Tomoko Toyota

6.5k total citations
87 papers, 2.8k citations indexed

About

Tomoko Toyota is a scholar working on Molecular Biology, Genetics and Cellular and Molecular Neuroscience. According to data from OpenAlex, Tomoko Toyota has authored 87 papers receiving a total of 2.8k indexed citations (citations by other indexed papers that have themselves been cited), including 47 papers in Molecular Biology, 45 papers in Genetics and 24 papers in Cellular and Molecular Neuroscience. Recurrent topics in Tomoko Toyota's work include Genetics and Neurodevelopmental Disorders (28 papers), Genetic Associations and Epidemiology (15 papers) and Autism Spectrum Disorder Research (13 papers). Tomoko Toyota is often cited by papers focused on Genetics and Neurodevelopmental Disorders (28 papers), Genetic Associations and Epidemiology (15 papers) and Autism Spectrum Disorder Research (13 papers). Tomoko Toyota collaborates with scholars based in Japan, United States and Australia. Tomoko Toyota's co-authors include Takeo Yoshikawa, Kazuo Yamada, Yoshimi Iwayama, Tetsuo Ohnishi, Norio Mori, Eiji Hattori, Motoko Maekawa, Hisako Ohba, Yoshio Minabe and Kazuhiko Nakamura and has published in prestigious journals such as Proceedings of the National Academy of Sciences, SHILAP Revista de lepidopterología and PLoS ONE.

In The Last Decade

Tomoko Toyota

84 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
Tomoko Toyota Japan 31 1.5k 850 818 398 344 87 2.8k
Rami Abou Jamra Germany 29 1.4k 0.9× 1.1k 1.3× 544 0.7× 244 0.6× 407 1.2× 99 2.8k
Koko Ishizuka United States 21 1.4k 0.9× 431 0.5× 714 0.9× 247 0.6× 218 0.6× 59 2.5k
J. Kirsty Millar United Kingdom 32 3.8k 2.6× 1.4k 1.6× 1.1k 1.4× 471 1.2× 534 1.6× 49 4.9k
Steven J. Clapcote United Kingdom 25 1.5k 1.1× 574 0.7× 806 1.0× 331 0.8× 216 0.6× 49 2.5k
Miki Bundo Japan 29 2.3k 1.6× 1.3k 1.5× 471 0.6× 266 0.7× 639 1.9× 70 3.6k
Hanna Jaaro-Peled United States 22 1.2k 0.8× 339 0.4× 867 1.1× 327 0.8× 226 0.7× 36 2.1k
Sharon L. Eastwood United Kingdom 24 1000 0.7× 275 0.3× 1.3k 1.6× 529 1.3× 329 1.0× 36 2.1k
James Auta United States 22 1.2k 0.8× 533 0.6× 1.3k 1.6× 488 1.2× 241 0.7× 50 2.8k
Guomei Tang United States 20 1.2k 0.8× 519 0.6× 784 1.0× 504 1.3× 228 0.7× 43 2.9k
Toshifumi Tomoda United States 29 2.1k 1.5× 502 0.6× 949 1.2× 246 0.6× 156 0.5× 51 3.3k

