Jeffrey M. Gross

2.7k total citations
77 papers, 2.0k citations indexed

About

Jeffrey M. Gross is a scholar working on Molecular Biology, Cell Biology and Ophthalmology. According to data from OpenAlex, Jeffrey M. Gross has authored 77 papers receiving a total of 2.0k indexed citations (citations by other indexed papers that have themselves been cited), including 63 papers in Molecular Biology, 23 papers in Cell Biology and 12 papers in Ophthalmology. Recurrent topics in Jeffrey M. Gross's work include Retinal Development and Disorders (35 papers), Zebrafish Biomedical Research Applications (18 papers) and Developmental Biology and Gene Regulation (12 papers). Jeffrey M. Gross is often cited by papers focused on Retinal Development and Disorders (35 papers), Zebrafish Biomedical Research Applications (18 papers) and Developmental Biology and Gene Regulation (12 papers). Jeffrey M. Gross collaborates with scholars based in United States, China and France. Jeffrey M. Gross's co-authors include David R. McClay, Rosa A. Uribe, Jiwoon Lee, Richard J. Nuckels, Brian D. Perkins, Chi‐Fai Ng, Rachel K. Tittle, Jonathan Bibliowicz, Chanjae Lee and Tristan Darland and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Biological Chemistry and Development.

In The Last Decade

Jeffrey M. Gross

73 papers receiving 2.0k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Jeffrey M. Gross United States 30 1.6k 577 327 242 210 77 2.0k
Juan Ramón Martínez‐Morales Spain 21 1.7k 1.1× 458 0.8× 409 1.3× 155 0.6× 498 2.4× 46 2.0k
Muriel Perron France 27 2.4k 1.5× 600 1.0× 317 1.0× 231 1.0× 671 3.2× 60 2.6k
Ryan Thummel United States 26 1.6k 1.0× 734 1.3× 218 0.7× 175 0.7× 231 1.1× 56 2.0k
Minh‐Thanh Nguyen United States 14 1.5k 1.0× 506 0.9× 356 1.1× 102 0.4× 204 1.0× 15 1.9k
Thomas S. Vihtelic United States 22 1.5k 0.9× 748 1.3× 171 0.5× 195 0.8× 389 1.9× 34 1.8k
Nadean L. Brown United States 27 2.1k 1.3× 489 0.8× 253 0.8× 294 1.2× 611 2.9× 50 2.3k
Cheryl Y. Gregory‐Evans Canada 28 2.0k 1.3× 330 0.6× 469 1.4× 668 2.8× 420 2.0× 67 2.7k
Bharesh K. Chauhan United States 20 1.1k 0.7× 324 0.6× 261 0.8× 138 0.6× 118 0.6× 28 1.4k
Sabine Fuhrmann United States 20 1.5k 0.9× 279 0.5× 331 1.0× 263 1.1× 485 2.3× 35 1.7k
Penny Rashbass United Kingdom 16 2.4k 1.5× 495 0.9× 520 1.6× 145 0.6× 414 2.0× 22 2.8k

Countries citing papers authored by Jeffrey M. Gross

Since Specialization
Citations

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

Fields of papers citing papers by Jeffrey M. Gross

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Jeffrey M. Gross. 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 Jeffrey M. Gross. The network helps show where Jeffrey M. Gross may publish in the future.

