Ikue Hata

1.1k total citations
39 papers, 811 citations indexed

About

Ikue Hata is a scholar working on Molecular Biology, Clinical Biochemistry and Physiology. According to data from OpenAlex, Ikue Hata has authored 39 papers receiving a total of 811 indexed citations (citations by other indexed papers that have themselves been cited), including 23 papers in Molecular Biology, 20 papers in Clinical Biochemistry and 14 papers in Physiology. Recurrent topics in Ikue Hata's work include Metabolism and Genetic Disorders (19 papers), Mitochondrial Function and Pathology (13 papers) and Nitric Oxide and Endothelin Effects (7 papers). Ikue Hata is often cited by papers focused on Metabolism and Genetic Disorders (19 papers), Mitochondrial Function and Pathology (13 papers) and Nitric Oxide and Endothelin Effects (7 papers). Ikue Hata collaborates with scholars based in Japan, Netherlands and Russia. Ikue Hata's co-authors include Yosuke Shigematsu, Seiji Yamaguchi, Masakatsu Sudo, Hirokazu Tsukahara, Yukië Tanaka, Nobuo Sakura, Go Tajima, Mitsufumi Mayumi, T. Tajima and Satoko Hirano and has published in prestigious journals such as Journal of Biological Chemistry, The American Journal of Human Genetics and American Journal of Physiology-Endocrinology and Metabolism.

In The Last Decade

Ikue Hata

39 papers receiving 775 citations

Peers

Ikue Hata

PHYSI

PPCH

RHEUM

P Parvy France

Claude Sansaricq United States

Jean-Marie Saudubray France

Arianna Maiorana Italy

John F. Nicholson United States

Mei Tran United States

Wulf Röschinger Germany

Wiesław Tarnowski Poland

Ali Hariri United States

Kensuke Asaba Japan

P Parvy France

Ikue Hata

565 ×1.2

404 ×1.0

188 ×0.9

PHYSI

194 ×1.2

PPCH

148 ×1.9

RHEUM

Citations per year, relative to Ikue Hata Ikue Hata (= 1×) peers P Parvy

Countries citing papers authored by Ikue Hata

Since Specialization

Citations

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

Fields of papers citing papers by Ikue Hata

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Ikue Hata

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

Kobayashi, Hironori, Go Tajima, Keiichi Hara, et al.. (2022). The frequencies of very long-chain acyl-CoA dehydrogenase deficiency genetic variants in Japan have changed since the implementation of expanded newborn screening. Molecular Genetics and Metabolism. 136(1). 74–79. 6 indexed citations

Hata, Ikue, Yusei Ohshima, Takashi Hamazaki, et al.. (2022). Severity estimation of very-long-chain acyl-CoA dehydrogenase deficiency via 13C-fatty acid loading test. Pediatric Research. 92(5). 1391–1399. 1 indexed citations

Hata, Ikue, et al.. (2019). Evaluation of Metabolic Defects in Fatty Acid Oxidation Using Peripheral Blood Mononuclear Cells Loaded with Deuterium-Labeled Fatty Acids. Disease Markers. 2019. 1–11. 6 indexed citations

Igarashi, Aiko, et al.. (2018). A case of an infant with extremely low birth weight and hypothyroidism associated with massive cutaneous infantile hemangioma. Journal of Pediatric Endocrinology and Metabolism. 31(12). 1377–1380. 4 indexed citations

Yamada, Kenji, Hironori Kobayashi, Jamiyan Purevsuren, et al.. (2017). Clinical and molecular investigation of 14 Japanese patients with complete TFP deficiency: a comparison with Caucasian cases. Journal of Human Genetics. 62(9). 809–814. 20 indexed citations

Hara, Keiichi, Go Tajima, Satoshi Okada, et al.. (2015). Significance of ACADM mutations identified through newborn screening of MCAD deficiency in Japan. Molecular Genetics and Metabolism. 118(1). 9–14. 14 indexed citations

Yasutomi, Motoko, et al.. (2014). Cytokine profiles in Mycoplasma pneumoniae infection-associated hemophagocytic lymphohistiocytosis. Journal of Microbiology Immunology and Infection. 49(5). 813–816. 13 indexed citations

Sakai, Hidemasa, Ryuta Nishikomori, Koichi Oshima, et al.. (2011). Novel mutations of MVK gene in Japanese family members affected with hyperimmunoglobulinemia D and periodic fever syndrome. Rheumatology International. 32(12). 3761–3764. 4 indexed citations

Okada, Satoshi, Go Tajima, Miyuki Tsumura, et al.. (2010). Molecular pathogenesis of a novel mutation, G108D, in short-chain acyl-CoA dehydrogenase identified in subjects with short-chain acyl-CoA dehydrogenase deficiency. Human Genetics. 127(6). 619–628. 21 indexed citations

10.

