Alexis L Norris
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Explore the profile of Alexis L Norris including associated specialties, affiliations and a list of published articles.
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18
Citations
543
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Recent Articles
1.
2.
Duggirala H, Johnson J, Tadesse D, Hsu C, Norris A, Faust J, et al.
Am J Vet Res
. 2025 Jan;
1-6.
PMID: 39819607
The US FDA's Center for Veterinary Medicine (CVM) is advancing its leadership in veterinary science by integrating AI and machine learning (ML) into its regulatory framework and scientific initiatives. This...
3.
Kiesler P, Lee S, Norris A, Miller M, Mercado C, Moyer A, et al.
STAR Protoc
. 2024 Oct;
5(4):103385.
PMID: 39392744
Genome editing technology is being used in animals for a variety of purposes, including improvement of animal and public health outcomes. Characterization of genome editing reagents and anticipated genomic alterations...
4.
Gilpatrick T, Wang J, Weiss D, Norris A, Eshleman J, Timp W
bioRxiv
. 2023 Feb;
PMID: 36798399
Generating high-coverage sequencing coverage at select genomic loci has extensive applications in both research science and genetic medicine. Long-read sequencing technologies (e.g. nanopore sequencing) have expanded our ability to generate...
5.
Kondo M, Norris A, Yang K, Cheshire M, Newkirk I, Chen X, et al.
Neurosci Res
. 2022 Sep;
185:67-72.
PMID: 36162734
Here we re-analyze RNA-sequencing data from the anterior cingulate cortex (ACC) of SZ patients using recent methods to improve accuracy and sensitivity of results, such as the quality surrogate variable...
6.
Endothelial p.R183Q Increases ANGPT2 (Angiopoietin-2) and Drives Formation of Enlarged Blood Vessels
Huang L, Bichsel C, Norris A, Thorpe J, Pevsner J, Alexandrescu S, et al.
Arterioscler Thromb Vasc Biol
. 2021 Oct;
42(1):e27-e43.
PMID: 34670408
Objective: Capillary malformation (CM) occurs sporadically and is associated with Sturge-Weber syndrome. The somatic mosaic mutation in (c.548G>A, p.R183Q) is enriched in endothelial cells (ECs) in skin CM and Sturge-Weber...
7.
Osei-Owusu I, Norris A, Joynt A, Thorpe J, Cho S, Tierney E, et al.
Cold Spring Harb Mol Case Stud
. 2020 Dec;
6(6).
PMID: 33335013
Chromosomal structural variation can cause severe neurodevelopmental and neuropsychiatric phenotypes. Here we present a nonverbal female adolescent with severe stereotypic movement disorder with severe problem behavior (e.g., self-injurious behavior, aggression,...
8.
Marti-Carreras J, Rafael Gener A, D Miller S, Brito A, Camacho C, Connor R, et al.
Viruses
. 2020 Dec;
12(12).
PMID: 33322070
Viruses represent important test cases for data federation due to their genome size and the rapid increase in sequence data in publicly available databases. However, some consequences of previously decentralized...
9.
Norris A, Lee S, Greenlees K, Tadesse D, Miller M, Lombardi H
Nat Biotechnol
. 2020 Mar;
38(4):503.
PMID: 32139895
An amendment to this paper has been published and can be accessed via a link at the top of the paper.
10.
Norris A, Lee S, Greenlees K, Tadesse D, Miller M, Lombardi H
Nat Biotechnol
. 2020 Feb;
38(2):163-164.
PMID: 32034391
No abstract available.