Whole genome sequencing in psychiatric disorders: the WGSPD consortium.
Review and Opinion Articles
Brain evolution and uniqueness in the human genome.
Fragile X: translation in action.
Role for metabotropic glutamate receptor 5 ( mGluR5 ) in the pathogenesis of fragile X syndrome.
Failure of neuronal homeostasis results in common neuropsychiatric phenotypes.
Neuroligins and neurexins link synaptic function to cognitive disease.
Advances in understanding visual cortex plasticity.
The origins of social impairments in autism spectrum disorder: studies of infants at risk.
Allelic diversity in human developmental neurogenetics: insights into biology and disease.
MicroRNAs in psychiatric and neurodevelopmental disorders.
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