Keisuke Nagasaki

Researcher Name Resolver ID ORCID

Publication Activity (10 Years)

Years Active: 2018-2024
Publications (10 Years): 41

Top Topics

Polycystic Kidney Disease

Top Venues

American journal of medical genetics. Part A

Congenital anomalies

BMJ case reports

Nature genetics

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

Publications

Satoshi Narumi, Keisuke Nagasaki, Mitsuo Kiriya, Erika Uehara, Kazuhisa Akiba, Kanako Tanase-Nakao, Kazuhiro Shimura, Kiyomi Abe, Chiho Sugisawa, Tomohiro Ishii, Kenichi Miyako, Yukihiro Hasegawa, Yoshihiro Maruo, Koji Muroya, Natsuko Watanabe, Eijun Nishihara, Yuka Ito, Takahiko Kogai, Kaori Kameyama, Kazuhiko Nakabayashi, Kenichiro Hata, Maki Fukami, Hirohito Shima, Atsuo Kikuchi, Jun Takayama, Gen Tamiya, Tomonobu Hasegawa
Functional variants in a TTTG microsatellite on 15q26.1 cause familial nonautoimmune thyroid abnormalities. Nature genetics 56 (5) (2024)
Takuya Fuse, Yuta Aizawa, Hiromi Nyuzuki, Kentaro Sawano, Keisuke Nagasaki, Akihiko Saitoh
Hypocarnitinemia in twins after maternal pivalate-conjugated antibiotic therapy. Pediatrics international : official journal of the Japan Pediatric Society 66 (1) (2024)
Noboru Uchida, Tomohiro Ishii, Gen Nishimura, Takeshi Sato, Gen Kuratsuji, Keisuke Nagasaki, Yuki Hosokawa, Eriko Adachi, Kei Takasawa, Kenichi Kashimada, Yuko Tsujioka, Tomonobu Hasegawa
RMRP-related short stature: A report of six additional Japanese individuals with cartilage hair hypoplasia and literature review. American journal of medical genetics. Part A 194 (6) (2024)
Nao Shibata, Chikahiko Numakura, Takashi Hamajima, Kenichi Miyako, Ikuma Fujiwara, Jun Mori, Akihiko Saitoh, Keisuke Nagasaki
Clinical and molecular analyses of isolated central congenital hypothyroidism based on a survey conducted in Japan. Endocrine journal 71 (5) (2024)
Nao Shibata, Chikahiko Numakura, Takashi Hamajima, Kenichi Miyako, Ikuma Fujiwara, Jun Mori, Akihiko Saitoh, Keisuke Nagasaki
Clinical and molecular analyses of isolated central congenital hypothyroidism based on a survey conducted in Japan. Endocrine journal (2024)
Hiromi Nyuzuki, Junichi Ozawa, Keisuke Nagasaki, Yosuke Nishio, Tomoo Ogi, Jun Tohyama, Takeshi Ikeuchi
A severe case of cardiospondylocarpofacial syndrome with a novel MAP3K7 variant. Human genome variation 11 (1) (2024)
Takanori Onuki, Tadokoro Hiroaki, Kentaro Sawano, Nao Shibata, Hiromi Nyuzuki, Yohei Ogawa, Masayasu Okada, Hirohito Sone, Keisuke Nagasaki
Robust growth hormone responses to GH-releasing peptide 2 in adolescents. Journal of pediatric endocrinology & metabolism : JPEM 37 (8) (2024)
Takanori Onuki, Tadokoro Hiroaki, Kentaro Sawano, Nao Shibata, Hiromi Nyuzuki, Yohei Ogawa, Masayasu Okada, Hirohito Sone, Keisuke Nagasaki
Robust growth hormone responses to GH-releasing peptide 2 in adolescents. Journal of pediatric endocrinology & metabolism : JPEM (2024)
Noboru Uchida, Tomohiro Ishii, Gen Nishimura, Takeshi Sato, Gen Kuratsuji, Keisuke Nagasaki, Yuki Hosokawa, Eriko Adachi, Kei Takasawa, Kenichi Kashimada, Yuko Tsujioka, Tomonobu Hasegawa
RMRP-related short stature: A report of six additional Japanese individuals with cartilage hair hypoplasia and literature review. American journal of medical genetics. Part A (2024)
Hiroyuki Saitou, Taichi Kitaoka, Takuo Kubota, Junko Kanno, Hiroshi Mochizuki, Toshimi Michigami, Kosei Hasegawa, Ikuma Fujiwara, Takashi Hamajima, Daisuke Harada, Yuko Seki, Keisuke Nagasaki, Sumito Dateki, Noriyuki Namba, Hirofumi Tokuoka, Jeanne M Pimenta, Shelda Cohen, Keiichi Ozono
