I. Iuchi

724 total citations
45 papers, 435 citations indexed

About

I. Iuchi is a scholar working on Genetics, Cell Biology and Molecular Biology. According to data from OpenAlex, I. Iuchi has authored 45 papers receiving a total of 435 indexed citations (citations by other indexed papers that have themselves been cited), including 25 papers in Genetics, 18 papers in Cell Biology and 13 papers in Molecular Biology. Recurrent topics in I. Iuchi's work include Hemoglobinopathies and Related Disorders (25 papers), Hemoglobin structure and function (18 papers) and Cholinesterase and Neurodegenerative Diseases (10 papers). I. Iuchi is often cited by papers focused on Hemoglobinopathies and Related Disorders (25 papers), Hemoglobin structure and function (18 papers) and Cholinesterase and Neurodegenerative Diseases (10 papers). I. Iuchi collaborates with scholars based in Japan, United Kingdom and United States. I. Iuchi's co-authors include Takaoki Miyaji, S. Shibata, Howard B. Hamilton, Susumu Shibata, Kazuo Hidaka, T Miyaji, Lorraine M. Kraus, Alfred Kraus, Shuichi Ueda and Lynn Ten Eyck and has published in prestigious journals such as Nature, Science and Journal of Clinical Investigation.

In The Last Decade

I. Iuchi

45 papers receiving 404 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
I. Iuchi Japan 11 247 228 114 112 109 45 435
Richmond Danso‐Danquah United States 11 186 0.8× 152 0.7× 72 0.6× 53 0.5× 59 0.5× 19 360
SABURO YAMAZOE Japan 7 43 0.2× 69 0.3× 294 2.6× 81 0.7× 43 0.4× 11 480
Y Derrien France 9 55 0.2× 42 0.2× 35 0.3× 13 0.1× 38 0.3× 43 345
Richard P. McPartland United States 13 99 0.4× 19 0.1× 36 0.3× 26 0.2× 21 0.2× 23 434
Leanne K. Winner Australia 8 24 0.1× 46 0.2× 106 0.9× 35 0.3× 6 0.1× 11 331
Monita Muralidharan India 10 25 0.1× 49 0.2× 37 0.3× 13 0.1× 19 0.2× 21 225
M. S. Rashed Saudi Arabia 12 17 0.1× 14 0.1× 79 0.7× 82 0.7× 10 0.1× 24 519
Anna D. Cunningham United States 8 24 0.1× 15 0.1× 43 0.4× 81 0.7× 7 0.1× 8 313
Yoshiteru Kamiyama Japan 9 17 0.1× 33 0.1× 12 0.1× 57 0.5× 36 0.3× 9 331
YiQing Lü China 9 7 0.0× 36 0.2× 23 0.2× 27 0.2× 17 0.2× 19 377

Countries citing papers authored by I. Iuchi

Since Specialization
Citations

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

Fields of papers citing papers by I. Iuchi

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of I. Iuchi

This figure shows the co-authorship network connecting the top 25 collaborators of I. Iuchi. A scholar is included among the top collaborators of I. Iuchi 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 I. Iuchi. I. Iuchi 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.
Hidaka, Kazuo, Masanori Toyoda, Shoji Kuroda, et al.. (2001). Identification of missense mutation (G365R) of the butyrylcholinesterase (BCHE) gene in a Japanese patient with familial cholinesterasemia.. PubMed. 47(4). 153–60. 1 indexed citations
2.
Hidaka, Kazuo, Yoko Watanabe, Masafumi Tomita, et al.. (2001). Gene analysis of genomic DNA from stored serum by polymerase chain reaction: identification of three missense mutations in patients with cholinesterasemia and ABO genotyping. Clinica Chimica Acta. 303(1-2). 61–67. 8 indexed citations
3.
Hidaka, Kazuo, et al.. (1999). First case of missense mutation (LDH-H:R171P) in exon 4 of the lactate dehydrogenase gene detected in a Japanese patient. Journal of Human Genetics. 44(1). 69–72. 6 indexed citations
4.
Hidaka, Kazuo, Yoko Watanabe, Naonori Ueda, et al.. (1999). [Missense mutations of the butyrylcholinesterase gene in six Japanese patients with low cholinesterasemia: genetic analysis using sera stored in a freezer].. PubMed. 47(10). 980–2. 2 indexed citations
5.
6.
Hidaka, Kazuo, et al.. (1997). Nonsense mutation in exon 2 of the butyrylcholinesterase gene: a case of familial cholinesterasemia. Clinica Chimica Acta. 261(1). 27–34. 8 indexed citations
7.
Hidaka, Kazuo, I. Iuchi, Yoko Watanabe, et al.. (1997). Genetic analysis of a Japanese patient with butyrylcholinesterase deficiency. Annals of Human Genetics. 61(6). 491–496. 7 indexed citations
8.
Hidaka, Kazuo, et al.. (1990). Hb Fukutomi [α126(H9)Asp → Val]: A New Hemoglobin Vart with High Oxygen Affinity. Hemoglobin. 14(5). 499–509. 4 indexed citations
9.
Hidaka, Kazuo, et al.. (1989). HB F-Fukuyama orAγT43(CD2)ASP→ASN. Hemoglobin. 13(1). 93–96. 5 indexed citations
10.
Hidaka, Kazuo, et al.. (1988). HB Fukuyama [β77(EF1)HIS→TYR]: A New Abnormal Hemoglobin Discovered in a Japanese. Hemoglobin. 12(4). 391–394. 15 indexed citations
11.
12.
Ohba, Yusuke, et al.. (1978). Occurrence of Hemoglobin G Cousha in Japan. Hemoglobin. 2(5). 437–441. 5 indexed citations
13.
Iuchi, I., et al.. (1978). Short Communications: Characterization of Hb Ube-4: Alpha 116 (Gh4) Glu → Ala. Hemoglobin. 2(2). 181–186. 6 indexed citations
14.
Iuchi, I., et al.. (1969). Survey of Atypical Pseudocholinesterasemia in Okayama District (Preliminary report) and a New Method for Its Detection. 16(1). 35–44. 3 indexed citations
15.
Nakamura, Katsumi, et al.. (1969). Hemoglobin M Disease Discovered in Yonago- the Second Instance in Japanese Families of M Saskatoon Hemoglobinopathy. Proceedings of the Japan Academy. 45(7). 613–617. 1 indexed citations
16.
Iuchi, I.. (1968). Symposium: Hemoglobinopathies in Japan. 1. Abnormal hemoglobin in Japan. Biochemical and epidemiologic characters of abnormal hemoglobin in Japan.. PubMed. 31(5). 842–51. 2 indexed citations
17.
Miyaji, T, et al.. (1968). Japanese Haemoglobin Variant. Nature. 217(5123). 89–90. 26 indexed citations
18.
19.
Kraus, A., T Miyaji, I. Iuchi, & Lorraine M. Kraus. (1967). Hemoglobin Memphis/S. A new variant of sickle cell anemia.. PubMed. 80. 297–304. 2 indexed citations
20.

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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