Masato Mori

1.3k total citations
31 papers, 720 citations indexed

About

Masato Mori is a scholar working on Molecular Biology, Genetics and Clinical Biochemistry. According to data from OpenAlex, Masato Mori has authored 31 papers receiving a total of 720 indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Molecular Biology, 10 papers in Genetics and 9 papers in Clinical Biochemistry. Recurrent topics in Masato Mori's work include Mitochondrial Function and Pathology (9 papers), Metabolism and Genetic Disorders (9 papers) and Genetics and Neurodevelopmental Disorders (7 papers). Masato Mori is often cited by papers focused on Mitochondrial Function and Pathology (9 papers), Metabolism and Genetic Disorders (9 papers) and Genetics and Neurodevelopmental Disorders (7 papers). Masato Mori collaborates with scholars based in Japan, United States and China. Masato Mori's co-authors include Takanori Yamagata, Mariko Y. Momoi, Hong Li, Masaya Kubota, Takashi Ichiyama, Jun Tohyama, Hiroshi Isumi, Naoko Suenaga, Susumu Furukawa and Madoka Kajimoto and has published in prestigious journals such as PLoS ONE, Scientific Reports and Journal of Investigative Dermatology.

In The Last Decade

Masato Mori

30 papers receiving 703 citations

Peers

Countries citing papers authored by Masato Mori

Since Specialization

Citations

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

Fields of papers citing papers by Masato Mori

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Masato Mori

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

#	Work	Indexed citations
1	Transient Pseudohypoaldosteronism Secondary to Group B Streptococcus Pyelonephritis 2021 ·Cureus ·(unknown), (unknown), (unknown), Masato Mori, (unknown)	2
2	A simple method for sequencing the whole human mitochondrial genome directly from samples and its application to genetic testing 2019 ·Scientific Reports ·Yue Yao, Motoi Nishimura, Kei Murayama, (unknown), (unknown), Minako Beppu, Takayuki Ishige, Sakae Itoga, Sachio Tsuchida, Masato Mori, Masaki Takayanagi, Masataka Yokoyama, Kazuyuki Yamagata, Yoshihito Kishita, Yasushi Okazaki, Fumio Nomura, Kazuyuki Matsushita, Tomoaki Tanaka	22
3	The association of GPR85 with PSD-95-neuroligin complex and autism spectrum disorder: a molecular analysis 2015 ·Molecular Autism ·(unknown), Yuko Tanabe, Zhi‐Ling Yu, Karin Kojima, Masato Mori, Hong Li, Sadahiko Iwamoto, Takanori Yamagata, Mariko Y. Momoi, Takashi Momoi	35
4	Late-onset Leigh syndrome with myoclonic epilepsy with ragged-red fibers 2012 ·Brain and Development ·Yukifumi Monden, Masato Mori, (unknown), (unknown), Takanori Yamagata, Mariko Y. Momoi	14
5	Mutation in Parkinson Disease-Associated, G-Protein-Coupled Receptor 37 (GPR37/PaelR) Is Related to Autism Spectrum Disorder 2012 ·PLoS ONE ·(unknown), Zhi‐Ling Yu, Hong Li, Takanori Yamagata, Masato Mori, Takashi Momoi, Mariko Y. Momoi	46
6	Subtelomeric deletions of 1q43q44 and severe brain impairment associated with delayed myelination 2012 ·Journal of Human Genetics ·Keiko Shimojima, Nobuhiko Okamoto, Yume Suzuki, Mari Saito, Masato Mori, (unknown), Mariko Y. Momoi, Hideji Hattori, Yoshiyuki Okano, Ken Hisata, Akihisa Okumura, Toshiyuki Yamamoto	16
