Hirotake Sawada

604 total citations
19 papers, 336 citations indexed

About

Hirotake Sawada is a scholar working on Molecular Biology, Endocrinology, Diabetes and Metabolism and Physiology. According to data from OpenAlex, Hirotake Sawada has authored 19 papers receiving a total of 336 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Molecular Biology, 6 papers in Endocrinology, Diabetes and Metabolism and 5 papers in Physiology. Recurrent topics in Hirotake Sawada's work include Glycogen Storage Diseases and Myoclonus (3 papers), Magnesium in Health and Disease (3 papers) and Ion channel regulation and function (3 papers). Hirotake Sawada is often cited by papers focused on Glycogen Storage Diseases and Myoclonus (3 papers), Magnesium in Health and Disease (3 papers) and Ion channel regulation and function (3 papers). Hirotake Sawada collaborates with scholars based in Japan, United States and Canada. Hirotake Sawada's co-authors include Hiroyuki Nunoi, Yoshiro Suzuki, Makoto Tominaga, Fumio Endo, Sumito Dateki, Gen Nishimura, Takahito Inoue, Shinichi Hirose, Hiroshi Mizumoto and Go Tajima and has published in prestigious journals such as Endocrinology, The American Journal of Human Genetics and BMJ Open.

In The Last Decade

Hirotake Sawada

18 papers receiving 332 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Hirotake Sawada Japan 12 115 82 61 59 58 19 336
Bin-Xian Zhang United States 12 222 1.9× 42 0.5× 26 0.4× 105 1.8× 29 0.5× 16 413
Dahee Choi South Korea 9 321 2.8× 49 0.6× 40 0.7× 69 1.2× 26 0.4× 14 448
Liangjie Jia China 5 213 1.9× 60 0.7× 30 0.5× 107 1.8× 36 0.6× 8 436
Masahiro Takei Japan 10 186 1.6× 170 2.1× 9 0.1× 55 0.9× 124 2.1× 27 471
Mohanad Gabani United States 11 160 1.4× 49 0.6× 31 0.5× 83 1.4× 34 0.6× 15 372
Sebastián Susperreguy Argentina 10 138 1.2× 26 0.3× 44 0.7× 45 0.8× 103 1.8× 14 360
Fan Fan United States 9 221 1.9× 45 0.5× 19 0.3× 51 0.9× 10 0.2× 12 466
Dorothy Sears Worrall United States 8 299 2.6× 107 1.3× 13 0.2× 165 2.8× 44 0.8× 8 606
Anie Azroyan France 9 264 2.3× 22 0.3× 9 0.1× 33 0.6× 34 0.6× 10 404
Ganesh Pathare Germany 15 260 2.3× 34 0.4× 11 0.2× 48 0.8× 60 1.0× 22 430

