Verneri Anttila

Summary

Affiliation: Wellcome Trust Genome Campus
Country: UK

Publications

  1. ncbi Genome-wide association study of migraine implicates a common susceptibility variant on 8q22.1
    Verneri Anttila
    Wellcome Trust Sanger Institute, Wellcome Trust Genome Campus, Cambridge, UK
    Nat Genet 42:869-73. 2010
  2. ncbi Towards an understanding of genetic predisposition to migraine
    Verneri Anttila
    Wellcome Trust Sanger Institute, Wellcome Trust Genome Campus, CB10 1SA, Hinxton, UK
    Genome Med 3:17. 2011
  3. ncbi European lactase persistence genotype shows evidence of association with increase in body mass index
    Johannes Kettunen
    Wellcome Trust Sanger Institute, Wellcome Trust Genome Campus, Hinxton, Cambridge CB10 1HH, UK
    Hum Mol Genet 19:1129-36. 2010

Detail Information

Publications3

  1. ncbi Genome-wide association study of migraine implicates a common susceptibility variant on 8q22.1
    Verneri Anttila
    Wellcome Trust Sanger Institute, Wellcome Trust Genome Campus, Cambridge, UK
    Nat Genet 42:869-73. 2010
    ..96 × 10??, permuted threshold for genome-wide significance 7.7 × 10??. To our knowledge, our data establish rs1835740 as the first genetic risk factor for migraine...
  2. ncbi Towards an understanding of genetic predisposition to migraine
    Verneri Anttila
    Wellcome Trust Sanger Institute, Wellcome Trust Genome Campus, CB10 1SA, Hinxton, UK
    Genome Med 3:17. 2011
    ..This putative mechanism, regulating the expression of the primary glutamate transporter in the brain, EAAT2/GLT-1, has interesting implications bridging the gap between Mendelian and common forms in this key group of disorders...
  3. ncbi European lactase persistence genotype shows evidence of association with increase in body mass index
    Johannes Kettunen
    Wellcome Trust Sanger Institute, Wellcome Trust Genome Campus, Hinxton, Cambridge CB10 1HH, UK
    Hum Mol Genet 19:1129-36. 2010
    ..In this study, we highlight issues in model selection in the genome-wide association studies and problems in imputation of these special genomic regions...