Impact Factor
2.02
Journal Citation Impact
Estimated influence, citation density, publishing volume, and citation integrity from the analytics table.
Citation rate
1.38
28 total citations
h5-index
6
h5 depth signal
Cited share
38.1%
8 of 21
Total citations
28
Citation footprint
Metric signal
0.57
External metric anchor
Self-citation
3.6%
1 self-citations
Citations Trend
Monthly Publications Cadence
Citing Geographic Demographics
United States
38
China
24
United Kingdom
6
France
5
Morocco
4
Citing Fields of Research
Genetics & Genomics
97
Statistical Methods
20
Evolutionary Genomics
8
Lung Cancer
7
AI & Machine Learning
7
Publishing Activity & Reach
Volume, recency, access pattern, and citing-community signals from the journal analytics record.
All-time article footprint
4,265
Articles tracked across the journal lifetime
Indexed publication set
21
8 cited publications
Last 12 months
6
1.2 publications/month
Open access share
100.0%
6 OA publications in the last year
Leading citing country
United States
38 citing publications
Leading citing field
Genetics & Genomics
97 citing publications
Latest tracked publication
10 October 2026
10 recent records available
Coverage & Indexing History
v19n1, 1969-
v19n1, 1969-
Active Coverage
Research Focus & Classification
Indexed Subjects
Genetics & Genomics
Lung Cancer
Musculoskeletal Disorders
Mitochondria
Cardiology
Broad Categories
Genetics, Medical
Genetics & Genomics
Musculoskeletal Disorders
Lung Cancer
Neurodegenerative Disorders
MeSH Descriptors
Genetics, Medical
Latest Publications
Recent article records with DOI-first linking and condensed abstracts.
01
DOI 10.1159/hhe/adcag001
Open DOI
Association between ABCB1 gene polymorphism and response to levetiracetam treatment in focal epilepsy: a prospective case-control study in a Chinese population
Background Epilepsy affects millions of people worldwide, and drug-resistant epilepsy (DRE) poses significant challenges. This investigation examined the relationship between ABCB1 gene variations and the efficacy of levetiracetam (LEV) ...
02
DOI 10.1159/000553247
Open DOI
A frequentist test of proportional colocalization after selecting relevant genetic variants
Colocalization analyses assess whether two traits are affected by the same or distinct causal genetic variants in a single gene region. A class of Bayesian enumeration colocalization tests are now routinely used in practice; for example,...
03
DOI 10.1159/000552488
Open DOI
Comparative profiles of pediatric Mendeliome: A Single-Centre 572-Whole-Exome Sequencing Study in Xinjiang
Objective: To compare the diagnostic yields and utility of whole-exome sequencing (WES) for Mendelian disorders in pediatric patients of different ethnic backgrounds in Xinjiang. Methods: A retrospective analysis of 572 pediatric patient...
04
DOI 10.1159/000553528
Open DOI
Investigation of the Effects of Noncoding LDLR Variants on Hyperlipidaemia risk
Introduction: Coding and noncoding variants of the LDLR gene have been reported to cause familial hyperlipidaemia (FH) and rare coding variants have been shown to increase risk of hyperlipidaemia in the general population. Methods: Hyper...
05
06
DOI 10.1159/000549745
Open DOI
Exploratory Analysis of HMGB1 Genetic Variants and Their Potential Association with Lung Cancer Susceptibility and Chemotherapy Response in a Chinese Population
Background High-mobility group box 1 (HMGB1) protein plays a significant role in cancer development and treatment response. The current research on the role of HMGB1 in lung cancer and its treatment outcomes is limited and inconsistent. ...
07
DOI 10.1159/000549053
Open DOI
Generalized Stable Population and Agent-Based Models of Phenotypic Transmission in Human Populations, with an Application to Body Size
Introduction: We show that generalizations of stable population (GSPM) and agent-based models (ABMs) are useful tools to simulate trajectories of human phenotypes. Although mathematically very different, both classes of models can simult...
08
DOI 10.1159/000549356
Open DOI
Acknowledgement to Reviewers
09
DOI 10.1159/000549644
Open DOI
Weighted Burden Analysis of Rare Genetic Variants Identifies Novel Genes with Effects on BMI
Introduction: A previous study of 200,000 exome-sequenced UK Biobank participants investigating the association between rare coding variants and BMI had implicated two genes, MC4R and PCSK1, at exome-wide significance. In addition, furth...
10
DOI 10.1159/000547925
Open DOI
Proteinase-Activated Receptor 2 Expression and F2RL1 Genetic Variants Are Associated with Asthma: A Case-Control Study in the Chinese Population
Introduction: Asthma is a chronic respiratory disorder characterized by airway inflammation, hyperresponsiveness, and reversible airflow obstruction. Despite therapeutic strategies, asthma remains inadequately controlled in many patients...
Bibliographical & Catalog Notes
Print issues ceased with 2021.
Also available online.
Continues Acta genetica et statistica medica.
Vol. 37, no. 1 (1987)19920828 Notice published Printed on acid-free paper