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Common genetic variants on chromosome 9p21 confers risk of ischemic stroke: A large-scale genetic association study
Missense variant in interleukin-6 signal transducer identified as susceptibility locus for rheumatoid arthritis in Chinese patients
Genome-Wide association between EYA1 and Aspirin-induced peptic ulceration
Systematic population-based identification of NTRK and RET fusion-positive thyroid cancers
Bronchopulmonary dysplasia and wnt pathway-associated single nucleotide polymorphisms
Filaggrin gene polymorphisms are associated with atopic dermatitis in women but not in men in the Caucasian population of Central Russia
Pharmacogenomic Single Nucleotide Polymorphism (SNP) Variants As Predictors of Toxicity Phenotypes in the Treatment of Acute Childhood Leukemia
Advanced glycation end‐products (AGEs) are lower in prostate tumor tissue and inversely related to proportion of West African ancestry
MALDI MS-Based Investigations for SARS-CoV-2 Detection
A functionally impaired missense variant identified in French Canadian families implicates FANCI as a candidate ovarian cancer-predisposing gene