Coppola, Giovanni

Association of Cognitive and Behavioral Features Between Adults With Tuberous Sclerosis and Frontotemporal Dementia

Liu, A. J., Staffaroni, A. M., Rojas-Martinez, J. C., Olney, N. T., Alquezar-Burillo, C., Ljubenkov, P. A., La Joie, R., Fong, J. C., Taylor, J., Karydas, A., et al. (2020) · JAMA Neurology

Tuberous Sclerosis Complex ResearchDementia and Cognitive Impairment Research

Cited by 18

Linking tuberous sclerosis complex, excessive mTOR signaling, and age-related neurodegeneration: a new association between TSC1 mutation and frontotemporal dementia

Olney, N. T., Alquezar, C., Ramos, E. M., Nana, A. L., Fong, J. C., Karydas, A. M., Taylor, J. B., Stephens, M. L., Argouarch, A. R., Van Berlo, V. A., et al. (2017) · Acta Neuropathologica

Tuberous Sclerosis Complex ResearchAlzheimer's disease research and treatments

Cited by 15

Technology Insight: querying the genome with microarrays—progress and hope for neurological disease

Coppola, G., & Geschwind, D. H. (2006) · Nature Clinical Practice Neurology

Gene expression and cancer classificationGenetic Associations and Epidemiology

Cited by 12

Identification of a rare coding variant in TREM2 in a Chinese individual with Alzheimer’s disease

Bonham, L. W., Sirkis, D. W., Fan, J., Aparicio, R. E., Tse, M., Ramos, E. M., Wang, Q., Coppola, G., Rosen, H. J., Miller, B. L., et al. (2017) · Neurocase

Alzheimer's disease research and treatmentsNeuroinflammation and Neurodegeneration Mechanisms

Cited by 10

AD-linked R47H- TREM2 mutation induces disease-enhancing proinflammatory microglial states in mice and humans

Sayed, F. A., Kodama, L., Udeochu, J. C., Fan, L., Carling, G. K., Le, D., Li, Q., Zhou, L., Mathys, H., Wang, M., et al. (2020) · bioRxiv (Cold Spring Harbor Laboratory)

Neuroinflammation and Neurodegeneration MechanismsAlzheimer's disease research and treatments

Cited by 3

De Novo Coding Variants Are Strongly Associated with Tourette Syndrome

Willsey, J., Fernandez, T., Yu, D., King, R., Dietrich, A., Xing, J., Sanders, S., Mandell, J., Neale, B., Coppola, G., et al. (2019) · European Neuropsychopharmacology

Obsessive-Compulsive Spectrum DisordersGenomics and Rare Diseases

Cited by 2