Joachim Hallmayer

Publication Details

• Intronic single nucleotide polymorphisms of engrailed homeobox 2 modulate the disease vulnerability of autism in a han chinese population.

  Yang P, Shu BC, Hallmayer JF, Lung FW. Neuropsychobiology. 2010; 62 (2): 104-15

  Autism is a neurodevelopmental disorder with a strong genetic background that has been suggested to be associated with a susceptibility gene, engrailed homeobox 2(EN2), which maps to chromosome 7q36. Our study was aimed to explore the association between EN2 intronic single nucleotide polymorphisms (SNPs) with autism in an ethnic Han Chinese population.

  PubMedID: 20523082