Jun Tohyama

5.7k citations
108 papers · 2.8k · h-index 29

Impact in

Papers in

    • Genetics and Neurodevelopmental Disorders 24
    • Genomics and Rare Diseases 11
    • Genomic variations and chromosomal abnormalities 10

Jun Tohyama

102 papers receiving 2.7k citations

Peers

Jun Tohyama
Comparison fields: 5 of 105
  • Psychiatry and Mental health 751
  • Clinical Biochemistry 243
  • Genetics 992
  • Cellular and Molecular Neuroscience 520
  • Pediatrics, Perinatology and Child Health 458
Replace Davide Mei with:
Davide Mei Italy
Raffaella Cusmai Italy
Sarah Weckhuysen Belgium
Eric Leguern France
Elena Parrini Italy
Agathe Roubertie France
Anna‐Elina Lehesjoki Finland
E. Andermann Canada
Michael C. Kruer United States
Byung Chan Lim South Korea
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Citations per field
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Davide Mei · 1×
Citations per year

Countries citing papers authored by Jun Tohyama

Since Specialization
Citations

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

Fields of papers citing papers by Jun Tohyama

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 25 scholars most cited alongside Jun Tohyama, 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 Jun Tohyama Line = papers co-authored together Jun Tohyama links everyone, so they are left out of the graph.

All Works

20 of 20 papers shown

Showing the 20 most-cited of 108 papers — load more, or switch the sort, to bring in the rest.

#Work
1 2008383
2 2015136
3 2007131
4 2007105
5 2006100
6 199790
7 199289
8 200787
9 200983
10 200671
11 200764
12 201563
13 201857
14 201454
15 201553
16 201951
17 201551
18 201147
19 201143
20 201443

About Jun Tohyama

Jun Tohyama is a scholar working on Molecular Biology, Genetics, Psychiatry and Mental health, Pediatrics, Perinatology and Child Health and Cellular and Molecular Neuroscience, having authored 108 papers that have together received 2.8k indexed citations. Recurring topics across this work include Epilepsy research and treatment (30 papers), Genetics and Neurodevelopmental Disorders (24 papers), Neuroscience and Neuropharmacology Research (13 papers), Genomics and Rare Diseases (11 papers), Pharmacological Effects and Toxicity Studies (10 papers), Lysosomal Storage Disorders Research (10 papers), Genomic variations and chromosomal abnormalities (10 papers) and Neonatal and fetal brain pathology (8 papers). The work is most often cited by research in Psychiatry and Mental health (751 citations), Clinical Biochemistry (243 citations), Genetics (992 citations), Cellular and Molecular Neuroscience (520 citations) and Pediatrics, Perinatology and Child Health (458 citations). Jun Tohyama has collaborated with scholars based in Japan, United States and France. Frequent co-authors include Mitsuhiro Kato, Naomichi Matsumoto, Hirotomo Saitsu, Noriyuki Akasaka, Kiyoshi Hayasaka, Mitsuko Nakashima, Kazuhiro Ogata, Osamu Kanazawa, Noriko Miyake and Yu Kobayashi. Their work appears in journals such as Brain and Development, Human Genetics, Epilepsia, Pediatric Neurology and Epileptic Disorders.

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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