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Use of Sequenom Sample ID PlusÂ® SNP Genotyping in Identification of FFPE Tumor Samples
Utilizing Multiple in Silico Analyses to Identify Putative Causal SCN5A Variants in Brugada Syndrome
Validation of 58 autosomal individual identification SNPs in three Chinese populations
Validation of DNA Methylation Biomarkers for Diagnosis of Acute Lymphoblastic Leukemia
Validation of ZAP-70 methylation and its relative significance in predicting outcome in chronic lymphocytic leukemia
Variants in the ATM-CHEK2-BRCA1 axis determine genetic predisposition and clinical presentation of papillary thyroid carcinoma
Targeted resequencing of the microRNAome and 3’UTRome reveals functional germline DNA variants with altered prevalence in epithelial ovarian cancer
Targeting of multiple myeloma-related angiogenesis by miR- 199a-5p mimics: in vitro and in vivo anti-tumor activity
The 9p21 Locus Is Associated with Coronary Artery Disease and Cardiovascular Events in the Presence (but Not in the Absence) of Coronary Calcification
The association between sex-related interleukin-6 gene polymorphisms and the risk for cerebral palsy