Naomi Tsuchida

1.7k total citations
49 papers, 391 citations indexed

About

Naomi Tsuchida is a scholar working on Molecular Biology, Rheumatology and Genetics. According to data from OpenAlex, Naomi Tsuchida has authored 49 papers receiving a total of 391 indexed citations (citations by other indexed papers that have themselves been cited), including 20 papers in Molecular Biology, 16 papers in Rheumatology and 16 papers in Genetics. Recurrent topics in Naomi Tsuchida's work include Genetics and Neurodevelopmental Disorders (13 papers), Genomics and Rare Diseases (11 papers) and Genomic variations and chromosomal abnormalities (7 papers). Naomi Tsuchida is often cited by papers focused on Genetics and Neurodevelopmental Disorders (13 papers), Genomics and Rare Diseases (11 papers) and Genomic variations and chromosomal abnormalities (7 papers). Naomi Tsuchida collaborates with scholars based in Japan, Malaysia and United States. Naomi Tsuchida's co-authors include Naomichi Matsumoto, Yohei Kirino, Hideaki Nakajima, Yuri Uchiyama, Ryusuke Yoshimi, Yosuke Kunishita, Kaoru Takase‐Minegishi, Satoko Miyatake, Takeshi Mizuguchi and Masataka Taguri and has published in prestigious journals such as SHILAP Revista de lepidopterología, PLoS ONE and Genome Research.

In The Last Decade

Naomi Tsuchida

44 papers receiving 389 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Naomi Tsuchida Japan 11 175 143 115 90 59 49 391
Fátima Godinho Portugal 7 171 1.0× 190 1.3× 29 0.3× 52 0.6× 88 1.5× 12 389
Vasilios Zachariadis Sweden 11 38 0.2× 157 1.1× 38 0.3× 90 1.0× 36 0.6× 20 392
Gary J. Mack Canada 7 98 0.6× 365 2.6× 66 0.6× 68 0.8× 26 0.4× 8 522
Stephan A. Müller Germany 4 89 0.5× 65 0.5× 114 1.0× 15 0.2× 29 0.5× 4 296
Sara N. Stahley United States 10 92 0.5× 177 1.2× 114 1.0× 13 0.1× 16 0.3× 14 444
G. Sellar United Kingdom 8 41 0.2× 247 1.7× 23 0.2× 110 1.2× 158 2.7× 11 472
Elizabeth Nacheva United Kingdom 11 46 0.3× 161 1.1× 108 0.9× 99 1.1× 6 0.1× 16 410
Gregory D. Gregory United States 8 34 0.2× 413 2.9× 83 0.7× 67 0.7× 194 3.3× 9 674
Paola Valentino Italy 12 103 0.6× 80 0.6× 37 0.3× 10 0.1× 146 2.5× 26 490
Can Koşukçu Türkiye 12 40 0.2× 156 1.1× 19 0.2× 123 1.4× 72 1.2× 31 337

