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Human GeneticsSCIE

国际简称：HUM GENET 参考译名：人类遗传学

中科院分区
2区
CiteScore分区
Q1
JCR分区
Q2

基本信息：: ISSN：0340-6717; E-ISSN：1432-1203; 是否OA：未开放; 是否预警：否; TOP期刊：是

出版信息：: 出版地区：UNITED STATES; 出版商：Springer Berlin Heidelberg; 出版语言：English; 出版周期：Monthly; 出版年份：1964; 研究方向：生物-遗传学

评价信息：: 影响因子：3.8; H-index：126; CiteScore指数：10.8; SJR指数：2.049; SNIP指数：1.627

发文数据：: Gold OA文章占比：37.64%; 研究类文章占比：79.25%; 年发文量：106; 自引率：0.0377...; 开源占比：0.303; 出版撤稿占比：0; 出版国人文章占比：0.07; OA被引用占比：0.2666...

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英文简介期刊介绍 CiteScore数据中科院SCI分区 JCR分区发文数据常见问题

英文简介Human Genetics期刊介绍

Human Genetics is a monthly journal publishing original and timely articles on all aspects of human genetics. The Journal particularly welcomes articles in the areas of Behavioral genetics, Bioinformatics, Cancer genetics and genomics, Cytogenetics, Developmental genetics, Disease association studies, Dysmorphology, ELSI (ethical, legal and social issues), Evolutionary genetics, Gene expression, Gene structure and organization, Genetics of complex diseases and epistatic interactions, Genetic epidemiology, Genome biology, Genome structure and organization, Genotype-phenotype relationships, Human Genomics, Immunogenetics and genomics, Linkage analysis and genetic mapping, Methods in Statistical Genetics, Molecular diagnostics, Mutation detection and analysis, Neurogenetics, Physical mapping and Population Genetics. 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 reporting 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, and papers that report meta-analyses of previously published datasets will normally not be accepted.

The Journal typically will not 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 particular interest or is a candidate gene involved in a human trait or disorder.

期刊简介Human Genetics期刊介绍

《Human Genetics》自1964出版以来，是一本生物学优秀杂志。致力于发表原创科学研究结果，并为生物学各个领域的原创研究提供一个展示平台，以促进生物学领域的的进步。该刊鼓励先进的、清晰的阐述，从广泛的视角提供当前感兴趣的研究主题的新见解，或审查多年来某个重要领域的所有重要发展。该期刊特色在于及时报道生物学领域的最新进展和新发现新突破等。该刊近一年未被列入预警期刊名单，目前已被权威数据库SCIE收录，得到了广泛的认可。

该期刊投稿重要关注点：

预计审稿时间：约1月
国际TOP期刊
生物学
GENETICS & HEREDITY
SCIE
中科院2区
非预警

Cite Score数据（2024年最新版）Human Genetics Cite Score数据

CiteScore：10.8
SJR：2.049
SNIP：1.627

学科类别	分区	排名	百分位
大类：Medicine 小类：Genetics (clinical)	Q1	7 / 99	93%
大类：Medicine 小类：Genetics	Q1	39 / 347	88%

CiteScore 是由Elsevier(爱思唯尔)推出的另一种评价期刊影响力的文献计量指标。反映出一家期刊近期发表论文的年篇均引用次数。CiteScore以Scopus数据库中收集的引文为基础，针对的是前四年发表的论文的引文。CiteScore的意义在于，它可以为学术界提供一种新的、更全面、更客观地评价期刊影响力的方法，而不仅仅是通过影响因子(IF)这一单一指标来评价。

历年Cite Score趋势图

中科院SCI分区Human Genetics 中科院分区

中科院 2023年12月升级版 综述期刊：否 Top期刊：否

大类学科	分区	小类学科	分区
生物学	2区	GENETICS & HEREDITY 遗传学	2区

中科院分区表 是以客观数据为基础，运用科学计量学方法对国际、国内学术期刊依据影响力进行等级划分的期刊评价标准。它为我国科研、教育机构的管理人员、科研工作者提供了一份评价国际学术期刊影响力的参考数据，得到了全国各地高校、科研机构的广泛认可。

中科院分区表 将所有期刊按照一定指标划分为1区、2区、3区、4区四个层次，类似于“优、良、及格”等。最开始，这个分区只是为了方便图书管理及图书情报领域的研究和期刊评估。之后中科院分区逐步发展成为了一种评价学术期刊质量的重要工具。

历年中科院分区趋势图

JCR分区Human Genetics JCR分区

2023-2024 年最新版

按JIF指标学科分区	收录子集	分区	排名	百分位
学科：GENETICS & HEREDITY	SCIE	Q2	49 / 191	74.6%

按JCI指标学科分区	收录子集	分区	排名	百分位
学科：GENETICS & HEREDITY	SCIE	Q1	43 / 191	77.75%

JCR分区的优势在于它可以帮助读者对学术文献质量进行评估。不同学科的文章引用量可能存在较大的差异，此时单独依靠影响因子(IF)评价期刊的质量可能是存在一定问题的。因此，JCR将期刊按照学科门类和影响因子分为不同的分区，这样读者可以根据自己的研究领域和需求选择合适的期刊。

