Arif O. Khan - Concepedia

Author

Arif O. Khan

King Khaled Eye Specialist Hospital ORCID

Also Known As

A O Khan, A. O Khan, A.O. Khan, Arif Khan, Arif O Khan, Arif O. Khan

113

Publications

1.9K

Citations

H-Index

Concepts

All Affiliations

King Khaled Eye Specialist Hospital King Faisal Specialist Hospital & Research Centre King Saud University University Hospital Cologne University of Cologne

About

Arif O. Khan is an author at King Khaled Eye Specialist Hospital specializing in medicine, ophthalmology, and genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	12	12	732
2	Molecular Genetics	3	3	123
3	Molecular Medicine	2	2	120
4	Public Health	1	1	81
5	Molecular Biology	1	1	52

Arif O. Khan

Publications

1.6K

Citations

H-Index

Page 1

	Year	Citations
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 Tobias Eisenberger, Christine Neuhaus, Arif O. Khan, PLoS ONE Cnv AnalysisGeneticsGenetic EpidemiologyPathologyDisease Gene Identification	2013	225
Expanding the clinical, allelic, and locus heterogeneity of retinal dystrophies Nisha Patel, Mohammed A. Aldahmesh, Hisham Alkuraya, Genetics in Medicine Ocular DiseaseRetinaOphthalmologyGeneticsLocus Heterogeneity	2015	109
The distinct ophthalmic phenotype of Knobloch syndrome in children Arif O. Khan, Mohammed A. Aldahmesh, Jawahir Y. Mohamed, British Journal of Ophthalmology Ocular DiseaseGeneticsGenetic EpidemiologyPathologyRetinal Therapies	2012	81
Molecular characterization of retinitis pigmentosa in Saudi Arabia. Mohammed A. Aldahmesh, Leen Abu Safieh, Hisham Alkuraya, PubMed	2009	80
Recessive Congenital Total Cataract with Microcornea and Heterozygote Carrier Signs Caused by a Novel Missense CRYAA Mutation (R54C) Arif O. Khan, Mohammed A. Aldahmesh, Brian F. Meyer American Journal of Ophthalmology Ocular DiseaseOphthalmologyGeneticsGlaucomaHeterozygote Carrier Signs	2007	65
Next-generation sequencing reveals the mutational landscape of clinically diagnosed Usher syndrome: copy number variations, phenocopies, a predominant target for translational read-through, and<i>PEX26</i>mutated in Heimler syndrome Christine Neuhaus, Tobias Eisenberger, Christian Decker, Molecular Genetics & Genomic Medicine	2017	62
Severe Molecular Defects of a Novel<i>FOXC1 W152G</i>Mutation Result in Aniridia Yoko Itō, Tim Footz, Fred B. Berry, Investigative Ophthalmology & Visual Science	2009	58
New Findings in a Global Approach to Dissect the Whole Phenotype of PLA2G6 Gene Mutations Mustafa A. Salih, Emeline Mundwiller, Arif O. Khan, PLoS ONE GeneticsMolecular BiologyBrain Iron AccumulationMolecular GeneticsDisease Gene Identification	2013	52
<i>C21orf2</i>is mutated in recessive early-onset retinal dystrophy with macular staphyloma and encodes a protein that localises to the photoreceptor primary cilium Arif O. Khan, Tobias Eisenberger, Kerstin Nagel‐Wolfrum, British Journal of Ophthalmology	2015	43
Ophthalmic features of ataxia telangiectasia–like disorder Arif O. Khan, Darren T. Oystreck, Mustafa A. Salih Journal of American Association for Pediatric Ophthalmology and Strabismus Ocular DiseaseOphthalmologyOcular PathologyNeuropathologyMedicine	2007	40

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