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Putative regulatory functions of SNPs associated with bronchial asthma, arterial hypertension and their comorbid phenotype
Significance of screening sensitive methylation sites using whole-genome sequencing in early diagnosis of non-small cell lung cancer
Limitation of standard pseudoisochromatic plates in identifying colour vision deficiencies when compared with genetic testing
miR-30a-5p promotes glomerular podocyte apoptosis via DNMT1-mediated hypermethylation under hyperhomocysteinemia
BRAF Immunoexpression Can Be Intralesionally Heterogeneous but BRAF V600E Mutation Status Is Intralesionally Homogeneous and Interlesionally Concordant in Melanoma: A Study of 140 Lesions From 98 Patients
Leveraging large observational studies to discover genetic determinants of drug concentrations: A proof‐of‐concept study
Physiological levels of 25‐hydroxyvitamin D3 induce a suppressive CD4+ T cell phenotype not reflected in the epigenetic landscape
Associations of CXCL12 polymorphisms with clinicopathological features in breast cancer: a case-control study
Dietary patterns and cognitive function in older New Zealand adults: the REACH study
Association between Maternal Drug Use and Cytochrome P450 Genetic Polymorphisms and the Risk of Congenital Heart Defects in Offspring