Asami Mori

707 total citations
17 papers, 549 citations indexed

About

Asami Mori is a scholar working on Molecular Biology, Pediatrics, Perinatology and Child Health and Pulmonary and Respiratory Medicine. According to data from OpenAlex, Asami Mori has authored 17 papers receiving a total of 549 indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Molecular Biology, 12 papers in Pediatrics, Perinatology and Child Health and 9 papers in Pulmonary and Respiratory Medicine. Recurrent topics in Asami Mori's work include Neonatal Health and Biochemistry (12 papers), Heme Oxygenase-1 and Carbon Monoxide (8 papers) and Methemoglobinemia and Tumor Lysis Syndrome (8 papers). Asami Mori is often cited by papers focused on Neonatal Health and Biochemistry (12 papers), Heme Oxygenase-1 and Carbon Monoxide (8 papers) and Methemoglobinemia and Tumor Lysis Syndrome (8 papers). Asami Mori collaborates with scholars based in Japan, Türkiye and United States. Asami Mori's co-authors include Yoshihiro Maruo, Yoshihiro Takeuchi, Hiroshi Satō, Masaru Iwai, Hiroko Takahashi, Yu Mimura, Katsuyuki Matsui, Hirokazu Okamoto, Tomoyuki Okuda and Hiroshi Sato and has published in prestigious journals such as The Journal of Clinical Endocrinology & Metabolism, Journal of Controlled Release and The Journal of Pediatrics.

In The Last Decade

Asami Mori

17 papers receiving 533 citations

Peers

Asami Mori

PPCH

PRM

EDM

PHARM

Neilann K. Horner United States

Sahar M. El-Haggar Egypt

J. K. McKenzie Canada

Takao Morinobu Japan

G. E. Hoffmann Germany

N C R Räihä Finland

Radosław Jaźwiec Poland

Maja Malenica Bosnia and Herzegovina

Inger Holmberg Sweden

Rein Seensalu Sweden

Neilann K. Horner United States

Asami Mori

137 ×0.5

117 ×0.5

PPCH

36 ×0.2

PRM

43 ×0.3

EDM

72 ×0.9

PHARM

Citations per year, relative to Asami Mori Asami Mori (= 1×) peers Neilann K. Horner

Countries citing papers authored by Asami Mori

Since Specialization

Citations

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

Fields of papers citing papers by Asami Mori

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Asami Mori

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

All Works

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17 of 17 papers shown

Maruo, Yoshihiro, et al.. (2016). Successful every-other-day liothyronine therapy for severe resistance to thyroid hormone beta with a novel THRB mutation; case report. BMC Endocrine Disorders. 16(1). 1–1. 32 indexed citations

Maruo, Yoshihiro, Keisuke Nagasaki, Katsuyuki Matsui, et al.. (2016). Natural course of congenital hypothyroidism by dual oxidase 2 mutations from the neonatal period through puberty. European Journal of Endocrinology. 174(4). 453–463. 35 indexed citations

Maruo, Yoshihiro, Hiroshi Fujito, Katsuyuki Matsui, et al.. (2014). Bilirubin Uridine Diphosphate-Glucuronosyltransferase Variation Is a Genetic Basis of Breast Milk Jaundice. The Journal of Pediatrics. 165(1). 36–41.e1. 40 indexed citations

Maruo, Yoshihiro, Funda Özgenç, Yu Mimura, et al.. (2011). Compound Heterozygote of a Novel Missense Mutation (p.K402T) and a Double Missense Mutation (p.[G71R;Y486D]) in Type II Crigler‐Najjar Syndrome. Journal of Pediatric Gastroenterology and Nutrition. 52(3). 362–365. 7 indexed citations

Mohri, Kohta, Tomoyuki Okuda, Asami Mori, Kazumi Danjo, & Hirokazu Okamoto. (2010). Optimized pulmonary gene transfection in mice by spray–freeze dried powder inhalation. Journal of Controlled Release. 144(2). 221–226. 59 indexed citations

