| Rapid whole-genome sequencing for genetic disease diagnosis in neonatal intensive care units CJ Saunders, NA Miller, SE Soden, DL Dinwiddie, A Noll, NA Alnadi, ... Science translational medicine 4 (154), 154ra135-154ra135, 2012 | 681 | 2012 |
| Effectiveness of exome and genome sequencing guided by acuity of illness for diagnosis of neurodevelopmental disorders SE Soden, CJ Saunders, LK Willig, EG Farrow, LD Smith, JE Petrikin, ... Science translational medicine 6 (265), 265ra168-265ra168, 2014 | 527 | 2014 |
| Whole-genome sequencing for identification of Mendelian disorders in critically ill infants: a retrospective analysis of diagnostic and clinical findings LK Willig, JE Petrikin, LD Smith, CJ Saunders, I Thiffault, NA Miller, ... The Lancet Respiratory Medicine 3 (5), 377-387, 2015 | 371 | 2015 |
| Aneuploidy underlies rapid adaptive evolution of yeast cells deprived of a conserved cytokinesis motor G Rancati, N Pavelka, B Fleharty, A Noll, R Trimble, K Walton, A Perera, ... Cell 135 (5), 879-893, 2008 | 356 | 2008 |
| Comparison of commercially available target enrichment methods for next-generation sequencing K Bodi, AG Perera, PS Adams, D Bintzler, K Dewar, DS Grove, ... Journal of biomolecular techniques: JBT 24 (2), 73, 2013 | 239 | 2013 |
| Identification of EMS-Induced Mutations in Drosophila melanogaster by Whole-Genome Sequencing JP Blumenstiel, AC Noll, JA Griffiths, AG Perera, KN Walton, WD Gilliland, ... Genetics 182 (1), 25-32, 2009 | 161 | 2009 |
| MMP21 is mutated in human heterotaxy and is required for normal left-right asymmetry in vertebrates A Guimier, GC Gabriel, F Bajolle, M Tsang, H Liu, A Noll, M Schwartz, ... Nature genetics 47 (11), 1260-1263, 2015 | 77 | 2015 |
| The Multiple Roles of Mps1 in Drosophila Female Meiosis WD Gilliland, SE Hughes, JL Cotitta, S Takeo, Y Xiang, RS Hawley PLoS genetics 3 (7), e113, 2007 | 61 | 2007 |
| A Whole-Chromosome Analysis of Meiotic Recombination in Drosophila melanogaster DE Miller, S Takeo, K Nandanan, A Paulson, MM Gogol, AC Noll, ... G3: Genes| Genomes| Genetics 2 (2), 249-260, 2012 | 60 | 2012 |
| Clinical detection of deletion structural variants in whole-genome sequences AC Noll, NA Miller, LD Smith, B Yoo, S Fiedler, LD Cooley, LK Willig, ... NPJ genomic medicine 1 (1), 1-11, 2016 | 34 | 2016 |
| Rapid whole-genome sequencing for genetic disease diagnosis in neonatal intensive care units. Sci Transl Med. 2012; 4: 154ra135 CJ Saunders, NA Miller, SE Soden, DL Dinwiddie, A Noll, NA Alnadi Medicinski podmladak, 2013 | 15 | 2013 |
| Low grade B cell lymphoma arising in a background of multifocal extra-adrenal myelolipoma A Noll, J Boone, M Cunningham, J Mammen, O Tawfik Annals of Clinical & Laboratory Science 43 (4), 441-446, 2013 | 8 | 2013 |
| Trends in the staff’s perception of patient safety culture in Romanian hospitals C Tereanu, A Noll, D Herghea, RI Malancea, A Tinca, I Eclemea, ... Current Health Sciences Journal 46 (3), 236, 2020 | 3 | 2020 |
| Comparison of commercially available target enrichment methods for next generation sequencing with Illumina platform PS Adams, D Bintzler, K Bodi, K Dewar, DS Grove, J Kieleczawa, ... Journal of Biomolecular Techniques: JBT 21 (3 Suppl), S17, 2010 | 1 | 2010 |
| Modeling heparin protocol dosing compliance using dynamic and static data to improve clinical outcomes Machine Learning in Healthcare, 2019 | | 2019 |
| DEFICIENCY OF ADENOSINE DEAMINASE 2: A RECENTLY DESCRIBED AUTOINFLAMMATORY DISEASE WITH NEUROLOGICAL MANIFESTATIONS (P1. 254) A Noll, E Kessler, S Gratton Neurology 88 (16 Supplement), 2017 | | 2017 |
| Whole-genome sequencing for identification of Mendelian disorders in critically ill infants L Steinmetz, JE Petrikin, LD Smith, CJ Saunders, I Thiffault, NA Miller, ... The Lancet Respiratory Medicine 3 (5), 377-387, 2015 | | 2015 |
| IDENTIFICATION AND CLINICAL ASSESSMENT OF DELETION STRUCTURAL VARIANTS IN WHOLE GENOME SEQUENCES OF ACUTELY ILL NEONATES AC Noll University of Kansas, 2014 | | 2014 |
| Identification of BCL9L as a Novel Heterotaxy Gene by Whole Genome Sequencing of a Quartet C Saunders, N Miller, S Soden, D Dinwiddie, A Noll, S Humphray, ... JOURNAL OF MOLECULAR DIAGNOSTICS 14 (6), 643-643, 2012 | | 2012 |
| A Whole-Chromosome Analysis of Meiotic DE Miller, S Takeo, K Nandanan, A Paulson, MM Gogol, AC Noll, ... | | 2012 |