Clinical outcomes and medical management of achondroplasia in Japanese children: A retrospective medical record review of clinical data. American journal of medical genetics. Part A 194 (8) (2024)
Noboru Uchida, Tomohiro Ishii, Gen Nishimura, Takeshi Sato, Gen Kuratsuji, Keisuke Nagasaki, Yuki Hosokawa, Eriko Adachi, Kei Takasawa, Kenichi Kashimada, Yuko Tsujioka, Tomonobu Hasegawa
RMRP-related short stature: A report of six additional Japanese individuals with cartilage hair hypoplasia and literature review. American journal of medical genetics. Part A 194 (6) (2024)
Hiromi Nyuzuki, Junichi Ozawa, Keisuke Nagasaki, Yosuke Nishio, Tomoo Ogi, Jun Tohyama, Takeshi Ikeuchi
A severe case of cardiospondylocarpofacial syndrome with a novel MAP3K7 variant. Human genome variation 11 (1) (2024)
Satoshi Narumi, Keisuke Nagasaki, Mitsuo Kiriya, Erika Uehara, Kazuhisa Akiba, Kanako Tanase-Nakao, Kazuhiro Shimura, Kiyomi Abe, Chiho Sugisawa, Tomohiro Ishii, Kenichi Miyako, Yukihiro Hasegawa, Yoshihiro Maruo, Koji Muroya, Natsuko Watanabe, Eijun Nishihara, Yuka Ito, Takahiko Kogai, Kaori Kameyama, Kazuhiko Nakabayashi, Kenichiro Hata, Maki Fukami, Hirohito Shima, Atsuo Kikuchi, Jun Takayama, Gen Tamiya, Tomonobu Hasegawa
Functional variants in a TTTG microsatellite on 15q26.1 cause familial nonautoimmune thyroid abnormalities. Nature genetics 56 (5) (2024)
Noboru Uchida, Tomohiro Ishii, Gen Nishimura, Takeshi Sato, Gen Kuratsuji, Keisuke Nagasaki, Yuki Hosokawa, Eriko Adachi, Kei Takasawa, Kenichi Kashimada, Yuko Tsujioka, Tomonobu Hasegawa
RMRP-related short stature: A report of six additional Japanese individuals with cartilage hair hypoplasia and literature review. American journal of medical genetics. Part A 194 (6) (2024)
Satoshi Narumi, Keisuke Nagasaki, Mitsuo Kiriya, Erika Uehara, Kazuhisa Akiba, Kanako Tanase-Nakao, Kazuhiro Shimura, Kiyomi Abe, Chiho Sugisawa, Tomohiro Ishii, Kenichi Miyako, Yukihiro Hasegawa, Yoshihiro Maruo, Koji Muroya, Natsuko Watanabe, Eijun Nishihara, Yuka Ito, Takahiko Kogai, Kaori Kameyama, Kazuhiko Nakabayashi, Kenichiro Hata, Maki Fukami, Hirohito Shima, Atsuo Kikuchi, Jun Takayama, Gen Tamiya, Tomonobu Hasegawa
Functional variants in a TTTG microsatellite on 15q26.1 cause familial nonautoimmune thyroid abnormalities. Nature genetics 56 (5) (2024)
Satoshi Narumi, Keisuke Nagasaki, Mitsuo Kiriya, Erika Uehara, Kazuhisa Akiba, Kanako Tanase-Nakao, Kazuhiro Shimura, Kiyomi Abe, Chiho Sugisawa, Tomohiro Ishii, Kenichi Miyako, Yukihiro Hasegawa, Yoshihiro Maruo, Koji Muroya, Natsuko Watanabe, Eijun Nishihara, Yuka Ito, Takahiko Kogai, Kaori Kameyama, Kazuhiko Nakabayashi, Kenichiro Hata, Maki Fukami, Hirohito Shima, Atsuo Kikuchi, Jun Takayama, Gen Tamiya, Tomonobu Hasegawa
Functional variants in a TTTG microsatellite on 15q26.1 cause familial nonautoimmune thyroid abnormalities. Nature genetics (2024)
Hiroyuki Saitou, Taichi Kitaoka, Takuo Kubota, Junko Kanno, Hiroshi Mochizuki, Toshimi Michigami, Kosei Hasegawa, Ikuma Fujiwara, Takashi Hamajima, Daisuke Harada, Yuko Seki, Keisuke Nagasaki, Sumito Dateki, Noriyuki Namba, Hirofumi Tokuoka, Jeanne M Pimenta, Shelda Cohen, Keiichi Ozono
Clinical outcomes and medical management of achondroplasia in Japanese children: A retrospective medical record review of clinical data. American journal of medical genetics. Part A (2024)
