N. Khan

发表

Worldwide Argus II implantation: recommendations to optimize patient outcomes

Jennifer I. Lim, Jessy D. Dorn, Suber S. Huang, 2016, BMC Ophthalmology.

CNGB3 achromatopsia with progressive loss of residual cone function and impaired rod-mediated function.

P. Sieving, N. Khan, B. Wissinger, 2007, Investigative ophthalmology & visual science.

Retinal safety evaluation of photoacoustic microscopy.

Yannis M. Paulus, Xueding Wang, Van Phuc Nguyen, 2020, Experimental eye research.

Distinct Signature of Altered Homeostasis in Aging Rod Photoreceptors: Implications for Retinal Diseases

A. Swaroop, S. Parapuram, S. Zareparsi, 2010, PloS one.

P23H rhodopsin transgenic rat: correlation of retinal function with histopathology.

P. Sieving, N. Khan, M. Kondo, 2000, Investigative ophthalmology & visual science.

Inhibiting autophagy reduces retinal degeneration caused by protein misfolding

D. Klionsky, N. Khan, D. Zacks, 2018, Autophagy.

Loss of Raf-1 kinase inhibitory protein delays early-onset severe retinal ciliopathy in Cep290rd16 mouse.

H. Khanna, N. Khan, Balajikarthick Subramanian, 2014, Investigative ophthalmology & visual science.

Clinical phenotypes and prognostic full-field electroretinographic findings in Stargardt disease.

J. Heckenlively, K. Branham, N. Khan, 2013, American journal of ophthalmology.

Erratum to: Worldwide Argus II implantation: recommendations to optimize patient outcomes

Jennifer I. Lim, Suber S. Huang, A. Ho, 2016, BMC Ophthalmology.

A specific phosphorylation regulates the protective role of αA-crystallin in diabetes.

P. Fort, K. Schey, N. Khan, 2018, JCI insight.

ISCEV extended protocol for the photopic On–Off ERG

J. Kremers, G. Holder, N. Khan, 2018, Documenta ophthalmologica. Advances in ophthalmology.

Autophagy-mediated catabolism of visual transduction proteins prevents retinal degeneration

D. Klionsky, N. Khan, D. Zacks, 2016, Autophagy.

Advancing therapeutic strategies for inherited retinal degeneration: recommendations from the Monaciano Symposium.

W. Hauswirth, J. Flannery, J. Heckenlively, 2015, Investigative ophthalmology & visual science.

Caspase Inhibition with XIAP as an Adjunct to AAV Vector Gene-Replacement Therapy: Improving Efficacy and Prolonging the Treatment Window

W. Hauswirth, N. Khan, D. Zacks, 2012, PloS one.

Rod differentiation factor NRL activates the expression of nuclear receptor NR2E3 to suppress the development of cone photoreceptors

A. Swaroop, N. Khan, Edwin C. T. Oh, 2008, Brain Research.

Diagnostic fundus autofluorescence patterns in achromatopsia.

J. Heckenlively, K. Branham, N. Khan, 2013, American journal of ophthalmology.

Peripheral Pigmented Retinal Lesions in Stargardt Disease.

J. Heckenlively, K. Branham, N. Khan, 2017, American journal of ophthalmology.

Double hyperautofluorescent ring on fundus autofluorescence in ABCA4

J. Heckenlively, K. Branham, N. Khan, 2018, Ophthalmic genetics.

The RUSH2A Study: Best-Corrected Visual Acuity, Full-Field Electroretinography Amplitudes, and Full-Field Stimulus Thresholds at Baseline

Christina Y Weng, Christina Y. Weng, Todd A. Durham, 2020, Translational vision science & technology.

Nrl-knockout mice deficient in Rpe65 fail to synthesize 11-cis retinal and cone outer segments.

E. Pugh, A. Swaroop, David S. Williams, 2008, Investigative ophthalmology & visual science.

Comparison of Fundus-Guided Microperimetry and Multifocal Electroretinography for Evaluating Hydroxychloroquine Maculopathy

Adrienne Chen, N. Khan, K. T. Jayasundera, 2019, Translational vision science & technology.

Autoimmune retinopathy associated with monoclonal gammopathy of undetermined significance: a case report

N. Khan, G. Abrams, Abigail T. Fahim, 2020, BMC ophthalmology.

Management of autoimmune retinopathies with immunosuppression.

S. He, J. Heckenlively, N. Khan, 2009, Archives of ophthalmology.

The Deubiquitinating Enzyme Ataxin-3 Regulates Ciliogenesis and Phagocytosis in the Retina

J. Abril, G. Marfany, N. Khan, 2020, Cell reports.

C2orf71 Mutations as a Frequent Cause of Autosomal-Recessive Retinitis Pigmentosa: Clinical Analysis and Presentation of 8 Novel Mutations.

