David Hicks

7.0k total citations · 1 hit paper
124 papers, 5.6k citations indexed

About

David Hicks is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Endocrine and Autonomic Systems. According to data from OpenAlex, David Hicks has authored 124 papers receiving a total of 5.6k indexed citations (citations by other indexed papers that have themselves been cited), including 103 papers in Molecular Biology, 64 papers in Cellular and Molecular Neuroscience and 26 papers in Endocrine and Autonomic Systems. Recurrent topics in David Hicks's work include Retinal Development and Disorders (87 papers), Photoreceptor and optogenetics research (39 papers) and Circadian rhythm and melatonin (26 papers). David Hicks is often cited by papers focused on Retinal Development and Disorders (87 papers), Photoreceptor and optogenetics research (39 papers) and Circadian rhythm and melatonin (26 papers). David Hicks collaborates with scholars based in France, United States and Germany. David Hicks's co-authors include José‐Alain Sahel, Colin J. Barnstable, Robert S. Molday, Yves Courtois, Christian P. Hamel, H. Dreyfus, Anita E. Hendrickson, Saddek Mohand‐Saïd, Valérie Forster and Norbert Kinkl and has published in prestigious journals such as Journal of Biological Chemistry, Nature Genetics and Journal of Neuroscience.

In The Last Decade

David Hicks

122 papers receiving 5.5k citations

Hit Papers

The Retinal Pigment Epithelium in Health and Disease 2010 2026 2015 2020 2010 100 200 300 400

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
David Hicks France 40 4.3k 2.2k 1.6k 696 659 124 5.6k
Charlotte E. Remé Switzerland 39 3.9k 0.9× 1.5k 0.7× 2.1k 1.3× 769 1.1× 519 0.8× 60 5.5k
Debora B. Farber United States 46 6.8k 1.6× 2.9k 1.3× 1.9k 1.2× 311 0.4× 540 0.8× 207 7.8k
Neal S. Peachey United States 54 6.3k 1.5× 3.8k 1.7× 2.3k 1.5× 318 0.5× 745 1.1× 206 8.3k
Ruben Adler United States 44 4.8k 1.1× 3.1k 1.4× 964 0.6× 260 0.4× 613 0.9× 124 6.4k
Steven Nusinowitz United States 38 4.1k 0.9× 1.3k 0.6× 2.2k 1.4× 220 0.3× 823 1.2× 99 5.2k
Ronald A. Bush United States 42 4.7k 1.1× 2.0k 0.9× 1.8k 1.2× 249 0.4× 893 1.4× 76 5.4k
William K. Stell Canada 46 4.3k 1.0× 3.5k 1.6× 1.4k 0.9× 339 0.5× 1.0k 1.5× 128 6.5k
Glen Jeffery United Kingdom 43 3.4k 0.8× 1.7k 0.8× 1.7k 1.1× 418 0.6× 954 1.4× 171 5.4k
Ann H. Milam United States 48 6.0k 1.4× 2.7k 1.2× 3.6k 2.3× 177 0.3× 1.1k 1.7× 84 7.9k
Elio Raviola United States 46 4.4k 1.0× 3.7k 1.7× 963 0.6× 690 1.0× 771 1.2× 75 6.8k

