日期 影响因子
日期:
2020 年 — 2026 年
2020
2021
2022
2023
2024
2025
2026
影响因子:
–

Correction: Clinical characterizations and molecular genetic study of two co-segregating variants in PDZD7 and PDE6C genes leading simultaneously to non-syndromic hearing loss and achromatopsia

更正：PDZD7 和 PDE6C 基因中两个共分离变异的临床特征和分子遗传学研究，这两个变异同时导致非综合征性听力损失和全色盲。

期刊:BMC Medical Genomics
影响因子:2
doi:10.1186/s12920-025-02197-2
Nouri, Zahra; Sarmadi, Akram; Narrei, Sina; Kianersi, Hamidreza; Kianersi, Farzan; Tabatabaiefar, Mohammad Amin
发表日期：2025
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Mono-allelic MUTYH mutation as the likely inherited etiology of hereditary breast cancer in a patient from a multi-cancer family- report of a family and literature review

单等位基因MUTYH突变可能是多癌家族患者遗传性乳腺癌的致病因素——家族病例报告及文献综述

期刊:BMC Medical Genomics
影响因子:2
doi:10.1186/s12920-025-02213-5
Sarmadi, Akram; Javanmard, Shaghayegh Haghjooy; Zeinalian, Mehrdad; Hosseinzadeh, Majid; Tabatabaiefar, Mohammad Amin
MUTYH
肿瘤
肿瘤免疫
乳腺癌
发表日期：2025
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Prevalence of Novel and Recurrent Pathogenic Variants in BRCA Genes in a Cohort of Iranian Hereditary Breast Cancer Patients

伊朗遗传性乳腺癌患者队列中BRCA基因新型和复发性致病变异的患病率

期刊:Advanced Biomedical Research
影响因子:1
doi:10.4103/abr.abr_681_24
Sarmadi, Akram; Haghjooy Javanmard, Shaghayegh; Zeinalian, Mehrdad; Hosseinzadeh, Majid; Tabatabaiefar, Mohammad Amin
肿瘤
肿瘤免疫
乳腺癌
发表日期：2025
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Evaluation of Apoptotic Effect of Transgenic Leishmania tropica Expressing MLLO-Bax-Smac Fusion Gene in Infected Macrophages, an In Vitro Study

体外研究：表达MLLO-Bax-Smac融合基因的转基因热带利什曼原虫对感染巨噬细胞凋亡效应的评价

期刊:Iranian Journal of Parasitology
影响因子:0.9
doi:10.18502/ijpa.v20i3.19611
Aghaei, Maryam; Khanahmad, Hossein; Aghaei, Shahrzad; Jalali, Akram; Shahmoradi, Zabihollah; Hashemi, Nooshin; Sarmadi, Akram; Aboutalebian, Shima; Mohammadi, Mohammad Ali; Hosseini, Sayed Mohsen; Hejazi, Seyed Hossein
巨噬细胞
凋亡
表观遗传
炎症/感染
巨噬细胞
细胞生物学
免疫/内分泌
发表日期：2025
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Clinical characterizations and molecular genetic study of two co-segregating variants in PDZD7 and PDE6C genes leading simultaneously to non-syndromic hearing loss and achromatopsia

对PDZD7和PDE6C基因中两个共分离变异的临床特征和分子遗传学研究，这两个变异同时导致非综合征性听力损失和全色盲。

期刊:BMC Medical Genomics
影响因子:2
doi:10.1186/s12920-024-01942-3
Nouri, Zahra; Sarmadi, Akram; Narrei, Sina; Kianersi, Hamidreza; Kianersi, Farzan; Tabatabaiefar, Mohammad Amin
发表日期：2024
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Knockdown of SOX12 Expression Induced Apoptotic Factors is Associated with TWIST1 and CTNNB1 Expression in Human Acute Myeloid Leukemia Cells

敲低SOX12表达诱导的凋亡因子与人急性髓系白血病细胞中TWIST1和CTNNB1的表达相关

期刊:International Journal of Molecular and Cellular Medicine
影响因子:0.8
doi:10.22088/IJMCM.BUMS.10.4.249
Dabiri, Arezou; Sharifi, Mohammadreza; Sarmadi, Akram
凋亡
SOX
表观遗传
IST1
白血病
Human
细胞生物学
发表日期：2021
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Molecular Genetic Study in a Cohort of Iranian Families Suspected to Maturity-Onset Diabetes of the Young, Reveals a Recurrent Mutation and a High-Risk Variant in the CEL Gene.

一项针对疑似患有青年起病型糖尿病的伊朗家庭队列的分子遗传学研究揭示了 CEL 基因中的复发性突变和高风险变异

期刊:Advanced Biomedical Research
影响因子:1
doi:10.4103/abr.abr_18_20
Sarmadi Akram, Mohammadi Aliasgar, Tabatabaei Fatemeh, Nouri Zahra, Chaleshtori Morteza Hashemzadeh, Tabatabaiefar Mohammad Amin
其它
发表日期：2020
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A novel pathogenic variant in the LRTOMT gene causes autosomal recessive non-syndromic hearing loss in an Iranian family

伊朗一个家族中发现LRTOMT基因的一种新型致病变异，导致常染色体隐性遗传性非综合征性听力损失。

期刊:BMC Medical Genetics
影响因子:
doi:10.1186/s12881-020-01061-7
Sarmadi, Akram; Nasrniya, Samane; Soleimani Farsani, Maryam; Narrei, Sina; Nouri, Zahra; Sepehrnejad, Mahsa; Nilforoush, Mohammad Hussein; Abtahi, Hamidreza; Tabatabaiefar, Mohammad Amin
发表日期：2020
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Alteration in CD8(+) T cell subsets in enterovirus-infected patients: An alarming factor for type 1 diabetes mellitus

肠道病毒感染患者CD8(+) T细胞亚群的改变：1型糖尿病的一个警示因素

期刊:Kaohsiung Journal of Medical Sciences
影响因子:3.1
doi:10.1016/j.kjms.2017.12.010
Zargari Samani, Omid; Mahmoodnia, Lila; Izad, Maryam; Shirzad, Hedayatollah; Jamshidian, Azam; Ghatrehsamani, Mahdi; Kheiri, Soleiman; Sadeghian, Ladan; Soltani, Amin; Sarmadi, Akram
T细胞
炎症/感染
CD8
代谢
微生物学
T细胞
糖尿病
细胞生物学
免疫/内分泌
发表日期：2018
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