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 2022-08-01 to 2026-08-01.)
ArticleCitations
Acknowledgement to Reviewers44
A Novel <i>PMVK </i>Variant Associated with Familial Porokeratosis5
A Common Variant in NID1 Gene Associated with the Prognosis of Heart Failure5
A Common Variant of ARRB2 Promoter Region Associated with the Prognosis of Heart Failure5
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 Participants4
Weighted Burden Analysis of Rare Genetic Variants Identifies Novel Genes with Effects on BMI3
The Diagnostic Value of miR-124a Expression in Peripheral Blood and Synovial Fluid of Patients with Rheumatoid Arthritis3
Reduction of Missed Diagnosis of G6PD Deficiency in Heterozygous Females by G6PD/6PGD Ratio Assay Combined with Amplification Refractory Mutation System PCR2
Investigation of the effects of non-coding LDLR variants on hyperlipidaemia risk2
Acknowledgement to Reviewers2
Polymorphisms of Placental Iodothyronine Deiodinase Genes in a Rural Area of Northern China with High Prevalence of Neural Tube Defects1
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 Hyperphenylalani1
Implications of the Co-Dominance Model for Hardy-Weinberg Testing in Genetic Association Studies1
Identification of a Hypoxia-Related Signature as Candidate Detector for Schizophrenia Based on Genome-Wide Gene Expression0
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
Erratum0
Joint Linkage and Association Analysis Using GENEHUNTER-MODSCORE with an Application to Familial Pancreatic Cancer0
Screening for Mitochondrial tRNA Variants in 200 Patients with Systemic Lupus Erythematosus0
Violation of the Constant Genetic Effect Assumption Can Result in Biased Estimates for Non-Linear Mendelian Randomization0
Acknowledgement to Reviewers0
A statistical testing strategy accounting for random and non-random (skewed) X-chromosome inactivation identifies lung cancer susceptibility loci among smokers0
Comparative Profiles of Pediatric Mendeliome: A Single-Center 572-Whole-Exome Sequencing Study in Xinjiang0
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
A Bibliometric Analysis of GWAS on Rheumatoid Arthritis from 2002 to 20240
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
Parental Consanguinity and Family History in Relation to Psoriasis and the Role of Sex: A Case-Control Study0
51st European Mathematical Genetics Meeting (EMGM) 20230
RNA-Based Next-Generation Sequencing Approach to Non-Small Cell Lung Cancer: A Single-Center Experience in Turkey0
Methods and Software to Analyze Gene-Environment Interactions under a Case-Mother-Control-Mother Design with Partially Missing Child Genotype0
Generalized Stable Population and Agent-Based Models of Phenotypic Transmission in Human Populations, with an Application to Body Size0
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