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Alice E Davidson

Showing results (41-50 of 66) with videos related to

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Ophthalmology|May 25, 2026
Genetic Prediction of Keratoplasty in Fuchs Endothelial Corneal DystrophySiyin Liu, Anita Szabo, Christina Zarouchlioti, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|August 10, 2011
Childhood-onset autosomal recessive bestrophinopathyArundhati Dev Borman, Alice E Davidson, James O'Sullivan, et al.
American Journal of Human Genetics|December 6, 2011
Biallelic mutations in PLA2G5, encoding group V phospholipase A2, cause benign fleck retinaPanagiotis I Sergouniotis, Alice E Davidson, Donna S Mackay, et al.
Translational Vision Science & Technology|June 6, 2025
Current Applications of Artificial Intelligence for Fuchs Endothelial Corneal Dystrophy: A Systematic ReviewSiyin Liu, Lynn Kandakji, Aleksander Stupnicki, et al.
American Journal of Human Genetics|March 3, 2018
Ectopic GRHL2 Expression Due to Non-coding Mutations Promotes Cell State Transition and Causes Posterior Polymorphous Corneal Dystrophy 4Petra Liskova, Lubica Dudakova, Cerys J Evans, et al.
Ophthalmology|October 24, 2013
Retinal structure and function in achromatopsia: implications for gene therapyVenki Sundaram, Caroline Wilde, Jonathan Aboshiha, et al.
Human Molecular Genetics|May 24, 2012
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, Jessica C Gardner, et al.
American Journal of Human Genetics|October 27, 2009
Missense mutations in a retinal pigment epithelium protein, bestrophin-1, cause retinitis pigmentosaAlice E Davidson, Ian D Millar, Jill E Urquhart, et al.
Experimental Eye Research|March 10, 2019
The utility of massively parallel sequencing for posterior polymorphous corneal dystrophy type 3 molecular diagnosisLubica Dudakova, Cerys J Evans, Nikolas Pontikos, et al.
JAMA Ophthalmology|June 28, 2019
Genetic Variants Associated With Corneal Biomechanical Properties and Potentially Conferring Susceptibility to Keratoconus in a Genome-Wide Association StudyAnthony P Khawaja, Karla E Rojas Lopez, Alison J Hardcastle, et al.
Pageof 7

Showing results (41-50 of 66) with videos related to

Sort By:
Pageof 7
Ophthalmology|May 25, 2026
Genetic Prediction of Keratoplasty in Fuchs Endothelial Corneal DystrophySiyin Liu, Anita Szabo, Christina Zarouchlioti, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|August 10, 2011
Childhood-onset autosomal recessive bestrophinopathyArundhati Dev Borman, Alice E Davidson, James O'Sullivan, et al.
American Journal of Human Genetics|December 6, 2011
Biallelic mutations in PLA2G5, encoding group V phospholipase A2, cause benign fleck retinaPanagiotis I Sergouniotis, Alice E Davidson, Donna S Mackay, et al.
Translational Vision Science & Technology|June 6, 2025
Current Applications of Artificial Intelligence for Fuchs Endothelial Corneal Dystrophy: A Systematic ReviewSiyin Liu, Lynn Kandakji, Aleksander Stupnicki, et al.
American Journal of Human Genetics|March 3, 2018
Ectopic GRHL2 Expression Due to Non-coding Mutations Promotes Cell State Transition and Causes Posterior Polymorphous Corneal Dystrophy 4Petra Liskova, Lubica Dudakova, Cerys J Evans, et al.
Ophthalmology|October 24, 2013
Retinal structure and function in achromatopsia: implications for gene therapyVenki Sundaram, Caroline Wilde, Jonathan Aboshiha, et al.
Human Molecular Genetics|May 24, 2012
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, Jessica C Gardner, et al.
American Journal of Human Genetics|October 27, 2009
Missense mutations in a retinal pigment epithelium protein, bestrophin-1, cause retinitis pigmentosaAlice E Davidson, Ian D Millar, Jill E Urquhart, et al.
Experimental Eye Research|March 10, 2019
The utility of massively parallel sequencing for posterior polymorphous corneal dystrophy type 3 molecular diagnosisLubica Dudakova, Cerys J Evans, Nikolas Pontikos, et al.
JAMA Ophthalmology|June 28, 2019
Genetic Variants Associated With Corneal Biomechanical Properties and Potentially Conferring Susceptibility to Keratoconus in a Genome-Wide Association StudyAnthony P Khawaja, Karla E Rojas Lopez, Alison J Hardcastle, et al.
Pageof 7