Deeann Wallis

Publication Activity (10 Years)

Years Active: 2018-2024
Publications (10 Years): 10

Top Topics

Inflammatory Response

Saccharomyces Cerevisiae

Extracellular Matrix

Top Venues

Acta neuropathologica communications

American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics

This page only lists publications with an associated author ORCID identifier.

Publications

Yunjia Chen, Yulong Fu, Magdalena Koczkowska, Tom Callens, Alicia Gomes, Jian Liu, William Bradley, Bryce Brown, Brandon Shaw, Daniela D'Agostino, Chuanhua Fu, Deeann Wallis
Genotype-Phenotype Correlation in Neurofibromatosis Type 1: Evidence for a Mild Phenotype Associated with Splicing Variants Leading to In-Frame Skipping of NF1 Exon 24 [19a]. Cancers 16 (13) (2024)
Cameron Church, Christian X Fay, Emil Kriukov, Hui Liu, Ashley Cannon, Lauren Ashley Baldwin, David K Crossman, Bruce Korf, Margaret R Wallace, Andrea M Gross, Brigitte C Widemann, Robert A Kesterson, Petr Baranov, Deeann Wallis
snRNA-seq of human cutaneous neurofibromas before and after selumetinib treatment implicates role of altered Schwann cell states, inter-cellular signaling, and extracellular matrix in treatment response. Acta neuropathologica communications 12 (1) (2024)
Yunjia Chen, Yulong Fu, Magdalena Koczkowska, Tom Callens, Alicia Gomes, Jian Liu, William Bradley, Bryce Brown, Brandon Shaw, Daniela D'Agostino, Chuanhua Fu, Deeann Wallis
Genotype-Phenotype Correlation in Neurofibromatosis Type 1: Evidence for a Mild Phenotype Associated with Splicing Variants Leading to In-Frame Skipping of NF1 Exon 24 [19a]. Cancers 16 (13) (2024)
Cameron Church, Christian X Fay, Emil Kriukov, Hui Liu, Ashley Cannon, Lauren Ashley Baldwin, David K Crossman, Bruce Korf, Margaret R Wallace, Andrea M Gross, Brigitte C Widemann, Robert A Kesterson, Petr Baranov, Deeann Wallis
snRNA-seq of human cutaneous neurofibromas before and after selumetinib treatment implicates role of altered Schwann cell states, inter-cellular signaling, and extracellular matrix in treatment response. Acta neuropathologica communications 12 (1) (2024)
Verena Staedtke, Kara Anstett, David Bedwell, Marco Giovannini, Kim Keeling, Robert Kesterson, YooRi Kim, Bruce Korf, André Leier, Miranda L McManus, Herb Sarnoff, Jeremie Vitte, James A Walker, Scott R Plotkin, Deeann Wallis
Gene-targeted therapy for neurofibromatosis and schwannomatosis: The path to clinical trials. Clinical trials (London, England) (2023)
Ashlee Long, Andrew Crouse, Robert A Kesterson, Matthew Might, Deeann Wallis
Functional characterization and potential therapeutic avenues for variants in the NTRK2 gene causing developmental and epileptic encephalopathies. American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics (2021)
Ashlee Long, Hui Liu, Jian Liu, Michael Daniel, David M Bedwell, Bruce Korf, Robert A Kesterson, Deeann Wallis
Analysis of patient-specific NF1 variants leads to functional insights for Ras signaling that can impact personalized medicine. Human mutation (2021)
Elias K Awad, Marc Moore, Hui Liu, Lukasz Ciszewski, Laura Lambert, Bruce R Korf, Linda J Popplewell, Robert A Kesterson, Deeann Wallis
Restoration of Normal NF1 Function with Antisense Morpholino Treatment of Recurrent Pathogenic Patient-Specific Variant c.1466A>G; p.Y489C. Journal of personalized medicine 11 (12) (2021)
Rachel M Carnes, Robert A Kesterson, Bruce R Korf, James A Mobley, Deeann Wallis
Affinity Purification of NF1 Protein-Protein Interactors Identifies Keratins and Neurofibromin Itself as Binding Partners. Genes 10 (9) (2019)
Deeann Wallis, Kairong Li, Hui Lui, Ke Hu, Mei-Jan Chen, Jing Li, Jungsoon Kang, Shamik Das, Bruce R Korf, Robert A Kesterson
Neurofibromin (NF1) genetic variant structure-function analyses using a full-length mouse cDNA. Human mutation 39 (6) (2018)