Mark A. McElwain

Truncating mutations of MAGEL2 cause Prader-Willi phenotypes and autism

Christian P. Schaaf, Manuel L. Gonzalez‐Garay, Fan Xia et al. · Nature Genetics · 2013 · 296 citations · Full text

Mendelian Disorder, Genetic Disorder, Genetics +4

Detection and phasing of single base de novo mutations in biopsies from human in vitro fertilized embryos by advanced whole-genome sequencing

Brock A. Peters, Bahram G. Kermani, Oleg Alferov et al. · Genome Research · 2015 · 58 citations · Full text

Genetic Testing, Genetics, Preimplantation Genetic Testing +27

Analysis of a Spindle Pole Body Mutant Reveals a Defect in Biorientation and Illuminates Spindle Forces

Tennessee J. Yoder, Mark A. McElwain, Susan E. Francis et al. · Molecular Biology of the Cell · 2004 · 27 citations · Full text

Bipolar Spindle, Cell Division, Protein Folding +14

A Suppressor/Enhancer Screen in Drosophila Reveals a Role for Wnt-Mediated Lipid Metabolism in Primordial Germ Cell Migration

Mark A. McElwain, Dennis C. Ko, Michael D. Gordon et al. · PLoS ONE · 2011 · 24 citations · Full text

Drosophila Reveals, Genetics, Wntd Signal Transduction +20

Long Fragment Read (LFR) Technology: Cost-Effective, High-Quality Genome-Wide Molecular Haplotyping

Mark A. McElwain, Rebecca Yu Zhang, Radoje Drmanac et al. · Methods in molecular biology · 2017 · 11 citations

Long-read Sequencing, Long Fragment Read, Dna Sequencing +13