Human Heredity

Papers
(The TQCC of Human Heredity is 2. 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 2021-09-01 to 2025-09-01.)
ArticleCitations
Acknowledgement to Reviewers31
A Common Variant of ARRB2 Promoter Region Associated with the Prognosis of Heart Failure6
A common variant in NID1 gene associated with the prognosis of heart failure4
comorbidPGS: an R package assessing shared predisposition between Phenotypes using Polygenic Scores4
A Novel <i>PMVK </i>Variant Associated with Familial Porokeratosis4
Investigation of Recessive Effects of Coding Variants on Common Clinical Phenotypes in Exome-Sequenced UK Biobank Participants3
Common Variants in Neuraminidase Genes Contribute to Predisposition to and Progression of Chronic Heart Failure2
Reduction of Missed Diagnosis of G6PD Deficiency in Heterozygous Females by G6PD/6PGD Ratio Assay Combined with Amplification Refractory Mutation System PCR2
The Diagnostic Value of miR-124a Expression in Peripheral Blood and Synovial Fluid of Patients with Rheumatoid Arthritis2
A Comprehensive Study of Disease-Causing Variants in <i>PAH</i>, <i>QDPR</i>, <i>PTS</i>, and <i>PCD</i> Genes in Iranian Patients with Hyperphenylalani2
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
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