Targeted long-read sequencing identifies missing disease-causing variation.
De novo variants in SNAP25 cause an early-onset developmental and epileptic encephalopathy.
The meaning of significant mean group differences for biomarker discovery.
Precise genome editing across kingdoms of life using retron-derived DNA.
Processing of social and monetary rewards in autism spectrum disorders.
Characterizing subcortical structural heterogeneity in autism.
Dynamics of BAF-Polycomb complex opposition on heterochromatin in normal and oncogenic states.
Smarca4 ATPase mutations disrupt direct eviction of PRC1 from chromatin.
Clustering autism: Using neuroanatomical differences in 26 mouse models to gain insight into the heterogeneity.
The autism inpatient collection: Methods and preliminary sample description.
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