Co-authorship network of co-authors of Jeffrey M. Gross

This figure shows the co-authorship network connecting the top 25 collaborators of Jeffrey M. Gross. A scholar is included among the top collaborators of Jeffrey M. Gross 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 Jeffrey M. Gross. Jeffrey M. Gross 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.
Kostka, Dennis, et al.. (2025). tet2 and tet3 regulate cell fate specification and differentiation events during retinal development. Scientific Reports. 15(1). 10404–10404. 1 indexed citations
2.
Leach, Lyndsay L., et al.. (2025). Macrophage/microglia-dependent mechanisms drive retinal pigment epithelium regeneration in zebrafish. Cell Reports. 44(10). 116325–116325.
3.
Raeisossadati, Reza, Emily Jane Davis, Bingjie Wang, et al.. (2024). A cis-regulatory module underlies retinal ganglion cell genesis and axonogenesis. Cell Reports. 43(6). 114291–114291. 3 indexed citations
4.
Kostka, Dennis, et al.. (2024). Isolation and Preparation of Embryonic Zebrafish Retinal Cells for Single-Cell RNA Sequencing. Methods in molecular biology. 2848. 85–103. 1 indexed citations
5.
Ausk, Brandon J., et al.. (2023). A microCT-based platform to quantify drug targeting. European Radiology Experimental. 7(1). 38–38.
6.
Leach, Lyndsay L., et al.. (2021). The immune response is a critical regulator of zebrafish retinal pigment epithelium regeneration. Proceedings of the National Academy of Sciences. 118(21). 31 indexed citations
7.
Chen, Si, Kira L. Lathrop, Takaaki Kuwajima, & Jeffrey M. Gross. (2021). Retinal ganglion cell survival after severe optic nerve injury is modulated by crosstalk between Jak/Stat signaling and innate immune responses in the zebrafish retina. Development. 149(8). 15 indexed citations
8.
Lu, Fangfang, et al.. (2021). The retinal pigment epithelium: Development, injury responses, and regenerative potential in mammalian and non-mammalian systems. Progress in Retinal and Eye Research. 85. 100969–100969. 58 indexed citations
9.
Lu, Fangfang, Jeffrey M. Gross, & Lyndsay L. Leach. (2021). mTOR signaling in zebrafish retinal pigment epithelium regeneration. Investigative Ophthalmology & Visual Science. 62(8). 2589–2589.
10.
Leach, Lyndsay L., Dwight K. Romanovicz, Ross F. Collery, et al.. (2019). Regeneration of the zebrafish retinal pigment epithelium after widespread genetic ablation. PLoS Genetics. 15(1). e1007939–e1007939. 41 indexed citations
11.
Gross, Jeffrey M., et al.. (2019). Genetic and epigenetic control of retinal development in zebrafish. Current Opinion in Neurobiology. 59. 120–127. 30 indexed citations
12.
Gautier‐Courteille, Carole, Deepti Anand, Atul Kakrana, et al.. (2018). The RNA-binding protein Celf1 post-transcriptionally regulates p27Kip1 and Dnase2b to control fiber cell nuclear degradation in lens development. PLoS Genetics. 14(3). e1007278–e1007278. 40 indexed citations
13.
Gross, Jeffrey M., et al.. (2018). The cellular bases of choroid fissure formation and closure. Developmental Biology. 440(2). 137–151. 33 indexed citations
14.
Tittle, Rachel K., Chi‐Fai Ng, Richard J. Nuckels, et al.. (2010). Uhrf1 and Dnmt1 are required for development and maintenance of the zebrafish lens. Developmental Biology. 350(1). 50–63. 67 indexed citations
15.
16.
Uribe, Rosa A. & Jeffrey M. Gross. (2007). Immunohistochemistry on Cryosections from Embryonic and Adult Zebrafish Eyes. Cold Spring Harbor Protocols. 2007(7). pdb.prot4779–pdb.prot4779. 41 indexed citations
17.
Gross, Jeffrey M. & John E. Dowling. (2005). Laminin Beta 1 and Laminin Gamma 1 Are Essential for Normal Lens and Retinal Development in Zebrafish. Investigative Ophthalmology & Visual Science. 46(13). 2441–2441. 1 indexed citations
18.
Robinson, Phyllis R., Kevin L. Griffith, Jeffrey M. Gross, & Michael C. O’Neill. (1999). A back-propagation neural network predicts absorption maxima of chimeric human red/green visual pigments. Vision Research. 39(9). 1707–1712. 2 indexed citations
19.
Thissen, Julia, et al.. (1997). Prenylation-dependent Association of Ki-Ras with Microtubules. Journal of Biological Chemistry. 272(48). 30362–30370. 106 indexed citations
20.
Gross, Jeffrey M., et al.. (1996). A quantitative and qualitative assessment of the NOVAWET-Perception bifocal contact lens.. PubMed. 22(2). 109–13. 2 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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