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. 2022 Sep 1;109(9):1620–1637. doi: 10.1016/j.ajhg.2022.07.011

Table 1.

Candidate directional anchor genes for schizophrenia and bipolar along with their associated drug-repurposing candidates

Gene Disorder Protective direction Repurposing candidates Sensitivity analyses
PCCB SZ increased expression biotin high-confidence causal gene from TWAS (PIP > 0.8), further supported by MR
FADS1 BIP increased expression icosapent, linolenic acid moderate-confidence causal gene from TWAS (PIP > 0.4, additionally supported by colocalization – PPH4 > 0.8), further supported by MR
GRIN2A SZ increased expression N-acetylcysteine, glycine high-confidence causal gene from TWAS (PIP > 0.8)
CACNA1C SZ increased expression ibutilide moderate-confidence causal gene from TWAS (PIP > 0.4, additionally supported by colocalization – PPH4 > 0.8)
RPS17 SZ increased expression artenimol moderate-confidence causal gene from TWAS (PIP > 0.4, additionally supported by colocalization – PPH4 > 0.8)
FES SZ decreased expression Fostamatinib, Lorlatinib high-confidence causal gene from TWAS (PIP > 0.8)