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A Multicenter Cross-Sectional Study on Assessment of Depression in Cardiac Patients

Journal of pharmacy & bioallied science, 2023-07, Vol.15 (5), p.616-S620

2023

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Exosomes: Isolation, characterization, and biomedical applications

Cell biology international, 2021-09, Vol.45 (9), p.1807-1831

2021

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Prevalence and risk factors of ibs among medical and nonmedical students in the jouf university

Nigerian journal of clinical practice, 2020-04, Vol.23 (4), p.555-560

2020

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A novel motivation for the unstable nonlinear Schrödinger equation through random inputs

AIP advances, 2024-02, Vol.14 (2), p.025146-025146-5

2024

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Efficient dye discoloration of modified Lamiaceae leaves

Materials research express, 2021-03, Vol.8 (3), p.35503

2021

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Frameshift variant in MITF gene in a large family with Waardenburg syndrome type II and a co-segregation of a C2orf74 variant

PloS one, 2021-02, Vol.16 (2), p.e0246607-e0246607

2021

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Epidemiology of childhood injuries in Saudi Arabia: a scoping review

BMC pediatrics, 2021-09, Vol.21 (1), p.1-14, Article 424

2021

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Multimodal Arabic Rumors Detection

IEEE access, 2023-01, Vol.11, p.1-1

2023

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KMT2C, a histone methyltransferase, is mutated in a family segregating non-syndromic primary failure of tooth eruption

Scientific reports, 2019-11, Vol.9 (1), p.16469-10, Article 16469

2019

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Geospatial Assessment of Ground Water Quality and Associated Health Problems in the Western Region of India

Water (Basel), 2022-02, Vol.14 (3), p.296

2022

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Integrability and Dynamic Behavior of a Piezoelectro-Magnetic Circular Rod

Mathematics (Basel), 2024-01, Vol.12 (2), p.236

2024

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Knowledge, attitude and practice of health care practitioners in Saudi Arabia, with regard to prevention of vitamin D deficiency in infancy

Saudi medical journal, 2018-06, Vol.39 (6), p.603-608

2018

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Whole genome SNP genotyping in a family segregating developmental dysplasia of the hip detected runs of homozygosity on chromosomes 15q13.3 and 19p13.2

Congenital anomalies, 2018-03, Vol.58 (2), p.56-61

2018

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Health outcomes and policy in pharmay curricula among Arab countries: An evaluation of 191 academic institutions

Saudi pharmaceutical journal, 2021-08, Vol.29 (8), p.799-806

2021

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Structural Elucidation of Rift Valley Fever Virus L Protein towards the Discovery of Its Potential Inhibitors

Pharmaceuticals (Basel, Switzerland), 2022-05, Vol.15 (6), p.659

2022

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Analyzing the U.S. Post-marketing safety surveillance of COVID-19 vaccines

Saudi pharmaceutical journal, 2022-02, Vol.30 (2), p.180-184

2022

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A homozygous potentially pathogenic variant in the PAXBP1 gene in a large family with global developmental delay and myopathic hypotonia

Clinical genetics, 2017-12, Vol.92 (6), p.579-586

2017

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Environmental Risk Factors and Health: An Umbrella Review of Meta-Analyses

International journal of environmental research and public health, 2021-01, Vol.18 (2), p.704

2021

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A novel missense variant in the RASGRP2 gene in patients with moderate to severe bleeding disorder

Platelets (Edinburgh), 2020-07, Vol.31 (5), p.646-651

2020

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Exome sequencing revealed a novel loss‐of‐function variant in the GLI3 transcriptional activator 2 domain underlies nonsyndromic postaxial polydactyly

Molecular genetics & genomic medicine, 2019-07, Vol.7 (7), p.e00627-n/a

2019

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Missense Mutations in the CTSC Gene in Saudi Families Segregating Papillon-Lefèvre Syndrome

Annals of Dermatology, 2020, 32(1), , pp.77-80

2020

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Saudi Expert Consensus-Based Autism Spectrum Disorder Statement: From Screening to Management

Children (Basel), 2022-08, Vol.9 (9), p.1269

2022

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Whole exome sequencing identified a novel single base pair insertion mutation in the EYS gene in a six generation family with retinitis pigmentosa

Congenital anomalies, 2018-01, Vol.58 (1), p.10-15

2018

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Melatonin ameliorates the adrenal and pancreatic alterations in streptozotocin-induced diabetic rats: Clinical, biochemical, and descriptive histopathological studies

Frontiers in veterinary science, 2022-10, Vol.9, p.1016312-1016312

2022

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A novel splice-site mutation in the ASPM gene underlies autosomal recessive primary microcephaly

Annals of Saudi medicine, 2016-11, Vol.36 (6), p.391-396

2016

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A Multicenter Cross-Sectional Study on Assessment of Depression in Cardiac Patients

Exosomes: Isolation, characterization, and biomedical applications

Prevalence and risk factors of ibs among medical and nonmedical students in the jouf university

A novel motivation for the unstable nonlinear Schrödinger equation through random inputs

Efficient dye discoloration of modified Lamiaceae leaves

Frameshift variant in MITF gene in a large family with Waardenburg syndrome type II and a co-segregation of a C2orf74 variant

Epidemiology of childhood injuries in Saudi Arabia: a scoping review

Multimodal Arabic Rumors Detection

KMT2C, a histone methyltransferase, is mutated in a family segregating non-syndromic primary failure of tooth eruption

Geospatial Assessment of Ground Water Quality and Associated Health Problems in the Western Region of India

Integrability and Dynamic Behavior of a Piezoelectro-Magnetic Circular Rod

Knowledge, attitude and practice of health care practitioners in Saudi Arabia, with regard to prevention of vitamin D deficiency in infancy

Whole genome SNP genotyping in a family segregating developmental dysplasia of the hip detected runs of homozygosity on chromosomes 15q13.3 and 19p13.2

Health outcomes and policy in pharmay curricula among Arab countries: An evaluation of 191 academic institutions

Structural Elucidation of Rift Valley Fever Virus L Protein towards the Discovery of Its Potential Inhibitors

Analyzing the U.S. Post-marketing safety surveillance of COVID-19 vaccines

A homozygous potentially pathogenic variant in the PAXBP1 gene in a large family with global developmental delay and myopathic hypotonia

Environmental Risk Factors and Health: An Umbrella Review of Meta-Analyses

A novel missense variant in the RASGRP2 gene in patients with moderate to severe bleeding disorder

Exome sequencing revealed a novel loss‐of‐function variant in the GLI3 transcriptional activator 2 domain underlies nonsyndromic postaxial polydactyly

Missense Mutations in the CTSC Gene in Saudi Families Segregating Papillon-Lefèvre Syndrome

Saudi Expert Consensus-Based Autism Spectrum Disorder Statement: From Screening to Management

Whole exome sequencing identified a novel single base pair insertion mutation in the EYS gene in a six generation family with retinitis pigmentosa

Melatonin ameliorates the adrenal and pancreatic alterations in streptozotocin-induced diabetic rats: Clinical, biochemical, and descriptive histopathological studies

A novel splice-site mutation in the ASPM gene underlies autosomal recessive primary microcephaly

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