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Role of Functional IFNL4, IFNLR1, IFNA, IFNAR2 Polymorphisms in Hepatitis B virus‐related liver disease in Han Chinese population
Segregating polymorphism in the NMDA receptor gene GRIN2A, schizotypy, and mental rotation among healthy individuals
Superior cognitive goal maintenance in carriers of genetic markers linked to reduced striatal D2 receptor density (C957T and DRD2/ANKK1-TaqIA)
Genome-wide DNA methylation profiling in infants born to gestational diabetes mellitus
Histone modifier gene mutations in peripheral T-cell lymphoma not otherwise specified
Epigenetic modifications of human placenta associated with preterm birth: a systematic review
Novel subgroups of adult-onset diabetes and their association with outcomes: a data-driven cluster analysis of six variables
Allele-specific methylation in the FADS genomic region in DNA from human saliva, CD4+ cells, and total leukocytes
Single nucleotide polymorphisms in the MYLKP1 pseudogene are associated with increased colon cancer risk in African Americans
Pharmacogenetics analysis of serotonin receptor gene variants and clinical response to risperidone in Han Chinese schizophrenic patients