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High-throughput genetic screening of 51 pediatric cataract genes identifies causative mutations in inherited pediatric cataract in south eastern Australia
Exome array analysis identifies variants in SPOCD1 and BTN3A2 that affect risk for gastric cancer
Validating the use of STELA to measure placental telomere length
Gender differences in the association of ENPP1 polymorphisms with type 2 diabetes in a Chinese population
Functional polymorphisms in PD-L1 gene are associated with the prognosis of patients with early stage non-small cell lung cancer
Status and future perspectives of single nucleotide polymorphisms (SNPs) markers in farmed fishes: Way ahead using next generation sequencing
Structural characterization and association of ovine dickkopf-1 gene with wool production and quality traits in Chinese Merino
HOXB13 mutations and binding partners in prostate development and cancer: Function, clinical significance, and future directions
Reproducibility of methylated CpG typing with the Illumina MiSeq
A prospective study of dietary and supplemental zinc intake and risk of type 2 diabetes depending on genetic variation in SLC30A8