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Clinical characteristics, risk factors, and rate of severity of a nationwide COVID-19 Saudi cohort

Saudi journal of biological sciences, 2022-07, Vol.29 (7), p.103315-103315, Article 103315

2022

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Automated SARS-COV-2 RNA extraction from patient nasopharyngeal samples using a modified DNA extraction kit for high throughput testing

Annals of Saudi medicine, 2020-09, Vol.40 (5), p.373-381

2020

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Favipiravir Effectiveness and Safety in Hospitalized Moderate-Severe COVID-19 Patients: Observational Prospective Multicenter Investigation in Saudi Arabia

Frontiers in medicine, 2022-03, Vol.9, p.826247-826247

2022

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Exome sequencing identifies novel NTRK1 mutations in patients with HSAN‐IV phenotype

American journal of medical genetics. Part A, 2017-04, Vol.173 (4), p.1009-1016

2017

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Weak or no association of TCF7L2 variants with Type 2 diabetes risk in an Arab population

BMC medical genetics, 2008-07, Vol.9 (1), p.72-72, Article 72

2008

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Genetic Study of Saudi Diabetes (GSSD): significant association of the KCNJ11 E23K polymorphism with type 2 diabetes

Diabetes/metabolism research and reviews, 2008-02, Vol.24 (2), p.137-140

2008

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Molecular analysis of T-B-NK+ severe combined immunodeficiency and Omenn syndrome cases in Saudi Arabia

BMC medical genetics, 2009-11, Vol.10 (1), p.116-116, Article 116

2009

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Haplotypes Encompassing the KIAA0391 and PSMA6 Gene Cluster Confer a Genetic Link for Myocardial Infarction and Coronary Artery Disease

Annals of human genetics, 2009-09, Vol.73 (5), p.475-483

2009

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Comprehensive gene panels provide advantages over clinical exome sequencing for Mendelian diseases

Genome Biology, 2015-06, Vol.16 (1), p.134-134, Article 134

2015

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Global Healthspan Summit 2023: closing the gap between healthspan and lifespan

Nature aging, 2024-04, Vol.4 (4), p.445

2024

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Design of Arab Diabetes Gene-Centric Array (ADGCA) in population with an epidemic of Type 2 Diabetes: A population specific SNP evaluation

Gene, 2018-07, Vol.663, p.157-164

2018

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Full-in-House Method (FinHM) for SARS-COV-2 Automated Viral RNA Extraction, Followed by in-House ‘Primer-Probe’ Based RT-qPCR Detection; Low Cost Mass Testing

American journal of internal medicine (Print), 2021, Vol.9 (1), p.1

2021

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Molecular analysis of T.sup.-.sup.B.sup.-.sup.NK.sup.+ .sup.severe combined immunodeficiency and Omenn syndrome cases in Saudi Arabia

BMC medical genetics, 2009-11, Vol.10, p.116

2009

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Erratum to: Comprehensive gene panels provide advantages over clinical exome sequencing for Mendelian diseases

Genome Biology, 2015-10, Vol.16 (1), p.226-226, Article 226

2015

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Syndromic congenital sensorineural deafness, microtia and microdontia resulting from a novel homoallelic mutation in fibroblast growth factor 3 ( )

European journal of human genetics : EJHG, 2009-01, Vol.17 (1), p.14-21

2009

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The KIAA0391 and PSMA6 gene cluster confers a risk factor for coronary artery disease

The FASEB journal, 2009-04, Vol.23 (S1)

2009

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Haplotypes encompassing the PSMA6 and KIAA0391 Gene Cluster confer risk for Myocardial Infarction

The FASEB journal, 2009-04, Vol.23 (S1)

2009

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Social Reality of the Father's Wife in Saudi Society : Study Applied to a Sample of Wives of the Father in the Province of Abqaiq

Journal of Social Affairs, 2017-01, Vol.34 (136), p.239

Al-Harbi, Haya Saleh Saud

2017

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Computerized Tomography Use in Williams-Beuren Syndrome Aortopathy

