PTEN mutations in autism spectrum disorder and congenital hydrocephalus: developmental pleiotropy and therapeutic targets
Tyrone DeSpenza(Duke University Hospital), Kristopher T. Kahle(Massachusetts General Hospital), Seth L. Alper(Beth Israel Deaconess Medical Center), Kellen Mermin‐Bunnell(Yale University), Hannah Smith(Yale University), Ellen J. Hoffman(Yale University), Stephanie M. Robert(Yale University), Sheng Chih Jin(Yale University), Aladine A. Elsamadicy(Yale University), Shreyas Panchagnula(Yale University), Adam J. Kundishora(Yale University), Jack Ocken(Yale University), Benjamin C. Reeves(Yale University), Phan Q. Duy(Yale University), Marina Carlson(Yale University)
Cited by 41
Related Papers
Contribution of rare inherited and de novo variants in 2,871 congenital heart disease probands
|Nature Genetics|2017|927
De novo mutations in congenital heart disease with neurodevelopmental and other congenital anomalies
|Science|2015|886
A genome-wide association study of cleft lip with and without cleft palate identifies risk variants near MAFB and ABCA4
|Nature Genetics|2010|593
Inhibition of Ca(2+)-dependent K+ transport and cell dehydration in sickle erythrocytes by clotrimazole and other imidazole derivatives.
|Journal of Clinical Investigation|1993|364