Yoshihiro Maruo - Concepedia

Author

Yoshihiro Maruo

Shiga University of Medical Science ORCID

Also Known As

Maruo, Y., Maruo, Yoshihiro, Tatsuhiko Yagihashi, Y Maruo, Y. Maruo, YOSHIHIRO MARUO, Yoshihiro MARUO, Yoshihiro Maruo

142

Publications

2.6K

Citations

H-Index

Concepts

All Affiliations

Shiga University of Medical Science The University of Tokyo Tokyo Medical and Dental University Nihon University Teikyo University

About

Yoshihiro Maruo is an author at Shiga University of Medical Science specializing in medicine, pathology, and genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	14	19	865
2	Natural Sciences	4	4	437
3	Health Sciences	1	1	14
4	Public Health	1	1	12
5	Allergy	1	1	43

Yoshihiro Maruo

Publications

2.2K

Citations

H-Index

Page 1

	Year	Citations
A Novel Mechanism for the Inhibition of Hyaluronan Biosynthesis by 4-Methylumbelliferone Ikuko Kakizaki, Kaoru Kojima, Keiichi Takagaki, Journal of Biological Chemistry Chemoprevention StrategyChemical BiologyHa BiosynthesisMedicinal ChemistryBiosynthesis	2004	286
Association of Neonatal Hyperbilirubinemia With Bilirubin UDP-Glucuronosyltransferase Polymorphism Yoshihiro Maruo, Kashiro Nishizawa, Hiroshi Satō, PEDIATRICS	1999	171
Prolonged Unconjugated Hyperbilirubinemia Associated With Breast Milk and Mutations of the Bilirubin Uridine Diphosphate- Glucuronosyltransferase Gene Yoshihiro Maruo, Kashiro Nishizawa, Hiroshi Sato, PEDIATRICS	2000	121
Transient Congenital Hypothyroidism Caused by Biallelic Mutations of the Dual Oxidase 2 Gene in Japanese Patients Detected by a Neonatal Screening Program Yoshihiro Maruo, Hiroko Takahashi, Ikumi Soeda, The Journal of Clinical Endocrinology & Metabolism	2008	119
Genetic polymorphisms of bilirubin uridine diphosphate‐glucuronosyltransferase gene in Japanese patients with Crigler–Najjar syndrome or Gilbert's syndrome as well as in healthy Japanese subjects Keisuke Takeuchi, Yoshinao Kobayashi, Shigenori Tamaki, Journal of Gastroenterology and Hepatology	2004	96
Phosphatase and tensin homolog (PTEN) mutation can cause activated phosphatidylinositol 3-kinase δ syndrome–like immunodeficiency Yuki Tsujita, Kanako Mitsui‐Sekinaka, Kohsuke Imai, Journal of Allergy and Clinical Immunology	2016	96
Comprehensive molecular analysis of Japanese patients with pediatric-onset MODY-type diabetes mellitus Tohru Yorifuji, Rika Fujimaru, Yuki Hosokawa, Pediatric Diabetes	2011	86
Two linked polymorphic mutations (A(TA)7TAA and T-3279G) of UGT1A1 as the principal cause of Gilbert syndrome Yoshihiro Maruo, Carlos D′ Addario, Asami Mori, Human Genetics Mendelian DisorderGenetic DisorderMedicineGeneticsPrincipal Cause	2004	77
UDP-GLUCURONOSYLTRANSFERASE 1A4 POLYMORPHISMS IN A JAPANESE POPULATION AND KINETICS OF CLOZAPINE GLUCURONIDATION Asami Mori, Yoshihiro Maruo, Masaru Iwai, Drug Metabolism and Disposition	2005	76
Six novel UDP-glucuronosyltransferase (UGT1A3) polymorphisms with varying activity Masaru Iwai, Yoshihiro Maruo, Masaki Ito, Journal of Human Genetics Natural SciencesGeneticsHuman PolymorphismMolecular BiologyVarying Activity	2004	75

Page 1