Carlos D. Aizenman

3.7k total citations
40 papers, 2.8k citations indexed

About

Carlos D. Aizenman is a scholar working on Cellular and Molecular Neuroscience, Cognitive Neuroscience and Molecular Biology. According to data from OpenAlex, Carlos D. Aizenman has authored 40 papers receiving a total of 2.8k indexed citations (citations by other indexed papers that have themselves been cited), including 33 papers in Cellular and Molecular Neuroscience, 21 papers in Cognitive Neuroscience and 18 papers in Molecular Biology. Recurrent topics in Carlos D. Aizenman's work include Neuroscience and Neuropharmacology Research (28 papers), Neural dynamics and brain function (16 papers) and Photoreceptor and optogenetics research (13 papers). Carlos D. Aizenman is often cited by papers focused on Neuroscience and Neuropharmacology Research (28 papers), Neural dynamics and brain function (16 papers) and Photoreceptor and optogenetics research (13 papers). Carlos D. Aizenman collaborates with scholars based in United States, Canada and Switzerland. Carlos D. Aizenman's co-authors include David J. Linden, Hollis T. Cline, Kara G. Pratt, J. P. Donoghue, Grzegorz Hess, Alfredo Kirkwood, Mark F. Bear, Serena M. Dudek, Zheng Li and Paul B. Manis and has published in prestigious journals such as Science, Proceedings of the National Academy of Sciences and Neuron.

In The Last Decade

Carlos D. Aizenman

40 papers receiving 2.8k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Carlos D. Aizenman United States 23 1.9k 1.3k 943 806 262 40 2.8k
Bryan M. Hooks United States 20 1.7k 0.9× 1.5k 1.2× 703 0.7× 379 0.5× 104 0.4× 28 2.8k
Alev Erişir United States 32 2.3k 1.2× 1.3k 1.1× 1.3k 1.4× 327 0.4× 216 0.8× 70 3.6k
Ian Duguid United Kingdom 20 1.4k 0.7× 764 0.6× 669 0.7× 522 0.6× 282 1.1× 33 2.0k
Kerry D. Walton United States 23 1.9k 1.0× 775 0.6× 1.3k 1.4× 423 0.5× 219 0.8× 39 3.1k
Christopher S. Leonard United States 26 2.0k 1.0× 2.2k 1.7× 1.3k 1.4× 588 0.7× 285 1.1× 47 4.1k
Agnès Baude France 26 3.0k 1.6× 1.4k 1.1× 1.5k 1.6× 627 0.8× 133 0.5× 46 3.6k
Ken Sugino United States 28 2.4k 1.3× 1.5k 1.2× 2.0k 2.1× 598 0.7× 381 1.5× 33 4.7k
Małgorzata Kossut Poland 29 1.9k 1.0× 1.5k 1.2× 786 0.8× 361 0.4× 123 0.5× 135 3.0k
Elizabeth M. Quinlan United States 25 2.8k 1.5× 1.5k 1.2× 1.9k 2.0× 387 0.5× 170 0.6× 42 4.0k
Raphael Lamprecht Israel 22 1.6k 0.9× 910 0.7× 758 0.8× 319 0.4× 147 0.6× 51 2.4k

Countries citing papers authored by Carlos D. Aizenman

Since Specialization
Citations

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

Fields of papers citing papers by Carlos D. Aizenman

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Carlos D. Aizenman. 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 Carlos D. Aizenman. The network helps show where Carlos D. Aizenman may publish in the future.

