Yoshiro Koda

3.9k total citations
149 papers, 3.1k citations indexed

About

Yoshiro Koda is a scholar working on Molecular Biology, Cell Biology and Physiology. According to data from OpenAlex, Yoshiro Koda has authored 149 papers receiving a total of 3.1k indexed citations (citations by other indexed papers that have themselves been cited), including 95 papers in Molecular Biology, 30 papers in Cell Biology and 29 papers in Physiology. Recurrent topics in Yoshiro Koda's work include Glycosylation and Glycoproteins Research (38 papers), Blood groups and transfusion (27 papers) and Erythrocyte Function and Pathophysiology (22 papers). Yoshiro Koda is often cited by papers focused on Glycosylation and Glycoproteins Research (38 papers), Blood groups and transfusion (27 papers) and Erythrocyte Function and Pathophysiology (22 papers). Yoshiro Koda collaborates with scholars based in Japan, United States and Poland. Yoshiro Koda's co-authors include Mikiko Soejima, Hiroshi Kimurâ, Makoto Tsuneoka, Hao Pang, Kwesi Teye, Hidenori Tachida, Christopher H.S. McIntosh, Cuilan Nian, Sujin Kim and Baojie Wang and has published in prestigious journals such as Journal of Biological Chemistry, Blood and The Journal of Clinical Endocrinology & Metabolism.

In The Last Decade

Yoshiro Koda

144 papers receiving 3.0k citations

Peers

Yoshiro Koda
Mikiko Soejima Japan
Shih-Feng Tsai Taiwan
Fumio Kishi Japan
Jane-Jane Chen United States
Osamu Hashimoto Japan
Jeffrey Teckman United States
Johng S. Rhim United States
Nicola K. Gray United Kingdom
Julie Lekstrom-Himes United States
Jean‐Philippe Salier France
Mikiko Soejima Japan
Yoshiro Koda
Citations per year, relative to Yoshiro Koda Yoshiro Koda (= 1×) peers Mikiko Soejima

Countries citing papers authored by Yoshiro Koda

Since Specialization
Citations

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

Fields of papers citing papers by Yoshiro Koda

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Yoshiro Koda

This figure shows the co-authorship network connecting the top 25 collaborators of Yoshiro Koda. A scholar is included among the top collaborators of Yoshiro Koda 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 Yoshiro Koda. Yoshiro Koda 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.
Sugita, Yasuo, Takuya Furuta, Kenji Takahashi, et al.. (2025). Alzheimer's Disease With Cardiac Transthyretin Amyloidosis: A Clinicopathological Study of Autopsy Cases. Neuropathology. 45(4). e70011–e70011.
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Soejima, Mikiko & Yoshiro Koda. (2024). Identification and Diagnosis of Complete Haptoglobin Gene Deletion, One of the Genes Responsible for Adverse Posttransfusion Reactions. Biomedicines. 12(4). 790–790. 2 indexed citations
4.
Soejima, Mikiko & Yoshiro Koda. (2023). FUT1 variants responsible for Bombay or para-Bombay phenotypes in a database. Scientific Reports. 13(1). 17447–17447. 3 indexed citations
5.
Nakayama, Yosuke, Mikiko Soejima, Junko Yano, et al.. (2020). Effect of tolvaptan on renal involvement in patients with autosomal dominant polycystic kidney disease according to different gene mutations. Clinical and Experimental Nephrology. 25(3). 251–260. 1 indexed citations
6.
Soejima, Mikiko, Kwesi Teye, & Yoshiro Koda. (2018). The haptoglobin promoter polymorphism rs5471 is the most definitive genetic determinant of serum haptoglobin level in a Ghanaian population. Clinica Chimica Acta. 483. 303–307. 5 indexed citations
7.
Fujihara, Junko, Misuzu Ueki, Toshihiro Yasuda, et al.. (2011). Functional and Genetic Survey of All Known Single-Nucleotide Polymorphisms Within the Human Deoxyribonuclease I Gene in Wide-Ranging Ethnic Groups. DNA and Cell Biology. 30(4). 205–217. 6 indexed citations
8.
Koda, Yoshiro, et al.. (2011). EVALUATION OF TWO REAL-TIME PCR METHODS FOR DETECTION OF HPdel, A RISK MUTATION FOR ANAPHYLACTIC SHOCK, BEFORE TRANSFUSION. Japanese Journal of Transfusion and Cell Therapy. 57(1). 34–38.
9.
Nakayama, Kazuhiro, Yoshiko Yanagisawa, Ayumi Ogawa, et al.. (2011). High prevalence of an anti-hypertriglyceridemic variant of the MLXIPL gene in Central Asia. Journal of Human Genetics. 56(12). 828–833. 15 indexed citations
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Soejima, Mikiko, Hao Pang, & Yoshiro Koda. (2006). Genetic variation of FUT2 in a Ghanaian population: identification of four novel mutations and inference of balancing selection. Annals of Hematology. 86(3). 199–204. 25 indexed citations
12.
Tsuneoka, Makoto, Yoshitake Nishimune, Keisuke Ohta, et al.. (2005). Expression of Mina53, a product of a Myc target gene in mouse testis. International Journal of Andrology. 29(2). 323–330. 23 indexed citations
13.
Yamagishi, Sho‐ichi, et al.. (2002). Pigment epithelium-derived factor Met72Thr polymorphism in patients with diabetic microangiopathy.. PubMed. 22(3-4). 67–71. 11 indexed citations
14.
Nakayama, Kazuhiro, Shoji Fukamachi, Hiroshi Kimura, et al.. (2002). Distinctive distribution of AIM1 polymorphism among major human populations with different skin color. Journal of Human Genetics. 47(2). 92–94. 52 indexed citations
15.
Soejima, Mikiko, et al.. (1999). Functional analysis of the 5′‐flanking region of FTA for expression of rat GDP‐L‐fucose:β‐D‐galactoside 2‐α‐L‐fucosyltransferase. European Journal of Biochemistry. 266(1). 274–281. 7 indexed citations
16.
Koda, Yoshiro, et al.. (1998). [Anhaptoglobinemia and hypohaptoglobinemia].. PubMed. 676–8. 2 indexed citations
17.
Koda, Yoshiro, Mikiko Soejima, Naofumi Yoshioka, & Hiroshi Kimurâ. (1998). The Haptoglobin-Gene Deletion Responsible for Anhaptoglobinemia. The American Journal of Human Genetics. 62(2). 245–252. 56 indexed citations
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Koda, Yoshiro, Mikiko Soejima, & Hiroshi Kimurâ. (1997). Structure and Expression of H-type GDP-L-Fucose:β-D-Galactoside 2-α-L-Fucosyltransferase Gene (FUT1). Journal of Biological Chemistry. 272(11). 7501–7505. 35 indexed citations
20.
Kimurâ, Hiroshi, Yohko Ito, Yoshiro Koda, & Yutaka Hase. (1993). Rubinstein–Taybi syndrome with thymic hypoplasia. American Journal of Medical Genetics. 46(3). 293–296. 12 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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