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Genetics of type 1A diabetes.
Reduced Neutrophil Count in People of African Descent Is Due To a Regulatory Variant in the Duffy Antigen Receptor for Chemokines Gene
Genetic Loci associated with C-reactive protein levels and risk of coronary heart disease.
A Genome-Wide Association Study in Chronic Obstructive Pulmonary Disease (COPD): Identification of Two Major Susceptibility Loci
HHEX-IDE polymorphism is associated with low birth weight in offspring with a family history of type 1 diabetes.
A Genome-Wide Association Study Confirms VKORC1, CYP2C9, and CYP4F2 as Principal Genetic Determinants of Warfarin Dose
MALDI-TOF MS in Prenatal Genomics
Genetic polymorphisms in chronic hyperplastic sinusitis with nasal polyposis.
Genetic variation in CRTh2 influences development of allergic phenotypes.
Genetic variation in CYP27B1 is associated with congestive heart failure in patients with hypertension