Countries citing papers authored by Naomi Tsuchida

Since Specialization
Citations

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

Fields of papers citing papers by Naomi Tsuchida

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Naomi Tsuchida

This figure shows the co-authorship network connecting the top 25 collaborators of Naomi Tsuchida. A scholar is included among the top collaborators of Naomi Tsuchida 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 Naomi Tsuchida. Naomi Tsuchida 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.
Mizuguchi, Takeshi, Keisuke Hamada, Kotaro Yuge, et al.. (2025). Hemizygous SMARCA1 variants cause X-linked intellectual disability. Journal of Human Genetics. 70(7). 359–363.
2.
Koshimizu, Eriko, Mitsuhiro Kato, Kazuharu Misawa, et al.. (2024). Detection of hidden intronic DDC variant in aromatic L-amino acid decarboxylase deficiency by adaptive sampling. Journal of Human Genetics. 69(3-4). 153–157. 1 indexed citations
3.
Fu, Lina, Yuka Yamamoto, Takashi Yao, et al.. (2024). Biallelic missense CEP55 variants cause prenatal MARCH syndrome. Journal of Human Genetics. 70(1). 63–66.
4.
Tsuchida, Naomi, Chong Ae Kim, Rachel Sayuri Honjo, et al.. (2024). Novel compound heterozygous ABCA2 variants cause IDPOGSA, a variable phenotypic syndrome with intellectual disability. Journal of Human Genetics. 69(3-4). 163–167. 2 indexed citations
5.
Yamaguchi, Midori, Kaoru Takase‐Minegishi, Yohei Kirino, et al.. (2023). Pregnancy outcomes in patients with familial Mediterranean fever: systematic review and meta-analysis. Lara D. Veeken. 63(2). 277–284. 4 indexed citations
6.
Kurosawa, Kenji, Kazuhiro Iwama, Nobuhiko Okamoto, et al.. (2023). A heterozygous germline deletion within USP8 causes severe neurodevelopmental delay with multiorgan abnormalities. Journal of Human Genetics. 69(2). 85–90. 1 indexed citations
7.
Fukuda, Hiromi, Takeshi Mizuguchi, Hiroshi Doi, et al.. (2023). Long-read sequencing revealing intragenic deletions in exome-negative spastic paraplegias. Journal of Human Genetics. 68(10). 689–697. 3 indexed citations
8.
Uchiyama, Yuri, Kohei Hamanaka, Atsushi Fujita, et al.. (2023). Distal arthrogryposis in a girl arising from a novel TNNI2 variant inherited from paternal somatic mosaicism. Journal of Human Genetics. 68(5). 363–367. 3 indexed citations
9.
Mizuguchi, Takeshi, Tomoko Toyota, Eriko Koshimizu, et al.. (2023). Complete SAMD12 repeat expansion sequencing in a four-generation BAFME1 family with anticipation. Journal of Human Genetics. 68(12). 875–878. 1 indexed citations
10.
Kido, Jun, Kimiyasu Egami, Yohei Misumi, et al.. (2023). X-linked intellectual disability related to a novel variant of KLHL15. Human Genome Variation. 10(1). 21–21.
11.
Mizuguchi, Takeshi, Hiroshi Doi, Shigeru Koyano, et al.. (2022). Patients with biallelic GGC repeat expansions in NOTCH2NLC exhibiting a typical neuronal intranuclear inclusion disease phenotype. Genomics. 114(5). 110469–110469. 4 indexed citations
12.
Kobayashi, Daisuke, Gen Nakamura, Takeshi Okamoto, et al.. (2022). Acute heart failure due to left common iliac arteriovenous fistula: A case of VEXAS syndrome. Modern Rheumatology Case Reports. 7(1). 327–333. 10 indexed citations
13.
Okamoto, Nobuhiko, Eriko Koshimizu, Naomi Tsuchida, et al.. (2022). A novel homozygous CHMP1A variant arising from segmental uniparental disomy causes pontocerebellar hypoplasia type 8. Journal of Human Genetics. 68(4). 247–253. 2 indexed citations
14.
Kato, Tomohiro, Naomi Tsuchida, Ayaka Maeda, et al.. (2022). Clinical images: VEXAS syndrome presenting as treatment‐refractory polyarteritis nodosa. Arthritis & Rheumatology. 74(11). 1863–1864. 14 indexed citations
15.
Tsuchida, Naomi, Yosuke Kunishita, Yuri Uchiyama, et al.. (2021). Pathogenic UBA1 variants associated with VEXAS syndrome in Japanese patients with relapsing polychondritis. Annals of the Rheumatic Diseases. 80(8). 1057–1061. 82 indexed citations
16.
Itai, Toshiyuki, Satoko Miyatake, Naomi Tsuchida, et al.. (2021). Novel CLTC variants cause new brain and kidney phenotypes. Journal of Human Genetics. 67(1). 1–7. 6 indexed citations
17.
Tsuchida, Naomi, Y. Okada, Sonoko Sakata, et al.. (2021). Two families with TET3-related disorder showing neurodevelopmental delay with craniofacial dysmorphisms. Journal of Human Genetics. 67(3). 157–164. 13 indexed citations
18.
Tsuchida, Naomi, Yohei Kirino, Masafumi Onodera, et al.. (2019). Haploinsufficiency of A20 caused by a novel nonsense variant or entire deletion of TNFAIP3 is clinically distinct from Behçet’s disease. Arthritis Research & Therapy. 21(1). 137–137. 43 indexed citations
19.
Tsuchida, Naomi, Keisuke Hamada, Masaaki Shiina, et al.. (2018). GRIN2D variants in three cases of developmental and epileptic encephalopathy. Clinical Genetics. 94(6). 538–547. 16 indexed citations
20.
Tsuchida, Naomi, Mitsuko Nakashima, Akihiko Miyauchi, et al.. (2017). Novel biallelic SZT2 mutations in 3 cases of early‐onset epileptic encephalopathy. Clinical Genetics. 93(2). 266–274. 23 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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