تصفح حسب المؤلف "Al-Shafai, Mashael"
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Association of Vitamin D Genetic Risk Score with Noncommunicable Diseases: A Systematic Review
Almaghrbi, Heba; Al-Shafai, Mashael; Al-Asmakh, Maha; Bawadi, Hiba ( MDPI , 2023 , Article)Background and Aims: The genetic risk score (GRS) is an important tool for estimating the total genetic contribution or susceptibility to a certain outcome of interest in an individual, taking into account their genetic ... -
The genetic basis and the diagnostic yield of genetic testing related to nonsyndromic hearing loss in Qatar
Alkhidir, Shaza; El-Akouri, Karen; Al-Dewik, Nader; Khodjet-El-khil, Houssein; Okashah, Sarah; Islam, Nazmul; Ben-Omran, Tawfeg; Al-Shafai, Mashael... more authors ... less authors ( Springer Nature , 2024 , Article)Hearing loss is the most predominant sensory defect occurring in pediatrics, of which, 66% cases are attributed to genetic factors. The prevalence of hereditary hearing loss increases in consanguineous populations, and the ... -
The genetic elucidation of monogenic obesity in the Arab world: a systematic review
Abouhashem, Nadien; Al-Shafai, Kholoud; Al-Shafai, Mashael ( J Pediatr Endocrinol Metab , 2022 , Article)Background: Investigation of monogenic obesity (MO), a rare condition caused by a single gene variant(s), especially in consanguineous populations, is a powerful approach for obtaining novel insights into the genetic ... -
The Interplay Between Diet and the Epigenome in the Pathogenesis of Type-1 Diabetes
Kohil, Amira; Al-Asmakh, Maha; Al-Shafai, Mashael; Terranegra, Annalisa ( Frontiers , 2021 , Article Review)The autoimmune disease, Type 1 Diabetes Mellitus (T1DM), results in the destruction of pancreatic β-cells, and the International Diabetes Federation reports that its incidence is increasing worldwide. T1DM is a complex ... -
Investigation of Genetic Causes in Patients with Congenital Heart Disease in Qatar: Findings from the Sidra Cardiac Registry
Okashah, Sarah; Vasudeva, Dhanya; El Jerbi, Aya; Khodjet-El-khil, Houssein; Al-Shafai, Mashael; Syed, Najeeb; Kambouris, Marios; Udassi, Sharda; Saraiva, Luis R.; Al-Saloos, Hesham; Udassi, Jai; Al-Shafai, Kholoud N.... more authors ... less authors ( Multidisciplinary Digital Publishing Institute (MDPI) , 2022 , Article)Congenital heart disease (CHD) is one of the most common forms of birth defects worldwide, with a prevalence of 1–2% in newborns. CHD is a multifactorial disease partially caused by genetic defects, including chromosomal ... -
Knowledge and Perception of and Attitude toward a Premarital Screening Program in Qatar: A Cross-Sectional Study
Al-Shafai, Mashael; Al-Romaihi, Aisha; Al-Hajri, Noora; Islam, Nazmul; Adawi, Karam ( MDPI , 2022 , Article)Premarital screening (PMS) is a primary preventive measure to decrease the incidence of certain genetic disorders and sexually transmitted diseases. This study aimed to explore the knowledge and perception of and the ... -
Legal approaches to risk of harm in genetic counseling: perspectives from Quebec and Qatar
Patrinos, Dimitri; Ghaly, Mohammed; Al-Shafai, Mashael; Zawati, Ma’n H. ( Frontiers Media SA , 2023 , Article)Genetic counseling is a fast-growing profession worldwide, with genetic counselors taking on increasingly comprehensive and autonomous roles in the healthcare sector. However, the absence of appropriate legal frameworks ... -
The role of genetic and epigenetic GNAS alterations in the development of early-onset obesity
Alaa, Abbas; Hammad, Ayat S; Al-Shafai, Mashael ( Elsevier , 2023 , Article)BackgroundGNAS (guanine nucleotide-binding protein, alpha stimulating) is an imprinted gene that encodes Gsα, the α subunit of the heterotrimeric stimulatory G protein. This subunit mediates the signalling of a diverse ... -
The Special Features of Prenatal and Preimplantation Genetic Counseling in Arab Countries.
Malik, Shaza D; Al-Shafai, Mashael; Abdallah, Atiyeh M ( MDPI , 2022 , Article Review)Genetic counseling services have only recently been introduced in most Arab countries, and their utilization is increasing. Prenatal genetic counseling is essential, particularly in the Arab context, which is characterized ... -
Understanding the genetics of early onset obesity in a cohort of children from Qatar.
Mohammed, Idris; Haris, Basma; Al-Barazenji, Tara; Vasudeva, Dhanya; Tomei, Sara; Al Azwani, Iman; Dauleh, Hajar; Shehzad, Saira; Chirayath, Shiga; Mohamadsalih, Ghassan; Petrovski, Goran; Khalifa, Amel; Love, Donald R; Al-Shafai, Mashael; Hussain, Khalid... more authors ... less authors ( Oxford University Press , 2023 , Article)Monogenic obesity is a rare form of obesity due to pathogenic variants in genes implicated in the leptin-melanocortin signaling pathway and accounts for around 5% of severe early onset obesity. Mutations in the genes ...