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.
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.
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.
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.
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.
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.
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.
