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Author

Matt Wilsey

Observed name: Wilsey, Matt
Observed institution: Grace Science Foundation
ORCID: 0000-0001-9418-7010
Observed ORCID: 0000-0001-9418-7010
OpenAlex ID: A5077892538
The shifting model in clinical diagnostics: how next-generation sequencing and families are altering the way rare diseases are discovered, studied, and treated
2014 · Matthew Might, Matt Wilsey · Genetics in Medicine · 80
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NGLY1 deficiency: estimated incidence, clinical features, and genotypic spectrum from the NGLY1 Registry
2022 · Caroline R. Stanclift, Selina S. Dwight, et al. · Orphanet Journal of Rare Diseases · 28
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GlcNAc-Asn is a biomarker for NGLY1 deficiency
2021 · William F Mueller, Lei Zhu, et al. · The Journal of Biochemistry · 27
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AAV9-NGLY1 gene replacement therapy improves phenotypic and biomarker endpoints in a rat model of NGLY1 Deficiency
2022 · Lei Zhu, Brandon Tan, et al. · Molecular Therapy — Methods & Clinical Development · 24
NGLY1 deficiency: a prospective natural history study
2023 · Sandra Tong, Pamela Ventola, et al. · Human Molecular Genetics · 17
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Preclinical pharmacology and safety studies to support an AAV9 NGLY1 gene therapy clinical trial for the treatment of NGLY1 deficiency
2025 · Lei Zhu, Jennifer W. Cook, et al. · Molecular Therapy — Methods & Clinical Development · 2
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Natural history of NGLY1 deficiency: motor function & clinical features
2026 · Grace Morrison, Selina Dwight, et al. · Human Molecular Genetics · 1
MRI Characterization of Structural Brain Abnormalities in NGLY1 Deficiency
2026 · Emily L. Dennis, Lei Zhu, et al. · International Journal of Developmental Neuroscience
In This Issue
2014 · Matthew Might, Matt Wilsey · Genetics in Medicine
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Works count: 11
Citation count: 179
H-index: 5
I10-index: 5
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