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Personalized Medicine

IF1.8
论文数32
被引数1
期刊论文 32
发表时间
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Strengthening the evidence base for precision medicine through the utilization of real-world data and real-world evidence: a narrative review from the US perspective通过利用真实世界数据和真实世界证据加强精准医学的证据基础：基于美国视角的叙事性综述
deletePersonalized Medicine
IF1.8
delete2026-05-01
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PREAI
deleteNagel, Emily; Roman, Youssef M.
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The norepinephrine dosing dilemma in septic shock: a narrative review脓毒性休克中去甲肾上腺素剂量使用的困境：一篇叙事性综述
deletePersonalized Medicine
IF1.8
delete2026-05-01
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PREAI
deleteAkbari, Negin; Shaban, Fatemeh; Malekzadeh, Jawad; Moghaddam, Ahmad Bagheri
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Genome diagnostics: a pillar of twenty-first century healthcare and precision medicine基因组诊断：21世纪医疗保健和精准医学的基石
deletePersonalized Medicine
IF1.8
delete2026-04-01
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PREAI
deleteDammalli, Manjunath; Bhavya, S. G.; Maruthi, K. R.; Rangaswamy, B. E.; Yaraguppi, Deepak A.
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The role of real-world data and real-world evidence in advancing regulatory science and targeted therapeutics: a narrative review from the United States perspective真实世界数据与真实世界证据在推进监管科学和靶向治疗中的作用：基于美国视角的叙事性综述
deletePersonalized Medicine
IF1.8
delete2026-04-01
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PREAI
deleteNagel, Emily; Roman, Youssef M.
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Association between polymorphisms in microRNA biosynthesis genes and acute lymphoblastic leukemia susceptibility in Chinese children and adolescents微RNA生物合成基因多态性与中国儿童和青少年急性淋巴细胞白血病易感性的关联
deletePersonalized Medicine
IF1.8
delete2026-04-01
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PREAI
deleteCao, Xiaoqing; Wang, Lingyun; Kang, Yurou; Tai, Ping; Chen, Nayun; Liu, Yang; Yang, Yanli; Fang, Daihua; He, Bangshun
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Association of a common SOD gene variant with ARHL risk: analysis by age, hearing threshold, and enzyme activity常见SOD基因变异与ARHL风险的关联：基于年龄、听阈和酶活性的分析
deletePersonalized Medicine
IF1.8
delete2026-03-04
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PREAI
deleteMorabbi, Ali; Balali, Hasti; Karimian, Ali
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An integrated triple approach - TPMT phenotype, NUDT-15 genotype, and therapeutic drug monitoring of thiopurine metabolites for optimal clinical efficacy: a case series整合三重方法——TPMT表型、NUDT-15基因型及硫嘌呤代谢物治疗药物监测以实现最佳临床疗效：病例系列
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IF1.8
delete2026-03-04
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PREAI
deleteJoseph, Silvia; Prabha, Ratna; Mathew Thomas, David; Joseph, A. J.
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Assessment of exonic polymorphism of IDH2, KRAS1, TP53, and BRAF2 using PCR-RFLP in hepatocellular carcinoma: a case-control study from Arunachal Pradesh and Sikkim
deletePersonalized Medicine
IF1.8
delete2026-03-04
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PREAI
deleteChauhan, Chetan; Kumar, Vishal; Narain, Kanwar; Phukan, Sanjib K.; Kakoty, Santanu; Tawsik, Sopai; Bhutia, Chewang D.; Devi, Kangjam Rekha
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From genomes to metabolomes: adaptive science in personalized medicine从基因组到代谢组：个性化医学中的适应性科学
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IF1.8
delete2026-03-04
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PREAI
deleteRichard, Melina
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Integrating host genetics in Helicobacter pylori infection: clinical insights for personalized eradication strategies整合幽门螺杆菌感染中的宿主遗传学：个性化根除策略的临床见解
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delete2026-03-04
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PREAI
deleteKhazali, Nazanin; Ghadersoltani, Paria; Saniee, Parastoo
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Prevalence and correlates of pharmacotherapy metabolized by CYP2C19, CYP2C9, CYP2D6, and UGT1A1 in the population sampleCYP2C19、CYP2C9、CYP2D6和UGT1A1代谢的药物疗法在人群样本中的患病率及其相关因素
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IF1.8
delete2026-03-04
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deleteAnfinogenova, Nina D.; Stepanov, Vadim A.; Kuznetsova, Alina D.; Chesalov, Nazary P.; Popov, Sergey V.; Repin, Alexey N.
