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A. Noll · SciRah

Researcher profile · Semantic Scholar

A. Noll

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A. Noll — researcher profile on SciRah

h-index: 9
Works: 15
Citations: 2,295

Most-cited papers

Rapid Whole-Genome Sequencing for Genetic Disease Diagnosis in Neonatal Intensive Care Units
C. Saunders, Neil A. Miller, S. Soden, D. Dinwiddie +19 more
2012Science Translational Medicine637 citations Open access
Semantic Scholar
Effectiveness of exome and genome sequencing guided by acuity of illness for diagnosis of neurodevelopmental disorders
S. Soden, C. Saunders, L. Willig, E. Farrow +23 more
2014Science Translational Medicine537 citations Open access
Semantic Scholar
Whole-genome sequencing for identification of Mendelian disorders in critically ill infants: a retrospective analysis of diagnostic and clinical findings
L. Willig, J. Petrikin, Laurie D. Smith, C. Saunders +20 more
2015The Lancet Respiratory Medicine340 citations Open access
Semantic Scholar
Aneuploidy and polyploidy underlie adaptive evolution of yeast cells deprived of a conserved cytokinesis motor
Giulia Rancati, Norman Pavelka, Brian Fleharty, A. Noll +6 more
2008Cell330 citations Open access
Semantic Scholar
Identification of EMS-Induced Mutations in Drosophila melanogaster by Whole-Genome Sequencing
J. Blumenstiel, A. Noll, J. Griffiths, Anoja Perera +4 more
2009Genetics140 citations Open access
Semantic Scholar
Comparison of commercially available target enrichment methods for next-generation sequencing.
K. Bodi, Anoja Perera, P. Adams, D. Bintzler +9 more
2013Journal of Biomolecular Techniques125 citations Open access
Semantic Scholar
MMP21 is mutated in human heterotaxy and is required for normal left-right asymmetry in vertebrates
A. Guimier, George C. Gabriel, F. Bajolle, Michael Tsang +32 more
2015Nature Genetics84 citations Open access
Semantic Scholar
A Whole-Chromosome Analysis of Meiotic Recombination in Drosophila melanogaster
Danny E. Miller, Takeo Satomi, Kavyasree Nandanan, A. Paulson +9 more
2012G3: Genes, Genomes, Genetics65 citations Open access
Semantic Scholar
Clinical detection of deletion structural variants in whole-genome sequences
A. Noll, Neil A. Miller, Laurie D. Smith, B. Yoo +12 more
2016npj Genomic Medicine30 citations Open access
Semantic Scholar
Establishment of F1 hybrid mortality in real time
Ashley Saulsberry, Marisa Pinchas, A. Noll, J. Lynch +2 more
2017BMC Evolutionary Biology3 citations Open access
Semantic Scholar
Comparison of Custom Target Enrichment Methods: Agilent vs. Nimblegen
K. Bodi, P. Adams, D. Bintzler, K. Dewar +9 more
20111 citations
Semantic Scholar
Comparison of Commercially Available Target Enrichment Methods for Next Generation Sequencing with Illumina Platform.
P. Adams, D. Bintzler, K. Bodi, K. Dewar +8 more
20101 citations
Semantic Scholar
IDENTIFICATION AND CLINICAL ASSESSMENT OF DELETION STRUCTURAL VARIANTS IN WHOLE GENOME SEQUENCES OF ACUTELY ILL NEONATES
A. Noll
20140 citations
Semantic Scholar
Neonatal Intensive Care Units Rapid Whole-Genome Sequencing for Genetic Disease Diagnosis in
C. Saunders, Neil A. Miller, S. Soden, D. Dinwiddie +19 more
20120 citations
Semantic Scholar
Genomic Variation Research Group (GVRG): Analysis of Copy Number Variation in C. elegans using Next Generation Sequencing
B. Kingham, Sean M. Blake, A. Noll, C. Dagnall +6 more
20100 citations
Semantic Scholar

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