1.7k 0.9× 1.4k 0.9× 290 0.3× 737 1.1× 135 7.2k
Jeff S. Mumm 4.4k 0.8× 1.2k 0.6× 1.5k 0.9× 632 0.6× 548 0.8× 60 6.9k
Claudia A. O. Stuermer 3.5k 0.6× 2.1k 1.1× 2.5k 1.5× 1.2k 1.2× 271 0.4× 111 5.8k
D. Dahl 3.8k 0.7× 2.8k 1.5× 1.8k 1.1× 1.9k 1.9× 334 0.5× 114 7.6k
Solon Thanos 3.8k 0.7× 3.8k 2.0× 683 0.4× 1.9k 1.8× 245 0.4× 192 7.9k

Countries citing papers authored by Daniel Goldman

Since Specialization
Citations

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

Fields of papers citing papers by Daniel Goldman

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Daniel Goldman

This figure shows the co-authorship network connecting the top 25 collaborators of Daniel Goldman. A scholar is included among the top collaborators of Daniel Goldman 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 Daniel Goldman. Daniel Goldman 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
3.
Devi, Sulochana, et al.. (2022). Vegf signaling between Müller glia and vascular endothelial cells is regulated by immune cells and stimulates retina regeneration. Proceedings of the National Academy of Sciences. 119(50). e2211690119–e2211690119. 18 indexed citations
4.
Devi, Sulochana, et al.. (2021). Notch signaling via Hey1 and Id2b regulates Müller glia's regenerative response to retinal injury. Glia. 69(12). 2882–2898. 30 indexed citations
5.
Chong, Baxi, et al.. (2018). The importance of body-limb coordination in a walking tetrapod. Bulletin of the American Physical Society. 2018. 1 indexed citations
6.
Elsaeidi, Fairouz, Peter Macpherson, Elizabeth Mills, et al.. (2018). Notch Suppression Collaborates with Ascl1 and Lin28 to Unleash a Regenerative Response in Fish Retina, But Not in Mice. Journal of Neuroscience. 38(9). 2246–2261. 65 indexed citations
8.
Zhao, Xiao‐Feng & Daniel Goldman. (2014). A New Transgenic Line Reporting pStat3 Signaling in Glia. Zebrafish. 11(6). 588–589. 1 indexed citations
10.
Aravantinou, Meropi, Nina Derby, Giulia Calenda, et al.. (2012). The Nonnucleoside Reverse Transcription Inhibitor MIV-160 Delivered from an Intravaginal Ring, But Not from a Carrageenan Gel, Protects Against Simian/Human Immunodeficiency Virus-RT Infection. AIDS Research and Human Retroviruses. 28(11). 1467–1475. 23 indexed citations
11.
Wan, Jin, Rajesh Ramachandran, & Daniel Goldman. (2012). HB-EGF Is Necessary and Sufficient for Müller Glia Dedifferentiation and Retina Regeneration. Developmental Cell. 22(2). 334–347. 209 indexed citations
12.
Ramachandran, Rajesh, et al.. (2012). Insm1a-mediated gene repression is essential for the formation and differentiation of Müller glia-derived progenitors in the injured retina. Nature Cell Biology. 14(10). 1013–1023. 87 indexed citations
13.
Powell, Curtis, Fairouz Elsaeidi, & Daniel Goldman. (2012). Injury-Dependent Müller Glia and Ganglion Cell Reprogramming during Tissue Regeneration Requires Apobec2a and Apobec2b. Journal of Neuroscience. 32(3). 1096–1109. 66 indexed citations
14.
Ghiasvand, Noor M., et al.. (2011). Deletion of a remote enhancer near ATOH7 disrupts retinal neurogenesis, causing NCRNA disease. Nature Neuroscience. 14(5). 578–586. 110 indexed citations
15.
Ramachandran, Rajesh, Xiao‐Feng Zhao, & Daniel Goldman. (2011). Ascl1a/Dkk/β-catenin signaling pathway is necessary and glycogen synthase kinase-3β inhibition is sufficient for zebrafish retina regeneration. Proceedings of the National Academy of Sciences. 108(38). 15858–15863. 169 indexed citations
16.
Ramachandran, Rajesh, Blake V. Fausett, & Daniel Goldman. (2010). Ascl1a regulates Müller glia dedifferentiation and retinal regeneration through a Lin-28-dependent, let-7 microRNA signalling pathway. Nature Cell Biology. 12(11). 1101–1107. 279 indexed citations
17.
Tang, Huibin, Peter Macpherson, Eric S. Meadows, et al.. (2008). A Histone Deacetylase 4/Myogenin Positive Feedback Loop Coordinates Denervation-dependent Gene Induction and Suppression. Molecular Biology of the Cell. 20(4). 1120–1131. 115 indexed citations
18.
Goldman, Daniel, et al.. (2006). A reporter-assisted mutagenesis screen using α1-tubulin-GFP transgenic zebrafish uncovers missteps during neuronal development and axonogenesis. Developmental Biology. 296(1). 29–47. 40 indexed citations
19.
Allison, W. Ted, Linda K. Barthel, Kuang Chen, et al.. (2005). Genetic Analysis of the Cone Photoreceptor Mosaic in Zebrafish. Investigative Ophthalmology & Visual Science. 46(13). 3962–3962. 1 indexed citations
20.
Gilmour, Brian P., et al.. (1995). Electrical Activity Suppresses Nicotinic Acetylcholine Receptor γ Subunit Promoter Activity. Developmental Biology. 168(2). 416–428. 21 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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