Countries citing papers authored by Tomoko Toyota

Since Specialization
Citations

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

Fields of papers citing papers by Tomoko Toyota

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Tomoko Toyota

This figure shows the co-authorship network connecting the top 25 collaborators of Tomoko Toyota. A scholar is included among the top collaborators of Tomoko Toyota 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 Tomoko Toyota. Tomoko Toyota 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.
Niitsu, Tomihisa, Kengo Oishi, Jing Liu, et al.. (2023). Taq1A polymorphism in patients with bipolar disorder: A candidate gene study based on the dopamine hypothesis. SHILAP Revista de lepidopterología. 3(2). 100124–100124. 2 indexed citations
2.
Uezato, Akihito, S. Dai, Naoki Yamamoto, et al.. (2022). Differential genetic associations and expression of PAPST1/SLC35B2 in bipolar disorder and schizophrenia. Journal of Neural Transmission. 129(7). 913–924. 2 indexed citations
3.
Balan, Shabeesh, Tetsuo Ohnishi, Akiko Watanabe, et al.. (2021). Role of an Atypical Cadherin Gene, Cdh23 in Prepulse Inhibition, and Implication of CDH23 in Schizophrenia. Schizophrenia Bulletin. 47(4). 1190–1200. 11 indexed citations
4.
Nakaya, Akihiro, Kayoko Esaki, Shabeesh Balan, et al.. (2020). Lipid Pathology of the Corpus Callosum in Schizophrenia and the Potential Role of Abnormal Gene Regulatory Networks with Reduced Microglial Marker Expression. Cerebral Cortex. 31(1). 448–462. 20 indexed citations
5.
Balan, Shabeesh, Yoshimi Iwayama, Tomoko Toyota, et al.. (2014). 22q11.2 deletion carriers and schizophrenia-associated novel variants. The British Journal of Psychiatry. 204(5). 398–399. 15 indexed citations
6.
Shimamoto, Chie, Tetsuo Ohnishi, Motoko Maekawa, et al.. (2014). Functional characterization of FABP3, 5 and 7 gene variants identified in schizophrenia and autism spectrum disorder and mouse behavioral studies. Human Molecular Genetics. 23(24). 6495–6511. 80 indexed citations
7.
Balan, Shabeesh, Yoshimi Iwayama, Kazuo Yamada, et al.. (2014). Sequencing and expression analyses of the synaptic lipid raft adapter gene PAG1 in schizophrenia. Journal of Neural Transmission. 122(3). 477–485. 3 indexed citations
8.
Kondo, Kenji, Masashi Ikeda, Takeo Saito, et al.. (2013). Genetic Variants on 3q21 and in the Sp8 Transcription Factor Gene (SP8) as Susceptibility Loci for Psychotic Disorders: A Genetic Association Study. PLoS ONE. 8(8). e70964–e70964. 16 indexed citations
9.
Kondo, Kenji, Takeo Saito, Yoshimi Iwayama, et al.. (2013). Genetic association study between the detected risk variants based upon type II diabetes GWAS and psychotic disorders in the Japanese population. Journal of Human Genetics. 59(1). 54–56. 8 indexed citations
10.
Ohnishi, Tetsuo, Kazuo Yamada, Akiko Watanabe, et al.. (2011). Ablation of Mrds1/Ofcc1 Induces Hyper-γ-Glutamyl Transpeptidasemia without Abnormal Head Development and Schizophrenia-Relevant Behaviors in Mice. PLoS ONE. 6(12). e29499–e29499. 7 indexed citations
11.
Yamada, Kazuo, Yoshimi Iwayama, Tomoko Toyota, et al.. (2011). Association study of the KCNJ3 gene as a susceptibility candidate for schizophrenia in the Chinese population. Human Genetics. 131(3). 443–451. 41 indexed citations
12.
Thanseem, Ismail, Kazuhiko Nakamura, Ayyappan Anitha, et al.. (2011). Association of Transcription Factor Gene LMX1B with Autism. PLoS ONE. 6(8). e23738–e23738. 7 indexed citations
13.
Maekawa, Motoko, Tomoko Toyota, Yoshimi Iwayama, et al.. (2011). Schizophrenia with the 22q11.2 deletion and additional genetic defects: case history. The British Journal of Psychiatry. 199(3). 245–246. 28 indexed citations
14.
Maekawa, Motoko, Yoshimi Iwayama, Ryoichi Arai, et al.. (2010). Polymorphism screening of brain-expressed FABP7, 5 and 3 genes and association studies in autism and schizophrenia in Japanese subjects. Journal of Human Genetics. 55(2). 127–130. 33 indexed citations
15.
Nakamura, Kazuhiko, Ayyappan Anitha, Kazuo Yamada, et al.. (2008). Genetic and expression analyses reveal elevated expression of syntaxin 1A ( STX1A) in high functioning autism. The International Journal of Neuropsychopharmacology. 11(8). 1073–1073. 62 indexed citations
16.
Ikeda, Yumiko, Noriaki Yahata, Masatoshi Nagano, et al.. (2008). Low serum levels of brain-derived neurotrophic factor and epidermal growth factor in patients with chronic schizophrenia. Schizophrenia Research. 101(1-3). 58–66. 124 indexed citations
17.
Yamada, Kazuo, Tomoko Toyota, Yoshio Minabe, et al.. (2006). A novel scale including strabismus and ‘cuspidal ear’ for distinguishing schizophrenia patients from controls using minor physical anomalies. Psychiatry Research. 145(2-3). 249–258. 22 indexed citations
18.
Ide, Masayuki, Kazuo Yamada, Tomoko Toyota, et al.. (2005). Genetic association analyses of PHOX2B and ASCL1 in neuropsychiatric disorders: evidence for association of ASCL1 with Parkinson’s disease. Human Genetics. 117(6). 520–527. 23 indexed citations
19.
Aoki, Mika, Kazuo Yamada, Yoshimi Iwayama‐Shigeno, et al.. (2004). Case-control association study of human netrin G1 gene in Japanese schizophrenia.. PubMed. 51(2). 121–8. 12 indexed citations
20.
Kockelkorn, Thessa T. J. P., Makoto Arai, Hiroyuki Matsumoto, et al.. (2004). Association study of polymorphisms in the 5′ upstream region of human DISC1 gene with schizophrenia. Neuroscience Letters. 368(1). 41–45. 49 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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