Mohamed Abouelhoda
Overview
Explore the profile of Mohamed Abouelhoda including associated specialties, affiliations and a list of published articles.
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80
Citations
1916
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Recent Articles
1.
AlAbdi L, Maddirevula S, Aljamal B, Hamid H, Almulhim A, Hashem M, et al.
Med
. 2024 Nov;
6(3):100528.
PMID: 39504961
Background: Founder variants are ancestral variants shared by individuals who are not closely related. The large effect size of some of these variants in the context of Mendelian disorders offers...
2.
Abouelhoda M, Almuqati N, Abogosh A, Alfraih F, Maddirevula S, Alkuraya F
Hum Genet
. 2023 Dec;
143(2):125-136.
PMID: 38159139
Pharmacogenomics (PGx) is a promising field of precision medicine where efficacy of drugs is maximized while side effects are minimized for individual patients. Knowledge of the frequency of PGx-relevant variants...
3.
Al Eissa M, Alotibi R, Alhaddad B, Aloraini T, Samman M, Alasiri A, et al.
Front Genet
. 2023 Nov;
14:1250317.
PMID: 38028588
Physicians face diagnostic dilemmas upon reports indicating disease variants of unknown significance (VUS). The most puzzling cases are patients with rare diseases, where finding another matched genotype and phenotype to...
4.
Shim I, Kuwahara H, Chen N, Hashem M, AlAbdi L, Abouelhoda M, et al.
Nat Commun
. 2023 Oct;
14(1):6535.
PMID: 37852978
Arabs account for 5% of the world population and have a high burden of cardiometabolic disease, yet clinical utility of polygenic risk prediction in Arabs remains understudied. Among 5399 Arab...
5.
Monies D, Goljan E, Assoum M, Albreacan M, Binhumaid F, Subhani S, et al.
Genome Med
. 2023 Jun;
15(1):44.
PMID: 37344829
Background: The clinical utility of exome sequencing is now well documented. Rapid exome sequencing (RES) is more resource-intensive than regular exome sequencing and is typically employed in specialized clinical settings...
6.
Alswailem M, Alghamdi B, AlOtaibi A, Aljomiah A, Al-Hindi H, Murugan A, et al.
J Clin Endocrinol Metab
. 2023 Mar;
108(9):e704-e711.
PMID: 36995892
Context: Diffuse sclerosing papillary thyroid cancer (DSPTC) is rare, with limited data on its molecular genetics. Objective: We studied the molecular genetics of a cohort of DSPTC. Methods: DNA was...
7.
Alkhamis F, Alabdali M, AlSulaiman A, Alamri A, Alali R, Akhtar M, et al.
Funct Integr Genomics
. 2023 Mar;
23(2):102.
PMID: 36973604
Ischemic stroke represents a significant societal burden across the globe. Rare high penetrant monogenic variants and less pathogenic common single nucleotide polymorphisms (SNPs) have been described as being associated with...
8.
Nassar A, Zekri A, Elberry M, Lymona A, Lotfy M, Abouelhoda M, et al.
Curr Issues Mol Biol
. 2022 Dec;
44(12):5890-5901.
PMID: 36547062
This study aimed to investigate the impact of somatic mutations on various interleukin signaling pathways associated with grade II invasive breast cancer (BC) in Egyptian patients to broaden our understanding...
9.
Al-Hamed M, Hussein M, Shah Y, Al-Mojalli H, Alsabban E, Alshareef T, et al.
Hum Mutat
. 2022 Sep;
43(12):e24-e37.
PMID: 36177613
The use of genetic testing within nephrology is increasing and its diagnostic yield depends on the methods utilized, patient selection criteria, and population characteristics. We performed exome sequencing (ES) analysis...
10.
Tegally H, San J, Cotten M, Moir M, Tegomoh B, Mboowa G, et al.
Science
. 2022 Sep;
378(6615):eabq5358.
PMID: 36108049
Investment in severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) sequencing in Africa over the past year has led to a major increase in the number of sequences that have been...