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A high throughput panel for identifying clinically-relevant mutation profiles in melanoma
Pretreatment Epidermal Growth Factor Receptor (EGFR) T790M Mutation Predicts Shorter EGFR Tyrosine Kinase Inhibitor Response Duration in Patients With Nonâ€“Small-Cell Lung Cancer
A Novel Mass Spectrometry Based Assay for Diagnosis of EML4-ALK Positive Non-Small Cell Lung Cancer
Quantitative DNA Methylation Analysis Identifies a Single CpG Dinucleotide Important for ZAP-70 Expression and Predictive of Prognosis in Chronic Lymphocytic Leukemia
Interaction between maternal BMI and angiogenic gene polymorphisms associates with the risk of spontaneous preterm birth
Single nucleotide polymorphisms in the NOS2 and NOS3 genes are associated with exhaled nitric oxide
Combined genomarkers approach to Salmonella characterization reveals that nucleotide sequence differences in the phase 1 flagellin gene fliC are markers for variation within serotypes
Umbilical cord PUFA are determined by maternal and child fatty acid desaturase (FADS) genetic variants in the Avon Longitudinal Study of Parents and Children (ALSPAC)
Racial differences in oncogene mutations detected in early-stage low-grade endometrial cancers
Genome-wide association study of plasma efavirenz pharmacokinetics in AIDS Clinical Trials Group protocols implicates several CYP2B6 variants