Human Heredity

Papers
(The TQCC of Human Heredity is 1. The table below lists those papers that are above that threshold based on CrossRef citation counts [max. 250 papers]. The publications cover those that have been published in the past four years, i.e., from 2021-04-01 to 2025-04-01.)
ArticleCitations
Acknowledgement to Reviewers19
Family History of Breast Cancer Is Associated with Elevated Risk of Prostate Cancer: Evidence for Shared Genetic Risks4
A Common Variant of ARRB2 Promoter Region Associated with the Prognosis of Heart Failure2
51st European Mathematical Genetics Meeting (EMGM) 20232
The Mitochondrial tRNA<sup>Asp</sup> T7561C, tRNA<sup>His</sup> C12153T, and A12172G Mutations May Be Associated with Essential Hypertension in a Han Chinese Pedigree2
The Diagnostic Value of miR-124a Expression in Peripheral Blood and Synovial Fluid of Patients with Rheumatoid Arthritis2
Mutational Screening for Mitochondrial tRNA Genes in 100 Women with Pre-Eclampsia2
Two novel variants of the CAPN3 gene in Chinese patients with Limb-Girdle Muscular Dystrophy Recessive 11
Genetic Analyses of Enamel Hypoplasia in Multiethnic Cohorts1
50th European Mathematical Genetics Meeting (EMGM) 20221
A Novel <i>PMVK </i>Variant Associated with Familial Porokeratosis1
Common Variants in Neuraminidase Genes Contribute to Predisposition to and Progression of Chronic Heart Failure1
A Novel c.3636-4 A&gt;G Mutation in the <i>CCDC88C</i> Plays a Causative Role in Familial Spinocerebellar Ataxia1
Violation of the Constant Genetic Effect Assumption Can Result in Biased Estimates for Non-Linear Mendelian Randomization1
Identification of a Novel Mutation in Patients with Type A Insulin Resistance Syndrome1
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