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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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PGx

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Mutation Profiling

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Methylation

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  • Diagnostic Performance of Nucleotide MALDI-TOF-MS for the Rapid Diagnosis of Pulmonary Tuberculosis and the Detection of Drug Resistance
  • Multiple polygenic score approach in colorectal cancer risk prediction
  • Trans-QTL Alliance of HKT1 and PHL7 Modulate Salinity Stress Tolerance and Enhance Crop Yield Endurance
  • Evaluating the Influence of CHI3L1 and PI3 Methylation in Allergic and Nonallergic Asthma
  • Next-Generation Sequencing for Cystic Fibrosis: Florida Newborn Screening Experience
  • Navigating therapeutic challenges: Voriconazole pharmacokinetics and CYP2C19 genetic polymorphism—A case report and literature review
  • Maternal vitamin D and genetic variants determine cord blood vitamin D levels in newborn
  • A MGMT Enhancer Variant is Associated with Glioma Susceptibility and Progression
  • High-grade glioma, IDH-and H3-wildtype in young adults: a rare condition with a distinct epigenetic landscape
  • Harmonization of Reporting for Detection of ALK Genetic Alterations in Neuroblastoma: A SIOPEN Biology Study
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