Alice E. Davidson - Concepedia

Author

Alice E. Davidson

Also Known As

A Davidson, A E Davidson, A. DAVIDSON, A. Davidson, A. E. Davidson, Alice Davidson, Alice E Davidson, Alice E. Davidson, Alice E Davidson, Alice E. Davidson

106

Publications

3.3K

Citations

H-Index

Concepts

All Affiliations

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

About

Alice E. Davidson is an author at University College London specializing in medicine, genetics, and ophthalmology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	17	21	1.5K
2	Public Health	3	3	150
3	Natural Sciences	1	1	18
4	Anatomy	1	1	174
5	Biochemistry	1	1	18

Alice E. Davidson

Publications

2.4K

Citations

H-Index

Page 1

	Year	Citations
Missense Mutations in a Retinal Pigment Epithelium Protein, Bestrophin-1, Cause Retinitis Pigmentosa Alice E. Davidson, I. D. Millar, Jill Urquhart, The American Journal of Human Genetics Missense MutationsOcular DiseaseRetinaOphthalmologyPathology	2009	180
Retinal Structure and Function in Achromatopsia Venki Sundaram, Caroline Wilde, Jonathan Aboshiha, Ophthalmology RetinaOphthalmologyRetinal StructureAnatomyGlaucoma	2013	174
A Longitudinal Study of Stargardt Disease: Clinical and Electrophysiologic Assessment, Progression, and Genotype Correlations Kaoru Fujinami, Noemi Lois, Alice E. Davidson, American Journal of Ophthalmology PathologyGenotype CorrelationsNeuropathologyMedicineStargardt Disease	2013	151
Deep intronic mutation in OFD1, identified by targeted genomic next-generation sequencing, causes a severe form of X-linked retinitis pigmentosa (RP23) Tom R. Webb, David A. Parfitt, J.C. Gardner, Human Molecular Genetics	2012	151
Recessive Mutations in KCNJ13, Encoding an Inwardly Rectifying Potassium Channel Subunit, Cause Leber Congenital Amaurosis Panagiotis I. Sergouniotis, Alice E. Davidson, Donna S. Mackay, The American Journal of Human Genetics Molecular NeuroscienceDevelopmental BiologyHyperpolarization (Biology)Genetic DisorderGenetics	2011	140
Retinal Structure, Function, and Molecular Pathologic Features in Gyrate Atrophy Panagiotis I. Sergouniotis, Alice E. Davidson, Eva Lenassi, Ophthalmology Ocular DiseaseRetinaOphthalmologyRetinal StructureMolecular Biology	2011	116
Clinical and Molecular Analysis of Stargardt Disease With Preserved Foveal Structure and Function Kaoru Fujinami, Panagiotis I. Sergouniotis, Alice E. Davidson, American Journal of Ophthalmology OphthalmologyPreserved Foveal StructureMolecular AnalysisPathologyScleroderma	2013	116
<i>RP1L1</i>Variants are Associated with a Spectrum of Inherited Retinal Diseases Including Retinitis Pigmentosa and Occult Macular Dystrophy Alice E. Davidson, Panagiotis I. Sergouniotis, Donna S. Mackay, Human Mutation Ocular DiseaseFamily MembersGeneticsGenetic EpidemiologyPathology	2012	101
Antisense Therapy for a Common Corneal Dystrophy Ameliorates TCF4 Repeat Expansion-Mediated Toxicity Christina Zarouchlioti, Beatriz Sanchez-Pintado, Nathaniel J. Hafford‐Tear, The American Journal of Human Genetics	2018	90
CRISPR/Cas9-targeted enrichment and long-read sequencing of the Fuchs endothelial corneal dystrophy–associated TCF4 triplet repeat Nathaniel J. Hafford‐Tear, Yu‐Chih Tsai, Amanda N. Sadan, Genetics in Medicine	2019	83

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