Koko Ishizuka

3.4k total citations
59 papers, 2.5k citations indexed

About

Koko Ishizuka is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Sensory Systems. According to data from OpenAlex, Koko Ishizuka has authored 59 papers receiving a total of 2.5k indexed citations (citations by other indexed papers that have themselves been cited), including 32 papers in Molecular Biology, 14 papers in Cellular and Molecular Neuroscience and 13 papers in Sensory Systems. Recurrent topics in Koko Ishizuka's work include Phosphodiesterase function and regulation (17 papers), Olfactory and Sensory Function Studies (13 papers) and Receptor Mechanisms and Signaling (10 papers). Koko Ishizuka is often cited by papers focused on Phosphodiesterase function and regulation (17 papers), Olfactory and Sensory Function Studies (13 papers) and Receptor Mechanisms and Signaling (10 papers). Koko Ishizuka collaborates with scholars based in United States, Japan and United Kingdom. Koko Ishizuka's co-authors include Akira Sawa, Atsushi Kamiya, Saurav Seshadri, Taihei Miyakawa, Takemi Kimura, Shoichi Katsuragi, Junichi Takamatsu, Susumu Mori, Ruriko Igata‐Yi and Akiko Hayashi‐Takagi and has published in prestigious journals such as Nature, Proceedings of the National Academy of Sciences and Journal of Biological Chemistry.

In The Last Decade

Koko Ishizuka

58 papers receiving 2.5k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Koko Ishizuka United States	21	1.4k	714	431	330	306	59	2.5k
Minae Niwa Japan	27	862 0.6×	893 1.3×	213 0.5×	315 1.0×	208 0.7×	56	2.0k
Hanna Jaaro-Peled United States	22	1.2k 0.9×	867 1.2×	339 0.8×	353 1.1×	115 0.4×	36	2.1k
Pawel Licznerski United States	19	1.4k 1.0×	979 1.4×	288 0.7×	591 1.8×	259 0.8×	24	3.0k
Steven J. Clapcote United Kingdom	25	1.5k 1.1×	806 1.1×	574 1.3×	112 0.3×	164 0.5×	49	2.5k
Tomoko Toyota Japan	31	1.5k 1.1×	818 1.1×	850 2.0×	322 1.0×	218 0.7×	87	2.8k
John Marshall United States	28	1.8k 1.3×	1.3k 1.8×	286 0.7×	245 0.7×	210 0.7×	44	2.9k
Robin J. Kleiman United States	26	1.7k 1.3×	625 0.9×	259 0.6×	146 0.4×	195 0.6×	45	2.5k
Ana M.D. Carneiro United States	18	754 0.6×	748 1.0×	244 0.6×	251 0.8×	96 0.3×	27	1.7k
Luisa Iacovelli Italy	28	1.7k 1.2×	1.2k 1.7×	249 0.6×	144 0.4×	284 0.9×	58	2.6k
Vivi M. Heine Netherlands	26	1.6k 1.2×	683 1.0×	382 0.9×	299 0.9×	283 0.9×	66	3.3k

Countries citing papers authored by Koko Ishizuka

Since Specialization

Citations

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

Fields of papers citing papers by Koko Ishizuka

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Koko Ishizuka

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

Faghiri, Ashkan, Kun Yang, Andréia V. Faria, et al.. (2024). Frequency modulation increases the specificity of time-resolved connectivity: A resting-state fMRI study. Network Neuroscience. 8(3). 734–761. 2 indexed citations

Yang, Kun, Yuto Hasegawa, Janardhan P. Bhattarai, et al.. (2024). Inflammation-related pathology in the olfactory epithelium: its impact on the olfactory system in psychotic disorders. Molecular Psychiatry. 29(5). 1453–1464. 9 indexed citations

Calhoun, Vince D., Zening Fu, Kun Yang, et al.. (2024). A whole-brain neuromark resting-state fMRI analysis of first-episode and early psychosis: Evidence of aberrant cortical-subcortical-cerebellar functional circuitry. NeuroImage Clinical. 41. 103584–103584. 7 indexed citations

Mihaljević, Marina, Max Lam, Carlos A. Ayala‐Grosso, et al.. (2023). Olfactory neuronal cells as a promising tool to realize the “druggable genome” approach for drug discovery in neuropsychiatric disorders. Frontiers in Neuroscience. 16. 1081124–1081124. 6 indexed citations

