Eishin Ogawa

1.5k total citations
39 papers, 1.1k citations indexed

About

Eishin Ogawa is a scholar working on Molecular Biology, Endocrinology, Diabetes and Metabolism and Genetics. According to data from OpenAlex, Eishin Ogawa has authored 39 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 25 papers in Molecular Biology, 11 papers in Endocrinology, Diabetes and Metabolism and 9 papers in Genetics. Recurrent topics in Eishin Ogawa's work include Sexual Differentiation and Disorders (10 papers), Metabolism and Genetic Disorders (5 papers) and Growth Hormone and Insulin-like Growth Factors (5 papers). Eishin Ogawa is often cited by papers focused on Sexual Differentiation and Disorders (10 papers), Metabolism and Genetic Disorders (5 papers) and Growth Hormone and Insulin-like Growth Factors (5 papers). Eishin Ogawa collaborates with scholars based in Japan, New Zealand and Australia. Eishin Ogawa's co-authors include Hiroko Kodama, Toshihiro Ohura, Takahiro Matsuki, T. Hara, Ikuma Fujiwara, Hiroshi Mori, Kazuya Yamamoto, Takuji Yamada, Satoshi Matsumoto and Ken Kurokawa and has published in prestigious journals such as Nature Communications, The Journal of Clinical Endocrinology & Metabolism and Endocrinology.

