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Aaron Noll
Aaron Noll
Data Scientist Cerner Corporation
Verified email at cerner.com
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Cited by
Year
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
5942012
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
4632014
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
3222008
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
2962015
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
2152013
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
1502009
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
702015
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
562007
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
532012
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
272016
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
222013
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
82013
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
12020
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
12010
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
Decipher the transcriptome during mouse liver development by RNA-Seq
JY Cui, A Noll, S Gunewardena, B Yoo, H Lu, X Zhong, C Klaassen
DRUG METABOLISM REVIEWS 43, 33-33, 2011
2011
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