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Resveratrol and Ophthalmic Diseases

Nutrients, 2016-04, Vol.8 (4), p.200-200

2016

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Utility of Circulating MicroRNAs as Clinical Biomarkers for Cardiovascular Diseases

BioMed research international, 2015-01, Vol.2015 (2015), p.1-10

2015

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The clinical spectrum of homozygous HOXA1 mutations

American journal of medical genetics. Part A, 2008-05, Vol.146A (10), p.1235-1240

2008

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Carriers of mitochondrial DNA macrohaplogroup L3 basal lineages migrated back to Africa from Asia around 70,000 years ago

BMC evolutionary biology, 2018-06, Vol.18 (1), Article 98

2018

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Mutations in FBXL4 Cause Mitochondrial Encephalopathy and a Disorder of Mitochondrial DNA Maintenance

American journal of human genetics, 2013-09, Vol.93 (3), p.471-481

2013

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Mutation of C20orf7 Disrupts Complex I Assembly and Causes Lethal Neonatal Mitochondrial Disease

American journal of human genetics, 2008-10, Vol.83 (4), p.468-478

2008

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Carriers of Mitochondrial DNA Macrohaplogroup N Lineages Reached Australia around 50,000 Years Ago following a Northern Asian Route

PloS one, 2015-06, Vol.10 (6), p.e0129839-e0129839

2015

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Genetics of Keratoconus: Where Do We Stand?

Journal of Ophthalmology, 2014-01, Vol.2014 (3), p.1-11

2014

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MicroRNA profiling in intraocular medulloepitheliomas

PloS one, 2015-03, Vol.10 (3), p.e0121706

2015

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Carriers of mitochondrial DNA macrohaplogroup R colonized Eurasia and Australasia from a southeast Asia core area

BMC evolutionary biology, 2017-05, Vol.17 (1), p.115, Article 115

2017

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Parent's attitude toward prenatal diagnosis and termination of pregnancy could be influenced by other factors rather than by the severity of the condition

Prenatal diagnosis, 2013-03, Vol.33 (3), p.257-261

2013

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Attitudes to prenatal diagnosis and termination of pregnancy for 30 conditions among women in Saudi Arabia and the UK

Prenatal diagnosis, 2012-11, Vol.32 (11), p.1109-1113

2012

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Leber congenital amaurosis: Current genetic basis, scope for genetic testing and personalized medicine

Experimental eye research, 2019-12, Vol.189, p.107834-107834, Article 107834

2019

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Mitochondrial DNA structure in the Arabian Peninsula

BMC evolutionary biology, 2008-02, Vol.8 (1), p.45, Article 45

2008

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Plexin domain containing 2 (PLXDC2) gene polymorphism rs7081455 may not influence POAG risk in a Saudi cohort

BMC research notes, 2018-10, Vol.11 (1), p.733-5, Article 733

2018

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Deep Capillary Macular Perfusion Indices Obtained with OCT Angiography Correlate with Degree of Nonproliferative Diabetic Retinopathy

European journal of ophthalmology, 2017-11, Vol.27 (6), p.716-729

2017

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Keratoconus is associated with increased copy number of mitochondrial DNA

Molecular vision, 2014-08, Vol.20, p.1203-1208

2014

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Polymorphism rs13334190 in zinc finger protein 469 (ZNF469) is not a risk factor for keratoconus in a Saudi cohort

BMC research notes, 2017-11, Vol.10 (1), p.652-652, Article 652

2017

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Mitochondrial Abnormalities in Patients with Primary Open-Angle Glaucoma

Investigative ophthalmology & visual science, 2006-06, Vol.47 (6), p.2533-2541

2006

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Attitudes of Saudi parents with a deaf child towards prenatal diagnosis and termination of pregnancy

Prenatal diagnosis, 2014-02, Vol.34 (2), p.153-158

2014

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Eurasian and African mitochondrial DNA influences in the Saudi Arabian population

BMC evolutionary biology, 2007-03, Vol.7, p.32

2007

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A microdeletion in the GRHL2 Gene in two unrelated patients with congenital fibrosis of the extra ocular muscles

BMC research notes, 2017-11, Vol.10 (1), p.562-562, Article 562

2017

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Neurometabolic Disorders-Related Early Childhood Epilepsy: A Single-Center Experience in Saudi Arabia

Pediatrics and neonatology, 2015-12, Vol.56 (6), p.393-401

2015

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Mitochondrial lineage M1 traces an early human backflow to Africa

BMC genomics, 2007-07, Vol.8 (1), p.223-223

2007

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The genetics of nonsyndromic bilateral Duane retraction syndrome

Journal of AAPOS, 2016-10, Vol.20 (5), p.396-400.e2

2016

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Resveratrol and Ophthalmic Diseases

Utility of Circulating MicroRNAs as Clinical Biomarkers for Cardiovascular Diseases

The clinical spectrum of homozygous HOXA1 mutations

Carriers of mitochondrial DNA macrohaplogroup L3 basal lineages migrated back to Africa from Asia around 70,000 years ago

Mutations in FBXL4 Cause Mitochondrial Encephalopathy and a Disorder of Mitochondrial DNA Maintenance

Mutation of C20orf7 Disrupts Complex I Assembly and Causes Lethal Neonatal Mitochondrial Disease

Carriers of Mitochondrial DNA Macrohaplogroup N Lineages Reached Australia around 50,000 Years Ago following a Northern Asian Route

Genetics of Keratoconus: Where Do We Stand?

MicroRNA profiling in intraocular medulloepitheliomas

Carriers of mitochondrial DNA macrohaplogroup R colonized Eurasia and Australasia from a southeast Asia core area

Parent's attitude toward prenatal diagnosis and termination of pregnancy could be influenced by other factors rather than by the severity of the condition

Attitudes to prenatal diagnosis and termination of pregnancy for 30 conditions among women in Saudi Arabia and the UK

Leber congenital amaurosis: Current genetic basis, scope for genetic testing and personalized medicine

Mitochondrial DNA structure in the Arabian Peninsula

Plexin domain containing 2 (PLXDC2) gene polymorphism rs7081455 may not influence POAG risk in a Saudi cohort

Deep Capillary Macular Perfusion Indices Obtained with OCT Angiography Correlate with Degree of Nonproliferative Diabetic Retinopathy

Keratoconus is associated with increased copy number of mitochondrial DNA

Polymorphism rs13334190 in zinc finger protein 469 (ZNF469) is not a risk factor for keratoconus in a Saudi cohort

Mitochondrial Abnormalities in Patients with Primary Open-Angle Glaucoma

Attitudes of Saudi parents with a deaf child towards prenatal diagnosis and termination of pregnancy

Eurasian and African mitochondrial DNA influences in the Saudi Arabian population

A microdeletion in the GRHL2 Gene in two unrelated patients with congenital fibrosis of the extra ocular muscles

Neurometabolic Disorders-Related Early Childhood Epilepsy: A Single-Center Experience in Saudi Arabia

Mitochondrial lineage M1 traces an early human backflow to Africa

The genetics of nonsyndromic bilateral Duane retraction syndrome

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