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Identification of MFRP and the secreted serine proteases PRSS56 and ADAMTS19 as part of a molecular network involved in ocular growth regulation

PLoS genetics, 2021-03, Vol.17 (3), p.e1009458-e1009458

2021

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A Nonlinear High-Gain Observer for Systems With Measurement Noise in a Feedback Control Framework

IEEE transactions on automatic control, 2013-03, Vol.58 (3), p.569-580

2013

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DNA Methylation Status of the Interspersed Repetitive Sequences for LINE-1, Alu, HERV-E, and HERV-K in Trabeculectomy Specimens from Glaucoma Eyes

Journal of ophthalmology, 2018-01, Vol.2018, p.9171536-10

2018

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Association of Genes in the High-Density Lipoprotein Metabolic Pathway with Polypoidal Choroidal Vasculopathy in Asian Population: A Systematic Review and Meta-Analysis

Journal of ophthalmology, 2018-01, Vol.2018, p.9538671-14

2018

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Molecular Genetics of Pigment Dispersion Syndrome and Pigmentary Glaucoma: New Insights into Mechanisms

Journal of ophthalmology, 2018-01, Vol.2018, p.5926906-11

2018

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Evaluation of TGF-Beta 2 and VEGFα Gene Expression Levels in Epiretinal Membranes and Internal Limiting Membranes in the Course of Retinal Detachments, Proliferative Diabetic Retinopathy, Macular Holes, and Idiopathic Epiretinal Membranes

Journal of ophthalmology, 2018-01, Vol.2018, p.8293452-6

2018

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Tracking performance of a high-gain observer in the presence of measurement noise

International journal of adaptive control and signal processing, 2016-08, Vol.30 (8-10), p.1228-1243

2016

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Organization of the work of feldshers at the Middle Asian Railway

Fel'dsher i akusherka, 1971-03, Vol.36 (3), p.6

1971

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Pushing the envelope of retinal ganglion cell genesis: Context dependent function of Math5 (Atoh7)

Developmental biology, 2012-08, Vol.368 (2), p.214-230

2012

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Math5 defines the ganglion cell competence state in a subpopulation of retinal progenitor cells exiting the cell cycle

Developmental biology, 2012-05, Vol.365 (2), p.395-413

2012

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Dynamic expression of ganglion cell markers in retinal progenitors during the terminal cell cycle

Molecular and cellular neuroscience, 2012-06, Vol.50 (2), p.160-168

2012

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eP217: Ophthalmology genetics clinic in the times of COVID-19: A hybrid model

Genetics in medicine, 2022-03, Vol.24 (3), p.S135-S135

2022

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Glaucoma Syndromes: Insights into Glaucoma Genetics and Pathogenesis from Monogenic Syndromic Disorders

Genes, 2021-09, Vol.12 (9), p.1403

2021

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Nanophthalmos: A Review of the Clinical Spectrum and Genetics

Journal of ophthalmology, 2018-01, Vol.2018, p.2735465-9

2018

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PRINCIPLES AND PROBLEMS OF FINANCIAL PROVISION OF EDUCATION TO PERSONS SENTENCED TO IMPRISONMENT

Baltic Journal of Economic Studies, 2020-01, Vol.6 (4), p.141-148

2020

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PROCEDURE AND PROBLEMS OF FINANCING PROVISION OF HEALTH CARE TO THE IMPRISONED PERSONS

Baltic Journal of Economic Studies, 2020-01, Vol.6 (3), p.114-123

2020

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Design and Outcomes of a Novel Multidisciplinary Ophthalmic Genetics Clinic

Genes, 2023-03, Vol.14 (3), p.726

2023

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Immunogenetics of the Ocular Anterior Segment: Lessons from Inherited Disorders

Journal of ophthalmology, 2021-06, Vol.2021, p.6691291-19

2021

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Specific Deoxyceramide Species Correlate with Expression of Macular Telangiectasia Type 2 (MacTel2) in a SPTLC2 Carrier HSAN1 Family

