Koichi Nakanishi

ORCID

Publication Activity (10 Years)

Years Active: 2016-2024
Publications (10 Years): 25

Top Venues

Pediatric nephrology (Berlin, Germany)

Journal of human genetics

Clinical and experimental nephrology

Human genome variation

This page only lists publications with an associated author ORCID identifier.

Publications

Wataru Shimabukuro, Yasutsugu Chinen, Naoya Imanaga, Kumiko Yanagi, Tadashi Kaname, Koichi Nakanishi
Renal coloboma syndrome/dominant optic atrophy with severe retinal atrophy and de novo digenic mutations in PAX2 and OPA1. Pediatric nephrology (Berlin, Germany) 39 (8) (2024)
Wataru Shimabukuro, Yasutsugu Chinen, Naoya Imanaga, Kumiko Yanagi, Tadashi Kaname, Koichi Nakanishi
Renal coloboma syndrome/dominant optic atrophy with severe retinal atrophy and de novo digenic mutations in PAX2 and OPA1. Pediatric nephrology (Berlin, Germany) (2024)
Wataru Shimabukuro, Yasutsugu Chinen, Naoya Imanaga, Kumiko Yanagi, Tadashi Kaname, Koichi Nakanishi
Renal coloboma syndrome/dominant optic atrophy with severe retinal atrophy and de novo digenic mutations in PAX2 and OPA1. Pediatric nephrology (Berlin, Germany) 39 (8) (2024)
Wataru Shimabukuro, Shogo Nakada, Kohei Shimada, Mayumi Tsukayama, Kazuya Hamada, Hideki Goya, Noriko Kinjo, Tomohide Yoshida, Keiko Mekaru, Koichi Nakanishi
Relationship between the serum creatinine concentrations of preterm neonates within 24 h of birth and their mothers before delivery. Clinical and experimental nephrology 28 (4) (2023)
Wataru Shimabukuro, Shogo Nakada, Kohei Shimada, Mayumi Tsukayama, Kazuya Hamada, Hideki Goya, Noriko Kinjo, Tomohide Yoshida, Keiko Mekaru, Koichi Nakanishi
Relationship between the serum creatinine concentrations of preterm neonates within 24 h of birth and their mothers before delivery. Clinical and experimental nephrology 28 (4) (2023)
Wataru Shimabukuro, Shogo Nakada, Kohei Shimada, Mayumi Tsukayama, Kazuya Hamada, Hideki Goya, Noriko Kinjo, Tomohide Yoshida, Keiko Mekaru, Koichi Nakanishi
Relationship between the serum creatinine concentrations of preterm neonates within 24 h of birth and their mothers before delivery. Clinical and experimental nephrology (2023)
Wataru Shimabukuro, Satoru Hamada, Tokiko Oshiro, Shougo Nakada, Nobuyuki Hyakuna, Koichi Nakanishi
High serum cystatin C levels in juvenile myelomonocytic leukemia patients without abnormal kidney function. Pediatric nephrology (Berlin, Germany) 37 (7) (2022)
Yasutsugu Chinen, Sadao Nakamura, Kumiko Yanagi, Takuya Kaneshi, Hideki Goya, Tomohide Yoshida, Kazuhito Satou, Tadashi Kaname, Kenji Naritomi, Koichi Nakanishi
Additional findings of tibial dysplasia in a male with orofaciodigital syndrome type XVI. Human genome variation 9 (1) (2022)
Nana Sakakibara, Kandai Nozu, Tomohiko Yamamura, Tomoko Horinouchi, China Nagano, Ming Juan Ye, Shinya Ishiko, Yuya Aoto, Rini Rossanti, Riku Hamada, Nobuhiko Okamoto, Yuko Shima, Koichi Nakanishi, Masafumi Matsuo, Kazumoto Iijima, Naoya Morisada
Comprehensive genetic analysis using next-generation sequencing for the diagnosis of nephronophthisis-related ciliopathies in the Japanese population. Journal of human genetics 67 (7) (2022)
