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Cerebellum & Ataxias|October 22, 2019
Spinocerebellar Ataxia type 29 in a family of Māori descentKathie J Ngo, Gemma Poke, Katherine Neas, et al.Iscience|March 30, 2023
Alterations in oligodendrocyte transcriptional networks reveal region-specific vulnerabilities to neurological diseaseDario Tommasini, Rachel Fox, Kathie J Ngo, et al.Journal of Medical Case Reports|April 26, 2023
Spinocerebellar ataxia type 14 (SCA14) in an Argentinian family: a case reportNiharika Duggirala, Kathie J Ngo, Sabrina M Pagnoni, et al.Plant Physiology|February 19, 2013
Production of a high-efficiency TILLING population through polyploidizationHelen Tsai, Victor Missirian, Kathie J Ngo, et al.Stroke|February 9, 2026
Cortical Oscillations as an Endophenotype Mediating ApoE-ε2 Effects on Poststroke Functional StatusCélia Delcamp, Anne Schwarz, Kathie J Ngo, et al.NPJ Parkinson'S Disease|April 25, 2024
Lysosomal genes contribute to Parkinson's disease near agriculture with high intensity pesticide useKathie J Ngo, Kimberly C Paul, Darice Wong, et al.Scientific Reports|May 11, 2021
A TILLING by sequencing approach to identify induced mutations in sunflower genesValentina Fanelli, Kathie J Ngo, Veronica L Thompson, et al.The Plant Cell|April 15, 2014
Efficient Genome-Wide Detection and Cataloging of EMS-Induced Mutations Using Exome Capture and Next-Generation SequencingIsabelle M Henry, Ugrappa Nagalakshmi, Meric C Lieberman, et al.Acta Neuropathologica Communications|December 19, 2021
De novo pathogenic variant in SETX causes a rapidly progressive neurodegenerative disorder of early childhood-onset with severe axonal polyneuropathyAristides Hadjinicolaou, Kathie J Ngo, Daniel Y Conway, et al.Plant Physiology|May 3, 2011
Discovery of rare mutations in populations: TILLING by sequencingHelen Tsai, Tyson Howell, Rebecca Nitcher, et al.Pageof 2