In The Last Decade

Eishin Ogawa

38 papers receiving 1.0k citations

Peers

Countries citing papers authored by Eishin Ogawa

Since Specialization

Citations

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

Fields of papers citing papers by Eishin Ogawa

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Eishin Ogawa

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

#	Work	Indexed citations
1	Longitudinal Glycaemic Profiles during Remission in 6q24-Related Transient Neonatal Diabetes Mellitus 2021 ·Hormone Research in Paediatrics ·(unknown), Tsuyoshi Isojima, (unknown), (unknown), (unknown), Eishin Ogawa, Hiroko Kodama, Tohru Yorifuji, Masakazu Mimaki	1
2	Unbalanced Y;7 Translocation between Two Low-Similarity Sequences Leading to SRY-Positive 45,X Testicular Disorders of Sex Development 2019 ·Cytogenetic and Genome Research ·(unknown), Atsushi Hattori, Hirohito Shima, Akira Ishiguro, Yu Abe, Tsutomu Ogata, Eishin Ogawa, Maki Fukami	2
3	Effects of Zinc Acetate on Serum Zinc Concentrations in Chronic Liver Diseases: a Multicenter, Double-Blind, Randomized, Placebo-Controlled Trial and a Dose Adjustment Trial 2019 ·Biological Trace Element Research ·Kazuhiro Katayama, Atsushi Hosui, Yoshiyuki Sakai, Minoru Itou, Yasushi Matsuzaki, Yoriyuki Takamori, Keiko Hosho, Tomomi Tsuru, Yasuhiro Takikawa, Kojiro Michitaka, Eishin Ogawa, Yoko Miyoshi, Toshifumi Ito, Shinobu Ida, (unknown), (unknown), Hiroko Kodama, Tetsuo Takehara	19
4	A key genetic factor for fucosyllactose utilization affects infant gut microbiota development 2016 ·Nature Communications ·Takahiro Matsuki, (unknown), Hiroshi Mori, Hoshitaka Matsumoto, T. Hara, (unknown), Eishin Ogawa, Hiroko Kodama, Kazuya Yamamoto, Takuji Yamada, Satoshi Matsumoto, Ken Kurokawa	271
5	Lactate and Pyruvate Levels in Blood and Cerebrospinal Fluid in Patients with Menkes Disease 2014 ·The Journal of Pediatrics ·Yan‐Hong Gu, Hiroko Kodama, Eishin Ogawa, (unknown)	7
6	Changes in body weight and height in survivors of Menkes disease 2014 ·Journal of Trace Elements in Medicine and Biology ·Yan‐Hong Gu, Hiroko Kodama, Eishin Ogawa, (unknown), (unknown), Mariko Yagi, Sayaka Yoshida, Takayoshi Ohkubo	2
7	Interaction of PICK1 with C-Terminus of Growth Hormone–Releasing Hormone Receptor (GHRHR) Modulates Trafficking and Signal Transduction of Human GHRHR 2013 ·Journal of Pharmacological Sciences ·Yuriko Katsushima, Takeya Sato, (unknown), (unknown), Yuki Suzuki, Eishin Ogawa, (unknown), Jun Sukegawa, Kohji Fukunaga, Teruyuki Yanagisawa	4
8	Combined linkage analysis and exome sequencing identifies novel genes for familial goiter 2013 ·Journal of Human Genetics ·Junxia Yan, Tsutomu Takahashi, Toshihiro Ohura, (unknown), Ikuko Takahashi, Eishin Ogawa, Hiroko Okuda, Hatasu Kobayashi, Toshiaki Hitomi, Wanyang Liu, Kouji H. Harada, Akio Koizumi	18
9	Effect of copper and disulfiram combination therapy on the macular mouse, a model of Menkes disease 2012 ·Journal of Trace Elements in Medicine and Biology ·(unknown), Hiroko Kodama, Chie Fujisawa, (unknown), Eishin Ogawa	16
10	Influences of p53 deficiency on the apoptotic response, DNA damage removal and mutagenesis in UVB-exposed mouse skin 2010 ·Mutagenesis ·Hironobu Ikehata, Ryuhei Okuyama, Eishin Ogawa, Shingo Nakamura, (unknown), Toshio Mori, Koji Tanaka, Setsuya Aiba, Tetsuo Ono	20
11	Novel CYP17A1 mutation in a Japanese patient with combined 17α-hydroxylase/17,20-lyase deficiency 2009 ·Metabolism ·Noriyuki Katsumata, Eishin Ogawa, Ikuma Fujiwara, (unknown)	18
12	Subacute Thyroiditis in Children: Patient Report and Review of the Literature 2003 ·Journal of Pediatric Endocrinology and Metabolism ·Eishin Ogawa, Yuriko Katsushima, Ikuma Fujiwara, Koji Iinuma	21
13	Hypophosphatemia in juvenile patients with systemic lupus erythematosus 2003 ·Pediatrics International ·Ikuma Fujiwara, Eishin Ogawa, Yoshiaki Kondo, Toshihiro Ohura, Kazuie Iinuma	8
14	Compound Heterozygous Mutations in the Cholesterol Side-Chain Cleavage Enzyme Gene (CYP11A) Cause Congenital Adrenal Insufficiency in Humans 2002 ·The Journal of Clinical Endocrinology & Metabolism ·Noriyuki Katsumata, Masatoshi Ohtake, (unknown), Eishin Ogawa, Takayuki Hara, Naoko Sato, Toshiaki Tanaka	77
15	Three Families with Autosomal Dominant Nephrogenic Diabetes Insipidus Caused by Aquaporin-2 Mutations in the C-Terminus 2001 ·The American Journal of Human Genetics ·Michio Kuwahara, Kazuyuki Iwai, (unknown), Takashi Igarashi, Eishin Ogawa, Yuriko Katsushima, (unknown), Shinichi Uchida, Yoshio Terada, Marie‐Françoise Arthus, Michèle Lonergan, Takuya Fujiwara, Daniel G. Bichet, Fumiaki Marumo, Sei Sasaki	109
16	A novel intronic mutation of the TAZ ( G4.5 ) gene in a patient with Barth syndrome: creation of a 5' splice donor site with variant GC consensus and elongation of the upstream exon 2001 ·Human Genetics ·Osamu Sakamoto, Toshihiro Ohura, Yuriko Katsushima, Ikuma Fujiwara, Eishin Ogawa, Shigeaki Miyabayashi, Kazuie Iinuma	19
17	Mutation Analysis of the GLUT2 Gene in Patients with Fanconi-Bickel Syndrome 2000 ·Pediatric Research ·Osamu Sakamoto, Eishin Ogawa, Toshihiro Ohura, Yutaka Igarashi, Yoichi Matsubara, Kuniaki Narisawa, (unknown)	49
18	Molecular analysis of Japanese patients with steroid 21-hydroxylase deficiency 1999 ·Journal of Human Genetics ·(unknown), T. Ohura, Eishin Ogawa, Sachiko Sato, Yutaka Igarashi, Yoichi Matsubara, Kazuie Iinuma	40
19	Ovine placental lactogen lacks direct somatogenic and anticatabolic actions in the postnatal lamb 1995 ·Journal of Endocrinology ·Eishin Ogawa, Bernhard H. Breier, (unknown), P. D. Gluckman	11
20	Effects of Individual Mutations in the P-450(C21) Pseudogene on the P-450(C21) Activity and Their Distribution in the Patient Genomes of Congenital Steroid 21-Hydroxylase Deficiency1 1991 ·The Journal of Biochemistry ·Yujiro Higashi, (unknown), Ayako Tanae, (unknown), Jun Nakura, Takuma Kondo, Toshihiro Ohura, Eishin Ogawa, Kazuo Nakayama, Yoshiaki Fujii‐Kuriyama	161

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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