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ACS Central Science|April 3, 2019
Large-Scale Production of 119mTe and 119Sb for Radiopharmaceutical ApplicationsKevin T Bennett, Sharon E Bone, Andrew C Akin, et al.Biorxiv : the Preprint Server for Biology|April 27, 2026
Long-read MitoScope reveals tissue-resolved somatic mitochondrial variation and landscape of nuclear-embedded mitochondrial sequencesChristina Zakarian, Joshua D Smith, Chee Hong Wong, et al.BMJ Open|March 25, 2022
Association of the Intermountain Risk Score with major adverse health events in patients positive for COVID-19: an observational evaluation of a US cohortBenjamin D Horne, Joseph R Bledsoe, Joseph B Muhlestein, et al.American Journal of Human Genetics|April 16, 2019
Homozygous Mutations in CSF1R Cause a Pediatric-Onset Leukoencephalopathy and Can Result in Congenital Absence of MicrogliaNynke Oosterhof, Irene J Chang, Ehsan Ghayoor Karimiani, et al.Journal of Medical Genetics|January 4, 2014
Whole exome sequencing identifies de novo mutations in GATA6 associated with congenital diaphragmatic herniaLan Yu, James T Bennett, Julia Wynn, et al.Journal of Medical Genetics|June 9, 2017
Loss of function in ROBO1 is associated with tetralogy of Fallot and septal defectsPaul Kruszka, Pranoot Tanpaiboon, Katherine Neas, et al.Inorganic Chemistry|April 18, 2020
A Solid-State Support for Separating Astatine-211 from BismuthDavid H Woen, Cecilia Eiroa-Lledo, Andrew C Akin, et al.Circulation|December 16, 2021
DREAM-ICD-II StudyChristian Steinberg, Nicolas Dognin, Amit Sodhi, et al.The Journal of Pediatrics|June 20, 2020
The Impact of Rapid Exome Sequencing on Medical Management of Critically Ill ChildrenAmanda S Freed, Sarah V Clowes Candadai, Megan C Sikes, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|April 20, 2018
Analysis of 17 genes detects mutations in 81% of 811 patients with lissencephalyNataliya Di Donato, Andrew E Timms, Kimberly A Aldinger, et al.Pageof 76