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 2022-01-01 to 2026-01-01.)
ArticleCitations
Acknowledgement to Reviewers38
A Common Variant of ARRB2 Promoter Region Associated with the Prognosis of Heart Failure6
A Novel <i>PMVK </i>Variant Associated with Familial Porokeratosis5
comorbidPGS: an R package assessing shared predisposition between Phenotypes using Polygenic Scores4
A Common Variant in NID1 Gene Associated with the Prognosis of Heart Failure4
Investigation of Recessive Effects of Coding Variants on Common Clinical Phenotypes in Exome-Sequenced UK Biobank Participants3
The Diagnostic Value of miR-124a Expression in Peripheral Blood and Synovial Fluid of Patients with Rheumatoid Arthritis3
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 Pedigree3
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
Common Variants in Neuraminidase Genes Contribute to Predisposition to and Progression of Chronic Heart Failure2
Acknowledgement to Reviewers2
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 O2
Weighted Burden Analysis of Rare Genetic Variants Identifies Novel Genes with Effects on BMI2
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