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Human Genomics
ISSN：1473-9542

Human Genomics

HUM GENOMICS
学科领域：医学
是否预警：不在预警名单内
是否OA：是
录用周期：11 Weeks
新锐分区：医学2区
年发文量：136
影响因子：4.3
JCR分区：Q1

基本信息

《人类基因组学》是一本同行评审、开放获取的在线期刊，重点关注基因组分析在人类健康和疾病各个方面的应用，以及药物疗效和安全性的基因组分析和比较基因组学。该期刊涵盖的主题包括但不限于：药物基因组学、全基因组关联研究、全基因组测序、外显子组测序、下一代深度测序、功能基因组学、表观基因组学、翻译基因组学、表达谱分析、蛋白质组学、生物信息学、动物模型、统计遗传学、遗传流行病学、人类群体遗传学和比较基因组学。
1473-9542SCIE/Scopus收录/DOAJ开放期刊
4.3
点击查看最新影响趋势>
4
新
2026年3月发布
点击查看历史分区趋势    >
大类学科小类学科Top期刊综述期刊
医学2区
GENETICS & HEREDITY 遗传学
2区
否
N/A
新
WOS期刊SCI分区  2024-2025最新升级版
按JIF指标学科分区收集子录JIF分区JIF排名百分位
学科：GENETICS & HEREDITY
SCIE
Q1
38/192
按JCR指标学科分区收集子录JCR分区JCR排名百分位
学科：GENETICS & HEREDITY
SCIE
Q1
37/192
49
136
点击查看年发文量趋势图>
13%-11 WeeksGBP2390; USD3190; EUR2690GENETICS & HEREDITY-
2.3%
点击查看自引率趋势图>
时间预警情况
2026年03月发布的新锐学术版不在预警名单中
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
91.18%100%2.5%
CiteScore：5.40
SJR：1.381
SNIP：0.979
学科类别分区排名百分位
大类：Biochemistry, Genetics and Molecular Biology
小类：Genetics
Q2
143 / 348
大类：Biochemistry, Genetics and Molecular Biology
小类：Drug Discovery
Q2
68 / 156
大类：Biochemistry, Genetics and Molecular Biology
小类：Molecular Biology
Q3
219 / 410
大类：Biochemistry, Genetics and Molecular Biology
小类：Molecular Medicine
Q3
98 / 177

