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Involvement of hypertrophic cardiomyopathy genes in sudden infant death syndrome (SID)
The -9247 T/C polymorphism in the SOST upstream regulatory region that potentially affects C/EBPalpha and FOXA1 binding is associated with osteoporosis.
Development and evaluation of a PCR and mass spectroscopy (PCR-MS)-based method for quantitative, type-specific detection of human papillomavirus.
GATA-2 L359 V mutation is exclusively associated with CML progression but not other hematological malignancies and GATA-2 P250A is a novel single nucleotide polymorphism.
The role of cell-free circulating DNA in the diagnosis and prognosis of prostate cancer
Sequenom MassARRAY application in the long QT syndromeÂ mutation detection
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