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Genetic Association and Altered Gene Expression of Osteoprotegerin in Otosclerosis Patients
Homozygous Sequence Variants in the NPR2 Gene Underlying Acromesomelic Dysplasia Maroteaux Type (AMDM) in Consanguineous Families
Classical and Atypical Fibrodysplasia Ossificans Progressiva in India
Joint Effect of Unlinked Genotypes: Application to Type 2 Diabetes in the EPIC-Potsdam Case-Cohort Study
Trans-Ethnic Meta-Analysis Identifies Common and Rare Variants Associated with Hepatocyte Growth Factor Levels in the Multi-Ethnic Study of Atherosclerosis (MESA)
Analysis of Human Triallelic SNPs by Next-Generation Sequencing
Statistical Methods for Association Tests of Multiple Continuous Traits in Genome-Wide Association Studies
SVSI: Fast and Powerful Set-Valued System Identification Approach to Identifying Rare Variants in Sequencing Studies for Ordered Categorical Traits
Novel A219P Mutation of Hydroxymethylbilane Synthase Identified in a Chinese Woman with Acute Intermittent Porphyria and Syndrome of Inappropriate Antidiuretic Hormone