Botir T. Sagdullaev

3.3k total citations · 1 hit paper
63 papers, 2.4k citations indexed

About

Botir T. Sagdullaev is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Ophthalmology. According to data from OpenAlex, Botir T. Sagdullaev has authored 63 papers receiving a total of 2.4k indexed citations (citations by other indexed papers that have themselves been cited), including 45 papers in Molecular Biology, 30 papers in Cellular and Molecular Neuroscience and 9 papers in Ophthalmology. Recurrent topics in Botir T. Sagdullaev's work include Retinal Development and Disorders (35 papers), Photoreceptor and optogenetics research (24 papers) and Neuroscience and Neuropharmacology Research (17 papers). Botir T. Sagdullaev is often cited by papers focused on Retinal Development and Disorders (35 papers), Photoreceptor and optogenetics research (24 papers) and Neuroscience and Neuropharmacology Research (17 papers). Botir T. Sagdullaev collaborates with scholars based in United States, Uzbekistan and China. Botir T. Sagdullaev's co-authors include Elena Ivanova, Maureen A. McCall, Christopher Yee, Abduqodir Toychiev, Peter D. Lukasiewicz, Daniel H. Geschwind, Saravanan S. Karuppagounder, Rajiv R. Ratan, John W. Cave and Tamás Kovács‐Öller and has published in prestigious journals such as Cell, Proceedings of the National Academy of Sciences and Nature Communications.

In The Last Decade

Botir T. Sagdullaev

60 papers receiving 2.4k citations

Hit Papers

Selenium Drives a Transcriptional Adaptive Program to Blo... 2019 2026 2021 2023 2019 250 500 750

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Botir T. Sagdullaev United States 24 1.6k 907 520 392 298 63 2.4k
Elena Ivanova United States 21 1.2k 0.8× 576 0.6× 518 1.0× 388 1.0× 234 0.8× 42 1.9k
Maurizio Cammalleri Italy 24 938 0.6× 608 0.7× 157 0.3× 123 0.3× 199 0.7× 80 2.0k
Yoshiaki Tagawa Japan 24 1.2k 0.7× 947 1.0× 71 0.1× 438 1.1× 66 0.2× 63 2.6k
Marie‐Pierre Junier France 32 1.3k 0.8× 704 0.8× 97 0.2× 388 1.0× 262 0.9× 71 2.8k
Jan Christoph Koch Germany 30 1.1k 0.7× 928 1.0× 31 0.1× 136 0.3× 349 1.2× 66 2.6k
Laura Contreras Spain 21 1.2k 0.8× 515 0.6× 38 0.1× 172 0.4× 115 0.4× 37 1.8k
Arantxa Tabernero Spain 35 1.8k 1.1× 763 0.8× 80 0.2× 230 0.6× 322 1.1× 74 2.8k
Kazuhiko Namekata Japan 33 1.9k 1.2× 595 0.7× 44 0.1× 100 0.3× 468 1.6× 87 3.4k
Tetsuya Nagayama United States 22 1.2k 0.8× 753 0.8× 107 0.2× 183 0.5× 400 1.3× 38 2.6k
Sumiko Kiryu‐Seo Japan 30 1.3k 0.8× 898 1.0× 39 0.1× 152 0.4× 278 0.9× 64 2.5k

Countries citing papers authored by Botir T. Sagdullaev

Since Specialization
Citations

This map shows the geographic impact of Botir T. Sagdullaev'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 Botir T. Sagdullaev with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Botir T. Sagdullaev more than expected).

Fields of papers citing papers by Botir T. Sagdullaev

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Botir T. Sagdullaev. 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 Botir T. Sagdullaev. The network helps show where Botir T. Sagdullaev may publish in the future.

