Kotoko Kosuge

473 total citations
20 papers, 365 citations indexed

About

Kotoko Kosuge is a scholar working on Endocrinology, Diabetes and Metabolism, Cardiology and Cardiovascular Medicine and Molecular Biology. According to data from OpenAlex, Kotoko Kosuge has authored 20 papers receiving a total of 365 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Endocrinology, Diabetes and Metabolism, 8 papers in Cardiology and Cardiovascular Medicine and 7 papers in Molecular Biology. Recurrent topics in Kotoko Kosuge's work include Hormonal Regulation and Hypertension (7 papers), Heart Failure Treatment and Management (5 papers) and Renin-Angiotensin System Studies (5 papers). Kotoko Kosuge is often cited by papers focused on Hormonal Regulation and Hypertension (7 papers), Heart Failure Treatment and Management (5 papers) and Renin-Angiotensin System Studies (5 papers). Kotoko Kosuge collaborates with scholars based in Japan and United States. Kotoko Kosuge's co-authors include Masayoshi Soma, Noriko Aoi, Tomohiro Nakayama, Mikano Sato, Koichí Matsumoto, Shinichiro Kokubun, Katsuo Kanmatsuse, Dolkun Rahmutula, Yoichi Izumi and Junko Honye and has published in prestigious journals such as Biochemical and Biophysical Research Communications, American Heart Journal and Journal of Hypertension.

In The Last Decade

Kotoko Kosuge

19 papers receiving 353 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Kotoko Kosuge Japan	13	120	116	97	62	54	20	365
Ajeeth K. Pingili United States	13	97 0.8×	81 0.7×	107 1.1×	33 0.5×	39 0.7×	18	348
Anika Götz Germany	9	145 1.2×	137 1.2×	93 1.0×	76 1.2×	36 0.7×	9	395
Björn Wahlstrand Sweden	11	104 0.9×	122 1.1×	151 1.6×	65 1.0×	16 0.3×	13	404
Karin Simon Brazil	13	60 0.5×	53 0.5×	146 1.5×	34 0.5×	21 0.4×	27	455
Valeria Berruti Italy	9	93 0.8×	161 1.4×	71 0.7×	22 0.4×	34 0.6×	11	427
H.-U. Häring Germany	13	182 1.5×	51 0.4×	154 1.6×	56 0.9×	52 1.0×	29	493
A. Şükrü Aynacıoğlu Türkiye	12	38 0.3×	58 0.5×	112 1.2×	33 0.5×	36 0.7×	16	377
B Łacka Poland	10	146 1.2×	144 1.2×	99 1.0×	106 1.7×	29 0.5×	24	424
Jean-François Thibodeau Canada	11	67 0.6×	68 0.6×	189 1.9×	28 0.5×	36 0.7×	21	454
Hyun Wha Chung South Korea	9	214 1.8×	78 0.7×	227 2.3×	23 0.4×	53 1.0×	13	574

Countries citing papers authored by Kotoko Kosuge

Since Specialization

Citations

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

Fields of papers citing papers by Kotoko Kosuge

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Kotoko Kosuge

This figure shows the co-authorship network connecting the top 25 collaborators of Kotoko Kosuge. A scholar is included among the top collaborators of Kotoko Kosuge 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 Kotoko Kosuge. Kotoko Kosuge 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

Soma, Masayoshi, Tomohiro Nakayama, Kotoko Kosuge, et al.. (2012). Association between SIRT2 gene polymorphism and height in healthy, elderly Japanese subjects. Translational research. 161(1). 57–58. 7 indexed citations

Aoi, Noriko, Tomohiro Nakayama, Masayoshi Soma, et al.. (2012). The insulin-like growth factor-1 gene is associated with cerebral infarction in Japanese subjects. Hereditas. 149(5). 153–162. 2 indexed citations

Hayashi, Kentaro, et al.. (2011). Disseminated Gonococcal Infection in Japan: A Case Report and Literature Review. Internal Medicine. 50(18). 2039–2043. 29 indexed citations

Aoi, Noriko, Tomohiro Nakayama, Masayoshi Soma, et al.. (2010). Association of the insulin-like growth factor1 gene with myocardial infarction in Japanese subjects. Hereditas. 147(5). 215–224. 11 indexed citations

Ueno, Takahiro, Yasuharu Tabara, Noboru Fukuda, et al.. (2009). Association of SLC6A9 Gene Variants with Human Essential Hypertension. Journal of Atherosclerosis and Thrombosis. 16(3). 201–206. 6 indexed citations