Satoshi Narumi, Keisuke Nagasaki, Mitsuo Kiriya, Erika Uehara, Kazuhisa Akiba, Kanako Tanase-Nakao, Kazuhiro Shimura, Kiyomi Abe, Chiho Sugisawa, Tomohiro Ishii, Kenichi Miyako, Yukihiro Hasegawa, Yoshihiro Maruo, Koji Muroya, Natsuko Watanabe, Eijun Nishihara, Yuka Ito, Takahiko Kogai, Kaori Kameyama, Kazuhiko Nakabayashi, Kenichiro Hata, Maki Fukami, Hirohito Shima, Atsuo Kikuchi, Jun Takayama, Gen Tamiya, Tomonobu Hasegawa
Functional variants in a TTTG microsatellite on 15q26.1 cause familial nonautoimmune thyroid abnormalities. Nature genetics 56 (5) (2024)
Mayumi Hosokawa, Yosuke Ichihashi, Yasunori Sato, Nao Shibata, Keisuke Nagasaki, Kento Ikegawa, Yukihiro Hasegawa, Takashi Hamajima, Fusa Nagamatsu, Shigeru Suzuki, Chikahiko Numakura, Naoko Amano, Goro Sasaki, Keiko Nagahara, Shun Soneda, Daisuke Ariyasu, Miwako Maeda, Hotaka Kamasaki, Keiko Aso, Tomonobu Hasegawa, Tomohiro Ishii
Incidence and Risk Factors for Adrenal Crisis in Pediatric-onset Adrenal Insufficiency: A Prospective Study. The Journal of clinical endocrinology and metabolism 109 (8) (2024)
Hiroyuki Saitou, Taichi Kitaoka, Takuo Kubota, Junko Kanno, Hiroshi Mochizuki, Toshimi Michigami, Kosei Hasegawa, Ikuma Fujiwara, Takashi Hamajima, Daisuke Harada, Yuko Seki, Keisuke Nagasaki, Sumito Dateki, Noriyuki Namba, Hirofumi Tokuoka, Jeanne M Pimenta, Shelda Cohen, Keiichi Ozono
Clinical outcomes and medical management of achondroplasia in Japanese children: A retrospective medical record review of clinical data. American journal of medical genetics. Part A 194 (8) (2024)
Kyoko Fukahori, Jun Nirei, Kaoru Yamawaki, Keisuke Nagasaki
Cyclic intravenous pamidronate for an infant with osteogenesis imperfecta type II. BMJ case reports 16 (5) (2023)
Yugo Kawakami, Kentaro Sawano, Nao Shibata, Takayuki Kaneko, Keisuke Nagasaki
Klinefelter syndrome with penoscrotal transposition and diphallia: A case study. Congenital anomalies (2023)
Kyoko Fukahori, Jun Nirei, Kaoru Yamawaki, Keisuke Nagasaki
Cyclic intravenous pamidronate for an infant with osteogenesis imperfecta type II. BMJ case reports 16 (5) (2023)
Takanori Onuki, Shota Hiroshima, Kentaro Sawano, Nao Shibata, Yohei Ogawa, Keisuke Nagasaki, Hiromi Nyuzuki
A Study of Maternal Patients Diagnosed with Inborn Errors of Metabolism Due to Positive Newborn Mass Screening in Their Newborns. Children (Basel, Switzerland) 10 (8) (2023)
Kyoko Fukahori, Jun Nirei, Kaoru Yamawaki, Keisuke Nagasaki
Cyclic intravenous pamidronate for an infant with osteogenesis imperfecta type II. BMJ case reports 16 (5) (2023)
Mayumi Hosokawa, Yosuke Ichihashi, Yasunori Sato, Nao Shibata, Keisuke Nagasaki, Kento Ikegawa, Yukihiro Hasegawa, Takashi Hamajima, Fusa Nagamatsu, Shigeru Suzuki, Chikahiko Numakura, Naoko Amano, Goro Sasaki, Keiko Nagahara, Shun Soneda, Daisuke Ariyasu, Miwako Maeda, Hotaka Kamasaki, Keiko Aso, Tomonobu Hasegawa, Tomohiro Ishii
Incidence and Risk Factors for Adrenal Crisis in Pediatric-onset Adrenal Insufficiency: A Prospective Study. The Journal of clinical endocrinology and metabolism (2023)
Kyoko Fukahori, Kentaro Sawano, Hiroshi Yoshida, Keisuke Nagasaki
Asymmetrical Graves' disease in children: potential usefulness of potassium iodide monotherapy. BMJ case reports 15 (4) (2022)
Shota Hiroshima, Chihiro Taniguchi, Mika Inoue, Hirohito Sone, Keisuke Nagasaki
Two cases of 22q11.2 deletion syndrome with decreased serum calcium during recovery following thyrotoxicosis. Congenital anomalies 62 (6) (2022)
Kazutaka Morota, Hiroaki Tadokoro, Kentaro Sawano, Kenichi Watanabe, Naoko Iwata, Haruki Fujisawa, Atsushi Suzuki, Yoshihisa Sugimura, Keisuke Nagasaki
