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M. Ali
M. Ali
University of Texas Health Science Center at Houston
Biology
Genetics
Cancer research
Anatomy
Dominance (genetics)
5
Papers
59
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Recessive mutations in TSPAN12 cause retinal dysplasia and severe familial exudative vitreoretinopathy (FEVR).
2012
Investigative Ophthalmology & Visual Science
James A. Poulter
Alice E. Davidson
M. Ali
David F. Gilmour
David A. Parry
Helen A. Mintz-Hittner
Ian M. Carr
Helen M. Bottomley
Vernon Long
Louise Downey
Panagiotis I. Sergouniotis
Genevieve A. Wright
Robert E. MacLaren
Anthony T. Moore
Andrew R. Webster
Chris F. Inglehearn
Carmel Toomes
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Citations (57)
Identification of 3 Novel Mutations in LCA5 (Lebercilin) in Leber’s Congenital Amaurosis Families
2010
Investigative Ophthalmology & Visual Science
Musallam Al-Araimi
James A. Poulter
Martin McKibbin
Adam D. Booth
M. N. Mohammed
Hussain Jafri
Yasmin Rashid
M. Ali
Chris F. Inglehearn
Carmel Toomes
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Foveal Hypoplasia, Chiasmal Misrouting and Anterior Segment Dysgenesis in the Absence of Albinism
2009
Investigative Ophthalmology & Visual Science
David F. Gilmour
Musallam Al-Araimi
Bishwanath Pal
Moin D. Mohamed
John Bradbury
M M van Genderen
M. Ali
Carmel Toomes
Chris F. Inglehearn
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Confirmation of a Locus for Primary Congenital Glaucoma (PCG) on Chromosome 14q24 in a Pakistani Pedigree
2008
Investigative Ophthalmology & Visual Science
Adam P. Booth
A.-L. Murphy
G. Williams
M. Ali
Carmel Toomes
H. Jaffri
Yasmin Rashid
Martin McKibbin
Chris F. Inglehearn
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A missense mutation (p.R106S) in the nuclear localization signal sequence of CERKL causes autosomal recessive retinal degeneration
2008
M. Ali
Vedam L. Ramprasad
Nagasamy Soumittra
Moin Mohamed
Hussain Jafri
Yasmin Rashid
Michael Danciger
Martin McKibbin
Govindasamy Kumaramanickavel
Chris F. Inglehearn
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