GetPortalImpactFactorByIdResp(projectId=1, id=b0722756, cover=https://img.medsci.cn/images/journal/cover/2021/Hpv_202109271315128050.jpg, fullname=HUMAN GENETICS, abbr=HUM GENET, pyear=1976, frequence=Monthly, articleNumbers=1893, citedSelf2015=3.4, acceptanceRate=null, submissionToAcceptance=null, averageReviewTime=平均1.75月, reviewFee=null, pageFee=null, 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=0340-6717, greenSci=https://www.greensci.net/search?kw=0340-6717, scijournal=https://www.scijournal.org/impact-factor-of-HUM-GENET.shtml, medsciHotlightString=null, medsciHotlightRealtime=6.096, medsciHotlight=4.678, medsciHotlight5year=5.75591, citescore=9.5, hIndex=137, impactFactor=5.3, orgnization=Springer Verlag, orgnizationUrl=http://springerlink.com, country=Germany, countryCn=德国, isOa=0, isOaString=否, sciScie=Science Citation Index|Science Citation Index Expanded|Current Contents - Life Sciences|BIOSIS Previews, bigclassCas=生物 2区, smallclassCas=生物 2 区, website=https://link.springer.com/journal/439, websiteHits=9500, guideForAuthor=null, guideForAuthorHits=12, submitWebsite=https://www.editorialmanager.com/huge/default.aspx, submitWebsiteHits=2203, content=Human Genetics is a monthly journal publishing original and timely articles on all aspects of human genetics. The Journal welcomes articles in the areas of Gene structure and organization Gene expression Mutation detection and analysis Linkage analysis and genetic mapping Physical mapping Cytogenetics and Genomic Imaging Genome structure and organisation Disease association studies Molecular diagnostics Genetic epidemiology Evolutionary genetics Developmental genetics Genotype-phenotype relationships Molecular genetics of tumorigenesis Genetics of complex diseases and epistatic interactions and Bioinformatics. Articles reporting animal models relevant to human biology or disease are also welcome. Preference will be given to those articles which address clinically relevant questions or which provide new insights into human biology. Unless they report entirely novel and unusual aspects of a topic clinical case reports cytogenetic case reports papers on descriptive population genetics articles dealing with the frequency of polymorphisms or additional mutations within genes in which numerous lesions have already been described will normally not be accepted. The Journal will not normally consider for publication manuscripts that report merely the isolation map position structure and tissue expression profile of a gene of unknown function unless the gene is of unusual interest or is a candidate gene involved in a human trait or disorder. Data on novel pathological mutations may be submitted to Human Genetics Online the electronic mutation data submission system administered by Springer-Verlag (, totalCites=10034, brief=HUM GENET杂志生物行业，“<strong><a target="_blank" href="/sci/index.do?smallclass=遗传学" >遗传学</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=HUM GENET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='https://www.medsci.cn/sci/submit.do?id=b0722756'>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=230, tagName=遗传学, createdHits=1), ImpactFactorTagDto(id=42146, tagName=分子流行病学, createdHits=1), ImpactFactorTagDto(id=33291, tagName=分子遗传学, createdHits=1), ImpactFactorTagDto(id=35453, tagName=基因功能, createdHits=1), ImpactFactorTagDto(id=313, tagName=临床, createdHits=1)], citeScoreList=[GetImpactFactorCiteScoreListResponse(year=2016, citescore=4.55), GetImpactFactorCiteScoreListResponse(year=2017, citescore=4.37), GetImpactFactorCiteScoreListResponse(year=2018, citescore=4.34), GetImpactFactorCiteScoreListResponse(year=2019, citescore=9.4), GetImpactFactorCiteScoreListResponse(year=2020, citescore=9.5)], medsciIndexList=[GetImpactFactorMedsciIndexListResponse(year=2020, medsciHotlight=6.889), GetImpactFactorMedsciIndexListResponse(year=2021, medsciHotlight=5.402), GetImpactFactorMedsciIndexListResponse(year=2022, medsciHotlight=5.336), GetImpactFactorMedsciIndexListResponse(year=2023, medsciHotlight=6.584), GetImpactFactorMedsciIndexListResponse(year=2024, medsciHotlight=6.096)], citeScoreGradeList=[GetImpactFactorCiteScoreGradeResponse(smallClass=Medicine - Genetics (clinical) , rank=15/91), GetImpactFactorCiteScoreGradeResponse(smallClass=Biochemistry, Genetics and Molecular Biology - Genetics , rank=51/318)], totalJcrAreaList=[GetImpactFactorCiteScoreGradeResponse(smallClass=GENETICS & HEREDITY, rank=Q1)], pmcUrl=https://www.ncbi.nlm.nih.gov/nlmcatalog?term=0340-6717[ISSN], pubmedUrl=https://www.ncbi.nlm.nih.gov/pubmed?cmd=search&term=HUMAN GENETICS[ta], article_number=146, article_number_cn=12, earlyWarning=null, linkOutUrl=null, isJournalMember=false, unscrambleContent=null, dayViewCount=false, endexampletyle=暂无数据)