Tajima, Go, Nobuo Sakura, Satoshi Okada, et al.. (2008). Development of a New Enzymatic Diagnosis Method for Very-long-chain Acyl-CoA Dehydrogenase Deficiency by Detecting 2-Hexadecenoyl-CoA Production and its Application in Tandem Mass Spectrometry-based Selective Screening and Newborn Screening in Japan. Pediatric Research. 64(6). 667–672. 22 indexed citations

11.

Shigematsu, Yosuke, Ikue Hata, Yukië Tanaka, et al.. (2005). Stable-isotope dilution gas chromatography–mass spectrometric measurement of 3-hydroxyglutaric acid, glutaric acid and related metabolites in body fluids of patients with glutaric aciduria type 1 found in newborn screening. Journal of Chromatography B. 823(1). 7–12. 10 indexed citations

12.

Yoshino, Makoto, Yoriko Watanabe, Ichiro Yoshida, et al.. (2003). Effect of supplementation with l-carnitine at a small dose on acylcarnitine profiles in serum and urine and the renal handling of acylcarnitines in a patient with multiple acyl-coenzyme A dehydrogenation defect. Journal of Chromatography B. 792(1). 73–82. 3 indexed citations

13.

Miyazaki, Toru, Toshihiro Ohura, Makio Kobayashi, et al.. (2001). Fatal Propionic Acidemia in Mice Lacking Propionyl-CoA Carboxylase and Its Rescue by Postnatal, Liver-specific Supplementation via a Transgene. Journal of Biological Chemistry. 276(38). 35995–35999. 51 indexed citations

14.

Tsukahara, Hirokazu, Chikahide Hori, Ikue Hata, et al.. (1998). Assessment of endogenous nitric oxide formation in children: Measurement of urinary excretion of nitrite/nitrate.. Japanese journal of pediatric nephrology. 11(1). 79–83. 2 indexed citations

15.

Tsukahara, Hirokazu, Masahiro Hiraoka, Chikahide Hori, et al.. (1997). Urinary nitrite/nitrate excretion in infancy: comparison between term and preterm infants. Early Human Development. 47(1). 51–56. 23 indexed citations

16.

Tsukahara, Hirokazu, Kiyoshi Kikuchi, Masakazu Saito, et al.. (1997). Endogenous nitric oxide production in Kawasaki disease. Scandinavian Journal of Clinical and Laboratory Investigation. 57(1). 43–47. 19 indexed citations

17.

Tsukahara, Hirokazu, Kiyoshi Kikuchi, Kouki Kimura, et al.. (1997). Experimentally induced acute hyperinsulinemia stimulates endogenous nitric oxide production in humans: Detection using urinary excretion. Metabolism. 46(4). 406–409. 18 indexed citations

18.

Tsukahara, Hirokazu, Masahiro Hiraoka, Chikahide Hori, et al.. (1997). Chronic erythropoietin treatment enhances endogenous nitric oxide production in rats. Scandinavian Journal of Clinical and Laboratory Investigation. 57(6). 487–493. 24 indexed citations

19.

Kikawa, Yoshiharu, Manabu Inuzuka, Junichi Koga, et al.. (1997). Identification of Genetic Mutations in Japanese Patients with Fructose-1, 6-Bisphosphatase Deficiency. The American Journal of Human Genetics. 61(4). 852–861. 49 indexed citations

20.

Shigematsu, Yosuke, Ikue Hata, Akio Nakai, et al.. (1996). Prenatal Diagnosis of Organic Acidemias Based on Amniotic Fluid Levels of Acylcarnitines. Pediatric Research. 39(4). 680–684. 41 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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