Inglehearn, Chris F.

Top Publications

Top Publications Authored or Co-Authored by "Inglehearn, Chris F."

• Mutations in the pre-mRNA splicing factor gene PRPC8 in autosomal dominant retinitis pigmentosa (RP13)

  Human Molecular Genetics, Volume 10, No. 15, Year 2001, Citations 284
• Mutations in TMEM216 perturb ciliogenesis and cause Joubert, Meckel and related syndromes

  Nature Genetics, Volume 42, No. 7, Year 2010, Citations 265
• An siRNA-based functional genomics screen for the identification of regulators of ciliogenesis and ciliopathy genes

  Nature Cell Biology, Volume 17, No. 8, Year 2015, Citations 206
• Mutations in a novel retina-specific gene cause autosomal dominant retinitis pigmentosa

  Nature Genetics, Volume 22, No. 3, Year 1999, Citations 162
• Disrupted alternative splicing for genes implicated in splicing and ciliogenesis causes PRPF31 retinitis pigmentosa

  Nature Communications, Volume 9, No. 1, Article 4234, Year 2018, Citations 147