Predictive impact of rare genomic copy number variations in siblings of individuals with autism spectrum disorders.
Research Articles
Deciphering the biological mechanisms underlying the genome-wide associations between computerized device use and psychiatric disorders.
Dynamics of social representation in the mouse prefrontal cortex.
Selfish mutations dysregulating RAS-MAPK signaling are pervasive in aged human testes.
Feasibility of conducting autism biomarker research in the clinical setting.
Compromising the phosphodependent regulation of the GABAAR β3 subunit reproduces the core phenotypes of autism spectrum disorders.
Mirror extreme BMI phenotypes associated with gene dosage at the chromosome 16p11.2 locus.
KCTD13 is a major driver of mirrored neuroanatomical phenotypes of the 16p11.2 copy number variant.
Identification of a RAI1-associated disease network through integration of exome sequencing, transcriptomics, and 3D genomics.
Psychotic symptoms in 16p11.2 copy-number variant carriers.
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