Human Heredity

Papers
(The median citation count of Human Heredity is 0. 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 Novel <i>PMVK </i>Variant Associated with Familial Porokeratosis4
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
Investigation of Recessive Effects of Coding Variants on Common Clinical Phenotypes in Exome-Sequenced UK Biobank Participants3
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
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
Polymorphisms of Placental Iodothyronine Deiodinase Genes in a Rural Area of Northern China with High Prevalence of Neural Tube Defects1
Identification of a Novel Mutation in Patients with Type A Insulin Resistance Syndrome1
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
Family History of Breast Cancer Is Associated with Elevated Risk of Prostate Cancer: Evidence for Shared Genetic Risks1
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
Joint Linkage and Association Analysis Using GENEHUNTER-MODSCORE with an Application to Familial Pancreatic Cancer0
51st European Mathematical Genetics Meeting (EMGM) 20230
Place of Concordance-Discordance Model in Evaluating Next-Generation Sequencing Performance0
Screening for Mitochondrial tRNA Mutations in 318 Patients with Dilated Cardiomyopathy0
Penalized Logistic Regression Analysis for Genetic Association Studies of Binary Phenotypes0
The Prevalence of <b><i>JAK2</i></b> Exon 12 Mutations in Vietnamese Patients with <b><i>JAK2</i></b> V617F-Negative Polycythemia Vera: Frequent or Rare0
Violation of the Constant Genetic Effect Assumption Can Result in Biased Estimates for Non-Linear Mendelian Randomization0
Identification of a Hypoxia-Related Signature as Candidate Detector for Schizophrenia Based on Genome-Wide Gene Expression0
50th European Mathematical Genetics Meeting (EMGM) 20220
Molecular Characterization of Two Hypertension Pedigrees Carrying Mitochondrial tRNAGln 4386T>C Mutation0
Two novel variants of the CAPN3 gene in Chinese patients with Limb-Girdle Muscular Dystrophy Recessive 10
Methods and Software to Analyze Gene-Environment Interactions under a Case-Mother-Control-Mother Design with Partially Missing Child Genotype0
Screening for Mitochondrial tRNA Variants in 200 Patients with Systemic Lupus Erythematosus0
A Bibliometric Analysis of GWAS on Rheumatoid Arthritis from 2002 to 20240
Easy-PSAP: An Integrated Workflow to Prioritize Pathogenic Variants in Sequence Data from a Single Individual0
A statistical testing strategy accounting for random and non-random (skewed) X-chromosome inactivation identifies lung cancer susceptibility loci among smokers0
Parental Consanguinity and Family History in Relation to Psoriasis and the Role of Sex: A Case-Control Study0
Mutational Screening for Mitochondrial tRNA Genes in 100 Women with Pre-Eclampsia0
RNA-Based Next-Generation Sequencing Approach to Non-Small Cell Lung Cancer: A Single-Center Experience in Turkey0
Genetic Analyses of Enamel Hypoplasia in Multiethnic Cohorts0
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