Hamad Alzaidan
Overview
Explore the profile of Hamad Alzaidan including associated specialties, affiliations and a list of published articles.
Author names and details appear as published. Due to indexing inconsistencies, multiple individuals may share a name, and a single author may have variations. MedLuna displays this data as publicly available, without modification or verification
Snapshot
Snapshot
Articles
26
Citations
432
Followers
0
Related Specialties
Related Specialties
Top 10 Co-Authors
Top 10 Co-Authors
Published In
Published In
Affiliations
Affiliations
Soon will be listed here.
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.
Del-Pozo-Rodriguez J, Tilly P, Lecat R, Vaca H, Mosser L, Brivio E, et al.
medRxiv
. 2024 Mar;
PMID: 38496416
The ADAT2/ADAT3 complex catalyzes the adenosine to inosine modification at the wobble position of eukaryotic tRNAs. Mutations in , the catalytically inactive subunit of the ADAT2/ADAT3 complex, have been identified...
3.
Alhudaithi A, Alsughier Z, Alzaidan H, Aldhelai T
Cureus
. 2023 Nov;
15(10):e47947.
PMID: 38034196
Background: Dental caries is a disease that is quite common in children and has a negative impact on their oral health, mental health, and quality of life. This study aimed...
4.
Gracia-Diaz C, Zhou Y, Yang Q, Maroofian R, Espana-Bonilla P, Lee C, et al.
Nat Commun
. 2023 Jul;
14(1):4109.
PMID: 37433783
Genetic variants in chromatin regulators are frequently found in neurodevelopmental disorders, but their effect in disease etiology is rarely determined. Here, we uncover and functionally define pathogenic variants in the...
5.
AlQudairy H, Aldhalaan H, AlRuways S, Almutairi N, AlNakiyah M, AlGhofaili R, et al.
Front Pediatr
. 2023 Mar;
10:1051534.
PMID: 36923948
Background: (solute carrier family 13, member 5) encodes sodium/citrate cotransporter, which mainly localizes in cellular plasma membranes in the frontal cortex, retina, and liver. Pathogenic variants of the gene cause...
6.
Shamseldin H, Derar N, Alzaidan H, Alhathal N, Alfalah A, Abdulwahab F, et al.
Hum Genet
. 2023 Jan;
142(4):477-482.
PMID: 36715754
Ichthyosis is a genetically heterogeneous genodermatosis characterized by severely rough, dry and scaly skin. We report two consanguineous families with congenital ichthyosis. Combined positional mapping and exome sequencing of the...
7.
Saida K, Maroofian R, Sengoku T, Mitani T, Pagnamenta A, Marafi D, et al.
Genet Med
. 2022 Nov;
25(1):90-102.
PMID: 36318270
Purpose: Brain monoamine vesicular transport disease is an infantile-onset movement disorder that mimics cerebral palsy. In 2013, the homozygous SLC18A2 variant, p.Pro387Leu, was first reported as a cause of this...
8.
Altassan R, Sulaiman R, Alfalah A, Alwagiat W, Megdad E, Alqasabi D, et al.
Eur J Med Genet
. 2022 Sep;
65(11):104602.
PMID: 36049607
Patients with certain inherited metabolic disorders (IMD) are at high risk for metabolic decompensation with exposure to infections. The COVID-19 pandemic has been particularly challenging for health care providers dealing...
9.
Shamseldin H, Shaheen R, Ewida N, Bubshait D, Alkuraya H, Almardawi E, et al.
Genet Med
. 2022 Apr;
24(4):966.
PMID: 35394428
No abstract available.
10.
Alghamdi M, Tohary M, Alzaidan H, Imtiaz F, Al-Hassnan Z
JIMD Rep
. 2021 Nov;
62(1):91-96.
PMID: 34765403
Succinyl-CoA:3-ketoacid CoA transferase (SCOT) deficiency is an inherited metabolic disease caused by mutated OXCT1 gene resulting in recurrent ketoacidosis. Analysis of longitudinal data in such an ultra-rare disease is warranted...