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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
PTPN22 -1123G?>?C polymorphism is associated with susceptibility to primary immune thrombocytopenia in Chinese population
A Common Genetic Variant of FCN3/CD164L2 Is Associated with Essential Hypertension in a Chinese Population
Ten SNPs of PAX6, Lumican, and MYOC genes are not associated with high myopia in Han Chinese
Low-Level Environmental Cadmium Exposure is Associated with DNA Hypomethylation in Argentinean Women