Toshiyuki Itai

417 total citations
15 papers, 39 citations indexed

About

Toshiyuki Itai is a scholar working on Molecular Biology, Genetics and Cardiology and Cardiovascular Medicine. According to data from OpenAlex, Toshiyuki Itai has authored 15 papers receiving a total of 39 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Molecular Biology, 5 papers in Genetics and 3 papers in Cardiology and Cardiovascular Medicine. Recurrent topics in Toshiyuki Itai's work include Genomics and Rare Diseases (3 papers), Cellular transport and secretion (2 papers) and RNA modifications and cancer (2 papers). Toshiyuki Itai is often cited by papers focused on Genomics and Rare Diseases (3 papers), Cellular transport and secretion (2 papers) and RNA modifications and cancer (2 papers). Toshiyuki Itai collaborates with scholars based in Japan, United States and Brazil. Toshiyuki Itai's co-authors include Satoko Miyatake, Naomichi Matsumoto, Hiroshi Ishikawa, Yuri Uchiyama, Naomi Tsuchida, Zhongming Zhao, Futoshi Sekiguchi, Hiromi Nagase, Takeshi Mizuguchi and Atsushi Fujita and has published in prestigious journals such as Scientific Reports, BMC Cancer and American Journal of Medical Genetics Part B Neuropsychiatric Genetics.

In The Last Decade

Toshiyuki Itai

10 papers receiving 38 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Toshiyuki Itai Japan 5 13 12 11 11 6 15 39
Anya Revah‐Politi United States 4 22 1.7× 19 1.6× 30 2.7× 20 1.8× 9 1.5× 5 74
Seiichiro Yoshioka Japan 5 8 0.6× 9 0.8× 11 1.0× 18 1.6× 3 0.5× 8 43
Somayeh Bakhtiari United States 5 6 0.5× 16 1.3× 9 0.8× 5 0.5× 5 0.8× 11 43
María Pérez-Poyato Spain 5 6 0.5× 20 1.7× 15 1.4× 9 0.8× 6 1.0× 6 83
Julie McCarrier United States 5 10 0.8× 22 1.8× 37 3.4× 4 0.4× 5 0.8× 10 73
Judith Kalser Switzerland 4 11 0.8× 11 0.9× 18 1.6× 22 2.0× 10 1.7× 9 46
Johanna Jähn Germany 5 8 0.6× 16 1.3× 32 2.9× 12 1.1× 2 0.3× 5 54
Ali Al‐Otaibi Saudi Arabia 5 19 1.5× 9 0.8× 8 0.7× 26 2.4× 3 0.5× 12 43
Philip Milburn‐McNulty United Kingdom 5 21 1.6× 8 0.7× 5 0.5× 24 2.2× 15 2.5× 10 39
Steffen Syrbe Germany 2 6 0.5× 19 1.6× 18 1.6× 10 0.9× 2 0.3× 3 49

Countries citing papers authored by Toshiyuki Itai

Since Specialization
Citations

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

Fields of papers citing papers by Toshiyuki Itai

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Toshiyuki Itai

This figure shows the co-authorship network connecting the top 25 collaborators of Toshiyuki Itai. A scholar is included among the top collaborators of Toshiyuki Itai 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 Toshiyuki Itai. Toshiyuki Itai is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

15 of 15 papers shown
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Itai, Toshiyuki, Andi Liu, Sarah W. Curtis, et al.. (2024). Investigating gene functions and single-cell expression profiles of de novo variants in orofacial clefts. Human Genetics and Genomics Advances. 5(3). 100313–100313.
5.
Dai, Yulin, Toshiyuki Itai, Guangsheng Pei, et al.. (2024). DeepFace: Deep-learning-based framework to contextualize orofacial-cleft-related variants during human embryonic craniofacial development. Human Genetics and Genomics Advances. 5(3). 100312–100312. 4 indexed citations
6.
Hamada, Keisuke, Kohei Hamanaka, Keita Miyoshi, et al.. (2023). Novel missense variants cause intermediate phenotypes in the phenotypic spectrum of SLC5A6-related disorders. Journal of Human Genetics. 69(2). 69–77. 5 indexed citations
7.
Kawano, Osamu, Takashi Saito, Eri Takeshita, et al.. (2023). Skeletal anomaly and opisthotonus in early-onset epileptic encephalopathy with KCNQ2 abnormality. Brain and Development. 45(4). 231–236.
8.
Itai, Toshiyuki, Peilin Jia, Yulin Dai, et al.. (2023). De novo mutations disturb early brain development more frequently than common variants in schizophrenia. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 192(3-4). 62–70. 1 indexed citations
9.
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
10.
Nakamura, Yuko, Tohru Okanishi, Tetsuya Okazaki, et al.. (2021). Progressive cerebral atrophies in three children with COL4A1 mutations. Brain and Development. 43(10). 1033–1038. 1 indexed citations
11.
Itai, Toshiyuki, Satoko Miyatake, Taku Hatano, et al.. (2021). Cerebrovascular diseases in two patients with entire NSD1 deletion. Human Genome Variation. 8(1). 20–20. 2 indexed citations
12.
Yamamoto, Ayako, Yoshiaki Saito, Yoshitaka Oyama, et al.. (2020). Effect of total callosotomy on KCNQ2-related intractable epilepsy. Brain and Development. 42(8). 612–616. 3 indexed citations
13.
Ishikawa, Nobutsune, Yoshiyuki Kobayashi, Toshiyuki Itai, et al.. (2019). Successful treatment of intractable life-threatening seizures with perampanel in the first case of early myoclonic encephalopathy with a novel de novo SCN1A mutation. Seizure. 71. 20–23. 8 indexed citations
14.
Itai, Toshiyuki, et al.. (2018). A case of prenatal chronic intestinal pseudo‐obstruction associated with Leigh syndrome. Clinical Case Reports. 6(8). 1474–1477. 3 indexed citations
15.
Ishikawa, Hiroshi, et al.. (2018). Predicting the intrauterine fetal death of fetuses with cystic hygroma in early pregnancy. Congenital Anomalies. 58(5). 167–170. 6 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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