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TRPM8 genetic variant is associated with chronic migraine and allodynia
PCSK9 E670G polymorphism increases risk of coronary artery disease in a Chinese Han population
Identification of susceptibility locus shared by IgA nephropathy and inflammatory bowel disease in a Chinese Han population
A diabetes‐associated genetic variant is associated with diastolic dysfunction and cardiovascular disease
Anxiety risk SNPs on chromosome 2 modulate arousal in children in a fear generalization paradigm
Genome-wide association study in Chinese cohort identifies one novel hypospadias risk associated locus at 12q13.13
Genome-wide association study of morbid obesity in Han Chinese
Genetic variations associated with spleen-Yang deficiency pattern of non-alcoholic fatty liver disease: a candidate gene study
Dusp8 affects hippocampal size and behavior in mice and humans
Association of Genetic Variation With Keratoconus