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Genetic susceptibility to hepatic sinusoidal obstruction syndrome in pediatric patients undergoing HSCT
TLR4 polymorphisms may increase susceptibility to periodontitis in Pg-positive individuals
Genetic variant rs72613567 of HSD17B13 gene reduces alcohol‐related liver disease risk in Chinese Han population
Orthostatic hypotension and novel blood pressure associated gene variants in older adults: data from the TILDA Study
Assessment for familial pattern and association of polymorphisms in KIAA0319 gene with specific reading disorder in children from North India visiting a tertiary care centre: A case–control study
Single Nucleotide Polymorphisms in Thyroid Hormone Transporter Genes MCT8, MCT10 and Deiodinase DIO2 Contribute to Inter-Individual Variance of Executive Functions and Personality Traits
Non-Syndromic Cleft Lip with or without Cleft Palate: Genome-Wide Association Study in Europeans Identifies a Suggestive Risk Locus at 16p12.1 and Supports SH3PXD2A as a Clefting Susceptibility Gene
Dataset of allele and genotype frequencies of five polymorphisms candidate genes analyzed for association with body mass index in Russian women
XRCC1 Arg194Trp polymorphism and thyroid cancer
Functional Genetic Polymorphisms in the IL1RL1-IL18R1 Region Confer Risk for Ocular Behçet’s Disease in a Chinese Han Population