Follow
Adam O'Neill
Adam O'Neill
University of Otago
No verified email
Title
Cited by
Cited by
Year
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
1472019
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
972015
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
502018
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
462018
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
422014
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
412020
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
362018
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
352020
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
342022
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
322021
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
272013
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
242020
Spatial centrosome proteomic profiling of human iPSC-derived neural cells
F Uzbas, AC O’Neill
Bio-protocol 13 (17), 2023
22023
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
12020
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
The system can't perform the operation now. Try again later.
Articles 1–16