Takayuki Yokoi

Publication Activity (10 Years)

Years Active: 2018-2021
Publications (10 Years): 6

Top Topics

Intellectual Disability

Autism Spectrum Disorder

Top Venues

Pediatrics international : official journal of the Japan Pediatric Society

Congenital anomalies

American journal of medical genetics. Part A

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

Publications

Takayuki Yokoi, Yumi Enomoto, Yoshinori Tsurusaki, Noriaki Harada, Toshiyuki Saito, Jun-Ichi Nagai, Takuya Naruto, Kenji Kurosawa
An efficient genetic test flow for multiple congenital anomalies and intellectual disability. Pediatrics international : official journal of the Japan Pediatric Society 62 (5) (2021)
Takayuki Yokoi, Yumi Enomoto, Yoshinori Tsurusaki, Kenji Kurosawa
Siblings with vascular Ehlers-Danlos syndrome inherited via maternal mosaicism. Congenital anomalies 61 (3) (2021)
Hiroaki Murakami, Yoshinori Tsurusaki, Keisuke Enomoto, Yukiko Kuroda, Takayuki Yokoi, Noritaka Furuya, Hiroshi Yoshihashi, Mari Minatogawa, Chihiro Abe-Hatano, Ikuko Ohashi, Naoto Nishimura, Tatsuro Kumaki, Yumi Enomoto, Takuya Naruto, Fuminori Iwasaki, Noriaki Harada, Aki Ishikawa, Hiroshi Kawame, Kiyoko Sameshima, Yu Yamaguchi, Masahisa Kobayashi, Makiko Tominaga, Satoshi Ishikiriyama, Toshiaki Tanaka, Hiroshi Suzumura, Shinsuke Ninomiya, Akane Kondo, Tadashi Kaname, Kenjiro Kosaki, Mitsuo Masuno, Yoshikazu Kuroki, Kenji Kurosawa
Update of the genotype and phenotype of KMT2D and KDM6A by genetic screening of 100 patients with clinically suspected Kabuki syndrome. American journal of medical genetics. Part A 182 (10) (2020)
Takayuki Yokoi, Yumi Enomoto, Yoshinori Tsurusaki, Takuya Naruto, Kenji Kurosawa
Cantú syndrome with novel pathogenic variant in nucleotide-binding domain 1 of ABCC9. Pediatrics international : official journal of the Japan Pediatric Society 62 (10) (2020)
Takayuki Yokoi, Kenshi Sei, Yumi Enomoto, Takuya Naruto, Kenji Kurosawa
Somatic mosaicism of a heterogeneous mutation of ACTA1 in nemaline myopathy. Pediatrics international : official journal of the Japan Pediatric Society 61 (11) (2019)
Takayuki Yokoi, Toshiyuki Saito, Jun-Ichi Nagai, Kenji Kurosawa
17q21.32-q22 Deletion in a girl with osteogenesis imperfecta, tricho-dento-osseous syndrome, and intellectual disability. Congenital anomalies 59 (2) (2018)