Vinit B. Mahajan

Microarray analysis of corneal fibroblast gene expression after interleukin-1 treatment.

Tissue-specific gene expression of head and neck squamous cell carcinoma in vivo by complementary DNA microarray analysis.

Estrogen receptor alpha and matrix metalloproteinase 2 polymorphisms and age-related maculopathy in older women.

A head-tilt test for hypopyon after intravitreal triamcinolone.

Management of sympathetic ophthalmia with the fluocinolone acetonide implant.

A new macular dystrophy with anomalous vascular development, pigment spots, cystic spaces, and neovascularization.

Erythropoetin receptor expression in the human diabetic retina.

Effects of vitrectomy on age-related macular degeneration.

Automated early detection of diabetic retinopathy.

T-cell infiltration in autosomal dominant neovascular inflammatory vitreoretinopathy.

Patients with an acute zonal occult outer retinopathy-like illness rapidly improve with valacyclovir treatment.

Collagen XVIII mutation in Knobloch syndrome with acute lymphoblastic leukemia.

Intravitreal bevacizumab during pregnancy.

Bilateral intravitreal injection of antivascular endothelial growth factor therapy.

Intraoperative choroidal detachment during 23-gauge vitrectomy.

Mutations in prickle orthologs cause seizures in flies, mice, and humans.

Seroreactivity against aqueous-soluble and detergent-soluble retinal proteins in posterior uveitis.

Sutureless triplanar sclerotomy for 23-gauge vitrectomy.

Intravitreal bevacizumab for treatment of proliferative and nonproliferative type 2 idiopathic macular telangiectasia.

Uveitis following intravitreal bevacizumab: a non-infectious cluster.

Automated discovery and quantification of image-based complex phenotypes: a twin study of drusen phenotypes in age-related macular degeneration.

Correspondence.

Infrared Imaging and Optical Coherence Tomography Reveal Early-Stage Astrocytic Hamartomas Not Detectable by Fundoscopy.

Unexpected mutations after CRISPR-Cas9 editing in vivo.

CRISPR-Cas Genome Surgery in Ophthalmology.

Limbal Trocar-Cannulas for Complex Vitrectomy Surgery.

Retinal and choroidal angiogenesis: a review of new targets.

Retrospective Analysis of Structural Disease Progression in Retinitis Pigmentosa Utilizing Multimodal Imaging.

Electroretinography Reveals Difference in Cone Function between Syndromic and Nonsyndromic USH2A Patients.

CRISPR-mediated Ophthalmic Genome Surgery.

Signal Normalization Reduces Image Appearance Disparity Among Multiple Optical Coherence Tomography Devices.

Calpain-5 gene expression in the mouse eye and brain.

Gene Therapy Restores Mfrp and Corrects Axial Eye Length.

CRISPR Repair Reveals Causative Mutation in a Preclinical Model of Retinitis Pigmentosa: A Brief Methodology.

Personalized Proteomics in Proliferative Vitreoretinopathy Implicate Hematopoietic Cell Recruitment and mTOR as a Therapeutic Target.

Genome Surgery and Gene Therapy in Retinal Disorders.

Therapeutic drug repositioning using personalized proteomics of liquid biopsies.

Autologous stem cell therapy for inherited and acquired retinal disease.

Bevacizumab Injection in Patients with Neovascular Age-Related Macular Degeneration Increases Angiogenic Biomarkers.

Proteomic analysis of the human retina reveals region-specific susceptibilities to metabolic- and oxidative stress-related diseases.

A novel de novo mutation in a patient with inflammatory vitreoretinopathy, hearing loss, and developmental delay.

Caring for Hereditary Childhood Retinal Blindness.

Acute vitreoretinal trauma and inflammation after traumatic brain injury in mice.

HTRA1, an age-related macular degeneration protease, processes extracellular matrix proteins EFEMP1 and TSP1.

CRISPR GENOME SURGERY IN THE RETINA IN LIGHT OF OFF-TARGETING.

Deferoxamine-induced electronegative ERG responses.

Gene therapy and genome surgery in the retina.

Translation of CRISPR Genome Surgery to the Bedside for Retinal Diseases.

Extracellular superoxide dismutase (SOD3) regulates oxidative stress at the vitreoretinal interface.

Rates of Bone Spicule Pigment Appearance in Patients With Retinitis Pigmentosa Sine Pigmento.

Missense mutation in SLIT2 associated with congenital myopia, anisometropia, connective tissue abnormalities, and obesity.

Quantitative progression of retinitis pigmentosa by optical coherence tomography angiography.

Personalized Proteomics for Precision Health: Identifying Biomarkers of Vitreoretinal Disease.

PROGRESSION OF SCOTOPIC SINGLE-FLASH ELECTRORETINOGRAPHY IN THE STAGES OF CAPN5 VITREORETINOPATHY.

ProSave: an application for restoring quantitative data to manipulated subsets of protein lists.

Review of Ocular Manifestations of Joubert Syndrome.

SCAPER-associated nonsyndromic autosomal recessive retinitis pigmentosa.

In Vivo Expression of Mutant Calpains in the Eye Using Lentivirus.

Viral Delivery Systems for CRISPR.

Fundus autofluorescence and ellipsoid zone (EZ) line width can be an outcome measurement in RHO-associated autosomal dominant retinitis pigmentosa.

VCAN Canonical Splice Site Mutation is Associated With Vitreoretinal Degeneration and Disrupts an MMP Proteolytic Site.

Optical Coherence Tomography Angiography of RPGR-Associated Retinitis Pigmentosa Suggests Foveal Avascular Zone is a Biomarker for Vision Loss.

Traumatic chorioretinitis sclopetaria: Risk factors, management, and prognosis.