Countries citing papers authored by David Hicks

Since Specialization
Citations

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

Fields of papers citing papers by David Hicks

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of David Hicks

This figure shows the co-authorship network connecting the top 25 collaborators of David Hicks. A scholar is included among the top collaborators of David Hicks 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 David Hicks. David Hicks 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.
Roux, Michel J., et al.. (2024). Hyperglycemia and circadian disruption lead to retinal dysfunction in a stabilized colony of the fat sand rat Psammomys obesus. Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. 1870(4). 167118–167118.
2.
3.
Hicks, David, et al.. (2017). Melatonin signaling affects the timing in the daily rhythm of phagocytic activity by the retinal pigment epithelium. Experimental Eye Research. 165. 90–95. 35 indexed citations
4.
Sandu, Cristina, et al.. (2013). Prolonged light exposure induces widespread phase shifting in the circadian clock and visual pigment gene expression of the Arvicanthis ansorgei retina.. PubMed. 19. 1060–73. 16 indexed citations
5.
Sandu, Cristina, David Hicks, & Marie‐Paule Felder‐Schmittbuhl. (2011). Rat photoreceptor circadian oscillator strongly relies on lighting conditions. European Journal of Neuroscience. 34(3). 507–516. 39 indexed citations
6.
Mendoza, Jorge, et al.. (2009). Loss of photic entrainment at low illuminances in rats with acute photoreceptor degeneration. European Journal of Neuroscience. 30(8). 1527–1536. 22 indexed citations
7.
Tezcaner, Ayşen & David Hicks. (2007). In vitro characterization of micropatterned PLGA‐PHBV8 blend films as temporary scaffolds for photoreceptor cells. Journal of Biomedical Materials Research Part A. 86A(1). 170–181. 16 indexed citations
9.
Delyfer, Marie‐Noëlle, Thierry Léveillard, Saddek Mohand‐Saïd, et al.. (2004). Inherited retinal degenerations: therapeutic prospects. Biology of the Cell. 96(4). 261–269. 96 indexed citations
10.
Cinaroglu, Ayca, Anıl Özdemir, Ceren Ergorul, et al.. (2004). Expression and possible function of fibroblast growth factor 9 (FGF9) and its cognate receptors FGFR2 and FGFR3 in postnatal and adult retina. Journal of Neuroscience Research. 79(3). 329–339. 22 indexed citations
11.
Kinkl, Norbert, José‐Alain Sahel, & David Hicks. (2001). Alternate FGF2-ERK1/2 Signaling Pathways in Retinal Photoreceptor and Glial Cells in Vitro. Journal of Biological Chemistry. 276(47). 43871–43878. 66 indexed citations
13.
Dreyfus, H., et al.. (1998). Excitotoxic damage of retinal glial cells depends upon normal neuron-glial interactions. Glia. 23(2). 146–155. 18 indexed citations
14.
Buğra, Kuyaş & David Hicks. (1997). Acidic and basic fibroblast growth factor messenger RNA and protein show increased expression in adult compared to developing normal and dystrophic rat retina. Journal of Molecular Neuroscience. 9(1). 13–25. 22 indexed citations
15.
Hicks, David, Bernard Guérold, & H. Dreyfus. (1996). Stimulation of endogenous ganglioside metabolism by neurotrophic growth factors in cultured retinal M�ller glia. Glia. 16(4). 316–324. 11 indexed citations
16.
Hicks, David & Terry A. Krulwich. (1995). The respiratory chain of alkaliphilic bacteria. Biochimica et Biophysica Acta (BBA) - Bioenergetics. 1229(3). 303–314. 39 indexed citations
17.
Becquet, F., Olivier Goureau, G. Soubrane, et al.. (1994). Superoxide Inhibits Proliferation and Phagocytic Internalization of Photoreceptor Outer Segments by Bovine Retinal Pigment Epithelium in Vitro. Experimental Cell Research. 212(2). 374–382. 27 indexed citations
18.
Malecaze, François, André Mathis, Jean-Louis Arné, et al.. (1991). Localization of acidic fibroblast growth factor in proliferative vitreoretinopathy membranes. Current Eye Research. 10(8). 719–729. 27 indexed citations
19.
Akagawa, Kimio, David Hicks, & Colin J. Barnstable. (1987). Histiotypic organization and cell differentiation in rat retinal reaggregate cultures. Brain Research. 437(2). 298–308. 49 indexed citations
20.
Hicks, David, Nathan Nelson, & Charles F. Yocum. (1986). Cyanobacterial and chloroplast F1-ATPases: cross-reconstitution of photophosphorylation and subunit immunological relationships. Biochimica et Biophysica Acta (BBA) - Bioenergetics. 851(2). 217–222. 5 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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