Kenji Naritomi

4.5k total citations
58 papers, 689 citations indexed

About

Kenji Naritomi is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Kenji Naritomi has authored 58 papers receiving a total of 689 indexed citations (citations by other indexed papers that have themselves been cited), including 44 papers in Genetics, 26 papers in Molecular Biology and 9 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Kenji Naritomi's work include Genomic variations and chromosomal abnormalities (16 papers), Genetic Syndromes and Imprinting (9 papers) and Genetics and Neurodevelopmental Disorders (9 papers). Kenji Naritomi is often cited by papers focused on Genomic variations and chromosomal abnormalities (16 papers), Genetic Syndromes and Imprinting (9 papers) and Genetics and Neurodevelopmental Disorders (9 papers). Kenji Naritomi collaborates with scholars based in Japan, United States and Germany. Kenji Naritomi's co-authors include Yoshinori Izumikawa, Kumiko Yanagi, Yasutsugu Chinen, Tadashi Kaname, Norio Niikawa, Yoshimitsu Fukushima, Takaya Tohma, Keiko Wakui, Shigetoshi Nagataki and Kiyoshi Imaizumi and has published in prestigious journals such as SHILAP Revista de lepidopterología, Biochemical and Biophysical Research Communications and The American Journal of Human Genetics.

In The Last Decade

Kenji Naritomi

51 papers receiving 675 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Kenji Naritomi Japan 17 463 400 133 65 52 58 689
Fabienne Giuliano France 17 549 1.2× 698 1.7× 80 0.6× 118 1.8× 38 0.7× 38 1.1k
Sabine Endele Germany 14 309 0.7× 701 1.8× 52 0.4× 51 0.8× 20 0.4× 22 908
E. M. Bleeker‐Wagemakers Netherlands 17 235 0.5× 719 1.8× 46 0.3× 104 1.6× 36 0.7× 50 904
Pamela Magini Italy 16 349 0.8× 347 0.9× 53 0.4× 27 0.4× 52 1.0× 38 717
J. Kunze Germany 14 226 0.5× 328 0.8× 57 0.4× 60 0.9× 48 0.9× 40 577
Elisa Tassano Italy 15 272 0.6× 310 0.8× 46 0.3× 18 0.3× 47 0.9× 54 596
Julien Thévenon France 15 474 1.0× 450 1.1× 54 0.4× 78 1.2× 27 0.5× 51 798
Vanna Pecile Italy 17 499 1.1× 443 1.1× 175 1.3× 31 0.5× 32 0.6× 54 825
Lukrecija Brečević Switzerland 17 479 1.0× 361 0.9× 174 1.3× 27 0.4× 31 0.6× 31 749
Bérengère de Martinville United States 17 389 0.8× 616 1.5× 83 0.6× 50 0.8× 56 1.1× 27 980

