Vera Alexeeva

1.3k total citations
26 papers, 1.0k citations indexed

About

Vera Alexeeva is a scholar working on Cellular and Molecular Neuroscience, Molecular Biology and Surgery. According to data from OpenAlex, Vera Alexeeva has authored 26 papers receiving a total of 1.0k indexed citations (citations by other indexed papers that have themselves been cited), including 18 papers in Cellular and Molecular Neuroscience, 11 papers in Molecular Biology and 4 papers in Surgery. Recurrent topics in Vera Alexeeva's work include Neurobiology and Insect Physiology Research (15 papers), Photoreceptor and optogenetics research (4 papers) and CRISPR and Genetic Engineering (4 papers). Vera Alexeeva is often cited by papers focused on Neurobiology and Insect Physiology Research (15 papers), Photoreceptor and optogenetics research (4 papers) and CRISPR and Genetic Engineering (4 papers). Vera Alexeeva collaborates with scholars based in United States, Russia and China. Vera Alexeeva's co-authors include Ferdinand S. Vilim, Klaudiusz R. Weiss, Jonathan V. Sweedler, Jian Jing, Stanislav S. Rubakhin, Nikolai Dembrow, Irving Kupfermann, L. Li, Charles C. Horn and Elena V. Romanova and has published in prestigious journals such as Journal of Biological Chemistry, Journal of Neuroscience and PLoS ONE.

In The Last Decade

Vera Alexeeva

26 papers receiving 1.0k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Vera Alexeeva United States	20	655	355	177	155	138	26	1.0k
Willem C. Wildering Canada	19	638 1.0×	340 1.0×	116 0.7×	147 0.9×	84 0.6×	38	1.1k
Nikolai Dembrow United States	18	920 1.4×	390 1.1×	490 2.8×	104 0.7×	100 0.7×	22	1.3k
Yasuo Furukawa Japan	20	705 1.1×	659 1.9×	57 0.3×	89 0.6×	155 1.1×	71	1.3k
Petra Skiebe Germany	13	640 1.0×	166 0.5×	86 0.5×	59 0.4×	70 0.5×	16	710
Ildikó Kemenes United Kingdom	21	696 1.1×	276 0.8×	349 2.0×	24 0.2×	102 0.7×	43	1.1k
L. Li United States	9	363 0.6×	171 0.5×	67 0.4×	84 0.5×	72 0.5×	13	542
Vatsala Thirumalai India	17	623 1.0×	219 0.6×	372 2.1×	40 0.3×	58 0.4×	26	991
PE Lloyd United States	13	749 1.1×	301 0.8×	141 0.8×	24 0.2×	124 0.9×	14	862
Yuko Fujisawa Japan	20	763 1.2×	497 1.4×	35 0.2×	63 0.4×	205 1.5×	39	1.7k
Mingming Ma China	18	887 1.4×	423 1.2×	28 0.2×	189 1.2×	41 0.3×	40	1.4k

Countries citing papers authored by Vera Alexeeva

Since Specialization

Citations

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

Fields of papers citing papers by Vera Alexeeva

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Vera Alexeeva

This figure shows the co-authorship network connecting the top 25 collaborators of Vera Alexeeva. A scholar is included among the top collaborators of Vera Alexeeva 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 Vera Alexeeva. Vera Alexeeva 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

Stegen, Sjoukje J. C. van der, Roseanna M. Petrovic, Hongyao Xie, et al.. (2022). Generation of T-cell-receptor-negative CD8αβ-positive CAR T cells from T-cell-derived induced pluripotent stem cells. Nature Biomedical Engineering. 6(11). 1284–1297. 49 indexed citations

Alexeeva, Vera, et al.. (2020). A human H1-HBB11-GFP reporter embryonic stem cell line (WAe001-A-2) generated using TALEN-based genome editing. Stem Cell Research. 45. 101837–101837. 1 indexed citations

Zhang, Guo, Ferdinand S. Vilim, Elena V. Romanova, et al.. (2017). Discovery of leucokinin-like neuropeptides that modulate a specific parameter of feeding motor programs in the molluscan model, Aplysia. Journal of Biological Chemistry. 292(46). 18775–18789. 18 indexed citations

Alexeeva, Vera, Sunita L. D’Souza, & Christoph Schaniel. (2016). A human MIXL1 green fluorescent protein reporter embryonic stem cell line engineered using TALEN-based genome editing. Stem Cell Research. 17(1). 93–96. 1 indexed citations

