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

Molecular Variations in Glycoprotein B of Asian Human Cytomegalovirus: Potential Impact on Virus Entry and Immune Evasion in Ocular Diseases

亚洲人巨细胞病毒糖蛋白B的分子变异:对病毒入侵和眼部疾病免疫逃逸的潜在影响

Lestari, Tantri; Yawata, Nobuyo; Gonzalez, Gabriel; Miyadera, Hiroko; Motooka, Daisuke; Imamura, Yuko; Oki, Hiroya; Mori, Yasuo; Shirane, Mariko; Khor, Seik-Soon; Omae, Yosuke; Shimada, Mihoko; Windy, Dyah Ayu; Nakano, Satoko; Tsutsui, Hiroki; Kuramoto, Shiori; Fukui, Chihiro; Nakamura, Riku; Yamana, Satoshi; Kaburaki, Toshikatsu; Mashimo, Hisashi; Takase, Hiroshi; Yanai, Ryoji; Hasegawa, Eiichi; Shibata, Kensuke; Yawata, Makoto; Tokunaga, Katsushi; Ohguro, Nobuyuki; Sonoda, Koh-Hei

Novel Genetic Loci for Nontuberculous Mycobacterial Pulmonary Disease and Potential Protective Effect of Body Mass Index

非结核分枝杆菌肺病的新基因位点及体重指数的潜在保护作用

Park, Kyungtaek; Kim, Hyejin; Huh, Hee Jae; Namkoong, Ho; Hasegawa, Naoki; Nishimura, Tomoyasu; Asakura, Takanori; Morimoto, Kozo; Kurashima, Atsuyuki; Omae, Yosuke; Kawai, Yosuke; Tokunaga, Katsushi; Berghout, Joanne; Fennelly, Kevin P; Holland, Steven M; Cho, Jaeyoung; Yim, Jae-Joon; Won, Sungho; Jhun, Byung Woo; Won, Hong-Hee

Impact of germline variants on breast and ovarian cancer risk in Japanese women: an original cohort study and meta-analysis

生殖系变异对日本女性乳腺癌和卵巢癌风险的影响:一项原创队列研究和荟萃分析

Yazaki, Shu; Hori, Megumi; Aiba, Hisaki; Momozawa, Yukihide; Yoshida, Masayuki; Shiino, Sho; Harano, Kenichi; Yamauchi, Chisako; Yamanaka, Takashi; Miwa, Maiko; Matsuda, Koichi; Kawai, Yosuke; Kobayashi-Kato, Mayumi; Kitagawa, Masakazu; Saito, Motonobu; Nakagomi, Hiroshi; Tachibana, Kazunoshin; Sakamoto, Ikuko; Takahashi, Kazuaki; Asami, Yuka; Katanoda, Kota; Kuchiba, Aya; Yoshida, Hiroshi; Ishikawa, Mitsuya; Shimoi, Tastunori; Sudo, Kazuki; Shimizu, Chikako; Shimomura, Akihiko; Murata, Takeshi; Yamashita, Yuji; Kogawa, Takahiro; Fujiwara, Saori; Saji, Haruya; Kato, Hisamori; Miyagi, Etsuko; Iwasaki, Yusuke; Aoi, Tomomi; Takata, Sadaaki; Ogasawara, Aiko; Ohtake, Tohru; Fujimori, Keiya; Hirotsu, Yosuke; Nagashima, Minoru; Komatsu, Masaaki; Hamamoto, Ryuji; Hirata, Makoto; Yoshida, Teruhiko; Honda, Takayuki; Hiranuma, Kengo; Matsuda, Maiko; Shimada, Yoko; Sunami, Kuniko; Noiri, Eisei; Omae, Yosuke; Matsumoto, Koji; Okamoto, Aikou; Omata, Masao; Watanabe, Takafumi; Miyagi, Yohei; Murakami, Yoshinori; Tokunaga, Katsushi; Hasegawa, Kosei; Kato, Tomoyasu; Onishi, Tatsuya; Yamashita, Toshinari; Naito, Yoichi; Suto, Akihiko; Yonemori, Kan; Kohno, Takashi; Shiraisihi, Kouya

Genome sequencing provides high diagnostic yield and new etiological insights for intellectual disability and developmental delay

