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IL10 low‐frequency variants in Behçet’s disease patients
HLA‐DPB 1 variant rs3117242 is associated with anti‐neutrophil cytoplasmic antibody‐associated vasculitides in a Han Chinese population
The genetic architecture of Stargardt macular dystrophy (STGD1): a longitudinal 40-year study in a genetic isolate
Family-based association study identifies SNAP25 as a susceptibility gene for autism in the Han Chinese population
An exploratory study of host polymorphisms in genes that clinically characterize breast cancer tumors and pretreatment cognitive performance in breast …
Maternal bonding style, cholinergic receptor gene polymorphisms in association with smoking-related depressive symptoms
Association of IL-8-251T/A,+ 781C/T and+ 396T/G genetic polymorphisms and haplotypes with breast cancer risk in a Northern Chinese population
Variant of EOMES Associated with Increasing Risk in Chinese Patients with Relapsing-remitting Multiple Sclerosis
Effect of AMP‐activated protein kinase subunit alpha 2 (PRKAA2) genetic polymorphisms on susceptibility to type 2 diabetes mellitus and diabetic nephropathy in a …
Diagnostic markers in the pathogenesis of parkinsonism syndrome development in chronic brain ischemia