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C. Nagano · SciRah

Researcher profile · Semantic Scholar

C. Nagano

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C. Nagano — researcher profile on SciRah

h-index: 21
Works: 160
Citations: 1,444

Most-cited papers

Multi-population genome-wide association study implicates immune and non-immune factors in pediatric steroid-sensitive nephrotic syndrome
Alexandra Barry, M. McNulty, Xiaoyuan Jia, Y. Gupta +66 more
2023Nature Communications49 citations Open access
Semantic Scholar
Examination of the predicted prevalence of Gitelman syndrome by ethnicity based on genome databases
Atsushi Kondo, C. Nagano, Shinya Ishiko, Takashi Omori +16 more
2021Scientific Reports38 citations Open access
Semantic Scholar
Last Nucleotide Substitutions of COL4A5 Exons Cause Aberrant Splicing
Yuya Aoto, T. Horinouchi, Tomohiko Yamamura, Atsushi Kondo +13 more
2021Kidney International Reports35 citations Open access
Semantic Scholar
A multicenter retrospective study of calcineurin inhibitors in nephrotic syndrome secondary to podocyte gene variants.
Georgia Malakasioti, D. Iancu, A. Milovanova, A. Tsygin +34 more
2023Kidney International32 citations Open access
Semantic Scholar
Detecting MUC1 variants in patients clinicopathologically diagnosed with ADTKD
Eri Okada, N. Morisada, T. Horinouchi, Hideki Fujii +22 more
2022Kidney International Reports22 citations Open access
Semantic Scholar
Comprehensive genetic analysis using next-generation sequencing for the diagnosis of nephronophthisis-related ciliopathies in the Japanese population
N. Sakakibara, K. Nozu, Tomohiko Yamamura, T. Horinouchi +12 more
2022Journal of Human Genetics21 citations Open access
Semantic Scholar
Clinical, Pathological, and Genetic Characteristics in Patients with Focal Segmental Glomerulosclerosis
C. Nagano, S. Hara, N. Yoshikawa, A. Takeda +24 more
2022Kidney36015 citations Open access
Semantic Scholar
Minimal residual disease in high-risk neuroblastoma shows a dynamic and disease burden-dependent correlation between bone marrow and peripheral blood
Kyaw San Lin, Suguru Uemura, Khin Kyae Mon Thwin, Naoko Nakatani +12 more
2021Translational Oncology15 citations Open access
Semantic Scholar
BCS1L mutations produce Fanconi syndrome with developmental disability
Kojima Kanako, N. Sakakibara, K. Murayama, Koji Nagatani +15 more
2021Journal of Human Genetics14 citations Open access
Semantic Scholar
A review of the genetic background in complicated WT1-related disorders
C. Nagano, K. Nozu
2024Clinical and Experimental Nephrology13 citations Open access
Semantic Scholar
Anti-nephrin antibodies in steroid-sensitive nephrotic syndrome in Japanese children
T. Horinouchi, C. Nagano, A. Watts
2023Pediatric nephrology (Berlin, West)12 citations Open access
Semantic Scholar
Limited correlation between tumor markers and minimal residual disease detected by seven neuroblastoma-associated mRNAs in high-risk neuroblastoma patients.
Suguru Uemura, Kyaw San Lin, Khin Kyae Mon Thwin, Naoko Nakatani +12 more
2021Molecular and clinical oncology11 citations Open access
Semantic Scholar
Systematic Review of Clinical Characteristics and Genotype-Phenotype Correlation in LAMB2-Associated Disease
Ryota Suzuki, N. Sakakibara, Yuta Ichikawa, Hideaki Kitakado +11 more
2023Kidney International Reports9 citations Open access
Semantic Scholar
Clinical and Biochemical Characteristics of Pseudohypoaldosteronism Type 1 with and Without Genetic Mutations: A Literature Review
Yuki Nakata, C. Nagano, Yukihito Imagawa, Keisuke Shirai +5 more
2025Journal of Clinical Medicine8 citations Open access
Semantic Scholar
Phenotype and genotype of autosomal dominant tubulointerstitial kidney disease in a Japanese cohort
Yu Tanaka, C. Nagano, N. Sakakibara, Eri Okada +12 more
2025Clinical and Experimental Nephrology8 citations Open access
Semantic Scholar
All reported non-canonical splice site variants in GLA cause aberrant splicing
Eri Okada, T. Horinouchi, Tomohiko Yamamura, Yuya Aoto +14 more
2023Clinical and Experimental Nephrology8 citations Open access
Semantic Scholar
Multivariate analysis of the impact of weather and air pollution on emergency department visits for night-time headaches among children: retrospective, clinical observational study
H. Yamaguchi, K. Nozu, Shinya Ishiko, Hiroaki Nagase +8 more
2021BMJ Open8 citations Open access
Semantic Scholar
