References:
1. Singh T, Walters JTR, Johnstone M, et al. The contribution of rare variants to risk of schizophrenia in individuals with and without intellectual disability. Nat Genet 2017; 49: 1167–1173.
2. Tansey KE, Rees E, Linden DE, et al. Common alleles contribute to schizophrenia in CNV carriers. Mol Psychiatry 2016; 21: 1085–1089.
3. Szecówka K, Misiak B, Łaczmańska I, et al. Copy number variations and schizophrenia. Mol Neurobiol 2022; 60: 1854–1864.
Rare genetic variants in the risk of schizophrenia
