Satoru Takahashi

ORCID

Publication Activity (10 Years)

Years Active: 2019-2024
Publications (10 Years): 6

Top Venues

Congenital anomalies

Molecular genetics & genomic medicine

Neurology

Human genome variation

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

Publications

Toshio Okamoto, Ken Nagaya, Mitsumaro Nii, Satoru Takahashi
Non-progressive hepatic tumor with high levels of serum alpha-fetoprotein in two infants with trisomy 18. Congenital anomalies (2024)
Rina Imanishi, Kouichi Nakau, Sorachi Shimada, Hideharu Oka, Ryo Takeguchi, Ryosuke Tanaka, Tatsutoshi Sugiyama, Mitsumaro Nii, Toshio Okamoto, Ken Nagaya, Yoshio Makita, Kumiko Yanagi, Tadashi Kaname, Satoru Takahashi
A novel HECW2 variant in an infant with congenital long QT syndrome. Human genome variation 10 (1) (2023)
Yukihiro Sato, Eiji Yoshioka, Yasuaki Saijo, Yasuhito Kato, Ken Nagaya, Satoru Takahashi, Yoshiya Ito, Sumitaka Kobayashi, Yu Ait Bamai, Keiko Yamazaki, Sachiko Itoh, Chihiro Miyashita, Atsuko Ikeda-Araki, Reiko Kishi, null null
Associated congenital anomalies and syndromes of 248 infants with orofacial clefts born between 2011 and 2014 in the Japan environment and children's study. Congenital anomalies (2022)
Tomohiro Wakabayashi, Shinobu Fukumura, Satoru Takahashi, Kenji Kurosawa, Shuichi Miyamoto, Kosuke Tsuchida, Shinsuke Kato, Takeshi Tsugawa, Yoshiyuki Sakai, Yukihiko Kawasaki
Stereotyped Upper Limb Movement in MECP2 Duplication Syndrome. Neurology 97 (2) (2021)
Satoru Takahashi, Ryo Takeguchi, Mami Kuroda, Ryosuke Tanaka
Atypical Rett syndrome in a girl with mosaic triple X and MECP2 variant. Molecular genetics & genomic medicine 8 (3) (2020)
Ryo Takeguchi, Satoru Takahashi, Mami Kuroda, Ryosuke Tanaka, Nao Suzuki, Yuko Tomonoh, Yukiko Ihara, Nobuyoshi Sugiyama, Masayuki Itoh
MeCP2_e2 partially compensates for lack of MeCP2_e1: A male case of Rett syndrome. Molecular genetics & genomic medicine 8 (2) (2019)

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Publication Activity (10 Years)

Top Topics

Top Venues

Satoru Takahashi