Mechanisms of neurodegeneration in a preclinical autosomal dominant retinitis pigmentosa knock-in model with a Rho mutation.

Early Onset Neovascular Inflammatory Vitreoretinopathy Due to a Mutation: Report of a Case.

Therapeutic Window for Phosphodiesterase 6-Related Retinitis Pigmentosa.

Silicone oil-induced ocular hypertension and glaucomatous neurodegeneration in mouse.

Proteomic insight into the pathogenesis of CAPN5-vitreoretinopathy.

Gain-of-function mutations in a member of the Src family kinases cause autoinflammatory bone disease in mice and humans.

Bilateral Endophthalmitis after Immediately Sequential Bilateral Cataract Surgery.

In trans variant calling reveals enrichment for compound heterozygous variants in genes involved in neuronal development and growth.

CRISPR Base Editing in Induced Pluripotent Stem Cells.

Comparison of structural progression between ciliopathy and non-ciliopathy associated with autosomal recessive retinitis pigmentosa.

Opposing T cell responses in experimental autoimmune encephalomyelitis.

CAPN5 genetic inactivation phenotype supports therapeutic inhibition trials.

Hypoxic drive caused Type 3 neovascularization in a preclinical model of exudative age-related macular degeneration.

Novel REEP6 gene mutation associated with autosomal recessive retinitis pigmentosa.

Compound heterozygous novel frameshift variants in the gene result in Leber congenital amaurosis.

Novel mutations in the 3-box motif of the BACK domain of KLHL7 associated with nonsyndromic autosomal dominant retinitis pigmentosa.

Structural Insights into the Unique Activation Mechanisms of a Non-classical Calpain and Its Disease-Causing Variants.

Fundoscopy-directed genetic testing to re-evaluate negative whole exome sequencing results.

Metabolite therapy guided by liquid biopsy proteomics delays retinal neurodegeneration.

Modulation of Post-Traumatic Immune Response Using the IL-1 Receptor Antagonist Anakinra for Improved Visual Outcomes.

Phenotypic variance in Calpain-5 retinal degeneration.

Proteomic analysis of intermediate uveitis suggests myeloid cell recruitment and implicates IL-23 as a therapeutic target.

Reply.

Optical Gap Biomarker in Cone-Dominant Retinal Dystrophy.

Quantitative Autofluorescence Following Gene Therapy With Voretigene Neparvovec.

Sex Differences in the Repair of Retinal Detachments in the United States.

Whole-Exome Sequencing of Patients With Posterior Segment Uveitis.

Intravitreal methotrexate and fluocinolone acetonide implantation for Vogt-Koyanagi-Harada uveitis.

Sex Does Not Influence Visual Outcomes After Blast-Mediated Traumatic Brain Injury but IL-1 Pathway Mutations Confer Partial Rescue.

Retinal Manifestations of Mitochondrial Oxidative Phosphorylation Disorders.

Molecular Surgery: Proteomics of a Rare Genetic Disease Gives Insight into Common Causes of Blindness.

Liquid biopsy proteomics of uveal melanoma reveals biomarkers associated with metastatic risk.

Peptidomimetics Therapeutics for Retinal Disease.

Telegenetics for inherited retinal diseases in the COVID-19 environment.

Structure-based phylogeny identifies avoralstat as a TMPRSS2 inhibitor that prevents SARS-CoV-2 infection in mice.

Genetics of Uveitis.

Molecular Characterization of a Rare Case of Bilateral Vitreoretinal T Cell Lymphoma through Vitreous Liquid Biopsy.

The Present and Future of Mitochondrial-Based Therapeutics for Eye Disease.

Proteomics in uveal melanoma.

An intravitreal implant injection method for sustained drug delivery into mouse eyes.

A protocol to inject ocular drug implants into mouse eyes.

Investigation of Cas9 antibodies in the human eye.

Surgical management of acanthamoeba chorioretinitis.

New COL6A6 Variant Causes Autosomal Dominant Retinitis Pigmentosa in a Four-Generation Family.

Expanding the phenotype of TTLL5-associated retinal dystrophy: a case series.

Retinal artery and vein occlusion in calciphylaxis.

Author Correction: Investigation of Cas9 antibodies in the human eye.

Multimodal imaging reveals retinoschisis masquerading as retinal detachment in patients with choroideremia.

Proteomic analysis of autoimmune retinopathy implicates NrCAM as a potential biomarker.

Calpains as mechanistic drivers and therapeutic targets for ocular disease.

Bacillary Layer Detachment after Photodynamic Therapy.

Predicting Systemic Health Features from Retinal Fundus Images Using Transfer-Learning-Based Artificial Intelligence Models.

REPRODUCTIVE OPHTHALMOLOGY: The Intersection of Inherited Eye Diseases and Reproductive Technologies.

Clinical characteristics of high myopia in female carriers of pathogenic mutations: a case series and review of the literature.

Protocol to quantify enzymatic effects on vitreous liquefaction in porcine eyes using a transwell-plate system.

Chorioretinal atrophy following voretigene neparvovec despite the presence of fundus autofluorescence.

Conjunctival Swabs Reveal Higher Detection Rate Compared to Schirmer Strips for SARS-CoV-2 RNA Detection in Tears of Hospitalized COVID-19 Patients.

Intravitreal Fluocinolone Acetonide (Retisert) Implantation Using a Keratome Blade.

Cilia-associated wound repair mediated by IFT88 in retinal pigment epithelium.

Hardwiring tissue-specific AAV transduction in mice through engineered receptor expression.

AI-Human Hybrid Workflow Enhances Teleophthalmology for the Detection of Diabetic Retinopathy.