Fabiana Longo
Assistant Project Scientist, Department of Pathology & Lab Medicine, School of Medicine
Biography
Fabiana Longo, Ph.D., is an Assistant Project Scientist in the Department of Pathology and Laboratory Medicine at the University of California, Irvine. She received her Ph.D. in Experimental and Translational Medicine with a curriculum in Neuroscience from the University of Insubria in 2019, completing her doctoral research at San Raffaele Scientific Institute in Milan, Italy. Her research focuses on understanding the molecular mechanisms of neurodegeneration in genetic diseases and developing targeted translational approaches for treatment.
Longo's work at UCI centers on spinocerebellar ataxias, particularly Spinocerebellar Ataxia Type 7 (SCA7), where she investigates alterations in GABAergic inhibitory transmission and their role in disease progression. Her research employs both pharmacological and genetic approaches to modulate cerebellar circuitry, with findings that may extend to other polyglutamine ataxias. She has contributed to research demonstrating that zebrin-II cell subtype dysregulation is a shared feature across multiple polyglutamine ataxia mouse models and patients. Her earlier work in Italy examined the pathophysiology of Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay (ARSACS), including the discovery that co-translational degradation of mutant sacsin explains the lack of genotype-phenotype correlation in ARSACS patients.
Longo has published first-author papers in journals including Neurology and Human Molecular Genetics, and has contributed to research published in Science Translational Medicine and the Journal of Clinical Investigation. She has presented her research at international conferences including the Gordon Research Conference on CAG Triplet Repeat Disorders and the International Congress for Ataxia Research. At UCI, she mentors undergraduate and graduate students through the Biological Sciences Undergraduate Research Program and has served as a wet lab instructor for diversity initiatives.
Return to topEducation
- PhD in Experimental and Translational Medicine, curriculum of Neuroscience, University of Insubria, 2019
- Master's Degree in Medical Biotechnology and Molecular Medicine, curriculum of Neuroscience, University of Milan, 2014
- Bachelor's Degree in Biotechnology, University of Parma, 2012
Distinctions
- Fondazione Centro San Raffaele research fellowship, 2018 FCSR FELLOWSHIP PROGRAM, 2018
- Post graduate research fellowship, San Raffaele Scientific Institute, 2015
- Winner of the best poster, CHOC & UCI Rare Disease Symposium & Family Conference, 2025
- Winner of the best oral presentation, Division of Genetics and Cell Biology Retreat of San Raffaele Institute, 2018
Areas of Expertise
- Neurodegenerative Disease Mechanisms
- Mitochondrial Dysfunction in Ataxias
- Calcium Homeostasis in Neurons
- Protein Quality Control Pathways
- GABAergic Inhibitory Transmission Modulation
- Purkinje Cell Electrophysiology
- Zebrin Striping Pattern Disruption
Recent Publications
- Battaglini M, Schiavone F, Carmignani A, Marino A, Naef V, Petretto A, Bartolucci M, Longo F, Maltecca F, Santorelli FM, Ciofani G, “Polydopamine Nanoparticles as a Potential Non-Pharmaceutical Antioxidant Tool against Mitochondrial Disorder” (opens in new tab), ACS Applied Nano Materials, vol. 8, pp. 16540-16552, 2025.
- Gromova A, Cha B, Nguyen N, Garg D, Coscolluella C, Strickland LM, Luong D, Longo F, Sopher BL, ElMallah MK, La Spada A, “Neuromuscular junction transcriptome analysis of spinal and bulbar muscular atrophy mice implicates sarcomere gene expression and calcium flux dysregulation in disease pathogenesis” (opens in new tab), Human Molecular Genetics, vol. 34, pp. 1238-1251, 2025.
- Bartelt LC, Switonski PM, Adamek G, Longo F, Carvalho J, Duvick LA, Jarrah SI, McLoughlin HS, Scoles DR, Pulst SM, Orr HT, Hull C, Lowe CB, La Spada AR, “Dysregulation of zebrin-II cell subtypes in the cerebellum is a shared feature across polyglutamine ataxia mouse models and patients” (opens in new tab), Science Translational Medicine, vol. 16, 2024.
- Zaghi M, Longo F, Massimino L, Rubio A, Bido S, Mazzara PG, Bellini E, Banfi F, Podini P, Maltecca F, Zippo A, Broccoli V, Sessa A, “SETD5 haploinsufficiency affects mitochondrial compartment in neural cells” (opens in new tab), Molecular Autism, vol. 14, 2023.
- Del Bondio A, Longo F, De Ritis D, Spirito E, Podini P, Brais B, Bachi A, Quattrini A, Maltecca F, “Restoring calcium homeostasis in Purkinje cells arrests neurodegeneration and neuroinflammation in the ARSACS mouse model” (opens in new tab), Journal of Clinical Investigation, vol. 8, 2023.
- Longo F, De Ritis D, Miluzio A, Fraticelli D, Baets J, Scarlato M, Santorelli FM, Biffo S, Maltecca F, “Assessment of sacsin turnover in ARSACS patients: implications for molecular diagnosis and pathogenesis” (opens in new tab), Neurology, vol. 97, pp. E2315-E2327, 2021.
- Longo F, Benedetti S, Zambon A A, Natali Sora M G, Di Resta C, De Ritis D, Quattrini A, Maltecca F, Ferrari M, Previtali S C, “Impaired turnover of hyperfused mitochondria in severe axonal neuropathy due to a novel DRP1 mutation” (opens in new tab), Human Molecular Genetics, vol. 29, pp. 177-188, 2020.
- Duncan EJ, Larivière R, Bradshaw TY, Longo F, Sgarioto N, Hayes MJ, Romano LEL, Nethisinghe S, Giunti P, Bruntraeger MB, Durham HD, Brais B, Maltecca F, Gentil BJ, Chapple JP, “Altered organisation of the intermediate filament cytoskeleton and relocalisation of proteostasis modulators in cells lacking the ataxia protein sacsin” (opens in new tab), Human Molecular Genetics, vol. 26, pp. 3130-3143, 2017.
- Folci A, Murru L, Vezzoli E, Ponzoni L, Gerosa L, Moretto E, Longo F, Zapata J, Braida D, Pistillo F, Bähler M, Francolini M, Sala M, Bassani S, “Myosin IXa Binds AMPAR and Regulates Synaptic Structure, LTP, and Cognitive Function” (opens in new tab), Frontiers in Molecular Neuroscience, vol. 9, 2016.
Contact Information
Email: flongo@uci.edu
Phone: (949) 824-7407
Address: 419 S. Circle View Dr. ISEB, Rm. 2500, Irvine, CA 92697-4629
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Last updated on 2/20/2026.