Eric Weh

703 total citations
22 papers, 486 citations indexed

About

Eric Weh is a scholar working on Molecular Biology, Ophthalmology and Genetics. According to data from OpenAlex, Eric Weh has authored 22 papers receiving a total of 486 indexed citations (citations by other indexed papers that have themselves been cited), including 17 papers in Molecular Biology, 12 papers in Ophthalmology and 6 papers in Genetics. Recurrent topics in Eric Weh's work include Retinal Development and Disorders (15 papers), Retinal Diseases and Treatments (9 papers) and Cancer, Hypoxia, and Metabolism (6 papers). Eric Weh is often cited by papers focused on Retinal Development and Disorders (15 papers), Retinal Diseases and Treatments (9 papers) and Cancer, Hypoxia, and Metabolism (6 papers). Eric Weh collaborates with scholars based in United States, Türkiye and Portugal. Eric Weh's co-authors include Elena V. Semina, Joseph Carroll, Daniel W. Odell, Melissa Wagner-Schuman, Adam M. Dubis, Yuming Lei, Alfredo Dubra, Yusufu N. Sulai, Linda M. Reis and Cagri G. Besirli and has published in prestigious journals such as SHILAP Revista de lepidopterología, PLoS ONE and Scientific Reports.

In The Last Decade

Eric Weh

22 papers receiving 478 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Eric Weh United States	11	266	219	194	100	45	22	486
Christopher J. Layton Australia	14	352 1.3×	328 1.5×	124 0.6×	75 0.8×	26 0.6×	31	597
Mohamed F. El-Ashry United Kingdom	15	336 1.3×	349 1.6×	319 1.6×	108 1.1×	30 0.7×	25	731
Janmeet S. Saini United States	8	170 0.6×	382 1.7×	105 0.5×	46 0.5×	23 0.5×	9	476
Tasneem P. Sharma United States	9	204 0.8×	309 1.4×	113 0.6×	55 0.6×	13 0.3×	17	473
Megan Riker United States	12	207 0.8×	463 2.1×	129 0.7×	40 0.4×	12 0.3×	17	574
Denise J. Morgan United States	7	189 0.7×	274 1.3×	109 0.6×	25 0.3×	9 0.2×	11	421
Ilaria Passerini Italy	15	318 1.2×	452 2.1×	118 0.6×	67 0.7×	11 0.2×	49	574
Cristina Martínez-Fernández de la Cámara United Kingdom	16	265 1.0×	500 2.3×	78 0.4×	106 1.1×	20 0.4×	25	582
Ponugoti Vasantha Rao United States	14	154 0.6×	472 2.2×	82 0.4×	42 0.4×	32 0.7×	43	607
Dan Yi Wang Hong Kong	15	689 2.6×	432 2.0×	255 1.3×	110 1.1×	28 0.6×	16	923

Countries citing papers authored by Eric Weh

Since Specialization

Citations

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

Fields of papers citing papers by Eric Weh

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Eric Weh

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

All Works

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20 of 20 papers shown

Goswami, Moloy T., Eric Weh, Katherine M. Weh, et al.. (2025). Glutamine catabolism supports amino acid biosynthesis and suppresses the integrated stress response to promote photoreceptor survival. eLife. 13. 1 indexed citations

Wubben, Thomas J., Eric Weh, & Cagri G. Besirli. (2025). Photoreceptor Degeneration: More Than a Bystander in Age-Related Macular Degeneration. Advances in experimental medicine and biology. 1468. 27–31. 1 indexed citations

Pan, Warren W., Katherine M. Weh, Sraboni Chaudhury, et al.. (2025). A Novel, Long-Acting, Small Molecule PKM2 Activator and Its Potential Broad Application Against Photoreceptor Degeneration. Translational Vision Science & Technology. 14(7). 26–26. 1 indexed citations

Goswami, Moloy T., Eric Weh, Katherine M. Weh, et al.. (2024). Glutamine catabolism supports amino acid biosynthesis and suppresses the integrated stress response to promote photoreceptor survival. eLife. 13. 2 indexed citations

Fernando, Roshini, et al.. (2023). Flow cytometric method for the detection and quantification of retinal cell death and oxidative stress. Experimental Eye Research. 233. 109563–109563. 3 indexed citations

