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Cytokine Genetic Variants and Health-Related Quality of Life in Crohn’s Disease: An Exploratory Study
STX1A gene variations contribute to the susceptibility of children attention-deficit/hyperactivity disorder: a case–control association study
Genetic aspects of idiopathic paediatric uveitis and juvenile idiopathic arthritis associated uveitis in Chinese Han
Investigating the role of microRNA-27a gene polymorphisms and its interactive effect with risk factors in gastrointestinal cancers
Mutated ATP10B increases Parkinson’s disease risk by compromising lysosomal glucosylceramide export
PNPLA3 rs738409 is not associated with the risk of hepatocellular carcinoma and persistent infection of hepatitis B virus (HBV) in HBV-related subjects: A case-control study and meta-analysis on Asians
Association of Polymorphisms in the Kisspeptin/GPR54 Pathway Genes With Risk of Early Puberty in Chinese Girls
Associations among Genetic Variants and Intracranial Aneurysm in a Chinese Population
DHA intake interacts with ELOVL2 and ELOVL5 genetic variants to influence polyunsaturated fatty acids in human milk
Association between IL1B gene and cervical cancer susceptibility in Chinese Uygur Population: A Case–Control study