历年影响因子趋势图

发文数据

2023-2024 年国家/地区发文量统计

国家/地区数量
USA180
England54
France54
CHINA MAINLAND53
GERMANY (FED REP GER)40
Canada32
Italy24
Netherlands23
Japan17
Australia16

本刊中国学者近年发表论文

1、Comprehensive interpretation of single-nucleotide substitutions in GJB2 reveals the genetic and phenotypic landscape of GJB2-related hearing loss
Author: Xiang, Jiale; Sun, Xiangzhong; Song, Nana; Ramaswamy, Sathishkumar; Abou Tayoun, Ahmad N.; Peng, Zhiyu

Journal: HUMAN GENETICS. 2023; Vol. 142, Issue 1, pp. 33-43. DOI: 10.1007/s00439-022-02479-0
2、Dissection of mendelian predisposition and complex genetic architecture of craniovertebral junction malformation
Author: Liu, Zhenlei; Du, Huakang; Zhao, Hengqiang; Cai, Siyi; Zhao, Sen; Niu, Yuchen; Li, Xiaoxin; Liu, Bowen; Huang, Yingzhao; Shao, Jiashen; Liu, Lian; Tian, Ye; Wu, Zhihong; Wu, Hao; Hu, Yue; Zhang, Terry Jianguo; Jian, Fengzeng; Wu, Nan

Journal: HUMAN GENETICS. 2023; Vol. 142, Issue 1, pp. 89-101. DOI: 10.1007/s00439-022-02474-5
3、Truncation mutations in MYRF underlie primary angle closure glaucoma
Author: Ouyang, Jiamin; Sun, Wenmin; Shen, Huangxuan; Liu, Xing; Wu, Yingchen; Jiang, Hongmei; Li, Xueqing; Wang, Yingwei; Jiang, Yi; Li, Shiqiang; Xiao, Xueshan; Hejtmancik, J. Fielding; Tan, Zhiqun; Zhang, Qingjiong

Journal: HUMAN GENETICS. 2023; Vol. 142, Issue 1, pp. 103-123. DOI: 10.1007/s00439-022-02487-0
4、Common genetic risk factors in ASD and ADHD co-occurring families
Author: Zhou, Anbo; Cao, Xiaolong; Mahaganapathy, Vaidhyanathan; Azaro, Marco; Gwin, Christine; Wilson, Sherri; Buyske, Steven; Bartlett, Christopher W.; Flax, Judy F.; Brzustowicz, Linda M.; Xing, Jinchuan

Journal: HUMAN GENETICS. 2023; Vol. 142, Issue 2, pp. 217-230. DOI: 10.1007/s00439-022-02496-z
5、Profiling human pathogenic repeat expansion regions by synergistic and multi-level impacts on molecular connections
Author: Fan, Cong; Chen, Ken; Wang, Yukai; Ball, Edward, V; Stenson, Peter D.; Mort, Matthew; Bacolla, Albino; Kehrer-Sawatzki, Hildegard; Tainer, John A.; Cooper, David N.; Zhao, Huiying

Journal: HUMAN GENETICS. 2023; Vol. 142, Issue 2, pp. 245-274. DOI: 10.1007/s00439-022-02500-6
6、Identifying shared genetic factors underlying epilepsy and congenital heart disease in Europeans
Author: Wu, Yiming; Bayrak, Cigdem Sevim; Dong, Bosi; He, Shixu; Stenson, Peter D.; Cooper, David N.; Itan, Yuval; Chen, Lei

Journal: HUMAN GENETICS. 2023; Vol. 142, Issue 2, pp. 275-288. DOI: 10.1007/s00439-022-02502-4
7、Variations in mitochondrial DNA coding and d-loop region are associated with early embryonic development defects in infertile women
Author: Liu, Yuqing; Zhao, Shuai; Chen, Xiaolei; Bian, Yuehong; Cao, Yongzhi; Xu, Peiwen; Zhang, Changming; Zhang, Jiangtao; Zhao, Shigang; Zhao, Han

Journal: HUMAN GENETICS. 2023; Vol. 142, Issue 2, pp. 193-200. DOI: 10.1007/s00439-022-02505-1
8、Hearing of Otof-deficient mice restored by trans-splicing of N- and C-terminal otoferlin
Author: Tang, Honghai; Wang, Hui; Wang, Shengyi; Hu, Shao Wei; Lv, Jun; Xun, Mengzhao; Gao, Kaiyu; Wang, Fang; Chen, Yuxin; Wang, Daqi; Wang, Wuqing; Li, Huawei; Shu, Yilai

Journal: HUMAN GENETICS. 2023; Vol. 142, Issue 2, pp. 289-304. DOI: 10.1007/s00439-022-02504-2