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22q11.2 Deletion Syndrome as a Neural Model for Schizophrenia

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      References

        • Kraguljac N.V.
        • McDonald W.M.
        • Widge A.S.
        • Rodriguez C.I.
        • Tohen M.
        • Nemeroff C.B.
        Neuroimaging biomarkers in schizophrenia.
        Am J Psychiatry. 2021; 178: 509-521
        • Tiwari A.K.
        • Zai C.C.
        • Müller D.J.
        • Kennedy J.L.
        Genetics in schizophrenia: Where are we and what next?.
        Dialogues Clin Neurosci. 2010; 12: 289-303
        • Galderisi S.
        • Giordano G.M.
        We are not ready to abandon the current schizophrenia construct, but should be prepared to do so.
        Schizophr Res. 2022; 242: 30-34
        • Zinkstok J.
        • Schmitz N.
        • van Amelsvoort T.
        • Moeton M.
        • Baas F.
        • Linszen D.
        Genetic variation in COMT and PRODH is associated with brain anatomy in patients with schizophrenia.
        Genes Brain Behav. 2008; 7: 61-69
        • Francisco A.A.
        • Foxe J.J.
        • Horsthuis D.J.
        • DeMaio D.
        • Molholm S.
        Assessing auditory processing endophenotypes associated with schizophrenia in individuals with 22q11. 2 deletion syndrome.
        Transl Psychiatry. 2020; 10: 85
        • Francisco A.A.
        • Foxe J.J.
        • Horsthuis D.J.
        • Molholm S.
        Early visual processing and adaptation as markers of disease, not vulnerability: EEG evidence from 22q11. 2 deletion syndrome, a population at high risk for schizophrenia.
        NPJ Schizophr. 2022; 8: 28
        • Biria M.
        • Tomescu M.I.
        • Custo A.
        • Cantonas L.M.
        • Song K.W.
        • Schneider M.
        • et al.
        Visual processing deficits in 22q11. 2 deletion syndrome.
        Neuroimage Clin. 2018; 17: 976-986
        • Francisco A.A.
        • Horsthuis D.J.
        • Popiel M.
        • Foxe J.J.
        • Molholm S.
        Atypical response inhibition and error processing in 22q11. 2 deletion syndrome and schizophrenia: Towards neuromarkers of disease progression and risk.
        Neuroimage Clin. 2020; 27102351
        • Mancini V.
        • Rochas V.
        • Seeber M.
        • Grent-'t-Jong T.
        • Rihs T.A.
        • Latrèche C.
        • et al.
        Oscillatory neural signatures of visual perception across developmental stages in individuals with 22q11.2 deletion syndrome.
        Biol Psychiatry. 2022; 92: 407-418
        • Mancini V.
        • Rochas V.
        • Seeber M.
        • Roehri N.
        • Rihs T.A.
        • Ferat V.
        • et al.
        Aberrant developmental patterns of gamma-band response and long-range communication disruption in youths with 22q11.2 deletion syndrome.
        Am J Psychiatry. 2022; 179: 204-215

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