References

A selection of publications including the use of ECACC HRC DNA:

• Identification of FOXP2 truncation as a novel cause of developmental speech and language deficits.
  MacDermot et al: American Journal of Human Genetics, 2005, Vol. 76, 1074

• A genome annotation-driven approach to cloning the human ORFeome
  Collins et al:Genome Biology 2004, Vol. 5, R84

• The impact of SNP density on fine-scale patterns of linkage disequilibrium
  Ke et al:  Human Molecular Genetics, 2004, Vol. 13, 577-588

• An association between variants in the IGF2 gene and Beckwith–Wiedemann syndrome: interaction between genotype and epigenotype
  Murrell et al: Human Molecular Genetics, 2004, Vol. 13, 247-255

• A 77-Kilobase region of chromosome 6p22.2 Is associated with dyslexia in families from the United Kingdom and from the United States
  Francks et al: American Journal of Human. Genetics, 2004, Vol. 75, 1046–1058
  
• Association and haplotype analysis of the insulin-degrading enzyme (IDE) gene, a strong positional and biological candidate for type 2 diabetes susceptibility
  Groves et al: Diabetes, 2003, Vol. 52, 1300-1305

• Large-scale association studies of variants in genes encoding the pancreatic beta-cell KATP channel subunits Kir6.2 (KCNJ11) and SUR1 (ABCC8) confirm that the KCNJ11 E23K variant is associated with type 2 diabetes.
  Gloyn et al.  Diabetes, 2003 Vol. 2, 568-572

• Meta-analysis and a large association study confirm a role for calpain-10 variation in type 2 diabetes susceptibility.
  Weedon et al. American Journal of Human Genetics, 2003, Vol. 73, 1208-12

• Use of European Collection of Cell Cultures (ECACC) DNA Control Panels (HRC-1) in the quality control of high throughput SNP Studies at MRC geneservice.
  Andrew Dearlove and Justin Brooking