Human Heredity

Papers
(The median citation count 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 2021-05-01 to 2025-05-01.)
ArticleCitations
Acknowledgement to Reviewers26
A Common Variant of ARRB2 Promoter Region Associated with the Prognosis of Heart Failure5
A Novel <i>PMVK </i>Variant Associated with Familial Porokeratosis4
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
comorbidPGS: an R package assessing shared predisposition between Phenotypes using Polygenic Scores2
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 Diagnostic Value of miR-124a Expression in Peripheral Blood and Synovial Fluid of Patients with Rheumatoid Arthritis2
Common Variants in Neuraminidase Genes Contribute to Predisposition to and Progression of Chronic Heart Failure2
Investigation of Recessive Effects of Coding Variants on Common Clinical Phenotypes in Exome-Sequenced UK Biobank Participants2
Reduction of Missed Diagnosis of G6PD Deficiency in Heterozygous Females by G6PD/6PGD Ratio Assay Combined with Amplification Refractory Mutation System PCR1
Mutational Screening for Mitochondrial tRNA Genes in 100 Women with Pre-Eclampsia1
Family History of Breast Cancer Is Associated with Elevated Risk of Prostate Cancer: Evidence for Shared Genetic Risks1
Polymorphisms of Placental Iodothyronine Deiodinase Genes in a Rural Area of Northern China with High Prevalence of Neural Tube Defects1
Implications of the Co-Dominance Model for Hardy-Weinberg Testing in Genetic Association Studies1
A Novel c.3636-4 A&gt;G Mutation in the <i>CCDC88C</i> Plays a Causative Role in Familial Spinocerebellar Ataxia1
Identification of <b><i>CHEK2</i></b> Germline Mutations in <b><i>BRCA1/2-</i></b> and <b><i>PALB2</i></b>-Negative Breast and O1
Acknowledgement to Reviewers1
Identification of a Novel Mutation in Patients with Type A Insulin Resistance Syndrome1
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