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Type I interferon receptor variants in gene regulatory regions are associated with susceptibility to cerebral malaria in Malawi
Genome-wide association study identifies a new locus at 7q21. 13 associated with hepatitis B virus–related hepatocellular carcinoma
Matrix‐assisted laser desorption/ionization time‐of‐flight mass spectrometry analysis of 36 blood group alleles among 396 T hai samples reveals region‐specific …
Replication Study Confirms the Association of the Common rs1800629 Variant of the TNFα Gene with Postmenopausal Osteoporosis Susceptibility in the Han …
Genetic variation in the von Willebrand factor gene in Swedish von Willebrand disease patients
Exome sequencing study in patients with multiple sclerosis reveals variants associated with disease course
Quantitative Measurement of PARD3 Copy Number Variations in Human Neural Tube Defects
Association of TERT polymorphisms with chronic hepatitis B in a Chinese Han population
Neurexin gene family variants as risk factors for autism spectrum disorder
IL-17A gene polymorphism rs2275913 is associated with the development of asthma after bronchiolitis in infancy