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European Journal of Human Genetics : EJHG|November 6, 2009
Five novel loci for inherited hearing loss mapped by SNP-based homozygosity profiles in Palestinian familiesHashem Shahin, Tom Walsh, Amal Abu Rayyan, et al.
Scientific Reports|October 8, 2024
Frequency and spectrum of mutations in human sperm measured using duplex sequencing correlate with trio-based de novo mutation analysesJonatan Axelsson, Danielle LeBlanc, Habiballah Shojaeisaadi, et al.
Haematologica|August 3, 2023
Quantification of measurable residual disease using duplex sequencing in adults with acute myeloid leukemiaLaura W Dillon, Jake Higgins, Hassan Nasif, et al.
Regulatory Toxicology and Pharmacology : RTP|November 10, 2025
Application of error-corrected sequencing technologies for in vivo regulatory mutagenicity assessmentCarole L Yauk, Anthony M Lynch, Vasily N Dobrovolsky, et al.
Blood Cancer Journal|May 28, 2020
Ultra-accurate Duplex Sequencing for the assessment of pretreatment ABL1 kinase domain mutations in Ph+ ALLNicholas J Short, Hagop Kantarjian, Rashmi Kanagal-Shamanna, et al.
Environmental and Molecular Mutagenesis|June 30, 2025
Transferability, Reproducibility and Sensitivity of Mutation Quantification by Duplex SequencingShaofei Zhang, Barbara L Parsons, Devon Fitzgerald, et al.
JAMA Oncology|May 2, 2024
Measurable Residual FLT3 Internal Tandem Duplication Before Allogeneic Transplant for Acute Myeloid LeukemiaLaura W Dillon, Gege Gui, Niveditha Ravindra, et al.
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