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

Uncovering the Hidden Connections Between PCOS and Alzheimer's Disease: A Two-Sample Mendelian Randomization Perspective

揭示多囊卵巢综合征与阿尔茨海默病之间的隐秘联系：基于双样本孟德尔随机化的视角

期刊:International Journal of Endocrinology and Metabolism
影响因子:1.8
doi:10.5812/ijem-159124
Motafeghi, Farzaneh Sadat; Akbarzadeh, Mahdi; Talebi, Samaneh; Habibi, Danial; Tehrani Fateh, Sahand; Alavi Majd, Hamid; Hedayati, Mehdi; Azizi, Fereidoun; Sadat Daneshpour, Maryam; Ramezani Tehrani, Fahimeh
阿尔茨海默症
多囊卵巢综合征
免疫/内分泌
发表日期：2025
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Clinical Features and Genetic Characteristics of XLID Patients With KDM5C Gene Mutations: Insights on Phenotype-Genotype Correlations From 175 Previous Cases and Identification of a Novel Variant

KDM5C基因突变型X连锁智力障碍患者的临床特征和遗传特征：基于175例既往病例的表型-基因型相关性研究及新变异的鉴定

期刊:Molecular Genetics & Genomic Medicine
影响因子:1.6
doi:10.1002/mgg3.70057
Ghasemi, Mohammad-Reza; Esmaeilizadeh, Zahra; Tehrani Fateh, Sahand; Sadeghi, Hossein; Bagheri, Saman; Hashemi-Gorji, Farzad; Sheikhi Nooshabadi, Morteza; Madannezhad, Rasoul; Tavabe Ghavami, Toktam Sadat; Mirfakhraie, Reza; Miryounesi, Mohammad
发表日期：2025
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Non-coding RNAs as potential therapeutic targets for receptor tyrosine kinase signaling in solid tumors: current status and future directions

非编码RNA作为实体瘤受体酪氨酸激酶信号通路潜在治疗靶点：现状与展望

期刊:Cancer Cell International
影响因子:6
doi:10.1186/s12935-023-03203-2
Moeinafshar, Aysan; Nouri, Mohammad; Shokrollahi, Nima; Masrour, Mahdi; Behnam, Amirmohammad; Tehrani Fateh, Sahand; Sadeghi, Hossein; Miryounesi, Mohammad; Ghasemi, Mohammad-Reza
信号转导
发表日期：2024
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Insights into additional lactone-based signaling circuits in Streptomyces: existence of acyl-homoserine lactones and LuxI/LuxR homologs in six Streptomyces species

深入了解链霉菌中其他基于内酯的信号传导回路：六种链霉菌中存在酰基高丝氨酸内酯和 LuxI/LuxR 同源物

期刊:Frontiers in Microbiology
影响因子:4
doi:10.3389/fmicb.2024.1342637
Amir Salehi-Najafabadi, Sepand Tehrani Fateh, Ghasem Amoabediny, Javad Hamedi
信号转导
发表日期：2024
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Examining the clinical and genetic spectrum of maturity-onset diabetes of the young (MODY) in Iran

对伊朗青年起病型糖尿病（MODY）的临床和遗传谱进行研究

期刊:Scientific Reports
影响因子:3.9
doi:10.1038/s41598-024-70864-y
Asgarian, Sara; Lanjanian, Hossein; Rahimipour Anaraki, Shiva; Hadaegh, Farzad; Moazzam-Jazi, Maryam; Najd-Hassan-Bonab, Leila; Masjoudi, Sajedeh; Zahedi, Asiyeh Sadat; Zarkesh, Maryam; Shalbafan, Bita; Akbarzadeh, Mahdi; Tehrani Fateh, Sahand; Khalili, Davood; Momenan, Amirabbas; Sarbazi, Narges; Hedayati, Mehdi; Azizi, Fereidoun; Daneshpour, Maryam S
糖尿病
代谢
发表日期：2024
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Identification of novel mutations in TPK1 and SLC19A3 genes in families exhibiting thiamine metabolism dysfunction syndrome

