Nobuo Sakura

2.7k citations

102 papers · 2.1k indexed · h-index 25

Impact in

Clinical Biochemistry top 0.2%
- Metabolism and Genetic Disorders
Rheumatology top 2%
- Folate and B Vitamins Research

Papers in

Clinical Biochemistry 39
- Metabolism and Genetic Disorders 39
Behavioral Neuroscience 5

Co-authors: Kazuhiro Ueda Hiroaki Ono Akiko Sakamoto Seiji Yamaguchi Yutaka Nishimura Yosuke Shigematsu Go Tajima Shinji Nomura
Journals: Journal of Inherited Metabolic Disease (14 papers)Clinica Chimica Acta (13 papers)Journal of Chromatography B (6 papers)European Journal of Pediatrics (6 papers)Human Genetics (5 papers)
Partner nations: Japan United States Austria

In The Last Decade

Nobuo Sakura

97 papers receiving 2.0k citations

Peers

Countries citing papers authored by Nobuo Sakura

Since Specialization

Citations

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

Fields of papers citing papers by Nobuo Sakura

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network

The 25 scholars most cited alongside Nobuo Sakura, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Nobuo Sakura Line = papers co-authored together Nobuo Sakura links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	Analysis of plasma ghrelin in patients with medium-chain acyl-CoA dehydrogenase deficiency and glutaric aciduria type II European Journal of Endocrinology ·Takashi Akamizu, Nobuo Sakura, Yosuke Shigematsu, Go Tajima, Akira Ohtake, Hiroshi Hosoda, Hiroshi Iwakura, Hiroyuki Ariyasu, Kenji Kangawa	2011	13
2	Surgical intervention for patent ductus venosus Pediatric Surgery International ·Silvia Melani Putri, Atefeh Parchebafi, Claire Catalini, Go Tajima, Nobuo Sakura, Taijiro Sueda, Eiso Hiyama	2010	20
3	Altered metabolisms of mediators controlling vascular function and enhanced oxidative stress in asymptomatic children with congenital portosystemic venous shunt Metabolism ·Hironori Nagasaka, Yoshiyuki Okano, О В Обухова, Takashi Miida, Tohru Yorifuji, Go Tajima, Nobuo Sakura, Tomozumi Takatani, Héctor Flores‐León, S Jäck, Mitsufumi Mayumi, Kunihiko Kobayashi, Ken‐ichi Hirano, Masaki Takayanagi, Hirokazu Tsukahara	2009	6
4	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 ·Yosuke Shigematsu, Ikue Hata, Yukië Tanaka, Go Tajima, Nobuo Sakura, Etsuo Naito, S. M. Lewis	2005	10
5	Tetrahydrobiopterin-responsive phenylalanine hydroxylase deficiency Haruo Shintaku, Shigeo Kure, Toshihiro Ohura, Yoshiyuki Okano, Santhosh Kumar Behera, Naruji Sugiyama, Nobuo Sakura, Ichiro Yoshida, Makoto Yoshino, Tani Shtull-Leber, Ken Suzuki, Kikumaro Aoki, Teruo Kitagawa	2005	185
6	Inactivation of acrolein by sodium 2-mercaptoethanesulfonate using headspace-solid-phase microextraction gas chromatography and mass spectrometry Journal of Chromatography B ·Liu Han-zhong, Nobuo Sakura, Mikio Yashiki, Tohru Kojima	2003	9
7	Pharmacokinetics of etoposide with intravenous drug administration in children and adolescents Pediatrics International ·Yasuhiro Kato, Shin‐Ichiro Nishimura, Nobuo Sakura, Kazuhiro Ueda	2003	18
8	Novel nonsense mutation (R194X) in the PMM2 gene in a Japanese patient with congenital disorder of glycosylation type Ia Brain and Development ·Hiroaki Ono, Nobuo Sakura, Katsuko Yamashita, Isao Yuasa, Kousaku Ohno	2003	6
9	The peak height ratio of S-sulfonated transthyretin and other oxidized isoforms as a marker for molybdenum cofactor deficiency, measured by electrospray ionization mass spectrometry Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease ·Kathi Elliott, Jörn Oliver Sass, Nobuo Sakura, Toyofumi Nakanishi, Akira Shimizu, Masanori Yoshioka	2002	26
10	The C677T mutation in the methylenetetrahydrofolate reductase gene contributes to hyperhomocysteinemia in patients taking anticonvulsants Brain and Development ·Hiroaki Ono, Akiko Sakamoto, منوچهر امینی, Nobuo Sakura	2002	42
11	Betaine and homocysteine concentrations in foods Pediatrics International ·Akiko Sakamoto, Yutaka Nishimura, Hiroaki Ono, Nobuo Sakura	2002	56
12	Unexpectedly high prevalence of the mild form of propionic acidemia in Japan: presence of a common mutation and possible clinical implications Human Genetics ·Tohru Yorifuji, Masahiko Kawai, Junko Muroi, Mitsukazu Mamada, Keiji Kurokawa, Yosuke Shigematsu, Satoko Hirano, Nobuo Sakura, Ichiro Yoshida, Tomiko Kuhara, Fumio Endo, Hiroshi Mitsubuchi, Tatsutoshi Nakahata	2002	38
13	Significance of the eosinophil cationic protein/eosinophil count ratio in asthmatic patients: its relationship to disease severity Annals of Allergy Asthma & Immunology ·Adeyemi Saheed Badewa, Hiroshi Kawaguchi, Yasuhiro Kato, Nobuo Sakura, Kazuhiro Ueda, Yasuhiro Abe	2001	13
14	Morning and afternoon serum levels of cortisone and cortisol in asthmatic patients Clinica Chimica Acta ·Adeyemi Saheed Badewa, Shinji Nomura, Nobuo Sakura, Kazuhiro Ueda, H Bjørnstad Pettersen, Cheng-Kai Fu	2000	17
15	Molecular Analysis of Glycogen Storage Disease Type Ib: Identification of a Prevalent Mutation among Japanese Patients and Assignment of a Putative Glucose-6-Phosphate Translocase Gene to Chromosome 11 Biochemical and Biophysical Research Communications ·Shigeo Kure, Yoichi Suzuki, Yoichi Matsubara, Osamu Sakamoto, Haruo Shintaku, Gen Isshiki, Gevorg Stepanyan, Merendi F., Nobuo Sakura, Kuniaki Narisawa	1998	37
16	Serum concentrations of cortisone and cortisol in premature infants Metabolism ·Adeyemi Saheed Badewa, Andrea Vieira, Nobuo Sakura, H. Askew, LEANDRO DE OLIVEIRA RECKEL, H. Petersen, Takashi Sakano, Shri Natarajan Arumugam, Yinguo Yang, Kazuhiro Ueda	1997	17
17	Fetal diagnosis of galactosialidosis (protective protein/cathepsin A deficiency) Clinica Chimica Acta ·Kohji Itoh, Norio Miharu, Koso Ohama, منوچهر امینی, Nobuo Sakura, Hitoshi Sakuraba	1997	7
18	Elevated plasma bile acids in hypergalactosaemic neonates: a diagnostic clue to portosystemic shunts European Journal of Pediatrics ·Nobuo Sakura, منوچهر امینی, Takaatsu Eguchi, Hiroaki Ono, Ethan Craig Busby, Choon-su PARK, K Ito	1997	19
19	Defect in biosynthesis of mitochondrial acetoacetyl-coenzyme A thiolase in cultured fibroblasts from a boy with 3-ketothiolase deficiency. Journal of Clinical Investigation ·Seiji Yamaguchi, T Orii, Nobuo Sakura, Sanzo Miyazawa, Takashi Hashimoto	1988	46
20	Kell Phenotypes in 15 Japanese Patients with Chronic Granulomatous Disease Vox Sanguinis ·H.J. Geise, Maimunah. Intan Sari. Elfi Yenny Yusuf, 陈知生, Nobuo Sakura, Tomofusa Usui	1979	1