基因组测序能够提供高诊断率,并为智力障碍和发育迟缓的病因学研究提供新的见解。

Hamanaka, Kohei; Fujita, Atsushi; Miyatake, Satoko; Misawa, Kazuharu; Koshimizu, Eriko; Uchiyama, Yuri; Tsuchida, Naomi; Seyama, Rie; Sakamoto, Masamune; Iwama, Kazuhiro; Nishimura, Naoto; Utsuno, Yasuhiro; Fu, Li; Takizawa, Marina; Liang, Qiaowei; Itai, Toshiyuki; Saida, Ken; Ohori, Sachiko; Kameyama, Shinichi; Fukuda, Hiromi; Hayashi, Yukina; Inoue, Yuta; Goto, Tomohide; Ichikawa, Kazushi; Kuki, Ichiro; Fukuoka, Masataka; Kim, Kiyohiro; Shiohama, Tadashi; Shimoda, Konomi; Otsuka, Kosuke; Ueda, Yuki; Cho, Kazutoshi; Yuge, Kotaro; Tachi, Nobutada; Yoshida, Masaki; Daida, Atsuro; Hirasawa, Kyoko; Yanagishita, Tomoe; Yamamoto, Toshiyuki; Shirai, Kentaro; Mehr, Tammar Fixler; Fattal-Valevski, Aviva; Lev, Dorit; Yokoyama, Haruna; Iwabuchi, Emi; Saito, Yoshihiko; Miura, Masaki; Sugai, Kenji; Ishiyama, Akihiko; Sasaki, Masayuki; Watanabe, Yoshihiro; Takanashi, Jun-Ichi; Kim, Chong Ae; Yokochi, Kenji; Tohyama, Jun; Mori, Tatsuo; Izumi, Yuishin; Hasegawa, Yuiko; Okamoto, Nobuhiko; Ikeda, Takahiro; Osaka, Hitoshi; Kawai, Yosuke; Omae, Yosuke; Tokunaga, Katsushi; Kato, Mitsuhiro; Mizuguchi, Takeshi; Matsumoto, Naomichi

Genome-wide association study of common side effects following COVID-19 booster vaccination in a cohort of corporate employees in Japan

日本企业员工群体中新冠加强疫苗接种后常见副作用的全基因组关联研究

Omae, Yosuke; Khor, Seik-Soon; Shimada, Mihoko; Kawai, Yosuke; Yamaguchi, Taihei; Yagi, Maiko; Ebisawa, Masashi; Takeuchi, Junko S; Mizoue, Tetsuya; Sugiura, Wataru; Tokunaga, Katsushi

Identification of region-specific gene isoforms in the human brain using long-read transcriptome sequencing

利用长读长转录组测序技术鉴定人脑中区域特异性基因异构体

Shimada, Mihoko; Omae, Yosuke; Kakita, Akiyoshi; Gabdulkhaev, Ramil; Hitomi, Yuki; Miyagawa, Taku; Honda, Makoto; Fujimoto, Akihiro; Tokunaga, Katsushi

Identification of the hybrid gene LILRB5-3 by long-read sequencing and implication of its novel signaling function

利用长读长测序技术鉴定杂合基因LILRB5-3及其新型信号传导功能

Hirayasu, Kouyuki; Khor, Seik-Soon; Kawai, Yosuke; Shimada, Mihoko; Omae, Yosuke; Hasegawa, Gen; Hashikawa, Yuko; Tanimoto, Hiromu; Ohashi, Jun; Hosomichi, Kazuyoshi; Tajima, Atsushi; Nakamura, Hiroyuki; Nakamura, Minoru; Tokunaga, Katsushi; Hanayama, Rikinari; Nagasaki, Masao

Large-Scale Whole-Genome Analysis of HTLV-1-Associated Myelopathy Identified Hereditary Spastic Paraplegias

HTLV-1相关脊髓病的大规模全基因组分析发现了遗传性痉挛性截瘫

Takao, Naoki; Yagishita, Naoko; Araya, Natsumi; Aratani, Satoko; Yamauchi, Junji; Takahashi, Katsunori; Kunitomo, Yasuo; Sato, Tomoo; Nakamori, Masahiro; Kawai, Yosuke; Omae, Yosuke; Tokunaga, Katsushi; Matsuda, Fumihiko; Mitsuhashi, Satomi; Yamano, Yoshihisa

Association study of GBA1 variants with MSA based on comprehensive sequence analysis -Pitfalls in short-read sequence analysis depending on the human reference genome

基于全面序列分析的GBA1变异与MSA关联研究——依赖人类参考基因组的短读长序列分析的陷阱

Orimo, Kenta; Mitsui, Jun; Matsukawa, Takashi; Tanaka, Masaki; Nomoto, Junko; Ishiura, Hiroyuki; Omae, Yosuke; Kawai, Yosuke; Tokunaga, Katsushi; Toda, Tatsushi; Tsuji, Shoji

Correction: Association study of GBA1 variants with MSA based on comprehensive sequence analysis -Pitfalls in short-read sequence analysis depending on the human reference genome

更正:基于全面序列分析的GBA1变异与MSA关联研究——依赖人类参考基因组的短读长序列分析的缺陷

Orimo, Kenta; Mitsui, Jun; Matsukawa, Takashi; Tanaka, Masaki; Nomoto, Junko; Ishiura, Hiroyuki; Omae, Yosuke; Kawai, Yosuke; Tokunaga, Katsushi; Toda, Tatsushi; Tsuji, Shoji