In steroid-resistant nephrotic syndrome that meets the strict definition, monogenic variants are less common than expected
Yuta Ichikawa, N. Sakakibara, C. Nagano, Y. Inoki +8 more
2024Pediatric nephrology (Berlin, West)7 citations Open access
Semantic Scholar
Genotype and X-chromosome inactivation are associated with disease severity in females with X-linked Alport syndrome.
Ryota Suzuki, N. Sakakibara, Sae Murakami, Yuta Ichikawa +13 more
2024Nephrology, Dialysis and Transplantation7 citations
Semantic Scholar
Detecting MUC1 Variants in Patients Clinicopathologically Diagnosed With Having Autosomal Dominant Tubulointerstitial Kidney Disease
Eri Okada, N. Morisada, T. Horinouchi, Hideki Fujii +22 more
2022Kidney International Reports6 citations Open access
Semantic Scholar
Use of renin-angiotensin system inhibitors as initial therapy in children with Henoch–Schönlein purpura nephritis of moderate severity
Sadayuki Nagai, T. Horinouchi, T. Ninchoji, Atsushi Kondo +15 more
2022Pediatric nephrology (Berlin, West)6 citations Open access
Semantic Scholar
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
K. Iijima, Mayumi Sako, T. Horinouchi, Tomoyuki Sakai +49 more
2025Scientific Reports5 citations Open access
Semantic Scholar
Clinical and Genetic Insights Into Isolated Proteinuria With CUBN Variants
N. Sakakibara, Shinya Ishiko, Yuriko Tanaka, Y. Inoki +14 more
2025Kidney International Reports5 citations Open access
Semantic Scholar
Detecting pathogenic deep intronic variants in Gitelman syndrome
Rini Rossanti, T. Horinouchi, N. Sakakibara, Tomohiko Yamamura +10 more
2022American Journal of Medical Genetics. Part A5 citations
Semantic Scholar
Beneficial screening of Fabry disease in patients with hypohidrosis
Megumi Nagai-Sangawa, A. Fukunaga, C. Takeuchi, S. Nishiyama +5 more
2021Journal of dermatology (Print)5 citations Open access
Semantic Scholar
Evaluation of Suspected Autosomal Alport Syndrome Synonymous Variants
Rini Rossanti, T. Horinouchi, Tomohiko Yamamura, C. Nagano +18 more
2021Kidney3605 citations Open access
Semantic Scholar
Impact of Age-3 Urine Screening on Diagnosis and Treatment Timing in Alport Syndrome
Hideaki Kitakado, Shingo Ishimori, Shuhei Aoyama, Yuka Kimura +8 more
2025Kidney International Reports4 citations Open access
Semantic Scholar
Co-localization of IgG with nephrin in immune-mediated idiopathic nephrotic syndrome
Yuta Ichikawa, N. Sakakibara, Shuhei Aoyama, Yuka Kimura +14 more
2025Clinical and Experimental Nephrology4 citations Open access
Semantic Scholar
A case of pseudo-Bartter/Gitelman syndrome caused by long-term laxative abuse, leading to end-stage kidney disease
Atsushi Kondo, K. Yoshiya, N. Sakakibara, C. Nagano +2 more
2024CEN Case Reports4 citations Open access
Semantic Scholar
Maturity‐onset diabetes of the young type 5, presenting as diabetic ketoacidosis with alkalemia: A report of a case
Akiko Hayakawa-Iwamoto, Daisuke Aotani, Yuki Shimizu, S. Kakoi +11 more
2021Journal of Diabetes Investigation4 citations Open access
Semantic Scholar
Familial focal segmental glomerulosclerosis with Alport-like glomerular basement changes caused by paired box protein 2 gene variant
Y. Yamada, Hiroki Yokoyama, Ryo Kinoshita, K. Kitamoto +6 more
2023CEN Case Reports3 citations Open access
Semantic Scholar
Epidemiological impact of universal varicella vaccination on consecutive emergency department visits for varicella and its economic impact among children in Kobe City, Japan.
H. Yamaguchi, K. Nozu, Shinya Ishiko, Hiroaki Nagase +8 more
2021Journal of Infection and Chemotherapy3 citations Open access
Semantic Scholar
Comprehensive Splice Pattern Analysis for Previously Reported OCRL Splicing Variants and Their Phenotypic Contributions
Rini Rossanti, Eri Okada, N. Sakakibara, Ryota Suzuki +12 more
2025Kidney International Reports2 citations Open access
Semantic Scholar
Clinical use of the VNtyper-Kestrel pipeline for MUC1 variant detection in autosomal-dominant tubulointerstitial kidney disease
C. Nagano, N. Morisada, Y. Inoki, Yuriko Tanaka +9 more
2025Clinical and Experimental Nephrology2 citations Open access
Semantic Scholar
Early use of renin–angiotensin–aldosterone system inhibitors and stable renal function in familial focal segmental glomerulosclerosis with ACTN4 mutation: a case report and literature review
Kisho Miyasako, Yujiro Maeoka, Yuho Adachi, Ryo Tamura +4 more
