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| 近期推荐: | 热 Wiley 2026暑期线上学习营 | 报名正式开启! | 新 Springer Nature生物医学与生命科学资源合集 | 附免费书单 | 热 全流程投稿协助套餐服务 |
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| 基本信息 | 登录收藏 | |||||||||||||||||||||||||||||
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期刊名字![]() | PSYCHIATRIC GENETICS PSYCHIAT GENET (此期刊被最新的JCR期刊SCIE收录) LetPub评分 5.1
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声誉 6.4 影响力 3.6 速度 7.0 | |||||||||||||||||||||||||||||
| 期刊ISSN | 0955-8829 | 安装APP,查看期刊最新消息
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| E-ISSN | 1473-5873 | |||||||||||||||||||||||||||||
| 2025-2026最新IF (数据来源于网友提供) | 注册或登录后,查看IF | |||||||||||||||||||||||||||||
| 实时影响因子 | 截止2026年5月06日:1.34 | |||||||||||||||||||||||||||||
| 2025-2026自引率 | 7.1%点击查看自引率趋势图 | |||||||||||||||||||||||||||||
| 五年IF (数据来源于网友提供) | 1.396数据由网友[软萌故事]收集提供 | |||||||||||||||||||||||||||||
| h-index | 56 | |||||||||||||||||||||||||||||
| CiteScore ( 2026年6月最新版) |
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| 期刊简介 |
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| 期刊官方网站 | http://journals.lww.com/psychgenetics/pages/default.aspx | |||||||||||||||||||||||||||||
期刊投稿格式模板 VIP专享 |
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| 期刊投稿网址 | https://www.editorialmanager.com/PG | |||||||||||||||||||||||||||||
| 该期刊中国学者近期发文 - New | Prenatal diagnosis and genetic counselling of a rare de-novo 12p13.33p13.32 deletion and 15q26.2q26.3 duplication in a Chinese family Author: Zhang, Zhenzhen; Wang, Wei; Xiong, Jin; Xia, Qi Journal: PSYCHIATRIC GENETICS. 2026; Vol. 36, Issue 2, pp. 90-94. DOI: 10.1097/YPG.0000000000000412 The clinical significance of miR-484 in depression of older people with Alzheimer's disease and its potential role on depressive behavior Author: Teng, Shuai; Li, Ying; Wang, Xichun; Jiang, Pingjing Journal: PSYCHIATRIC GENETICS. 2026; Vol. 36, Issue 2, pp. 69-80. DOI: 10.1097/YPG.0000000000000411 Genetic correlation between inflammatory bowel disease and educational attainment: unveiling shared genetic mechanisms Author: Hong, Zhonghua; Yin, Hezhai Journal: PSYCHIATRIC GENETICS. 2026; Vol. 36, Issue 2, pp. 95-105. DOI: 10.1097/YPG.0000000000000416 Prenatal diagnosis and genetic counseling for three cases of fetuses with low-level mosaic Turner syndrome Author: Dai, Hongbo; Li, Quanlun; Quan, Yan Journal: PSYCHIATRIC GENETICS. 2026; Vol. 36, Issue 2, pp. 106-109. DOI: 10.1097/YPG.0000000000000414 | |||||||||||||||||||||||||||||
| 期刊语言要求 | 经LetPub语言功底雄厚的美籍native English speaker精心编辑的稿件,不仅能满足PSYCHIATRIC GENETICS的语言要求,还能让PSYCHIATRIC GENETICS编辑和审稿人得到更好的审稿体验,让稿件最大限度地被PSYCHIATRIC GENETICS编辑和审稿人充分理解和公正评估。LetPub的专业SCI论文编辑服务(包括SCI论文英语润色,同行资深专家修改润色,SCI论文专业翻译,SCI论文格式排版,专业学术制图等)帮助作者准备稿件,已助力全球15万+作者顺利发表论文。部分发表范例可查看:服务好评 论文致谢 。
提交文稿 | |||||||||||||||||||||||||||||
| 是否OA开放访问 | No | |||||||||||||||||||||||||||||
| 通讯方式 | LIPPINCOTT WILLIAMS & WILKINS, 530 WALNUT ST, PHILADELPHIA, USA, PA, 19106-3621 | |||||||||||||||||||||||||||||
| 出版商 | Lippincott Williams and Wilkins Ltd. | |||||||||||||||||||||||||||||
| 涉及的研究方向 | 医学-神经科学 | |||||||||||||||||||||||||||||
| 出版国家或地区 | UNITED STATES | |||||||||||||||||||||||||||||
| 出版语言 | English | |||||||||||||||||||||||||||||
| 出版周期 | Quarterly | |||||||||||||||||||||||||||||
| 出版年份 | 1990 | |||||||||||||||||||||||||||||
| 年文章数 | 23点击查看年文章数趋势图 | |||||||||||||||||||||||||||||
| Gold OA文章占比 | 17.14% | |||||||||||||||||||||||||||||
| 研究类文章占比: 文章 ÷(文章 + 综述) | 91.30% | |||||||||||||||||||||||||||||
| WOS期刊JCR分区 ( 2025-2026年最新版) | 注册或登录后,查看WOS分区等级 | |||||||||||||||||||||||||||||
| 期刊分区表预警名单 | 2026年03月发布的新锐学术版:不在预警名单中 2025年03月发布的2025版:不在预警名单中 2024年02月发布的2024版:不在预警名单中 2023年01月发布的2023版:不在预警名单中 2021年12月发布的2021版:不在预警名单中 2020年12月发布的2020版:不在预警名单中 | |||||||||||||||||||||||||||||