Genes, 2023-04, Vol.14 (4), p.931

2023

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ATOH7 mutations cause autosomal recessive persistent hyperplasia of the primary vitreous

Human molecular genetics, 2012-08, Vol.21 (16), p.3681-3694

2012

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Math5 (Atoh7) gene dosage limits retinal ganglion cell genesis

Neuroreport, 2012-07, Vol.23 (10), p.631-634

2012

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The Repeat-In-Toxin Family Member TosA Mediates Adherence of Uropathogenic Escherichia coli and Survival during Bacteremia

Infection and Immunity, 2012-02, Vol.80 (2), p.493-505

2012

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P488: Interrogating the pathologic noncoding genome with tissue-specific multiomics

Genetics in Medicine Open, 2023, Vol.1 (1), p.100535, Article 100535

2023

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A Novel 13q12 Microdeletion Associated with Familial Syndromic Corneal Opacification

Genes, 2023-05, Vol.14 (5), p.1034

2023

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Identification of MFRP and the secreted serine proteases PRSS56 and ADAMTS19 as part of a molecular network involved in ocular growth regulation

A Nonlinear High-Gain Observer for Systems With Measurement Noise in a Feedback Control Framework

DNA Methylation Status of the Interspersed Repetitive Sequences for LINE-1, Alu, HERV-E, and HERV-K in Trabeculectomy Specimens from Glaucoma Eyes

Association of Genes in the High-Density Lipoprotein Metabolic Pathway with Polypoidal Choroidal Vasculopathy in Asian Population: A Systematic Review and Meta-Analysis

Molecular Genetics of Pigment Dispersion Syndrome and Pigmentary Glaucoma: New Insights into Mechanisms

Evaluation of TGF-Beta 2 and VEGFα Gene Expression Levels in Epiretinal Membranes and Internal Limiting Membranes in the Course of Retinal Detachments, Proliferative Diabetic Retinopathy, Macular Holes, and Idiopathic Epiretinal Membranes

Tracking performance of a high-gain observer in the presence of measurement noise

Organization of the work of feldshers at the Middle Asian Railway

Pushing the envelope of retinal ganglion cell genesis: Context dependent function of Math5 (Atoh7)

Math5 defines the ganglion cell competence state in a subpopulation of retinal progenitor cells exiting the cell cycle

Dynamic expression of ganglion cell markers in retinal progenitors during the terminal cell cycle

eP217: Ophthalmology genetics clinic in the times of COVID-19: A hybrid model

Glaucoma Syndromes: Insights into Glaucoma Genetics and Pathogenesis from Monogenic Syndromic Disorders

Nanophthalmos: A Review of the Clinical Spectrum and Genetics

PRINCIPLES AND PROBLEMS OF FINANCIAL PROVISION OF EDUCATION TO PERSONS SENTENCED TO IMPRISONMENT

PROCEDURE AND PROBLEMS OF FINANCING PROVISION OF HEALTH CARE TO THE IMPRISONED PERSONS

Design and Outcomes of a Novel Multidisciplinary Ophthalmic Genetics Clinic

Immunogenetics of the Ocular Anterior Segment: Lessons from Inherited Disorders

Specific Deoxyceramide Species Correlate with Expression of Macular Telangiectasia Type 2 (MacTel2) in a SPTLC2 Carrier HSAN1 Family

ATOH7 mutations cause autosomal recessive persistent hyperplasia of the primary vitreous

Math5 (Atoh7) gene dosage limits retinal ganglion cell genesis

The Repeat-In-Toxin Family Member TosA Mediates Adherence of Uropathogenic Escherichia coli and Survival during Bacteremia

P488: Interrogating the pathologic noncoding genome with tissue-specific multiomics

A Novel 13q12 Microdeletion Associated with Familial Syndromic Corneal Opacification

Variants in myelin regulatory factor (MYRF) cause autosomal dominant and syndromic nanophthalmos in humans and retinal degeneration in mice

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