Jing, Jian, Vera Alexeeva, Michael R. Due, et al.. (2015). Functional Characterization of a Vesicular Glutamate Transporter in an Interneuron That Makes Excitatory and Inhibitory Synaptic Connections in a Molluscan Neural Circuit. Journal of Neuroscience. 35(24). 9137–9149. 10 indexed citations

Mormone, Elisabetta, et al.. (2014). “Footprint-Free” Human Induced Pluripotent Stem Cell-Derived Astrocytes for In Vivo Cell-Based Therapy. Stem Cells and Development. 23(21). 2626–2636. 25 indexed citations

Bai, Lu, Elena V. Romanova, Vera Alexeeva, et al.. (2013). Characterization of GdFFD, a d-Amino Acid-containing Neuropeptide That Functions as an Extrinsic Modulator of the Aplysia Feeding Circuit. Journal of Biological Chemistry. 288(46). 32837–32851. 42 indexed citations

Romanova, Elena V., Kosei Sasaki, Vera Alexeeva, et al.. (2012). Urotensin II in Invertebrates: From Structure to Function in Aplysia californica. PLoS ONE. 7(11). e48764–e48764. 29 indexed citations

Vilim, Ferdinand S., Kosei Sasaki, Jürgen Rybak, et al.. (2010). Distinct Mechanisms Produce Functionally Complementary Actions of Neuropeptides That Are Structurally Related But Derived from Different Precursors. Journal of Neuroscience. 30(1). 131–147. 43 indexed citations

10.

Jing, Jian, Jonathan V. Sweedler, Elizabeth C. Cropper, et al.. (2010). Feedforward Compensation Mediated by the Central and Peripheral Actions of a Single Neuropeptide Discovered Using Representational Difference Analysis. Journal of Neuroscience. 30(49). 16545–16558. 40 indexed citations

11.

Jing, Jian, Ferdinand S. Vilim, Charles C. Horn, et al.. (2007). From Hunger to Satiety: Reconfiguration of a Feeding Network by Aplysia Neuropeptide Y. Journal of Neuroscience. 27(13). 3490–3502. 86 indexed citations

12.

Proekt, Alex, Ferdinand S. Vilim, Vera Alexeeva, et al.. (2005). Identification of a New Neuropeptide Precursor Reveals a Novel Source of Extrinsic Modulation in the Feeding System ofAplysia. Journal of Neuroscience. 25(42). 9637–9648. 34 indexed citations

13.

Furukawa, Yasuo, Yuko Fujisawa, Hiroyuki Minakata, et al.. (2003). PRQFVamide, a Novel Pentapeptide Identified From the CNS and Gut ofAplysia. Journal of Neurophysiology. 89(6). 3114–3127. 32 indexed citations

14.

Orekhova, Irina V., Vera Alexeeva, Paul J. Church, Klaudiusz R. Weiss, & Vladimír Březina. (2003). Multiple Presynaptic and Postsynaptic Sites of Inhibitory Modulation by Myomodulin at ARC Neuromuscular Junctions ofAplysia. Journal of Neurophysiology. 89(3). 1488–1502. 14 indexed citations

15.

Sweedler, Jonathan V., L. Li, Stanislav S. Rubakhin, et al.. (2002). Identification and characterization of the feeding circuit-activating peptides, a novel neuropeptide family of aplysia.. PubMed. 22(17). 7797–808. 72 indexed citations

16.

Li, L., Philip D. Floyd, Stanislav S. Rubakhin, et al.. (2001). Cerebrin prohormone processing, distribution and action in Aplysia californica. Journal of Neurochemistry. 77(6). 1569–1580. 37 indexed citations

17.

Vilim, Ferdinand S., Vera Alexeeva, Leonid L. Moroz, et al.. (2001). Cloning, expression and processing of the CP2 neuropeptide precursor of Aplysia. Peptides. 22(12). 2027–2038. 31 indexed citations

18.

Floyd, Philip D., Lingjun Li, Stanislav S. Rubakhin, et al.. (1999). Insulin Prohormone Processing, Distribution, and Relation to Metabolism inAplysia californica. Journal of Neuroscience. 19(18). 7732–7741. 103 indexed citations

19.

Floyd, Philip D., L. Li, Stanislav S. Rubakhin, et al.. (1999). Insulin prohormone processing, distribution, and relation to metabolism in Aplysia californica.. PubMed. 19(18). 7732–41. 107 indexed citations

20.

Alexeeva, Vera, et al.. (1998). Effect of a Serotonergic Extrinsic Modulatory Neuron (MCC) on Radula Mechanoafferent Function inAplysia. Journal of Neurophysiology. 80(4). 1609–1622. 10 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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