期刊高被引文献

Translating pharmacogenomics into clinical decisions: do not let the perfect be the enemy of the good
来源期刊：Human GenomicsDOI：10.1186/s40246-019-0229-z
Noninvasive prenatal testing for chromosome aneuploidies and subchromosomal microdeletions/microduplications in a cohort of 42,910 single pregnancies with different clinical features
来源期刊：Human GenomicsDOI：10.1186/s40246-019-0250-2
Interplay Between the Host, the Human Microbiome, and Drug Metabolism
来源期刊：Human GenomicsDOI：10.1186/s40246-019-0211-9
Noninvasive prenatal testing for chromosome aneuploidies and subchromosomal microdeletions/microduplications in a cohort of 8141 single pregnancies
来源期刊：Human GenomicsDOI：10.1186/s40246-019-0198-2
What influences public views on forensic DNA testing in the criminal field? A scoping review of quantitative evidence
来源期刊：Human GenomicsDOI：10.1186/s40246-019-0207-5
SLC39A8 gene encoding a metal ion transporter: discovery and bench to bedside
来源期刊：Human GenomicsDOI：10.1186/s40246-019-0233-3
Essential genetic findings in neurodevelopmental disorders
来源期刊：Human GenomicsDOI：10.1186/s40246-019-0216-4
Evidence that DNA repair genes, a family of tumor suppressor genes, are associated with evolution rate and size of genomes
来源期刊：Human GenomicsDOI：10.1186/s40246-019-0210-x
Mutations in ATP13A2 (PARK9) are associated with an amyotrophic lateral sclerosis-like phenotype, implicating this locus in further phenotypic expansion
来源期刊：Human GenomicsDOI：10.1186/s40246-019-0203-9
lncRNA TUG1 modulates proliferation, apoptosis, invasion, and angiogenesis via targeting miR-29b in trophoblast cells
来源期刊：Human GenomicsDOI：10.1186/s40246-019-0237-z
Genome-wide association study identifies novel loci for type 2 diabetes-attributed end-stage kidney disease in African Americans
来源期刊：Human GenomicsDOI：10.1186/s40246-019-0205-7
Size matters: how sample size affects the reproducibility and specificity of gene set analysis
来源期刊：Human GenomicsDOI：10.1186/s40246-019-0226-2
Considerations for the use of Cre recombinase for conditional gene deletion in the mouse lens
来源期刊：Human GenomicsDOI：10.1186/s40246-019-0192-8
Transcriptome-wide analysis of differentially expressed chemokine receptors, SNPs, and SSRs in the age-related macular degeneration
来源期刊：Human GenomicsDOI：10.1186/s40246-019-0199-1
A novel knowledge-derived data potentizing method revealed unique liver cancer-associated genetic variants
来源期刊：Human GenomicsDOI：10.1186/s40246-019-0213-7
Shared genetic underpinnings of childhood obesity and adult cardiometabolic diseases
来源期刊：Human GenomicsDOI：10.1186/s40246-019-0202-x
EFTUD2 gene deficiency disrupts osteoblast maturation and inhibits chondrocyte differentiation via activation of the p53 signaling pathway
来源期刊：Human GenomicsDOI：10.1186/s40246-019-0238-y
The multi-faceted functioning portrait of LRF/ZBTB7A
来源期刊：Human GenomicsDOI：10.1186/s40246-019-0252-0
The evolutionary genetics of lactase persistence in seven ethnic groups across the Iranian plateau
来源期刊：Human GenomicsDOI：10.1186/s40246-019-0195-5
Downregulation of miR-542-3p promotes osteogenic transition of vascular smooth muscle cells in the aging rat by targeting BMP7
来源期刊：Human GenomicsDOI：10.1186/s40246-019-0245-z
Investigating RNA expression profiles altered by nicotinamide mononucleotide therapy in a chronic model of alcoholic liver disease
来源期刊：Human GenomicsDOI：10.1186/s40246-019-0251-1
Genome-wide enriched pathway analysis of acute post-radiotherapy pain in breast cancer patients: a prospective cohort study
来源期刊：Human GenomicsDOI：10.1186/s40246-019-0212-8
Identification and potential mechanisms of a 4-lncRNA signature that predicts prognosis in patients with laryngeal cancer
来源期刊：Human GenomicsDOI：10.1186/s40246-019-0230-6
Toward a clinical diagnostic pipeline for SPINK1 intronic variants
来源期刊：Human GenomicsDOI：10.1186/s40246-019-0193-7
The significance of trisomy 7 mosaicism in noninvasive prenatal screening
来源期刊：Human GenomicsDOI：10.1186/s40246-019-0201-y
Identification of key candidate genes and molecular pathways in white fat browning: an anti-obesity drug discovery based on computational biology
