Mitsuhiro Kato

288 papers receiving 11.0k citations

Mitsuhiro Kato's Hit Papers

GWAS meta-analysis of over 29,000 people with epilepsy identifies 26 risk loci and subtype-specific genetic architecture 2023 · 129 citations
1290+8+16Years since publication100200300400500

Peers

Mitsuhiro Kato
Comparison fields: 5 of 89
  • Psychiatry and Mental health 2.7k
  • Developmental Neuroscience 288
  • Clinical Biochemistry 264
  • Genetics 1.7k
  • Pediatrics, Perinatology and Child Health 582
Replace Hirotomo Saitsu with:
Hirotomo Saitsu Japan
Nadia Bahi‐Buisson France
Grazia M. S. Mancini Netherlands
Richard Jacob Leventer Australia
Heather C. Mefford United States
V. des Portes France
Jacques L. Michaud Canada
Boris Keren France
Cyril Mignot France
Anna‐Elina Lehesjoki Finland
Mitsuhiro Kato relative to Hirotomo Saitsu Japan Hirotomo Saitsu's profile →
Citations per field
00.5×1.5×1.9×
Hirotomo Saitsu · 1×
Citations per year

Countries citing papers authored by Mitsuhiro Kato

Since Specialization
Citations

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

Fields of papers citing papers by Mitsuhiro Kato

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 25 scholars most cited alongside Mitsuhiro Kato, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Mitsuhiro Kato Line = papers co-authored together Mitsuhiro Kato links everyone, so they are left out of the graph.

All Works

20 of 20 papers shown

Showing the 20 most-cited of 298 papers — load more, or switch the sort, to bring in the rest.

#Work
1
Mutation of ARX causes abnormal development of forebrain and testes in mice and X-linked lissencephaly with abnormal genitalia in humans
Hit paper breakdown →
2002593
2 2008463
3 2012422
4
De novo mutations in the autophagy gene WDR45 cause static encephalopathy of childhood with neurodegeneration in adulthood
Hit paper breakdown →
2013390
5 2004266
6 2003261
7 2006212
8 2013196
9 2013189
10 2010186
11 2013173
12 2015164
13 2007156
14 2013152
15 2010139
16 2012138
17 2018133
18 2005129
19
GWAS meta-analysis of over 29,000 people with epilepsy identifies 26 risk loci and subtype-specific genetic architecture
Hit paper breakdown →
2023129
20 2007127

About Mitsuhiro Kato

Mitsuhiro Kato is a scholar working on Psychiatry and Mental health, Pediatrics, Perinatology and Child Health, Genetics, Clinical Biochemistry and Cellular and Molecular Neuroscience, having authored 298 papers that have together received 11.3k indexed citations. Recurring topics across this work include Epilepsy research and treatment (74 papers), Fetal and Pediatric Neurological Disorders (31 papers), Genetics and Neurodevelopmental Disorders (18 papers), Genomic variations and chromosomal abnormalities (12 papers), Genomics and Rare Diseases (11 papers), Hereditary Neurological Disorders (7 papers), Metabolism and Genetic Disorders (7 papers) and Sleep and Wakefulness Research (4 papers). The work is most often cited by research in Psychiatry and Mental health (2.7k citations), Developmental Neuroscience (288 citations), Clinical Biochemistry (264 citations), Genetics (1.7k citations) and Pediatrics, Perinatology and Child Health (582 citations). Mitsuhiro Kato has collaborated with scholars based in Japan, United States and Malaysia. Frequent co-authors include Naomichi Matsumoto, Hirotomo Saitsu, Kiyoshi Hayasaka, Jun Tohyama, Mitsuko Nakashima, Noriko Miyake, William B. Dobyns, Yoshinori Tsurusaki, Hitoshi Osaka and Shinji Saitoh. Their work appears in journals such as Brain and Development, Epilepsia, Clinical Genetics, The American Journal of Human Genetics and Scientific Reports.

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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