Schizophrenia-associated somatic copy number variants from 12,834 cases reveal contribution to risk and recurrent, isoform-specific NRXN1 disruptions

Citation:

Maury EA, Sherman MA, Genovese G, Gilgenast TG, Rajarajan P, Flaherty E, Akbarian S, Chess A, McCarroll SA, Loh P-R, Phillips-Cremins JE, Brennand KJ, Walters JTR, O’ Donovan M, Sullivan P, and workgroup PGCSCNV, and workgroup PGCSCNV, Sebat J, Lee EA, Walsh CA. Schizophrenia-associated somatic copy number variants from 12,834 cases reveal contribution to risk and recurrent, isoform-specific NRXN1 disruptions [Internet]. medRxiv Submitted;