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The contribution of rare variants to risk of schizophrenia in individuals with and without intellectual disability.
Singh T, Walters JTR, Johnstone M, Curtis D, Suvisaari J, Torniainen M, Rees E, Iyegbe C, Blackwood D, McIntosh AM, Kirov G, Geschwind D, Murray RM, Di Forti M, Bramon E, Gandal M, Hultman CM, Sklar P; INTERVAL Study; UK10K Consortium; Palotie A, Sullivan PF, O'Donovan MC, Owen MJ, Barrett JC. Singh T, et al. Among authors: bramon e. Nat Genet. 2017 Aug;49(8):1167-1173. doi: 10.1038/ng.3903. Epub 2017 Jun 26. Nat Genet. 2017. PMID: 28650482 Free PMC article.
Mismatch negativity in schizophrenia: a family study.
Bramon E, Croft RJ, McDonald C, Virdi GK, Gruzelier JG, Baldeweg T, Sham PC, Frangou S, Murray RM. Bramon E, et al. Schizophr Res. 2004 Mar 1;67(1):1-10. doi: 10.1016/s0920-9964(03)00132-4. Schizophr Res. 2004. PMID: 14741319
Association between BDNF val66 met genotype and episodic memory.
Dempster E, Toulopoulou T, McDonald C, Bramon E, Walshe M, Filbey F, Wickham H, Sham PC, Murray RM, Collier DA. Dempster E, et al. Among authors: bramon e. Am J Med Genet B Neuropsychiatr Genet. 2005 Apr 5;134B(1):73-5. doi: 10.1002/ajmg.b.30150. Am J Med Genet B Neuropsychiatr Genet. 2005. PMID: 15719396
217 results