Human Heredity

Papers
(The median citation count of Human Heredity is 1. 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 2020-11-01 to 2024-11-01.)
ArticleCitations
Violation of the Constant Genetic Effect Assumption Can Result in Biased Estimates for Non-Linear Mendelian Randomization19
Screening for Mitochondrial tRNA Mutations in 318 Patients with Dilated Cardiomyopathy4
Association of <b><i>PNPLA3</i></b> I148M with Liver Disease Biomarkers in Latinos4
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
Genetic Analyses of Enamel Hypoplasia in Multiethnic Cohorts2
PhosSNPs-Regulated Gene Network and Pathway Significant for Rheumatoid Arthritis2
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
Family History of Breast Cancer Is Associated with Elevated Risk of Prostate Cancer: Evidence for Shared Genetic Risks2
Meta-Analysis of Joint Test of SNP and SNP-Environment Interaction with Heterogeneity2
The Diagnostic Value of miR-124a Expression in Peripheral Blood and Synovial Fluid of Patients with Rheumatoid Arthritis2
Identification of a Hypoxia-Related Signature as Candidate Detector for Schizophrenia Based on Genome-Wide Gene Expression1
Methods and Software to Analyze Gene-Environment Interactions under a Case-Mother-Control-Mother Design with Partially Missing Child Genotype1
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
A Common Variant of ARRB2 Promoter Region Associated with the Prognosis of Heart Failure1
Reduction of Missed Diagnosis of G6PD Deficiency in Heterozygous Females by G6PD/6PGD Ratio Assay Combined with Amplification Refractory Mutation System PCR1
A Novel <i>PMVK </i>Variant Associated with Familial Porokeratosis1
Exome-Wide Pan-Cancer Analysis of Germline Variants in 8,719 Individuals Finds Little Evidence of Rare Variant Associations1
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