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Kiyomi Abe

Acylated delphinidin glucosides and flavonols from Clitoria ternatea
1985 · Norio Saitô, Kiyomi Abe, et al. · Phytochemistry · 62
Thyroid hormone treatment activates protective pathways in both in vivo and in vitro models of neuronal injury
2017 · Jianrong Li, Ines Donangelo, et al. · Molecular and Cellular Endocrinology · 56
Thyroid Hormone Protects Primary Cortical Neurons Exposed to Hypoxia by Reducing DNA Methylation and Apoptosis
2019 · Jianrong Li, Kiyomi Abe, et al. · Endocrinology · 36
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Living Donor Liver Transplantation for Glycogen Storage Disease Type Ib
2009 · Mureo Kasahara, Reiko Horikawa, et al. · Liver Transplantation · 35
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Association between monoallelic TSHR mutations and congenital hypothyroidism: a statistical approach
2017 · Kiyomi Abe, Satoshi Narumi, et al. · European Journal of Endocrinology · 27
Combined Growth Hormone and Thyroid-Stimulating Hormone Deficiency in a Japanese Patient with a Novel Frameshift Mutation in IGSF1
2015 · Yumi Asakura, Kiyomi Abe, et al. · Hormone Research in Paediatrics · 25
Genetics of Congenital Isolated TSH Deficiency: Mutation Screening of the Known Causative Genes and a Literature Review
2019 · Chiho Sugisawa, Tetsuya Takamizawa, et al. · The Journal of Clinical Endocrinology & Metabolism · 23
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Functional variants in a TTTG microsatellite on 15q26.1 cause familial nonautoimmune thyroid abnormalities
2024 · Satoshi Narumi, Keisuke Nagasaki, et al. · Nature Genetics · 17
Mild thyroid peroxidase deficiency caused by TPO mutations with residual activity: Correlation between clinical phenotypes and enzymatic activity
2017 · Satoshi Narumi, Larry A Fox, et al. · Endocrine Journal · 16
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Homozygous DUOXA2 mutation (p.Tyr138*) in a girl with congenital hypothyroidism and her apparently unaffected brother: Case report and review of the literature
2017 · Chiho Sugisawa, Shinji Higuchi, et al. · Endocrine Journal · 15
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Thyroid Hormone–mediated Histone Modification Protects Cortical Neurons From the Toxic Effects of Hypoxic Injury
2022 · Kiyomi Abe, Jianrong Li, et al. · Journal of the Endocrine Society · 14
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Transient congenital hypothyroidism caused by compound heterozygous mutations affecting the NADPH-oxidase domain of DUOX2
2015 · Atsuko Yoshizawa-Ogasawara, Kiyomi Abe, et al. · Journal of Pediatric Endocrinology and Metabolism · 14
Thyroid hormone receptor β sumoylation is required for thyrotropin regulation and thyroid hormone production
2021 · Sujie Ke, Yan-Yun Liu, et al. · JCI Insight · 13
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Pseudodominant inheritance in a family with nonautoimmune hypothyroidism due to biallelic DUOX 2 mutations
2014 · Kiyomi Abe, Satoshi Narumi, et al. · Clinical Endocrinology · 12
GWAS of thyroid dysgenesis identifies a risk locus at 2q33.3 linked to regulation of Wnt signaling
2022 · Satoshi Narumi, Robert Opitz, et al. · Human Molecular Genetics · 9
Thyroid hormone receptor alpha sumoylation modulates white adipose tissue stores
2021 · Yan-Yun Liu, Jingjing Jiang, et al. · Scientific Reports · 9
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Identification of compound heterozygous TSHR mutations (R109Q and R450H) in a patient with nonclassic TSH resistance and functional characterization of the mutant receptors
2018 · Chiho Sugisawa, Kiyomi Abe, et al. · Clinical Pediatric Endocrinology · 8
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Molecular and Clinical Features of Congenital Hypothyroidism Due to Multiple DUOX2 Variants
2024 · Erika Uehara, Kiyomi Abe, et al. · Thyroid · 7
Biotin Deficiency in a Glycogen Storage Disease Type 1b Girl Fed Only with Glycogen Storage Disease‐Related Formula
2011 · Kenji IHARA, KIYOMI ABE, et al. · Pediatric Dermatology · 7
A patient with congenital hypothyroidism due to a PAX8 frameshift variant accompanying a urogenital malformation
2022 · Kanako Tanase-Nakao, Koji Muroya, et al. · Clinical Pediatric Endocrinology · 5
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Wide Range of Biotin (Vitamin H) Content in Foodstuffs and Powdered Milks as Assessed by High-performance Affinity Chromatography
2009 · Kou Hayakawa, Noriyuki Katsumata, et al. · Clinical Pediatric Endocrinology · 5
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Genotype–Phenotype Correlations in 30 Japanese Patients With Congenital Hypothyroidism Attributable to TG Defects
2024 · Kanako Tanase-Nakao, Megumi Iwahashi-Odano, et al. · The Journal of Clinical Endocrinology & Metabolism · 4
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Familial Non-Autoimmune Hyperthyroidism Caused by an Extracellular Domain Variant (p.Leu267Phe) of the TSH Receptor
2025 · Kazuhiro Shimura, Yosuke Ichihashi, et al. · Hormone Research in Paediatrics · 2
A study of the etiology of transient congenital hypothyroidism in Niigata Prefecture, Japan
2013 · Keisuke Nagasaki, Satoshi Narumi, et al. · International Journal of Pediatric Endocrinology · 2
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Bidirectional changes in serum 25-hydroxyvitamin D in newborns during the first four days of life: A longitudinal cohort study
2026 · Kazushige Ikeda, Kaori Hara-Isono, et al. · Clinical Nutrition ESPEN · 1
Works count: 32
Citation count: 429
H-index: 13
I10-index: 14
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