Norio Mori

10.8k total citations
172 papers, 7.1k citations indexed

About

Norio Mori is a scholar working on Cellular and Molecular Neuroscience, Molecular Biology and Cognitive Neuroscience. According to data from OpenAlex, Norio Mori has authored 172 papers receiving a total of 7.1k indexed citations (citations by other indexed papers that have themselves been cited), including 68 papers in Cellular and Molecular Neuroscience, 53 papers in Molecular Biology and 49 papers in Cognitive Neuroscience. Recurrent topics in Norio Mori's work include Neuroscience and Neuropharmacology Research (47 papers), Autism Spectrum Disorder Research (40 papers) and Genetics and Neurodevelopmental Disorders (35 papers). Norio Mori is often cited by papers focused on Neuroscience and Neuropharmacology Research (47 papers), Autism Spectrum Disorder Research (40 papers) and Genetics and Neurodevelopmental Disorders (35 papers). Norio Mori collaborates with scholars based in Japan, United Kingdom and United States. Norio Mori's co-authors include Katsuaki Suzuki, Kazuhiko Nakamura, Yasuhide Iwata, Nori Takei, Kenji J. Tsuchiya, Yoshimoto Sekine, Hideo Matsuzaki, Masatsugu Tsujii, Yasuomi Ouchi and Yoshio Minabe and has published in prestigious journals such as Journal of Clinical Investigation, Journal of Neuroscience and SHILAP Revista de lepidopterología.

In The Last Decade

Norio Mori

172 papers receiving 6.9k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Norio Mori Japan 43 2.1k 2.1k 2.1k 1.5k 1.1k 172 7.1k
Mary M. Herman United States 55 3.3k 1.5× 1.7k 0.8× 3.9k 1.9× 1.2k 0.8× 1.3k 1.1× 179 10.5k
Ryota Hashimoto Japan 52 2.6k 1.2× 2.1k 1.0× 3.2k 1.5× 1.9k 1.3× 2.5k 2.2× 314 10.0k
S. Hossein Fatemi United States 54 2.1k 1.0× 3.1k 1.5× 2.7k 1.3× 2.8k 1.9× 1.3k 1.1× 117 9.2k
Robert H. Lipsky United States 44 2.5k 1.2× 970 0.5× 2.6k 1.2× 806 0.5× 962 0.8× 112 8.1k
Andrew J. Dwork United States 50 3.0k 1.4× 1.7k 0.8× 3.5k 1.7× 1.2k 0.8× 1.2k 1.1× 140 10.4k
Yoshio Minabe Japan 39 2.0k 1.0× 2.0k 0.9× 1.6k 0.8× 772 0.5× 884 0.8× 216 5.5k
Rajiv P. Sharma United States 36 1.3k 0.6× 905 0.4× 3.3k 1.6× 2.0k 1.3× 1.2k 1.1× 128 6.4k
Anat Biegon United States 55 3.5k 1.7× 1.1k 0.5× 2.2k 1.1× 616 0.4× 806 0.7× 187 8.4k
Ian Everall United Kingdom 57 2.0k 0.9× 1.7k 0.8× 2.8k 1.3× 1.2k 0.8× 1.3k 1.2× 217 10.4k
Steven A. Kushner Netherlands 44 2.0k 0.9× 1.6k 0.7× 2.0k 0.9× 874 0.6× 642 0.6× 137 6.7k

Countries citing papers authored by Norio Mori

Since Specialization
Citations

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

Fields of papers citing papers by Norio Mori

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Norio Mori

This figure shows the co-authorship network connecting the top 25 collaborators of Norio Mori. A scholar is included among the top collaborators of Norio Mori 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 Norio Mori. Norio Mori 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
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2.
Makinodan, Manabu, Keiko Iwata, Daisuke Ikawa, et al.. (2016). Tumor necrosis factor-alpha expression in peripheral blood mononuclear cells correlates with early childhood social interaction in autism spectrum disorder. Neurochemistry International. 104. 1–5. 10 indexed citations
3.
Takagai, Shu, Kenji J. Tsuchiya, Hiroaki Itoh, et al.. (2015). Cohort Profile: Hamamatsu Birth Cohort for Mothers and Children (HBC Study). International Journal of Epidemiology. 45(2). 333–342. 37 indexed citations
4.
Takagai, Shu, et al.. (2014). Abnormal sucking behavior in infants as a predictor of developmental delay at 18-month or 3-year of age. 43. 5–23. 1 indexed citations
5.
Thanseem, Ismail, Ayyappan Anitha, Kazuhiko Nakamura, et al.. (2011). Elevated Transcription Factor Specificity Protein 1 in Autistic Brains Alters the Expression of Autism Candidate Genes. Biological Psychiatry. 71(5). 410–418. 39 indexed citations
6.
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
7.
Kushima, Itaru, Branko Aleksić, Yoshihito Ito, et al.. (2010). Association study of ubiquitin-specific peptidase 46 (USP46) with bipolar disorder and schizophrenia in a Japanese population. Journal of Human Genetics. 55(3). 133–136. 15 indexed citations
8.
Miyachi, Taishi, Hideo Matsuzaki, Keiko Iwata, et al.. (2009). Serum levels of platelet-derived growth factor BB homodimers are increased in male children with autism. Progress in Neuro-Psychopharmacology and Biological Psychiatry. 34(1). 154–158. 32 indexed citations
9.
Suzuki, Katsuaki, Genichi Sugihara, Kazuhiko Nakamura, et al.. (2009). Metabolite alterations in the hippocampus of high-functioning adult subjects with autism. The International Journal of Neuropsychopharmacology. 13(4). 529–529. 23 indexed citations
10.
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
11.
Tsuchiya, Kenji J., Kaori Matsumoto, Taishi Miyachi, et al.. (2008). Paternal age at birth and high-functioning autistic-spectrum disorder in offspring. The British Journal of Psychiatry. 193(4). 316–321. 51 indexed citations
12.
Kakiuchi, Chihiro, Mizuho Ishiwata, Shinichiro Nanko, et al.. (2007). Association analysis of ATF4 and ATF5, genes for interacting-proteins of DISC1, in bipolar disorder. Neuroscience Letters. 417(3). 316–321. 15 indexed citations
13.
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
14.
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
15.
Tani, Kunihiko, Nori Takei, Masayoshi Kawai, et al.. (2004). Augmentation of milnacipran by risperidone in treatment for major depression. The International Journal of Neuropsychopharmacology. 7(1). 55–58. 14 indexed citations
16.
Iyo, Masaomi, Yoshimoto Sekine, & Norio Mori. (2004). Neuromechanism of Developing Methamphetamine Psychosis: A Neuroimaging Study. Annals of the New York Academy of Sciences. 1025(1). 288–295. 34 indexed citations
17.
Mori, Norio, et al.. (2002). THE EFFECT OF THE DESTRUCTION OF THE CAUDATE-PUTAMEN ON THE DEVELOPMENT OF AMYGDALOID KINDLING AND KINDLED SEIZURES. FUKUSHIMA JOURNAL OF MEDICAL SCIENCE. 48(1). 39–50. 1 indexed citations
18.
Ohara, Koichi, Norio Mori, Yasuo Suzuki, et al.. (1997). Anticipation and Imprinting in Schizophrenia. Biological Psychiatry. 42(9). 760–766. 35 indexed citations
19.
Mori, Norio, et al.. (1995). Liposome-entrapped phenytoin locally suppresses amygdaloid epileptogenic focus created by db-cAMP/EDTA in rats. Brain Research. 703(1-2). 184–190. 24 indexed citations
20.

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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