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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
Genetic variant rs72613567 of HSD17B13 gene reduces alcohol‐related liver disease risk in Chinese Han population
Association of single nucleotide polymorphism in NLRC3, NLRC5, HIP1, and LRP8 genes with fecal egg counts in goats naturally infected with Haemonchus contortus
Development and analytical validation of a 29 gene clinical pharmacogenetic genotyping panel: Multi‐ethnic allele and copy number variant detection
Approaches to Tumor Classification in Pulmonary Sarcomatoid Carcinoma
The role of NAT2 polymorphism and methylation in anti‐tuberculosis drug‐induced liver injury in Mongolian tuberculosis patients
A novel multi‐locus genetic risk score identifies patients with higher risk of generalized aggressive periodontitis
Imprinting aberrations of SNRPN, ZAC1 and INPP5F genes involved in the pathogenesis of congenital heart disease with extracardiac malformations
Relation of promoter methylation of the structural oxytocin gene to critical life events in Major Depression: A case control study
DNA methylation of the INSR gene as a mediator of the association between prenatal exposure to famine and adulthood waist circumference