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Dysbindin gene (DTNBP1) in major depressive disorder (MDD) patients: Lack of association with clinical phenotypes
Detailed investigation of the role of common and low frequency WFS1 variants in type 2 diabetes risk
Fine-mapping quantitative trait loci for twinning rate on BTA14 in North American Holsteins
Re-sequencing and analysis of variation in the TCF7L2 gene in African Americans suggests the SNP rs7903146 is the causal diabetes susceptibility variant
Obesity susceptibility genetic variants identified from recent genome-wide association studies: Implications in a Chinese population
Association of genetic variants in the adiponectin gene with adiponectin level and hypertension in Hong Kong Chinese
Robust hepatitis B virus genotyping by mass spectrometry
WNT receptors, bone mass and fractures: gene-wide association analysis of LRP5 and LRP6 polymorphisms with replication
Replacing reverse line-blot hybridization spoligotyping of the Mycobacterium tuberculosis complex
Association of a melatonin receptor 1B (MTNR1B) gene variant with fasting glucose and HOMA-B in children and adolescents of high BMI-SDS groups