Co-authorship network of co-authors of Carlos D. Aizenman

This figure shows the co-authorship network connecting the top 25 collaborators of Carlos D. Aizenman. A scholar is included among the top collaborators of Carlos D. Aizenman 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 Carlos D. Aizenman. Carlos D. Aizenman 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.
2.
Aizenman, Carlos D., et al.. (2021). Early Developmental Exposure to Fluoxetine and Citalopram Results in Different Neurodevelopmental Outcomes. Neuroscience. 467. 110–121. 4 indexed citations
3.
Aizenman, Carlos D., et al.. (2017). A cellular mechanism for inverse effectiveness in multisensory integration. eLife. 6. 19 indexed citations
4.
5.
Liu, Zhenyu, et al.. (2016). A population of gap junction-coupled neurons drives recurrent network activity in a developing visual circuit. Journal of Neurophysiology. 115(3). 1477–1486. 6 indexed citations
6.
Gu, Jenny, et al.. (2015). Valproate-Induced Neurodevelopmental Deficits inXenopus laevisTadpoles. Journal of Neuroscience. 35(7). 3218–3229. 29 indexed citations
7.
Aizenman, Carlos D., et al.. (2011). A neuroprotective role for polyamines in a Xenopus tadpole model of epilepsy. Nature Neuroscience. 14(4). 505–512. 45 indexed citations
8.
Aizenman, Carlos D., et al.. (2011). Sensory modality–specific homeostatic plasticity in the developing optic tectum. Nature Neuroscience. 14(5). 548–550. 31 indexed citations
9.
Xu, Heng, et al.. (2011). Visual Experience-Dependent Maturation of Correlated Neuronal Activity Patterns in a Developing Visual System. Journal of Neuroscience. 31(22). 8025–8036. 21 indexed citations
10.
Lee, Ryan, Elizabeth Mills, Neil Schwartz, et al.. (2010). Neurodevelopmental effects of chronic exposure to elevated levels of pro-inflammatory cytokines in a developing visual system. Neural Development. 5(1). 2–2. 51 indexed citations
11.
Xu, Heng, Kristina Davitt, Wei Dong, et al.. (2008). Combining Multicore Imaging Fiber With Matrix Addressable Blue/Green LED Arrays for Spatiotemporal Photonic Excitation at Cellular Level. IEEE Journal of Selected Topics in Quantum Electronics. 14(1). 167–170. 11 indexed citations
12.
Keuren‐Jensen, Kendall Van, et al.. (2008). Roles of NR2A and NR2B in the Development of Dendritic Arbor MorphologyIn Vivo. Journal of Neuroscience. 28(4). 850–861. 80 indexed citations
13.
Xu, Heng, Kristina Davitt, Wei Dong, et al.. (2008). Integration of a matrix addressable blue/green LED array with multicore imaging fiber for spatiotemporal excitation in endoscopic biomedical applications. Physica status solidi. C, Conferences and critical reviews/Physica status solidi. C, Current topics in solid state physics. 5(6). 2299–2302. 2 indexed citations
14.
Aizenman, Carlos D. & Hollis T. Cline. (2007). Enhanced Visual Activity In Vivo Forms Nascent Synapses in the Developing Retinotectal Projection. Journal of Neurophysiology. 97(4). 2949–2957. 49 indexed citations
15.
Aizenman, Carlos D., et al.. (2003). Visually Driven Regulation of Intrinsic Neuronal Excitability Improves Stimulus Detection In Vivo. Neuron. 39(5). 831–842. 120 indexed citations
16.
Aizenman, Carlos D., et al.. (2002). Visually Driven Modulation of Glutamatergic Synaptic Transmission Is Mediated by the Regulation of Intracellular Polyamines. Neuron. 34(4). 623–634. 86 indexed citations
17.
Li, Zheng, Carlos D. Aizenman, & Hollis T. Cline. (2002). Regulation of Rho GTPases by Crosstalk and Neuronal Activity In Vivo. Neuron. 33(5). 741–750. 186 indexed citations
18.
Ji, Ru‐Rong, Thomas E. Schläepfer, Carlos D. Aizenman, et al.. (1998). Repetitive transcranial magnetic stimulation activates specific regions in rat brain. Proceedings of the National Academy of Sciences. 95(26). 15635–15640. 155 indexed citations
19.
Aizenman, Carlos D., Paul B. Manis, & David J. Linden. (1998). Polarity of Long-Term Synaptic Gain Change Is Related to Postsynaptic Spike Firing at a Cerebellar Inhibitory Synapse. Neuron. 21(4). 827–835. 181 indexed citations
20.
Aizenman, Carlos D., Alfredo Kirkwood, & Mark F. Bear. (1996). A Current Source Density Analysis of Evoked Responses in Slices of Adult Rat Visual Cortex: Implications for the Regulation of Long-Term Potentiation. Cerebral Cortex. 6(6). 751–758. 47 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

Breakdown of academic impact, for papers by Bryan M. Hooks Breakdown of academic impact, for papers by Alev Erişir Breakdown of academic impact, for papers by Ian Duguid Breakdown of academic impact, for papers by Kerry D. Walton Breakdown of academic impact, for papers by Christopher S. Leonard Breakdown of academic impact, for papers by Agnès Baude Breakdown of academic impact, for papers by Ken Sugino Breakdown of academic impact, for papers by Małgorzata Kossut Breakdown of academic impact, for papers by Elizabeth M. Quinlan Breakdown of academic impact, for papers by Raphael Lamprecht
Rankless by CCL
2026