Taruna Ikrar

1.5k total citations
31 papers, 972 citations indexed

About

Taruna Ikrar is a scholar working on Cellular and Molecular Neuroscience, Molecular Biology and Cognitive Neuroscience. According to data from OpenAlex, Taruna Ikrar has authored 31 papers receiving a total of 972 indexed citations (citations by other indexed papers that have themselves been cited), including 18 papers in Cellular and Molecular Neuroscience, 12 papers in Molecular Biology and 10 papers in Cognitive Neuroscience. Recurrent topics in Taruna Ikrar's work include Neuroscience and Neuropharmacology Research (13 papers), Neural dynamics and brain function (8 papers) and Photoreceptor and optogenetics research (7 papers). Taruna Ikrar is often cited by papers focused on Neuroscience and Neuropharmacology Research (13 papers), Neural dynamics and brain function (8 papers) and Photoreceptor and optogenetics research (7 papers). Taruna Ikrar collaborates with scholars based in United States, Indonesia and Japan. Taruna Ikrar's co-authors include Xiangmin Xu, Nicholas D. Olivas, Joshua T. Trachtenberg, Elaine Tring, Sandra J. Kuhlman, René Hen, B Antoine, Kaiwen He, Alexis S. Hill and Hey‐Kyoung Lee and has published in prestigious journals such as Nature, Nature Communications and Neuron.

In The Last Decade

Taruna Ikrar

27 papers receiving 959 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Taruna Ikrar United States	13	661	466	260	197	134	31	972
Gail D. Stevenson United States	12	666 1.0×	390 0.8×	362 1.4×	148 0.8×	135 1.0×	14	1.2k
Jenq‐Wei Yang Germany	18	635 1.0×	519 1.1×	208 0.8×	141 0.7×	89 0.7×	30	982
Nóra Szilágyi Hungary	15	578 0.9×	450 1.0×	280 1.1×	99 0.5×	108 0.8×	33	1.2k
Yuri Gonchar United States	13	1.1k 1.7×	746 1.6×	487 1.9×	199 1.0×	185 1.4×	13	1.4k
Rylan S. Larsen United States	16	694 1.0×	437 0.9×	439 1.7×	80 0.4×	98 0.7×	23	1.1k
Kazuhiro Sohya Japan	17	724 1.1×	468 1.0×	368 1.4×	145 0.7×	118 0.9×	24	1.1k
János Fuzik Sweden	15	457 0.7×	300 0.6×	366 1.4×	91 0.5×	145 1.1×	19	1.1k
Patrik Krieger Germany	19	719 1.1×	495 1.1×	407 1.6×	52 0.3×	82 0.6×	40	1.1k
Ilya Kruglikov United States	15	962 1.5×	619 1.3×	667 2.6×	178 0.9×	355 2.6×	26	1.8k
F.H. Lopes da Silva Netherlands	10	867 1.3×	1.1k 2.3×	161 0.6×	105 0.5×	160 1.2×	10	1.5k

Countries citing papers authored by Taruna Ikrar

Since Specialization

Citations

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

Fields of papers citing papers by Taruna Ikrar

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Taruna Ikrar

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

Wargasetia, Teresa Liliana, et al.. (2024). The Art of Bioimmunogenomics (BIGs) 5.0 in CAR-T Cell Therapy for Lymphoma Management. Advanced Pharmaceutical Bulletin. 14(2). 314–330.

Ikrar, Taruna, et al.. (2021). The Art of Oncoimmunovaccinomics. 11(4). 50–66.

