Migraine: a complex genetic disorder

This publication has 145 references indexed in Scilit:

• Trait Components Provide Tools to Dissect the Genetic Susceptibility of Migraine
  American Journal of Human Genetics, 2006
• Minor Head Trauma–Induced Sporadic Hemiplegic Migraine Coma
  Pediatric Neurology, 2006
• A haplotype map of the human genome
  Nature, 2005
• Association between migraine and HLA–DRB1 gene polymorphisms
  The Journal of Headache and Pain, 2005
• The estrogen receptor 1 G594A polymorphism is associated with migraine susceptibility in two independent case/control groups
  neurogenetics, 2004
• No Mutations in CACNA1A and ATP1A2 in Probands With Common Types of Migraine
  Archives of Neurology, 2004
• A novel missense ATP1A2 mutation in a Finnish family with familial hemiplegic migraine type 2
  neurogenetics, 2004
• Update on the genetics of migraine
  Human Genetics, 2004
• Is the CACNA1A gene involved in familial migraine with aura?
  Neurological Sciences, 2002
• Autosomal dominant cerebellar ataxia (SCA6) associated with small polyglutamine expansions in the α1A-voltage-dependent calcium channel
  Nature Genetics, 1997