Avril Kennan

Identification of an IMPDH1 mutation in autosomal dominant retinitis pigmentosa (RP10) revealed following comparative microarray analysis of transcripts derived from retinas of wild-type and Rho-/- mice

Avril Kennan · Human Molecular Genetics · 2002 · 171 citations

Medicine, Genetics, Molecular Genetics +16

Retinitis Pigmentosa and Progressive Sensorineural Hearing Loss Caused by a C12258A Mutation in the Mitochondrial MTTS2 Gene

Fiona C. Mansergh, Sophia Millington‐Ward, Avril Kennan et al. · The American Journal of Human Genetics · 1999 · 103 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

Toward a Gene Therapy for Dominant Disease: Validation of an RNA Interference-Based Mutation-Independent Approach

Anna‐Sophia Kiang, Arpad Palfi, Marius Ader et al. · Molecular Therapy · 2005 · 82 citations · Full text

Life Sciences, Genetics, Molecular Biology +14

Therapeutic benefit derived from RNAi-mediated ablation of IMPDH1 transcripts in a murine model of autosomal dominant retinitis pigmentosa (RP10)

Lawrence C. S. Tam, Anna‐Sophia Kiang, Avril Kennan et al. · Human Molecular Genetics · 2008 · 63 citations · Full text

Medicine, Molecular Biology, Ophthalmology +17

Characterization of RP1L1, a highly polymorphic paralog of the retinitis pigmentosa 1 (RP1) gene.

Sara J. Bowne, Stephen P. Daiger, Heckenlively et al. · PubMed · 2003 · 51 citations · Full text

Medicine, Genetics, Molecular Genetics +14