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Journal of Human Genetics|January 22, 2020
Molecular mechanisms determining severity in patients with Pierson syndromeShogo Minamikawa, Saori Miwa, Tetsuji Inagaki, et al.
Kidney International Reports|June 12, 2026
Genetic Screening of Patients With Inherited Fanconi SyndromeYuta Inoki, Nana Sakakibara, Asahi Yamamoto, et al.
Kidney International Reports|May 2, 2022
Detecting MUC1 Variants in Patients Clinicopathologically Diagnosed With Having Autosomal Dominant Tubulointerstitial Kidney DiseaseEri Okada, Naoya Morisada, Tomoko Horinouchi, et al.
Kidney International Reports|May 14, 2023
Corrigendum to "Detecting MUC1 Variants in Patients Clinicopathologically Diagnosed With Having Autosomal Dominant Tubulointerstitial Kidney Disease"Kidney International Reports, Volume 7, Issue 4, April 2022, Pages 857-866Eri Okada, Naoya Morisada, Tomoko Horinouchi, et al.
Clinical and Experimental Nephrology|May 28, 2019
Clinical characteristics of HNF1B-related disorders in a Japanese populationChina Nagano, Naoya Morisada, Kandai Nozu, et al.
Scientific Reports|October 10, 2025
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 studyKazumoto Iijima, Mayumi Sako, Tomoko Horinouchi, et al.
Kidney360|September 30, 2022
Clinical, Pathological, and Genetic Characteristics in Patients with Focal Segmental GlomerulosclerosisChina Nagano, Shigeo Hara, Norishige Yoshikawa, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|September 29, 2021
Identification of novel OCRL isoforms associated with phenotypic differences between Dent disease-2 and Lowe syndromeNana Sakakibara, Takeshi Ijuin, Tomoko Horinouchi, et al.
Nature Communications|June 4, 2020
Development of an exon skipping therapy for X-linked Alport syndrome with truncating variants in COL4A5Tomohiko Yamamura, Tomoko Horinouchi, Tomomi Adachi, et al.
Kidney International|March 10, 2023
A multicenter retrospective study of calcineurin inhibitors in nephrotic syndrome secondary to podocyte gene variantsGeorgia Malakasioti, Daniela Iancu, Anastasiia Milovanova, et al.
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