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Functional variants in the sucrase–isomaltase gene associate with increased risk of irritable bowel syndrome
Investigation of dominant and recessive inheritance models in genome‐wide association studies data of nonsyndromic cleft lip with or without cleft palate
The Interaction of TPH1 A779C Polymorphism and Maternal Authoritarianism on Creative Potential
Association of IL-10 rs1800871 and rs1800872 Polymorphisms with Breast Cancer Risk: A Systematic Review and Meta-Analysis
Single-nucleotide and Copy-number variance related to severity of Hypospadias
A common DIO2 polymorphism and Alzheimer disease dementia in African and European Americans
Single nucleotide polymorphisms in the acylphosphatase 2 gene and the SNP-SNP interactions on the risk of breast cancer in Chinese Han women
Associations between sun sensitive pigmentary genes and serum prostate specific antigen levels
Improvement in the sensitivity of newborn screening for Fabry disease among females through the use of a high-throughput and cost-effective method, DNA mass …
Genetic variation in TCF7L2 rs7903146 and history of GDM negatively and independently impact on diabetes-associated metabolic traits