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 2021-02-01 to 2025-02-01.)
ArticleCitations
Acknowledgement to Reviewers19
Family History of Breast Cancer Is Associated with Elevated Risk of Prostate Cancer: Evidence for Shared Genetic Risks4
The Diagnostic Value of miR-124a Expression in Peripheral Blood and Synovial Fluid of Patients with Rheumatoid Arthritis2
Mutational Screening for Mitochondrial tRNA Genes in 100 Women with Pre-Eclampsia2
A Common Variant of ARRB2 Promoter Region Associated with the Prognosis of Heart Failure2
51st European Mathematical Genetics Meeting (EMGM) 20232
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
A Novel <i>PMVK </i>Variant Associated with Familial Porokeratosis1
50th European Mathematical Genetics Meeting (EMGM) 20221
A Novel c.3636-4 A&gt;G Mutation in the <i>CCDC88C</i> Plays a Causative Role in Familial Spinocerebellar Ataxia1
Violation of the Constant Genetic Effect Assumption Can Result in Biased Estimates for Non-Linear Mendelian Randomization1
Genetic Analyses of Enamel Hypoplasia in Multiethnic Cohorts1
Two novel variants of the CAPN3 gene in Chinese patients with Limb-Girdle Muscular Dystrophy Recessive 11
Identification of a Novel Mutation in Patients with Type A Insulin Resistance Syndrome1
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
Implications of the Co-Dominance Model for Hardy-Weinberg Testing in Genetic Association Studies0
Screening for Mitochondrial tRNA Mutations in 318 Patients with Dilated Cardiomyopathy0
Common Variants in Neuraminidase Genes Contribute to Predisposition to and Progression of Chronic Heart Failure0
Joint Linkage and Association Analysis Using GENEHUNTER-MODSCORE with an Application to Familial Pancreatic Cancer0
comorbidPGS: an R package assessing shared predisposition between Phenotypes using Polygenic Scores0
Penalized Logistic Regression Analysis for Genetic Association Studies of Binary Phenotypes0
Identification of a Hypoxia-Related Signature as Candidate Detector for Schizophrenia Based on Genome-Wide Gene Expression0
Acknowledgement to Reviewers0
Place of Concordance-Discordance Model in Evaluating Next-Generation Sequencing Performance0
Methods and Software to Analyze Gene-Environment Interactions under a Case-Mother-Control-Mother Design with Partially Missing Child Genotype0
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 Hyperphenylalani0
Parental consanguinity and family history in relation to psoriasis and the role of sex: a case-control study0
Polymorphisms of Placental Iodothyronine Deiodinase Genes in a Rural Area of Northern China with High Prevalence of Neural Tube Defects0
Investigation of Recessive Effects of Coding Variants on Common Clinical Phenotypes in Exome-Sequenced UK Biobank Participants0
Screening for Mitochondrial tRNA Variants in 200 Patients with Systemic Lupus Erythematosus0
A statistical testing strategy accounting for random and non-random (skewed) X-chromosome inactivation identifies lung cancer susceptibility loci among smokers0
Reduction of Missed Diagnosis of G6PD Deficiency in Heterozygous Females by G6PD/6PGD Ratio Assay Combined with Amplification Refractory Mutation System PCR0
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 O0
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