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Suboptimal maternal and cord plasma pyridoxal 5? phosphate concentrations are uncommon in a cohort of Canadian pregnant women and newborn infants
Sulfatase modifying factor 1 (SUMF1) is associated with Chronic Obstructive Pulmonary Disease
Suppression of indoleamine-2,3-dioxygenase 1 expression by promoter hypermethylation in ER-positive breast cancer
Targeted sequencing of ABCA7 identifies splicing, stop-gain and intronic risk variants for Alzheimer disease
TEX15: A DNA repair gene associated with prostate cancer risk in Han Chinese
The Association of Chemokine Gene Polymorphisms with VKH and Behcet’s Disease in a Chinese Han Population
Rare coding variants in PLCG2, ABI3, and TREM2implicate microglial-mediated innate immunity in Alzheimer’s disease
Serum high-sensitive C-reactive protein (hsCRP) level and CRP genetic polymorphisms are associated with abdominal aortic aneurysm
Rare mutations and potentially damaging missense variants in genes encoding fibrillar collagens and proteins involved in their production are candidates for risk for preterm premature rupture of membranes
Single nucleotide polymorphisms for DNA typing in the domestic horse