Akinari Sekine, Sumi Hidaka, Tomofumi Moriyama, Yasuto Shikida, Keiji Shimazu, Eiji Ishikawa, Kiyotaka Uchiyama, Hiroshi Kataoka, Haruna Kawano, Mahiro Kurashige, Mai Sato, Tatsuya Suwabe, Shinya Nakatani, Tadashi Otsuka, Hirayasu Kai, Kan Katayama, Shiho Makabe, Shun Manabe, Wataru Shimabukuro, Koichi Nakanishi, Saori Nishio, Fumihiko Hattanda, Kazushige Hanaoka, Kenichiro Miura, Hiroki Hayashi, Junichi Hoshino, Ken Tsuchiya, Toshio Mochizuki, Shigeo Horie, Ichiei Narita, Satoru Muto
Cystic Kidney Diseases That Require a Differential Diagnosis from Autosomal Dominant Polycystic Kidney Disease (ADPKD). Journal of clinical medicine 11 (21) (2022)
Nobuo Kanazawa, Hiroaki Hemmi, Noriko Kinjo, Hidenori Ohnishi, Jun Hamazaki, Hiroyuki Mishima, Akira Kinoshita, Tsunehiro Mizushima, Satoru Hamada, Kazuya Hamada, Norio Kawamoto, Saori Kadowaki, Yoshitaka Honda, Kazushi Izawa, Ryuta Nishikomori, Miyuki Tsumura, Yusuke Yamashita, Shinobu Tamura, Takashi Orimo, Toshiya Ozasa, Takashi Kato, Izumi Sasaki, Yuri Fukuda-Ohta, Naoko Wakaki-Nishiyama, Yutaka Inaba, Kayo Kunimoto, Satoshi Okada, Takeshi Taketani, Koichi Nakanishi, Shigeo Murata, Koh-Ichiro Yoshiura, Tsuneyasu Kaisho
Heterozygous missense variant of the proteasome subunit β-type 9 causes neonatal-onset autoinflammation and immunodeficiency. Nature communications 12 (1) (2021)
Rini Rossanti, Tomoko Horinouchi, Tomohiko Yamamura, China Nagano, Nana Sakakibara, Shinya Ishiko, Yuya Aoto, Atsushi Kondo, Sadayuki Nagai, Eri Okada, Shingo Ishimori, Hiroaki Nagase, Satoshi Matsui, Keiichi Tamagaki, Yoshifumi Ubara, Masahiko Nagahama, Yuko Shima, Koichi Nakanishi, Takeshi Ninchoji, Masafumi Matsuo, Kazumoto Iijima, Kandai Nozu
Evaluation of Suspected Autosomal Alport Syndrome Synonymous Variants. Kidney360 3 (3) (2021)
Yasutsugu Chinen, Kumiko Yanagi, Sadao Nakamura, Noriko Nakayama, Motoko Kamiya, Mami Nakayashiro, Tadashi Kaname, Kenji Naritomi, Koichi Nakanishi
A novel homozygous missense SLC25A20 mutation in three CACT-deficient patients: clinical and autopsy data. Human genome variation 7 (2020)
Yuko Shima, Koichi Nakanishi, Hironobu Mukaiyama, Yu Tanaka, Takuzo Wada, Ryojiro Tanaka, Hiroshi Kaito, Kandai Nozu, Mayumi Sako, Kazumoto Iijima, Norishige Yoshikawa
Clinicopathological significance of glomerular capillary IgA deposition in childhood IgA nephropathy. Pediatric nephrology (Berlin, Germany) 36 (4) (2020)
Yuko Shima, Koichi Nakanishi, Taketsugu Hama, Hironobu Mukaiyama, Masashi Sato, Yu Tanaka, Ryojiro Tanaka, Hiroshi Kaito, Kandai Nozu, Mayumi Sako, Kazumoto Iijima, Norishige Yoshikawa
Crescentic IgA nephropathy in children. Pediatric nephrology (Berlin, Germany) 35 (6) (2020)
Tomohide Yoshida, Hideki Goya, Nobuhiro Iida, Mayumi Arakaki, Naoya Sanabe, Koichi Nakanishi
Early parenteral nutrition in neonates with congenital diaphragmatic hernia. Pediatrics international : official journal of the Japan Pediatric Society 62 (2) (2020)
Shogo Minamikawa, Saori Miwa, Tetsuji Inagaki, Kei Nishiyama, Hiroshi Kaito, Takeshi Ninchoji, Tomohiko Yamamura, China Nagano, Nana Sakakibara, Shingo Ishimori, Shigeo Hara, Norishige Yoshikawa, Daishi Hirano, Ryoko Harada, Riku Hamada, Natsuki Matsunoshita, Michio Nagata, Yuko Shima, Koichi Nakanishi, Hiroaki Nagase, Hiroki Takeda, Naoya Morisada, Kazumoto Iijima, Kandai Nozu
