GetPortalImpactFactorByIdResp(projectId=1, id=ad505214, cover=https://img.medsci.cn/images/journal/cover/2021/Kyi_202109271316159840.jpg, fullname=Orphanet Journal of Rare Diseases, abbr=ORPHANET J RARE DIS, pyear=2006, frequence=Irregular, articleNumbers=3559, citedSelf2015=5.6, acceptanceRate=null, submissionToAcceptance=null, averageReviewTime=平均4.56月, reviewFee=null, pageFee=2680.0, publishedRatio=2023年中国人文章占该期刊总数量暂无数据 (2022年为100.00%), issn=1750-1172, greenSci=https://www.greensci.net/search?kw=1750-1172, scijournal=https://www.scijournal.org/impact-factor-of-ORPHANET-J-RARE-DIS.shtml, medsciHotlightString=null, medsciHotlightRealtime=8.718, medsciHotlight=7.383, medsciHotlight5year=7.10153, citescore=6.3, hIndex=110, impactFactor=3.7, orgnization=BioMed Central Ltd., orgnizationUrl=http://www.biomedcentral.com/, country=United Kingdom, countryCn=英国, isOa=1, isOaString=是, sciScie=Science Citation Index Expanded|BIOSIS Previews|BIOSIS Reviews Reports And Meetings, bigclassCas=医学 2区, smallclassCas=医学 3 区, website=http://www.ojrd.com/, websiteHits=7827, guideForAuthor=null, guideForAuthorHits=23, submitWebsite=https://www.ojrd.com/manuscript, submitWebsiteHits=2557, content=Published by BioMed Central. ISSN: 1750-1172.<br /><br />Orphanet Journal of Rare Diseases is an open access, peer-reviewed online journal that encompasses all aspects of rare diseases and orphan drugs. The journal welcomes high quality review articles encompassing all aspects of diagnosis, clinical description, clinical work-up and management as well as aetiopathogenesis, *epidemiology, and genetic counselling of rare diseases. It brings together knowledge of basic research and clinical practice. By providing this information, crucial for optimised diagnosis and management, the Orphanet Journal of Rare Diseases aims to contribute to the improved care of patients affected by rare diseases. The journal provides researchers and clinicians with the opportunity to publish state of the art developments in the area of rare diseases and orphan drugs as well as to publish new syndromes and results of clinical trials including those with negative results., totalCites=13170, brief=ORPHANET J RARE DIS杂志医学行业，“<strong><a target="_blank" href="/sci/index.do?smallclass=医学：研究与实验" >医学：研究与实验</a></strong>”子行业的中等级别杂志, articleType=论著，综述各类型文章都接收, medsciHeat=<span style="color: #990000;">暗红</span>, medsciComment=ORPHANET J RARE DIS杂志级别还可以，但是相对来说，比较冷门，关注人数偏少，有些可能是国内不太熟悉，但该杂志在国际仍然有相当知晓度的。因为缺少中国人投稿，稿源可能未必丰富，发表有可能有很大的机会哦。, medsciExplanation=MedSci期刊指数是根据中国科研工作者（含医学临床，基础，生物，化学等学科）对SCI杂志的认知度，熟悉程度，以及投稿的量等众多指标综合评定而成。当然，具体的，您还可以结合“<a href='//www.nyrain.com/sci/submit.do?id=ad505214'>投稿经验系统</a>”，进行综合判断，这更是大家的实战经验，值得分享和参考。<br> 注意，上述MedSci期刊指数采用MedSci专利技术，由计算机系统自动计算，并给出建议，存在不准确的可能，仅供您投稿选择杂志时参考。, tags=[ImpactFactorTagDto(id=471, tagName=遗传, createdHits=5), ImpactFactorTagDto(id=593, tagName=血管, createdHits=2), ImpactFactorTagDto(id=10637, tagName=罕见病, createdHits=2), ImpactFactorTagDto(id=19493, tagName=血管畸形, createdHits=1), ImpactFactorTagDto(id=5132, tagName=出生缺陷, createdHits=1), ImpactFactorTagDto(id=266, tagName=心血管, createdHits=1)], citeScoreList=[GetImpactFactorCiteScoreListResponse(year=2017, citescore=3.35), GetImpactFactorCiteScoreListResponse(year=2018, citescore=4.06), GetImpactFactorCiteScoreListResponse(year=2019, citescore=5.0), GetImpactFactorCiteScoreListResponse(year=2020, citescore=5.2), GetImpactFactorCiteScoreListResponse(year=2023, citescore=6.3)], medsciIndexList=[GetImpactFactorMedsciIndexListResponse(year=2020, medsciHotlight=6.753), GetImpactFactorMedsciIndexListResponse(year=2021, medsciHotlight=7.081), GetImpactFactorMedsciIndexListResponse(year=2022, medsciHotlight=7.751), GetImpactFactorMedsciIndexListResponse(year=2023, medsciHotlight=9.383), GetImpactFactorMedsciIndexListResponse(year=2024, medsciHotlight=8.718)], citeScoreGradeList=[GetImpactFactorCiteScoreGradeResponse(smallClass=Medicine - Pharmacology (medical) , rank=24/232), GetImpactFactorCiteScoreGradeResponse(smallClass=Medicine - Genetics (clinical) , rank=17/91)], totalJcrAreaList=[GetImpactFactorCiteScoreGradeResponse(smallClass=GENETICS & HEREDITY, rank=Q2), GetImpactFactorCiteScoreGradeResponse(smallClass=MEDICINE, RESEARCH & EXPERIMENTAL, rank=Q1)], pmcUrl=https://www.ncbi.nlm.nih.gov/nlmcatalog?term=1750-1172[ISSN], pubmedUrl=https://www.ncbi.nlm.nih.gov/pubmed?cmd=search&term=ORPHANET JOURNAL OF RARE DISEASES[ta], article_number=451, article_number_cn=86, earlyWarning=null, linkOutUrl=null, isJournalMember=false, unscrambleContent=null, dayViewCount=false, endexampletyle=暂无数据)