Recurrent de novo mutations in neurodevelopmental disorders: Properties and clinical implications.
Review and Opinion Articles
Cell biology of astrocyte-synapse interactions.
Microglia emerge as central players in brain disease.
NKCC1 chloride importer antagonists attenuate many neurological and psychiatric disorders.
Evolution of the human nervous system function, structure, and development.
Brain carnitine deficiency causes nonsyndromic autism with an extreme male bias: A hypothesis.
Whole genome sequencing in psychiatric disorders: the WGSPD consortium.
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.
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