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Specific molecular signatures predict decitabine response in chronic myelomonocytic leukemia
F2RL3 methylation, lung cancer incidence and mortality
Susceptibility to Invasive Meningococcal Disease: Polymorphism of Complement System Genes and Neisseria meningitidis Factor H Binding Protein
An efficient screening method for simultaneous detection of recurrent copy number variants associated with psychiatric disorders
The Study to Understand the Genetics of the Acute Response to Metformin and Glipizide in Humans (SUGAR-MGH): Design of a pharmacogenetic Resource for Type 2 Diabetes
Genetic variants in de novo lipogenic pathway genes predict the prognosis of surgically-treated hepatocellular carcinoma
Assessing the clinical value of targeted massively parallel sequencing in a longitudinal, prospective population-based study of cancer patients.
Associations of IL-2 and IL-4 expression and polymorphisms with the risks of Mycoplasma pneumoniae infection and asthma in children.
Association between VEGF polymorphisms (936c/t, -460t/c and -634g/c) with haplotypes and coronary heart disease susceptibility.
Strong effect of SNP rs4988300 of the LRP5 gene on bone phenotype of Caucasian postmenopausal women.
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