Kenji Naritomi

4.5k citations
58 papers · 689 indexed · h-index 17
Topics
Genomic variations and chromosomal abnormalities (16 papers)Genetic Syndromes and Imprinting (9 papers)Genetics and Neurodevelopmental Disorders (9 papers)

In The Last Decade

Kenji Naritomi

51 papers receiving 675 citations

Peers

Kenji Naritomi
Comparison fields: 5 of 71
  • Genetics 463
  • Molecular Biology 400
  • Pediatrics, Perinatology and Child Health 133
  • Cell Biology 65
  • Genetics 52
Replace Fabienne Giuliano with:
Fabienne Giuliano France
J. Kunze Germany
Elisa Tassano Italy
E. M. Bleeker‐Wagemakers Netherlands
Sabine Endele Germany
Pamela Magini Italy
Vanna Pecile Italy
Joanna Wiszniewska United States
Alma Kuechler Germany
Pietro Palumbo Italy
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Citations per field
00.5×1.7×
Fabienne Giuliano · 1×
Citations per year

Countries citing papers authored by Kenji Naritomi

Since Specialization
Citations

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

Fields of papers citing papers by Kenji Naritomi

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Kenji Naritomi

This figure shows the co-authorship network connecting the top 25 collaborators of Kenji Naritomi. A scholar is included among the top collaborators of Kenji Naritomi 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 Kenji Naritomi. Kenji Naritomi 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
#WorkIndexed citations
1 2
2 10
3 46
4 27
5 1
6 31
7 4
8
[Oro-cranio-digital syndrome].
0
9 2
10 1
11 4
12 12
13 10
14 12
15 0
16 33
17 16
18 19
19 17
20 11

About Kenji Naritomi

Kenji Naritomi is a scholar working on Genetics, Developmental Biology and Immunology and Allergy, having authored 58 papers that have together received 689 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (16 papers), Genetic Syndromes and Imprinting (9 papers) and Genetics and Neurodevelopmental Disorders (9 papers). The work is most often cited by research in Genetics (463 citations), Developmental Biology (28 citations) and Pediatrics, Perinatology and Child Health (133 citations). Kenji Naritomi has collaborated with scholars based in Japan, United States and Germany. Frequent co-authors include Yoshinori Izumikawa, Kumiko Yanagi, Yasutsugu Chinen, Tadashi Kaname, Norio Niikawa, Yoshimitsu Fukushima, Takaya Tohma, Keiko Wakui, Shigetoshi Nagataki and Kiyoshi Imaizumi. Their work appears in journals such as SHILAP Revista de lepidopterología, Biochemical and Biophysical Research Communications and The American Journal of Human Genetics.

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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