Hatsue Tsuneyama

494 total citations
40 papers, 331 citations indexed

About

Hatsue Tsuneyama is a scholar working on Hematology, Physiology and Genetics. According to data from OpenAlex, Hatsue Tsuneyama has authored 40 papers receiving a total of 331 indexed citations (citations by other indexed papers that have themselves been cited), including 39 papers in Hematology, 29 papers in Physiology and 9 papers in Genetics. Recurrent topics in Hatsue Tsuneyama's work include Blood groups and transfusion (39 papers), Erythrocyte Function and Pathophysiology (29 papers) and Hemoglobinopathies and Related Disorders (8 papers). Hatsue Tsuneyama is often cited by papers focused on Blood groups and transfusion (39 papers), Erythrocyte Function and Pathophysiology (29 papers) and Hemoglobinopathies and Related Disorders (8 papers). Hatsue Tsuneyama collaborates with scholars based in Japan, Sweden and United Kingdom. Hatsue Tsuneyama's co-authors include Makoto Uchikawa, Kenichi Ogasawara, Kazumi Isa, Kenji Tadokoro, Masahiro Satake, Kana Sasaki, Takeo Juji, Yoshihiko Kominato, Rie Sano and Yōichirō Takahashi and has published in prestigious journals such as Blood, Transfusion and Vox Sanguinis.

In The Last Decade

Hatsue Tsuneyama

37 papers receiving 325 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Hatsue Tsuneyama Japan	12	284	210	104	76	45	40	331
Núria Nogués Spain	13	240 0.8×	142 0.7×	72 0.7×	104 1.4×	58 1.3×	32	390
Kathryn R. Girard‐Pierce United States	9	302 1.1×	240 1.1×	94 0.9×	68 0.9×	43 1.0×	11	377
Susanne Kilga‐Nogler Austria	7	278 1.0×	213 1.0×	64 0.6×	104 1.4×	24 0.5×	10	329
D Tripodi United States	6	161 0.6×	69 0.3×	43 0.4×	51 0.7×	37 0.8×	22	268
Andrea Doescher Germany	8	281 1.0×	208 1.0×	77 0.7×	101 1.3×	15 0.3×	19	308
Jonathan S. Smythe United Kingdom	9	231 0.8×	288 1.4×	100 1.0×	45 0.6×	59 1.3×	10	371
Sandra J. Nance United States	10	448 1.6×	323 1.5×	108 1.0×	148 1.9×	17 0.4×	25	502
J.H. Maas Germany	8	352 1.2×	243 1.2×	103 1.0×	104 1.4×	18 0.4×	12	398
P. Morel United States	9	372 1.3×	293 1.4×	222 2.1×	55 0.7×	56 1.2×	13	446
Geetha Puthenveetil United States	8	105 0.4×	46 0.2×	134 1.3×	149 2.0×	165 3.7×	16	352

Countries citing papers authored by Hatsue Tsuneyama

Since Specialization

Citations

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

Fields of papers citing papers by Hatsue Tsuneyama

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Hatsue Tsuneyama

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

All Works

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20 of 20 papers shown

Isa, Kazumi, Hiromi Takeda, Hatsue Tsuneyama, et al.. (2023). Two new JK silencing alleles identified by single molecule sequencing with 20‐Kb long‐reads. Transfusion. 63(8). 1441–1446. 2 indexed citations

Watanabe‐Okochi, Naoko, Makoto Uchikawa, Hatsue Tsuneyama, et al.. (2022). Genetic background of anti‐Xg^a producers in Japanese blood donors. Vox Sanguinis. 117(10). 1235–1239. 2 indexed citations

Hayakawa, Akira, Rie Sano, Yōichirō Takahashi, et al.. (2021). Reduction of blood group A antigen on erythrocytes in a patient with myelodysplastic syndrome harboring somatic mutations in RUNX1 and GATA2. Transfusion. 62(2). 469–480. 2 indexed citations

Watanabe‐Okochi, Naoko, Hatsue Tsuneyama, Kazumi Isa, et al.. (2020). Novel hybrid genes and a splice site mutation encoding the St^a antigen among Japanese blood donors. Vox Sanguinis. 115(8). 756–766.

