Taylor, Graham Roy

Top Publications

Top Publications Authored or Co-Authored by "Taylor, Graham Roy"

• Mutations causing familial biparental hydatidiform mole implicate C6orf221 as a possible regulator of genomic imprinting in the human oocyte

  American Journal of Human Genetics, Volume 89, No. 3, Year 2011, Citations 213
• Mutational spectrum of the oral-facial-digital type I syndrome: A study on a large collection of patients

  Human Mutation, Volume 29, No. 10, Year 2008, Citations 100
• Mutations in MEGF10, a regulator of satellite cell myogenesis, cause early onset myopathy, areflexia, respiratory distress and dysphagia (EMARDD)

  Nature Genetics, Volume 43, No. 12, Year 2011, Citations 89
• Mutations in C4orf26, encoding a peptide with in vitro hydroxyapatite crystal nucleation and growth activity, cause amelogenesis imperfecta

  American Journal of Human Genetics, Volume 91, No. 3, Year 2012, Citations 88
• Prostaglandin transporter mutations cause pachydermoperiostosis with myelofibrosis

  Human Mutation, Volume 33, No. 8, Year 2012, Citations 74