来源期刊：Human GenomicsDOI：10.1186/s40246-019-0239-x
Three miRNAs cooperate with host genes involved in human cardiovascular disease
来源期刊：Human GenomicsDOI：10.1186/s40246-019-0232-4
Association of HTRA1 and ARMS2 gene polymorphisms with response to intravitreal ranibizumab among neovascular age-related macular degenerative subjects
来源期刊：Human GenomicsDOI：10.1186/s40246-019-0197-3
A semi-supervised machine learning framework for microRNA classification
来源期刊：Human GenomicsDOI：10.1186/s40246-019-0221-7
Human mitochondrial genome compression using machine learning techniques
来源期刊：Human GenomicsDOI：10.1186/s40246-019-0225-3
Association between polymorphism in CDKN2B-AS1 gene and its interaction with smoking on the risk of lung cancer in a Chinese population
来源期刊：Human GenomicsDOI：10.1186/s40246-019-0240-4
Factors affecting cell-free DNA fetal fraction: statistical analysis of 13,661 maternal plasmas for non-invasive prenatal screening
来源期刊：Human GenomicsDOI：10.1186/s40246-019-0244-0
Copy number of 8q24.3 drives HSF1 expression and patient outcome in cancer: an individual patient data meta-analysis
来源期刊：Human GenomicsDOI：10.1186/s40246-019-0241-3
Studies of liver tissue identify functional gene regulatory elements associated to gene expression, type 2 diabetes, and other metabolic diseases
来源期刊：Human GenomicsDOI：10.1186/s40246-019-0204-8
Helicobacter pylori infection, serum pepsinogens as markers of atrophic gastritis, and leukocyte telomere length: a population-based study
来源期刊：Human GenomicsDOI：10.1186/s40246-019-0217-3
Robust hypergraph regularized non-negative matrix factorization for sample clustering and feature selection in multi-view gene expression data
来源期刊：Human GenomicsDOI：10.1186/s40246-019-0222-6
Human genetics and genomics research in Ecuador: historical survey, current state, and future directions
来源期刊：Human GenomicsDOI：10.1186/s40246-019-0249-8
Transcriptome-wide association study of multiple myeloma identifies candidate susceptibility genes
来源期刊：Human GenomicsDOI：10.1186/s40246-019-0231-5
vi-HMM: a novel HMM-based method for sequence variant identification in short-read data
来源期刊：Human GenomicsDOI：10.1186/s40246-019-0194-6
Novel analytical methods to interpret large sequencing data from small sample sizes
来源期刊：Human GenomicsDOI：10.1186/s40246-019-0235-1
An embedded method for gene identification problems involving unwanted data heterogeneity
来源期刊：Human GenomicsDOI：10.1186/s40246-019-0228-0
Prediction of microbial communities for urban metagenomics using neural network approach
来源期刊：Human GenomicsDOI：10.1186/s40246-019-0224-4
HMNPPID—human malignant neoplasm protein–protein interaction database
来源期刊：Human GenomicsDOI：10.1186/s40246-019-0223-5
Correction to: The evolutionary genetics of lactase persistence in seven ethnic groups across the Iranian plateau
来源期刊：Human GenomicsDOI：10.1186/s40246-019-0200-z
Identification of a novel long non-coding RNA within RUNX1 intron 5
来源期刊：Human GenomicsDOI：10.1186/s40246-019-0219-1
Genetics and functions of the retinoic acid pathway, with special emphasis on the eye
来源期刊：Human GenomicsDOI：10.1186/s40246-019-0248-9
Common polymorphic inversions at 17q21.31 and 8p23.1 associate with cancer prognosis
来源期刊：Human GenomicsDOI：10.1186/s40246-019-0242-2
Diversity of ATM gene variants: a population-based genome data analysis for precision medicine
来源期刊：Human GenomicsDOI：10.1186/s40246-019-0234-2
Statement on bioinformatics and capturing the benefits of genome sequencing for society
来源期刊：Human GenomicsDOI：10.1186/s40246-019-0208-4
Genetic variants of VEGFR-1 gene promoter in acute myocardial infarction
来源期刊：Human GenomicsDOI：10.1186/s40246-019-0243-1

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学科领域：医学
影响因子：3.1
中科院分区： 2区
论文发表 2-4个月录用 7500+文章录用 不成功可退款
新
2026年3月发布（新锐分区）
大类学科小类学科Top期刊综述期刊
医学2区
GENETICS & HEREDITY 遗传学
2区
否
N/A
2025年3月升级版
大类学科小类学科Top期刊综述期刊
医学2区
GENETICS & HEREDITY 遗传学
2区
否
否
2023年12月旧的升级版
大类学科小类学科Top期刊综述期刊
医学3区
GENETICS & HEREDITY 遗传学
3区
否
否