HUMAN HEREDITY

HUMAN HEREDITY

HUM HERED
影响因子:1.5
是否综述期刊:
是否预警:不在预警名单内
是否OA:
出版国家/地区:SWITZERLAND
出版社:S. Karger AG
发刊时间:1969
发刊频率:Bimonthly
收录数据库:SCIE/Scopus收录
ISSN:0001-5652

期刊介绍

Gathering original research reports and short communications from all over the world, 'Human Heredity' is devoted to methodological and applied research on the genetics of human populations, association and linkage analysis, genetic mechanisms of disease, and new methods for statistical genetics, for example, analysis of rare variants and results from next generation sequencing. The value of this information to many branches of medicine is shown by the number of citations the journal receives in fields ranging from immunology and hematology to epidemiology and public health planning, and the fact that at least 50% of all 'Human Heredity' papers are still cited more than 8 years after publication (according to ISI Journal Citation Reports). Special issues on methodological topics (such as ‘Consanguinity and Genomics’ in 2014; ‘Analyzing Rare Variants in Complex Diseases’ in 2012) or reviews of advances in particular fields (‘Genetic Diversity in European Populations: Evolutionary Evidence and Medical Implications’ in 2014; ‘Genes and the Environment in Obesity’ in 2013) are published every year. Renowned experts in the field are invited to contribute to these special issues.
《人类遗传学》汇集了世界各地的原创研究报告和简短通讯,致力于人类群体遗传学、关联和连锁分析、疾病的遗传机制以及统计遗传学的新方法(例如罕见变异分析和下一代测序结果)的方法学和应用研究。这些信息对许多医学分支的价值体现在该杂志在免疫学、血液学、流行病学和公共卫生规划等领域收到的引用数量上,以及至少50%的“人类遗传学”论文在发表8年后仍被引用的事实(根据ISI期刊引用报告)。方法学专题专刊(如2014年的“血缘与基因组学”;“分析复杂疾病中的罕见变异”)或特定领域的进展综述(“欧洲人群的遗传多样性:2014年《进化证据与医学意义》; 2013年出版的《肥胖中的基因与环境》)每年出版。邀请该领域的著名专家对这些专题作出贡献。
年发文量 8
国人发稿量 6.22
国人发文占比 0.78%
自引率 -
平均录取率0
平均审稿周期 >12周,或约稿
版面费 -
偏重研究方向 生物-遗传学
期刊官网 http://www.karger.com/Journal/Home/224250
投稿链接 http://www.karger.com/Journal/Guidelines/224250

期刊高被引文献

Mathematical Properties of Linkage Disequilibrium Statistics Defined by Normalization of the Coefficient D = pAB – pApB
来源期刊:Human HeredityDOI:10.1159/000504171
Influence of Estrogen Receptor Alpha Polymorphism on Bone Mineral Density in Iranian Children
来源期刊:Human HeredityDOI:10.1159/000502230
Power and Sample Size Calculations for Genetic Association Studies in the Presence of Genetic Model Misspecification
来源期刊:Human HeredityDOI:10.1159/000508558
Novel IDS Variants Identified in Three Unrelated Pakistani Patients Affected with Mucopolysaccharidosis Type II (Hunter Syndrome)
来源期刊:Human HeredityDOI:10.1159/000510065
A Novel Feature Selection Method for High-Dimensional Biomedical Data Based on an Improved Binary Clonal Flower Pollination Algorithm
来源期刊:Human HeredityDOI:10.1159/000501652
The Contribution Plot: Decomposition and Graphical Display of the RV Coefficient, with Application to Genetic and Brain Imaging Biomarkers of Alzheimer’s Disease
来源期刊:Human HeredityDOI:10.1159/000501334
Further Evidence for the Implication of the MET Gene in Non-Syndromic Autosomal Recessive Deafness
来源期刊:Human HeredityDOI:10.1159/000503450
Meta-Analysis of SNP-Environment Interaction with Heterogeneity
来源期刊:Human HeredityDOI:10.1159/000504170
A Bayesian Hierarchical Framework for Pathway Analysis in Genome-Wide Association Studies
来源期刊:Human HeredityDOI:10.1159/000508664
Principal Component Analysis Based on Graph Laplacian and Double Sparse Constraints for Feature Selection and Sample Clustering on Multi-View Data
来源期刊:Human HeredityDOI:10.1159/000501653
Prediction of the RNA Secondary Structure Using a Multi-Population Assisted Quantum Genetic Algorithm
来源期刊:Human HeredityDOI:10.1159/000501480
The Association of Partial Azoospermia Factor C Deletions and Male Infertility in Northwestern China
来源期刊:Human HeredityDOI:10.1159/000504607
Heritability and Sex-Specific Genetic Effects of Self-Reported Physical Activity in a Brazilian Highly Admixed Population
来源期刊:Human HeredityDOI:10.1159/000506007
Estimating Uterine Fibroid SNP-Based Heritability in European American Women with Imaging-Confirmed Fibroids
来源期刊:Human HeredityDOI:10.1159/000501335
Frequency of BRCA1 and BRCA2 Mutations in Individuals with Breast and Ovarian Cancer in a Chinese Hakka Population Using Next-Generation Sequencing
来源期刊:Human HeredityDOI:10.1159/000505268
PSO-CFDP: A Particle Swarm Optimization-Based Automatic Density Peaks Clustering Method for Cancer Subtyping
来源期刊:Human HeredityDOI:10.1159/000501481
A Low-Rank Representation Method Regularized by Dual-Hypergraph Laplacian for Selecting Differentially Expressed Genes
来源期刊:Human HeredityDOI:10.1159/000501482
Estimating Additive Interaction Effect in Stratified Two-Phase Case-Control Design
来源期刊:Human HeredityDOI:10.1159/000502738
The Role of miR-210 in the Biological System: A Current Overview
来源期刊:Human HeredityDOI:10.1159/000509280
Test Gene-Environment Interactions for Multiple Traits in Sequencing Association Studies
来源期刊:Human HeredityDOI:10.1159/000506008
A Homozygous RAG1 Gene Mutation in a Case of Combined Immunodeficiency: Clinical, Molecular, and Computational Analysis
来源期刊:Human HeredityDOI:10.1159/000510062
Contents Vol. 84, 2019
来源期刊:Human HeredityDOI:10.1159/000512546
Unbalanced Sample Size Introduces Spurious Correlations to Genome-Wide Heterozygosity Analyses
来源期刊:Human HeredityDOI:10.1159/000507576
Front & Back Matter
来源期刊:Human HeredityDOI:10.1159/000510011

质量指标占比

研究类文章占比 OA被引用占比 撤稿占比 出版后修正文章占比
100.00%92.86%--

相关指数

影响因子
影响因子
年发文量
自引率
Cite Score

预警情况

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时间 预警情况
2025年03月发布的2025版不在预警名单中
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
*来源:中科院《 国际期刊预警名单》

JCR分区

WOS分区等级:Q4区
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WOS期刊SCI分区
WOS期刊SCI分区是指SCI官方(Web of Science)为每个学科内的期刊按照IF数值排 序,将期刊按照四等分的方法划分的Q1-Q4等级,Q1代表质量最高,即常说的1区期刊。
(2024-2025年最新版)
GENETICS & HEREDITY
Q4

中科院分区

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版本 大类学科 小类学科 Top期刊 综述期刊
2025年3月最新升级版
生物学4区
GENETICS & HEREDITY 遗传学
4区
2023年12月升级版
生物学4区
GENETICS & HEREDITY 遗传学
4区
2022年12月旧的升级版
生物学4区
GENETICS & HEREDITY 遗传学
4区