Works by Zhao, Rongjuan


Results: 21
    1
    2
    3

    autism risk gene CNTN4 modulates dendritic spine formation.

    Published in:
    Human Molecular Genetics, 2022, v. 31, n. 2, p. 207, doi. 10.1093/hmg/ddab233
    By:
    • Zhao, Rongjuan;
    • Zhu, Tengfei;
    • Liu, Qiong;
    • Tian, Qi;
    • Wang, Meng;
    • Chen, Jingjing;
    • Tong, Dali;
    • Yu, Bin;
    • Guo, Hui;
    • Xia, Kun;
    • Qiu, Zilong;
    • Hu, Zhengmao
    Publication type:
    Article
    4
    5
    6
    7
    8
    9
    10
    11
    12

    Disruptive mutations in TANC2 define a neurodevelopmental syndrome associated with psychiatric disorders.

    Published in:
    Nature Communications, 2019, v. 10, n. 1, p. N.PAG, doi. 10.1038/s41467-019-12435-8
    By:
    • Guo, Hui;
    • Bettella, Elisa;
    • Marcogliese, Paul C.;
    • Zhao, Rongjuan;
    • Andrews, Jonathan C.;
    • Nowakowski, Tomasz J.;
    • Gillentine, Madelyn A.;
    • Hoekzema, Kendra;
    • Wang, Tianyun;
    • Wu, Huidan;
    • Jangam, Sharayu;
    • Liu, Cenying;
    • Ni, Hailun;
    • Willemsen, Marjolein H.;
    • van Bon, Bregje W.;
    • Rinne, Tuula;
    • Stevens, Servi J. C.;
    • Kleefstra, Tjitske;
    • Brunner, Han G.;
    • Yntema, Helger G.
    Publication type:
    Article
    13
    14
    15
    16
    17
    18

    Biallelic loss-of-function variants in NEMF cause central nervous system impairment and axonal polyneuropathy.

    Published in:
    Human Genetics, 2021, v. 140, n. 4, p. 579, doi. 10.1007/s00439-020-02226-3
    By:
    • Ahmed, Ashfaque;
    • Wang, Meng;
    • Bergant, Gaber;
    • Maroofian, Reza;
    • Zhao, Rongjuan;
    • Alfadhel, Majid;
    • Nashabat, Marwan;
    • AlRifai, Muhammad Talal;
    • Eyaid, Wafaa;
    • Alswaid, Abdulrahman;
    • Beetz, Christian;
    • Qin, Yan;
    • Zhu, Tengfei;
    • Tian, Qi;
    • Xia, Lu;
    • Wu, Huidan;
    • Shen, Lu;
    • Dong, Shanshan;
    • Yang, Xinyi;
    • Liu, Cenying
    Publication type:
    Article
    19
    20
    21