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MARK2 variants cause autism spectrum disorder via the downregulation of WNT/β-catenin signaling pathway

  • Maolei Gong
  • , Jiayi Li
  • , Zailong Qin
  • , Matheus Vernet Machado Bressan Wilke
  • , Yijun Liu
  • , Qian Li
  • , Haoran Liu
  • , Chen Liang
  • , Joel A. Morales-Rosado
  • , Ana S.A. Cohen
  • , Susan S. Hughes
  • , Bonnie R. Sullivan
  • , Valerie Waddell
  • , Marie José H. van den Boogaard
  • , Richard H. van Jaarsveld
  • , Ellen van Binsbergen
  • , Koen L. van Gassen
  • , Tianyun Wang
  • , Susan M. Hiatt
  • , Michelle D. Amaral
    • Whitley V. Kelley, Jianbo Zhao, Weixing Feng, Changhong Ren, Yazhen Yu, Nicole J. Boczek, Matthew J. Ferber, Carrie Lahner, Sherr Elliott, Yiyan Ruan, Cyril Mignot, Boris Keren, Hua Xie, Xiaoyan Wang, Bernt Popp, Christiane Zweier, Juliette Piard, Christine Coubes, Frederic Tran Mau-Them, Hana Safraou, A. Micheil Innes, Julie Gauthier, Jacques L. Michaud, Daniel C. Koboldt, Odent Sylvie, Marjolaine Willems, Wen Hann Tan, Benjamin Cogne, Claudine Rieubland, Dominique Braun, Scott Douglas McLean, Konrad Platzer, Pia Zacher, Henry Oppermann, Lucie Evenepoel, Pierre Blanc, Laïla El Khattabi, Neshatul Haque, Nikita R. Dsouza, Michael T. Zimmermann, Raul Urrutia, Eric W. Klee, Yiping Shen, Hongzhen Du, Leonard Rappaport, Chang Mei Liu, Xiaoli Chen

Research output: Contribution to journal › Article › peer-review

14 Scopus citations

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Biochemistry, Genetics and Molecular Biology