| Literature DB >> 21445958 |
E K Green1, D Grozeva, R Sims, R Raybould, L Forty, K Gordon-Smith, E Russell, D St Clair, A H Young, I N Ferrier, G Kirov, I Jones, L Jones, M J Owen, M C O'Donovan, N Craddock.
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).Entities:
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Year: 2011 PMID: 21445958 DOI: 10.1002/ajmg.b.31187
Source DB: PubMed Journal: Am J Med Genet B Neuropsychiatr Genet ISSN: 1552-4841 Impact factor: 3.568