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Epigenome‐wide analysis of methylation changes in the sequence of gallstone disease, dysplasia, and gallbladder cancer
MICA polymorphisms associated with antithyroid drug‐induced agranulocytosis in the Chinese Han population
Auditory brainstem measures and genotyping boost the prediction of literacy: A longitudinal study on early markers of dyslexia
Exploratory genome-wide interaction analysis of non-steroidal anti-inflammatory drugs and predicted gene expression on colorectal cancer risk
Candidate genes-based investigation of susceptibility to Human African Trypanosomiasis in Côte d’Ivoire
A polymorphism in the haptoglobin, haptoglobin related protein locus is associated with risk of human sleeping sickness within Cameroonian populations
Association of Maternal Diabetes Mellitus and Polymorphisms of the NKX2.5 Gene in Children with Congenital Heart Disease: A Single Centre-Based Case-Control Study
Interaction of CEND1 gene and life events in susceptibility to depressive symptoms in Chinese Han college students
CYP3A5 genetic variants and their associations with carbamazepine and valproic acid response in Malaysian epileptic patients
Association of ABCG1 gene methylation and its dynamic change status with incident type 2 diabetes mellitus: the Rural Chinese Cohort Study