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Genes 47
Showing records 1 to 25 | Display all abstracts in Genes107893 Whole Exome Sequencing Reveals Novel Candidate Genes in Familial Forms of Glaucomatous Neurodegeneration
Narta K
Genes 2023; 14:
108228 Comparing Gene Panels for Non-Retinal Indications: A Systematic Review
Procopio R
Genes 2023; 14:
108226 Causal Association between Iritis or Uveitis and Glaucoma: A Two-Sample Mendelian Randomisation Study
Seo JH
Genes 2023; 14:
108685 Mendelian Randomization and Transcriptome-Wide Association Analysis Identified Genes That Were Pleiotropically Associated with Intraocular Pressure
Yang Z
Genes 2023; 14:
107892 Advances in Ophthalmic Epigenetics and Implications for Epigenetic Therapies: A Review
Moore SM
Genes 2023; 14:
107891 Genetic Factors Implicated in the Investigation of Possible Connections between Alzheimer's Disease and Primary Open Angle Glaucoma
Kuang G
Genes 2023; 14:
107890 Exome Sequencing Reveals Variant Underlying Congenital Hereditary Endothelial Dystrophy (CHED2) Misdiagnosed as Congenital Glaucoma
Yousaf K
Genes 2023; 14:
108227 Lack of Association of Polymorphism Located Upstream of (rs2472493), in (rs7636836), and Near - Genes (rs61275591) in Primary Open-Angle Glaucoma Patients of Saudi Origin
Kondkar AA
Genes 2023; 14:
108685 Mendelian Randomization and Transcriptome-Wide Association Analysis Identified Genes That Were Pleiotropically Associated with Intraocular Pressure
Zhang Z
Genes 2023; 14:
107893 Whole Exome Sequencing Reveals Novel Candidate Genes in Familial Forms of Glaucomatous Neurodegeneration
Teltumbade MR
Genes 2023; 14:
108226 Causal Association between Iritis or Uveitis and Glaucoma: A Two-Sample Mendelian Randomisation Study
Lee Y
Genes 2023; 14:
107892 Advances in Ophthalmic Epigenetics and Implications for Epigenetic Therapies: A Review
Christoforidis JB
Genes 2023; 14:
108227 Lack of Association of Polymorphism Located Upstream of (rs2472493), in (rs7636836), and Near - Genes (rs61275591) in Primary Open-Angle Glaucoma Patients of Saudi Origin
Sultan T
Genes 2023; 14:
107890 Exome Sequencing Reveals Variant Underlying Congenital Hereditary Endothelial Dystrophy (CHED2) Misdiagnosed as Congenital Glaucoma
Naz S
Genes 2023; 14:
108228 Comparing Gene Panels for Non-Retinal Indications: A Systematic Review
Pulido JS
Genes 2023; 14:
107891 Genetic Factors Implicated in the Investigation of Possible Connections between Alzheimer's Disease and Primary Open Angle Glaucoma
Salowe R
Genes 2023; 14:
108685 Mendelian Randomization and Transcriptome-Wide Association Analysis Identified Genes That Were Pleiotropically Associated with Intraocular Pressure
Zhu Y
Genes 2023; 14:
107890 Exome Sequencing Reveals Variant Underlying Congenital Hereditary Endothelial Dystrophy (CHED2) Misdiagnosed as Congenital Glaucoma
Mushtaq A
Genes 2023; 14:
107893 Whole Exome Sequencing Reveals Novel Candidate Genes in Familial Forms of Glaucomatous Neurodegeneration
Vishal M
Genes 2023; 14:
107891 Genetic Factors Implicated in the Investigation of Possible Connections between Alzheimer's Disease and Primary Open Angle Glaucoma
O'Brien J
Genes 2023; 14:
108227 Lack of Association of Polymorphism Located Upstream of (rs2472493), in (rs7636836), and Near - Genes (rs61275591) in Primary Open-Angle Glaucoma Patients of Saudi Origin
Azad TA
Genes 2023; 14:
108228 Comparing Gene Panels for Non-Retinal Indications: A Systematic Review
Gunton KB
Genes 2023; 14:
108227 Lack of Association of Polymorphism Located Upstream of (rs2472493), in (rs7636836), and Near - Genes (rs61275591) in Primary Open-Angle Glaucoma Patients of Saudi Origin
Osman EA
Genes 2023; 14:
107893 Whole Exome Sequencing Reveals Novel Candidate Genes in Familial Forms of Glaucomatous Neurodegeneration
Sadaf S
Genes 2023; 14:
107890 Exome Sequencing Reveals Variant Underlying Congenital Hereditary Endothelial Dystrophy (CHED2) Misdiagnosed as Congenital Glaucoma
Wohler E
Genes 2023; 14:
