Nader Al-Dewik
Overview
Explore the profile of Nader Al-Dewik including associated specialties, affiliations and a list of published articles.
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Articles
42
Citations
441
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Recent Articles
1.
Younes S, Elkahlout R, Kilani H, Okashah S, Sharshani H, Rezoug Z, et al.
BMC Med Genomics
. 2025 Mar;
18(1):49.
PMID: 40082840
Background: Maple syrup urine disease (MSUD) is a hereditary metabolic disorder caused by a deficiency in the branched-chain α-keto acid dehydrogenase (BCKD) enzymatic complex. The Middle East and North Africa,...
2.
Razzaq A, Elkahlout R, Nasrallah G, Ibrahim F, Samara M, Zayed H, et al.
Lifestyle Genom
. 2025 Jan;
:1-23.
PMID: 39746347
Introduction: Preterm birth (PTB) is associated with newborn morbidity and mortality. DNA methylation plays an important role in the development of fetus, thus can also serve as an epigenetic biomarker....
3.
Al-Dewik N, Abuarja T, Younes S, Nasrallah G, Alsharshani M, Ibrahim F, et al.
Per Med
. 2024 Sep;
21(5):313-333.
PMID: 39347749
Precision Medicine (PM) is a transformative clinical medicine strategy that aims to revolutionize healthcare by leveraging biological information and biomarkers. In the context of maternal and neonatal health, PM enables...
4.
Farrell T, Minisha F, Khenyab N, Ali N, Al Obaidly S, Yaqoub S, et al.
J Perinat Med
. 2024 Aug;
52(8):878-885.
PMID: 39167534
Objectives: Customized birthweight centiles have improved the detection of small for gestational age (SGA) and large for gestational age (LGA) babies compared to existing population standards. This study used perinatal...
5.
Linga B, Mohammed S, Farrell T, Rifai H, Al-Dewik N, Qoronfleh M
Cancers (Basel)
. 2024 Jun;
16(11).
PMID: 38893137
As next-generation sequencing (NGS) has become more widely used, germline and rare genetic variations responsible for inherited illnesses, including cancer predisposition syndromes (CPSs) that account for up to 10% of...
6.
Younes S, Nicolai E, Pieri M, Bernardini S, Daas H, Al-Sadeq D, et al.
Influenza Other Respir Viruses
. 2024 May;
18(5):e13290.
PMID: 38706402
Background: Priming with ChAdOx1 followed by heterologous boosting is considered in several countries. Nevertheless, analyses comparing the immunogenicity of heterologous booster to homologous primary vaccination regimens and natural infection are...
7.
Al-Sadeq D, Conter C, Thanassoulas A, Al-Dewik N, Safieh-Garabedian B, Martinez-Cruz L, et al.
Biochem J
. 2024 Apr;
481(8):569-585.
PMID: 38563463
Homocystinuria is a rare disease caused by mutations in the CBS gene that results in a deficiency of cystathionine β-synthase (CBS). CBS is an essential pyridoxal 5'-phosphate (PLP)-dependent enzyme in...
8.
Alkhidir S, El-Akouri K, Al-Dewik N, Khodjet-El-Khil H, Okashah S, Islam N, et al.
Sci Rep
. 2024 Feb;
14(1):4202.
PMID: 38378725
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,...
9.
Vazhiyelethil J, Minisha F, Al Obaidly S, AlQubaisi M, Salama H, Ali N, et al.
Qatar Med J
. 2024 Jan;
2024(1):2.
PMID: 38264267
Background: Bariatric surgery is performed in obese women of reproductive age to help achieve a healthy prepregnancy weight to reduce the complications associated with obesity in pregnancy. However, these procedures...
10.
Nahas L, Datta A, Alsamman A, Adly M, Al-Dewik N, Sekaran K, et al.
Metab Brain Dis
. 2023 Dec;
39(1):29-42.
PMID: 38153584
Autism Spectrum Disorder (ASD) is a complex neurodevelopmental condition characterized by altered brain connectivity and function. In this study, we employed advanced bioinformatics and explainable AI to analyze gene expression...