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 2022-05-01 to 2026-05-01.)
ArticleCitations
Acknowledgement to Reviewers43
A Common Variant of ARRB2 Promoter Region Associated with the Prognosis of Heart Failure5
A Common Variant in NID1 Gene Associated with the Prognosis of Heart Failure5
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
The Diagnostic Value of miR-124a Expression in Peripheral Blood and Synovial Fluid of Patients with Rheumatoid Arthritis3
Acknowledgement to Reviewers2
Weighted Burden Analysis of Rare Genetic Variants Identifies Novel Genes with Effects on BMI2
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
Polymorphisms of Placental Iodothyronine Deiodinase Genes in a Rural Area of Northern China with High Prevalence of Neural Tube Defects1
Reduction of Missed Diagnosis of G6PD Deficiency in Heterozygous Females by G6PD/6PGD Ratio Assay Combined with Amplification Refractory Mutation System PCR1
Acknowledgement to Reviewers1
Implications of the Co-Dominance Model for Hardy-Weinberg Testing in Genetic Association Studies1
Parental Consanguinity and Family History in Relation to Psoriasis and the Role of Sex: A Case-Control Study0
Methods and Software to Analyze Gene-Environment Interactions under a Case-Mother-Control-Mother Design with Partially Missing Child Genotype0
RNA-Based Next-Generation Sequencing Approach to Non-Small Cell Lung Cancer: A Single-Center Experience in Turkey0
Violation of the Constant Genetic Effect Assumption Can Result in Biased Estimates for Non-Linear Mendelian Randomization0
Joint Linkage and Association Analysis Using GENEHUNTER-MODSCORE with an Application to Familial Pancreatic Cancer0
A Novel c.3636-4 A&gt;G Mutation in the <i>CCDC88C</i> Plays a Causative Role in Familial Spinocerebellar Ataxia0
Place of Concordance-Discordance Model in Evaluating Next-Generation Sequencing Performance0
Erratum0
51st European Mathematical Genetics Meeting (EMGM) 20230
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
Molecular Characterization of Two Hypertension Pedigrees Carrying Mitochondrial tRNA Gln 4386T>C Mutation0
Two novel variants of the CAPN3 gene in Chinese patients with Limb-Girdle Muscular Dystrophy Recessive 10
Proteinase-Activated Receptor 2 Expression and F2RL1 Genetic Variants Are Associated with Asthma: A Case-Control Study in the Chinese Population0
Exploratory Analysis of HMGB1 Genetic Variants and Their Potential Association with Lung Cancer Susceptibility and Chemotherapy Response in a Chinese Population0
Generalized Stable Population and Agent-Based Models of Phenotypic Transmission in Human Populations, with an Application to Body Size0
Identification of a Hypoxia-Related Signature as Candidate Detector for Schizophrenia Based on Genome-Wide Gene Expression0
A statistical testing strategy accounting for random and non-random (skewed) X-chromosome inactivation identifies lung cancer susceptibility loci among smokers0
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