在表现出硫胺素代谢功能障碍综合征的家族中鉴定出TPK1和SLC19A3基因的新突变

期刊:Heliyon
影响因子:3.6
doi:10.1016/j.heliyon.2024.e27434
Norouzi Rostami, Fatemeh; Sadeghi, Hossein; Hashemi-Gorji, Farzad; Tehrani Fateh, Sahand; Mirfakhraie, Reza; Karimzadeh, Parvaneh; Davarpanah, Milad; Jamshidi, Sanaz; Madannejad, Rasoul; Moghimi, Parinaz; Ekrami, Mahdis; Miryounesi, Mohammad; Ghasemi, Mohammad-Reza
代谢
发表日期：2024
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Novel TECPR2 variant in two cases of hereditary sensory and autonomic neuropathy type 9: insights from genetic characterization and comprehensive literature review

两例遗传性感觉和自主神经病9型病例中发现新型TECPR2变异：来自基因特征分析和文献综述的启示

期刊:BMC Neurology
影响因子:2.2
doi:10.1186/s12883-024-03963-y
Moeinafshar, Aysan; Tehrani Fateh, Sahand; Hashemi-Gorji, Farzad; Karimzadeh, Parvaneh; Gholibeglou, Elham; Rostami, Masoumeh; Sadeghi, Hossein; Miryounesi, Mohammad; Ghasemi, Mohammad-Reza
TEC
发表日期：2024
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Comprehensive review and expanding the genetic landscape of Cornelia-de-Lange spectrum: insights from novel mutations and skin biopsy in exome-negative cases

对科内莉亚-德-兰格综合征谱系进行全面回顾并拓展其遗传图谱：来自外显子组阴性病例的新突变和皮肤活检的启示

期刊:BMC Medical Genomics
影响因子:2
doi:10.1186/s12920-024-01798-7
Tehrani Fateh, Sahand; Mohammad Zadeh, Nadia; Salehpour, Shadab; Hashemi-Gorji, Farzad; Omidi, Ashkan; Sadeghi, Hossein; Mirfakhraie, Reza; Moghimi, Parinaz; Keyvanfar, Sepideh; Mohammadi Sarvaleh, Sepideh; Miryounesi, Mohammad; Ghasemi, Mohammad-Reza
发表日期：2024
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Broadening the phenotype and genotype spectrum of novel mutations in pontocerebellar hypoplasia with a comprehensive molecular literature review

通过全面的分子文献综述，拓宽脑桥小脑发育不全新突变的表型和基因型谱。

期刊:BMC Medical Genomics
影响因子:2
doi:10.1186/s12920-024-01810-0
Ghasemi, Mohammad-Reza; Tehrani Fateh, Sahand; Moeinafshar, Aysan; Sadeghi, Hossein; Karimzadeh, Parvaneh; Mirfakhraie, Reza; Rezaei, Mitra; Hashemi-Gorji, Farzad; Rezvani Kashani, Morteza; Fazeli Bavandpour, Fatemehsadat; Bagheri, Saman; Moghimi, Parinaz; Rostami, Masoumeh; Madannejad, Rasoul; Roudgari, Hassan; Miryounesi, Mohammad
发育与干细胞
神经科学
发表日期：2024
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Expanding genetic and clinical aspects of Schwartz-Jampel syndrome: A report of two cases with literature review

施瓦茨-詹佩尔综合征的遗传和临床研究进展：两例病例报告及文献综述

期刊:Molecular Genetics and Metabolism Reports
影响因子:1.9
doi:10.1016/j.ymgmr.2024.101125
Elahi Vahed, Iman; Tehrani Fateh, Sahand; Kamali, Melika; Hashemi-Gorji, Farzad; Esmaeilzadeh, Zahra; Sadeghi, Hossein; Miryounesi, Mohammad; Ghasemi, Mohammad-Reza
发表日期：2024
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