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Differential Gene Expression in Peripheral White Blood Cells with Permissive Underfeeding and Standard Feeding in Critically Ill Patients: A Descriptive Sub-study of the PermiT Randomized Controlled Trial

Scientific reports, 2018-12, Vol.8 (1), p.17984-8, Article 17984

2018

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Spinal muscular atrophy carrier frequency in Saudi Arabia

Molecular genetics & genomic medicine, 2022-11, Vol.10 (11), p.e2049-n/a

2022

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Genome-wide association study of chronic hepatitis B virus infection reveals a novel candidate risk allele on 11q22.3

Journal of medical genetics, 2013-11, Vol.50 (11), p.725-732

2013

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Alteration of Fatty-Acid-Metabolizing Enzymes Affects Mitochondrial Form and Function in Hereditary Spastic Paraplegia

American journal of human genetics, 2012-12, Vol.91 (6), p.1051-1064

2012

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A novel homozygous missense mutation (c.610G>A, p.Gly204Ser) in the WNT7A gene causes tetra‐amelia in two Saudi families

American journal of medical genetics. Part A, 2011-03, Vol.155 (3), p.599-604

2011

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Monomeric C-reactive protein and Notch-3 co-operatively increase angiogenesis through PI3K signalling pathway

Cytokine (Philadelphia, Pa.), 2014-10, Vol.69 (2), p.165-179

2014

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A novel mutation in the SHH long‐range regulator (ZRS) is associated with preaxial polydactyly, triphalangeal thumb, and severe radial ray deficiency

American journal of medical genetics. Part A, 2012-10, Vol.158A (10), p.2610-2615

2012

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Clinical characteristics and genetic subtypes of fanconi anemia in saudi patients

Cancer genetics, 2016-04, Vol.209 (4), p.171-176

2016

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Novel human pathological mutations. Gene symbol: EDAR. Disease: Ectodermal dysplasia, hypohidrotic

Human genetics, 2010-01, Vol.127 (1), p.123-123

2010

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Novel human pathological mutations

Human genetics, 2009-08, Vol.126 (2), p.353-353

2009

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Homozygous R396H mutation of the RAG1 gene in a Saudi infant with Omenn's syndrome: a case report

Cases journal, 2009-07, Vol.2 (1), p.8391-8391

2009

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Homozygous R396H mutation of the RAG1 gene in a Saudi infant with Omenn's syndrome: a case report

Cases journal, 2009, Vol.2 (1), p.8391

2009

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A novel mutation in the SHH long-range regulator (ZRS) is associated with preaxial polydactyly, triphalangeal thumb, and severe radial ray deficiency

American Journal of Medical Genetics Part A, 2012, Vol.158A (10), p.2610-2615

2012

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A novel homozygous missense mutation (c.610G>A, p.Gly204Ser) in the WNT7A gene causes tetra-amelia in two Saudi families

American Journal of Medical Genetics Part A, 2011, Vol.155A (3), p.599-604

2011

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Homozygous R396H mutation of the RAG1 gene in a Saudi infant with Omenn's syndrome: a case report

Cases journal, 2009, Vol.2, p.8391-8391

2009

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Differential antioxidative and biochemical responses to aluminium stress in Brassica juncea cultivars

Horticulture, 2018, Environment, and Biotechnology, 59(5), , pp.615-627

2018

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Proteomic and ecophysiological responses of soybean (Glycine max L.) root nodules to Pb and hg stress

BMC plant biology, 2018-11, Vol.18 (1), p.283-21, Article 283

2018

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Some pathological observations on the naturally infected dromedary camels (Camelus dromedarius) with the Middle East respiratory syndrome coronavirus (MERS-CoV) in Saudi Arabia 2018-2019

The Veterinary quarterly, 2020-01, Vol.40 (1), p.190-197

2020

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Scanning Electron Microscopic Findings on Respiratory Organs of Some Naturally Infected Dromedary Camels with the Lineage-B of the Middle East Respiratory Syndrome Coronavirus (MERS-CoV) in Saudi Arabia-2018

Pathogens (Basel), 2021-04, Vol.10 (4), p.420

2021

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Structural and Optical Properties of ZnO Nanostructures Synthesized by Hydrothermal Method at Different Conditions

