Human Genetics SCIE

国际简称：HUM GENET 参考译名：人类遗传学

主要研究方向：生物-遗传学非预警期刊审稿周期：约1月

《人类遗传学》(Human Genetics)是一本由Springer Berlin Heidelberg出版的以生物-遗传学为研究特色的国际期刊，发表该领域相关的原创研究文章、评论文章和综述文章，及时报道该领域相关理论、实践和应用学科的最新发现，旨在促进该学科领域科学信息的快速交流。该期刊是一本未开放期刊，近三年没有被列入预警名单。该期刊享有很高的科学声誉，影响因子不断增加，发行量也同样高。

2区中科院分区
Q2 JCR分区
106 年发文量
3.8 IF影响因子
未开放 是否OA
126 H-index
1964 创刊年份
Monthly 出版周期
English 出版语言

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.

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Human Genetics期刊信息

ISSN：0340-6717
出版语言：English
是否OA：未开放
E-ISSN：1432-1203
出版地区：UNITED STATES
是否预警：否
出版商：Springer Berlin Heidelberg
出版周期：Monthly
创刊时间：1964
开源占比：0.303
Gold OA文章占比：37.64%
OA被引用占比：0.2666...
出版国人文章占比：0.07
出版撤稿占比：0
研究类文章占比：79.25%

Human Genetics CiteScore评价数据（2024年最新版）

CiteScore

SJR

SNIP

CiteScore 指数

10.8

2.049

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%

名词解释：CiteScore 是衡量期刊所发表文献的平均受引用次数，是在 Scopus 中衡量期刊影响力的另一个指标。当年CiteScore 的计算依据是期刊最近4年（含计算年度）的被引次数除以该期刊近四年发表的文献数。例如，2022年的 CiteScore 计算方法为：2022年的 CiteScore =2019-2022年收到的对2019-2022年发表的文件的引用数量÷2019-2022年发布的文献数量注：文献类型包括：文章、评论、会议论文、书籍章节和数据论文。

Human Genetics中科院评价数据

中科院 2023年12月升级版

Top期刊	综述期刊	大类学科		小类学科
否	否	生物学	2区	GENETICS & HEREDITY 遗传学	2区

中科院 2022年12月升级版

Top期刊	综述期刊	大类学科		小类学科
否	否	生物学	2区	GENETICS & HEREDITY 遗传学	2区

中科院 2021年12月旧的升级版

Top期刊	综述期刊	大类学科		小类学科
否	否	生物学	2区	GENETICS & HEREDITY 遗传学	3区

中科院 2021年12月基础版

Top期刊	综述期刊	大类学科		小类学科
否	否	生物	2区	GENETICS & HEREDITY 遗传学	2区

中科院 2021年12月升级版

Top期刊	综述期刊	大类学科		小类学科
否	否	生物学	2区	GENETICS & HEREDITY 遗传学	3区

中科院 2020年12月旧的升级版

Top期刊	综述期刊	大类学科		小类学科
否	否	生物学	2区	GENETICS & HEREDITY 遗传学	2区

Human Genetics JCR评价数据（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%

Human Genetics历年数据统计

影响因子

中科院分区

Human Genetics中国学者发文选摘

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