Takahashi, Hiroko, Yoshihiro Maruo, Asami Mori, et al.. (2008). Effect of D256N and Y483D on Propofol Glucuronidation by Human Uridine 5′‐diphosphate Glucuronosyltransferase (UGT1A9). Basic & Clinical Pharmacology & Toxicology. 103(2). 131–136. 44 indexed citations

Maruo, Yoshihiro, Ishwar C. Verma, Katsuyuki Matsui, et al.. (2008). Conformational Change of UGT1A1 by a Novel Missense Mutation (p.L131P) Causing Crigler‐Najjar Syndrome Type I. Journal of Pediatric Gastroenterology and Nutrition. 46(3). 308–311. 10 indexed citations

Maruo, Yoshihiro, Hiroko Takahashi, Katsuyuki Matsui, et al.. (2008). Transient Congenital Hypothyroidism Caused by Biallelic Mutations of the Dual Oxidase 2 Gene in Japanese Patients Detected by a Neonatal Screening Program. The Journal of Clinical Endocrinology & Metabolism. 93(11). 4261–4267. 94 indexed citations

Sugita, Kenichi, Yoshihiro Maruo, Hidemitsu Kurosawa, et al.. (2007). Severe hyperbilirubinemia in a 10‐year‐old girl with a combined disorder of hereditary spherocytosis and Gilbert syndrome. Pediatrics International. 49(4). 540–542. 12 indexed citations

10.

Maruo, Yoshihiro, Hiroko Takahashi, Asami Mori, et al.. (2006). Crigler‐Najjar Syndrome Type II Caused by a Homozygous Triple Mutation [T‐3279G, A(TA)7TAA, and H39D] of UGT1A1. Journal of Pediatric Gastroenterology and Nutrition. 42(2). 236–239. 7 indexed citations

11.

Mori, Asami, Yoshihiro Maruo, Masaru Iwai, Hiroshi Satō, & Yoshihiro Takeuchi. (2005). UDP-GLUCURONOSYLTRANSFERASE 1A4 POLYMORPHISMS IN A JAPANESE POPULATION AND KINETICS OF CLOZAPINE GLUCURONIDATION. Drug Metabolism and Disposition. 33(5). 672–675. 59 indexed citations

12.

Maruo, Yoshihiro, Masaru Iwai, Asami Mori, Hiroshi Satō, & Yoshihiro Takeuchi. (2005). Polymorphism of UDP-Glucuronosyltransferase and Drug Metabolism. Current Drug Metabolism. 6(2). 91–99. 53 indexed citations

13.

Maruo, Yoshihiro, Asami Mori, Masaru Iwai, et al.. (2004). Two linked polymorphic mutations (A(TA)7TAA and T-3279G) of UGT1A1 as the principal cause of Gilbert syndrome. Human Genetics. 115(6). 525–526. 65 indexed citations

14.

Maruo, Yoshihiro, Erkin Serdaroğlu, Masaru Iwai, et al.. (2003). A Novel Missense Mutation of the Bilirubin UDP‐Glucuronosyltransferase Gene in a Turkish Patient With Crigler‐Najjar Syndrome Type 1. Journal of Pediatric Gastroenterology and Nutrition. 37(5). 627–630. 4 indexed citations

15.

Maruo, Yoshihiro, Erkin Serdaroğlu, Masaru Iwai, et al.. (2003). A Novel Missense Mutation of the Bilirubin UDP-Glucuronosyltransferase Gene in a Turkish Patient With Crigler-Najjar Syndrome Type 1. Journal of Pediatric Gastroenterology and Nutrition. 37(5). 627–630. 9 indexed citations

16.

Maruo, Yoshihiro, Masaki Ito, Masako Iwai, et al.. (2003). Co‐occurrence of three different mutations in the bilirubin UDP‐glucuronosyltransferase gene in a Chinese family with Crigler–Najjar syndrome type I and Gilbert's syndrome. Clinical Genetics. 64(5). 420–423. 10 indexed citations

17.

Mori, Asami, et al.. (1987). Effects of pulsatile cardiopulmonary bypass on carbohydrate and lipid metabolism.. The Journal of Cardiovascular Surgery. 28(6). 621–6. 9 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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