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A comparison of DP-TOF Mass Spectroscopy (MS) and Next Generation Sequencing (NGS) methods for detecting molecular mutations in thyroid nodules fine needle aspiration biopsies
Genetic variants of interleukin 1B and 6 are associated with clinical outcome of surgically treated lumbar degenerative disc disease
Mannose‐binding lectin genotype is associated with respiratory disease in young children: a multi‐centre cohort study
High-throughput sequencing analysis of nuclear-encoded mitochondrial genes reveals a genetic signature of human longevity
CYP2A6 and GABRA2 Gene Polymorphisms are Associated With Dexmedetomidine Drug Response
DIP2C Polymorphisms are Implicated in Susceptibility and Clinical Phenotypes of Autism Spectrum Disorder
Genetic Variants in Double-Strand Break Repair Pathway Genes to Predict Platinum-Based Chemotherapy Prognosis in Patients With Lung Cancer
TRIM26 inhibits hepatitis B virus replication by promoting HBx degradation and TRIM26 genetic polymorphism predicts PegIFNα treatment response of HBeAg-positive chronic hepatitis B Patients
Association of TLR9-1237T> C; rs5743836 polymorphism with increased risk of Hodgkin’s lymphoma: A case-control study
Genetic variations in UCA1, a lncRNA functioning as a miRNA sponge, determine endometriosis development and the potential associated infertility via regulating lipogenesis