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 2020-04-01 to 2024-04-01.)
ArticleCitations
Violation of the Constant Genetic Effect Assumption Can Result in Biased Estimates for Non-Linear Mendelian Randomization10
Association of <b><i>PNPLA3</i></b> I148M with Liver Disease Biomarkers in Latinos4
Screening for Mitochondrial tRNA Mutations in 318 Patients with Dilated Cardiomyopathy3
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
PhosSNPs-Regulated Gene Network and Pathway Significant for Rheumatoid Arthritis2
Family History of Breast Cancer Is Associated with Elevated Risk of Prostate Cancer: Evidence for Shared Genetic Risks2
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
Meta-Analysis of Joint Test of SNP and SNP-Environment Interaction with Heterogeneity1
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 Pedigree1
Importance of Family History in the Era of Exome Analysis: A Report of a Family with Multiple Concurrent Genetic Diseases1
Common Variants in Neuraminidase Genes Contribute to Predisposition to and Progression of Chronic Heart Failure1
Exome-Wide Pan-Cancer Analysis of Germline Variants in 8,719 Individuals Finds Little Evidence of Rare Variant Associations1
Methods and Software to Analyze Gene-Environment Interactions under a Case-Mother-Control-Mother Design with Partially Missing Child Genotype1
Genetic Analyses of Enamel Hypoplasia in Multiethnic Cohorts1
The Diagnostic Value of miR-124a Expression in Peripheral Blood and Synovial Fluid of Patients with Rheumatoid Arthritis1
A Novel <i>PMVK </i>Variant Associated with Familial Porokeratosis0
A Novel c.3636-4 A&gt;G Mutation in the <i>CCDC88C</i> Plays a Causative Role in Familial Spinocerebellar Ataxia0
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
Front & Back Matter0
50th European Mathematical Genetics Meeting (EMGM) 20220
A Common Variant of ARRB2 Promoter Region Associated with the Prognosis of Heart Failure0
Investigation of Recessive Effects of Coding Variants on Common Clinical Phenotypes in Exome-Sequenced UK Biobank Participants0
Polymorphisms of Placental Iodothyronine Deiodinase Genes in a Rural Area of Northern China with High Prevalence of Neural Tube Defects0
Reduction of Missed Diagnosis of G6PD Deficiency in Heterozygous Females by G6PD/6PGD Ratio Assay Combined with Amplification Refractory Mutation System PCR0
Penalized Logistic Regression Analysis for Genetic Association Studies of Binary Phenotypes0
Identification of a Novel Mutation in Patients with Type A Insulin Resistance Syndrome0
Mutational Screening for Mitochondrial tRNA Genes in 100 Women with Pre-Eclampsia0
Identification of a Hypoxia-Related Signature as Candidate Detector for Schizophrenia Based on Genome-Wide Gene Expression0
Acknowledgement to Reviewers0
Joint Linkage and Association Analysis Using GENEHUNTER-MODSCORE with an Application to Familial Pancreatic Cancer0
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