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DISC1 Exon 11 Rare Variants Found More Commonly in Schizoaffective Spectrum Cases Than Controls

  • EK Green
  • , D Grozeva
  • , R Sims
  • , R Raybould
  • , L Forty
  • , Katherine Gordon-Smith
  • , E Russell
  • , D St Clair
  • , AH Young
  • , IN Ferrier
  • , G Kirov
  • , I Jones
  • , Lisa Jones
  • , MJ Owen
  • , MC O'Donovan
  • , N Craddock

Research output: Contribution to journalArticle

17 Citations (Scopus)

Abstract

We previously performed a linkage study using families identified through probands meeting criteria for DSM-IV schizoaffective disorder, bipolar type (SABP) and observed a genome-wide significant signal (LOD = 3.54) at chromosome 1q42 close to DISC1. An initial sequencing study of DISC1 using 14 unrelated DSM-IV SABP samples from the linkage study identified 2 non-synonymous coding SNPs in exon 11 in 2 separate individuals. Here we provide evidence of additional rare coding SNPs within exon 11. In sequencing exon 11 in 506 cases and 1,211 controls for variants that occurred only once, 4 additional rare variants were found in cases (P-value = 0.008, Fisher's exact trend test). (C) 2011 Wiley-Liss, Inc.
Original languageEnglish
Pages (from-to)490-492
Number of pages3
JournalAmerican Journal of Medical Genetics Part B: Neuropsychiatric Genetics
Volume156B
Issue number4
DOIs
Publication statusPublished - 1 Jun 2011

Keywords

  • schizoaffective spectrum
  • DISC1
  • rare variants

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