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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 7.2 影响力 5.5 速度 9.0 | |||||||||||||||||||||||||||||||
| 期刊ISSN | 1750-1172 | 微信扫码收藏此期刊 | ||||||||||||||||||||||||||||||
| 2023-2024最新影响因子 （数据来源于搜索引擎） | 3.4 点击查看影响因子趋势图 | |||||||||||||||||||||||||||||||
| 实时影响因子 | 截止2024年10月29日：2.56 | |||||||||||||||||||||||||||||||
| 2023-2024自引率 | 5.90%点击查看自引率趋势图 | |||||||||||||||||||||||||||||||
| 五年影响因子 | 3.9 | |||||||||||||||||||||||||||||||
| JCI期刊引文指标 | 0.82 | |||||||||||||||||||||||||||||||
| h-index | 87 | |||||||||||||||||||||||||||||||
| CiteScore （ 2024年最新版） |
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| 期刊简介 |
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| 期刊官方网站 | http://ojrd.biomedcentral.com | |||||||||||||||||||||||||||||||
| 期刊投稿网址 | https://www.editorialmanager.com/ojrd | |||||||||||||||||||||||||||||||
| 作者指南网址 | http://ojrd.biomedcentral.com/submission-guidelines | |||||||||||||||||||||||||||||||
| 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 | 357点击查看年文章数趋势图 | |||||||||||||||||||||||||||||||
| Gold OA文章占比 | 99.52% | |||||||||||||||||||||||||||||||
| 研究类文章占比： 文章 ÷（文章 + 综述） | 80.67% | |||||||||||||||||||||||||||||||
| WOS期刊SCI分区 （ 2023-2024年最新版） | WOS分区等级：2区
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| 中国科学院《国际期刊预警 名单（试行）》名单 | 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 | |||||||||||||||||||||||||||||||
| 中国科学院SCI期刊分区 （ 2023年12月最新升级版） | 点击查看中国科学院SCI期刊分区趋势图
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| 中国科学院SCI期刊分区 （ 2022年12月升级版） |
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| 中国科学院SCI期刊分区 （ 2021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 | |||||||||||||||||||||||||||||||
| 期刊常用信息链接 |
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| 中国学者近期发表的论文 | |
| 1. | The clinical characteristics and outcomes of patients with systemic sclerosis with myocardial involvement Author: He, Huilin; Lai, Jinzhi; Zhou, Jiaxin; Hou, Yong; Xu, Dong; Li, Mengtao; Zeng, Xiaofeng Journal: ORPHANET JOURNAL OF RARE DISEASES. 2023; Vol. 18, Issue 1, pp. -. DOI: 10.1186/s13023-023-02699-1 PubMed DOI |
| 2. | Association between one-session bilateral whole-lung lavage and periprocedural complications in patients with pulmonary alveolar proteinosis: a retrospective cohort study Author: Xu, Xiaohan; Qiu, Huanrong; Chen, Fei; Zhang, Yuelun; Tian, Xinlun; Liu, Yongjian; Wang, Ping; Zhu, Bo; Huang, Yuguang Journal: ORPHANET JOURNAL OF RARE DISEASES. 2023; Vol. 18, Issue 1, pp. -. DOI: 10.1186/s13023-023-02691-9 PubMed DOI |
| 3. | The global prevalence and ethnic heterogeneity of iron-refractory iron deficiency anaemia Author: Fan, Shanghua; Zhao, Ting; Sun, Liu Journal: ORPHANET JOURNAL OF RARE DISEASES. 2023; Vol. 18, Issue 1, pp. -. DOI: 10.1186/s13023-022-02612-2 PubMed DOI |
| 4. | A patient advocating for transparent science in rare disease research Author: Yang, Richard Rui Journal: ORPHANET JOURNAL OF RARE DISEASES. 2023; Vol. 18, Issue 1, pp. -. DOI: 10.1186/s13023-022-02557-6 PubMed DOI |