Kosuge, Kotoko, Masayoshi Soma, Tomohiro Nakayama, et al.. (2008). Human uncoupling protein 2 and 3 genes are associated with obesity in Japanese. Endocrine. 34(1-3). 87–95. 20 indexed citations

Aoi, Noriko, Tomohiro Nakayama, Naoyuki Sato, et al.. (2008). Case-control Study of the Role of the Gitelman's Syndrome Gene in Essential Hypertension. Endocrine Journal. 55(2). 305–310. 11 indexed citations

Kosuge, Kotoko, Masayoshi Soma, Noriko Aoi, et al.. (2007). A Novel Variable Number of Tandem Repeat of the Natriuretic Peptide Precursor B gene's 5'-Flanking Region is Associated with Essential Hypertension among Japanese Females. International Journal of Medical Sciences. 4(3). 146–152. 12 indexed citations

Sato, Mikano, Tomohiro Nakayama, Masayoshi Soma, et al.. (2007). Association between prostaglandin E2 receptor gene and essential hypertension. Prostaglandins Leukotrienes and Essential Fatty Acids. 77(1). 15–20. 25 indexed citations

10.

Sato, Mikano, Masayoshi Soma, Tomohiro Nakayama, et al.. (2006). A Case of Adrenocorticotropin-independent Bilateral Adrenal Macronodular Hyperplasia (AIMAH) with Primary Hyperparathyroidism (PHPT). Endocrine Journal. 53(1). 111–117. 17 indexed citations

11.

Soma, Masayoshi, Tomohiro Nakayama, Mikano Sato, et al.. (2004). Two medium-chain acyl-coenzyme A synthetase genes, SAH and MACS1, are associated with plasma high-density lipoprotein cholesterol levels, but they are not associated with essential hypertension. Journal of Hypertension. 22(10). 1903–1907. 26 indexed citations

12.

Aoi, Noriko, Masayoshi Soma, Tomohiro Nakayama, et al.. (2004). Variable Number of Tandem Repeat of the 5'-Flanking Region of Type-C Human Natriuretic Peptide Receptor Gene Influences Blood Pressure Levels in Obesity-Associated Hypertension. Hypertension Research. 27(10). 711–716. 29 indexed citations

13.

Nakayama, Tomohiro, Masayoshi Soma, Noriko Aoi, et al.. (2003). Haplotype Analysis of the Prostacyclin Synthase Gene and Essential Hypertension. Hypertension Research. 26(7). 553–557. 14 indexed citations

14.

Nakayama, Tomohiro, Masayoshi Soma, Satoshi Saito, et al.. (2003). Missense mutation of exon 3 in the type A human natriuretic peptide receptor gene is associated with myocardial infarction.. PubMed. 9(12). CR505–10. 17 indexed citations

15.

Nakayama, Tomohiro, Masayoshi Soma, Dolkun Rahmutula, et al.. (2002). Association Study between a Novel Single Nucleotide Polymorphism of the Promoter Region of the Prostacyclin Synthase Gene and Essential Hypertension. Hypertension Research. 25(1). 65–68. 14 indexed citations

16.

Rahmutula, Dolkun, Tomohiro Nakayama, Masayoshi Soma, et al.. (2002). Structure and Polymorphisms of the Human Natriuretic Peptide Receptor C Gene. Endocrine. 17(2). 85–90. 14 indexed citations

17.

Soma, Masayoshi, Yoshihiro Mizutani, Xinjuan Xu, et al.. (2002). A Novel Missense Mutation of Exon 3 in the Type A Human Natriuretic Peptide Receptor Gene: Possible Association with Essential Hypertension.. Hypertension Research. 25(3). 395–401. 30 indexed citations

18.

Nakayama, Tomohiro, Masayoshi Soma, Buaijiaer Hasimu, et al.. (2002). Splicing mutation of the prostacyclin synthase gene in a family associated with hypertension. Biochemical and Biophysical Research Communications. 297(5). 1135–1139. 31 indexed citations

19.

Soma, Masayoshi, Satoshi Saito, Junko Honye, et al.. (2002). Association of a novel single nucleotide polymorphism of the prostacyclin synthase gene with myocardial infarction. American Heart Journal. 143(5). 797–801. 39 indexed citations

20.

Nakayama, Tomohiro, Michiyoshi Minato, Masayoshi Soma, et al.. (2001). A Novel Mutation in Ca<sup>2+</sup> -Sensing Receptor Gene in Familial Hypocalciuric Hypercalcemia. Endocrine. 15(3). 277–282. 11 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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