Works matching AU Liu, Yalan


Results: 138
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    Exome sequencing identifies a novel CEACAM16 mutation associated with autosomal dominant nonsyndromic hearing loss DFNA4B in a Chinese family.

    Published in:
    Journal of Human Genetics, 2015, v. 60, n. 3, p. 119, doi. 10.1038/jhg.2014.114
    By:
    • Wang, Honghan;
    • Wang, Xinwei;
    • He, Chufeng;
    • Li, Haibo;
    • Qing, Jie;
    • Grati, M'hamed;
    • Hu, Zhengmao;
    • Li, Jiada;
    • Hu, Yiqiao;
    • Xia, Kun;
    • Mei, Lingyun;
    • Wang, Xingwei;
    • Yu, Jianjun;
    • Chen, Hongsheng;
    • Jiang, Lu;
    • Liu, Yalan;
    • Men, Meichao;
    • Zhang, Hailin;
    • Guan, Liping;
    • Xiao, Jingjing
    Publication type:
    Article
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    Integrative proteogenomic characterization of early esophageal cancer.

    Published in:
    Nature Communications, 2023, v. 14, n. 1, p. 1, doi. 10.1038/s41467-023-37440-w
    By:
    • Li, Lingling;
    • Jiang, Dongxian;
    • Zhang, Qiao;
    • Liu, Hui;
    • Xu, Fujiang;
    • Guo, Chunmei;
    • Qin, Zhaoyu;
    • Wang, Haixing;
    • Feng, Jinwen;
    • Liu, Yang;
    • Chen, Weijie;
    • Zhang, Xue;
    • Bai, Lin;
    • Tian, Sha;
    • Tan, Subei;
    • Xu, Chen;
    • Song, Qi;
    • Liu, Yalan;
    • Zhong, Yunshi;
    • Chen, Tianyin
    Publication type:
    Article
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    Association of genetic variants of GRIN2B with autism.

    Published in:
    Scientific Reports, 2015, p. 8296, doi. 10.1038/srep08296
    By:
    • Pan, Yongcheng;
    • Chen, Jingjing;
    • Guo, Hui;
    • Ou, Jianjun;
    • Peng, Yu;
    • Liu, Qiong;
    • Shen, Yidong;
    • Shi, Lijuan;
    • Liu, Yalan;
    • Xiong, Zhimin;
    • Zhu, Tengfei;
    • Luo, Sanchuan;
    • Hu, Zhengmao;
    • Zhao, Jingping;
    • Xia, Kun
    Publication type:
    Article