Exome sequence analysis and follow up genotyping implicates rare ULK1 variants to be involved in susceptibility to schizophrenia

This is the peer reviewed version of the following article: Al Eissa, M. M., et al. (2018). "Exome sequence analysis and follow up genotyping implicates rare ULK1 variants to be involved in susceptibility to schizophrenia." Annals of Human Genetics 82(2): 88-92., which has been published in final form at DOI:10.1111/ahg.12226. This article may be used for non-commercial purposes in accordance with Wiley Terms and Conditions for Use of Self-Archived Versions ; UK Medical Research Council project grants G9623693N, G0500791,G0701007, and G1000708. MMAE is funded by a PhD studentship scholarship from the Kingdom of Saudi Arabia, Ministry of Health. Drs McQuillin and Bassare supported by the UCLH NIHR BRC. The UK10K project was funded by Wellcome Trust grant WT091310. NIMH grant R01MH077139, the Sylvan C. Herman Foundation, theStanley Medical Research Institute and The Swedish Research Council (grants 2009–4959 and 2011–4659). NIMH Grand Opportunity grant RCMH089905, the Sylvan C. Herman Foundation, a grant from the Stanley Medical Research Institute and multiplegifts to the Stanley Center for Psychiatric Research at the Broad Institute of MIT and Harvard