Heart views, 2017-01, Vol.18 (1), p.21-25

2017

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The World Federation of ADHD International Consensus Statement: 208 Evidence-based conclusions about the disorder

Neuroscience and biobehavioral reviews, 2021-09, Vol.128, p.789-818

2021

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Multiplexed detection of DOCK8, PGM3 and STAT3 proteins for the diagnosis of Hyper-Immunoglobulin E syndrome using gold nanoparticles-based immunosensor array platform

Biosensors & bioelectronics, 2018-10, Vol.117, p.613-619

2018

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Unbiased targeted next-generation sequencing molecular approach for primary immunodeficiency diseases

Journal of allergy and clinical immunology, 2016-06, Vol.137 (6), p.1780-1787

2016

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Computerized tomography use in Williams#8211;Beuren syndrome aortopathy

Heart views, 2017-01, Vol.18 (1), p.21

2017

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Computerized Tomography Use in Williams-Beuren Syndrome Aortopathy

Heart views : the official journal of the Gulf Heart Association, 2017, Vol.18 (1), p.21-25

2017

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Clinical characteristics, risk factors, and rate of severity of a nationwide COVID-19 Saudi cohort

Automated SARS-COV-2 RNA extraction from patient nasopharyngeal samples using a modified DNA extraction kit for high throughput testing

Favipiravir Effectiveness and Safety in Hospitalized Moderate-Severe COVID-19 Patients: Observational Prospective Multicenter Investigation in Saudi Arabia

Exome sequencing identifies novel NTRK1 mutations in patients with HSAN‐IV phenotype

Weak or no association of TCF7L2 variants with Type 2 diabetes risk in an Arab population

Genetic Study of Saudi Diabetes (GSSD): significant association of the KCNJ11 E23K polymorphism with type 2 diabetes

Molecular analysis of T-B-NK+ severe combined immunodeficiency and Omenn syndrome cases in Saudi Arabia

Haplotypes Encompassing the KIAA0391 and PSMA6 Gene Cluster Confer a Genetic Link for Myocardial Infarction and Coronary Artery Disease

Comprehensive gene panels provide advantages over clinical exome sequencing for Mendelian diseases

Global Healthspan Summit 2023: closing the gap between healthspan and lifespan

Design of Arab Diabetes Gene-Centric Array (ADGCA) in population with an epidemic of Type 2 Diabetes: A population specific SNP evaluation

Full-in-House Method (FinHM) for SARS-COV-2 Automated Viral RNA Extraction, Followed by in-House ‘Primer-Probe’ Based RT-qPCR Detection; Low Cost Mass Testing

Molecular analysis of T.sup.-.sup.B.sup.-.sup.NK.sup.+ .sup.severe combined immunodeficiency and Omenn syndrome cases in Saudi Arabia

Erratum to: Comprehensive gene panels provide advantages over clinical exome sequencing for Mendelian diseases

Syndromic congenital sensorineural deafness, microtia and microdontia resulting from a novel homoallelic mutation in fibroblast growth factor 3 ( )

The KIAA0391 and PSMA6 gene cluster confers a risk factor for coronary artery disease

Haplotypes encompassing the PSMA6 and KIAA0391 Gene Cluster confer risk for Myocardial Infarction

Social Reality of the Father's Wife in Saudi Society : Study Applied to a Sample of Wives of the Father in the Province of Abqaiq

Computerized Tomography Use in Williams-Beuren Syndrome Aortopathy

The World Federation of ADHD International Consensus Statement: 208 Evidence-based conclusions about the disorder

Multiplexed detection of DOCK8, PGM3 and STAT3 proteins for the diagnosis of Hyper-Immunoglobulin E syndrome using gold nanoparticles-based immunosensor array platform

Unbiased targeted next-generation sequencing molecular approach for primary immunodeficiency diseases

Computerized tomography use in Williams#8211;Beuren syndrome aortopathy

Computerized Tomography Use in Williams-Beuren Syndrome Aortopathy

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