MARK2 variants cause autism spectrum disorder via the downregulation of WNT/β-catenin signaling pathway
Maolei Gong(Aerospace Center Hospital), Dominique Braun(University of Bern), Ana S.A. Cohen(Children's Mercy Hospital), Boris Keren(Sorbonne Université), Yiyan Ruan(Dalian Institute of Chemical Physics), Juliette Piard(Centre Hospitalier Universitaire de Besançon), Christiane Zweier(University Hospital of Bern), Frédéric Tran Mau‐Them(Inserm), Changhong Ren(Capital Medical University), Daniel C. Koboldt(Nationwide Children's Hospital), Joel A. Morales‐Rosado(Vanderbilt University Medical Center), Marie‐José H. van den Boogaard(University Medical Center Utrecht), Weixing Feng(Capital Medical University), Koen L.I. van Gassen(University Medical Center Utrecht), Nicole J. Boczek(Mayo Clinic in Arizona), Bonnie Sullivan(Mercy Hospital), Christine Coubes, Marjolaine Willems(Université de Montpellier), Michelle D. Amaral(HudsonAlpha Institute for Biotechnology), Ellen van Binsbergen(University Medical Center Utrecht), A. Micheil Innes(University of Calgary), Wen‐Hann Tan(Boston Children's Hospital), Jacques L. Michaud(Centre Hospitalier Universitaire Sainte-Justine), Bernt Popp(Berlin Institute of Health at Charité - Universitätsmedizin Berlin), Claudine Rieubland(University of Bern), Whitley V. Kelley(HudsonAlpha Institute for Biotechnology), Jianbo Zhao(Capital Medical University), Cyril Mignot(Sorbonne Université), Carrie A. Lahner(Mayo Clinic), Richard H. van Jaarsveld(Utrecht University), Susan Hughes(Children's Mercy Hospital), Zailong Qin(Guangxi Maternal and Child Health Hospital), Matheus Vernet Machado Bressan Wilke(Washington University in St. Louis), Matthew J. Ferber(Mayo Clinic), Valerie Waddell(Children's Mercy Hospital), Liang Chen(Deyang Stomatological Hospital), Qian Li(Chinese Academy of Sciences), Xiaoyan Wang(East China Normal University), Haoran Liu(Qingdao University), Yazhen Yu, Hua Xie, Tianyun Wang(King University), Odent Sylvie(Centre National de la Recherche Scientifique), Yijun Liu(Institute of Zoology), Benjamin Cogné(Centre National de la Recherche Scientifique), Julie Gauthier(Centre Hospitalier Universitaire Sainte-Justine), Hana Safraou(Inserm), Sherr Elliott(University of California, San Francisco), Jiayi Li(Chinese Academy of Medical Sciences & Peking Union Medical College), Susan M. Hiatt(HudsonAlpha Institute for Biotechnology)
Cited by 19
Related Papers
De novo germline and postzygotic mutations in AKT3, PIK3R2 and PIK3CA cause a spectrum of related megalencephaly syndromes
|Nature Genetics|2012|752
Mutations in GRIN2A and GRIN2B encoding regulatory subunits of NMDA receptors cause variable neurodevelopmental phenotypes
|Nature Genetics|2010|509
Integrating de novo and inherited variants in 42,607 autism cases identifies mutations in new moderate-risk genes
|Nature Genetics|2022|475
High Rate of Recurrent De Novo Mutations in Developmental and Epileptic Encephalopathies
|The American Journal of Human Genetics|2017|456