Tsuneyama, Hatsue, Kazumi Isa, Naoko Watanabe‐Okochi, et al.. (2020). An unusual variant glycophorin expressing protease‐resistant M antigen encoded by the GYPB‐E(2‐4)‐B hybrid gene. Vox Sanguinis. 115(7). 579–585. 3 indexed citations

Hayakawa, Akira, Rie Sano, Yōichirō Takahashi, et al.. (2019). RUNX1 mutation in a patient with myelodysplastic syndrome and decreased erythrocyte expression of blood group A antigen. Transfusion. 60(1). 184–196. 12 indexed citations

Omae, Yosuke, Mayumi Takeuchi, Kazumi Isa, et al.. (2019). Integrative genome analysis identified the KANNO blood group antigen as prion protein. Transfusion. 59(7). 2429–2435. 11 indexed citations

Katsuragi, Shinji, Hitoshi Ohto, Atsushi Yoshida, et al.. (2019). Anemic Disease of the Newborn With Little Increase in Hemolysis and Erythropoiesis Due to Maternal Anti-Jra: A Case Study and Review of the Literature. Transfusion Medicine Reviews. 33(3). 183–188. 7 indexed citations

Kurita, Ryo, Kenichi Ogasawara, Kazumi Isa, et al.. (2018). Application of immortalized human erythroid progenitor cell line in serologic tests to detect red blood cell alloantibodies. Transfusion. 58(11). 2675–2682. 4 indexed citations

10.

Tanaka, Mitsunobu, Junko Takahashi, Kenichi Ogasawara, et al.. (2014). Novel alleles of Lan− in Japanese populations. Transfusion. 54(5). 1438–1439. 3 indexed citations

11.

Takahashi, Yōichirō, Kazumi Isa, Rie Sano, et al.. (2014). Presence of nucleotide substitutions in transcriptional regulatory elements such as the erythroid cell‐specific enhancer‐like element and theABOpromoter in individuals with phenotypes A₃and B₃, respectively. Vox Sanguinis. 107(2). 171–180. 26 indexed citations

12.

Takahashi, Yōichirō, Kazumi Isa, Rie Sano, et al.. (2013). Deletion of the RUNX1 binding site in the erythroid cell‐specific regulatory element of the ABO gene in two individuals with the A_m phenotype. Vox Sanguinis. 106(2). 167–175. 32 indexed citations

13.

Yasuda, Hiroyasu, et al.. (2011). SEROLOGIC REACTIVITY AND CLINICAL SIGNIFICANCE OF THE HIGH FREQUENCY ANTIGEN KANNO AND ITS ANTIBODY. Japanese Journal of Transfusion and Cell Therapy. 57(6). 478–483. 1 indexed citations

14.

Tilley, Louise, Joyce Poole, K. Ridgwell, et al.. (2009). A new blood group system, RHAG: three antigens resulting from amino acid substitutions in the Rh-associated glycoprotein. Vox Sanguinis. 98(2). 151–159. 30 indexed citations

15.

Tsuneyama, Hatsue. (2005). [Diego blood system and the antibodies].. PubMed. 63 Suppl 7. 692–4. 1 indexed citations

16.

Kashiwase, Kouichi, Yoshihide Ishikawa, Hironobu Hyodo, et al.. (2001). E variants found in Japanese and c antigenicity alteration without substitution in the second extracellular loop. Transfusion. 41(11). 1408–1412. 14 indexed citations

17.

Hyodo, Hironobu, Yoshihide Ishikawa, Koichi Kashiwase, et al.. (2000). Polymorphisms of RhD^Va and a New RhD^Va–Like Variant Found in Japanese Individuals. Vox Sanguinis. 78(2). 122–125. 15 indexed citations

18.

Hyodo, Hironobu, Yoshihide Ishikawa, Koichi Kashiwase, et al.. (2000). Polymorphisms of RhD<sup>Va</sup> and a New RhD<sup>Va</sup>–Like Variant Found in Japanese Individuals. Vox Sanguinis. 78(2). 122–125. 2 indexed citations

19.

Yasuda, Hiroyasu, Hitoshi Ohto, Osamu Yamaguchi, et al.. (2000). Three episodes of delayed hemolytic transfusion reactions due to multiple red cell antibodies, anti-Dia, anti-Jkb and anti-E. Transfusion Science. 23(2). 107–112. 5 indexed citations

20.

Suzuki, Hirotsugu, et al.. (1994). First Case of Hemolytic Disease of the Newborn due to Anti‐Ul^a Antibodies. Vox Sanguinis. 66(4). 293–294. 3 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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