Mianesaz Hamidreza

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Date range:

2018-2026

2026

Mianesaz, H., Göczi, L., Bojcsuk, D., Ghalamkari, S., Fadel, L., Póliska, S., Penyige, A., Nagy, L., Nagy, G., Vámosi, G., Széles, L.: Genome-wide chromatin profiling reveals a non-limiting role for RXR in macrophage-like cells stimulated with multiple nuclear receptor agonists.
J. Biol Chem. [Epub ahead of print], 2026.

DEA

Journal metrics:

Q1 Biochemistry (2025)

Q1 Cell Biology (2025)

Q1 Molecular Biology (2025)

2025

Mianesaz, H., Göczi, L., Nagy, G., Póliska, S., Fadel, L., Bojcsuk, D., Penyige, A., Szirák, K., AlHaman, F., Nagy, L., Vámosi, G., Széles, L.: Genomic regions occupied by both RARα and VDR are involved in the convergence and cooperation of retinoid and vitamin D signaling pathways.
Nucleic Acids Res. 53 (6), 1-20, (article identifier: 230), 2025.

doi DEA WoS Scopus

Journal metrics:

D1 Genetics

2024

Mianesaz, H., Ghalamkari, S., Abbasi, F., Razzaghy-Azar, M., Sayarifard, F., Vakili, R., Sedghi, M., Noroozi Asl, S., Hosseini, S., Amoli, M. M., Yaghootkar, H.: Genetic variant profiling of neonatal diabetes mellitus in Iranian patients: unveiling 58 distinct variants in 14 genes.
J of Diabetes Invest. 15 (10), 1390-1402, 2024.

doi DEA WoS Scopus

Journal metrics:

Q1 Endocrinology, Diabetes and Metabolism

Q1 Internal Medicine

Q1 Medicine (miscellaneous)

Ghalamkari, S., Mianesaz, H., Chitsaz, A., Ghazavi, M., Salehi, M.: Proband-Only Exome Sequencing for Intellectual Disability in Iran: Diagnostic Yield and Genetic Insights.
Am. J. Med. Genet. A. 197 (4), 1-9, (article identifier: 63915), 2024.

doi DEA WoS Scopus

Journal metrics:

Q2 Genetics

Q3 Genetics (clinical)

2023

Mianesaz, H., Ghalamkari, S., Salehi, M., Behnam, M., Hosseinzadeh, M., Basiri, K., Ghasemi, M., Sedghi, M., Ansari, B.: Causative variants linked with limb girdle muscular dystrophy in an Iranian population: 6 novel variants.
Molec Gen & Gen Med. 11 (2), 1-14, (article identifier: 2101), 2023.

doi DEA WoS Scopus

Journal metrics:

Q3 Genetics

Q3 Genetics (clinical)

Q3 Molecular Biology

2022

Göczi, L., Csumita, M., Horváth, A., Nagy, G., Póliska, S., Pigni, M., Thelemann, C., Dániel, B., Mianesaz, H., Varga, T., Sen, K., Raghav, S. K., Schoggins, J. W., Nagy, L., Acha-Orbea, H., Meissner, F., Reith, W., Széles, L.: A Multi-Omics Approach Reveals Features That Permit Robust and Widespread Regulation of IFN-Inducible Antiviral Effectors.
J. Immun. 209 (10), 1930-1941, 2022.

doi DEA WoS Scopus

Journal metrics:

Q1 Immunology

Q1 Immunology and Allergy

Sarmadi, M., Gheibi, A., Khanahmad, H., Khorramizadeh, M. R., Hejazi, S. H., Zahedi, N., Mianesaz, H., Kashfi, K.: Design and Characterization of a Recombinant Brucella abortus RB51 Vaccine That Elicits Enhanced T Cell-Mediated Immune Response.
Vaccines. 10 (3), 1-11, (article identifier: 388), 2022.

doi DEA WoS Scopus

Journal metrics:

D1 Drug Discovery

Q1 Immunology

Q1 Infectious Diseases

D1 Pharmacology

D1 Pharmacology (medical)

Hadi, N., Namazi, F., Ketabchi, F., Khosravian, F., Nateghi, B., Talebi, A., Baghi, M., Mianesaz, H., Zare, F., Salehi, M.: miR-574, miR-499, miR-125b, miR-106a, and miR-9 potentially target TGFBR-1 and TGFBR-2 genes involving in inflammatory response pathway: Potential novel biomarkers for chronic lymphocytic leukemia.
Pathol. Res. Pract. 238, 1-8, (article identifier: 154077), 2022.

doi DEA WoS Scopus

Journal metrics:

Q3 Cell Biology

Q2 Pathology and Forensic Medicine

2021

Ghalamkari, S., Alavi, S., Mianesaz, H., Khosravian, F., Bahreini, A., Salehi, M.: A novel carcinogenic PI3Kα mutation suggesting the role of helical domain in transmitting nSH2 regulatory signals to kinase domain.
Life Sci. 269, 1-7, (article identifier: 118759), 2021.

doi DEA WoS Scopus

Journal metrics:

Q1 Biochemistry, Genetics and Molecular Biology (miscellaneous)

Q1 Medicine (miscellaneous)

D1 Pharmacology, Toxicology and Pharmaceutics (miscellaneous)

2019

10.

Sedghi, M., Moslemi, A. R., Olive, M., Etemadifar, M., Ansari, B., Nasiri, J., Emrahi, L., Mianesaz, H., Laing, N. G., Tajsharghi, H.: Motor neuron diseases caused by a novel variant: A genotype/phenotype study.
Ann Clin Transl Neurol. 6 (11), 2197-2204, 2019.

doi DEA WoS Scopus

Journal metrics:

D1 Neurology (clinical)

Q1 Neuroscience (miscellaneous)

2018

11.

Ghalamkari, S., Khosravian, F., Mianesaz, H., Kazemi, M., Behjati, M., Hakimian, S. M., Salehi, M.: A Comparison Between Full-COLD PCR/HRM and PCR Sequencing for Detection of Mutations in Exon 9 of PIK3CA in Breast Cancer Patients.
Appl. Biochem. Biotechnol. 187 (3), 975-983, 2018.

doi DEA WoS Scopus

Journal metrics:

Q2 Applied Microbiology and Biotechnology

Q3 Biochemistry

Q2 Bioengineering

Q2 Biotechnology

Q2 Environmental Engineering

Q2 Medicine (miscellaneous)

Q3 Molecular Biology