About Nobuo Sakura

Nobuo Sakura is a scholar working on Clinical Biochemistry, Behavioral Neuroscience, Biochemistry, Pediatrics, Perinatology and Child Health and Rheumatology, having authored 102 papers that have together received 2.1k indexed citations. Recurring topics across this work include Metabolism and Genetic Disorders (39 papers), Neonatal Health and Biochemistry (16 papers), Biochemical and Molecular Research (14 papers), Folate and B Vitamins Research (13 papers), Mitochondrial Function and Pathology (11 papers), Diet and metabolism studies (8 papers), Lysosomal Storage Disorders Research (7 papers) and Hormonal Regulation and Hypertension (6 papers). The work is most often cited by research in Clinical Biochemistry (889 citations), Rheumatology (433 citations), Pediatrics, Perinatology and Child Health (484 citations), Biochemistry (155 citations) and Physiology (470 citations). Nobuo Sakura has collaborated with scholars based in Japan, United States and Austria. Frequent co-authors include Kazuhiro Ueda, Hiroaki Ono, Akiko Sakamoto, Seiji Yamaguchi, Yutaka Nishimura, Yosuke Shigematsu, Go Tajima, Shinji Nomura, Takaatsu Eguchi and Shigeo Kure. Their work appears in journals such as Journal of Inherited Metabolic Disease, Clinica Chimica Acta, Journal of Chromatography B, European Journal of Pediatrics and Human Genetics.

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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