James V. M. Hanson, W. Berger, B. Lam, 2017, Investigative ophthalmology & visual science.

Anti-retinal pigment epithelium antibodies in acute exudative polymorphous vitelliform maculopathy: a new hypothesis about disease pathogenesis.

S. He, J. Heckenlively, N. Khan, 2009, Archives of ophthalmology.

Two mouse models for recoverin-associated autoimmune retinopathy

S. He, J. Heckenlively, N. Khan, 2010, Molecular vision.

Excess cones in the retinal degeneration rd7 mouse, caused by the loss of function of orphan nuclear receptor Nr2e3, originate from early-born photoreceptor precursors.

A. Swaroop, N. Khan, J. Roger, 2011, Human molecular genetics.

Transformation of cone precursors to functional rod photoreceptors by bZIP transcription factor NRL

E. Strettoi, A. Swaroop, H. Khanna, 2007, Proceedings of the National Academy of Sciences.

A CTRP5 gene S163R mutation knock-in mouse model for late-onset retinal degeneration.

D. Bartsch, N. Khan, C. Cukras, 2011, Human molecular genetics.

INTRAVITREAL DAPTOMYCIN: A Safety and Efficacy Study

N. Khan, D. Zacks, V. Elner, 2011, Retina.

Acute panretinal structural and functional abnormalities after intravitreous ocriplasmin injection.

N. Khan, Mark W. Johnson, Abigail T. Fahim, 2014, JAMA ophthalmology.

Primate Retinal Signaling Pathways: Suppressing ON-Pathway Activity in Monkey With Glutamate Analogues Mimics Human CSNB1-NYX Genetic Night Blindness.

P. Sieving, N. Khan, M. Kondo, 2005, Journal of neurophysiology.

Establishing baseline rod electroretinogram values in achromatopsia and cone dystrophy

J. Heckenlively, K. Branham, N. Khan, 2012, Documenta Ophthalmologica.

Deletion of autophagy inducer RB1CC1 results in degeneration of the retinal pigment epithelium

S. Mitter, D. Klionsky, M. Boulton, 2015, Autophagy.

Detailed clinical characterisation, unique features and natural history of autosomal recessive RDH12-associated retinal degeneration

J. Heckenlively, K. Branham, N. Khan, 2019, British Journal of Ophthalmology.

Development of a gene-therapy vector for RDH12-associated retinal dystrophy.

Adrienne Chen, N. Khan, R. Ali, 2019, Human gene therapy.

Deciphering the genetic architecture and ethnographic distribution of IRD in three ethnic populations by whole genome sequence analysis

K. Frazer, P. Sieving, Andrew Huynh, 2021, PLoS genetics.

Rapid visual field constriction in a patient with retinitis pigmentosa and pituitary adenoma

S. Sullivan, J. Heckenlively, K. Branham, 2020, American journal of ophthalmology case reports.

Advancing Clinical Trials for Inherited Retinal Diseases: Recommendations from the Second Monaciano Symposium

P. Sieving, J. Sahel, A. Cideciyan, 2020, Translational vision science & technology.

Rd9 Is a Naturally Occurring Mouse Model of a Common Form of Retinitis Pigmentosa Caused by Mutations in RPGR-ORF15

A. Swaroop, Tiansen Li, H. Khanna, 2012, PloS one.

Clinical course and visual function in a family with mutations in the RPE65 gene.

P. Sieving, J. Felius, N. Khan, 2002, Archives of ophthalmology.

Macular hyperpigmentary changes in ABCA4-Stargardt disease

N. Khan, T. Jayasundera, M. F. Abalem, 2019, International Journal of Retina and Vitreous.

Renal-retinal ciliopathy gene Sdccag8 regulates DNA damage response signaling.

S. Bekker-Jensen, T. Hurd, A. Kispert, 2014, Journal of the American Society of Nephrology : JASN.

Analysis of photoreceptor function and inner retinal activity in juvenile X-linked retinoschisis

P. Sieving, N. Khan, J. Jamison, 2001, Vision Research.

Real-world outcomes of voretigene neparvovec treatment in pediatric patients with RPE65-associated Leber congenital amaurosis

K. Branham, N. Khan, Callie Deng, 2022, Graefe's Archive for Clinical and Experimental Ophthalmology.

Reliability of kinetic visual field testing in children with mutation-proven retinal dystrophies: Implications for therapeutic clinical trials

J. Heckenlively, K. Branham, N. Khan, 2016, Ophthalmic genetics.

Altered retinal structure and function in Spinocerebellar ataxia type 3

G. Marfany, E. Muñoz, N. Khan, 2022, Neurobiology of Disease.

X-Chromosome Inactivation Is a Biomarker of Clinical Severity in Female Carriers of RPGR-Associated X-Linked Retinitis Pigmentosa.

