Rare Maternally Inherited Coding Variants on Chromosome X Carry Predominantly Male Risk in Autism, Tourette Syndrome, and Attention-deficit/Hyperactivity Disorder

Sheng Wang,Belinda Wang,Vanessa Drury,Sam Drake,Nawei Sun, Hasan Alkhairo,Juan David Arbelaez,Clif Duhn,Vanessa H. Bal,Kate Langley,Joanna Martin,Jinchuan Xing,Gary A. Heiman,Jay A. Tischfield,Thomas Fernandez,Michael John Owen,Michael O’Donovan,Anita Thapar,Matthew W. State,A. Jeremy Willsey

medRxiv (Cold Spring Harbor Laboratory)（2022）

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关键词

X Chromosome Inactivation,Autism,Sexually Dimorphic Gene Expression,Fragile X Syndrome,Sex Determination

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