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Home / Resources / Publication Library

Publication Library

The MassARRAY® technology has been used in genetic research settings for almost 20 years and has been featured in over 4,000 peer-reviewed publications globally. It brings a proven level of technological performance for molecular analysis.

Featured Publications

Infectious Disease ,
Diagnostic Performance of Nucleotide MALDI-TOF-MS for the Rapid Diagnosis of Pulmonary Tuberculosis and the Detection of Drug Resistance
Infection and Drug Resistance 2025
Hereditary Genetics ,
Next-Generation Sequencing for Cystic Fibrosis: Florida Newborn Screening Experience
International Journal of Neonatal Screening 2025
Methylation ,
EpiClock; biological age measurement from blood DNA methylation using a minimal CpG marker set for high-throughput iPlex mass spectrometry assay for screening in drug development and pop...
Experimental Gerontology 2025
Hereditary Genetics ,
A cost-utility analysis of newborn screening for spinal muscular atrophy in Canada
Orphanet Journal of Rare Diseases 2025
Liquid Biopsy ,
Detection of actionable mutations in circulating tumor DNA for non-small cell lung cancer patients
Communications Medicine 2025
PGx ,
Development of an Ancestrally Inclusive Preemptive Pharmacogenetic Testing Panel
Clinical and Translational Science 2025

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  • Harmonization of Reporting for Detection of ALK Genetic Alterations in Neuroblastoma: A SIOPEN Biology Study
  • Evolution of large polymorphic inversions in a panmictic songbird
  • Relationships Between Expressions and Variants of the Myosin−Binding Protein C1 Gene and Fatty Acid Composition in Longissimus Thoracis Muscle of Grazing Sonid Sheep
  • Identification of rare genetic variants in familial forms and unrelated cases of bisphosphonates-associated atypical femur fracture
  • Association of inflammatory susceptibility genes with myopia in Chinese children
  • Association of single-nucleotide polymorphisms in SLC2A9, SLC22A12 and SLC22A11 genes with hyperuricemia in the Chinese Tibetan population
  • Multiplex detection and application of MALDI-TOF NAMS for porcine diarrheal pathogens
  • Genetic polymorphisms associated with metabolic dysfunction-associated steatotic liver disease and cardiometabolic risk susceptibility in the Chinese Han population
  • CYP2C9 polymorphism is associated with susceptibility to ischemic stroke in a Chinese population
  • Serum erythropoietin levels in 696 patients investigated for erythrocytosis with JAK2 mutation analysis
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