S. Daiger, S. Bowne, L. Sullivan, 2019, Ophthalmology. Retina.

Phenotypic conservation in patients with X-linked retinitis pigmentosa caused by RPGR mutations.

Anand Swaroop, Paul A Sieving, P. Sieving, 2013, JAMA ophthalmology.

Hereditary Cone Dystrophies

J. Heckenlively, N. Khan, P. Atmaca-Sonmez, 2008 .

Structural and functional rescue of murine rod photoreceptors by human rhodopsin transgene.

P. Sieving, N. Khan, P. Humphries, 1999, Human molecular genetics.

Ablation of the X-linked retinitis pigmentosa 2 (Rp2) gene in mice results in opsin mislocalization and photoreceptor degeneration.

A. Swaroop, H. Khanna, T. Hurd, 2013, Investigative ophthalmology & visual science.

Digital quantification of Goldmann visual fields (GVFs) as a means for genotype-phenotype comparisons and detection of progression in retinal degenerations.

J. Heckenlively, N. Khan, Sarwar Zahid, 2014, Advances in experimental medicine and biology.

Expansion of Severely Constricted Visual Field Using Google Glass.

Sayoko E Moroi, K. Branham, N. Khan, 2016, Ophthalmic surgery, lasers & imaging retina.

R. Klein, B. Klein, J. Heckenlively, 2008, Human molecular genetics.

Adherence and satisfaction in Argus II prosthesis users: a self determination theory model

K. Branham, N. Khan, K. T. Jayasundera, 2022, Ophthalmic genetics.

Characterization of a canine model of autosomal recessive retinitis pigmentosa due to a PDE6A mutation.

J. Steibel, N. Khan, M. Kiupel, 2009, Investigative ophthalmology & visual science.

Calculation of test-retest variability in phase I/IIa clinical trials for Inherited Retinal Degenerations

N. Khan, K. T. Jayasundera, D. Musch, 2021, Ophthalmic Genetics.

Prolonged Inner Retinal Photoreception Depends on the Visual Retinoid Cycle

Kwoon Y. Wong, N. Khan, W. Pack, 2016, The Journal of Neuroscience.

Cystoid macular changes on optical coherence tomography in a patient with maternally inherited diabetes and deafness (MIDD)-associated macular dystrophy

J. Heckenlively, K. Branham, N. Khan, 2017, Ophthalmic genetics.

A Mouse Model with Ablated Asparaginase and Isoaspartyl Peptidase 1 (Asrgl1) Develops Early Onset Retinal Degeneration (RD) Recapitulating the Human Phenotype

D. Bartsch, N. Khan, P. Raghavendra, 2022, Genes.

Prevalence of Antiretinal Antibodies in Acute Zonal Occult Outer Retinopathy: A Comprehensive Review of 25 Cases.

D. DeMill, J. Heckenlively, K. Branham, 2017, American journal of ophthalmology.

IFT88 mutations identified in individuals with non-syndromic recessive retinal degeneration result in abnormal ciliogenesis

K. Frazer, P. Sieving, A. Telenti, 2018, Human Genetics.

Contrast sensitivity deficits in patients with mutation-proven inherited retinal degenerations

K. Branham, N. Khan, T. Jayasundera, 2018, BMC Ophthalmology.

Elovl4 5-bp deletion knock-in mouse model for Stargardt-like macular degeneration demonstrates accumulation of ELOVL4 and lipofuscin.

N. Khan, J. Sparrow, R. Ayyagari, 2009, Experimental eye research.

Prevalence of anti-retinal antibodies in Acute Zonal Occult Outer Retinopathy (AZOOR): a comprehensive review of 25cases

D. DeMill, J. Heckenlively, N. Khan, 2019 .

Multifocal visual evoked potentials for early glaucoma detection.

N. Khan, D. Musch, Leslie Niziol, 2012, Ophthalmic surgery, lasers & imaging : the official journal of the International Society for Imaging in the Eye.

Characterization of a canine model of autosomal recessive retinitis pigmentosa due to a PDE6A mutation.

J. Steibel, N. Khan, M. Kiupel, 2009, Investigative ophthalmology & visual science.

Safety Evaluation of Photoacoustic Tomography System for Intraocular Tumors

Xueding Wang, N. Khan, H. Demirci, 2022, Translational vision science & technology.