Dr. Cicchetti obtained her Ph.D. in neurobiology from Laval University in Québec City (Canada) in 1998. In 2002, she completed a postdoctoral fellowship at Harvard Medical School in the field of cell replacement therapy for neurodegenerative disorders. She is now a professor for the department of Psychiatry & Neurosciences, of Laval University’s Medical School in Québec City. Dr. Cicchetti has published over 80 manuscripts in various high impact journals such as PNAS, Annals of Neurology, Acta Neuropathologica, Trends in Pharmacology, and Brain. She has received numerous awards and distinctions, including the Canadian Institutes of Health Research New Investigator Award (2007-2012), the Fonds de Recherche en Santé du Québec (FRSQ) Junior Research Award (2003-2006 and 2006-2007), Young Investigator Award from NARSAD (2006) and Parkinson Society Canada (2002) and more recently, the prestigious National Researcher award from FRQS (2014-2017), followed by an FRQS research Chair (2017-2021). Three of her recent publications (2014, 2015, 2016) have been awarded most influential papers in the field of Huntington’s disease. She is an active member of several scientific committees and editorial boards.
Our research program is built on 3 distinct themes: 1) to better understand the phenomena that may contribute to the development or the propagation of the pathological aspects found in neurodegenerative diseases (in particular Parkinson’s and Huntington’s) and related-cognitive features; 2) to develop therapeutic strategies that would allow an early or late intervention in the evolution of the disease; 3) to study the mechanisms of action underlying the beneficial and/or detrimental effects of current experimental therapies (cell transplantation and deep brain stimulation) in order to improve these methodologies for the clinic. Our research program is based on translational research, from the animal model to the clinic, with the goal of developing novel therapeutic targets for individuals suffering from Parkinson’s and/or Huntington’s diseases. With this research program, we have developed a considerable expertise in the animal models of these diseases, in imaging/microscopy in small animals, but more importantly in the histopathological analyses of human tissue. Our collaborations with various clinicians provide us invaluable access to human samples (blood, spinal cord, and brain), at times extremely rare (ex.: the brains of transplanted patients). Various pharmaceutical/industrial partners with whom we also collaborate will help us accelerate our findings to tangible clinical applications.
2705, boulevard Laurier
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Québec, Québec
Canada G1V 4G2
- Alves Martins Borba, Flavia NataleDoctoral studentCHUL+1 418-525-4444, extension 42296flavia.borba@crchudequebec.ulaval.ca
2705, boulevard Laurier
R-3701
Québec, QC
Canada G1V 4G2 - Cardim, ThyagoPostdoctoral fellowCHUL+1 418-525-4444, extension 42296thyago.cardim@crchudequebec.ulaval.ca
2705, boulevard Laurier
T2-50
Québec, QC
Canada G1V 4G2 - Cerquera Cleves, CatalinaDoctoral studentCHUL+1 418-525-4444, extension 42296catalina.cerquera-cleves@crchudequebec.ulaval.ca
2705, boulevard Laurier
T2-50
Québec, QC
Canada G1V 4G2 - Joseph, ThomsonPostdoctoral fellowCHUL+1 418-525-4444, extension 42296thomson.joseph@crchudequebec.ulaval.ca
2705, boulevard Laurier
T2-50
Québec, QC
Canada G1V 4G2 - Kopishinskaia, SvetlanaEmployeeCHUL+1 418-525-4444, extension 42296svetlana.kopishinskaia@crchudequebec.ulaval.ca
2705, boulevard Laurier
T2-50
Québec, QC
Canada G1V 4G2 - Lepinay, EvaDoctoral studentCHUL+1 418-525-4444, extension 42296eva.lepinay.1@ulaval.caeva.lepinay@crchudequebec.ulaval.ca
2705 Boulevard Laurier
T2-50
Québec, QC
Canada G1V 4G2 - Saint-Pierre, MartineEmployeeCHUL+1 418-525-4444, extension 42296 / 46204martine.saint-pierre@crchudequebec.ulaval.ca
2705, boulevard Laurier
T2-50
Québec, Québec
Canada G1V 4G2 - Salem, ShireenDoctoral studentCHUL+1 418-525-4444, extension 42296shireen.salem.1@ulaval.cashireen.salem@crchudequebec.ulaval.ca
2705, boulevard Laurier
T2-50
Québec, QC
Canada G1V 4G2 - Trabolsi, ChristineDoctoral studentCHUL+1 418-525-4444, extension 42296christine.trabolsi@crchudequebec.ulaval.ca
2705, boulevard Laurier
T2-50
Québec, QC
Canada G1V 4G2
The contribution of inflammatory astrocytes to BBB impairments in a brain-chip model of Parkinson's disease
Journal ArticleNat Commun, 14 (1), 2023.
Tau: a biomarker of Huntington's disease
Journal ArticleMol Psychiatry, 2023.
Corrigendum to "Understanding the role of the hematopoietic niche in Huntington's disease's phenotypic expression: In vivo evidence using a parabiosis model" [Neurobiol Dis. 2023 May;180:106091. doi:10.1016/j.nbd.2023.106091. Epub 2023 Mar 24]
Journal ArticleNeurobiol Dis, 187 , 2023.
Understanding the role of the hematopoietic niche in Huntington's disease's phenotypic expression: in vivo evidence using a parabiosis model
Journal ArticleNeurobiol Dis, 180 , 2023.
Untangling the Role of Tau in Huntington's Disease Pathology
Journal ArticleJ Huntingtons Dis, 12 (1), 2023.
Detection of antibodies against the huntingtin protein in human plasma
Journal ArticleCell Mol Life Sci, 80 (2), 2023.
Plasma GFAP and its association with disease severity in Huntington's disease
Journal ArticleJ Neurol, 2023.
A light-inducible protein clustering system for in vivo analysis of α-synuclein aggregation in Parkinson disease
Journal ArticlePLoS Biol, 20 (3), 2022.
Prion-like properties of the mutant huntingtin protein in living organisms: the evidence and the relevance
Journal ArticleMol Psychiatry, 27 (1), 2022.
Prompting endogenous repair of brain injury: science fiction or reality?
Journal ArticleMol Neurodegener, 17 (1), 2022.
Active projects
- Crosstalk at the blood-brain barrier: new insights into Parkinson's disease, from 2022-06-30 to 2024-06-30
- Les effets de la cystéamine chez les patients souffrant de la maladie de Huntington : Analyse des données cliniques, from 2023-01-01 to 2023-12-31
- Premier biomarqueur sanguin de la maladie de Parkinson : de la validation à la commercialisation, from 2022-09-14 to 2024-09-13
- Preventing pathological protein spread in Huntington's disease: relevance to pathology and treatment, from 2020-04-01 to 2025-03-31
- Preventing pathological protein spread in Huntington's disease: relevance to pathology and treatment, from 2021-12-20 to 2024-12-19
- Redefining PD pathophysiology mechanisms in the context of teterogeneous substantia nigra neuron subtypes, from 2021-09-01 to 2024-10-31
- Untangling tau contribution to cognitive impairments in Huntington’s disease., from 2019-04-01 to 2024-03-31
Recently finished projects
- CRISPR-Cas9 nickase as a new approach to treat Huntington’s disease, from 2019-07-01 to 2022-03-31
- Interrogating induced neuronal cells from Huntington’s disease patients to better understand cognitive impairments, from 2019-11-01 to 2023-06-30
- Projet de recherche clinique sur la maladie de Parkinson (Cystamine), from 2019-04-01 to 2022-03-31
- Targeting the neurovascular unit to prevent disease dissemination and progression, from 2021-01-01 to 2023-03-31