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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

Hereditary Genetics ,
Development and validation of a one-step SMN assay for genetic testing in spinal muscular atrophy via MALDI-TOF MS
Analyst 2024
Methylation ,
Urinary DNA-methylation and protein biomarkers identify urothelial carcinoma among other genitourinary diseases and cancer-free individuals
Journal of Translational Medicine 2024
Sample Integrity ,
Human identification of single hair shaft using a mass spectrometry mRNA typing system
Forensic Science International: Genetics 2024
PGx ,
DPYD Genotyping Recommendations: A Joint Consensus Recommendation of the Association for Molecular Pathology, American College of Medical Genetics and Genomics, Clinical Pharmacogenetics...
The Journal of Molecular Diagnostics 2024
Liquid Biopsy ,
Mutation analysis in individual circulating tumor cells depicts intratumor heterogeneity in melanoma
EMBO Molecular Medicine 2024
Infectious Disease ,
Diagnostic performance of matrix-assisted laser desorption ionization time-of-flight mass spectrometry (MALDI-TOF MS) in bronchoalveolar lavage fluid for pulmonary tuberculosis in HIV-in...
Journal of Clinical Tuberculosis and Other Mycobacterial Diseases 2024

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  • A Study Of the effect of Sex on drug dosing, concentrations, and pharmacogenomics in the Montreal Heart Institute Hospital Cohort (SOS-PGx): methodology and research progress
  • Multiplex panels of SNP markers based on single-base primer extension in the west Pacific pen shell Atrina lischkeana (Clessin, 1891)
  • PEAR1, PON1, CYP2C19, CYP1A2 and F2R Polymorphisms are Associated with MACE in Clopidogrel-Treated Patients with Acute Coronary Syndrome Undergoing Percutaneous Coronary Intervention
  • Pain in idiopathic scoliosis not associated with known genetic variants for pain
  • Efficacy and safety of rivaroxaban in preventing venous thromboembolism in postoperative patients with gynecological malignancies: protocol for a randomised controlled open-label trial (G-alfalfa trial)
  • iPhone-based anomaloscope for accessible, accurate color vision testing
  • Development and validation of a rapid point of care CYP2C19 genotyping platform
  • Interferon Gamma Gene Polymorphisms in Greek Primary Breast Cancer Patients
  • Association of iron homeostasis-related gene polymorphisms with pregnancy and neonatal outcomes in patients with gestational diabetes mellitus
  • RARB genetic variants might contribute to the risk of chronic obstructive pulmonary disease based on a case-control study
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With exception of the MassARRAY Dx, all other products are For Research Use Only. Not for use in diagnostic procedures.
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