| Altered neuronal migratory trajectories in human cerebral organoids derived from individuals with neuronal heterotopia J Klaus, S Kanton, C Kyrousi, AC Ayo-Martin, R Di Giaimo, S Riesenberg, ... Nature medicine 25 (4), 561-568, 2019 | 146 | 2019 |
| Mutations in DVL1 cause an osteosclerotic form of Robinow syndrome KJ Bunn, P Daniel, HS Rösken, AC O’Neill, SR Cameron-Christie, ... The American Journal of Human Genetics 96 (4), 623-630, 2015 | 97 | 2015 |
| De novo and inherited private variants in MAP1B in periventricular nodular heterotopia EL Heinzen, AC O'Neill, X Zhu, AS Allen, M Bahlo, J Chelly, MH Chen, ... PLoS genetics 14 (5), e1007281, 2018 | 49 | 2018 |
| A primate-specific isoform of PLEKHG6 regulates neurogenesis and neuronal migration AC O’Neill, C Kyrousi, J Klaus, RJ Leventer, EP Kirk, A Fry, DT Pilz, ... Cell reports 25 (10), 2729-2741. e6, 2018 | 46 | 2018 |
| Cohesin and CTCF differentially regulate spatiotemporal runx1 expression during zebrafish development J Marsman, AC O'Neill, BRY Kao, JM Rhodes, M Meier, J Antony, ... Biochimica et Biophysica Acta (BBA)-Gene Regulatory Mechanisms 1839 (1), 50-61, 2014 | 42 | 2014 |
| ECE 2 regulates neurogenesis and neuronal migration during human cortical development IY Buchsbaum, P Kielkowski, G Giorgio, AC O'Neill, R Di Giaimo, ... EMBO reports 21 (5), e48204, 2020 | 41 | 2020 |
| The X‐linked filaminopathies: Synergistic insights from clinical and molecular analysis EM Wade, BJ Halliday, ZA Jenkins, AC O'Neill, SP Robertson Human mutation 41 (5), 865-883, 2020 | 36 | 2020 |
| Mob2 insufficiency disrupts neuronal migration in the developing cortex AC O’Neill, C Kyrousi, M Einsiedler, I Burtscher, M Drukker, DM Markie, ... Frontiers in Cellular Neuroscience 12, 57, 2018 | 36 | 2018 |
| Spatial centrosome proteome of human neural cells uncovers disease-relevant heterogeneity AC O’Neill, F Uzbas, G Antognolli, F Merino, K Draganova, A Jäck, ... Science 376 (6599), eabf9088, 2022 | 32 | 2022 |
| Extracellular LGALS3BP regulates neural progenitor position and relates to human cortical complexity C Kyrousi, AC O’neill, A Brazovskaja, Z He, P Kielkowski, L Coquand, ... Nature Communications 12 (1), 6298, 2021 | 31 | 2021 |
| Human kidney cell reprogramming: applications for disease modeling and personalized medicine AC O’Neill, SD Ricardo Journal of the American Society of Nephrology 24 (9), 1347-1356, 2013 | 27 | 2013 |
| Nucleus size and DNA accessibility are linked to the regulation of paraspeckle formation in cellular differentiation M Grosch, S Ittermann, E Rusha, T Greisle, C Ori, DJJ Truong, AC O’Neill, ... BMC biology 18, 1-19, 2020 | 22 | 2020 |
| Spatial centrosome proteomic profiling of human iPSC-derived neural cells F Uzbas, AC O’Neill Bio-protocol 13 (17), 2023 | 2 | 2023 |
| Menke-Hennekam syndrome subtypes caused by variants in the Zinc finger domains ZZ and TAZ2 and the fourth intrinsically disordered linker of CBP and p300 LA Menke, ZA Jenkins, E Williams, G Gimenez, AC O'Neill, RC Hennekam, ... EUROPEAN JOURNAL OF HUMAN GENETICS 28 (SUPPL 1), 471-471, 2020 | 1 | 2020 |
| Rare Variants in Periventricular Neuronal Heterotopia A O'Neill University of Otago, 2016 | | 2016 |
| REPROGRAMMING HUMAN KIDNEY CELLS TO GENERATE PODOCYTE PROGENITORS: APPLICATIONS FOR DISEASE MODELLING AND CELLULAR REPLACEMENT SD Ricardo, BI Song, AM Smink, CV Jones, A O'Neill, AL Laslett, PG Kerr NEPHROLOGY 17, 61-61, 2012 | | 2012 |
