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GENETIC EPIDEMIOLOGY
ISSN：0741-0395

GENETIC EPIDEMIOLOGY

GENET EPIDEMIOL
学科领域：医学
是否预警：不在预警名单内
是否OA：否
录用周期：较慢,6-12周
新锐分区：医学4区
年发文量：42
影响因子：3.8
JCR分区：Q1

基本信息

《遗传流行病学》是一本同行评审期刊，讨论人类特征在家庭和人群中分布的遗传原因。遗传流行病学主要发表统计遗传学方面的论文，这是一个研究领域，主要关注发展统计学、生物信息学和计算模型来分析遗传数据。将基础生物学和群体遗传学纳入概念模型是有利的。该杂志寻求原创文章，包括应用研究或创新的统计，数学，计算，或基因组学方法，推进遗传流行病学的研究。鼓励其他类型的报告，如给编辑的信、主题评论和来自其他研究领域的观点，这些可能会丰富遗传流行病学领域。
0741-0395SCIE/Scopus收录
3.8
点击查看最新影响趋势>
3.3
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4区
GENETICS & HEREDITY 遗传学
3区
MATHEMATICAL & COMPUTATIONAL BIOLOGY 数学与计算生物学
3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
Q2
49/192
学科：MATHEMATICAL & COMPUTATIONAL BIOLOGY
SCIE
Q1
11/67
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
Q2
72/192
学科：MATHEMATICAL & COMPUTATIONAL BIOLOGY
SCIE
Q2
20/67
88
42
点击查看年发文量趋势图>
5%一般较慢,6-12周-医学-公共卫生、环境卫生与职业卫生
2.6%
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
97.62%44.95%-
CiteScore：4.10
SJR：0.970
SNIP：0.673
学科类别分区排名百分位
大类：Medicine
小类：Epidemiology
Q2
61 / 158
大类：Medicine
小类：Genetics (clinical)
Q3
54 / 100

