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Investigative Ophthalmology & Visual Science
|
March 20, 2012
Recessive mutations in TSPAN12 cause retinal dysplasia and severe familial exudative vitreoretinopathy (FEVR)
James A Poulter, Alice E Davidson, Manir Ali, et al.
Human Mutation
|
March 17, 2010
Prognosis for splicing factor PRPF8 retinitis pigmentosa, novel mutations and correlation between human and yeast phenotypes
Katherine V Towns, Athina Kipioti, Vernon Long, et al.
Neurosurgery
|
April 28, 2017
Results of the ANSWER Trial Using the PulseRider for the Treatment of Broad-Necked, Bifurcation Aneurysms
Alejandro M Spiotta, Colin P Derdeyn, Satoshi Tateshima, et al.
Ophthalmology
|
August 7, 2022
Late-Onset Autosomal Dominant Macular Degeneration Caused by Deletion of the CRX Gene
Samar Yahya, Claire E L Smith, James A Poulter, et al.
The British Journal of Ophthalmology
|
May 9, 2025
Inherited retinal disease pathway in the UK: a patient perspective and the potential of AI
Wendy Wong, Dayyanah Sumodhee, Tiyi Morris, et al.
JAMA Ophthalmology
|
March 3, 2017
Association of Steroid 5α-Reductase Type 3 Congenital Disorder of Glycosylation With Early-Onset Retinal Dystrophy
Rachel L Taylor, Gavin Arno, James A Poulter, et al.
Genome Medicine
|
December 12, 2018
Complex structural variants in Mendelian disorders: identification and breakpoint resolution using short- and long-read genome sequencing
Alba Sanchis-Juan, Jonathan Stephens, Courtney E French, et al.
Nature Medicine
|
May 20, 2020
A deep learning system for differential diagnosis of skin diseases
Yuan Liu, Ayush Jain, Clara Eng, et al.
Investigative Ophthalmology & Visual Science
|
June 7, 2017
Specific Alleles of CLN7/MFSD8, a Protein That Localizes to Photoreceptor Synaptic Terminals, Cause a Spectrum of Nonsyndromic Retinal Dystrophy
Kamron N Khan, Mohammed E El-Asrag, Cristy A Ku, et al.
Investigative Ophthalmology & Visual Science
|
September 9, 2025
Genome-Wide Insights Into the Genes and Pathways Shaping Human Foveal Development: Redefining the Genetic Landscape of Foveal Hypoplasia
Callum Hunt, Ha-Jun Yoon, Alvin Lirio, et al.
Page
of 125
Search research articles
Search
Showing results (1111-1120 of 1,250) with videos related to
Sort By:
Page
of 125
Investigative Ophthalmology & Visual Science
|
March 20, 2012
Recessive mutations in TSPAN12 cause retinal dysplasia and severe familial exudative vitreoretinopathy (FEVR)
James A Poulter, Alice E Davidson, Manir Ali, et al.
Human Mutation
|
March 17, 2010
Prognosis for splicing factor PRPF8 retinitis pigmentosa, novel mutations and correlation between human and yeast phenotypes
Katherine V Towns, Athina Kipioti, Vernon Long, et al.
Neurosurgery
|
April 28, 2017
Results of the ANSWER Trial Using the PulseRider for the Treatment of Broad-Necked, Bifurcation Aneurysms
Alejandro M Spiotta, Colin P Derdeyn, Satoshi Tateshima, et al.
Ophthalmology
|
August 7, 2022
Late-Onset Autosomal Dominant Macular Degeneration Caused by Deletion of the CRX Gene
Samar Yahya, Claire E L Smith, James A Poulter, et al.
The British Journal of Ophthalmology
|
May 9, 2025
Inherited retinal disease pathway in the UK: a patient perspective and the potential of AI
Wendy Wong, Dayyanah Sumodhee, Tiyi Morris, et al.
JAMA Ophthalmology
|
March 3, 2017
Association of Steroid 5α-Reductase Type 3 Congenital Disorder of Glycosylation With Early-Onset Retinal Dystrophy
Rachel L Taylor, Gavin Arno, James A Poulter, et al.
Genome Medicine
|
December 12, 2018
Complex structural variants in Mendelian disorders: identification and breakpoint resolution using short- and long-read genome sequencing
Alba Sanchis-Juan, Jonathan Stephens, Courtney E French, et al.
Nature Medicine
|
May 20, 2020
A deep learning system for differential diagnosis of skin diseases
Yuan Liu, Ayush Jain, Clara Eng, et al.
Investigative Ophthalmology & Visual Science
|
June 7, 2017
Specific Alleles of CLN7/MFSD8, a Protein That Localizes to Photoreceptor Synaptic Terminals, Cause a Spectrum of Nonsyndromic Retinal Dystrophy
Kamron N Khan, Mohammed E El-Asrag, Cristy A Ku, et al.
Investigative Ophthalmology & Visual Science
|
September 9, 2025
Genome-Wide Insights Into the Genes and Pathways Shaping Human Foveal Development: Redefining the Genetic Landscape of Foveal Hypoplasia
Callum Hunt, Ha-Jun Yoon, Alvin Lirio, et al.
Page
of 125