| Cancer/testis antigens: expression, regulation, tumor invasion, and use in immunotherapy of cancers A Salmaninejad, MR Zamani, M Pourvahedi, Z Golchehre, ... Immunological investigations 45 (7), 619-640, 2016 | 182 | 2016 |
| Molecular characterization of KRAS, BRAF, and EGFR genes in cases with prostatic adenocarcinoma; reporting bioinformatics description and recurrent mutations A Salmaninejad, S Ghadami, MZ Dizaji, Z Golchehre, MA Estiar, ... Clin Lab 61 (7), 749-59, 2015 | 15 | 2015 |
| CRB1-related Leber congenital amaurosis: reporting novel pathogenic variants and a brief review on mutations spectrum M Saberi, Z Golchehre, A Karamzade, M Entezam, Y Eshaghkhani, ... Iranian Biomedical Journal 23 (5), 362, 2019 | 11 | 2019 |
| A novel mutation in SNX10 gene causes malignant infantile osteopetrosis A Amirfiroozy, AA Hamidieh, Z Golchehre, A Rezamand, M Yahyaei, ... Avicenna Journal of Medical Biotechnology 9 (4), 205, 2017 | 11 | 2017 |
| First report of Klein-Waardenburg Syndrome in Iran and a novel pathogenic splice site variant in PAX3 gene M Saberi, Z Golchehre, H Salmani, A Karamzade, SZ Tabatabaie, ... International Journal of Pediatric Otorhinolaryngology 113, 229-233, 2018 | 6 | 2018 |
| Integrative genomic and transcriptomic analysis reveals genetic alterations associated with the early progression of follicular lymphoma F Gao, H Liu, X Meng, J Liu, J Wang, J Yu, X Liu, X Liu, L Li, L Qiu, Z Qian, ... British Journal of Haematology 202 (6), 1151-1164, 2023 | 5 | 2023 |
| Identification of a novel truncating variant in AHI1 gene and a brief review on mutations spectrum A Karamzade, M Babaei, M Saberi, N Golchin, ... Molecular biology reports 48 (6), 5339-5345, 2021 | 5 | 2021 |
| A rare immunological disease, caspase 8 deficiency: case report and literature review N Bazgir, A Tahvildari, Z Chavoshzade, M Jamee, Z Golchehre, A Karimi, ... Allergy, Asthma & Clinical Immunology 19 (1), 29, 2023 | 4 | 2023 |
| New Presentation of CD27 Deficiency; Coronary Ectasia and COVID-19 Z Golchehre, S Sharafian, N Momtazmanesh, Z Chavoshzadeh, A Karimi, ... Iranian Journal of Allergy, Asthma and Immunology 22 (1), 110-118, 2023 | 3 | 2023 |
| A novel mutation in the OXCT1 gene causing Succinyl-CoA: 3-Ketoacid CoA transferase (SCOT) deficiency starting with neurologic manifestations D Amirkashani, M Asadollahi, R Hosseini, S Talebi, Z Golchehre, ... Iranian Journal of Child Neurology 17 (2), 127, 2023 | 2 | 2023 |
| Cernunnos defect in an Iranian patient with T− B+ NK+ severe combined immunodeficiency: A case report and review of the literature M Jamee, N Khakbazan Fard, S Fallah, Z Golchehre, M Fallahi, ... Molecular Genetics & Genomic Medicine 10 (8), e1990, 2022 | 2 | 2022 |
| Next-generation sequencing identified novel truncating mutations in BBS9 causing Bardet Biedl syndrome in two Iranian consanguineous families S Akbaroghli, D Kooshavar, Z Golchehre, A Karamzade, M Saberi, ... Iranian Journal of Child Neurology 16 (1), 123, 2022 | 2 | 2022 |
| Whole-exome sequencing identified a novel variant (C. 405_422+ 39del) in DSP gene in an iranian pedigree with familial dilated cardiomyopathy Y Eshaghkhani, A Mohamadifar, M Asadollahi, M Taghizadeh, ... Reports of biochemistry & molecular biology 10 (2), 280, 2021 | 2 | 2021 |
| Intestinal hypomagnesemia in an Iranian patient with a novel TRPM6 variant: a case report and review of the literature F Kamali, M Jamee, JA Sayer, S Sadeghi-Bojd, Z Golchehre, ... CEN Case Reports 12 (4), 413-418, 2023 | | 2023 |
| A novel missense variant in EIF2B5 identified in a consanguineous Iranian family with vanishing white matter disease and a brief review of the literature P Nourmohammadi, M Asadollahi, A Karamzade, Y Eshaghkhani, ... Journal of Genetics 102 (2), 39, 2023 | | 2023 |
| Identification of multi-exon deletion in the COL7A1 gene underlying dystrophic epidermolysis bullosa by whole-exome sequencing M Taghizadeh, SM Derakhshan, MS Khaniani, Y Eshaghkhani, ... Our Dermatology Online/Nasza Dermatologia Online 12 (4), 2021 | | 2021 |
| Higher diagnostic yield can be achieved by using multigene NGS panel in testing patients with Marfan-related disorders A Karamzade, Z Golchehre, M Keramatipour, M Saberi, A Nasrollahzadeh, ... EUROPEAN JOURNAL OF HUMAN GENETICS 27, 117-118, 2019 | | 2019 |
| Experience learned from BRCA1 and BRCA2 screening in Iranian women M Keramatipour, Z Golchehre, A Nasrollahzadeh, M Arabpour, ... EUROPEAN JOURNAL OF HUMAN GENETICS 27, 403-403, 2019 | | 2019 |
| An introduction to expression and regulation of cancer/testis antigens (CTAs) A Salmaninejad, Z Golchehre, MB Eskandari, E Taghizadeh, A Shakoori Tehran University of Medical Sciences Journal 76 (1), 1-11, 2018 | | 2018 |
| An introduction to expression and regulation of testicular cancer antigens A Salmaninejad, Z Golchehre, MB Eskandari, E Taghizadeh, A Shakoori Tehran University Medical Journal 76 (1), 1-11, 2018 | | 2018 |
