Giovanni Coppola
Giovanni Coppola
Verified email at ucla.edu - Homepage
TitleCited byYear
Expanded GGGGCC Hexanucleotide Repeat in Noncoding Region of C9ORF72 Causes Chromosome 9p-Linked FTD and ALS
M DeJesus-Hernandez, IR Mackenzie, BF Boeve, AL Boxer, M Baker, ...
Neuron 72 (2), 245-256, 2011
30472011
Neuroprotective effects of brain-derived neurotrophic factor in rodent and primate models of Alzheimer's disease
AH Nagahara, DA Merrill, G Coppola, S Tsukada, BE Schroeder, ...
Nature medicine 15 (3), 331, 2009
7812009
Astrocyte scar formation aids central nervous system axon regeneration
MA Anderson, JE Burda, Y Ren, Y Ao, TM O’Shea, R Kawaguchi, ...
Nature 532 (7598), 195, 2016
5562016
Identification of common variants associated with human hippocampal and intracranial volumes
JL Stein, SE Medland, AA Vasquez, DP Hibar, RE Senstad, AM Winkler, ...
Nature genetics 44 (5), 552, 2012
5002012
Functional and evolutionary insights into human brain development through global transcriptome analysis
MB Johnson, YI Kawasawa, CE Mason, Ž Krsnik, G Coppola, ...
Neuron 62 (4), 494-509, 2009
4662009
Human-specific transcriptional regulation of CNS development genes by FOXP2
G Konopka, JM Bomar, K Winden, G Coppola, ZO Jonsson, F Gao, ...
Nature 462 (7270), 213, 2009
4092009
The ENIGMA Consortium: large-scale collaborative analyses of neuroimaging and genetic data
PM Thompson, JL Stein, SE Medland, DP Hibar, AA Vasquez, ...
Brain imaging and behavior 8 (2), 153-182, 2014
2952014
Identification of the Transcriptional Targets of FOXP2, a Gene Linked to Speech and Language, in Developing Human Brain
E Spiteri, G Konopka, G Coppola, J Bomar, M Oldham, J Ou, SC Vernes, ...
The American Journal of Human Genetics 81 (6), 1144-1157, 2007
2952007
The HDAC inhibitor 4b ameliorates the disease phenotype and transcriptional abnormalities in Huntington's disease transgenic mice
EA Thomas, G Coppola, PA Desplats, B Tang, E Soragni, R Burnett, ...
Proceedings of the National Academy of Sciences 105 (40), 15564-15569, 2008
2632008
Transcriptome analysis of embryonic and adult sensory axons reveals changes in mRNA repertoire localization
LF Gumy, GSH Yeo, YCL Tung, KH Zivraj, D Willis, G Coppola, BYH Lam, ...
Rna 17 (1), 85-98, 2011
2392011
Progranulin deficiency promotes circuit-specific synaptic pruning by microglia via complement activation
H Lui, J Zhang, SR Makinson, MK Cahill, KW Kelley, HY Huang, Y Shang, ...
Cell 165 (4), 921-935, 2016
2302016
An age-related sprouting transcriptome provides molecular control of axonal sprouting after stroke
S Li, JJ Overman, D Katsman, SV Kozlov, CJ Donnelly, JL Twiss, RJ Giger, ...
Nature neuroscience 13 (12), 1496, 2010
2252010
HDAC inhibitors correct frataxin deficiency in a Friedreich ataxia mouse model
M Rai, E Soragni, K Jenssen, R Burnett, D Herman, G Coppola, ...
PloS one 3 (4), e1958, 2008
2072008
Multiple chronic pain states are associated with a common amino acid–changing allele in KCNS1
M Costigan, I Belfer, RS Griffin, F Dai, LB Barrett, G Coppola, T Wu, ...
Brain 133 (9), 2519-2527, 2010
2012010
Combined intrinsic and extrinsic neuronal mechanisms facilitate bridging axonal regeneration one year after spinal cord injury
K Kadoya, S Tsukada, P Lu, G Coppola, D Geschwind, MT Filbin, ...
Neuron 64 (2), 165-172, 2009
1992009
Phenotypic variability associated with progranulin haploinsufficiency in patients with the common 1477C→ T (Arg493X) mutation: an international initiative
R Rademakers, M Baker, J Gass, J Adamson, ED Huey, P Momeni, ...
The Lancet Neurology 6 (10), 857-868, 2007
1982007
Genome-wide analyses of human perisylvian cerebral cortical patterning
BS Abrahams, D Tentler, JV Perederiy, MC Oldham, G Coppola, ...
Proceedings of the National Academy of Sciences 104 (45), 17849-17854, 2007
1932007
Network organization of the huntingtin proteomic interactome in mammalian brain
DI Shirasaki, ER Greiner, I Al-Ramahi, M Gray, P Boontheung, ...
Neuron 75 (1), 41-57, 2012
1792012
Efficient differentiation of human pluripotent stem cells to endothelial progenitors via small-molecule activation of WNT signaling
X Lian, X Bao, A Al-Ahmad, J Liu, Y Wu, W Dong, KK Dunn, EV Shusta, ...
Stem cell reports 3 (5), 804-816, 2014
1752014
Mutations in the gene encoding PDGF-B cause brain calcifications in humans and mice
A Keller, A Westenberger, MJ Sobrido, M García-Murias, A Domingo, ...
Nature genetics 45 (9), 1077, 2013
1752013
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Articles 1–20