Functional equivalence of genome sequencing analysis pipelines enables harmonized variant calling across human genetics projects.
Research Articles
Enhanced operant extinction and prefrontal excitability in a mouse model of Angelman syndrome.
Deep phenotyping of speech and language skills in individuals with 16p11.2 deletion.
Damaging de novo mutations diminish motor skills in children on the autism spectrum.
Normal CA1 place fields but discoordinated network discharge in a Fmr1-null mouse model of fragile X syndrome.
Network analysis of UBE3A/E6AP-associated proteins provides connections to several distinct cellular processes.
The bidirectional association between sleep problems and autism spectrum disorder: A population-based cohort study.
A longitudinal investigation of preferential attention to biological motion in 2- to 24-month-old infants.
Shared molecular neuropathology across major psychiatric disorders parallels polygenic overlap.
Rare variants in the genetic background modulate cognitive and developmental phenotypes in individuals carrying disease-associated variants.
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