Nano hybrids and composites, 2022-04, Vol.35, p.75-83

2022

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Public Awareness of and Action towards Heart Attack Symptoms: An Exploratory Study

International journal of environmental research and public health, 2020-12, Vol.17 (23), p.8982

2020

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Occurrence and characterisation of pathogenic Escherichia coli isolated from beef meat imported from South Africa and marketed in united Arab Emirates

AIP conference proceedings, 2018, Vol.1940 (1)

2018

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Epidemiology and antimicrobial resistance of Mycobacterium spp. in the United Arab Emirates: a retrospective analysis of 12 years of national antimicrobial resistance surveillance data

Frontiers in public health, 2024-06, Vol.12, p.1244353

2024

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Saudi orthopedic society guidelines for treating patients with bone and soft-tissue tumors during the COVID-19 pandemic

Journal of Musculoskeletal Surgery and Research, 2021-01, Vol.5 (1), p.10

2021

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The dipeptidyl peptidase-4 expression in some MERS-CoV naturally infected dromedary camels in Saudi Arabia 2018–2019

Virusdisease, 2020-06, Vol.31 (2), p.200-203

2020

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Differential Gene Expression in Peripheral White Blood Cells with Permissive Underfeeding and Standard Feeding in Critically Ill Patients: A Descriptive Sub-study of the PermiT Randomized Controlled Trial

Spinal muscular atrophy carrier frequency in Saudi Arabia

Genome-wide association study of chronic hepatitis B virus infection reveals a novel candidate risk allele on 11q22.3

Alteration of Fatty-Acid-Metabolizing Enzymes Affects Mitochondrial Form and Function in Hereditary Spastic Paraplegia

A novel homozygous missense mutation (c.610G>A, p.Gly204Ser) in the WNT7A gene causes tetra‐amelia in two Saudi families

Monomeric C-reactive protein and Notch-3 co-operatively increase angiogenesis through PI3K signalling pathway

A novel mutation in the SHH long‐range regulator (ZRS) is associated with preaxial polydactyly, triphalangeal thumb, and severe radial ray deficiency

Clinical characteristics and genetic subtypes of fanconi anemia in saudi patients

Novel human pathological mutations. Gene symbol: EDAR. Disease: Ectodermal dysplasia, hypohidrotic

Novel human pathological mutations

Homozygous R396H mutation of the RAG1 gene in a Saudi infant with Omenn's syndrome: a case report

Homozygous R396H mutation of the RAG1 gene in a Saudi infant with Omenn's syndrome: a case report

A novel mutation in the SHH long-range regulator (ZRS) is associated with preaxial polydactyly, triphalangeal thumb, and severe radial ray deficiency

A novel homozygous missense mutation (c.610G>A, p.Gly204Ser) in the WNT7A gene causes tetra-amelia in two Saudi families

Homozygous R396H mutation of the RAG1 gene in a Saudi infant with Omenn's syndrome: a case report

Differential antioxidative and biochemical responses to aluminium stress in Brassica juncea cultivars

Proteomic and ecophysiological responses of soybean (Glycine max L.) root nodules to Pb and hg stress

Some pathological observations on the naturally infected dromedary camels (Camelus dromedarius) with the Middle East respiratory syndrome coronavirus (MERS-CoV) in Saudi Arabia 2018-2019

Scanning Electron Microscopic Findings on Respiratory Organs of Some Naturally Infected Dromedary Camels with the Lineage-B of the Middle East Respiratory Syndrome Coronavirus (MERS-CoV) in Saudi Arabia-2018

Structural and Optical Properties of ZnO Nanostructures Synthesized by Hydrothermal Method at Different Conditions

Public Awareness of and Action towards Heart Attack Symptoms: An Exploratory Study

Occurrence and characterisation of pathogenic Escherichia coli isolated from beef meat imported from South Africa and marketed in united Arab Emirates

Epidemiology and antimicrobial resistance of Mycobacterium spp. in the United Arab Emirates: a retrospective analysis of 12 years of national antimicrobial resistance surveillance data

Saudi orthopedic society guidelines for treating patients with bone and soft-tissue tumors during the COVID-19 pandemic

The dipeptidyl peptidase-4 expression in some MERS-CoV naturally infected dromedary camels in Saudi Arabia 2018–2019

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