Countries citing papers authored by Hirotake Sawada

Since Specialization
Citations

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

Fields of papers citing papers by Hirotake Sawada

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Hirotake Sawada

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

All Works

19 of 19 papers shown
1.
Hasegawa, Yukihiro, Shinji Higuchi, Mari Satoh, et al.. (2022). Knowns and unknowns about congenital hypothyroidism: 2022 update. Clinical Pediatric Endocrinology. 32(1). 11–25. 1 indexed citations
2.
3.
Imai, Hissei, T. Goto, Yoshifumi Kido, et al.. (2022). Psychosocial interventions for community-dwelling individuals with schizophrenia: study protocol for a systematic review and meta-analysis. BMJ Open. 12(4). e057286–e057286. 2 indexed citations
4.
Suzuki, Yoshiro, Hirotake Sawada, Shigeru Suzuki, et al.. (2020). Novel TRPV6 mutations in the spectrum of transient neonatal hyperparathyroidism. The Journal of Physiological Sciences. 70(1). 33–33. 21 indexed citations
5.
Kido, Jun, Shinichiro Yoshida, Keishin Sugawara, et al.. (2020). Newborn screening for Fabry disease in the western region of Japan. Molecular Genetics and Metabolism Reports. 22. 100562–100562. 46 indexed citations
6.
Higuchi, Shinji, Keisuke Nagasaki, Mari Satoh, et al.. (2019). Levothyroxine Dosage as Predictor of Permanent and Transient Congenital Hypothyroidism: A Multicenter Retrospective Study in Japan. Hormone Research in Paediatrics. 92(1). 45–51. 17 indexed citations
7.
Mizumoto, Hiroshi, et al.. (2019). TRPV6 Gene Mutation in a Dizygous Twin With Transient Neonatal Hyperparathyroidism. Journal of the Endocrine Society. 3(3). 602–606. 20 indexed citations
8.
Suzuki, Yoshiro, David Chitayat, Hirotake Sawada, et al.. (2018). TRPV6 Variants Interfere with Maternal-Fetal Calcium Transport through the Placenta and Cause Transient Neonatal Hyperparathyroidism. The American Journal of Human Genetics. 102(6). 1104–1114. 54 indexed citations
9.
Ishii, Tomohiro, Masanori Adachi, Kei Takasawa, et al.. (2018). Incidence and Characteristics of Adrenal Crisis in Children Younger than 7 Years with 21-Hydroxylase Deficiency: A Nationwide Survey in Japan. Hormone Research in Paediatrics. 89(3). 166–171. 14 indexed citations
10.
Watanabe, Satoshi, Akiko Nakatomi, Tatsuro Kondoh, et al.. (2018). A hot-spot mutation in CDC42 (p.Tyr64Cys) and novel phenotypes in the third patient with Takenouchi-Kosaki syndrome. Journal of Human Genetics. 63(3). 387–390. 32 indexed citations
11.
Nagasaki, Keisuke, Takuo Kubota, Hironori Kobayashi, et al.. (2017). Clinical characteristics of septo-optic dysplasia accompanied by congenital central hypothyroidism in Japan. Clinical Pediatric Endocrinology. 26(4). 207–213. 9 indexed citations
12.
Sawada, Hirotake, et al.. (2017). Osteogenesis imperfecta complicated with renal hypoplasia leads to chronic kidney disease. Pediatrics International. 59(3). 369–370. 1 indexed citations
13.
Hashimoto, Yukiko, Sumito Dateki, Masakazu Hirose, et al.. (2016). Molecular and clinical features of KATP-channel neonatal diabetes mellitus in Japan. Pediatric Diabetes. 18(7). 532–539. 25 indexed citations
14.
Katakami, Hideki, et al.. (2015). Development of a novel ultrasensitive enzyme immunoassay for human glutamic acid decarboxylase 65 antibody. Annals of Clinical Biochemistry International Journal of Laboratory Medicine. 53(4). 495–503. 3 indexed citations
15.
Matsumoto, Shirou, Hirotake Sawada, Masaki Honda, et al.. (2015). Living donor liver transplantation from a heterozygous parent for classical maple syrup urine disease. Pediatric Transplantation. 19(3). E66–9. 11 indexed citations
16.
Tada, Hayato, Masa‐aki Kawashiri, Atsushi Imamura, et al.. (2015). Infantile Cases of Sitosterolaemia with Novel Mutations in the ABCG5 Gene: Extreme Hypercholesterolaemia is Exacerbated by Breastfeeding. JIMD Reports. 21(313). 115–122. 39 indexed citations
17.
Tanaka, Etsuko, et al.. (2014). Nephrotic syndrome complicated by idiopathic central diabetes insipidus. Pediatric Nephrology. 29(5). 927–930. 1 indexed citations
18.
Sawada, Hirotake, Hideki Yamaguchi, Takuya Shimbara, et al.. (2006). Central Effects of Calcitonin Receptor-Stimulating Peptide-1 on Energy Homeostasis in Rats. Endocrinology. 147(4). 2043–2050. 26 indexed citations
19.
Sawada, Hirotake, et al.. (2005). A novel mutation of the PHKA2 gene in a patient with X‐linked liver glycogenosis type 1. Pediatrics International. 47(6). 687–690. 14 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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