Author

Deemah Alwadaani

Observed names: D. Alwadaani, Deemah AlWadaani

Institutions: King Saud bin Abdulaziz University for Health Sciences, King Abdulaziz Medical City, King Abdullah International Medical Research Center, National Guard Health Affairs

Observed institutions: King Saud bin Abdulaziz University for Health Sciences, King Abdulaziz Medical City, King Abdullah International Medical Research Center, National Guard Health Affairs

ORCID: 0000-0001-6536-0777

Observed ORCID: 0000-0001-6536-0777

OpenAlex ID: A5019415062

Whole genome transcriptomic reveals heat stroke molecular signatures in humans

2023 · Abderrezak Bouchama, Mamoon Rashid, et al. · The Journal of Physiology · 27

Mutated RAP1GDS1 causes a new syndrome of dysmorphic feature, intellectual disability & speech delay

2020 · Abdulaziz Asiri, Essra Aloyouni, et al. · Annals of Clinical and Translational Neurology · 20

Pancytopenia, Recurrent Infection, Poor Wound Healing, Heterotopia of the Brain Probably Associated with A Candidate Novel de Novo CDC42 Gene Defect: Expanding the Molecular and Phenotypic Spectrum

2021 · Abdulaziz Asiri, Deemah Alwadaani, et al. · Genes · 15

Blockade of p38 MAPK overcomes AML stem cell line KG1a resistance to 5-Fluorouridine and the impact on miRNA profiling

2022 · Sabine Matou-Nasri, Maria Najdi, et al. · PLoS ONE · 14

Impact of Genetic Variations on Thromboembolic Risk in Saudis with Sickle Cell Disease

2023 · Mohammad A. Alshabeeb, Deemah Alwadaani, et al. · Genes · 6

Unraveling the Complex Genomic Interplay of Sickle Cell Disease Among the Saudi Population: A Case-Control GWAS Analysis

2025 · Ali Alghubayshi, Dayanjan Wijesinghe, et al. · International Journal of Molecular Sciences · 5

Differential Gene Expression in Peripheral White Blood Cells with Permissive Underfeeding and Standard Feeding in Critically Ill Patients: A Descriptive Sub-study of the PermiT Randomized Controlled Trial

2018 · Yaseen M. Arabi, Mohammed Al-Balwi, et al. · Scientific Reports · 5

Truncated SPAG9 as a novel candidate gene for a new syndrome: Coarse facial features, albinism, cataract and developmental delay (CACD syndrome)

2025 · Majid Alfadhel, Bashayr S. Alhubayshi, et al. · Genetics and Molecular Biology · 2

Unveiling the heritability of selected unexplored pharmacogenetic markers in the Saudi population

2025 · Mohammad A. Alshabeeb, Deemah Alwadaani, et al. · Frontiers in Pharmacology · 1

5566409 Impact of Genetic Variations on Thrombotic Risk of Sickle Cell Disease in Saudi Patients

2023 · M.A. Alshabeeb, D. Alwadaani, et al. · HemaSphere · 1

Differential Expression and Target Gene Analysis of PBMC-Derived microRNAs as Prognostic Biomarkers in Acute Lymphoblastic Leukemia

2026 · Fatemah S. Basingab, Hadil Alahdal, et al. · International Journal of Molecular Sciences

Identification of novel and recurrent mutations in nicotinamide nucleotide transhydrogenase (NNT) underlying familial glucocorticoid deficiency-type 4 in multiple Saudi families

2026 · Ibrahim Al Alwan, Raja Hussain Ali, et al. · Journal of Clinical & Translational Endocrinology

Impact of Genetic Variations on Thrombotic Risk in Saudis with Sickle Cell Disease

2023 · Farjah Algahtani, Mohammad Alshabeeb, et al. · Blood

Works count: 13

Citation count: 96

H-index: 5

I10-index: 4