| Discovery of rare mutations in populations: TILLING by sequencing H Tsai, T Howell, R Nitcher, V Missirian, B Watson, KJ Ngo, M Lieberman, ... Plant physiology 156 (3), 1257-1268, 2011 | 324 | 2011 |
| Efficient genome-wide detection and cataloging of EMS-induced mutations using exome capture and next-generation sequencing IM Henry, U Nagalakshmi, MC Lieberman, KJ Ngo, KV Krasileva, ... The Plant Cell 26 (4), 1382-1397, 2014 | 287 | 2014 |
| Evidence for carbon saturation in a highly structured and organic‐matter‐rich soil H Chung, KJ Ngo, A Plante, J Six Soil Science Society of America Journal 74 (1), 130-138, 2010 | 121 | 2010 |
| An intronic GAA repeat expansion in FGF14 causes the autosomal-dominant adult-onset ataxia SCA27B/ATX-FGF14 H Rafehi, J Read, DJ Szmulewicz, KC Davies, P Snell, LG Fearnley, ... The American Journal of Human Genetics 110 (1), 105-119, 2023 | 79 | 2023 |
| A diagnostic ceiling for exome sequencing in cerebellar ataxia and related neurological disorders KJ Ngo, JE Rexach, H Lee, LE Petty, S Perlman, JM Valera, JL Deignan, ... Human mutation 41 (2), 487-501, 2020 | 71 | 2020 |
| Production of a high-efficiency TILLING population through polyploidization H Tsai, V Missirian, KJ Ngo, RK Tran, SR Chan, V Sundaresan, L Comai Plant physiology 161 (4), 1604-1614, 2013 | 69 | 2013 |
| Early Disruption of Maternal–Zygotic Interaction and Activation of Defense-Like Responses in Arabidopsis Interspecific Crosses D Burkart-Waco, K Ngo, B Dilkes, C Josefsson, L Comai The Plant Cell 25 (6), 2037-2055, 2013 | 40 | 2013 |
| Perturbation of parentally biased gene expression during interspecific hybridization D Burkart-Waco, K Ngo, M Lieberman, L Comai PLoS One 10 (2), e0117293, 2015 | 35 | 2015 |
| Expanding the global prevalence of spinocerebellar ataxia type 42 K Ngo, M Aker, LE Petty, J Chen, F Cavalcanti, AB Nelson, S Hassin-Baer, ... Neurology: Genetics 4 (3), e232, 2018 | 16 | 2018 |
| A TILLING by sequencing approach to identify induced mutations in sunflower genes V Fanelli, KJ Ngo, VL Thompson, BR Silva, H Tsai, W Sabetta, ... Scientific reports 11 (1), 9885, 2021 | 13 | 2021 |
| Effectiveness of sodium azide alone compared to sodium azide in combination with methyl nitrosurea for rice mutagenesis TH Tai, A Chun, IM Henry, KJ Ngo, D Burkart-Waco Plant Breeding and Biotechnology 4 (4), 453-461, 2016 | 12 | 2016 |
| Next-generation sequencing for targeted discovery of rare mutations in rice D Burkart-Waco, H Tsai, K Ngo, IM Henry, L Comai, TH Tai Biotechnologies for plant mutation breeding, 323-340, 2017 | 11 | 2017 |
| Tilling by sequencing H Tsai, K Ngo, M Lieberman, V Missirian, L Comai Plant functional genomics: methods and protocols, 359-380, 2015 | 8 | 2015 |
| De novo pathogenic variant in SETX causes a rapidly progressive neurodegenerative disorder of early childhood-onset with severe axonal polyneuropathy A Hadjinicolaou, KJ Ngo, DY Conway, JP Provias, SK Baker, LI Brady, ... Acta Neuropathologica Communications 9 (1), 194, 2021 | 7 | 2021 |
| Lack of association between GBA mutations and motor complications in European and American Parkinson’s disease cohorts J Maple-Grødem, KC Paul, I Dalen, KJ Ngo, D Wong, AD Macleod, ... Journal of Parkinson's disease 11 (4), 1569-1578, 2021 | 6 | 2021 |
| miR-142-3p regulates cortical oligodendrocyte gene co-expression networks associated with tauopathy JD Hinman, KJ Ngo, D Kim, C Chen, CR Abraham, M Ghanbari, MA Ikram, ... Human molecular genetics 30 (1), 103-118, 2021 | 5 | 2021 |
| Spinocerebellar ataxia type 29 in a family of Māori descent KJ Ngo, G Poke, K Neas, BL Fogel Cerebellum & Ataxias 6, 1-4, 2019 | 3 | 2019 |
| Alterations in oligodendrocyte transcriptional networks reveal region-specific vulnerabilities to neurological disease D Tommasini, R Fox, KJ Ngo, JD Hinman, BL Fogel iScience 26 (4), 2023 | 1 | 2023 |
| Determining mutation density using restriction enzyme sequence comparative analysis (RESCAN) D Burkart-Waco, IM Henry, K Ngo, L Comai, TH Tai Biotechnologies for Plant Mutation Breeding: Protocols, 305-321, 2017 | 1 | 2017 |
| Cross-Sectional Analysis of Exome Sequencing Diagnosis in Patients With Neurologic Phenotypes Facing Barriers to Clinical Testing S Watson, KJ Ngo, HA Stevens, DY Wong, J Kim, Y Song, B Han, SI Hyun, ... Neurology: Genetics 10 (3), e200133, 2024 | | 2024 |