Jaaro-Peled, Hanna, Melissa A. Landek‐Salgado, Nicola G. Cascella, et al.. (2022). Sex-specific involvement of the Notch–JAG pathway in social recognition. Translational Psychiatry. 12(1). 99–99. 9 indexed citations

Namkung, Ho, Hiroshi Yukitake, Brian J. Lee, et al.. (2022). The miR-124-AMPAR pathway connects polygenic risks with behavioral changes shared between schizophrenia and bipolar disorder. Neuron. 111(2). 220–235.e9. 20 indexed citations

Hasegawa, Yuto, Ho Namkung, Amy Smith, et al.. (2021). Causal impact of local inflammation in the nasal cavity on higher brain function and cognition. Neuroscience Research. 172. 110–115. 13 indexed citations

Takayanagi, Yoichiro, Koko Ishizuka, Thomas Munk Laursen, et al.. (2020). From population to neuron: exploring common mediators for metabolic problems and mental illnesses. Molecular Psychiatry. 26(8). 3931–3942. 12 indexed citations

John, John P., et al.. (2019). An in-silico approach for discovery of microRNA-TF regulation of DISC1 interactome mediating neuronal migration. npj Systems Biology and Applications. 5(1). 17–17. 8 indexed citations

10.

Tharakan, Ravi, Simion Kreimer, Ceereena Ubaida‐Mohien, et al.. (2019). A methodology for discovering novel brain-relevant peptides: Combination of ribosome profiling and peptidomics. Neuroscience Research. 151. 31–37. 9 indexed citations

11.

Faust, Travis E., et al.. (2018). Dynamic Changes of the Mitochondria in Psychiatric Illnesses: New Mechanistic Insights From Human Neuronal Models. Biological Psychiatry. 83(9). 751–760. 43 indexed citations

12.

Wen, Zhexing, Shaolei Teng, Lingling Wang, et al.. (2017). Disrupted-in-Schizophrenia-1 (DISC1) protein disturbs neural function in multiple disease-risk pathways. Human Molecular Genetics. 26(14). 2634–2648. 19 indexed citations

13.

Jaaro-Peled, Hanna, Cara M. Altimus, Tara A. LeGates, et al.. (2016). Abnormal wake/sleep pattern in a novel gain-of-function model of DISC1. Neuroscience Research. 112. 63–69. 20 indexed citations

14.

Jones‐Brando, Lorraine, Claudia Bordón, Srona Sengupta, et al.. (2015). Infection and characterization of Toxoplasma gondii in human induced neurons from patients with brain disorders and healthy controls. Microbes and Infection. 18(2). 153–158. 15 indexed citations

15.

Barodia, Sandeep Kumar, Sang Ki Park, Koko Ishizuka, Akira Sawa, & Atsushi Kamiya. (2015). Half-life of DISC1 protein and its pathological significance under hypoxia stress. Neuroscience Research. 97. 1–6. 6 indexed citations

16.

Seshadri, Saurav, Travis E. Faust, Koko Ishizuka, et al.. (2015). Interneuronal DISC1 regulates NRG1-ErbB4 signalling and excitatory–inhibitory synapse formation in the mature cortex. Nature Communications. 6(1). 10118–10118. 49 indexed citations

17.

Seshadri, Saurav, Atsushi Kamiya, Yukako Yokota, et al.. (2010). Disrupted-in-Schizophrenia-1 expression is regulated by β-site amyloid precursor protein cleaving enzyme-1–neuregulin cascade. Proceedings of the National Academy of Sciences. 107(12). 5622–5627. 92 indexed citations

18.

Abazyan, Bagrat, Jun Nomura, Geetha Kannan, et al.. (2010). Prenatal Interaction of Mutant DISC1 and Immune Activation Produces Adult Psychopathology. Biological Psychiatry. 68(12). 1172–1181. 213 indexed citations

19.

Kamiya, Atsushi, Perciliz L. Tan, Ken‐ichiro Kubo, et al.. (2008). Recruitment of PCM1 to the Centrosome by the Cooperative Action of DISC1 and BBS4. Archives of General Psychiatry. 65(9). 996–996. 114 indexed citations

20.

Ishizuka, Koko, Takemi Kimura, Ruriko Igata‐Yi, et al.. (1997). Identification of monocyte chemoattractant protein‐1 in senile plaques and reactive microglia of Alzheimer's disease. Psychiatry and Clinical Neurosciences. 51(3). 135–138. 188 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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