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Yasufumi Ohtsuka

Observed names: Ohtsuka, Yasufumi, Y. Ohtsuka, YASUFUMI OHTSUKA
Observed institutions: Kurume University, Saga University, University of the Ryukyus, Saga Medical School Hospital, Shizuoka Children's Hospital, Kindai University, Kumamoto University
ORCID: 0000-0002-7292-649X
Observed ORCID: 0000-0002-7292-649X
OpenAlex ID: A5065837353
Clinical practice guideline for pediatric idiopathic nephrotic syndrome 2013: medical therapy
2015 · Kenji Ishikura, Shinsuke Matsumoto, et al. · Clinical and Experimental Nephrology · 105
Strong Association of the HLA-DR/DQ Locus with Childhood Steroid-Sensitive Nephrotic Syndrome in the Japanese Population
2018 · Xiaoyuan Jia, Tomoko Horinouchi, et al. · Journal of the American Society of Nephrology · 72
Common risk variants in NPHS1 and TNFSF15 are associated with childhood steroid-sensitive nephrotic syndrome
2020 · Xiaoyuan Jia, Tomohiko Yamamura, et al. · Kidney International · 71
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Mycophenolate Mofetil after Rituximab for Childhood-Onset Complicated Frequently-Relapsing or Steroid-Dependent Nephrotic Syndrome
2022 · Iijima, Kazumoto, 飯島, 一誠, et al. · Institutional Repositories DataBase (IRDB) · 54
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Clinically diverse phenotypes and genotypes of patients with branchio-oto-renal syndrome
2018 · Ai Unzaki, Naoya Morisada, et al. · Journal of Human Genetics · 51
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Autosomal recessive cystinuria caused by genome‐wide paternal uniparental isodisomy in a patient with Beckwith–Wiedemann syndrome
2014 · Y. Ohtsuka, K. Higashimoto, et al. · Clinical Genetics · 51
Clinical practice guideline for pediatric idiopathic nephrotic syndrome 2013: general therapy
2015 · Yoshitsugu Kaku, Yasufumi Ohtsuka, et al. · Clinical and Experimental Nephrology · 49
Comprehensive and quantitative multilocus methylation analysis reveals the susceptibility of specific imprinted differentially methylated regions to aberrant methylation in Beckwith–Wiedemann syndrome with epimutations
2014 · Toshiyuki Maeda, Ken Higashimoto, et al. · Genetics in Medicine · 39
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Early Elevation of Complement Factor Ba Is a Predictive Biomarker for Transplant-Associated Thrombotic Microangiopathy
2021 · Hiroshi Okamura, Hirohisa Nakamae, et al. · Frontiers in Immunology · 33
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A novel de novo point mutation of the OCT ‐binding site in the IGF2 / H19 ‐imprinting control region in a Beckwith–Wiedemann syndrome patient
2013 · K. Higashimoto, K. Jozaki, et al. · Clinical Genetics · 30
Homozygous deletion of DIS3L2 exon 9 due to non-allelic homologous recombination between LINE-1s in a Japanese patient with Perlman syndrome
2013 · Ken Higashimoto, Toshiyuki Maeda, et al. · European Journal of Human Genetics · 25
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Clinical Features, Molecular Genetics, and Long-Term Outcome in Congenital Chloride Diarrhea: A Nationwide Study in Japan
2019 · Ken-ichiro Konishi, Tatsuki Mizuochi, et al. · The Journal of Pediatrics · 24
Identification of consensus motifs associated with mitotic recombination and clinical characteristics in patients with paternal uniparental isodisomy of chromosome 11
2016 · Yasufumi Ohtsuka, Ken Higashimoto, et al. · Human Molecular Genetics · 21
Alport syndrome caused by a COL4A5 deletion and exonization of an adjacent AluY
2014 · Kandai Nozu, Kazumoto Iijima, et al. · Molecular Genetics & Genomic Medicine · 16
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Identification of novel OCRL isoforms associated with phenotypic differences between Dent disease-2 and Lowe syndrome
2021 · Nana Sakakibara, Takeshi Ijuin, et al. · Nephrology Dialysis Transplantation · 14
Aberrant hypomethylation at imprinted differentially methylated regions is involved in biparental placental mesenchymal dysplasia
2022 · Saori Aoki, Ken Higashimoto, et al. · Clinical Epigenetics · 11
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Association between Crohn’s disease and AarF domain-containing kinase 4 glomerulopathy
2019 · Toshihiko Kakiuchi, Yasufumi Ohtsuka, et al. · Clinical Journal of Gastroenterology · 11
Postoperative Atypical Hemolytic Uremic Syndrome Treated Successfully with Eculizumab
2016 · Shunichiro Yasuda, Masahide Yamamoto, et al. · Internal Medicine · 9
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Human uric acid transporter 1 gene analysis in familial renal hypo‐uricemia associated with exercise‐induced acute renal failure
2007 · YASUFUMI OHTSUKA, MASAFUMI ZAITSU, et al. · Pediatrics International · 9
Detection by multiplex ligation-dependent probe amplification of large deletion mutations in the COL4A5 gene in female patients with Alport syndrome
2009 · Kandai Nozu, Rafal Przybyslaw Krol, et al. · Pediatric Nephrology · 8
Rituximab in combination with cyclosporine and steroid pulse therapy for childhood-onset multidrug-resistant nephrotic syndrome: a multicenter single-arm clinical trial (JSKDC11 trial)
2023 · Kandai Nozu, Mayumi Sako, et al. · Clinical and Experimental Nephrology · 7
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Rituximab-induced long-term remission in childhood-onset, uncomplicated, frequently relapsing or steroid-dependent nephrotic syndrome: a randomized, placebo-controlled trial and a follow-up study
2025 · Kazumoto Iijima, Mayumi Sako, et al. · Scientific Reports · 5
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Successful Treatment of Transplantation-associated Atypical Hemolytic Uremic Syndrome With Eculizumab
2017 · Daiichiro Hasegawa, Atsuro Saito, et al. · Journal of Pediatric Hematology/Oncology · 5
Detection of large deletion mutations in the COL4A5 gene of female Alport syndrome patients
2008 · Kandai Nozu, Rafal Przybyslaw Krol, et al. · Pediatric Nephrology · 5
Kidney pathological findings of MYH9-related disease: a cross-sectional nationwide survey in Japan
2025 · Ryo Nakatani, Kenichiro Miura, et al. · Pediatric Nephrology · 4
Works count: 46
Citation count: 738
H-index: 14
I10-index: 17
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