Ryuichi Tsukino

720 total citations
10 papers, 155 citations indexed

About

Ryuichi Tsukino is a scholar working on Pediatrics, Perinatology and Child Health, Genetics and Molecular Biology. According to data from OpenAlex, Ryuichi Tsukino has authored 10 papers receiving a total of 155 indexed citations (citations by other indexed papers that have themselves been cited), including 4 papers in Pediatrics, Perinatology and Child Health, 4 papers in Genetics and 2 papers in Molecular Biology. Recurrent topics in Ryuichi Tsukino's work include Genomic variations and chromosomal abnormalities (4 papers), Prenatal Screening and Diagnostics (3 papers) and Chromosomal and Genetic Variations (2 papers). Ryuichi Tsukino is often cited by papers focused on Genomic variations and chromosomal abnormalities (4 papers), Prenatal Screening and Diagnostics (3 papers) and Chromosomal and Genetic Variations (2 papers). Ryuichi Tsukino collaborates with scholars based in Japan and United Kingdom. Ryuichi Tsukino's co-authors include Naoki Harada, Akira Yoshioka, Hidefumi Tonoki, Yoshimitsu Fukushima, Nobutake Matsuo, Kyohko Abe, Toshiro Nagai, Norio Niikawa, Kennichi Kakudo and Shan Liang and has published in prestigious journals such as Journal of Medical Genetics, Human Genetics and American Journal of Medical Genetics.

In The Last Decade

Ryuichi Tsukino

9 papers receiving 150 citations

Peers

Countries citing papers authored by Ryuichi Tsukino

Since Specialization

Citations

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

Fields of papers citing papers by Ryuichi Tsukino

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Ryuichi Tsukino

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

All Works

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10 of 10 papers shown

#	Work	Indexed citations
1	Successful Arthroscopic Treatment of Pigmented Villonodular Synovitis of the Knee in a Patient with Congenital Deficiency of Plasminogen Activator Inhibitor-1 and Recurrent Haemarthrosis 2001 ·Pathophysiology of Haemostasis and Thrombosis ·Hideto Matsui, Yukihiro Takahashi, Takeshi Matsunaga, (unknown), (unknown), Mitsuhiko Sugimoto, Ryuichi Tsukino, Yoshio Mii, J. C. Giddings, Akira Yoshioka	6
2	Allelic variants of human calcitonin receptor in the Japanese population 1996 ·Human Genetics ·Misa Nakamura, Zhiqiang Zhang, Shan Liang, Tomoyuki Hisa, (unknown), Ryuichi Tsukino, Toyoharu Yokoi, (unknown), Kennichi Kakudo	46
3	Mild form of beta‐ketothiolase deficiency (mitochondrial acetoacetyl‐CoA thiolase deficiency) in two Japanese siblings: identification of detectable residual activity and cross‐reactive material in EB‐transformed lymphocytes 1996 ·Clinical Genetics ·Toshiyuki Fukao, (unknown), (unknown), Ryuichi Tsukino, Shigeru Uemura, Xiang‐Qian Song, (unknown), Tomiko Kuhara, I. Matsumoto, Tadao Orii, Naomi Kondo	5
4	Molecular study of the Prader‐Willi syndrome: Deletion, RFLP, and phenotype analyses of 50 patients 1991 ·American Journal of Medical Genetics ·(unknown), Yoshimitsu Fukushima, Naoki Harada, Kyohko Abe, Nobutake Matsuo, Toshiro Nagai, Akira Yoshioka, Hidefumi Tonoki, Ryuichi Tsukino, Norio Niikawa	58
5	FAMILIAL OCCURRENCE OF OLIGOMEGANEPHRONIA 1985 ·Acta Pathologica Japonica ·(unknown), Ryuichi Tsukino, (unknown), Koichi Kuribayashi, Hiroyuki Katayama, (unknown), Koji Saito	10
6	Live varicella vaccine: prevention of nosocomial infection and protection of high risk infants from varicella infection. 1984 ·PubMed ·(unknown), Ryuichi Tsukino, Eikichi Miyashiro, (unknown), (unknown), Shigeru Uemura, (unknown)	8
7	A case of partial 3p trisomy (46,XY,-18,+der(18),t(3;18)(p24;q22)). 1981 ·Proceedings of the Japan Academy Series B ·Ryuichi Tsukino, (unknown), Shigeru Uemura, (unknown), Michio Koike	2
8	Ring chromosome 10: 46,XX,r(10)(p15→q26) 1980 ·Journal of Medical Genetics ·Ryuichi Tsukino, Naotake Tsuda, (unknown), Tetsuro Ishii, Masato Koike	19
9	A Female with Ring chromosome 18 1979 ·Pediatrics International ·Ryuichi Tsukino, (unknown), Eikichi Miyashiro, (unknown), (unknown), (unknown)	0
10	Recurrence Risk for the Second 21-Trisomic Children 1978 ·Proceedings of the Japan Academy Series B ·Hiroko Fujita, (unknown), T Sugawa, Sachio Ogita, (unknown), Ryuichi Tsukino	1

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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