Cerys J. Evans

Autosomal-Dominant Corneal Endothelial Dystrophies CHED1 and PPCD1 Are Allelic Disorders Caused by Non-coding Mutations in the Promoter of OVOL2

Alice E. Davidson, Petra Lišková, Cerys J. Evans et al. · The American Journal of Human Genetics · 2015 · 78 citations · Full text

Ectopic GRHL2 Expression Due to Non-coding Mutations Promotes Cell State Transition and Causes Posterior Polymorphous Corneal Dystrophy 4

Petra Lišková, Ľubica Ďuďáková, Cerys J. Evans et al. · The American Journal of Human Genetics · 2018 · 56 citations · Full text

Insulin-like actions of nickel and other transition-metal ions in rat fat-cells

E D Saggerson, Suren R. Sooranna, Cerys J. Evans · Biochemical Journal · 1976 · 42 citations · Full text

Decrease Lipolysis, Insulin Signaling, Metabolic Syndrome +17

Heterozygous deletions at the ZEB1 locus verify haploinsufficiency as the mechanism of disease for posterior polymorphous corneal dystrophy type 3

Petra Lišková, Cerys J. Evans, Alice E. Davidson et al. · European Journal of Human Genetics · 2015 · 34 citations · Full text

Ocular Disease, Mendelian Disorder, Ophthalmology +8

Identification of Six Novel Mutations in<i>ZEB1</i>and Description of the Associated Phenotypes in Patients with Posterior Polymorphous Corneal Dystrophy 3

Cerys J. Evans, Petra Lišková, Ľubica Ďuďáková et al. · Annals of Human Genetics · 2014 · 32 citations