Mark A. McElwain
Publications by Year
Research Areas
Cancer Genomics and Diagnostics, Acute Myeloid Leukemia Research, Genomic variations and chromosomal abnormalities, Advanced biosensing and bioanalysis techniques, RNA Interference and Gene Delivery
Most-Cited Works
- → Truncating mutations of MAGEL2 cause Prader-Willi phenotypes and autism(2013)299 cited
- → Detection and phasing of single base de novo mutations in biopsies from human in vitro fertilized embryos by advanced whole-genome sequencing(2015)58 cited
- → Analysis of a Spindle Pole Body Mutant Reveals a Defect in Biorientation and Illuminates Spindle Forces(2004)27 cited
- → A Suppressor/Enhancer Screen in Drosophila Reveals a Role for Wnt-Mediated Lipid Metabolism in Primordial Germ Cell Migration(2011)24 cited
- → Long Fragment Read (LFR) Technology: Cost-Effective, High-Quality Genome-Wide Molecular Haplotyping(2017)13 cited
- → A crucial role for lipid phosphorylation in WntD-mediated primordial germ cell migration(2010)1 cited
- → Analytical Validation of a Duplex Sequencing AML Assay with a Limit of Detection Below 0.01% VAF for SNVs and Indels(2023)1 cited
- → Accurate Sequencing and Haplotyping from 10 Cells Using Long Fragment Read (LFR) Technology(2022)1 cited
- → An AML Targeted Duplex Sequencing Assay That Can Detect Measurable Residual Disease (MRD) at a Sensitivity Better Than 0.01% Variant Allele Frequency(2024)
- Magel-cause-Prader-Willi-supplemental(2013)