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

Inflammatory bowel disease in a young female patient with a novel de novo TRAF3 frameshift variant responsive to ustekinumab: a case report

一例年轻女性患者，携带新型从头TRAF3移码突变，对乌司奴单抗治疗有反应，并患有炎症性肠病：病例报告

期刊:Intestinal Research
影响因子:3.9
doi:10.5217/ir.2024.00190
Takeuchi, Ichiro; Taniguchi, Kosuke; Arai, Katsuhiro; Uchiyama, Toru; Terao, Miho; Hori, Asuka; Kawai, Toshinao; Yoshioka, Takako; Kyodo, Reiko; Shimizu, Hirotaka; Fujita, Satoshi; Motomura, Kenichiro; Okazaki, Yuka; Ishikawa, Takashi; Ogura, Masao; Hayashi, Kentaro; Matsumoto, Kenji; Takada, Shuji; Onodera, Masafumi; Morita, Hideaki; Hata, Kenichiro
炎症/感染
炎症
TRAF3
发表日期：2026
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Culture Medium Enriched with Ultrafine Carbon Monoxide Bubbles Enhances In Vitro Blastocyst Formation of In Vivo-Fertilized Mouse Zygotes

富含超细一氧化碳气泡的培养基可增强体内受精小鼠合子的体外囊胚形成

期刊:Antioxidants
影响因子:6.6
doi:10.3390/antiox14060684
Hirakawa, Toyofumi; Nakabayashi, Kazuhiko; Ito, Noriko; Ishiwata, Keisuke; Urushiyama, Daichi; Miyata, Kohei; Baba, Tsukasa; Hata, Kenichiro; Yasunaga, Shin'ichiro; Yotsumoto, Fusanori; Tachibana, Katsuro; Miyamoto, Shingo
Mouse
发表日期：2025
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Genome-wide DNA methylation profiles in the raphe nuclei of patients with autism spectrum disorder

自闭症谱系障碍患者中缝核的全基因组DNA甲基化谱

期刊:Psychiatry and Clinical Neurosciences
影响因子:6.2
doi:10.1111/pcn.13830
Iwata, Keiko; Nakabayashi, Kazuhiko; Ishiwata, Keisuke; Nakamura, Kazuhiko; Kameno, Yosuke; Hata, Kenichiro; Matsuzaki, Hideo
自闭症
表观遗传
神经科学
DNA甲基化
发表日期：2025
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Maternal Vitamin D Deficiency Is a Risk Factor for Infants' Epigenetic Gestational Age Acceleration at Birth in Japan: A Cohort Study

日本一项队列研究表明，孕妇维生素D缺乏是婴儿出生时表观遗传胎龄加速的危险因素。

期刊:Nutrients
影响因子:5
doi:10.3390/nu17020368
Kawai, Tomoko; Jwa, Seung Chik; Ogawa, Kohei; Tanaka, Hisako; Aoto, Saki; Kamura, Hiromi; Morisaki, Naho; Fujiwara, Takeo; Hata, Kenichiro
表观遗传
发表日期：2025
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Comparative effectiveness of subcutaneous sarilumab 200 mg biweekly, subcutaneous Tocilizumab 162 mg biweekly, and intravenous Tocilizumab 8 mg/kg every 4 weeks in patients with rheumatoid arthritis: a prospective cohort study

皮下注射沙利珠单抗200 mg每两周一次、皮下注射托珠单抗162 mg每两周一次以及静脉注射托珠单抗8 mg/kg每4周一次在类风湿性关节炎患者中的疗效比较：一项前瞻性队列研究

期刊:Arthritis Research & Therapy
影响因子:4.6
doi:10.1186/s13075-025-03514-x
Onishi, Akira; Tanaka, Masao; Fujii, Takayuki; Murata, Koichi; Murakami, Kosaku; Hashimoto, Motomu; Watanabe, Ryu; Nozaki, Yuji; Ashida, Chisato; Yamamoto, Wataru; Yamada, Hirotaka; Sendo, Sho; Ebina, Kosuke; Makino, Hidehiko; Son, Yonsu; Wada, Yumiko; Hata, Kenichiro; Matsuda, Shuichi; Morinobu, Akio
关节炎
发表日期：2025
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Isolation of Nucleated Red Blood Cells With Intact Genomic DNA From Cord Blood by Applying G&T-Seq

利用G&T-Seq技术从脐带血中分离具有完整基因组DNA的有核红细胞

期刊:Reproductive Medicine and Biology
影响因子:3.3
doi:10.1002/rmb2.12671
Ito, Noriko; Fujii, Tatsuya; Taniguchi, Kosuke; Okazaki, Yuka; Ogata-Kawata, Hiroko; Sago, Haruhiko; Hata, Kenichiro; Nakabayashi, Kazuhiko
细胞生物学
红细胞
发表日期：2025
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Correction: Loss-of-function mutation of NSD2 is associated with abnormal placentation accompanied by fetal growth retardation in mice

更正：NSD2 功能缺失突变与小鼠胎盘异常形成及胎儿生长迟缓有关。

期刊:PLoS One
影响因子:2.6
doi:10.1371/journal.pone.0334633
Ohnishi, Eriko; Kinoshita, Shiori; Nakabayashi, Kazuhiko; Hata, Kenichiro; Kawai, Tomoko
NSD2
发表日期：2025
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Loss-of-function mutation of NSD2 is associated with abnormal placentation accompanied by fetal growth retardation in mice

小鼠NSD2功能缺失突变与胎盘异常形成及胎儿生长迟缓有关。

期刊:PLoS One
影响因子:2.6
doi:10.1371/journal.pone.0328243
Ohnishi, Eriko; Kinoshita, Shiori; Nakabayashi, Kazuhiko; Hata, Kenichiro; Kawai, Tomoko
NSD2
发表日期：2025
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Approaches to Evaluate Whole Exome Sequencing Data That Incorporate Genetic Intolerance Scores for Congenital Anomalies, Including Intronic Regions Adjacent to Exons

评估包含先天性异常遗传不耐受评分（包括外显子邻近内含子区域）的全外显子组测序数据的方法

期刊:Molecular Genetics & Genomic Medicine
影响因子:1.6
doi:10.1002/mgg3.70092
Taniguchi, Kosuke; Hasegawa, Fuyuki; Okazaki, Yuka; Hori, Asuka; Ogata-Kawata, Hiroko; Aoto, Saki; Migita, Ohsuke; Kawai, Tomoko; Nakabayashi, Kazuhiko; Okamura, Kohji; Fukui, Kana; Wada, Seiji; Ozawa, Katsusuke; Ito, Yushi; Sago, Haruhiko; Hata, Kenichiro
发表日期：2025
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DNA methylation data from Japanese patients with Rubinstein-Taybi syndrome

来自日本鲁宾斯坦-泰比综合征患者的DNA甲基化数据

期刊:Human Genome Variation
影响因子:1.3
doi:10.1038/s41439-025-00332-0
Kawai, Tomoko; Aoki, Taiga; Nakabayashi, Kazuhiko; Hata, Kenichiro; Kaname, Tadashi; Kosaki, Rika
表观遗传
DNA甲基化
发表日期：2025
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