Carr, Ian M.

Top Publications

Top Publications Authored or Co-Authored by "Carr, Ian M."

• 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
• 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
• The tudor SND1 protein is an m⁶a RNA reader essential for replication of kaposi’s sarcoma-associated herpesvirus

  eLife, Volume 8, Article e47261, Year 2019, Citations 74