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Takeshi Ninchoji

Observed names: Ninchoji, Takeshi, T Ninchoji, Takeshi NINCHOJI
Observed institutions: Nippon Steel (Japan), Kameda Medical Center, Himeji Medical Center, Toyohashi Municipal Hospital, Tsugaru General Hospital, Hyogo Prefectural Harima-Himeji General Medical Center, Kobe University
ORCID: 0000-0001-7590-1522
Observed ORCID: 0000-0001-7590-1522
OpenAlex ID: A5019540296
Genetic, Clinical, and Pathologic Backgrounds of Patients with Autosomal Dominant Alport Syndrome
2016 · Naohiro Kamiyoshi, Kandai Nozu, et al. · Clinical Journal of the American Society of Nephrology · 141
Genotype-phenotype correlations influence the response to angiotensin-targeting drugs in Japanese patients with male X-linked Alport syndrome
2020 · Tomohiko Yamamura, Tomoko Horinouchi, et al. · Kidney International · 122
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Natural History and Genotype–Phenotype Correlation in Female X-Linked Alport Syndrome
2017 · Tomohiko Yamamura, Kandai Nozu, et al. · Kidney International Reports · 96
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Milder clinical aspects of X-linked Alport syndrome in men positive for the collagen IV α5 chain
2013 · Yuya Hashimura, Kandai Nozu, et al. · Kidney International · 91
Differential diagnosis of Bartter syndrome, Gitelman syndrome, and pseudo–Bartter/Gitelman syndrome based on clinical characteristics
2015 · Natsuki Matsunoshita, Kandai Nozu, et al. · Genetics in Medicine · 86
Clinical and Genetic Characteristics in Patients With Gitelman Syndrome
2018 · Junya Fujimura, Kandai Nozu, et al. · Kidney International Reports · 76
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The Pharmacological Characteristics of Molecular-Based Inherited Salt-Losing Tubulopathies
2010 · Kandai Nozu, Kazumoto Iijima, et al. · The Journal of Clinical Endocrinology & Metabolism · 64
Examination of the predicted prevalence of Gitelman syndrome by ethnicity based on genome databases
2021 · Atsushi Kondo, China Nagano, et al. · Scientific Reports · 55
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Treatment strategies for Henoch-Schönlein purpura nephritis by histological and clinical severity
2011 · Takeshi Ninchoji, Hiroshi Kaito, et al. · Pediatric Nephrology · 54
Clinical and genetic variability of PAX2-related disorder in the Japanese population
2020 · Rini Rossanti, Naoya Morisada, et al. · Journal of Human Genetics · 32
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Characterization of contiguous gene deletions in COL4A6 and COL4A5 in Alport syndrome-diffuse leiomyomatosis
2017 · Kandai Nozu, Shogo Minamikawa, et al. · Journal of Human Genetics · 31
Prevalence of Wilson disease based on genome databases in Japan
2020 · Hiroshi Yamaguchi, Hiroaki Nagase, et al. · Pediatrics International · 25
Genetic background, recent advances in molecular biology, and development of novel therapy in Alport syndrome
2020 · Kandai Nozu, Yutaka Takaoka, et al. · Kidney Research and Clinical Practice · 25
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Metabolomics analysis of umbilical cord blood clarifies changes in saccharides associated with delivery method
2012 · Fusako Hashimoto, Shin Nishiumi, et al. · Early Human Development · 25
Congenital chloride diarrhea needs to be distinguished from Bartter and Gitelman syndrome
2018 · Natsuki Matsunoshita, Kandai Nozu, et al. · Journal of Human Genetics · 24
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Somatic mosaicism and variant frequency detected by next-generation sequencing in X-linked Alport syndrome
2015 · Xue Jun Fu, Kandai Nozu, et al. · European Journal of Human Genetics · 24
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Genotype-Phenotype Correlation in WT1 Exon 8 to 9 Missense Variants
2021 · China Nagano, Yutaka Takaoka, et al. · Kidney International Reports · 22
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Female X-linked Alport syndrome with somatic mosaicism
2016 · Kana Yokota, Kandai Nozu, et al. · Clinical and Experimental Nephrology · 21
The utility of urinary CD80 as a diagnostic marker in patients with renal diseases
2018 · Shogo Minamikawa, Kandai Nozu, et al. · Scientific Reports · 20
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Impact of the State of Emergency during the COVID-19 Pandemic in 2020 on Asthma Exacerbations among Children in Kobe City, Japan
2021 · Hiroshi Yamaguchi, Kandai Nozu, et al. · International Journal of Environmental Research and Public Health · 17
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A comparison of splicing assays to detect an intronic variant of the OCRL gene in Lowe syndrome
2017 · Keita Nakanishi, Kandai Nozu, et al. · European Journal of Medical Genetics · 17
Rituximab treatment for relapsed opsoclonus–myoclonus syndrome
2015 · Daisaku Toyoshima, Naoya Morisada, et al. · Brain and Development · 17
The relationship between arginine vasopressin levels and hyponatremia following a percutaneous renal biopsy in children receiving hypotonic or isotonic intravenous fluids
2010 · Kyoko Kanda, Kandai Nozu, et al. · Pediatric Nephrology · 17
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 · 16
An in vitro splicing assay reveals the pathogenicity of a novel intronic variant in ATP6V0A4 for autosomal recessive distal renal tubular acidosis
2017 · Tomohiko Yamamura, Kandai Nozu, et al. · BMC Nephrology · 16
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Works count: 84
Citation count: 1,390
H-index: 19
I10-index: 37
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