Showing 1–14 of 14 results
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Research | | Open
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Research | | Open
Rare genetic variants in the gene encoding histone lysine demethylase 4C (KDM4C) and their contributions to susceptibility to schizophrenia and autism spectrum disorder
- Hidekazu Kato
- , Itaru Kushima
- , Daisuke Mori
- , Akira Yoshimi
- , Branko Aleksic
- , Yoshihiro Nawa
- , Miho Toyama
- , Sho Furuta
- , Yanjie Yu
- , Kanako Ishizuka
- , Hiroki Kimura
- , Yuko Arioka
- , Keita Tsujimura
- , Mako Morikawa
- , Takashi Okada
- , Toshiya Inada
- , Masahiro Nakatochi
- , Keiko Shinjo
- , Yutaka Kondo
- , Kozo Kaibuchi
- , Yasuko Funabiki
- , Ryo Kimura
- , Toshimitsu Suzuki
- , Kazuhiro Yamakawa
- , Masashi Ikeda
- , Nakao Iwata
- , Tsutomu Takahashi
- , Michio Suzuki
- , Yuko Okahisa
- , Manabu Takaki
- , Jun Egawa
- , Toshiyuki Someya
- & Norio Ozaki
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Research | | Open
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Research |
De novo truncating variants in PHF21A cause intellectual disability and craniofacial anomalies
- Kohei Hamanaka
- , Yuji Sugawara
- , Takeyoshi Shimoji
- , Tone Irene Nordtveit
- , Mitsuhiro Kato
- , Mitsuko Nakashima
- , Hirotomo Saitsu
- , Toshimitsu Suzuki
- , Kazuhiro Yamakawa
- , Ingvild Aukrust
- , Gunnar Houge
- , Satomi Mitsuhashi
- , Atsushi Takata
- , Kazuhiro Iwama
- , Ahmed Alkanaq
- , Atsushi Fujita
- , Eri Imagawa
- , Takeshi Mizuguchi
- , Noriko Miyake
- , Satoko Miyatake
- & Naomichi Matsumoto
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Research |
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Research |
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Research | | Open
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Research | | Open
Nav1.2 haplodeficiency in excitatory neurons causes absence-like seizures in mice
- Ikuo Ogiwara
- , Hiroyuki Miyamoto
- , Tetsuya Tatsukawa
- , Tetsushi Yamagata
- , Tojo Nakayama
- , Nafiseh Atapour
- , Eriko Miura
- , Emi Mazaki
- , Sara J. Ernst
- , Dezhi Cao
- , Hideyuki Ohtani
- , Shigeyoshi Itohara
- , Yuchio Yanagawa
- , Mauricio Montal
- , Michisuke Yuzaki
- , Yushi Inoue
- , Takao K. Hensch
- , Jeffrey L. Noebels
- & Kazuhiro Yamakawa
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Research |
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Reviews |
EFHC1 variants in juvenile myoclonic epilepsy: reanalysis according to NHGRI and ACMG guidelines for assigning disease causality
- Julia N. Bailey
- , Christopher Patterson
- , Laurence de Nijs
- , Reyna M. Durón
- , Viet-Huong Nguyen
- , Miyabi Tanaka
- , Marco T. Medina
- , Aurelio Jara-Prado
- , Iris E. Martínez-Juárez
- , Adriana Ochoa
- , Yolli Molina
- , Toshimitsu Suzuki
- , María E. Alonso
- , Jenny E. Wight
- , Yu-Chen Lin
- , Laura Guilhoto
- , Elza Marcia Targas Yacubian
- , Jesús Machado-Salas
- , Andrea Daga
- , Kazuhiro Yamakawa
- , Thierry M. Grisar
- , Bernard Lakaye
- & Antonio V. Delgado-Escueta
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Research |
Elfn1 recruits presynaptic mGluR7 in trans and its loss results in seizures
- Naoko H. Tomioka
- , Hiroki Yasuda
- , Hiroyuki Miyamoto
- , Minoru Hatayama
- , Naoko Morimura
- , Yoshifumi Matsumoto
- , Toshimitsu Suzuki
- , Maya Odagawa
- , Yuri S. Odaka
- , Yoshimi Iwayama
- , Ji Won Um
- , Jaewon Ko
- , Yushi Inoue
- , Sunao Kaneko
- , Shinichi Hirose
- , Kazuyuki Yamada
- , Takeo Yoshikawa
- , Kazuhiro Yamakawa
- & Jun Aruga
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Research |
Singular localization of sodium channel β4 subunit in unmyelinated fibres and its role in the striatum
- Haruko Miyazaki
- , Fumitaka Oyama
- , Ritsuko Inoue
- , Toshihiko Aosaki
- , Takaya Abe
- , Hiroshi Kiyonari
- , Yoshihiro Kino
- , Masaru Kurosawa
- , Jun Shimizu
- , Ikuo Ogiwara
- , Kazuhiro Yamakawa
- , Yoshinori Koshimizu
- , Fumino Fujiyama
- , Takeshi Kaneko
- , Hideaki Shimizu
- , Katsuhiro Nagatomo
- , Katsuya Yamada
- , Tomomi Shimogori
- , Nobutaka Hattori
- , Masami Miura
- & Nobuyuki Nukina
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Research |
Mutations in EFHC1 cause juvenile myoclonic epilepsy
- Toshimitsu Suzuki
- , Antonio V Delgado-Escueta
- , Kripamoy Aguan
- , Maria E Alonso
- , Jun Shi
- , Yuji Hara
- , Motohiro Nishida
- , Tomohiro Numata
- , Marco T Medina
- , Tamaki Takeuchi
- , Ryoji Morita
- , Dongsheng Bai
- , Subramaniam Ganesh
- , Yoshihisa Sugimoto
- , Johji Inazawa
- , Julia N Bailey
- , Adriana Ochoa
- , Aurelio Jara-Prado
- , Astrid Rasmussen
- , Jaime Ramos-Peek
- , Sergio Cordova
- , Francisco Rubio-Donnadieu
- , Yushi Inoue
- , Makiko Osawa
- , Sunao Kaneko
- , Hirokazu Oguni
- , Yasuo Mori
- & Kazuhiro Yamakawa