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Novel sequence variants in the TLR6 gene associated with advanced breast cancer risk in the Saudi Arabian population

PloS one, 2018-11, Vol.13 (11), p.e0203376-e0203376

2018

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A novel homozygous SCN5A variant detected in sick sinus syndrome

Pacing and clinical electrophysiology, 2021-02, Vol.44 (2), p.380-384

2021

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Identification of TMC1 as a relatively common cause for nonsyndromic hearing loss in the Saudi population

American journal of medical genetics. Part B, Neuropsychiatric genetics, 2020-04, Vol.183 (3), p.172-180

2020

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The role of BRCA1/2 in hereditary and familial breast and ovarian cancers

Molecular genetics & genomic medicine, 2019-09, Vol.7 (9), p.e879-n/a

2019

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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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Camels' biological fluids contained nanobodies: promising avenue in cancer therapy

Cancer cell international, 2022-09, Vol.22 (1), p.279-279, Article 279

2022

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Identification of Novel CDH23 Variants Causing Moderate to Profound Progressive Nonsyndromic Hearing Loss

Genes, 2020-12, Vol.11 (12), p.1474

2020

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Correction: Camels' biological fluids contained nanobodies: promising avenue in cancer therapy

Cancer cell international, 2023-03, Vol.23 (1), p.56-56, Article 56

2023

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The protective effects of the methylenetetrahydrofolate reductase rs1801131 variant among Saudi smokers

Saudi journal of biological sciences, 2021-07, Vol.28 (7), p.3972-3980

2021

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Clinical, Endocrine, and Molecular Genetic Analysis of a Large Cohort of Saudi Arabian Patients with Laron Syndrome

Hormone research in paediatrics, 2017-01, Vol.88 (2), p.119-126

2017

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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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Assessing the Performance of Extended Half-Life Coagulation Factor VIII, FC Fusion Protein by Using Chromogenic and One-Stage Assays in Saudi Hemophilia A Patients

Advances in hematology, 2020, Vol.2020 (2020), p.1-7

2020

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Twenty novel mutations in BCKDHA, BCKDHB and DBT genes in a cohort of 52 Saudi Arabian patients with maple syrup urine disease

Molecular genetics and metabolism reports, 2017-06, Vol.11 (C), p.17-23

2017

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Correlation between genetic variation in thymine DNA glycosylase and smoking behavior

Gene, 2021-01, Vol.766, p.145092-145092, Article 145092

2021

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Prevalence of bleeding symptoms among young adults in Saudi Arabia, a national survey

Medicine (Baltimore), 2021-10, Vol.100 (43), p.e27513-e27513

2021

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The structural effects of mutations can aid in differential phenotype prediction of beta-myosin heavy chain (Myosin-7) missense variants

Bioinformatics (Oxford, England), 2016-10, Vol.32 (19), p.2947-2955

2016

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The SAAP pipeline and database: tools to analyze the impact and predict the pathogenicity of mutations

BMC genomics, 2013, Vol.14 Suppl 3 (Suppl 3), p.S4-S4, Article S4

2013

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First description of the molecular and clinical characterization of hereditary factor V deficiency in Saudi Arabia: report of four novel mutations

Blood coagulation & fibrinolysis, 2019-07, Vol.30 (5), p.224-232

2019

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Potential role of Toll-like receptor 2 expression and polymorphisms in colon cancer susceptibility in the Saudi Arabian population

OncoTargets and therapy, 2018-01, Vol.11, p.8127-8141

2018

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Evidence for an autosomal recessive pattern of inheritance in Keratitis-ichthyosis-deafness (KID) syndrome: Exome sequencing reveals a novel homozygous GJB2 mutation

Meta Gene, 2019-02, Vol.19, p.15-22

2019

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King Faisal Specialist Hospital and Research Centre Experience in Developing Point-of-Care Testing Program

