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

Genetic association between SORBS1 rs2274490 and INSR rs12971499 polymorphisms with polycystic ovary syndrome: A case-control study

SORBS1 rs2274490 和 INSR rs12971499 多态性与多囊卵巢综合征的遗传关联：一项病例对照研究

期刊:Journal of Education and Health Promotion
影响因子:1.3
doi:10.4103/jehp.jehp_1612_24
Ebrahimi, Amir Hossein; Shakib, Pegah; Yavari, Fereshteh; Sharafi, Zeinab; Morovvati, Abbas; Zarei, Mohammad Reza; Dirbaziyan, Ashkan; Movahhed, Tahereh Komeili
多囊卵巢综合征
INSR
免疫/内分泌
发表日期：2026
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The clinical and genetic spectrum of twenty-six individuals with hearing loss affected by MYO15A variants

26名受MYO15A变异影响的听力损失患者的临床和遗传谱

期刊:Scientific Reports
影响因子:3.9
doi:10.1038/s41598-025-99417-7
Morovvati, Saeid; Sarband, Mina Mohammadi; Doostmohammadi, Samaneh; Rayat, Sima; Emamdjomeh, Hessamaldin; Farhadi, Mohammad; Asghari, Alimohamad; Garshasbi, Masoud; Falah, Masoumeh
发表日期：2025
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Combination chemotherapy via poloxamer 188 surface-modified PLGA nanoparticles that traverse the blood-brain-barrier in a glioblastoma model

通过泊洛沙姆 188 表面改性 PLGA 纳米粒子在胶质母细胞瘤模型中穿过血脑屏障进行联合化疗

期刊:Scientific Reports
影响因子:3.8
doi:10.1038/s41598-024-69888-1
Fatemeh Madani, Hassan Morovvati, Thomas J Webster, Sareh Najaf Asaadi, Seyed Mahdi Rezayat, Mahmoudreza Hadjighassem, Masood Khosravani, Mahdi Adabi
神经
血脑屏障
其它细胞
发表日期：2024
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Providing predictive models for quality parameters of groundwater resources in arid areas of central Iran: A case study of kashan plain

构建伊朗中部干旱地区地下水资源质量参数预测模型：以卡尚平原为例

期刊:Heliyon
影响因子:3.6
doi:10.1016/j.heliyon.2024.e31493
Zarajabad, Aysan Morovvati; Hadi, Mahdi; Nodehi, Ramin Nabizadeh; Moradi, Mahsa; Ghalhari, Mohammad Rezvani; Zeraatkar, Abbas; Mahvi, Amir Hossein
发表日期：2024
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Association study between polymorphisms in MIA3, SELE, SMAD3 and CETP genes and coronary artery disease in an Iranian population

伊朗人群中MIA3、SELE、SMAD3和CETP基因多态性与冠状动脉疾病的关联研究

期刊:BMC Cardiovascular Disorders
影响因子:2.3
doi:10.1186/s12872-022-02695-6
Rayat, Sima; Ramezanidoraki, Nasim; Kazemi, Nima; Modarressi, Mohammad H; Falah, Masoumeh; Zardadi, Safoura; Morovvati, Saeid
MIA
SELE
SMAD3
发表日期：2022
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Analysis of TMIE gene mutations including the first large deletion of exon 1 with autosomal recessive non-syndromic deafness

TMIE基因突变分析，包括首例伴有常染色体隐性非综合征性耳聋的1号外显子大片段缺失

期刊:BMC Medical Genomics
影响因子:2
doi:10.1186/s12920-022-01287-9
Rayat, Sima; Farhadi, Mohammad; Emamdjomeh, Hessamaldin; Morovvati, Saeid; Falah, Masoumeh
发表日期：2022
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CAD gene and early infantile epileptic encephalopathy-50; three Iranian deceased patients and a novel mutation: case report

CAD基因与早期婴儿癫痫性脑病-50；三例伊朗死亡患者及一种新的突变：病例报告

期刊:BMC Pediatrics
影响因子:2
doi:10.1186/s12887-022-03195-4
Yarahmadi, Sepideh Gholami; Morovvati, Saeid
癫痫
神经科学
发表日期：2022
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Cystinosis and two rare mutations in CTNS gene: two case reports

胱氨酸病和CTNS基因的两种罕见突变：两例病例报告

期刊:Journal of Medical Case Reports
影响因子:0.8
doi:10.1186/s13256-022-03379-7
Gholami Yarahmadi, Sepideh; Sarlaki, Fatemeh; Morovvati, Saeid
发表日期：2022
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Novel mutation in TENM3 gene in an Iranian patient with colobomatous microphthalmia

伊朗一名患有缺损性小眼畸形的患者TENM3基因出现新突变

期刊:Clinical Case Reports
影响因子:0.6
doi:10.1002/ccr3.5532
Gholami Yarahmadi, Sepideh; Sarlaki, Fatemeh; Morovvati, Saeid
发表日期：2022
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Detection of Canine Parvovirus Type 2 by Designing Multiple Methods and Genetic Characterization in Iran

伊朗犬细小病毒2型检测：多种方法设计与基因特征分析

期刊:Archives of Razi Institute
影响因子:
doi:10.22092/ARI.2022.358646.2273
Morovvati, A; Keyvanfar, H; Zahraei Salehi, T; Mousavi Nasab, S D; Zargar, M
Canine
发表日期：2022
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