Transcriptomic and epigenomic consequences of heterozygous loss-of-function mutations in AKAP11, a shared risk gene for bipolar disorder and schizophrenia

作者：Nargess Farhangdoost, Calwing Liao, Yumin Liu, Daniel Rochefort, Farah Aboasali, Alessia Pietrantonio, Martin Alda, Patrick A. Dion, Boris Chaumette, Anouar Khayachi, Guy A. Rouleau · 发表于：Molecular Psychiatry · 年份：2025 · DOI：10.1038/s41380-025-03040-x · 被引用次数：8 · 研究领域：Genetics and Neurodevelopmental Disorders、Epigenetics and DNA Methylation、Bipolar Disorder and Treatment