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期刊名:Personalized medicine

缩写:PERS MED

ISSN:1741-0541

e-ISSN:1744-828X

IF/分区:1.8/Q3

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共收录本刊相关文章索引1276
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
Youssef Roman Youssef Roman
Precision medicine promises improved health outcomes by tailoring treatments to individual genetic and environmental factors. However, achieving this potential is hindered by persistent health disparities and the underrepresentation of raci...
Cole Ettingoff,Megan Von Isenburg,Drew Birrenkott et al. Cole Ettingoff et al.
Background: -Omics technologies - including genomics, transcriptomics, proteomics, and metabolomics - are increasingly used in acute care settings. However, the current extent of this research has not been systematically ...
Lu Tan,Ailing Chao,Heng Liang et al. Lu Tan et al.
Aim: Vancomycin dosing in neonates is challenging due to developmental pharmacokinetic variability. The study was to characterize vancomycin pharmacokinetics in a large cohort of preterm and term neonates and develop indi...
Ankit Dahiya,Kartikey Singh,Anunav Ashish et al. Ankit Dahiya et al.
Introduction: Advanced Therapy Medicinal Products (ATMPs), which include gene therapies, somatic cell therapies, and tissue-engineered products, are a new paradigm for treating previously intractable diseases. Their regen...
Gülcan Demir,Zeynep Yegin Gülcan Demir
This review comprehensively evaluates personalized public health strategies using artificial intelligence (AI) in disease prediction/management and genetic data analysis. In the field of healthcare, AI has achieved significant advancements ...
Francesco Pepe,Tancredi Didier Bazan Russo,Valerio Gristina et al. Francesco Pepe et al.
Lung cancer (LC) remains the leading cause of cancer-related mortality worldwide, with most cases diagnosed at advanced stages, resulting in poor survival rates. Early detection significantly improves outcomes, yet current screening methods...
Özkan Bağcı,Batuhan Şanlıtürk,Ebru Marzioğlu Özdemir et al. Özkan Bağcı et al.
Aim: In this study, we aimed to reveal the sequence analysis of 69 pharmacogenes in 635 patients and the clinical explanation of variants. Materials and m...
Haoyang Yan,Christine M Rini,Ann Katherine M Foreman et al. Haoyang Yan et al.
Purpose: To investigate patient reactions to and understanding of secondary genomic findings with limited to no medical actionability (LMA-SFs) from diagnostic genome sequencing. ...
Tiantian Wei,Jing Shen,Lijun He et al. Tiantian Wei et al.
Objectives: The genetic variant rs13137 of miR-21 is associated with susceptibility in many diseases. However, the association with cognitive dysfunction (CD) in Chinese patients with systemic lupus erythematosus (SLE) re...
Alice Kim,Amy Nisselle,Louise Keogh et al. Alice Kim et al.
Innovations, such as genomics, are expected to transform the practice of the healthcare workforce. Workplace learning is an established and fundamental component of healthcare workforce training. We propose that it can be leveraged to facil...