7	Liver-specific mitochondrial respiratory chain complex I deficiency in fatal influenza encephalopathy 2011 ·Brain and Development ·Chikako Arakawa, Ayumi Endo, (unknown), Yukihiko Fujita, Tatsuo Fuchigami, Hideo Mugishima, Akira Ohtake, Kei Murayama, Masato Mori, Rie Miyata, (unknown)	3
8	A case of ADEM with atypical MRI findings of a centrally-located long spinal cord lesion 2011 ·Brain and Development ·Yukifumi Monden, Takanori Yamagata, (unknown), Toshiyuki Takahashi, Masato Mori, Tokiko Fukuda, Hideo Sugie, (unknown)	7
9	Another promising treatment option for neuroblastoma-associated opsoclonus–myoclonus syndrome by oral high-dose dexamethasone pulse: Lymphocyte markers as disease activity 2011 ·Brain and Development ·(unknown), Akira Morimoto, Akiko Takada, (unknown), Tokiko Fukuda, Masato Mori, Takanori Yamagata, Hideo Sugie, Mariko Y. Momoi	9
10	Expression analysis and mutation detection of DLX5 and DLX6 in autism 2009 ·Brain and Development ·Naomi Nakashima, Takanori Yamagata, Masato Mori, (unknown), (unknown), Mariko Y. Momoi	25
11	Serum and CSF levels of cytokines in acute encephalopathy following prolonged febrile seizures 2007 ·Brain and Development ·Takashi Ichiyama, Naoko Suenaga, Madoka Kajimoto, Jun Tohyama, Hiroshi Isumi, Masaya Kubota, Masato Mori, Susumu Furukawa	87
12	Mutation analysis of methyl-CpG binding protein family genes in autistic patients 2005 ·Brain and Development ·Hong Li, Takanori Yamagata, Masato Mori, Akihiro Yasuhara, Mariko Y. Momoi	50
13	Early-Onset Ataxia With Oculomotor Apraxia With a Novel APTX Mutation 2005 ·Pediatric Neurology ·Aya Ito, Takanori Yamagata, Masato Mori, Mariko Y. Momoi	5
14	Two New XPD Patients Compound Heterozygous for the Same Mutation Demonstrate Diverse Clinical Features 2005 ·Journal of Investigative Dermatology ·Mitsuo Fujimoto, S. Leech, (unknown), Masato Mori, Heather Fawcett, Elena Botta, Yasuyuki Nozaki, Takanori Yamagata, Shinichi Moriwaki, Miria Stefanini, Mariko Y. Momoi, Hidemi Nakagawa, Sam Shuster, Celia Moss, Alan R. Lehmann	24
15	Absence of causative mutations and presence of autism-related allele in FOXP2 in Japanese autistic patients 2004 ·Brain and Development ·Hong Li, Takanori Yamagata, Masato Mori, Mariko Y. Momoi	34
16	Dichloroacetate treatment for mitochondrial cytopathy: long-term effects in MELAS 2004 ·Brain and Development ·Masato Mori, Takanori Yamagata, (unknown), (unknown), Mariko Y. Momoi	34
17	RSK2 gene mutations in Coffin–Lowry syndrome with drop episodes 2004 ·Brain and Development ·Miki Nakamura, Takanori Yamagata, Masato Mori, Mariko Y. Momoi	9
18	Absence of allelic loss in cytomegalic neurons of cortical tuber in the Eker rat model of tuberous sclerosis 2003 ·Acta Neuropathologica ·Masashi Mizuguchi, Masato Mori, Yasuyuki Nozaki, Mariko Y. Momoi, Masayuki Itoh, Sachio Takashima, Okio Hino	13
19	Mutational analysis of the BMP-1 gene in patients with gastroschisis 2001 ·Journal of Pediatric Surgery ·Hiroaki Komuro, Masato Mori, Yasuhide Hayashi, Masafumi Fukagawa, (unknown), Kazuhiko Takahara, Daniel S. Greenspan, Mariko Y. Momoi	20
20	Elastic fiber degeneration in Costello syndrome 1996 ·American Journal of Medical Genetics ·Masato Mori, Takanori Yamagata, (unknown), Mitsuhiro Nokubi, Ken Saito, Yoshimitsu Fukushima, Mariko Y. Momoi	46

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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