2025BMC Nephrology2 citations Open access
Semantic Scholar
Potential involvement of abnormal splicing in severe WT1-related disorders
C. Nagano, Masafumi Matuso, Y. Inoki, Yuriko Tanaka +8 more
2025Clinical and Experimental Nephrology2 citations Open access
Semantic Scholar
The first case of Al-Raqad syndrome in Japan is associated with a homozygous DCPS exonic variant resulting in aberrant splicing.
Haruka Nozaki, N. Sakakibara, Hiroaki Hanafusa, Y. Inoki +10 more
2025Brain & development (Tokyo. 1979)2 citations Open access
Semantic Scholar
COL4A5 Intronic Variants at Third to Fifth Nucleotides Cause Alport Syndrome
Hideaki Kitakado, T. Horinouchi, Shuhei Aoyama, Yuka Kimura +11 more
2024Kidney International Reports2 citations
Semantic Scholar
Nephronophthisis 13 caused by WDR19 variants with pancytopenia: case report
Yu Tanaka, T. Horinouchi, Y. Inoki, Yuta Ichikawa +9 more
2024CEN Case Reports2 citations Open access
Semantic Scholar
Corrigendum to "A multicenter retrospective study of calcineurin inhibitors in nephrotic syndrome secondary to podocyte gene variants." Kidney Int. 2023;103:962-972.
Georgia Malakasioti, Daniela Iancu, Anastasiia Milovanova, A. Tsygin +35 more
2024Kidney International2 citations Open access
Semantic Scholar
An extremely mild clinical course in a case with LAMB2-associated nephritis diagnosed with next-generation sequencing
Koji Sakuraya, K. Nozu, Hitohiko Murakami, C. Nagano +4 more
2021CEN Case Reports2 citations Open access
Semantic Scholar
Utility of glomerular Gd-IgA1 staining for indistinguishable cases of IgA nephropathy or Alport syndrome
Shinya Ishiko, A. Tanaka, A. Takeda, M. Hara +17 more
2021Clinical and Experimental Nephrology2 citations Open access
Semantic Scholar
Whole-genome sequencing identified a deep intronic COL4A5 variant causing aberrant splicing in a female patient with X-linked Alport syndrome
C. Nagano, Shuhei Aoyama, Yuka Kimura, Y. Inoki +5 more
2026CEN Case Reports1 citations
Semantic Scholar
12-Year-Old Girl with Systemic Lupus Erythematosus Complicated by Gangrene and Intermittent Claudication.
Takashi Uechi, T. Horinouchi, Y. Inoki, Yuriko Tanaka +6 more
2025Modern Rheumatology Case Reports1 citations
Semantic Scholar
Differences in kidney prognosis between congenital and infantile nephrotic syndrome
Y. Inoki, T. Horinouchi, Shuhei Aoyama, Yuka Kimura +18 more
2025Pediatric nephrology (Berlin, West)1 citations Open access
Semantic Scholar
WT1 exon 10 missense variant in a pediatric patient with focal segmental glomerulosclerosis with embryonal hyperplasia
Mari Kurokawa, Manao Nishimura, Kei Nishiyama, Kentaro Matsuoka +2 more
2024Pediatric nephrology (Berlin, West)1 citations Open access
Semantic Scholar
Severe Kidney Dysplastic Phenotypes Caused by WT1 Exon 9 Missense Variants
Huong Quynh Tran Thuy, Tuyen Thi Thanh Nguyen, K. Fukui, C. Nagano +3 more
2024Journal of the American Society of Nephrology1 citations
Semantic Scholar
Clinical, Pathological, and Genetic Characteristics of Patients with Digenic Alport Syndrome
Y. Inoki, T. Horinouchi, Tomohiko Yamamura, Shingo Ishimori +8 more
2024Kidney3601 citations Open access
Semantic Scholar
Anti-Nephrin Antibodies in Idiopathic Nephrotic Syndrome in Japanese Children
T. Horinouchi, A. Watts, C. Nagano, Yuta Ichikawa +11 more
2023Journal of the American Society of Nephrology1 citations
Semantic Scholar
Steroid- and immunosuppressant-based protocol of Henoch-Schönlein purpura nephritis without angiotensin inhibitors in the acute phase
K. Kasahara, Y. Gotoh, Yoshiyuki Kuroyanagi, C. Nagano +4 more
2023Minerva Pediatrica1 citations
Semantic Scholar

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K. Nozu×45
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K. Nozu — researcher profile on SciRah
T. Horinouchi×37
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N. Sakakibara×31
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K. Iijima — researcher profile on SciRah

Atsushi Kondo×20

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Shingo Ishimori×20

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Hideaki Kitakado×19

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Chika Ueda — researcher profile on SciRah

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Yuya Aoto — researcher profile on SciRah

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Y. Inoki — researcher profile on SciRah