
Academic Journal
Q4Human Heredity
About Human Heredity
Human Heredity is a scholarly journal published by S. Karger AG. SCImago 2025 lists it in Q4, with an SJR of 0.265 and H-index of 67.
Coverage: 1950-1954, 1956-2026. Research categories: Genetics (Q4); Genetics (clinical) (Q4).
Open-access policies and author information
Reported in the official DOAJ public CSV snapshot (2026-09-01), downloaded 2026-10-03. Record updated 2025-11-10. This snapshot does not establish today’s listing status or fee quotation.
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Source-backed journal facts
Topics in published research
Genetic Associations and Epidemiology; Genetic Mapping and Diversity in Plants and Animals; Diverse Scientific and Economic Studies; Blood groups and transfusion; Human auditory perception and evaluation; Hemoglobinopathies and Related Disorders.
OpenAlex classifies topics from published works. These topics are not the publisher’s official aims and scope.
Source: OpenAlex source record. Retrieved 2026-10-03. Source record updated 2026-10-02. OpenAlex metrics are different from SCImago metrics and the Clarivate Journal Impact Factor.
Journal Metrics
Quartile, SJR and the listed SCImago H-index use the 2025 imported SCImago dataset. A quartile may vary by subject category. Values without a source or reporting year are unverified historical entries. Verify the current Journal Impact Factor with Clarivate or the publisher before using it.
Aims & Scope
The publisher’s official aims and scope have not yet been verified for this profile. Use the journal website to check subject fit and accepted article types before submitting.
Recent Research Articles
Latest publications matched automatically by ISSN.
A frequentist test of proportional colocalization after selecting relevant genetic variants
Ashish Patel, John C. Whittaker, Stephen Burgess
2026-09-04 · DOI: 10.1159/000553247Investigation of the Effects of Noncoding LDLR Variants on Hyperlipidaemia risk
Daniela Rojano, David Curtis
2026-07-10 · DOI: 10.1159/000553528Comparative Profiles of Pediatric Mendeliome: A Single-Center 572-Whole-Exome Sequencing Study in Xinjiang
Yan Li, Chen Cao, Yanfei Luo, Guanghui Sun et al.
2026-05-20 · DOI: 10.1159/000552488Erratum
2026-03-18 · DOI: 10.1159/000551109Exploratory Analysis of HMGB1 Genetic Variants and Their Potential Association with Lung Cancer Susceptibility and Chemotherapy Response in a Chinese Population
Qing Li, Li Yan, Hongjing Li, Li Zhang et al.
2025-12-18 · DOI: 10.1159/000549745Acknowledgement to Reviewers
2025-12-17 · DOI: 10.1159/000549356Generalized Stable Population and Agent-Based Models of Phenotypic Transmission in Human Populations, with an Application to Body Size
Néstor Aldea, Aitor García-Aguirre, Hiram Beltrán-Sánchez, Sebastián Daza et al.
2025-11-28 · DOI: 10.1159/000549053Weighted Burden Analysis of Rare Genetic Variants Identifies Novel Genes with Effects on BMI
David Curtis
2025-11-19 · DOI: 10.1159/000549644Proteinase-Activated Receptor 2 Expression and F2RL1 Genetic Variants Are Associated with Asthma: A Case-Control Study in the Chinese Population
Guohuan Chen, Bizhi Zheng, Jinhe Cui
2025-08-19 · DOI: 10.1159/000547925A Common Variant in NID1 Gene Associated with the Prognosis of Heart Failure
Dong Hu, Jing Zhao, Dongyang Wu, Lei Xiao et al.
2025-08-14 · DOI: 10.1159/000547663Molecular Characterization of Two Hypertension Pedigrees Carrying Mitochondrial tRNA Gln 4386T>C Mutation
Zhongshun Luo, Jiayu Lin, Jiazhen Ji, Meixia Zhang et al.
2025-07-31 · DOI: 10.1159/000547311Easy-PSAP: An Integrated Workflow to Prioritize Pathogenic Variants in Sequence Data from a Single Individual
Marie-Sophie C. Ogloblinsky, Marc B. Gros-La-Faige, Daniel P. Lewinsohn, Mathilde Nguyen et al.
2025-06-10 · DOI: 10.1159/000543671A Bibliometric Analysis of GWAS on Rheumatoid Arthritis from 2002 to 2024
Wen-Hui Wang, Ming-Hui Xia, Xin-Ru Liu, Shu-Feng Lei et al.
2025-04-03 · DOI: 10.1159/000543947RNA-Based Next-Generation Sequencing Approach to Non-Small Cell Lung Cancer: A Single-Center Experience in Turkey
Orhan Gorukmez, Ozlem Gorukmez, Ali Topak
2025-02-13 · DOI: 10.1159/000544697Parental Consanguinity and Family History in Relation to Psoriasis and the Role of Sex: A Case-Control Study
Alanood N. AlKhas, Ali H. Ziyab
2024-12-31 · DOI: 10.1159/000543351Acknowledgement to Reviewers
2024-12-17 · DOI: 10.1159/000542124Screening for Mitochondrial tRNA Variants in 200 Patients with Systemic Lupus Erythematosus
Dan Xuan, Fuyong Qiang, Hui Xu, Li Wang et al.
2024-11-13 · DOI: 10.1159/000542357A statistical testing strategy accounting for random and non-random (skewed) X-chromosome inactivation identifies lung cancer susceptibility loci among smokers
Rodolphe Jantzen, Sophie Camilleri-Broët, Nicole Ezer, Philippe Broët et al.
2024-06-14 · DOI: 10.1159/000539520Two novel variants of the CAPN3 gene in Chinese patients with Limb-Girdle Muscular Dystrophy Recessive 1
Lulu Zhang, Yi Zhang, Chunru Han, Juean Jiang et al.
2024-06-05 · DOI: 10.1159/000539521comorbidPGS: an R package assessing shared predisposition between Phenotypes using Polygenic Scores
Vincent Pascat, Liudmila Zudina, Anna Ulrich, Jared G. Maina et al.
2024-05-13 · DOI: 10.1159/000539325Reviews
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Version History
October 4, 2026 at 9:32 pm
October 2, 2026