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Author

Ryojun Takeda

Observed name: R., Takeda
ORCID: 0000-0003-1654-9463
Observed ORCID: 0000-0003-1654-9463
OpenAlex ID: A5038722314
Hypertension is a characteristic complication of X-linked hypophosphatemia
2016 · Yoshie Nakamura, Masaki Takagi, et al. · Endocrine Journal · 42
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Efficacy and Safety of Denosumab Therapy for Osteogenesis Imperfecta Patients with Osteoporosis—Case Series
2018 · Tsukasa Kobayashi, Yukio Nakamura, et al. · Journal of Clinical Medicine · 38
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Clinical and molecular features of patients with COL1 ‐related disorders: Implications for the wider spectrum and the risk of vascular complications
2022 · Ryojun Takeda, Tomomi Yamaguchi, et al. · American Journal of Medical Genetics Part A · 23
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Missense Mutations in NKAP Cause a Disorder of Transcriptional Regulation Characterized by Marfanoid Habitus and Cognitive Impairment
2019 · Sarah K. Fiordaliso, Aiko Iwata-Otsubo, et al. · The American Journal of Human Genetics · 22
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Expanding the phenotypic spectrum of ARCN1-related syndrome
2022 · Alyssa L. Ritter, Jessica Gold, et al. · Genetics in Medicine · 18
Novel compound heterozygous mutations identified by whole exome sequencing in a Japanese patient with geroderma osteodysplastica
2017 · Ryojun Takeda, Masaki Takagi, et al. · European Journal of Medical Genetics · 12
White matter abnormality in Jacobsen syndrome assessed by serial MRI
2020 · Shuhei Fujino, Hiroshi Yoshihashi, et al. · Brain and Development · 9
A case of a Japanese patient with neonatal diabetes mellitus caused by a novel mutation in the ABCC8 gene and successfully controlled with oral glibenclamide
2015 · Ryojun Takeda, Masaki Takagi, et al. · Clinical Pediatric Endocrinology · 7
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A case of transient neonatal diabetes due to a novel mutation in ABCC8
2016 · Masaki Takagi, Ryojun Takeda, et al. · Clinical Pediatric Endocrinology · 4
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An association with hypopituitarism and 9q subtelomere deletion syndrome
2018 · Shinji Higuchi, Masaki Takagi, et al. · Clinical Case Reports · 3
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A case of spondyloepiphyseal dysplasia tarda caused by a novel intragenic deletion of TRAPPC2
2015 · Masaki Takagi, Hiroko Yagi, et al. · Clinical Pediatric Endocrinology · 2
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TmP/GFR is a Useful Marker in Making a Clinical Diagnosis of X-Linked Hypophosphataemic Rickets Caused by the PHEX Gene Mutation
2015 · Ryojun Takeda, K Miyai, et al. · 54th ESPE Meeting (ESPE 2015) · 2
Reanalysis of Chromosomal Microarray Data Using a Smaller Copy Number Variant Call Threshold Identifies Four Cases with Heterozygous Multiexon Deletions of ARID1B, EHMT1, and FOXP1 Genes
2023 · Noriko Kubota, Ryojun Takeda, et al. · Molecular Syndromology · 1
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[Updates on rickets and osteomalacia: pathogenesis and pathophysiology of rickets].
2013 · Yukihiro Hasegawa, Kentaro Miyai, et al. · PubMed · 1
A case report of Coffin-Siris syndrome and autism spectrum disorder in an extremely low birth weight infant with de novo ARID1B nonsense variant: The role of genetic analysis
2026 · Emi Kasai-Yoshida, Yoichiro Kawasaki, et al. · Brain and Development Case Reports
Supplementary Material for: Reanalysis of chromosomal microarray data using a smaller copy number variant call threshold identifies four cases with heterozygous multiexon deletions of ARID1B, EHMT1, and FOXP1 genes
2023 · N., Kubota, R., Takeda, et al. · Figshare
A case of a primary hypothyroidism diagnosis based on decreased renal function
2018 · Kazuna Yamamoto, Chikako Terano, et al. · Japanese journal of pediatric nephrology
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A case of unilateral and segmental localized polycystic kidney disease in a boy who was detected at a microscopic hematuria on a school urinary screening
2015 · Shohei Takahashi, Satsuki Okamoto, et al. · Japanese journal of pediatric nephrology
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Works count: 19
Citation count: 184
H-index: 7
I10-index: 6
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