Jeremy M. Hoffmann

544 total citations
10 papers, 409 citations indexed

About

Jeremy M. Hoffmann is a scholar working on Molecular Biology, Ophthalmology and Radiology, Nuclear Medicine and Imaging. According to data from OpenAlex, Jeremy M. Hoffmann has authored 10 papers receiving a total of 409 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Molecular Biology, 6 papers in Ophthalmology and 4 papers in Radiology, Nuclear Medicine and Imaging. Recurrent topics in Jeremy M. Hoffmann's work include Retinal Development and Disorders (8 papers), Retinal Diseases and Treatments (5 papers) and CRISPR and Genetic Engineering (3 papers). Jeremy M. Hoffmann is often cited by papers focused on Retinal Development and Disorders (8 papers), Retinal Diseases and Treatments (5 papers) and CRISPR and Genetic Engineering (3 papers). Jeremy M. Hoffmann collaborates with scholars based in United States, Singapore and Germany. Jeremy M. Hoffmann's co-authors include Edwin M. Stone, Robert F. Mullins, Budd A. Tucker, Adam P. DeLuca, Todd E. Scheetz, Val C. Sheffield, Rebecca M. Johnston, Samuel G. Jacobson, Elliott H. Sohn and D. Brice Critser and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Scientific Reports and Investigative Ophthalmology & Visual Science.

In The Last Decade

Jeremy M. Hoffmann

10 papers receiving 405 citations

Peers

Jeremy M. Hoffmann
Xuan Cui United States
Vinod Jaskula-Ranga United States
Kristin R. Anfinson United States
Wen-Hsuan Wu United States
Holly Y. Chen United States
Xuan Cui United States
Jeremy M. Hoffmann
Citations per year, relative to Jeremy M. Hoffmann Jeremy M. Hoffmann (= 1×) peers Xuan Cui

Countries citing papers authored by Jeremy M. Hoffmann

Since Specialization
Citations

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

Fields of papers citing papers by Jeremy M. Hoffmann

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Jeremy M. Hoffmann

This figure shows the co-authorship network connecting the top 25 collaborators of Jeremy M. Hoffmann. A scholar is included among the top collaborators of Jeremy M. Hoffmann 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 Jeremy M. Hoffmann. Jeremy M. Hoffmann is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

10 of 10 papers shown
1.
Fenner, Beau J., Jonathan F. Russell, Arlene V. Drack, et al.. (2023). Long-term functional and structural outcomes in X-linked retinoschisis: implications for clinical trials. Frontiers in Medicine. 10. 1204095–1204095. 10 indexed citations
2.
3.
Bowen, Randy C., H. Culver Boldt, Robert F. Mullins, et al.. (2021). Intrafamilial Variability of Ocular Manifestations of von Hippel-Lindau Disease. Ophthalmology Retina. 6(1). 89–91. 1 indexed citations
4.
Whitmore, S. Scott, Adam P. DeLuca, D. Brice Critser, et al.. (2020). Analysis of retinal sublayer thicknesses and rates of change in ABCA4-associated Stargardt disease. Scientific Reports. 10(1). 16576–16576. 14 indexed citations
5.
Hoffmann, Jeremy M., B Müller, Stefan Günther, et al.. (2018). Toward genome editing in X-linked RP—development of a mouse model with specific treatment relevant features. Translational research. 203. 57–72. 6 indexed citations
6.
Burnight, Erin R., Manav Gupta, Luke A. Wiley, et al.. (2017). Using CRISPR-Cas9 to Generate Gene-Corrected Autologous iPSCs for the Treatment of Inherited Retinal Degeneration. Molecular Therapy. 25(9). 1999–2013. 117 indexed citations
7.
Sohn, Elliott H., Kai Wang, Stewart Thompson, et al.. (2014). COMPARISON OF DRUSEN AND MODIFYING GENES IN AUTOSOMAL DOMINANT RADIAL DRUSEN AND AGE-RELATED MACULAR DEGENERATION. Retina. 35(1). 48–57. 28 indexed citations
8.
Abràmoff, Michael D., Robert F. Mullins, Kyungmoo Lee, et al.. (2013). Human Photoreceptor Outer Segments Shorten During Light Adaptation. Investigative Ophthalmology & Visual Science. 54(5). 3721–3721. 56 indexed citations
9.
Tucker, Budd A., Todd E. Scheetz, Robert F. Mullins, et al.. (2011). Exome sequencing and analysis of induced pluripotent stem cells identify the cilia-related gene male germ cell-associated kinase ( MAK ) as a cause of retinitis pigmentosa. Proceedings of the National Academy of Sciences. 108(34). E569–76. 172 indexed citations
10.
Fingert, John H., Rebecca M. Johnston, Christine Taylor, et al.. (2007). Variations in the TCF8 Gene Are Associated With a Posterior Polymorphous Corneal Dystrophy Phenotype. Investigative Ophthalmology & Visual Science. 48(13). 5848–5848. 1 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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