Omar Hamdan
Overview
Explore the profile of Omar Hamdan including associated specialties, affiliations and a list of published articles.
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Articles
19
Citations
352
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Recent Articles
1.
Hamdan O, Alshajrawi R, Mussa Q, Alajlouni Y, Dabbah Y, Fratekh R, et al.
Rheumatol Int
. 2025 Mar;
45(4):71.
PMID: 40072585
Background/objectives: Eosinophilic Fasciitis (EF) is a rare connective tissue disorder characterized by skin thickening. Few studies explored its characteristics and factors associated with treatment response. Methods: PubMed, CENTRAL, Web of...
2.
Alnaimat F, Hamdan O, Natsheh T, Hamad R, Amrieh Z, Ahmad D, et al.
BMC Rheumatol
. 2025 Feb;
9(1):26.
PMID: 40012000
Background: Systemic Lupus erythematosus (SLE) is an autoimmune disorder in which females are affected more commonly than males. In addition to the physical burden of the disease, patients with SLE...
3.
Alnaimat F, Alawneh K, AbuHelal A, Hamdan O, Alelaimat A, Al Mashaleh M, et al.
BMC Rheumatol
. 2025 Feb;
9(1):16.
PMID: 39962571
Background: Psoriatic arthritis (PsA) is a chronic, inflammatory rheumatic disease. We aim to describe the characteristics of PsA patients and examine factors affecting their psychological and physical well-being. Methods: This...
4.
Fehlings D, Zarrei M, Engchuan W, Sondheimer N, Thiruvahindrapuram B, MacDonald J, et al.
Nat Genet
. 2024 Mar;
56(4):585-594.
PMID: 38553553
We performed whole-genome sequencing (WGS) in 327 children with cerebral palsy (CP) and their biological parents. We classified 37 of 327 (11.3%) children as having pathogenic/likely pathogenic (P/LP) variants and...
5.
Mitina A, Khan M, Lesurf R, Yin Y, Engchuan W, Hamdan O, et al.
EBioMedicine
. 2024 Feb;
101:105027.
PMID: 38418263
Background: Cardiomyopathy is a clinically and genetically heterogeneous heart condition that can lead to heart failure and sudden cardiac death in childhood. While it has a strong genetic basis, the...
6.
Alzayadneh I, Hamdan O, Alzayadneh L, Al-Zubi B, Glikson E, Almusaileem N, et al.
Aesthet Surg J
. 2024 Jan;
44(6):588-596.
PMID: 38243582
Background: Musculoskeletal pain is a common occupational health problem among surgeons that can affect work productivity and quality of life. Objectives: The aim of the study was to investigate the...
7.
Hamdan O, Nowak K
J Clin Pathol
. 2023 Jan;
76(2):73-75.
PMID: 36600573
The partner and localiser of BRCA2 (PALB2) gene, located on chromosome 16, functions as a tumour suppressor that plays a critical role in homologous recombination repair after DNA double-strand breaks....
8.
Trost B, Thiruvahindrapuram B, Chan A, Engchuan W, Higginbotham E, Howe J, et al.
Cell
. 2022 Nov;
185(23):4409-4427.e18.
PMID: 36368308
Fully understanding autism spectrum disorder (ASD) genetics requires whole-genome sequencing (WGS). We present the latest release of the Autism Speaks MSSNG resource, which includes WGS data from 5,100 individuals with...
9.
Alrawashdeh H, Al-Habahbeh O, Naser A, Abu Serhan H, Hamdan O, Sweiss K, et al.
Cureus
. 2022 Apr;
14(2):e22669.
PMID: 35386174
Lichen planus is an autoimmune inflammatory disease that can be associated with infections, drugs, and vaccines. Recently, it has been reported to occur following mRNA-based COVID-19 vaccines, particularly the Pfizer/BioNTech...
10.
Reuter M, Chaturvedi R, Jobling R, Pellecchia G, Hamdan O, Sung W, et al.
Circ Genom Precis Med
. 2021 Jul;
14(4):e003410.
PMID: 34328347
Background: Tetralogy of Fallot (TOF)-the most common cyanotic heart defect in newborns-has evidence of multiple genetic contributing factors. Identifying variants that are clinically relevant is essential to understand patient-specific disease...