Sokhadze, Guela, et al.. (2020). Layer 4 Gates Plasticity in Visual Cortex Independent of a Canonical Microcircuit. Current Biology. 30(15). 2962–2973.e5. 10 indexed citations

Putranto, Terawan Agus, et al.. (2019). Introducing the tolerogenic macrophage therapy as an alternative approach to manage systemic lupus erythematosus: a case series. Hipogrifo Revista de literatura y cultural del Siglo de Oro. 8(3). 726–732. 1 indexed citations

García‐Junco‐Clemente, Pablo, Taruna Ikrar, Elaine Tring, et al.. (2017). An inhibitory pull–push circuit in frontal cortex. Nature Neuroscience. 20(3). 389–392. 66 indexed citations

Ikrar, Taruna, et al.. (2017). Bionanomedicine: A “Panacea” In Medicine?. SHILAP Revista de lepidopterología. 21(2). 1 indexed citations

Ikrar, Taruna. (2017). Amyotrophic Lateral Sclerosis: New Suggestions of Pathophysiology and Treatments. 3(2). 9–18. 2 indexed citations

Sun, Yanjun, Taruna Ikrar, Melissa F. Davis, et al.. (2016). Neuregulin-1/ErbB4 Signaling Regulates Visual Cortical Plasticity. Neuron. 92(1). 160–173. 89 indexed citations

Ikrar, Taruna, et al.. (2016). Pten and EphB4 regulate the establishment of perisomatic inhibition in mouse visual cortex. Nature Communications. 7(1). 12829–12829. 11 indexed citations

10.

Ikrar, Taruna, et al.. (2016). Nogo Receptor 1 Confines a Disinhibitory Microcircuit to the Critical Period in Visual Cortex. Journal of Neuroscience. 36(43). 11006–11012. 27 indexed citations

11.

Ikrar, Taruna, Nannan Guo, Kaiwen He, et al.. (2013). Adult neurogenesis modifies excitability of the dentate gyrus. Frontiers in Neural Circuits. 7. 204–204. 148 indexed citations

12.

Kuhlman, Sandra J., Nicholas D. Olivas, Elaine Tring, et al.. (2013). A disinhibitory microcircuit initiates critical-period plasticity in the visual cortex. Nature. 501(7468). 543–546. 303 indexed citations

13.

Ikrar, Taruna, Yulin Shi, Tomoko Velasquez, Martyn Goulding, & Xiangmin Xu. (2012). Cell-type specific regulation of cortical excitability through the allatostatin receptor system. Frontiers in Neural Circuits. 6. 2–2. 10 indexed citations

14.

Shi, Yulin, et al.. (2012). Optical stimulation and imaging of functional brain circuitry in a segmented laminar flow chamber. Lab on a Chip. 13(4). 536–541. 4 indexed citations

15.

Malerba, Monica, María Ramos, Taruna Ikrar, et al.. (2011). Oligodendrocytes as Regulators of Neuronal Networks during Early Postnatal Development. PLoS ONE. 6(5). e19849–e19849. 40 indexed citations

16.

Ikrar, Taruna, Nicholas D. Olivas, Yulin Shi, & Xiangmin Xu. (2011). Mapping Inhibitory Neuronal Circuits by Laser Scanning Photostimulation. Journal of Visualized Experiments. 4 indexed citations

17.

Xu, Xiangmin, Nicholas D. Olivas, Rafael Levi, Taruna Ikrar, & Zoran Nenadić. (2010). High Precision and Fast Functional Mapping of Cortical Circuitry Through a Novel Combination of Voltage Sensitive Dye Imaging and Laser Scanning Photostimulation. Journal of Neurophysiology. 103(4). 2301–2312. 35 indexed citations

18.

Ikrar, Taruna, Haruo Hanawa, Hiroshi Watanabe, et al.. (2008). Evaluation of channel function after alteration of amino acid residues at the pore center of KCNQ1 channel. Biochemical and Biophysical Research Communications. 378(3). 589–594. 2 indexed citations

19.

Ikrar, Taruna, Haruo Hanawa, Hiroshi Watanabe, et al.. (2008). A Double‐Point Mutation in the Selectivity Filter Site of the KCNQ1 Potassium Channel Results in a Severe Phenotype, LQT1, of Long QT Syndrome. Journal of Cardiovascular Electrophysiology. 19(5). 541–549. 8 indexed citations

20.

Ramadan, Mahmoud M., Makoto Kodama, Wataru Mitsuma, et al.. (2006). Impact of Percutaneous Coronary Intervention on the Levels of Interleukin-6 and C-Reactive Protein in the Coronary Circulation of Subjects With Coronary Artery Disease. The American Journal of Cardiology. 98(7). 915–917. 20 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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