Hiroyo Mabe

828 total citations
18 papers, 402 citations indexed

About

Hiroyo Mabe is a scholar working on Endocrinology, Diabetes and Metabolism, Molecular Biology and Surgery. According to data from OpenAlex, Hiroyo Mabe has authored 18 papers receiving a total of 402 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Endocrinology, Diabetes and Metabolism, 4 papers in Molecular Biology and 3 papers in Surgery. Recurrent topics in Hiroyo Mabe's work include Genetics and Neurodevelopmental Disorders (3 papers), Obsessive-Compulsive Spectrum Disorders (2 papers) and Cancer, Hypoxia, and Metabolism (2 papers). Hiroyo Mabe is often cited by papers focused on Genetics and Neurodevelopmental Disorders (3 papers), Obsessive-Compulsive Spectrum Disorders (2 papers) and Cancer, Hypoxia, and Metabolism (2 papers). Hiroyo Mabe collaborates with scholars based in Japan, Belgium and United States. Hiroyo Mabe's co-authors include Noritaka Iwatani, Teruhisa Miike, K Devriendt, Akemi Tomoda, Jun Takeda, Eiji Yamada, Takashi X. Fujisawa, Masato Masuda, Fuki Ikeda and Noriyuki Takubo and has published in prestigious journals such as PLoS ONE, The Journal of Clinical Endocrinology & Metabolism and Diabetes.

In The Last Decade

Hiroyo Mabe

16 papers receiving 385 citations

Peers

Hiroyo Mabe

GENET

SURGE

EDM

Andrea B. Schote Germany

Noritaka Iwatani Japan

Ulf Hannelius Sweden

Erik Wibowo New Zealand

Agnieszka Olszewska Germany

J Perry United Kingdom

Andrey Finegersh United States

Mary Cataletto United States

Cecilia E. Kim United States

Yoshifumi Mizuno Japan

Andrea B. Schote Germany

Hiroyo Mabe

118 ×0.7

78 ×0.6

GENET

39 ×0.3

SURGE

64 ×0.6

EDM

21 ×0.3

Citations per year, relative to Hiroyo Mabe Hiroyo Mabe (= 1×) peers Andrea B. Schote

Countries citing papers authored by Hiroyo Mabe

Since Specialization

Citations

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

Fields of papers citing papers by Hiroyo Mabe

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Hiroyo Mabe

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

All Works

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18 of 18 papers shown

Kimura, Noriko, Koji Muroya, Masato Yonamine, et al.. (2025). Clinicopathological and genomic analysis of pediatric pheochromocytoma and sympathetic paraganglioma. Endocrine Journal. 72(4). 399–412. 2 indexed citations

Shinojima, Naoki, Shigetoshi Yano, Hiroyo Mabe, et al.. (2024). Long-term outcomes of multidisciplinary treatment combining surgery and stereotactic radiotherapy with Novalis for craniopharyngioma. Journal of Clinical Neuroscience. 120. 138–146. 1 indexed citations

Shinojima, Naoki, Yutaka Ueda, Hiroyo Mabe, et al.. (2023). Two children with lymphocytic hypophysitis presenting with positive anti-rabphilin-3A antibody. Endocrine Journal. 70(7). 703–709. 2 indexed citations

Ohba, Takashi, Fumitaka Saito, Munekage Yamaguchi, et al.. (2023). Advantages and limitations of estrogen replacement therapy on hypogonadal survivors of childhood cancer. International Journal of Clinical Oncology. 28(11). 1563–1572.

Horikawa, Yukio, Mayumi Enya, Hiroyo Mabe, et al.. (2017). NEUROD1‐deficient diabetes ( MODY6 ): Identification of the first cases in Japanese and the clinical features. Pediatric Diabetes. 19(2). 236–242. 38 indexed citations

Hotta, Mari, Reiko Horikawa, Hiroyo Mabe, et al.. (2015). Epidemiology of anorexia nervosa in Japanese adolescents. BioPsychoSocial Medicine. 9(1). 17–17. 23 indexed citations

Fujisawa, Takashi X., et al.. (2015). Anorexia Nervosa during Adolescence Is Associated with Decreased Gray Matter Volume in the Inferior Frontal Gyrus. PLoS ONE. 10(6). e0128548–e0128548. 31 indexed citations

Santen, Gijs W.E., Yu Sun, Antoinet C.J. Gijsbers, et al.. (2012). Further delineation of the phenotype of chromosome 14q13 deletions: (positional) involvement of FOXG1 appears the main determinant of phenotype severity, with no evidence for a holoprosencephaly locus. Journal of Medical Genetics. 49(6). 366–372. 17 indexed citations

Nozu, Kandai, Kazumoto Iijima, Kyoko Kanda, et al.. (2010). The Pharmacological Characteristics of Molecular-Based Inherited Salt-Losing Tubulopathies. The Journal of Clinical Endocrinology & Metabolism. 95(12). E511–E518. 44 indexed citations

10.

Tomoda, Akemi, et al.. (2010). Pseudohypacusis in childhood and adolescence is associated with increased gray matter volume in the medial frontal gyrus and superior temporal gyrus. Cortex. 48(4). 492–503. 12 indexed citations

11.

Miike, Teruhisa, et al.. (2003). Learning and memorization impairment in childhood chronic fatigue syndrome manifesting as school phobia in Japan. Brain and Development. 26(7). 442–447. 39 indexed citations

12.

Terasaki, Tadashi, Yoichiro Hashimoto, Fumio Miyashita, et al.. (2002). [A case of Turner syndrome complicated with brain infarction].. PubMed. 42(2). 145–8. 1 indexed citations

13.

Iwatani, Noritaka, et al.. (2000). Deletion of NKX2.1 gene encoding thyroid transcription factor-1 in two siblings with hypothyroidism and respiratory failure. The Journal of Pediatrics. 137(2). 272–276. 122 indexed citations

14.

Ohyama, Kenji, Noritaka Iwatani, Yoshiko Nakagomi, et al.. (1999). Growth Hormone Advances Spermatogenesis in Premature Rats Treated with Gonadotropin-Releasing Hormone Agonist.. Endocrine Journal. 46(4). 555–562. 7 indexed citations

15.

Yamada, Shirou, Hideaki Tomura, Hidekazu Nishigori, et al.. (1999). Identification of mutations in the hepatocyte nuclear factor-1alpha gene in Japanese subjects with early-onset NIDDM and functional analysis of the mutant proteins.. Diabetes. 48(3). 645–648. 49 indexed citations

16.

Tomoda, Akemi, Teruhisa Miike, Noritaka Iwatani, et al.. (1999). Effect of long-term melatonin administration on school-phobic children and adolescents with sleep disturbances. Current Therapeutic Research. 60(11). 607–612. 6 indexed citations

17.

Iwatani, Noritaka, et al.. (1997). Glucoregulatory disorders in school refusal students. Clinical Endocrinology. 47(3). 273–278. 8 indexed citations

18.

Iwatani, Noritaka, Hiroyo Mabe, Teruhisa Miike, et al.. (1997). A Mutation in the GH-receptor Gene of a Japanese Patient with Laron Syndrome. Folia Endocrinologica Japonica. 73(6). 643–649.

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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