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| 基本信息 | 登录收藏 | |||||||||||||||||||||
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期刊名字![]() | Orphanet Journal of Rare Diseases ORPHANET J RARE DIS (此期刊被最新的JCR期刊SCIE收录) LetPub评分 6.5
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声誉 7.1 影响力 5.5 速度 8.4 | |||||||||||||||||||||
| 期刊ISSN | 1750-1172 | 安装APP,查看期刊最新消息
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| 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:3.6 | |||||||||||||||||||||
| 2025-2026自引率 | 5.6%点击查看自引率趋势图 | |||||||||||||||||||||
| 五年IF (数据来源于网友提供) | 4.204数据由网友[随缘湖泊]收集提供 | |||||||||||||||||||||
| h-index | 87 | |||||||||||||||||||||
| 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://ojrd.biomedcentral.com | |||||||||||||||||||||
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/ojrd | |||||||||||||||||||||
| 作者指南网址 | http://ojrd.biomedcentral.com/submission-guidelines | |||||||||||||||||||||
| 该期刊中国学者近期发文 - New | Living-donor liver transplantation in children with inherited metabolic and genetic cholestatic liver diseases: a single-center retrospective cohort study Author: Liu, Hui; Chen, Zhida; Li, Wanfu; Huxitaer, Halimulati; Maimaiti, Gulimiremu; Maimaijiang, Ayiguzaili; Jiayilawu, Yeliaman; Habuding, Aerxin; Xi, Runqi; Wang, Haoyu; Song, FangJuan Journal: ORPHANET JOURNAL OF RARE DISEASES. 2026; Vol. 21, Issue 1, pp. -. DOI: 10.1186/s13023-026-04369-4 The mutational burden in os odontoideum patients Author: Tian, Yinglun; Gao, Guodong; Fan, Dongwei; Xue, Shilin; Gao, Qiyue; Zhang, Cheng; Xu, Nanfang; Wang, Shenglin Journal: ORPHANET JOURNAL OF RARE DISEASES. 2026; Vol. 21, Issue 1, pp. -. DOI: 10.1186/s13023-026-04342-1 Attenuated dietary motivation in Wilson's disease correlates with clinical severity Author: Wang, Xue-Qiao; Wang, Yan-Xin; Ye, Zhao-Hao; Zhang, Zhi-Lin; Pan, Xun; Wang, Xi-Chen; Cen, Si-Fan Journal: ORPHANET JOURNAL OF RARE DISEASES. 2026; Vol. 21, Issue 1, pp. -. DOI: 10.1186/s13023-026-04263-z Orphan drug propranolol for infantile hemangioma: ten-year real-world safety data from the FAERS database Author: Li, Xuanjia; Zhao, Xingyu; Yang, Chengzhe; Chen, Anwei Journal: ORPHANET JOURNAL OF RARE DISEASES. 2026; Vol. 21, Issue 1, pp. -. DOI: 10.1186/s13023-026-04331-4 | |||||||||||||||||||||
| 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Orphanet Journal of Rare Diseases的语言要求,还能让Orphanet Journal of Rare Diseases编辑和审稿人得到更好的审稿体验,让稿件最大限度地被Orphanet Journal of Rare Diseases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(2篇) 。
提交文稿 | |||||||||||||||||||||
| 是否OA开放访问 | Yes | |||||||||||||||||||||
OA期刊相关信息![]() | 文章处理费:需要( GBP2090; USD2890; EUR2390; ) 文章处理费豁免:查看说明 其他费用:没有 期刊主题关键词:rare diseases、orphan drugs 相关链接:Aims & ScopeAuthor InstructionsEditorial BoardAnonymous peer review | |||||||||||||||||||||
| 通讯方式 | BIOMED CENTRAL LTD, 236 GRAYS INN RD, FLOOR 6, LONDON, ENGLAND, WC1X 8HL | |||||||||||||||||||||
| 出版商 | BioMed Central | |||||||||||||||||||||
| 涉及的研究方向 | 医学-医学:研究与实验 | |||||||||||||||||||||
| 出版国家或地区 | ENGLAND | |||||||||||||||||||||
| 出版语言 | English | |||||||||||||||||||||
| 出版周期 | Irregular | |||||||||||||||||||||
| 出版年份 | 2006 | |||||||||||||||||||||
| 年文章数 | 630点击查看年文章数趋势图 | |||||||||||||||||||||
| Gold OA文章占比 | 100.00% | |||||||||||||||||||||
| 研究类文章占比: 文章 ÷(文章 + 综述) | 85.40% | |||||||||||||||||||||
| 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) Directory of Open Access Journals (DOAJ) | |||||||||||||||||||||
| PubMed Central (PMC)链接 | http://www.ncbi.nlm.nih.gov/nlmcatalog?term=1750-1172%5BISSN%5D | |||||||||||||||||||||
| 平均审稿速度 | 网友分享经验: 偏慢,4-8周 | |||||||||||||||||||||
| 平均录用比例 | 网友分享经验: 一般 | |||||||||||||||||||||
