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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
Association of polymorphism in the VEGFA gene 3′‐UTR+ 936T/C with susceptibility to biliary atresia in a Southern Chinese Han population
Identification of expression quantitative trait loci of MTOR associated with the progression of glioma
No association between 5 new GWAS-linked loci in Parkinson’s disease and multiple system atrophy in a Chinese population
Single nucleotide polymorphisms in asthma candidate genes TBXA2R, ADAM33 FCER1B and ORMDL3 in Pakistani asthmatics a case control study
Allelic variation in dopamine D2 receptor gene is associated with attentional impulsiveness on the Barratt Impulsiveness Scale (BIS-11)