日期:
2020 年 — 2026 年
2020
2021
2022
2023
2024
2025
2026
影响因子:

Exome sequencing analysis of Japanese autism spectrum disorder case-control sample supports an increased burden of synaptic function-related genes

对日本自闭症谱系障碍病例对照样本的外显子组测序分析表明,突触功能相关基因的负担增加。

Kimura, Hiroki; Nakatochi, Masahiro; Aleksic, Branko; Guevara, James; Toyama, Miho; Hayashi, Yu; Kato, Hidekazu; Kushima, Itaru; Morikawa, Mako; Ishizuka, Kanako; Okada, Takashi; Tsurusaki, Yoshinori; Fujita, Atsushi; Miyake, Noriko; Ogi, Tomoo; Takata, Atsushi; Matsumoto, Naomichi; Buxbaum, Joseph; Ozaki, Norio; Sebat, Jonathan

Severe achondroplasia due to two de novo variants in the transmembrane domain of FGFR3 on the same allele: A case report.

同一等位基因上 FGFR3 跨膜结构域的两个新生变异导致的严重软骨发育不全:病例报告

Nagata Tadashi, Matsushita Masaki, Mishima Kenichi, Kamiya Yasunari, Kato Kohji, Toyama Miho, Ogi Tomoo, Ishiguro Naoki, Kitoh Hiroshi

Methylation analysis for postpartum depression: a case control study

产后抑郁症的甲基化分析:一项病例对照研究

Nakamura, Yukako; Nakatochi, Masahiro; Kunimoto, Shohko; Okada, Takashi; Aleksic, Branko; Toyama, Miho; Shiino, Tomoko; Morikawa, Mako; Yamauchi, Aya; Yoshimi, Akira; Furukawa-Hibi, Yoko; Nagai, Taku; Ohara, Masako; Kubota, Chika; Yamada, Kiyofumi; Ando, Masahiko; Ozaki, Norio