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

Structural remodeling of the mitochondrial protein biogenesis machinery under proteostatic stress

蛋白质稳态应激下线粒体蛋白质生物合成机制的结构重塑

期刊:Science Advances
影响因子:12.5
doi:10.1126/sciadv.aed3579
Ehses, Kenneth; López-Alonso, Jorge P; Antico, Odetta; Lang, Yannik; Rudack, Till; Azem, Abdussalam; Muqit, Miratul M K; Ubarretxena-Belandia, Iban; Fernández-Busnadiego, Rubén
蛋白质稳态
线粒体
发表日期：2026
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Intracellular vesicle-mediated biomineralization of arsenic and barium by a sponge symbiotic bacterium

海绵共生细菌通过细胞内囊泡介导的砷和钡的生物矿化作用

期刊:ISME Communications
影响因子:6.1
doi:10.1093/ismeco/ycag039
Shoham, Shani; Weiss, Celeste; Keren, Ray; Lavy, Adi; Polishchuk, Iryna; Pokroy, Boaz; Azem, Abdussalam; Ilan, Micha
微生物学
囊泡
细胞生物学
发表日期：2026
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Structural basis for ATP-driven double-ring assembly of the human mitochondrial Hsp60 chaperonin

人线粒体Hsp60分子伴侣ATP驱动双环组装的结构基础

期刊:
影响因子:
doi:10.1101/2025.10.04.680452
Tascón, Igor; López-Alonso, Jorge P; Shkolnisky, Yoel; Gil-Cartón, David; Vilchez-Garcia, Jesús; Berruezo, Alberto G; Gómez-Llorente, Yacob; Malik, Radhika; Jebara, Fady; Patra, Malay; Hirsch, Joel A; Azem, Abdussalam; Ubarretxena-Belandia, Iban
线粒体
发表日期：2025
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Hotspots for Disease-Causing Mutations in the Mitochondrial TIM23 Import Complex

线粒体TIM23导入复合物致病突变的热点区域

期刊:Genes
影响因子:2.8
doi:10.3390/genes15121534
Jain, Sahil; Paz, Eyal; Azem, Abdussalam
TIM23
线粒体
TIM
发表日期：2024
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SCAPER-Related Autosomal Recessive Retinitis Pigmentosa with Intellectual Disability: Confirming and Extending the Phenotypic Spectrum and Bioinformatics Analyses

SCAPER相关常染色体隐性遗传性视网膜色素变性伴智力障碍：表型谱的确认与扩展及生物信息学分析

期刊:Genes
影响因子:2.8
doi:10.3390/genes15060791
Sharkia, Rajech; Zalan, Abdelnaser; Kessel, Amit; Al-Shareef, Wasif; Zahalka, Hazar; Hengel, Holger; Schöls, Ludger; Azem, Abdussalam; Mahajnah, Muhammad
SCAP
发表日期：2024
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Editorial: A focus on chaperone clients

社论：重点关注陪护客户

期刊:Frontiers in Molecular Biosciences
影响因子:4
doi:10.3389/fmolb.2023.1180739
Horovitz, Amnon; Azem, Abdussalam
发表日期：2023
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PTRH2 Gene Variants: Recent Review of the Phenotypic Features and Their Bioinformatics Analysis

PTRH2基因变异：表型特征及其生物信息学分析的最新综述

期刊:Genes
影响因子:2.8
doi:10.3390/genes14051031
Sharkia, Rajech; Jain, Sahil; Mahajnah, Muhammad; Habib, Clair; Azem, Abdussalam; Al-Shareef, Wasif; Zalan, Abdelnaser
发表日期：2023
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Correction to: First-line exome sequencing in Palestinian and Israeli Arabs with neurological disorders is efficient and facilitates disease gene discovery

更正：对患有神经系统疾病的巴勒斯坦和以色列阿拉伯人进行一线外显子组测序是有效的，并有助于发现致病基因。

期刊:European Journal of Human Genetics
影响因子:4.6
doi:10.1038/s41431-021-00909-7
Hengel, Holger; Buchert, Rebecca; Sturm, Marc; Haack, Tobias B; Schelling, Yvonne; Mahajnah, Muhammad; Sharkia, Rajech; Azem, Abdussalam; Balousha, Ghassan; Ghanem, Zaid; Falana, Mohammed; Balousha, Osama; Ayesh, Suhail; Keimer, Reinhard; Deigendesch, Werner; Zaidan, Jimmy; Marzouqa, Hiyam; Bauer, Peter; Schöls, Ludger
发表日期：2022
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First-line exome sequencing in Palestinian and Israeli Arabs with neurological disorders is efficient and facilitates disease gene discovery

对患有神经系统疾病的巴勒斯坦和以色列阿拉伯人进行一线外显子组测序是高效且有助于发现致病基因的。

期刊:European Journal of Human Genetics
影响因子:4.6
doi:10.1038/s41431-020-0609-9
Hengel, Holger; Buchert, Rebecca; Sturm, Marc; Haack, Tobias B; Schelling, Yvonne; Mahajnah, Muhammad; Sharkia, Rajech; Azem, Abdussalam; Balousha, Ghassan; Ghanem, Zaid; Falana, Mohammed; Balousha, Osama; Ayesh, Suhail; Keimer, Reinhard; Deigendesch, Werner; Zaidan, Jimmy; Marzouqa, Hiyam; Bauer, Peter; Schöls, Ludger
发表日期：2020
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Unraveling the genetic cause of hereditary ophthalmic disorders in Arab societies from Israel and the Palestinian Authority

从以色列和巴勒斯坦权力机构的角度揭示阿拉伯社会遗传性眼病的基因病因

期刊:European Journal of Human Genetics
影响因子:4.6
doi:10.1038/s41431-019-0566-3
Mayer, Anja K; Balousha, Ghassan; Sharkia, Rajech; Mahajnah, Muhammad; Ayesh, Suhail; Schulze, Martin; Buchert, Rebecca; Zobor, Ditta; Azem, Abdussalam; Schöls, Ludger; Bauer, Peter; Wissinger, Bernd
发表日期：2020
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