Chan, Waiman

Top Publications

Top Publications Authored or Co-Authored by "Chan, Waiman"

• Mutations in a human ROBO gene disrupt hindbrain axon pathway crossing and morphogenesis

  Science, Volume 304, No. 5676, Year 2004, Citations 364
• Homozygous HOXA1 mutations disrupt human brainstem, inner ear, cardiovascular and cognitive development

  Nature Genetics, Volume 37, No. 10, Year 2005, Citations 267
• A novel syndrome caused by the E410K amino acid substitution in the neuronal β-tubulin isotype 3

  Brain, Volume 136, No. 2, Year 2013, Citations 96
• Identification of KIF21A mutations as a rare cause of congenital fibrosis of the extraocular muscles type 3 (CFEOM3)

  Investigative Ophthalmology and Visual Science, Volume 45, No. 7, Year 2004, Citations 79
• HOXB1 founder mutation in humans recapitulates the phenotype of Hoxb1 ^-/- mice

  American Journal of Human Genetics, Volume 91, No. 1, Year 2012, Citations 72