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

A maternal exon H splice-site variant leading to pseudohypoparathyroidism type 1B with broad methylation defects in GNAS-differentially methylated regions

母源外显子H剪接位点变异导致假性甲状旁腺功能减退症1B型，伴有GNAS差异甲基化区域的广泛甲基化缺陷

期刊:Clinical Epigenetics
影响因子:4.4
doi:10.1186/s13148-026-02107-y
Urakawa, Tatsuki; Huang, Haipeng; Nagai, Takuhito; Hattori, Atsushi; Kawasaki, Tomoyuki; Saitsu, Hirotomo; Akutsu, Hidenori; Fukami, Maki; Kagami, Masayo
表观遗传
发表日期：2026
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Methylation profile characteristics in the H19/IGF2:IG-DMR revealed by long-read sequencing analysis in patients with Beckwith-Wiedemann syndrome having defects in the OCT4/SOX2 binding site

通过长读长测序分析揭示了贝克威思-威德曼综合征患者H19/IGF2:IG-DMR区域的甲基化谱特征，这些患者的OCT4/SOX2结合位点存在缺陷。

期刊:Clinical Epigenetics
影响因子:4.4
doi:10.1186/s13148-026-02065-5
Masubuchi, Hayate; Urakawa, Tatsuki; Kosaki, Rika; Nishimura, Riki; Wada, Yasunori; Dateki, Sumito; Yagasaki, Hideaki; Kagawa, Reiko; Nishimura, Yutaka; Soejima, Hidenobu; Ogata, Tsutomu; Fukami, Maki; Kagami, Masayo
SOX2
SOX
表观遗传
DNA甲基化
发表日期：2026
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Real-world glucocorticoid prescription patterns in patients with lupus nephritis: A retrospective study using a healthcare insurance claims database

狼疮性肾炎患者糖皮质激素处方模式的真实世界研究：一项基于医疗保险索赔数据库的回顾性研究

期刊:Lupus
影响因子:1.9
doi:10.1177/09612033251408515
Atsumi, Tatsuya; Hanaoka, Hironari; Nishijima, Nobuo; Murakami, Kohji; Nio, Mariko; Urakawa, Tsutomu; Fujimura, Takaaki; Hayashi, Hiroki
肾炎
免疫/内分泌
发表日期：2026
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SPY-QP-guided perfusion assessment to prevent esophagogastric anastomotic leakage: protocol for the SPYMIE study

SPY-QP指导的灌注评估预防食管胃吻合口漏：SPYMIE研究方案

期刊:BMC Surgery
影响因子:1.8
doi:10.1186/s12893-026-03545-4
Aoki, Tomoaki; Goto, Hironobu; Koterazawa, Yasufumi; Ando, Masayuki; Sugita, Yutaka; Ikeda, Taro; Harada, Hitoshi; Otowa, Yasunori; Urakawa, Naoki; Hasegawa, Hiroshi; Kanaji, Shingo; Yamashita, Kimihiro; Matsuda, Takeru; Kakeji, Yoshihiro
发表日期：2026
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From "Black Box" to Learning System: Formative Viewpoint on Digital Health Governance for Childhood Cancer Information in Japan

从“黑箱”到学习系统：日本儿童癌症信息数字健康治理的形成性视角

期刊:JMIR Formative Research
影响因子:
doi:10.2196/86775
Kubota, Kazumi; Urakawa, Ryuta
肿瘤
肿瘤免疫
发表日期：2026
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A comprehensive long-read sequencing system to assess DNA methylation at differentially methylated regions and imprinting-disorder-related genes

一种用于评估差异甲基化区域和印记紊乱相关基因DNA甲基化的综合性长读长测序系统

期刊:Genome Medicine
影响因子:11.2
doi:10.1186/s13073-025-01559-w
Urakawa, Tatsuki; Hattori, Atsushi; Ogiwara, Yasuko; Masubuchi, Hayate; Igarashi, Mizuho; Nakamura, Sayuri; Hara-Isono, Kaori; Ishiwata, Keisuke; Ogata-Kawata, Hiroko; Kamura, Hiromi; Kuroki, Yoko; Nakabayashi, Kazuhiko; Fukami, Maki; Kagami, Masayo
表观遗传
DNA甲基化
发表日期：2025
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Fast and efficient room-temperature phosphorescence from metal-free organic molecular liquids

无金属有机分子液体的快速高效室温磷光

期刊:Chemical Science
影响因子:7.4
doi:10.1039/d5sc03768a
Tani, Yosuke; Oshima, Yuya; Okada, Rika; Fujimura, Jun; Miyazaki, Yuji; Nakano, Motohiro; Urakawa, Osamu; Inoue, Tadashi; Ehara, Takumi; Miyata, Kiyoshi; Onda, Ken; Ogawa, Takuji
发表日期：2025
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Inflammation-associated molecules in the glomerular-endothelium in mild IgA-nephropathy patients identified by single-cell and spatial transcriptome

通过单细胞和空间转录组学方法鉴定轻度IgA肾病患者肾小球内皮细胞中的炎症相关分子

期刊:Communications Biology
影响因子:5.1
doi:10.1038/s42003-025-08325-z
Hasegawa, Kumi; Kawashima, Nagako; Kawabata, Ayako; Sakakura, Megumi; Onoda, Naoki; Sano, Takashi; Urakawa, Itaru; Matsubara, Masahiro; Naito, Shokichi
IgA
炎症
炎症/感染
Immunology/Inflammation
内皮细胞
细胞生物学
单细胞
发表日期：2025
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Oncological Outcomes and Postoperative Complications for Localized Soft Tissue Sarcomas of the Extremities and Trunk Wall in Patients Aged 85 Years or Older

85岁及以上患者四肢及躯干壁局限性软组织肉瘤的肿瘤学预后及术后并发症

期刊:Cancers
影响因子:4.4
doi:10.3390/cancers17121940
Ikuta, Kunihiro; Sakai, Tomohisa; Koike, Hiroshi; Fujito, Takeo; Urakawa, Hiroshi; Nishida, Yoshihiro; Imagama, Shiro
肿瘤
肿瘤免疫
发表日期：2025
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Multi-locus methylation analyses reveal GNAS methylation defects in three patients with the Beckwith-Wiedemann syndrome phenotype and no molecular defects in the 11p15.5 imprinted region

多位点甲基化分析显示，三名具有贝克威思-威德曼综合征表型的患者存在GNAS甲基化缺陷，而11p15.5印记区未发现分子缺陷。

期刊:Clinical Epigenetics
影响因子:4.4
doi:10.1186/s13148-025-01907-y
Urakawa, Tatsuki; Kanamaru, Yuri; Amano, Naoko; Uchida, Akira; Fukami, Maki; Kagami, Masayo
表观遗传
发表日期：2025
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