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Study on miRNA-146a-5p rs2910164 polymorphism in attention deficit and hyperactive disorder occurrence and development注意缺陷多动障碍发生发展中miRNA-146a-5p rs2910164多态性的研究
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delete2026-03-01
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deleteZhuang, Wenmin; Ding, Xuemin; Luo, Haixia; Deng, Ludan
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Association of XRCC4 and XRCC5 gene polymorphisms with polycystic ovarian syndrome in an Indian cohortXRCC4和XRCC5基因多态性与印度队列中多囊卵巢综合征的关联
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IF1.8
delete2026-02-01
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deleteSridhar, Nikitha; Venkatakrishnan, Gayathri; Benjamin, Jiby Jolly; Ramaswamy, Padmavathi; Baijumon Bindhu, Sabari Krishnan; Antony, Sharon Benita; Tholath, Rahul Rajan Mathews; Koshy, Teena
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A review on prognostic biomarker and phytocompound-mediated modulation of signaling pathways in colorectal cancer结直肠癌中预后生物标志物及植物化合物介导的信号通路调控综述
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deleteKrishnakumar, Bhavyaa; Christopher Paul, Benedict; Evan Prince, Sabina; Lavinya B, Udhaya
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Machine learning-enabled early risk stratification of β-Iactam-induced electrolyte imbalances机器学习赋能的β-内酰胺诱导电解质失衡早期风险分层
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IF1.8
delete2026-02-01
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PREAI
deleteRyu, Inho; Lee, Da Hoon; Cho, Hyeonwoo; Yum, Yunpil; Yu, Jiwon; Cho, Yewon; Choi, Sooryeol; Nam, Ki Nam; Jeon, Yong Duk; Kim, Woorim
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OMICs data from Tunisian population: challenges and opportunities in the era of precision medicine突尼斯人群的组学数据：精准医学时代的挑战与机遇
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IF1.8
delete2026-02-01
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deleteHkimi, Chaima; Yaiche, Hamza; Kamoun, Selim; Ben Aissa-Haj, Jihenne; Boujemaa, Maroua; Abdelhak, Sonia; Ghedira, Kais; Hamdi, Yosr
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The association between DNA repair genes polymorphisms and cisplatin-induced ototoxicity in cancer patients: a systematic review癌症患者中DNA修复基因多态性与顺铂诱导耳毒性的关联：一项系统评价
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delete2026-01-01
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deleteOmar, Nabil E.; Mekkawi, Rana; Said, Salma; Abd Elrahman, Omar; Hawasly, Fatima; Hamad, Anas; Elewa, H.
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A population pharmacokinetic model for early follow-up dosing of tacrolimus in Tunisian kidney transplant recipients他克莫司在突尼斯肾移植受者早期随访给药的人口药代动力学模型
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delete2026-01-01
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deleteAbderahmene, Amani; Francke, Marith I.; Ammar, Meriam; Andrews, Louise M.; Hesselink, Dennis A.; Amor, Dorra; Sahtout, Wissal; Awatif, Azzabi; Bouslama, Ali; Zellama, Dorsaf; Omezzine, Asma; De Winter, Brenda C. M.
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Lineage-specific transcriptomic signatures and therapeutic target discovery in myeloid and lymphoid leukemias谱系特异性转录组特征以及髓系和淋巴系白血病的治疗靶点发现
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IF1.8
delete2025-12-01
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deleteOzay, Basak; Ates, Onur; Kiraz, Yagmur
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Study of association between rs72703442 and rs55683539 genetic variants in MIR31HG and the risk of breast cancer研究MIR31HG中rs72703442和rs55683539遗传变异与乳腺癌风险之间的关联
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IF1.8
delete2025-12-01
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deleteAl-Nasani, Omar Jamal Khalaf; Reiisi, Somayeh
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