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Replication Study Confirms the Association of the Common rs1800629 Variant of the TNFα Gene with Postmenopausal Osteoporosis Susceptibility in the Han …
c-MET Overexpression as a Poor Predictor of MET Amplifications or Exon 14 Mutations in Lung Sarcomatoid Carcinomas
Genetic variation in the von Willebrand factor gene in Swedish von Willebrand disease patients
Exome sequencing study in patients with multiple sclerosis reveals variants associated with disease course
Neurexin gene family variants as risk factors for autism spectrum disorder
Quantitative Measurement of PARD3 Copy Number Variations in Human Neural Tube Defects
Polymorphisms within the prolactin and growth hormone/insulin-like growth factor-1 functional pathways associated with fertility traits in Holstein cows raised in a hot-humid climate
IL1R1 and IL1R2 polymorphisms were associated with tuberculosis risk: A pilot study
Integrative expression quantitative trait locus–based analysis of colorectal cancer identified a functional polymorphism regulating SLC22A5 expression
SMAD7 methylation as a novel marker in atherosclerosis