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Genetic variants in RET, ARHGEF3 and CTNNAL1, and relevant interaction networks, contribute to the risk of Hirschsprung disease.
A New Risk Variant for Multiple Sclerosis at 11q23.3 Locus Is Associated with Expansion of CXCR5+ Circulating Regulatory T Cells
Development of a set of SNP markers for population genetics of the red gorgonian (Paramuricea clavata), an emblematic species of the Mediterranean coralligenous
Association of SCN1A, SCN2A, and UGT2B7 Polymorphisms with Responsiveness to Valproic Acid in the Treatment of Epilepsy
Primary qualities evoked by quinine, sucrose, and capsaicin associate with PROP bitterness, but not TAS2R38 genotype
Genetic determinants of gestational diabetes mellitus: a case–control study in two independent populations
Association between genetic variants in genes encoding Argonaute proteins and cancer risk: A meta-analysis
Genetic susceptibility to parenting style: DRD2 and COMT influence creativity
Hyperprogression under Immune Checkpoint Inhibitor: a potential role for germinal immunogenetics
Genetic Association Analysis of Cell Cycle Regulators Reveals YWHAZ Has Prognostic Significance in Prostate Cancer