期刊高被引文献

Generalizing polygenic risk scores from Europeans to Hispanics/Latinos
来源期刊：Genetic EpidemiologyDOI：10.1002/gepi.22166
The eMERGE genotype set of 83,717 subjects imputed to ~40\u2009million variants genome wide and association with the herpes zoster medical record phenotype
来源期刊：Genetic EpidemiologyDOI：10.1002/gepi.22167
Loss of function, missense, and intronic variants in NOTCH1 confer different risks for left ventricular outflow tract obstructive heart defects in two European cohorts
来源期刊：Genetic EpidemiologyDOI：10.1002/gepi.22176
Constrained instruments and their application to Mendelian randomization with pleiotropy
来源期刊：Genetic EpidemiologyDOI：10.1002/gepi.22184
Genetic overlap between autoimmune diseases and non‐Hodgkin lymphoma subtypes
来源期刊：Genetic EpidemiologyDOI：10.1002/gepi.22242
Ordered multinomial regression for genetic association analysis of ordinal phenotypes at Biobank scale
来源期刊：Genetic EpidemiologyDOI：10.1002/gepi.22276
Spinning convincing stories for both true and false association signals
来源期刊：Genetic EpidemiologyDOI：10.1002/gepi.22189
ComPaSS‐GWAS: A method to reduce type I error in genome‐wide association studies when replication data are not available
来源期刊：Genetic EpidemiologyDOI：10.1002/gepi.22168
An adaptive test for meta‐analysis of rare variant association studies
来源期刊：Genetic EpidemiologyDOI：10.1002/gepi.22273
Using GWAS top hits to inform priors in Bayesian fine‐mapping association studies
来源期刊：Genetic EpidemiologyDOI：10.1002/gepi.22212
Bayesian variable selection using partially observed categorical prior information in fine‐mapping association studies
来源期刊：Genetic EpidemiologyDOI：10.1002/gepi.22213
Using Bayes model averaging to leverage both gene main effects and G\u2009×\u2009\nE interactions to identify genomic regions in genome‐wide association studies
来源期刊：Genetic EpidemiologyDOI：10.1002/gepi.22171
Summary statistic analyses can mistake confounding bias for heritability
来源期刊：Genetic EpidemiologyDOI：10.1002/gepi.22259
Rare variant association testing for multicategory phenotype
来源期刊：Genetic EpidemiologyDOI：10.1002/gepi.22210
A comparison of popular TDT‐generalizations for family‐based association analysis
来源期刊：Genetic EpidemiologyDOI：10.1002/gepi.22181
Gene–environment interactions related to blood pressure traits in two community‐based Korean cohorts
来源期刊：Genetic EpidemiologyDOI：10.1002/gepi.22195
A novel association of rs13334070 in the RPGRIP1L gene with adiposity factors discovered by joint linkage and linkage disequilibrium analysis in Iranian pedigrees: Tehran Cardiometabolic Genetic Study (TCGS)
来源期刊：Genetic EpidemiologyDOI：10.1002/gepi.22179
Correlations between relatives: From Mendelian theory to complete genome sequence
来源期刊：Genetic EpidemiologyDOI：10.1002/gepi.22206
PAMAM: Power analysis in multiancestry admixture mapping
来源期刊：Genetic EpidemiologyDOI：10.1002/gepi.22216
System for Quality‐Assured Data Analysis: Flexible, reproducible scientific workflows
来源期刊：Genetic EpidemiologyDOI：10.1002/gepi.22178
Heritability analysis of nontraditional glycemic biomarkers in the Atherosclerosis Risk in Communities Study
来源期刊：Genetic EpidemiologyDOI：10.1002/gepi.22243
Population genetic simulation study of power in association testing across genetic architectures and study designs
来源期刊：Genetic EpidemiologyDOI：10.1002/gepi.22264
Powerful statistical method to detect disease‐associated genes using publicly available genome‐wide association studies summary data
来源期刊：Genetic EpidemiologyDOI：10.1002/gepi.22251
Extended methods for gene–environment‐wide interaction scans in studies of admixed individuals with varying degrees of relationships
来源期刊：Genetic EpidemiologyDOI：10.1002/gepi.22196
Effect of population stratification on SNP‐by‐environment interaction
来源期刊：Genetic EpidemiologyDOI：10.1002/gepi.22250
Exome chip‐driven association study of lipidemia in >14,000 Koreans and evaluation of genetic effect on identified variants between different ethnic groups
来源期刊：Genetic EpidemiologyDOI：10.1002/gepi.22208
Estimation of DNA contamination and its sources in genotyped samples
来源期刊：Genetic EpidemiologyDOI：10.1002/gepi.22257
Exact variance component tests for longitudinal microbiome studies
来源期刊：Genetic EpidemiologyDOI：10.1002/gepi.22185
Powerful rare variant association testing in a copula‐based joint analysis of multiple phenotypes
来源期刊：Genetic EpidemiologyDOI：10.1002/gepi.22265
Assessing potential shared genetic aetiology between body mass index and sleep duration in 142,209 individuals
来源期刊：Genetic EpidemiologyDOI：10.1002/gepi.22174
Analytical strategies to include the X‐chromosome in variance heterogeneity analyses: Evidence for trait‐specific polygenic variance structure
来源期刊：Genetic EpidemiologyDOI：10.1002/gepi.22247
Some statistical consideration in transcriptome‐wide association studies
来源期刊：Genetic EpidemiologyDOI：10.1002/gepi.22274
Presidential address: Six open questions to genetic epidemiologists
来源期刊：Genetic EpidemiologyDOI：10.1002/gepi.22191
Beyond the traditional simulation design for evaluating type 1 error control: From the “theoretical” null to “empirical” null
来源期刊：Genetic EpidemiologyDOI：10.1002/gepi.22172
A comparison of two workflows for regulome and transcriptome‐based prioritization of genetic variants associated with myocardial mass
来源期刊：Genetic EpidemiologyDOI：10.1002/gepi.22215
Transethnic meta‐analysis of metabolic syndrome in a multiethnic study
来源期刊：Genetic EpidemiologyDOI：10.1002/gepi.22267
Familial recurrence risk with varying amount of family history
来源期刊：Genetic EpidemiologyDOI：10.1002/gepi.22193
Multi‐ethnic analysis shows genetic risk and environmental predictors interact to influence 25(OH)D concentration and optimal vitamin D intake
来源期刊：Genetic EpidemiologyDOI：10.1002/gepi.22272
Joint analysis of multiple phenotypes using a clustering linear combination method based on hierarchical clustering
来源期刊：Genetic EpidemiologyDOI：10.1002/gepi.22263
Case‐control versus case‐only estimates of gene‐environment interactions with common and misclassified clinical diagnosis
来源期刊：Genetic EpidemiologyDOI：10.1002/gepi.22266
Critical evaluation of copy number variant calling methods using DNA methylation
来源期刊：Genetic EpidemiologyDOI：10.1002/gepi.22269
Leveraging cell‐specific differentially methylated regions to identify leukocyte infiltration in adipose tissue
来源期刊：Genetic EpidemiologyDOI：10.1002/gepi.22252
Meta‐MultiSKAT: Multiple phenotype meta‐analysis for region‐based association test
来源期刊：Genetic EpidemiologyDOI：10.1002/gepi.22248
Modelling RNA‐Seq data with a zero‐inflated mixture Poisson linear model
来源期刊：Genetic EpidemiologyDOI：10.1002/gepi.22246
A simple approximation to the bias of gene–environment interactions in case–control studies with silent disease
来源期刊：Genetic EpidemiologyDOI：10.1002/gepi.22186
Population‐wide copy number variation calling using variant call format files from 6,898 individuals
来源期刊：Genetic EpidemiologyDOI：10.1002/gepi.22260
Assessing pleiotropy and mediation in genetic loci associated with chronic obstructive pulmonary disease
来源期刊：Genetic EpidemiologyDOI：10.1002/gepi.22192
An efficient integrative resampling method for gene–trait association analysis
来源期刊：Genetic EpidemiologyDOI：10.1002/gepi.22271
iFunMed: Integrative functional mediation analysis of GWAS and eQTL studies
来源期刊：Genetic EpidemiologyDOI：10.1002/gepi.22217
Combining sequence data from multiple studies: Impact of analysis strategies on rare variant calling and association results
来源期刊：Genetic EpidemiologyDOI：10.1002/gepi.22261

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学科领域：医学
影响因子：0.4
中科院分区： 4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4区
GENETICS & HEREDITY 遗传学
3区
MATHEMATICAL & COMPUTATIONAL BIOLOGY 数学与计算生物学
3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4区
GENETICS & HEREDITY 遗传学
4区
MATHEMATICAL & COMPUTATIONAL BIOLOGY 数学与计算生物学
4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4区
GENETICS & HEREDITY 遗传学
4区
MATHEMATICAL & COMPUTATIONAL BIOLOGY 数学与计算生物学
4区
否
否