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Arif O Khan
Arif O Khan
Professor of Ophthalmology, Cleveland Clinic Abu Dhabi
Verified email at mssm.edu
Title
Cited by
Cited by
Year
Autozygome-guided exome sequencing in retinal dystrophy patients reveals pathogenetic mutations and novel candidate disease genes
L Abu-Safieh, M Alrashed, S Anazi, H Alkuraya, AO Khan, M Al-Owain, ...
Genome research 23 (2), 236-247, 2013
2892013
Increasing the yield in targeted next-generation sequencing by implicating CNV analysis, non-coding exons and the overall variant load: the example of retinal dystrophies
T Eisenberger, C Neuhaus, AO Khan, C Decker, MN Preising, ...
PloS one 8 (11), e78496, 2013
2392013
In search of triallelism in Bardet–Biedl syndrome
L Abu-Safieh, S Al-Anazi, L Al-Abdi, M Hashem, H Alkuraya, M Alamr, ...
European journal of human genetics 20 (4), 420-427, 2012
1472012
Comprehensive gene panels provide advantages over clinical exome sequencing for Mendelian diseases
Saudi Mendeliome Group falkuaya@ kfshrc. edu. sa
Genome biology 16, 1-14, 2015
1382015
Mutations in LRPAP1 are associated with severe myopia in humans
MA Aldahmesh, AO Khan, H Alkuraya, N Adly, S Anazi, AA Al-Saleh, ...
The American Journal of Human Genetics 93 (2), 313-320, 2013
1272013
Genetics of primary glaucoma
AO Khan
Current opinion in ophthalmology 22 (5), 347-355, 2011
1272011
Postoperative glaucoma following infantile cataract surgery: an individual patient data meta-analysis
A Mataftsi, AB Haidich, S Kokkali, PK Rabiah, E Birch, DR Stager, ...
JAMA ophthalmology 132 (9), 1059-1067, 2014
1132014
Expanding the clinical, allelic, and locus heterogeneity of retinal dystrophies
N Patel, MA Aldahmesh, H Alkuraya, S Anazi, H Alsharif, AO Khan, ...
Genetics in Medicine 18 (6), 554-562, 2016
1072016
Molecular characterization of retinitis pigmentosa in Saudi Arabia
MA Aldahmesh, LA Safieh, H Alkuraya, A Al-Rajhi, H Shamseldin, ...
Molecular vision 15, 2464, 2009
1042009
Two-year survival of Ahmed valve implantation in the first 2 years of life with and without intraoperative mitomycin-C
F Al-Mobarak, AO Khan
Ophthalmology 116 (10), 1862-1865, 2009
1012009
Identification of ADAMTS18 as a gene mutated in Knobloch syndrome
MA Aldahmesh, AO Khan, JY Mohamed, H Alkuraya, H Ahmed, S Bobis, ...
Journal of medical genetics 48 (9), 597-601, 2011
912011
Mutations in ARMC9, which encodes a basal body protein, cause Joubert syndrome in humans and ciliopathy phenotypes in zebrafish
JC Van De Weghe, TDS Rusterholz, B Latour, ME Grout, KA Aldinger, ...
The American Journal of Human Genetics 101 (1), 23-36, 2017
872017
Novel phenotypes and loci identified through clinical genomics approaches to pediatric cataract
N Patel, D Anand, D Monies, S Maddirevula, AO Khan, T Algoufi, ...
Human genetics 136, 205-225, 2017
872017
Recessive congenital total cataract with microcornea and heterozygote carrier signs caused by a novel missense CRYAA mutation (R54C)
AO Khan, MA Aldahmesh, B Meyer
American journal of ophthalmology 144 (6), 949-952. e2, 2007
782007
Identification of a truncation mutation of acylglycerol kinase (AGK) gene in a novel autosomal recessive cataract locus
MA Aldahmesh, AO Khan, JY Mohamed, MH Alghamdi, FS Alkuraya
Human mutation 33 (6), 960-962, 2012
772012
Nanoparticles for biomedical applications: An overview
HA Khan, MK Sakharkar, A Nayak, U Kishore, A Khan
Nanobiomaterials, 357-384, 2018
712018
Next‐generation sequencing reveals the mutational landscape of clinically diagnosed Usher syndrome: copy number variations, phenocopies, a predominant target for translational …
C Neuhaus, T Eisenberger, C Decker, S Nagl, C Blank, M Pfister, ...
Molecular genetics & genomic medicine 5 (5), 531-552, 2017
712017
Congenital megalocornea with zonular weakness and childhood lens-related secondary glaucoma-a distinct phenotype caused by recessive LTBP2 mutations
AO Khan, MA Aldahmesh, FS Alkuraya
Molecular vision 17, 2570, 2011
712011
WDR19: An ancient, retrograde, intraflagellar ciliary protein is mutated in autosomal recessive retinitis pigmentosa and in Senior‐Loken syndrome
RG Coussa, EA Otto, HY Gee, P Arthurs, H Ren, I Lopez, V Keser, Q Fu, ...
Clinical genetics 84 (2), 150-159, 2013
702013
Allelic heterogeneity in inbred populations: the Saudi experience with Alström syndrome as an illustrative example
MA Aldahmesh, L Abu‐Safieh, AO Khan, ZN Al‐Hassnan, R Shaheen, ...
American Journal of Medical Genetics Part A 149 (4), 662-665, 2009
702009
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