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Rare coding variants as risk modifiers of the 22q11.2 deletion implicate postnatal cortical development in syndromic schizophrenia.
Lin JR, Zhao Y, Jabalameli MR, Nguyen N, Mitra J; International 22q11.DS Brain and Behavior Consortium; Swillen A, Vorstman JAS, Chow EWC, van den Bree M, Emanuel BS, Vermeesch JR, Owen MJ, Williams NM, Bassett AS, McDonald-McGinn DM, Gur RE, Bearden CE, Morrow BE, Lachman HM, Zhang ZD. Lin JR, et al. Among authors: chow ewc. Mol Psychiatry. 2023 May;28(5):2071-2080. doi: 10.1038/s41380-023-02009-y. Epub 2023 Mar 3. Mol Psychiatry. 2023. PMID: 36869225
Increased head circumference in schizophrenia.
Bassett AS, Chow EW, Bury A, Ali F, Haylock CA, Smith GN, Lapointe JS, Honer WG. Bassett AS, et al. Biol Psychiatry. 1996 Dec 1;40(11):1173-5. doi: 10.1016/S0006-3223(96)00288-0. Biol Psychiatry. 1996. PMID: 8931921 Free PMC article. Clinical Trial. No abstract available.
22q11 deletion syndrome in adults with schizophrenia.
Bassett AS, Hodgkinson K, Chow EW, Correia S, Scutt LE, Weksberg R. Bassett AS, et al. Am J Med Genet. 1998 Jul 10;81(4):328-37. Am J Med Genet. 1998. PMID: 9674980 Free PMC article.
Phenotype of adults with the 22q11 deletion syndrome: A review.
Cohen E, Chow EW, Weksberg R, Bassett AS. Cohen E, et al. Am J Med Genet. 1999 Oct 8;86(4):359-65. doi: 10.1002/(sici)1096-8628(19991008)86:4<359::aid-ajmg10>3.0.co;2-v. Am J Med Genet. 1999. PMID: 10494092 Free PMC article. Review.
Chromosomal abnormalities and schizophrenia.
Bassett AS, Chow EW, Weksberg R. Bassett AS, et al. Am J Med Genet. 2000 Spring;97(1):45-51. doi: 10.1002/(sici)1096-8628(200021)97:1<45::aid-ajmg6>3.0.co;2-9. Am J Med Genet. 2000. PMID: 10813803 Free PMC article. Review.
106 results