| 《新锐期刊分区表》 ( 2026年3月发布) | 点击查看期刊分区表趋势图
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| 期刊分区表 ( 2025年3月升级版) |
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| 期刊分区表 ( 2023年12月旧的升级版) |
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| SCI期刊收录coverage | Science Citation Index Expanded (SCIE) (2020年1月,原SCI撤销合并入SCIE,统称SCIE) Scopus (CiteScore) | |||||||||||||||||||||||||||||
| PubMed Central (PMC)链接 | http://www.ncbi.nlm.nih.gov/nlmcatalog?term=0955-8829%5BISSN%5D | |||||||||||||||||||||||||||||
| 平均审稿速度 | 网友分享经验: >12周,或约稿 | |||||||||||||||||||||||||||||
| 平均录用比例 | 网友分享经验: 较易 | |||||||||||||||||||||||||||||
| LetPub助力发表 | 经LetPub编辑的稿件平均录用比例是未经润色的稿件的1.5倍,平均审稿时间缩短40%。众多作者在使用LetPub的专业SCI论文编辑服务(包括SCI论文英语润色,同行资深专家修改润色,SCI论文专业翻译,SCI论文格式排版,专业学术制图等)后论文在PSYCHIATRIC GENETICS顺利发表。
快看看作者怎么说吧:服务好评 论文致谢 。 提交文稿 | |||||||||||||||||||||||||||||
| 期刊常用信息链接 |
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| 中国学者近期发表的论文 | |
| 1. | Prenatal diagnosis and genetic counselling of a rare de-novo 12p13.33p13.32 deletion and 15q26.2q26.3 duplication in a Chinese family Author: Zhang, Zhenzhen; Wang, Wei; Xiong, Jin; Xia, Qi Journal: PSYCHIATRIC GENETICS. 2026; Vol. 36, Issue 2, pp. 90-94. DOI: 10.1097/YPG.0000000000000412 PubMed DOI |
| 2. | The clinical significance of miR-484 in depression of older people with Alzheimer's disease and its potential role on depressive behavior Author: Teng, Shuai; Li, Ying; Wang, Xichun; Jiang, Pingjing Journal: PSYCHIATRIC GENETICS. 2026; Vol. 36, Issue 2, pp. 69-80. DOI: 10.1097/YPG.0000000000000411 PubMed DOI |
| 3. | Genetic correlation between inflammatory bowel disease and educational attainment: unveiling shared genetic mechanisms Author: Hong, Zhonghua; Yin, Hezhai Journal: PSYCHIATRIC GENETICS. 2026; Vol. 36, Issue 2, pp. 95-105. DOI: 10.1097/YPG.0000000000000416 PubMed DOI |
| 4. | Prenatal diagnosis and genetic counseling for three cases of fetuses with low-level mosaic Turner syndrome Author: Dai, Hongbo; Li, Quanlun; Quan, Yan Journal: PSYCHIATRIC GENETICS. 2026; Vol. 36, Issue 2, pp. 106-109. DOI: 10.1097/YPG.0000000000000414 PubMed DOI |
| 5. | Dissecting the genetic interaction between breast cancer risk and schizophrenia: evidence from crosstrait genome-wide analysis Author: Zhang, Min; Wu, Yongli; Qin, Yujie Journal: PSYCHIATRIC GENETICS. 2026; Vol. 36, Issue 1, pp. 32-41. DOI: 10.1097/YPG.0000000000000410 PubMed DOI |
| 6. | Diagnosis and follow-up of a PCDH19 epilepsy patient Author: Chen, Yanzhao; Xia, Yaming; Chen, Lipeng; Liu, Zhiping; Li, Bo; Zhou, Keying; Yue, Yongjian Journal: PSYCHIATRIC GENETICS. 2026; Vol. 36, Issue 1, pp. 26-31. DOI: 10.1097/YPG.0000000000000404 PubMed DOI |
| 7. | The diagnostic significance of miR-20b-5p in schizophrenia and its impact on the symptoms of schizophrenia Author: Li, Jianhui; Cheng, Yao; Lu, Wei Journal: PSYCHIATRIC GENETICS. 2025; Vol. 35, Issue 3, pp. 51-57. DOI: 10.1097/YPG.0000000000000393 PubMed DOI |
| 8. | Prenatal diagnosis and genetic counseling of a Chinese family with inherited multiple chromosomal microduplications Author: Hu, Fang; Zhang, Guoqiong Journal: PSYCHIATRIC GENETICS. 2025; Vol. 35, Issue 3, pp. 69-74. DOI: 10.1097/YPG.0000000000000391 PubMed DOI |
| 9. | Identification of de-novo CREBBP gene variants in patients with Rubinstein-Taybi syndrome Author: Ji, Qinghong; Ma, Weihong; Xin, Gang; Xin, Qian; Duan, Shuhong; Ding, Mingxia; Dong, Lihua; Li, Zhiqiang; Hong, Fanzhen Journal: PSYCHIATRIC GENETICS. 2025; Vol. 35, Issue 1, pp. -. DOI: 10.1097/YPG.0000000000000381 PubMed DOI |
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