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期刊名:Personalized medicine

缩写:PERS MED

ISSN:1741-0541

e-ISSN:1744-828X

IF/分区:1.2/Q4

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共收录本刊相关文章索引1302条
Clinical Trial Case Reports Meta-Analysis RCT Review Systematic Review
Classical Article Case Reports Clinical Study Clinical Trial Clinical Trial Protocol Comment Comparative Study Editorial Guideline Letter Meta-Analysis Multicenter Study Observational Study Randomized Controlled Trial Review Systematic Review
Poh Kuan Wong,Saiful Effendi Syafruddin,Fook Choe Cheah et al. Poh Kuan Wong et al.
Aim: Rs16851030, a single-nucleotide variant located in the 3'-untranslated region of the ADORA1 gene, has been proposed as a potential marker of caffeine sensitivity in apnea of prematurity. Besides, it is associated with aspirin-induced a...
Hanxing Huang,Lihan Xiao,Min Xiao et al. Hanxing Huang et al.
Aim: This research examined the correlation between miR-559 rs58450758 and the clinical pathological characteristics and prognosis of CRC.Materials & methods: RT-qPCR was utilized to assess the miR-559 expression levels. Chi-square test was...
Shilin Xu,Xuemei Li,Xuguang Li et al. Shilin Xu et al.
Aim: MIR137 host gene (MIR137HG) variants were involved in a variety of diseases, but its role in high-altitude pulmonary edema (HAPE) has not been reported. The study aimed to study the association between MIR137HG single-nucleotide polymo...
Nader Al-Dewik,Tala Abuarja,Salma Younes et al. Nader Al-Dewik et al.
Precision Medicine (PM) is a transformative clinical medicine strategy that aims to revolutionize healthcare by leveraging biological information and biomarkers. In the context of maternal and neonatal health, PM enables personalized care f...
Yasser Bm Ali,Noura Ma Hasan,Eman A El-Maadawy et al. Yasser Bm Ali et al.
Aim: This study aimed to investigate the associations between single nucleotide polymorphisms (SNPs) of IL-6 (-174G/C), microRNA146a (rs2910164C/G) and MALAT1 (rs619586A/G) and susceptibility to rheumatoid arthritis (RA) in Egyptians.Method...
Linh Ba Tieu,Vinh Nhu Nguyen,Phu Gia Tran et al. Linh Ba Tieu et al.
Background: Family health history (FHH) is central to human genomic profiling construction; however, there is no protocol for documenting FHH in a pedigree format in Vietnam.Aim: A "Gia Su Suc Khoe" (GSSK) tool was developed to create a use...
Saeedeh Salimi,Abbas Mohammadpour-Gharehbagh,Mohaddeseh Hedayat et al. Saeedeh Salimi et al.
Aim: The authors designed a meta-analysis to find a comprehensive result of the impact of RNLS polymorphisms on preeclampsia (PE) susceptibility. Methods: The online databases PubMed, Scopus, and Google Scholar were employed for the purpose...
Mohamed Kamal,Mohamed Nagy,Omneya Hassanain Mohamed Kamal
The application of personalized medicine in developing countries is a major challenge, especially for those with poor economic status. A critical factor in improving the application of personalized medicine is the efficient allocation of re...
Francesco Andrea Causio,Flavia Beccia,Loes Lindiwe Kreeftenberg et al. Francesco Andrea Causio et al.
In the transformative landscape of healthcare, personalized medicine emerges as a pivotal shift, harnessing genetic, environmental and lifestyle data to tailor medical treatments for enhanced outcomes and cost efficiency. Central to its suc...
Rewan Gamal Mohamed,Rania Saber,Mohamed Ali Hussein et al. Rewan Gamal Mohamed et al.
Aim: Vancomycin, a crucial treatment for Gram-positive bacteria, necessitates therapeutic drug monitoring (TDM) to prevent treatment failures. We investigated the healthcare professional's compliance toward TDM of vancomycin recommendations...