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Association between SNPs of Circulating Vascular Endothelial Growth Factor Levels, Hypercholesterolemia and Metabolic Syndrome

Medicina (Kaunas, Lithuania), 2019-08, Vol.55 (8), p.464

2019

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CHM mutation spectrum and disease: An update at the time of human therapeutic trials

Human mutation, 2021-04, Vol.42 (4), p.323-341

2021

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APOE genotypes in Lebanon: distribution and association with hypercholesterolemia and Alzheimer's disease

Personalized medicine, 2019-01, Vol.16 (1), p.15-23

2019

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Peripheral blood mononuclear cells extracts VEGF protein levels and VEGF mRNA: Associations with inflammatory molecules in a healthy population

PloS one, 2019-08, Vol.14 (8), p.e0220902-e0220902

2019

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Whole-Exome Sequencing Identifies KIZ as a Ciliary Gene Associated with Autosomal-Recessive Rod-Cone Dystrophy

American journal of human genetics, 2014-04, Vol.94 (4), p.625-633

2014

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The rs3957357C>T SNP in GSTA1 Is Associated with a Higher Risk of Occurrence of Hepatocellular Carcinoma in European Individuals

PloS one, 2016-12, Vol.11 (12), p.e0167543

2016

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Is There a Link Between Nutrition, Genetics, and Cardiovascular Disease?

Journal of cardiovascular development and disease, 2020-09, Vol.7 (3), p.1

2020

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The Association of rs1898830 in Toll-Like Receptor 2 with Lipids and Blood Pressure

Journal of cardiovascular development and disease, 2020-09, Vol.7 (3), p.1

2020

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Next Generation Sequencing Identifies Five Novel Mutations in Lebanese Patients with Bardet-Biedl and Usher Syndromes

Genes, 2019-12, Vol.10 (12), p.1047

2019

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rs2569190A>G in CD14 is Independently Associated with Hypercholesterolemia: A Brief Report

Journal of cardiovascular development and disease, 2019-10, Vol.6 (4), p.37

2019

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rs622342 in SLC22A1, CYP2C92 and CYP2C93 and Glycemic Response in Individuals with Type 2 Diabetes Mellitus Receiving Metformin/Sulfonylurea Combination Therapy: 6-Month Follow-Up Study

Journal of personalized medicine, 2020-06, Vol.10 (2), p.53

2020

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Association of TLR4 Polymorphisms, Expression, and Vitamin D with Helicobacter pylori Infection

Journal of personalized medicine, 2019-01, Vol.9 (1), p.2

2019

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rs6837671A>G in FAM13A Is a Trans-Ethnic Genetic Variant Interacting with Vitamin D Levels to Affect Chronic Obstructive Pulmonary Disease

Journal of personalized medicine, 2021-01, Vol.11 (2), p.84

2021

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Novel Missense Mutations in BEST1 Are Associated with Bestrophinopathies in Lebanese Patients

Genes, 2019-02, Vol.10 (2), p.151

2019

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Editorial: The genetics of inherited retinal diseases in understudied ethnic groups: Novel associations, challenges, and perspectives

Frontiers in genetics, 2022-08, Vol.13, p.990782-990782

2022

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The genetics of rod-cone dystrophy in Arab countries: a systematic review

European journal of human genetics : EJHG, 2021-06, Vol.29 (6), p.897-910

2021

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rs622342A>C in SLC22A1 is associated with metformin pharmacokinetics and glycemic response

Drug metabolism and pharmacokinetics, 2020-02, Vol.35 (1), p.160-164

2020

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Analysis of rod-cone dystrophy genes reveals unique mutational patterns

BMJ open science, 2022-12, Vol.6 (1), p.e100291-e100291

2022

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MERTK mutation update in inherited retinal diseases

Human mutation, 2018-07, Vol.39 (7), p.887-913

2018

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Further Insights into the Ciliary Gene and Protein KIZ and Its Murine Ortholog PLK1S1 Mutated in Rod-Cone Dystrophy

Genes, 2017-10, Vol.8 (10), p.277

2017

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Genotype-phenotype associations in CRB1 bi-allelic patients: a novel mutation, a systematic review and meta-analysis

BMC ophthalmology, 2024-04, Vol.24 (1), p.167-167, Article 167

2024

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The research output of rod-cone dystrophy genetics

Orphanet journal of rare diseases, 2022-04, Vol.17 (1), p.175-175, Article 175

2022

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The genetic landscape of inherited retinal dystrophies in Arabs

BMC medical genomics, 2023-05, Vol.16 (1), p.89-89, Article 89

2023

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ABCA4-related retinopathies in Lebanon

Heliyon, 2024-05, Vol.10 (9), p.e30304-e30304, Article e30304

2024

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Association between SNPs of Circulating Vascular Endothelial Growth Factor Levels, Hypercholesterolemia and Metabolic Syndrome

CHM mutation spectrum and disease: An update at the time of human therapeutic trials

APOE genotypes in Lebanon: distribution and association with hypercholesterolemia and Alzheimer's disease

Peripheral blood mononuclear cells extracts VEGF protein levels and VEGF mRNA: Associations with inflammatory molecules in a healthy population

Whole-Exome Sequencing Identifies KIZ as a Ciliary Gene Associated with Autosomal-Recessive Rod-Cone Dystrophy

The rs3957357C>T SNP in GSTA1 Is Associated with a Higher Risk of Occurrence of Hepatocellular Carcinoma in European Individuals

Is There a Link Between Nutrition, Genetics, and Cardiovascular Disease?

The Association of rs1898830 in Toll-Like Receptor 2 with Lipids and Blood Pressure

Next Generation Sequencing Identifies Five Novel Mutations in Lebanese Patients with Bardet-Biedl and Usher Syndromes

rs2569190A>G in CD14 is Independently Associated with Hypercholesterolemia: A Brief Report

rs622342 in SLC22A1, CYP2C92 and CYP2C93 and Glycemic Response in Individuals with Type 2 Diabetes Mellitus Receiving Metformin/Sulfonylurea Combination Therapy: 6-Month Follow-Up Study

Association of TLR4 Polymorphisms, Expression, and Vitamin D with Helicobacter pylori Infection

rs6837671A>G in FAM13A Is a Trans-Ethnic Genetic Variant Interacting with Vitamin D Levels to Affect Chronic Obstructive Pulmonary Disease

Novel Missense Mutations in BEST1 Are Associated with Bestrophinopathies in Lebanese Patients

Editorial: The genetics of inherited retinal diseases in understudied ethnic groups: Novel associations, challenges, and perspectives

The genetics of rod-cone dystrophy in Arab countries: a systematic review

rs622342A>C in SLC22A1 is associated with metformin pharmacokinetics and glycemic response

Analysis of rod-cone dystrophy genes reveals unique mutational patterns

MERTK mutation update in inherited retinal diseases

Genome-wide meta-analysis points to CTC1 and ZNF676 as genes regulating telomere homeostasis in humans

Further Insights into the Ciliary Gene and Protein KIZ and Its Murine Ortholog PLK1S1 Mutated in Rod-Cone Dystrophy

Genotype-phenotype associations in CRB1 bi-allelic patients: a novel mutation, a systematic review and meta-analysis

The research output of rod-cone dystrophy genetics

The genetic landscape of inherited retinal dystrophies in Arabs

ABCA4-related retinopathies in Lebanon

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