Fiona C. Mansergh

Mutation of the calcium channel gene Cacna1f disrupts calcium signaling, synaptic transmission and cellular organization in mouse retina

Fiona C. Mansergh, Noelle C. Orton, John P. Vessey et al. · Human Molecular Genetics · 2005 · 265 citations

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 · 102 citations · Full text

C12258a Mutation, Mendelian Disorder, Mitochondrial Function +11

Novel mutations in the TIGR gene in early and late onset open angle glaucoma

Fiona C. Mansergh, Paul F. Kenna, Carmen Ayuso et al. · Human Mutation · 1998 · 70 citations

Ocular Disease, Genetics, Amino Acid Substitution +18

A mutation (met→arg) in the type I keratin (K14) gene responsible for autosomal dominant epidermolysis bullosa simplex

Marian M. Humphries, Denise M. Sheils, G. Jane Farrar et al. · Human Mutation · 1993 · 62 citations

Expression profiling and gene discovery in the mouse lens.

Michael A. Wride, Fiona C. Mansergh, Steffan Adams et al. · PubMed · 2003 · 60 citations