Aiden Eblimit

950 total citations
18 papers, 469 citations indexed

About

Aiden Eblimit is a scholar working on Molecular Biology, Ophthalmology and Cell Biology. According to data from OpenAlex, Aiden Eblimit has authored 18 papers receiving a total of 469 indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Molecular Biology, 8 papers in Ophthalmology and 8 papers in Cell Biology. Recurrent topics in Aiden Eblimit's work include Retinal Development and Disorders (12 papers), Retinal Diseases and Treatments (8 papers) and Photoreceptor and optogenetics research (5 papers). Aiden Eblimit is often cited by papers focused on Retinal Development and Disorders (12 papers), Retinal Diseases and Treatments (8 papers) and Photoreceptor and optogenetics research (5 papers). Aiden Eblimit collaborates with scholars based in United States, China and Russia. Aiden Eblimit's co-authors include Rui Chen, Yumei Li, Mingchu Xu, Haji Akber Aisa, Yongqiang Liu, Li Zhao, Graeme Mardon, Keqing Wang, Feng Wang and Sung Yun Jung and has published in prestigious journals such as Journal of Clinical Investigation, Journal of Neuroscience and The Journal of Cell Biology.

In The Last Decade

Aiden Eblimit

18 papers receiving 463 citations

Peers

Aiden Eblimit

OPHTH

GENET

CMN

Yoonhee Kim South Korea

Johanna Viiri Finland

Luc Farout France

Priscilla Chan United States

Rebecca L. Fitzsimmons Australia

Yu-Lai Wang Japan

Katelyn M. Green United States

Debasmita Pankaj Alone India

Vipul M. Parmar United States

Yoonhee Kim South Korea

Aiden Eblimit

411 ×1.3

60 ×0.4

121 ×1.3

OPHTH

22 ×0.3

GENET

44 ×0.7

CMN

Citations per year, relative to Aiden Eblimit Aiden Eblimit (= 1×) peers Yoonhee Kim

Countries citing papers authored by Aiden Eblimit

Since Specialization

Citations

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

Fields of papers citing papers by Aiden Eblimit

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Aiden Eblimit

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

All Works

Sort: Min cites: Since: Top N: Style:

18 of 18 papers shown

Eblimit, Aiden, Ryan Crane, Shannon M. Conley, et al.. (2021). Co-Injection of Sulfotyrosine Facilitates Retinal Uptake of Hyaluronic Acid Nanospheres Following Intravitreal Injection. Pharmaceutics. 13(9). 1510–1510. 7 indexed citations

Bajaj, Lakshya, Jai Prakash Sharma, Alberto di Ronza, et al.. (2020). A CLN6-CLN8 complex recruits lysosomal enzymes at the ER for Golgi transfer. Journal of Clinical Investigation. 130(8). 4118–4132. 51 indexed citations

Eblimit, Aiden, Wei Liu, Keqing Wang, et al.. (2018). NMNAT1 E257K variant, associated with Leber Congenital Amaurosis (LCA9), causes a mild retinal degeneration phenotype. Experimental Eye Research. 173. 32–43. 18 indexed citations

Eblimit, Aiden, Qingnan Liang, Hehe Liu, et al.. (2018). Gene Therapy Rescues Retinal Degeneration in Receptor Expression-Enhancing Protein 6 Mutant Mice. Human Gene Therapy. 30(3). 302–315. 9 indexed citations

Herman, Isabella, Zhandong Liu, Aiden Eblimit, et al.. (2018). POU6f1 Mediates Neuropeptide-Dependent Plasticity in the Adult Brain. Journal of Neuroscience. 38(6). 1443–1461. 15 indexed citations

Dharmat, Rachayata, Aiden Eblimit, Michael A. Robichaux, et al.. (2018). SPATA7 maintains a novel photoreceptor-specific zone in the distal connecting cilium. The Journal of Cell Biology. 217(8). 2851–2865. 35 indexed citations

Eblimit, Aiden, et al.. (2017). Conditional loss of Spata7 in photoreceptors causes progressive retinal degeneration in mice. Experimental Eye Research. 166. 120–130. 11 indexed citations

Agrawal, Smriti A., Thomas Burgoyne, Aiden Eblimit, et al.. (2017). REEP6 deficiency leads to retinal degeneration through disruption of ER homeostasis and protein trafficking. Human Molecular Genetics. 26(14). 2667–2677. 37 indexed citations

Dou, Jun, et al.. (2017). Isochlorogenic acid A promotes melanin synthesis in B16 cell through the β-catenin signal pathway. Acta Biochimica et Biophysica Sinica. 49(9). 800–807. 19 indexed citations

10.

Zhao, Li, Yiyun Chen, Aiden Eblimit, et al.. (2016). Integrative subcellular proteomic analysis allows accurate prediction of human disease-causing genes. Genome Research. 26(5). 660–669. 13 indexed citations

11.

Soens, Zachry T., Yuanyuan Li, Li Zhao, et al.. (2016). Hypomorphic mutations identified in the candidate Leber congenital amaurosis gene CLUAP1. Genetics in Medicine. 18(10). 1044–1051. 31 indexed citations

12.

Xu, Mingchu, Qing Fu, Yumei Li, et al.. (2016). Next-generation sequencing-based molecular diagnosis of 12 inherited retinal disease probands of Uyghur ethnicity. Scientific Reports. 6(1). 21384–21384. 16 indexed citations

13.

Xu, Mingchu, Zixi Sun, Aiden Eblimit, et al.. (2016). Mutations inPOMGNT1cause non-syndromic retinitis pigmentosa. Human Molecular Genetics. 25(8). 1479–1488. 29 indexed citations

14.

Jin, Meng, Aiden Eblimit, Merlyn Pulikkathara, et al.. (2016). Conditional knockout of retinal determination genes in differentiating cells in Drosophila. FEBS Journal. 283(15). 2754–2766. 7 indexed citations

15.

Zhong, Hua, Aiden Eblimit, Yalda Moayedi, et al.. (2015). AAV8(Y733F)-mediated gene therapy in a Spata7 knockout mouse model of Leber congenital amaurosis and retinitis pigmentosa. Gene Therapy. 22(8). 619–627. 19 indexed citations

16.

Xu, Mingchu, Violet Gelowani, Aiden Eblimit, et al.. (2015). ATF6Is Mutated in Early Onset Photoreceptor Degeneration With Macular Involvement. Investigative Ophthalmology & Visual Science. 56(6). 3889–3889. 45 indexed citations

17.

Xu, Mingchu, Aiden Eblimit, Jing Wang, et al.. (2015). ADIPOR1Is Mutated in Syndromic Retinitis Pigmentosa. Human Mutation. 37(3). 246–249. 37 indexed citations

18.

Liu, Yongqiang, et al.. (2014). Kaliziri extract upregulates tyrosinase, TRP-1, TRP-2 and MITF expression in murine B16 melanoma cells. BMC Complementary and Alternative Medicine. 14(1). 166–166. 70 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.

Explore authors with similar magnitude of impact