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Manir Ali

Showing results (51-60 of 80) with videos related to

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Genes|January 11, 2018
Identification of Inherited Retinal Disease-Associated Genetic Variants in 11 Candidate GenesGaluh D N Astuti, L Ingeborgh van den Born, M Imran Khan, et al.
Investigative Ophthalmology & Visual Science|April 9, 2011
Genetic heterogeneity for recessively inherited congenital cataract microcornea with corneal opacityKamron Khan, Ahmed Al-Maskari, Martin McKibbin, et al.
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.
American Journal of Human Genetics|June 3, 2017
Defects in the Cell Signaling Mediator β-Catenin Cause the Retinal Vascular Condition FEVREvangelia S Panagiotou, Carla Sanjurjo Soriano, James A Poulter, et al.
Ophthalmology|August 7, 2022
Late-Onset Autosomal Dominant Macular Degeneration Caused by Deletion of the CRX GeneSamar Yahya, Claire E L Smith, James A Poulter, et al.
JAMA Ophthalmology|March 3, 2017
Association of Steroid 5α-Reductase Type 3 Congenital Disorder of Glycosylation With Early-Onset Retinal DystrophyRachel L Taylor, Gavin Arno, James A Poulter, 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 DystrophyKamron N Khan, Mohammed E El-Asrag, Cristy A Ku, et al.
Molecular Vision|March 25, 2015
Novel C8orf37 mutations cause retinitis pigmentosa in consanguineous families of Pakistani originZeinab Ravesh, Mohammed E El Asrag, Nicole Weisschuh, et al.
Schizophrenia Bulletin|November 7, 2020
A Recessively Inherited Risk Locus on Chromosome 13q22-31 Conferring Susceptibility to SchizophreniaTariq Mahmood, Mohammed E El-Asrag, James A Poulter, et al.
American Journal of Human Genetics|April 14, 2009
Null mutations in LTBP2 cause primary congenital glaucomaManir Ali, Martin McKibbin, Adam Booth, et al.
Pageof 8

Showing results (51-60 of 80) with videos related to

Sort By:
Pageof 8
Genes|January 11, 2018
Identification of Inherited Retinal Disease-Associated Genetic Variants in 11 Candidate GenesGaluh D N Astuti, L Ingeborgh van den Born, M Imran Khan, et al.
Investigative Ophthalmology & Visual Science|April 9, 2011
Genetic heterogeneity for recessively inherited congenital cataract microcornea with corneal opacityKamron Khan, Ahmed Al-Maskari, Martin McKibbin, et al.
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.
American Journal of Human Genetics|June 3, 2017
Defects in the Cell Signaling Mediator β-Catenin Cause the Retinal Vascular Condition FEVREvangelia S Panagiotou, Carla Sanjurjo Soriano, James A Poulter, et al.
Ophthalmology|August 7, 2022
Late-Onset Autosomal Dominant Macular Degeneration Caused by Deletion of the CRX GeneSamar Yahya, Claire E L Smith, James A Poulter, et al.
JAMA Ophthalmology|March 3, 2017
Association of Steroid 5α-Reductase Type 3 Congenital Disorder of Glycosylation With Early-Onset Retinal DystrophyRachel L Taylor, Gavin Arno, James A Poulter, 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 DystrophyKamron N Khan, Mohammed E El-Asrag, Cristy A Ku, et al.
Molecular Vision|March 25, 2015
Novel C8orf37 mutations cause retinitis pigmentosa in consanguineous families of Pakistani originZeinab Ravesh, Mohammed E El Asrag, Nicole Weisschuh, et al.
Schizophrenia Bulletin|November 7, 2020
A Recessively Inherited Risk Locus on Chromosome 13q22-31 Conferring Susceptibility to SchizophreniaTariq Mahmood, Mohammed E El-Asrag, James A Poulter, et al.
American Journal of Human Genetics|April 14, 2009
Null mutations in LTBP2 cause primary congenital glaucomaManir Ali, Martin McKibbin, Adam Booth, et al.
Pageof 8