Molecular mechanisms determining severity in patients with Pierson syndrome. Journal of human genetics 65 (4) (2020)
Yasutsugu Chinen, Sadao Nakamura, Takuya Kaneshi, Mami Nakayashiro, Kumiko Yanagi, Tadashi Kaname, Kenji Naritomi, Koichi Nakanishi
A novel nonsense SMC1A mutation in a patient with intractable epilepsy and cardiac malformation. Human genome variation 6 (2019)
Yuko Shima, Koichi Nakanishi, Yoshitsugu Kaku, Kenji Ishikura, Hiroshi Hataya, Takeshi Matsuyama, Masataka Honda, Mayumi Sako, Kandai Nozu, Ryojiro Tanaka, Kazumoto Iijima, Norishige Yoshikawa, null null
Combination therapy with or without warfarin and dipyridamole for severe childhood IgA nephropathy: an RCT. Pediatric nephrology (Berlin, Germany) 33 (11) (2018)
Taketsugu Hama, Koichi Nakanishi, Kenji Ishikura, Shuichi Ito, Hidefumi Nakamura, Mayumi Sako, Mari Saito-Oba, Kandai Nozu, Yuko Shima, Kazumoto Iijima, Norishige Yoshikawa, null null
Study protocol: high-dose mizoribine with prednisolone therapy in short-term relapsing steroid-sensitive nephrotic syndrome to prevent frequent relapse (JSKDC05 trial). BMC nephrology 19 (1) (2018)
Shogo Minamikawa, Kandai Nozu, Yoshimi Nozu, Tomohiko Yamamura, Mariko Taniguchi-Ikeda, Keita Nakanishi, Junya Fujimura, Tomoko Horinouchi, Yuko Shima, Koichi Nakanishi, Masuji Hattori, Kyoko Kanda, Ryojiro Tanaka, Naoya Morisada, China Nagano, Nana Sakakibara, Hiroaki Nagase, Ichiro Morioka, Hiroshi Kaito, Kazumoto Iijima
Development of ultra-deep targeted RNA sequencing for analyzing X-chromosome inactivation in female Dent disease. Journal of human genetics 63 (5) (2018)
Yuko Shima, Koichi Nakanishi, Mayumi Sako, Mari Saito-Oba, Yuko Hamasaki, Hiroshi Hataya, Masataka Honda, Koichi Kamei, Kenji Ishikura, Shuichi Ito, Hiroshi Kaito, Ryojiro Tanaka, Kandai Nozu, Hidefumi Nakamura, Yasuo Ohashi, Kazumoto Iijima, Norishige Yoshikawa, null null
Lisinopril versus lisinopril and losartan for mild childhood IgA nephropathy: a randomized controlled trial (JSKDC01 study). Pediatric nephrology (Berlin, Germany) 34 (5) (2018)
Nana Sakakibara, Naoya Morisada, Kandai Nozu, Koji Nagatani, Toshiyuki Ohta, Junya Shimizu, Takuzo Wada, Yuko Shima, Tomohiko Yamamura, Shogo Minamikawa, Junya Fujimura, Tomoko Horinouchi, China Nagano, Akemi Shono, Ming Juan Ye, Yoshimi Nozu, Koichi Nakanishi, Kazumoto Iijima
Clinical spectrum of male patients with OFD1 mutations. Journal of human genetics 64 (1) (2018)
Taketsugu Hama, Koichi Nakanishi, Masashi Sato, Hironobu Mukaiyama, Hiroko Togawa, Yuko Shima, Masayasu Miyajima, Kandai Nozu, Shizuko Nagao, Hisahide Takahashi, Mayumi Sako, Kazumoto Iijima, Norishige Yoshikawa, Hiroyuki Suzuki
Aberrant Smad3 phosphoisoforms in cyst-lining epithelial cells in the cpk mouse, a model of autosomal recessive polycystic kidney disease. American journal of physiology. Renal physiology 313 (6) (2017)
Yuko Shima, Koichi Nakanishi, Masashi Sato, Taketsugu Hama, Hironobu Mukaiyama, Hiroko Togawa, Ryojiro Tanaka, Kandai Nozu, Mayumi Sako, Kazumoto Iijima, Hiroyuki Suzuki, Norishige Yoshikawa
IgA nephropathy with presentation of nephrotic syndrome at onset in children. Pediatric nephrology (Berlin, Germany) 32 (3) (2016)

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Publication Activity (10 Years)

Top Topics

Top Venues

Koichi Nakanishi