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A functional variant in SLC1A3 influences ADHD risk by disrupting a hsa‐miR‐3171 binding site: A two‐stage association study
Influence of E‐cadherin genetic variation in canine mammary tumor risk, clinicopathological features and prognosis
Association of Candidate Gene Polymorphisms with Chronic Kidney Disease: Results of a Case-Control Analysis in the Nefrona Cohort
Genetic polymorphisms of PAX1 are functionally associated with different PUMC types of adolescent idiopathic scoliosis in a northern Chinese Han population
Association between the BANK1 rs3733197 polymorphism and polymyositis/dermatomyositis in a Chinese Han population
Forensic Epigenetic Analysis: The Path Ahead
Class 1, 2, and 3 BRAF-Mutated Metastatic Colorectal Cancer: A Detailed Clinical, Pathologic, and Molecular Characterization
Obesity increases the risk of chronic pain development after motor vehicle collision
Genome‐wide association study of statin‐induced myopathy in patients recruited using the UK clinical practice research datalink
Polymorphisms in potential mercury transporter ABCC2 and neurotoxic symptoms in populations exposed to mercury vapor from goldmining