Co-authorship network of co-authors of Botir T. Sagdullaev

This figure shows the co-authorship network connecting the top 25 collaborators of Botir T. Sagdullaev. A scholar is included among the top collaborators of Botir T. Sagdullaev 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 Botir T. Sagdullaev. Botir T. Sagdullaev 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.
Kulkarni, Nishant S., Alexander Josowitz, Roshan James, et al.. (2025). Latest trends & strategies in ocular drug delivery. Methods. 235. 100–117. 2 indexed citations
2.
Kumar, Amit, Saravanan S. Karuppagounder, Yingxin Chen, et al.. (2023). 2-Deoxyglucose drives plasticity via an adaptive ER stress-ATF4 pathway and elicits stroke recovery and Alzheimer’s resilience. Neuron. 111(18). 2831–2846.e10. 30 indexed citations
3.
Yang, Yun, Vı́ctor Tapias, Diana Acosta, et al.. (2022). Altered succinylation of mitochondrial proteins, APP and tau in Alzheimer’s disease. Nature Communications. 13(1). 159–159. 72 indexed citations
4.
Mills, Samuel A., Andrew I. Jobling, Michael Dixon, et al.. (2021). Fractalkine-induced microglial vasoregulation occurs within the retina and is altered early in diabetic retinopathy. Proceedings of the National Academy of Sciences. 118(51). 80 indexed citations
5.
Kovács‐Öller, Tamás, et al.. (2020). Imatinib Sets Pericyte Mosaic in the Retina. International Journal of Molecular Sciences. 21(7). 2522–2522. 7 indexed citations
6.
Ivanova, Elena, et al.. (2020). Optogenetic Stimulation of Cholinergic Amacrine Cells Improves Capillary Blood Flow in Diabetic Retinopathy. Investigative Ophthalmology & Visual Science. 61(10). 44–44. 8 indexed citations
7.
Sagdullaev, Botir T., et al.. (2017). STUDY OF TECHNOLOGICAL PROPERTIES OF SUBSTANCE AND BASIC COMPOSITION FOR OBTAINING THE DRUG PRODUCT OF “BIOMAYRIN”. Pharmacy & Pharmacology. 5(6). 532–542. 1 indexed citations
8.
Yee, Christopher, Elena Ivanova, & Botir T. Sagdullaev. (2015). Homologous network interactions between AII amacrine cells are essential for aberrant activity in RD. Investigative Ophthalmology & Visual Science. 56(7). 3230–3230. 1 indexed citations
9.
Ivanova, Elena, et al.. (2015). Aberrant activity in retinal degeneration impairs central visual processing and relies on Cx36-containing gap junctions. Experimental Eye Research. 150. 81–89. 42 indexed citations
10.
Yee, Christopher, Abduqodir Toychiev, Elena Ivanova, & Botir T. Sagdullaev. (2014). Aberrant synaptic input to retinal ganglion cells varies with morphology in a mouse model of retinal degeneration. The Journal of Comparative Neurology. 522(18). 4085–4099. 14 indexed citations
11.
Toychiev, Abduqodir, et al.. (2013). A time and cost efficient approach to functional and structural assessment of living neuronal tissue. Journal of Neuroscience Methods. 214(1). 105–112. 20 indexed citations
12.
Tschetter, Wayne W., N. M. Alam, Christopher Yee, et al.. (2013). Experience-Enabled Enhancement of Adult Visual Cortex Function. Journal of Neuroscience. 33(12). 5362–5366. 9 indexed citations
13.
Vaithianathan, Thirumalini & Botir T. Sagdullaev. (2010). Functional Remodeling of Inner Retinal Synaptic Transmission During Photoreceptor Degeneration. Investigative Ophthalmology & Visual Science. 51(13). 2483–2483. 4 indexed citations
14.
Song, Yijun, Katherine D. Cygnar, Botir T. Sagdullaev, et al.. (2008). Olfactory CNG Channel Desensitization by Ca2+/CaM via the B1b Subunit Affects Response Termination but Not Sensitivity to Recurring Stimulation. Neuron. 58(3). 374–386. 70 indexed citations
15.
Eggers, Erika D., et al.. (2006). Retinal GABA receptors and visual processing: a model system for presynaptic inhibition. Ocular Oncology and Pathology. 1(1). 1–1. 7 indexed citations
16.
Sagdullaev, Botir T.. (2005). Cleaning of Microfiltration Membranes for Filtration of Aqueous Extract of Marsh Mallow. Russian Journal of Applied Chemistry. 78(2). 329–332. 1 indexed citations
17.
Lukasiewicz, Peter D., Erika D. Eggers, Botir T. Sagdullaev, & Maureen A. McCall. (2004). GABAC receptor-mediated inhibition in the retina. Vision Research. 44(28). 3289–3296. 76 indexed citations
18.
Seiler, Magdalene J., Botir T. Sagdullaev, Gustaw Woch, & R.B. Aramant. (2003). Tracing With Pseudorabies Virus Shows Synaptic Connectivity of Retinal Transplants With Degenerated Host Retina. Investigative Ophthalmology & Visual Science. 44(13). 490–490. 1 indexed citations
19.
Sagdullaev, Botir T. & Maureen A. McCall. (2003). Effects of Stimulus Size on Ganglion Cell Responses in the Light Adapted Murine Retina. Investigative Ophthalmology & Visual Science. 44(13). 5193–5193. 1 indexed citations
20.
McCall, Maureen A. & Botir T. Sagdullaev. (2003). GABAC Receptor-mediated Inhibition Shapes Retinal Ganglion Cell Visual Responses. Investigative Ophthalmology & Visual Science. 44(13). 3235–3235. 3 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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