| 版面费/APC文章处理费信息 | 文章处理费:需要( GBP2090; USD2890; EUR2390; ) 文章处理费豁免:查看说明 其他费用:没有 LetPub提供文章处理费(APC)支持服务,可以用人民币支付版面费啦! | |||||||||||||||||||||
| 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Orphanet Journal of Rare Diseases顺利发表。
快看看作者怎么说吧:服务好评 论文致谢(2篇) 。 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. | Living-donor liver transplantation in children with inherited metabolic and genetic cholestatic liver diseases: a single-center retrospective cohort study Author: Liu, Hui; Chen, Zhida; Li, Wanfu; Huxitaer, Halimulati; Maimaiti, Gulimiremu; Maimaijiang, Ayiguzaili; Jiayilawu, Yeliaman; Habuding, Aerxin; Xi, Runqi; Wang, Haoyu; Song, FangJuan Journal: ORPHANET JOURNAL OF RARE DISEASES. 2026; Vol. 21, Issue 1, pp. -. DOI: 10.1186/s13023-026-04369-4 PubMed DOI |
| 2. | The mutational burden in os odontoideum patients Author: Tian, Yinglun; Gao, Guodong; Fan, Dongwei; Xue, Shilin; Gao, Qiyue; Zhang, Cheng; Xu, Nanfang; Wang, Shenglin Journal: ORPHANET JOURNAL OF RARE DISEASES. 2026; Vol. 21, Issue 1, pp. -. DOI: 10.1186/s13023-026-04342-1 PubMed DOI |
| 3. | Attenuated dietary motivation in Wilson's disease correlates with clinical severity Author: Wang, Xue-Qiao; Wang, Yan-Xin; Ye, Zhao-Hao; Zhang, Zhi-Lin; Pan, Xun; Wang, Xi-Chen; Cen, Si-Fan Journal: ORPHANET JOURNAL OF RARE DISEASES. 2026; Vol. 21, Issue 1, pp. -. DOI: 10.1186/s13023-026-04263-z PubMed DOI |
| 4. | Orphan drug propranolol for infantile hemangioma: ten-year real-world safety data from the FAERS database Author: Li, Xuanjia; Zhao, Xingyu; Yang, Chengzhe; Chen, Anwei Journal: ORPHANET JOURNAL OF RARE DISEASES. 2026; Vol. 21, Issue 1, pp. -. DOI: 10.1186/s13023-026-04331-4 PubMed DOI |
| 5. | Optimizing regional rare disease management systems within China's policy framework: practical insights from the shantou experience Author: Wu, Beiyan; Wang, Yali; Liu, Chao; Wang, Qilin; Gong, Mengchun; Chen, Yongsong Journal: ORPHANET JOURNAL OF RARE DISEASES. 2026; Vol. 21, Issue 1, pp. -. DOI: 10.1186/s13023-026-04340-3 PubMed DOI |
| 6. | WFS1-related isolated diabetes induced by a WFS1 missense mutation: focus on the isolated diabetes phenotype Author: Huang, Mei; Wei, Qianying; Qin, Yao; Qin, Lu; Shao, Ying; Wang, Suyu; Qu, Xinyi; Yang, Tao; Zhang, Mei Journal: ORPHANET JOURNAL OF RARE DISEASES. 2026; Vol. 21, Issue 1, pp. -. DOI: 10.1186/s13023-026-04291-9 PubMed DOI |
| 7. | SERPINC1 mutations and thrombotic events in inherited antithrombin deficiency: a study on the han population of East China Author: Xu, Fei; Chen, Xiaoli; Xu, Qiyu; Zou, Anqing; Li, Xiaolong; Wang, Mingshan; Yang, Lihong; Xie, Haixiao Journal: ORPHANET JOURNAL OF RARE DISEASES. 2026; Vol. 21, Issue 1, pp. -. DOI: 10.1186/s13023-026-04200-0 PubMed DOI |
| 8. | Targeted therapy for Langerhans cell histiocytosis with maxillofacial involvement in 20 children Author: Jiang, Yang; Li, Zhigang; Yang, Ying; Zhang, Rui; Wang, Tianyou; Yu, Guoxia Journal: ORPHANET JOURNAL OF RARE DISEASES. 2026; Vol. 21, Issue 1, pp. -. DOI: 10.1186/s13023-026-04301-w PubMed DOI |
| 9. | Pulmonary hemorrhage as an early clue: an integrated clinical-imaging-genetic diagnostic insight for vascular Ehlers-Danlos syndrome Author: Wang, Yaqi; Xie, Huaiya; Song, Lan; Xu, Kexin; Fan, Junping; Wang, Ping; Wu, Nan; Zhang, Ting; Shi, Juhong; Xu, Kai-Feng; Tian, Xinlun; Zhang, Xue Journal: ORPHANET JOURNAL OF RARE DISEASES. 2026; Vol. 21, Issue 1, pp. -. DOI: 10.1186/s13023-026-04327-0 PubMed DOI |
| 10. | Advances in hereditary angioedema in the modern treatment era in China: a focus on diagnosis, treatment, and prognosis Author: Zhao, Ye; Zou, Duowu Journal: ORPHANET JOURNAL OF RARE DISEASES. 2026; Vol. 21, Issue 1, pp. -. DOI: 10.1186/s13023-026-04314-5 PubMed DOI |
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