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
1.
Chinen, Yasutsugu, Sadao Nakamura, Kumiko Yanagi, et al.. (2022). Additional findings of tibial dysplasia in a male with orofaciodigital syndrome type XVI. Human Genome Variation. 9(1). 9–9. 2 indexed citations
2.
Kaname, Tadashi, Kumiko Yanagi, & Kenji Naritomi. (2014). A commentary on the promise of whole-exome sequencing in medical genetics. Journal of Human Genetics. 59(3). 117–118. 10 indexed citations
3.
Saitsu, Hirotomo, Yoshio Makita, Akie Miyamoto, et al.. (2012). Missense mutations in the DNA-binding/dimerization domain of NFIX cause Sotos-like features. Journal of Human Genetics. 57(3). 207–211. 46 indexed citations
4.
Yoshiura, Koh-ichiro, Tatsuro Kondoh, Hirofumi Ohashi, et al.. (2009). Molecular karyotyping in 17 patients and mutation screening in 41 patients with Kabuki syndrome. Journal of Human Genetics. 54(5). 304–309. 27 indexed citations
5.
Sato, Daisuke, Koh‐ichiro Yoshiura, Hirofumi Ohashi, et al.. (2008). No mutation in RAS‐MAPK pathway genes in 30 patients with Kabuki syndrome. American Journal of Medical Genetics Part A. 146A(14). 1893–1896. 1 indexed citations
6.
Maehara, Hiroki, Tadashi Kaname, Kumiko Yanagi, et al.. (2007). Midkine as a novel target for antibody therapy in osteosarcoma. Biochemical and Biophysical Research Communications. 358(3). 757–762. 31 indexed citations
7.
Yanagi, Kumiko, Tadashi Kaname, Yasutsugu Chinen, & Kenji Naritomi. (2004). Novel alternative splicing of human faciogenital dysplasia 1 gene. Congenital Anomalies. 44(3). 137–141. 4 indexed citations
8.
Naritomi, Kenji. (2001). [Oro-cranio-digital syndrome].. PubMed. 398–9.
9.
Morimoto, Junko, Hidetoshi Kaneoka, Toshiaki Murata, et al.. (2001). Proximal symphalangism with ?coarse? facial appearance, mixed hearing loss, and chronic renal failure: New malformation syndrome?. American Journal of Medical Genetics. 98(3). 269–272. 2 indexed citations
10.
Hyakuna, Nobuyuki, et al.. (1998). Retrospective analysis of clonality and detection of residual disease in myeloid leukemia by FISH on long‐term stored bone marrow smears. Pediatrics International. 40(4). 318–323. 1 indexed citations
11.
Naritomi, Kenji, Yasutsugu Chinen, & Takaya Tohma. (1997). Megalocornea-mental retardation syndrome: An additional case report. The Japanese Journal of Human Genetics. 42(3). 461–465. 4 indexed citations
12.
Takeshima, Yasuhiro, Hajime Nakamura, Kenji Naritomi, et al.. (1996). Japanese Cases of Type 1 Thanatophoric Dysplasia Exclusively Carry a C to T Transition at Nucleotide 742 of the Fibroblast Growth Factor Receptor 3 Gene. Biochemical and Biophysical Research Communications. 227(1). 236–239. 12 indexed citations
13.
Chinen, Yasutsugu, et al.. (1996). Small interstitial deletion of the long arm of chromosome 2 (2q24.3): Further delineation of 2q medial monosomy syndrome. The Japanese Journal of Human Genetics. 41(3). 323–328. 10 indexed citations
14.
Chinen, Yasutsugu & Kenji Naritomi. (1995). Malpuech facial clefting syndrome in a Japanese boy with cardiac defects. The Japanese Journal of Human Genetics. 40(4). 335–338. 12 indexed citations
15.
Naritomi, Kenji, et al.. (1994). Delineatino of the da‐Silva syndrome. American Journal of Medical Genetics. 49(3). 313–316.
16.
Imaizumi, Kiyoshi, et al.. (1990). Cytogenetic and molecular study of the Angelman syndrome. American Journal of Medical Genetics. 35(3). 314–318. 33 indexed citations
17.
Naritomi, Kenji, et al.. (1989). Gene assignment of Zellweger syndrome to 7q11.23: report of the second case associated with a pericentric inversion of chromosome 7. Human Genetics. 84(1). 79–80. 16 indexed citations
18.
Naritomi, Kenji, et al.. (1988). Zellweger syndrome and a microdeletion of the proximal long arm of chromosome 7. Human Genetics. 80(2). 201–202. 19 indexed citations
19.
Naritomi, Kenji, et al.. (1988). 16q21 is critical for 16q deletion syndrome. Clinical Genetics. 33(5). 372–375. 17 indexed citations
20.
Narisawa, Kuniaki, Hiroshi Hayakawa, Nobutake Matsuo, et al.. (1983). Diagnosis of variant forms of hyperphenylalaninemia using filter paper spots of urine. The Journal of Pediatrics. 103(4). 577–579. 11 indexed citations

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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