Goswami, Moloy T., Nicholas J. Miller, Eric Weh, et al.. (2023). Rod photoreceptor-specific deletion of cytosolic aspartate aminotransferase, GOT1, causes retinal degeneration. SHILAP Revista de lepidopterología. 3. 3 indexed citations

Weh, Eric, Moloy T. Goswami, Sraboni Chaudhury, et al.. (2023). Metabolic Alterations Caused by Simultaneous Loss of HK2 and PKM2 Leads to Photoreceptor Dysfunction and Degeneration. Cells. 12(16). 2043–2043. 6 indexed citations

Wubben, Thomas J., Sraboni Chaudhury, Jeanne A. Stuckey, et al.. (2023). Development of Novel Small-Molecule Activators of Pyruvate Kinase Muscle Isozyme 2, PKM2, to Reduce Photoreceptor Apoptosis. Pharmaceuticals. 16(5). 705–705. 6 indexed citations

Mei, Ling, Minzhi Yu, Yayuan Liu, et al.. (2022). Synthetic high-density lipoprotein nanoparticles delivering rapamycin for the treatment of age-related macular degeneration. Nanomedicine Nanotechnology Biology and Medicine. 44. 102571–102571. 15 indexed citations

10.

Weh, Eric, et al.. (2021). Dark-reared rd10 mice experience rapid photoreceptor degeneration with short exposure to room-light during in vivo retinal imaging. Experimental Eye Research. 215. 108913–108913. 11 indexed citations

11.

Wubben, Thomas J., et al.. (2020). Development of novel pyruvate kinase muscle isoform 2 (PKM2) activators for photoreceptor neuroprotection. Investigative Ophthalmology & Visual Science. 61(7). 4938–4938. 1 indexed citations

12.

Wubben, Thomas J., Mercy Pawar, Eric Weh, et al.. (2020). Small molecule activation of metabolic enzyme pyruvate kinase muscle isozyme 2, PKM2, circumvents photoreceptor apoptosis. Scientific Reports. 10(1). 2990–2990. 30 indexed citations

13.

Weh, Eric, Andrew D. Smith, Heather Hager, et al.. (2020). Hexokinase 2 is dispensable for photoreceptor development but is required for survival during aging and outer retinal stress. Cell Death and Disease. 11(6). 422–422. 29 indexed citations

14.

Weh, Eric, Hideyuki Takeuchi, Sanaa Muheisen, Robert S. Haltiwanger, & Elena V. Semina. (2017). Functional characterization of zebrafish orthologs of the human Beta 3-Glucosyltransferase B3GLCT gene mutated in Peters Plus Syndrome. PLoS ONE. 12(9). e0184903–e0184903. 13 indexed citations

15.

Protas, Meredith, Eric Weh, Tim Footz, et al.. (2017). Mutations of conserved non-coding elements of PITX2 in patients with ocular dysgenesis and developmental glaucoma. Human Molecular Genetics. 26(18). 3630–3638. 27 indexed citations

16.

Happ, Hannah C., Kala F. Schilter, Eric Weh, Linda M. Reis, & Elena V. Semina. (2016). 8q21.11 microdeletion in two patients with syndromic peters anomaly. American Journal of Medical Genetics Part A. 170(9). 2471–2475. 16 indexed citations

17.

Happ, Hannah C., Eric Weh, Deborah M. Costakos, Linda M. Reis, & Elena V. Semina. (2016). Case report of homozygous deletion involving the first coding exons of GCNT2 isoforms A and B and part of the upstream region of TFAP2A in congenital cataract. BMC Medical Genetics. 17(1). 64–64. 6 indexed citations

18.

Weh, Eric, Linda M. Reis, Hannah C. Happ, et al.. (2014). Whole exome sequence analysis of Peters anomaly. Human Genetics. 133(12). 1497–1511. 53 indexed citations

19.

Weh, Eric, Linda M. Reis, Rebecca C. Tyler, et al.. (2013). Novel B3GALTL mutations in classic Peters plus syndrome and lack of mutations in a large cohort of patients with similar phenotypes. Clinical Genetics. 86(2). 142–148. 33 indexed citations

20.

Wagner-Schuman, Melissa, Adam M. Dubis, Yuming Lei, et al.. (2010). Race- and Sex-Related Differences in Retinal Thickness and Foveal Pit Morphology. Investigative Ophthalmology & Visual Science. 52(1). 625–625. 206 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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