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Author Details

Giovanni Coppola
David Geffen School of Medicine, University of California los angeles
1999
323
85
Nevan J Krogan (CM4AI)
PMIDPaper TitleJournal TitlePublished Year
37887329Astrocytes Undergo Metabolic Reprogramming in the Multiple Sclerosis Animal Model.Cells2023
32830380Genetic and functional analysis of a Pacific hagfish opioid system.J Neurosci Res2022
36261683Elk-1 regulates retinal ganglion cell axon regeneration after injury.Sci Rep2022
36261010A molecular interactome of the glioblastoma perivascular niche reveals integrin binding sialoprotein as a mediator of tumor cell migration.Cell Rep2022
35981026Functional regulatory variants implicate distinct transcriptional networks in dementia.Science2022
35226409Remote blood collection from older adults in the Brain Health Registry for plasma biomarker and genetic analysis.Alzheimers Dement2022
35063084Tau interactome maps synaptic and mitochondrial processes associated with neurodegeneration.Cell2022
35114102Uninterrupted CAG repeat drives striatum-selective transcriptionopathy and nuclear pathogenesis in human Huntingtin BAC mice.Neuron2022
34591235Epigenetic clock and methylation studies in vervet monkeys.Geroscience2022
34554282IAPP-induced beta cell stress recapitulates the islet transcriptome in type 2 diabetes.Diabetologia2022
33247623Brain volumetric deficits in MAPT mutation carriers: a multisite study.Ann Clin Transl Neurol2021
33674450Selective axonal translation of the mRNA isoform encoding prenylated Cdc42 supports axon growth.J Cell Sci2021
33555315miR-142-3p regulates cortical oligodendrocyte gene co-expression networks associated with tauopathy.Hum Mol Genet2021
34851693AD-linked R47H-<i>TREM2</i> mutation induces disease-enhancing microglial states via AKT hyperactivation.Sci Transl Med2021
34496254Topoisomerase I inhibition and peripheral nerve injury induce DNA breaks and ATF3-associated axon regeneration in sensory neurons.Cell Rep2021
34380036Molecular and functional properties of cortical astrocytes during peripherally induced neuroinflammation.Cell Rep2021
34727153ERAP1, ERAP2, and Two Copies of HLA-Aw19 Alleles Increase the Risk for Birdshot Chorioretinopathy in HLA-A29 Carriers.Invest Ophthalmol Vis Sci2021
34662886Exome sequencing and analysis of 454,787 UK Biobank participants.Nature2021
34841284Transcriptomic profiling of whole blood in 22q11.2 reciprocal copy number variants reveals that cell proportion highly impacts gene expression.Brain Behav Immun Health2021
34515347The glycine arginine-rich domain of the RNA-binding protein nucleolin regulates its subcellular localization.EMBO J2021
34397420HDinHD: A Rich Data Portal for Huntington's Disease Research.J Huntingtons Dis2021
34128833GADD45A is a protective modifier of neurogenic skeletal muscle atrophy.JCI Insight2021
34210852Sequencing of 640,000 exomes identifies <i>GPR75</i> variants associated with protection from obesity.Science2021
34139149Specific and behaviorally consequential astrocyte G<sub>q</sub> GPCR signaling attenuation in vivo with iβARK.Neuron2021
33199433Plasma Tau and Neurofilament Light in Frontotemporal Lobar Degeneration and Alzheimer Disease.Neurology2021
33310624Reaction time and response inhibition in autosomal dominant Alzheimer's disease.Brain Cogn2021
31500805Synaptic and Gene Regulatory Mechanisms in Schizophrenia, Autism, and 22q11.2 Copy Number Variant-Mediated Risk for Neuropsychiatric Disorders.Biol Psychiatry2020
32088381DYNLRB1 is essential for dynein mediated transport and neuronal survival.Neurobiol Dis2020
31784375Clinical and volumetric changes with increasing functional impairment in familial frontotemporal lobar degeneration.Alzheimers Dement2020
31805439DNA Methylation Analysis Validates Organoids as a Viable Model for Studying Human Intestinal Aging.Cell Mol Gastroenterol Hepatol2020
31636026The longitudinal evaluation of familial frontotemporal dementia subjects protocol: Framework and methodology.Alzheimers Dement2020
31720731Activation of the HIF1α/PFKFB3 stress response pathway in beta cells in type 1 diabetes.Diabetologia2020
31860018Association of Cognitive and Behavioral Features Between Adults With Tuberous Sclerosis and Frontotemporal Dementia.JAMA Neurol2020
31914230Assessment of executive function declines in presymptomatic and mildly symptomatic familial frontotemporal dementia: NIH-EXAMINER as a potential clinical trial endpoint.Alzheimers Dement2020
31914218Utility of the global CDR[®] plus NACC FTLD rating and development of scoring rules: Data from the ARTFL/LEFFTDS Consortium.Alzheimers Dement2020
31914217Genetic screening of a large series of North American sporadic and familial frontotemporal dementia cases.Alzheimers Dement2020
32103041Immunosuppressive effect and global dysregulation of blood transcriptome in response to psychosocial stress in vervet monkeys (Chlorocebus sabaeus).Sci Rep2020
32094344Contribution of common and rare variants to bipolar disorder susceptibility in extended pedigrees from population isolates.Transl Psychiatry2020
31972607Lack of Association Between the CCR5-delta32 Polymorphism and Neurodegenerative Disorders.Alzheimer Dis Assoc Disord2020
33087929Exome sequencing and characterization of 49,960 individuals in the UK Biobank.Nature2020
33086039Context-Specific Striatal Astrocyte Molecular Responses Are Phenotypically Exploitable.Neuron2020
33065005A Ca<sup>2+</sup>-Dependent Switch Activates Axonal Casein Kinase 2α Translation and Drives G3BP1 Granule Disassembly for Axon Regeneration.Curr Biol2020
33001981Altered expression of genes regulating inflammation and synaptogenesis during regrowth of afferent neurons to cochlear hair cells.PLoS One2020
32913184DNA methylation study of Huntington's disease and motor progression in patients and in animal models.Nat Commun2020
32656921Quality of life and caregiver burden in familial frontotemporal lobar degeneration: Analyses of symptomatic and asymptomatic individuals within the LEFFTDS cohort.Alzheimers Dement2020
32699140Familial language network vulnerability in primary progressive aphasia.Neurology2020
32446642Epilepsy and Electroencephalographic Abnormalities in SATB2-Associated Syndrome.Pediatr Neurol2020
32180125Temporal variant of frontotemporal dementia in C9orf72 repeat expansion carriers: two case studies.Brain Imaging Behav2020
32203496Astrocyte layers in the mammalian cerebral cortex revealed by a single-cell in situ transcriptomic map.Nat Neurosci2020
32376949Injured adult neurons regress to an embryonic transcriptional growth state.Nature2020
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University of Pennsylvania
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Indiana University School of Medicine
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University of British Columbia
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