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Author Details
Full Name
Giovanni Coppola
Affiliation
David Geffen School of Medicine, University of California los angeles
ORCID
Career Start Year
1999
Papers
323
H Index
85
Expertise
CM4AI Collaborator
Nevan J Krogan (CM4AI)
PMID
Paper Title
Journal Title
Published Year
37887329
Astrocytes Undergo Metabolic Reprogramming in the Multiple Sclerosis Animal Model.
Cells
2023
32830380
Genetic and functional analysis of a Pacific hagfish opioid system.
J Neurosci Res
2022
36261683
Elk-1 regulates retinal ganglion cell axon regeneration after injury.
Sci Rep
2022
36261010
A molecular interactome of the glioblastoma perivascular niche reveals integrin binding sialoprotein as a mediator of tumor cell migration.
Cell Rep
2022
35981026
Functional regulatory variants implicate distinct transcriptional networks in dementia.
Science
2022
35226409
Remote blood collection from older adults in the Brain Health Registry for plasma biomarker and genetic analysis.
Alzheimers Dement
2022
35063084
Tau interactome maps synaptic and mitochondrial processes associated with neurodegeneration.
Cell
2022
35114102
Uninterrupted CAG repeat drives striatum-selective transcriptionopathy and nuclear pathogenesis in human Huntingtin BAC mice.
Neuron
2022
34591235
Epigenetic clock and methylation studies in vervet monkeys.
Geroscience
2022
34554282
IAPP-induced beta cell stress recapitulates the islet transcriptome in type 2 diabetes.
Diabetologia
2022
33247623
Brain volumetric deficits in MAPT mutation carriers: a multisite study.
Ann Clin Transl Neurol
2021
33674450
Selective axonal translation of the mRNA isoform encoding prenylated Cdc42 supports axon growth.
J Cell Sci
2021
33555315
miR-142-3p regulates cortical oligodendrocyte gene co-expression networks associated with tauopathy.
Hum Mol Genet
2021
34851693
AD-linked R47H-<i>TREM2</i> mutation induces disease-enhancing microglial states via AKT hyperactivation.
Sci Transl Med
2021
34496254
Topoisomerase I inhibition and peripheral nerve injury induce DNA breaks and ATF3-associated axon regeneration in sensory neurons.
Cell Rep
2021
34380036
Molecular and functional properties of cortical astrocytes during peripherally induced neuroinflammation.
Cell Rep
2021
34727153
ERAP1, ERAP2, and Two Copies of HLA-Aw19 Alleles Increase the Risk for Birdshot Chorioretinopathy in HLA-A29 Carriers.
Invest Ophthalmol Vis Sci
2021
34662886
Exome sequencing and analysis of 454,787 UK Biobank participants.
Nature
2021
34841284
Transcriptomic profiling of whole blood in 22q11.2 reciprocal copy number variants reveals that cell proportion highly impacts gene expression.
Brain Behav Immun Health
2021
34515347
The glycine arginine-rich domain of the RNA-binding protein nucleolin regulates its subcellular localization.
EMBO J
2021
34397420
HDinHD: A Rich Data Portal for Huntington's Disease Research.
J Huntingtons Dis
2021
34128833
GADD45A is a protective modifier of neurogenic skeletal muscle atrophy.
JCI Insight
2021
34210852
Sequencing of 640,000 exomes identifies <i>GPR75</i> variants associated with protection from obesity.
Science
2021
34139149
Specific and behaviorally consequential astrocyte G<sub>q</sub> GPCR signaling attenuation in vivo with iβARK.
Neuron
2021
33199433
Plasma Tau and Neurofilament Light in Frontotemporal Lobar Degeneration and Alzheimer Disease.
Neurology
2021
33310624
Reaction time and response inhibition in autosomal dominant Alzheimer's disease.
Brain Cogn
2021
31500805
Synaptic and Gene Regulatory Mechanisms in Schizophrenia, Autism, and 22q11.2 Copy Number Variant-Mediated Risk for Neuropsychiatric Disorders.
Biol Psychiatry
2020
32088381
DYNLRB1 is essential for dynein mediated transport and neuronal survival.
Neurobiol Dis
2020
31784375
Clinical and volumetric changes with increasing functional impairment in familial frontotemporal lobar degeneration.
Alzheimers Dement
2020
31805439
DNA Methylation Analysis Validates Organoids as a Viable Model for Studying Human Intestinal Aging.
Cell Mol Gastroenterol Hepatol
2020
31636026
The longitudinal evaluation of familial frontotemporal dementia subjects protocol: Framework and methodology.
Alzheimers Dement
2020
31720731
Activation of the HIF1α/PFKFB3 stress response pathway in beta cells in type 1 diabetes.
Diabetologia
2020
31860018
Association of Cognitive and Behavioral Features Between Adults With Tuberous Sclerosis and Frontotemporal Dementia.
JAMA Neurol
2020
31914230
Assessment of executive function declines in presymptomatic and mildly symptomatic familial frontotemporal dementia: NIH-EXAMINER as a potential clinical trial endpoint.
Alzheimers Dement
2020
31914218
Utility of the global CDR[®] plus NACC FTLD rating and development of scoring rules: Data from the ARTFL/LEFFTDS Consortium.
Alzheimers Dement
2020
31914217
Genetic screening of a large series of North American sporadic and familial frontotemporal dementia cases.
Alzheimers Dement
2020
32103041
Immunosuppressive effect and global dysregulation of blood transcriptome in response to psychosocial stress in vervet monkeys (Chlorocebus sabaeus).
Sci Rep
2020
32094344
Contribution of common and rare variants to bipolar disorder susceptibility in extended pedigrees from population isolates.
Transl Psychiatry
2020
31972607
Lack of Association Between the CCR5-delta32 Polymorphism and Neurodegenerative Disorders.
Alzheimer Dis Assoc Disord
2020
33087929
Exome sequencing and characterization of 49,960 individuals in the UK Biobank.
Nature
2020
33086039
Context-Specific Striatal Astrocyte Molecular Responses Are Phenotypically Exploitable.
Neuron
2020
33065005
A Ca<sup>2+</sup>-Dependent Switch Activates Axonal Casein Kinase 2α Translation and Drives G3BP1 Granule Disassembly for Axon Regeneration.
Curr Biol
2020
33001981
Altered expression of genes regulating inflammation and synaptogenesis during regrowth of afferent neurons to cochlear hair cells.
PLoS One
2020
32913184
DNA methylation study of Huntington's disease and motor progression in patients and in animal models.
Nat Commun
2020
32656921
Quality of life and caregiver burden in familial frontotemporal lobar degeneration: Analyses of symptomatic and asymptomatic individuals within the LEFFTDS cohort.
Alzheimers Dement
2020
32699140
Familial language network vulnerability in primary progressive aphasia.
Neurology
2020
32446642
Epilepsy and Electroencephalographic Abnormalities in SATB2-Associated Syndrome.
Pediatr Neurol
2020
32180125
Temporal variant of frontotemporal dementia in C9orf72 repeat expansion carriers: two case studies.
Brain Imaging Behav
2020
32203496
Astrocyte layers in the mammalian cerebral cortex revealed by a single-cell in situ transcriptomic map.
Nat Neurosci
2020
32376949
Injured adult neurons regress to an embryonic transcriptional growth state.
Nature
2020
1 - 50 of 323
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