Expansion of the GRIA2 phenotypic representation: a novel de novo loss of function mutation in a case with childhood onset schizophrenia

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Allelic Variant, Sequence Variants, Medicine +11

Analysis of protein-coding genetic variation in 60,706 humans

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Phenotypic Variation, Protein-coding Genetic Variation, Genetics +5

Genic Intolerance to Functional Variation and the Interpretation of Personal Genomes

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Genetics, Genetic Foundation, Genomics +19

Epigenomic Profiling Reveals DNA-Methylation Changes Associated with Major Psychosis

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Major Psychosis, Psychiatry, Psychotic Disorder +7

Clinical application of exome sequencing in undiagnosed genetic conditions

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