A 7-year-old boy with central diabetes insipidus presenting with thickened pituitary stalk and anti-rabphilin-3A antibody positivity. Journal of pediatric endocrinology & metabolism : JPEM 35 (5) (2022)
Mizuki Tani, Shota Hiroshima, Hidetoshi Sato, Kentaro Sawano, Yohei Ogawa, Masaru Imamura, Makoto Oishi, Keisuke Nagasaki
Infantile-Onset Isolated Neurohypophyseal Langerhans Cell Histiocytosis with Central Diabetes Insipidus: A Case Report. Children (Basel, Switzerland) 9 (5) (2022)
Kyoko Fukahori, Kaori Yamoto, Hirotomo Saitsu, Tsutomu Ogata, Keisuke Nagasaki
PORCN-related microphthalmia with limb anomalies: Case report and literature review. American journal of medical genetics. Part A (2022)
Keisuke Nagasaki, Hidetoshi Sato, Sunao Sasaki, Hiromi Nyuzuki, Nao Shibata, Kentaro Sawano, Shota Hiroshima, Tadashi Asami
Re-Evaluation of the Prevalence of Permanent Congenital Hypothyroidism in Niigata, Japan: A Retrospective Study. International journal of neonatal screening 7 (2) (2021)
Shota Hiroshima, Hiromi Nyuzuki, Sunao Sasaki, Yohei Ogawa, Keisuke Nagasaki
Regulation of Serum Sodium Levels during Chemotherapy Using Selective Arginine Vasopressin V2-Receptor Antagonist Tolvaptan in a Four-Year-Old Girl with a Suprasellar Germ Cell Tumor. Children (Basel, Switzerland) 8 (4) (2021)
Takanori Onuki, Yoshiaki Ohtsu, Shota Hiroshima, Kentaro Sawano, Keisuke Nagasaki
Two cases of cytochrome P450 oxidoreductase deficiency with severe scoliosis and surgery requirement. Congenital anomalies 61 (5) (2021)
Kentaro Sawano, Keisuke Nagasaki
Carotenoderma with hypothyroidism. Archives of disease in childhood (2021)
Shota Hiroshima, Yushi Ueki, Keisuke Yamazaki, Keisuke Nagasaki
Graves' disease in children: an enlarged goitre causes severe tracheal stenosis. BMJ case reports 14 (11) (2021)
Takanori Onuki, Nao Shibata, Shota Hiroshima, Kentaro Sawano, Keisuke Nagasaki
A Japanese family with a heterozygous novel mutation in the Indian hedgehog gene exhibiting a broad spectrum of clinical features and radiological findings. Congenital anomalies (2021)
Yukie Izumita, Satsuki Nishigaki, Mari Satoh, Noriyuki Takubo, Chikahiko Numakura, Ikuko Takahashi, Shun Soneda, Yoshifusa Abe, Hotaka Kamasaki, Yoshiaki Ohtsu, Junko Igaki, Yukihiro Hasegawa, Keisuke Nagasaki
Retrospective study of the renal function using estimated glomerular filtration rate and congenital anomalies of the kidney-urinary tract in pediatric Turner syndrome. Congenital anomalies 60 (6) (2020)
Mami Miyado, Maki Fukami, Shuji Takada, Miho Terao, Kazuhiko Nakabayashi, Kenichiro Hata, Yoichi Matsubara, Yoko Tanaka, Goro Sasaki, Keisuke Nagasaki, Masaaki Shiina, Kazuhiro Ogata, Youhei Masunaga, Hirotomo Saitsu, Tsutomu Ogata
Germline-Derived Gain-of-Function Variants of Gsα-Coding GNAS Gene Identified in Nephrogenic Syndrome of Inappropriate Antidiuresis. Journal of the American Society of Nephrology : JASN 30 (5) (2019)
Keisuke Nagasaki, Gen Nishimura, Toru Kikuchi, Hiromi Nyuzuki, Sunao Sasaki, Yohei Ogawa, Akihiko Saitoh
Nonsense mutations in FZD2 cause autosomal-dominant omodysplasia: Robinow syndrome-like phenotypes. American journal of medical genetics. Part A 176 (3) (2018)
Hiromi Nyuzuki, Takahiko Kogai, Akira Hishinuma, Yohei Ogawa, Akihiko Saitoh, Keisuke Nagasaki
PTEN mutation in a Japanese boy with autonomously functioning thyroid nodule. Pediatrics international : official journal of the Japan Pediatric Society 59 (11) (2018)