Cerys J. Evans - Concepedia

Author

Cerys J. Evans

University College London ORCID

Also Known As

C EVANS, C J Evans, C J. Evans, C. Evans, Cerys J Evans, Cerys J. Evans, Cerys J. Evans

Publications

347

Citations

H-Index

Concepts

All Affiliations

University College London Charles University Moorfields Eye Hospital General University Hospital in Prague Moorfields Eye Hospital NHS Foundation Trust

About

Cerys J. Evans is an author at University College London specializing in medicine, ophthalmology, and pathology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	5	5	131
2	Health Sciences	2	2	60
3	Biochemistry	2	2	60
4	Diabetes	1	1	42
5	Endocrinology	1	1	42

Cerys J. Evans

Publications

333

Citations

H-Index

Page 1

	Year	Citations
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, The American Journal of Human Genetics	2015	78
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, The American Journal of Human Genetics	2018	56
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 Decrease LipolysisInsulin SignalingMetabolic SyndromeRat Fat-cellsMetabolic State	1976	42
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, European Journal of Human Genetics Ocular DiseaseMendelian DisorderOphthalmologyGenetic DisorderCorneal Dystrophy	2015	34
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, Annals of Human Genetics	2014	32
Genotype-Phenotype Correlation for<i>TGFBI</i>Corneal Dystrophies Identifies p.(G623D) as a Novel Cause of Epithelial Basement Membrane Dystrophy Cerys J. Evans, Alice E. Davidson, Nicole Carnt, Investigative Ophthalmology & Visual Science Tgfbi MutationsOcular DiseaseMendelian DisorderOphthalmologyHuman Growth	2016	26
Paraproteinemic keratopathy associated with monoclonal gammopathy of undetermined significance (<scp>MGUS</scp>): clinical findings in twelve patients including recurrence after keratoplasty Pavlína Skalická, Ľubica Ďuďáková, Michalis Palos, Acta Ophthalmologica	2019	20
The activities and intracellular distribution of nicotinamide-adenine dinucleotide phosphate-malate dehydrogenase, phosphoenolpyruvate carboxykinase and pyruvate carboxylase in rat, guinea-pig and rabbit tissues David Saggerson, Cerys J. Evans Biochemical Journal Phosphoenolpyruvate CarboxykinaseIntracellular DistributionOxidative StressRabbit TissuesMetabolic State	1975	18
Schnyder corneal dystrophy and associated phenotypes caused by novel and recurrent mutations in the UBIAD1 gene Cerys J. Evans, Ľubica Ďuďáková, Pavlína Skalická, BMC Ophthalmology	2018	16
The utility of massively parallel sequencing for posterior polymorphous corneal dystrophy type 3 molecular diagnosis Ľubica Ďuďáková, Cerys J. Evans, Nikolas Pontikos, Experimental Eye Research Molecular DiagnosisMolecular Diagnostic TechniquesOcular DiseaseOphthalmologyCorneal Dystrophy	2019	11

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