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

Spatially resolved atlas of breast cancer uncovers intercellular machinery of venular niche governing lymphocyte extravasation.

乳腺癌的空间分辨图谱揭示了控制淋巴细胞渗出的静脉微环境细胞间机制

Wang Xin, Wang Zhanyu, Liao Qijun, Yuan Pei, Mei Junpu, Zhang Yin, Wu Chao, Kang Xiyu, Zheng Sufei, Yang Chenxuan, Liu Jiaxiang, Shang Qingyao, Li Jiangtao, Wang Bingning, Li Liangyu, Liu Hui, Hu Weining, Dong Zhensheng, Zhao Jie, Wang Linying, Liu Tao, Den Yusheng, Wang Chengrui, Han Lijuan, Chen Qianjun, Yang Huanming, Xu Xun, He Jie, Yue Zhen, Sun Nan, Fang Xiaodong, Ying Jianming

Integrative single-cell and spatial transcriptome analysis reveals heterogeneity of human liver progenitor cells

整合单细胞和空间转录组分析揭示了人肝脏祖细胞的异质性

Liu, Chuanjun; Wang, Kai; Mei, Junpu; Zhao, Ruizhen; Shen, Juan; Zhang, Wei; Li, Liangyu; Roy, Bhaskar; Fang, Xiaodong

Genome-Wide Association Study of Smoking Behavior Traits in a Chinese Han Population

中国汉族人群吸烟行为特征的全基因组关联研究

Li, Meng; Chen, Ying; Yao, Jianhua; Lu, Sheming; Guan, Ying; Xu, Yuqiong; Liu, Qiang; Sun, Silong; Mi, Qili; Mei, Junpu; Li, Xuemei; Miao, Mingming; Zhao, Shancen; Zhu, Zhouhai

PEAR1 gene polymorphism in a Chinese pedigree with pulmonary thromboembolism

中国肺血栓栓塞家系中的PEAR1基因多态性

Fu, Yingyun; Sun, Silong; Liang, Jie; Liu, Shengguo; Jiang, Yiqi; Xu, Lan; Mei, Junpu

New loci and coding variants confer risk for age-related macular degeneration in East Asians

新的基因位点和编码变异会增加东亚人群患年龄相关性黄斑变性的风险

Cheng, Ching-Yu; Yamashiro, Kenji; Chen, Li Jia; Ahn, Jeeyun; Huang, Lulin; Huang, Lvzhen; Cheung, Chui Ming G; Miyake, Masahiro; Cackett, Peter D; Yeo, Ian Y; Laude, Augustinus; Mathur, Ranjana; Pang, Junxiong; Sim, Kar Seng; Koh, Adrian H; Chen, Peng; Lee, Shu Yen; Wong, Doric; Chan, Choi Mun; Loh, Boon Kwang; Sun, Yaoyao; Davila, Sonia; Nakata, Isao; Nakanishi, Hideo; Akagi-Kurashige, Yumiko; Gotoh, Norimoto; Tsujikawa, Akitaka; Matsuda, Fumihiko; Mori, Keisuke; Yoneya, Shin; Sakurada, Yoichi; Iijima, Hiroyuki; Iida, Tomohiro; Honda, Shigeru; Lai, Timothy Yuk Yau; Tam, Pancy Oi Sin; Chen, Haoyu; Tang, Shibo; Ding, Xiaoyan; Wen, Feng; Lu, Fang; Zhang, Xiongze; Shi, Yi; Zhao, Peiquan; Zhao, Bowen; Sang, Jinghong; Gong, Bo; Dorajoo, Rajkumar; Yuan, Jian-Min; Koh, Woon-Puay; van Dam, Rob M; Friedlander, Yechiel; Lin, Ying; Hibberd, Martin L; Foo, Jia Nee; Wang, Ningli; Wong, Chang Hua; Tan, Gavin S; Park, Sang Jun; Bhargava, Mayuri; Gopal, Lingam; Naing, Thet; Liao, Jiemin; Ong, Peng Guan; Mitchell, Paul; Zhou, Peng; Xie, Xuefeng; Liang, Jinlong; Mei, Junpu; Jin, Xin; Saw, Seang-Mei; Ozaki, Mineo; Mizoguchi, Takanori; Kurimoto, Yasuo; Woo, Se Joon; Chung, Hum; Yu, Hyeong-Gon; Shin, Joo Young; Park, Dong Ho; Kim, In Taek; Chang, Woohyok; Sagong, Min; Lee, Sang-Joon; Kim, Hyun Woong; Lee, Ji Eun; Li, Yi; Liu, Jianjun; Teo, Yik Ying; Heng, Chew Kiat; Lim, Tock Han; Yang, Suk-Kyun; Song, Kyuyoung; Vithana, Eranga N; Aung, Tin; Bei, Jin Xin; Zeng, Yi Xin; Tai, E Shyong; Li, Xiao Xin; Yang, Zhenglin; Park, Kyu-Hyung; Pang, Chi Pui; Yoshimura, Nagahisa; Wong, Tien Yin; Khor, Chiea Chuen

Detection of clinically relevant genetic variants in autism spectrum disorder by whole-genome sequencing

利用全基因组测序检测自闭症谱系障碍中具有临床意义的遗传变异

Jiang, Yong-hui; Yuen, Ryan K C; Jin, Xin; Wang, Mingbang; Chen, Nong; Wu, Xueli; Ju, Jia; Mei, Junpu; Shi, Yujian; He, Mingze; Wang, Guangbiao; Liang, Jieqin; Wang, Zhe; Cao, Dandan; Carter, Melissa T; Chrysler, Christina; Drmic, Irene E; Howe, Jennifer L; Lau, Lynette; Marshall, Christian R; Merico, Daniele; Nalpathamkalam, Thomas; Thiruvahindrapuram, Bhooma; Thompson, Ann; Uddin, Mohammed; Walker, Susan; Luo, Jun; Anagnostou, Evdokia; Zwaigenbaum, Lonnie; Ring, Robert H; Wang, Jian; Lajonchere, Clara; Wang, Jun; Shih, Andy; Szatmari, Peter; Yang, Huanming; Dawson, Geraldine; Li, Yingrui; Scherer, Stephen W