Mallory Owen

An automated 13.5 hour system for scalable diagnosis and acute management guidance for genetic diseases

Mallory Owen, Sébastien Lefebvre, Christian Holm Hansen et al. · Nature Communications · 2022 · 70 citations · Full text

Measurement of genetic diseases as a cause of mortality in infants receiving whole genome sequencing

Stephen F. Kingsmore, Audrey J. Henderson, Mallory Owen et al. · npj Genomic Medicine · 2020 · 56 citations · Full text

Reclassification of the Etiology of Infant Mortality With Whole-Genome Sequencing

Mallory Owen, Meredith S. Wright, Serge Batalov et al. · JAMA Network Open · 2023 · 44 citations · Full text

Scalable, high quality, whole genome sequencing from archived, newborn, dried blood spots

Yan Ding, Mallory Owen, Jennie Le et al. · npj Genomic Medicine · 2023 · 28 citations · Full text

Improving the efficacy of exome sequencing at a quaternary care referral centre: novel mutations, clinical presentations and diagnostic challenges in rare neurogenetic diseases

Christopher Grunseich, Nathan Sarkar, Joyce Lu et al. · Journal of Neurology Neurosurgery & Psychiatry · 2021 · 21 citations · Full text