of risk SNPs to reveal biological subcategories of schizophrenia [ 56 ], (b) due to unequal distribution of risk-allele presence (only 11 participants homozygous for the non-risk allele), replication of the finding with pre-selection of participants depending on their genotype, (c) replicating the marginally significant association of positive symptoms and right pSTS activation with different approaches to assess schizotypy, such as the Oxford-Liverpool Inventory of Feelings and Experiences [ 57 ], (d) targeting not only right pSTS activation and connectivity, but also of further regions that are central for social-cognitive processing (e.g., amygdala, MPFC).
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Hyperfunctioning of the right posterior superior temporal sulcus in response to neutral facial expressions presents an endophenotype of schizophrenia.
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