| 5. | Prevalence of depression and anxiety, and their relationship to social support among patients and family caregivers of rare bone diseases Author: Lai, Xuefeng; Jiang, Yuling; Sun, Yue; Zhang, Zhijun; Wang, Shengfeng Journal: ORPHANET JOURNAL OF RARE DISEASES. 2023; Vol. 18, Issue 1, pp. -. DOI: 10.1186/s13023-022-02611-3 PubMed DOI |
| 6. | Glutamate dehydrogenase hyperinsulinism: mechanisms, diagnosis, and treatment Author: Zeng, Qiao; Sang, Yan-Mei Journal: ORPHANET JOURNAL OF RARE DISEASES. 2023; Vol. 18, Issue 1, pp. -. DOI: 10.1186/s13023-023-02624-6 PubMed DOI |
| 7. | Effects of early recombinant human growth hormone treatment in young Chinese children with Prader-Willi syndrome Author: Gao, Ying; Yang, Li-Li; Dai, Yang-Li; Shen, Zheng; Zhou, Qiong; Zou, Chao-Chun Journal: ORPHANET JOURNAL OF RARE DISEASES. 2023; Vol. 18, Issue 1, pp. -. DOI: 10.1186/s13023-023-02615-7 PubMed DOI |
| 8. | Ultrasound-guided interlaminar approach for nusinersen administration in patients with spinal muscular atrophy with spinal fusion or severe scoliosis Author: Wei, Cuijie; Liang, Zhenwei; Wu, Ying; Liu, Shan; Qiu, Jianxing; Meng, Lingchao; Li, Chunde; Li, Shuang; Bao, Xinhua; Wang, Zhaoxia; Chen, Luzeng; Xiong, Hui Journal: ORPHANET JOURNAL OF RARE DISEASES. 2023; Vol. 18, Issue 1, pp. -. DOI: 10.1186/s13023-023-02630-8 PubMed DOI |
| 9. | Mitochondrial diseases in Hong Kong: prevalence, clinical characteristics and genetic landscape Author: Wong, Tsz-sum; Belaramani, Kiran M.; Chan, Chun-kong; Chan, Wing-ki; Chan, Wai-lun Larry; Chang, Shek-kwan; Cheung, Sing-ngai; Cheung, Ka-yin; Cheung, Yuk-fai; Chong, Shuk-ching Josephine; Chow, Chi-kwan Jasmine; Chung, Hon-yin Brian; Fan, Sin-ying Florence; Fok, Wai-ming Joshua; Fong, Ka-wing; Fung, Tsui-hang Sharon; Hui, Kwok-fai; Hui, Ting-hin; Hui, Joannie; Ko, Chun-hung; Kwan, Min-chung; Kwok, Mei-kwan Anne; Kwok, Sung-shing Jeffrey; Lai, Moon-sing; Lam, Yau-on; Lam, Ching-wan; Lau, Ming-chung; Law, Chun-yiu Eric; Lee, Wing-cheong; Lee, Han-chih Hencher; Lee, Chin-nam; Leung, Kin-hang; Leung, Kit-yan; Li, Siu-hung; Ling, Tsz-ki Jacky; Liu, Kam-tim Timothy; Lo, Fai-man; Lui, Hiu-tung; Luk, Ching-on; Luk, Ho-ming; Ma, Che-kwan; Ma, Karen; Ma, Kam-hung; Mew, Yuen-ni; Mo, Alex; Ng, Sui-fun; Poon, Wing-kit Grace; Rodenburg, Richard; Sheng, Bun; Smeitink, Jan; Szeto, Cheuk-ling Charing; Tai, Shuk-mui; Tse, Choi-ting Alan; Tsung, Li-yan Lilian; Wong, Ho-ming June; Wong, Wing-yin Winnie; Wong, Kwok-kui; Wong, Suet-na Sheila; Wong, Chun-nei Virginia; Wong, Wai-shan Sammy; Wong, Chi-kin Felix; Wu, Shun-ping; Wu, Hiu-fung Jerome; Yau, Man-mut; Yau, Kin-cheong Eric; Yeung, Wai-lan; Yeung, Hon-ming Jonas; Yip, Kin-keung Edwin; Young, Pui-hong Terence; Yuan, Gao; Yuen, Yuet-ping Liz; Yuen, Chi-lap; Fung, Cheuk-wing Journal: ORPHANET JOURNAL OF RARE DISEASES. 2023; Vol. 18, Issue 1, pp. -. DOI: 10.1186/s13023-023-02632-6 PubMed DOI |
| 10. | Identification of a novel de novo mutation of SETBP1 and new findings of SETBP1 in tumorgenesis Author: Wang, Hongdan; Gao, Yue; Qin, Litao; Zhang, Mengting; Shi, Weili; Feng, Zhanqi; Guo, Liangjie; Zhu, Bofeng; Liao, Shixiu Journal: ORPHANET JOURNAL OF RARE DISEASES. 2023; Vol. 18, Issue 1, pp. -. DOI: 10.1186/s13023-023-02705-6 PubMed DOI |
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