Hamid Galehdari

Shahid Chamran University of Ahvaz — IR

Medicine · Health Sciences

24h-index2.8kcitations269works2.32yr avg
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Research Topics

Hemoglobinopathies and Related Disorders(24), Iron Metabolism and Disorders(20), Genomics and Rare Diseases(19), Genetics and Neurodevelopmental Disorders(15), RNA modifications and cancer(14)

Publications269 total

Synergistic chemo-photothermal therapy using doxorubicin-loaded gold nanorods for enhanced apoptosis in lung cancer cells
Scientific Reports·2025· 1 citedOpen Access
Sialic Acid Modulation of HMGA1 and HMGA2 Gene Expression in Human Astrocytoma Cells
Asian Journal of Biochemistry Genetics and Molecular Biology·2025Open Access
Synergistic Chemo-Photothermal Therapy Using Doxorubicin-Loaded Gold Nanorods for Enhanced Apoptosis in Lung Cancer Cells
2025Open Access
Association of sperm protamine1 and protamine2 transcript content with paternal age: A cross-sectional study
International Journal of Reproductive BioMedicine (IJRM)·2025Open Access
Investigating the Efficacy of the CRISPR/Cas9 Gene-Editing System for Targeting the HBB FSC 36-37 (-T) Mutation Locus in Hematopoietic Stem Cells
Molecular Biotechnology·2025
Identification of Reliable Housekeeping Genes for qRT-PCR Normalization in Neuroblastoma and Glioblastoma Cell Lines Infected with Lentivirus
Gene Cell and Tissue·2025Open Access
Bi-allelic pathogenic variants in TRMT1 disrupt tRNA modification and induce a neurodevelopmental disorder
The American Journal of Human Genetics·2025· 5 citedOpen Access
Some miRNA signatures associated with the use of Etomidate and Propofol and their implications for cardiac surgery
2025Open Access
Hematologic Parameters Cut-off Assessment of Adult Alpha-Thalassemia Patients in Iran
International Journal of Hematology-Oncology and Stem Cell Research·2024Open Access
Elucidating the clinical and genetic spectrum of inositol polyphosphate phosphatase INPP4A-related neurodevelopmental disorder
Genetics in Medicine·2024· 7 citedOpen Access
Biallelic pathogenic variants in TRMT1 disrupt tRNA modification and induce a syndromic neurodevelopmental disorder
2024· 1 citedOpen Access
Biallelic <i>ZBTB11</i> Variants: A Neurodevelopmental Condition with Progressive Complex Movement Disorders
Movement Disorders·2024· 3 citedOpen Access
Corrigendum to “Ex vivo expansion of hematopoietic stem cells in two/three-dimensional co-cultures with various source of stromal cells” [Tissue Cell 87 (2024) 102331]
Tissue and Cell·2024
Analysis of Factors Affecting Fetal Fraction in Cell-Free DNA Test
Jentashapir Journal of Cellular and Molecular Biology·2024Open Access
PKHD1L1, a gene involved in the stereocilia coat, causes autosomal recessive nonsyndromic hearing loss
Human Genetics·2024· 6 citedOpen Access
Overexpression and Downregulation of HOTAIR Influence the Stemness Markers in Gastric Cancer Cell Lines
Gene Cell and Tissue·2024· 1 citedOpen Access
Exploring the Influence of Sialic Acid on Drug Resistance in Glioma: A Focus on ABCB1 and ABCC1 Transporter Genes Expression
Jentashapir Journal of Cellular and Molecular Biology·2024Open Access
Ex vivo expansion of hematopoietic stem cells in two/ three-dimensional co-cultures with various source of stromal cells
Tissue and Cell·2024· 1 cited
Identification of new variants in patients with mucopolysaccharidosis in consanguineous Iranian families
Frontiers in Genetics·2024· 2 citedOpen Access
Development of a potent recombinant scFv antibody against the SARS-CoV-2 by in-depth bioinformatics study: Paving the way for vaccine/diagnostics development
Computers in Biology and Medicine·2024· 3 cited
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Frequent Co-authors

Reza Maroofian(19), Gholamreza Shariati(17), Neda Mazaheri(16), Henry Houlden(12), Reza Azizi Malamiri(9), Alireza Sedaghat(9), Maha S. Zaki(6), James R. Lupski(6), Mina Zamani(6), Yalda Jamshidi(5), Davut Pehli̇van(4), Mahnaz Kesmati(4), Stéphanie Efthymiou(4), Mohammad Yahya Vahidi Mehrjardi(4), Jawaher Zeighami(4), Alistair T. Pagnamenta(4), Christian Beetz(4), Peter Bauer(4), Amir Jalali(4), Wolff Schmiegel(3)