A reference haplotype panel for genome-wide imputation of short tandem repeats.
Research Articles
Identification of common genetic risk variants for autism spectrum disorder.
Enhanced population coding for rewarded choices in the medial frontal cortex of the mouse.
A genome-wide association study of shared risk across psychiatric disorders implicates gene regulation during fetal neurodevelopment.
Recessive rare variants in deoxyhypusine synthase, an enzyme involved in the synthesis of hypusine, are associated with a neurodevelopmental disorder.
Increased excitation-inhibition ratio stabilizes synapse and circuit excitability in four autism mouse models.
Predicting splicing from primary sequence with deep learning.
Psychiatric disorders in children with 16p11.2 deletion and duplication.
Both rare and common genetic variants contribute to autism in the Faroe Islands.
Smartphone measures of day-to-day behavior changes in children with autism.
- Previous Page
- Viewing
- Next Page