Point of care, 2008-12, Vol.7 (4), p.243-245

2008

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Genotype Hemophilia Screening Program Identified 2 Novel Variants Including a Novel Variant (c.5816-2A > G) Causing a Pathogenic Variant of the Factor 8 Gene

Clinical and applied thrombosis/hemostasis, 2023-01, Vol.29, p.10760296231182410-10760296231182410

2023

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Iron Deficiency and Iron Deficiency Anemia Are Common Epidemiological Conditions in Saudi Arabia: Report of the National Epidemiological Survey

Anemia, 2020-12, Vol.2020 (2020), p.1-8

2020

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Punicalagin and Ketogenic Amino Acids Loaded Organic Lipid Carriers Enhance the Bioavailability, Mitochondrial β-Oxidation, and Ketogenesis in Maturing Adipocytes

Nanomaterials (Basel, Switzerland), 2022-01, Vol.12 (3), p.368

2022

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PHENOTYPE/ GENOTYPE SCREENING PATTERN OF HEMOPHILIA A AND B IN SAUDI ARAB

Hematology, Transfusion and Cell Therapy, 2022-10, Vol.44, p.S28-S29

2022

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Novel sequence variants in the TLR6 gene associated with advanced breast cancer risk in the Saudi Arabian population

A novel homozygous SCN5A variant detected in sick sinus syndrome

Identification of TMC1 as a relatively common cause for nonsyndromic hearing loss in the Saudi population

The role of BRCA1/2 in hereditary and familial breast and ovarian cancers

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

Camels' biological fluids contained nanobodies: promising avenue in cancer therapy

Identification of Novel CDH23 Variants Causing Moderate to Profound Progressive Nonsyndromic Hearing Loss

Correction: Camels' biological fluids contained nanobodies: promising avenue in cancer therapy

The protective effects of the methylenetetrahydrofolate reductase rs1801131 variant among Saudi smokers

Clinical, Endocrine, and Molecular Genetic Analysis of a Large Cohort of Saudi Arabian Patients with Laron Syndrome

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

Assessing the Performance of Extended Half-Life Coagulation Factor VIII, FC Fusion Protein by Using Chromogenic and One-Stage Assays in Saudi Hemophilia A Patients

Twenty novel mutations in BCKDHA, BCKDHB and DBT genes in a cohort of 52 Saudi Arabian patients with maple syrup urine disease

Correlation between genetic variation in thymine DNA glycosylase and smoking behavior

Prevalence of bleeding symptoms among young adults in Saudi Arabia, a national survey

The structural effects of mutations can aid in differential phenotype prediction of beta-myosin heavy chain (Myosin-7) missense variants

The SAAP pipeline and database: tools to analyze the impact and predict the pathogenicity of mutations

First description of the molecular and clinical characterization of hereditary factor V deficiency in Saudi Arabia: report of four novel mutations

Potential role of Toll-like receptor 2 expression and polymorphisms in colon cancer susceptibility in the Saudi Arabian population

Evidence for an autosomal recessive pattern of inheritance in Keratitis-ichthyosis-deafness (KID) syndrome: Exome sequencing reveals a novel homozygous GJB2 mutation

King Faisal Specialist Hospital and Research Centre Experience in Developing Point-of-Care Testing Program

Genotype Hemophilia Screening Program Identified 2 Novel Variants Including a Novel Variant (c.5816-2A > G) Causing a Pathogenic Variant of the Factor 8 Gene

Iron Deficiency and Iron Deficiency Anemia Are Common Epidemiological Conditions in Saudi Arabia: Report of the National Epidemiological Survey

Punicalagin and Ketogenic Amino Acids Loaded Organic Lipid Carriers Enhance the Bioavailability, Mitochondrial β-Oxidation, and Ketogenesis in Maturing Adipocytes

PHENOTYPE/ GENOTYPE SCREENING PATTERN OF HEMOPHILIA A AND B IN SAUDI ARAB

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