https://novaprd-lb.newcastle.edu.au/vital/access/manager/Index en-au 5 Meta-analysis of genome-wide association studies identifies common susceptibility polymorphisms for colorectal and endometrial cancer near SH2B3 and TSHZ1 https://novaprd-lb.newcastle.edu.au/vital/access/manager/Repository/uon:26195 Wed 11 Apr 2018 15:00:42 AEST ]]> Genome-wide association study of endometrial cancer in E2C2 https://novaprd-lb.newcastle.edu.au/vital/access/manager/Repository/uon:20989 Wed 11 Apr 2018 11:20:08 AEST ]]> Polymorphisms in a putative enhancer at the 10q21.2 breast cancer risk locus regulate NRBF2 expression https://novaprd-lb.newcastle.edu.au/vital/access/manager/Repository/uon:28231 Wed 01 Aug 2018 14:52:20 AEST ]]> A systematic, large-scale resequencing screen of X-chromosome coding exons in mental retardation https://novaprd-lb.newcastle.edu.au/vital/access/manager/Repository/uon:7942 Sat 24 Mar 2018 08:34:59 AEDT ]]> Genome-wide association study identifies a possible susceptibility locus for endometrial cancer https://novaprd-lb.newcastle.edu.au/vital/access/manager/Repository/uon:17481 Sat 24 Mar 2018 08:04:10 AEDT ]]> Genome-wide association study identifies novel breast cancer susceptibility loci https://novaprd-lb.newcastle.edu.au/vital/access/manager/Repository/uon:3776 0.5. SNPs in five novel independent loci exhibited strong and consistent evidence of association with breast cancer (P < 10⁻⁷). Four of these contain plausible causative genes (FGFR2, TNRC9, MAP3K1 and LSP1). At the second stage, 1,792 SNPs were significant at the P < 0.05 level compared with an estimated 1,343 that would be expected by chance, indicating that many additional common susceptibility alleles may be identifiable by this approach.]]> Sat 24 Mar 2018 07:21:45 AEDT ]]>