Pharmacogenomics & Personalized Medicine

Pharmacogenomics & Personalized Medicine

药物基因组学和个性化医学

  • 4区 中科院分区
  • Q3 JCR分区

期刊简介

《Pharmacogenomics & Personalized Medicine》是由Dove Medical Press出版社创办的英文国际期刊(ISSN: 1178-7066,E-ISSN: 1178-7066),该期刊长期致力于药学领域的创新研究,主要研究方向为Biochemistry, Genetics and Molecular Biology-Molecular Medicine。作为SCI、SCIE收录期刊(JCR分区 Q3,中科院 4区),本刊采用OA开放获取模式(OA占比1%),以发表药学领域等方向的原创性研究为核心(研究类文章占比78.26%%)。凭借严格的同行评审与高效编辑流程,期刊年载文量精选控制在23篇,确保学术质量与前沿性。成果覆盖Web of ScienceWeb of Science、Scopus等国际权威数据库,为学者提供推动医学领域高水平交流平台。

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投稿提示

Pharmacogenomics & Personalized Medicine审稿周期约为16 Weeks。该刊近年未被列入国际预警名单,年发文量约23篇,录用竞争适中,主题需确保紧密契合医学前沿。投稿策略提示:避开学术会议旺季投稿以缩短周期,语言建议专业润色提升可读性。

  • 医学 大类学科
  • English 出版语言
  • 是否预警
  • SCI、SCIE 期刊收录
  • 23 发文量

中科院分区

《新锐期刊分区表》(2026年3月发布)

Top期刊 综述期刊 大类学科 小类学科
医学
4区
PHARMACOLOGY & PHARMACY 药学
3区

期刊分区表(2025年3月升级版)

Top期刊 综述期刊 大类学科 小类学科
医学
4区
PHARMACOLOGY & PHARMACY 药学
4区

期刊分区表(2023年12月升级版)

Top期刊 综述期刊 大类学科 小类学科
医学
4区
PHARMACOLOGY & PHARMACY 药学
4区

期刊分区表(2022年12月升级版)

Top期刊 综述期刊 大类学科 小类学科
医学
4区
PHARMACOLOGY & PHARMACY 药学
4区

期刊分区表(2021年12月升级版)

Top期刊 综述期刊 大类学科 小类学科
医学
3区
PHARMACOLOGY & PHARMACY 药学
3区

JCR分区

2025-2026年最新版

按JCI指标学科分区 收录子集 分区 排名 百分位
学科:PHARMACOLOGY & PHARMACY SCIE Q3 215 / 356

39.7

学科:PHARMACOLOGY & PHARMACY SCIE Q3 215 / 356

39.75

2023-2024年最新版

按JCI指标学科分区 收录子集 分区 排名 百分位
学科:PHARMACOLOGY & PHARMACY SCIE Q3 240 / 354

32.3

学科:PHARMACOLOGY & PHARMACY SCIE Q3 215 / 354

39.41

CiteScore(2026年6月最新版)

CiteScore SJR SNIP CiteScore 排名
CiteScore:4.8 SJR:0.73 SNIP:0.74
学科类别 分区 排名 百分位
大类:Pharmacology, Toxicology and Pharmaceutics 小类:Pharmacology Q2 155 / 328

52%

大类:Pharmacology, Toxicology and Pharmaceutics 小类:Molecular Medicine Q3 109 / 179

39%

期刊发文

  • Construction and Validation of Multi-Omics Predictive Models for Colorectal Cancer Using Machine-Learning Approache

    Author: Lu, Zhenhuan; Li, Xiaowen; Liang, Zhiping; Zhang, Xiaocong; Tan, Yiyan; Kuang, Yinglan; Li, Kang; Zhu, Xiaofeng

    Journal: PHARMACOGENOMICS & PERSONALIZED MEDICINE. 2026; Vol. 19, Issue , pp. -. DOI: 10.2147/PGPM.S566928

  • Massive Hepatocellular Carcinoma with Insufficient Future Liver Remnant Achieved Complete Response After Two-Stage Hepatectomy Combined with Hepatic Arterial Infusion Chemotherapy and Lenvatinib-sintilimab: A Case Repor

    Author: Xu, Ruoxiang; Zhang, Mingrui; Zeng, Zhiming; Wei, Yongguang; Liao, Xiwen; Yang, Chengkun; Peng, Tao; Su, Hao

    Journal: PHARMACOGENOMICS & PERSONALIZED MEDICINE. 2026; Vol. 19, Issue , pp. -. DOI: 10.2147/PGPM.S578577

  • Post-Translational Modifications of Histones and Non-Histones in Liver Disease and Traditional Chinese Medicine Treatment: A Narrative Revie

    Author: Xie, Zhuohua; Deng, Yanting; Zhang, Xinru; Chen, Jieyi; Deng, Jiasheng; Fang, Yibin; Ye, Xiaoxue; Zhou, Zhipin

    Journal: PHARMACOGENOMICS & PERSONALIZED MEDICINE. 2026; Vol. 19, Issue , pp. -. DOI: 10.2147/PGPM.S555701

  • Clinical Outcomes of Osimertinib Combined with Platinum-Based Chemotherapy in EGFR-Mutant Non-Small Cell Lung Cancer: A Retrospective Stud

    Author: Han, Ruixue; Yu, Xin

    Journal: PHARMACOGENOMICS & PERSONALIZED MEDICINE. 2026; Vol. 19, Issue , pp. -. DOI: 10.2147/PGPM.S566952

  • Bioinformatic Identification and Preliminary Validation of TP53, TGFB1, and NFE2L2 as Potential Ferroptosis-Related Regulators in Pancreatic Adenocarcinom

    Author: Li, Shouying; Zhang, Chunfang; Lv, Shengxiang; Zhang, Zhimei; Xu, Dazhou; Xu, Tonglei

    Journal: PHARMACOGENOMICS & PERSONALIZED MEDICINE. 2026; Vol. 19, Issue , pp. -. DOI: 10.2147/PGPM.S562602

  • Associations Between FTO Polymorphisms and Neuroblastoma Risk in Chinese Childre

    Author: Liu, Peiqi; Li, Yue; Li, Yong; Li, Li; Cheng, Jiwen; Li, Suhong; Zhang, Jiao; Zhou, Haixia; Huo, Yunlong; Yang, Zhonghua; He, Jing; Zhang, Ran

    Journal: PHARMACOGENOMICS & PERSONALIZED MEDICINE. 2025; Vol. 18, Issue , pp. 143-151. DOI: 10.2147/PGPM.S488314

  • Molecular Genetic Analysis of a DMD Frameshift Mutation in a Boy with Duchenne Muscular Dystrophy by MLPA and Sanger Sequencin

    Author: Chen, Qianwen; Zhang, Wenjuan; Zha, Lingfeng

    Journal: PHARMACOGENOMICS & PERSONALIZED MEDICINE. 2025; Vol. 18, Issue , pp. 153-162. DOI: 10.2147/PGPM.S514145

  • Novel SLC16A2 Frameshift Mutation as a Cause of Allan-Herndon-Dudley Syndrome and its Implications for Carrier Screenin

    Author: Lin, Peng; Liu, Huituan; Lou, Jiwu; Lyu, Guizhen; Li, Yanwei; He, Peiqing; Fu, Youqing; Zhang, Ronghua; Zhang, Yuqiong; Yan, Tizhen

    Journal: PHARMACOGENOMICS & PERSONALIZED MEDICINE. 2025; Vol. 18, Issue , pp. 85-94. DOI: 10.2147/PGPM.S492647