Veronique V. Belzil, Ph.D.
Affiliations: | 2012 | Physiology | Université de Montréal, Montréal, Canada |
Area:
NeurogeneticsGoogle:
"Veronique Belzil"Mean distance: 19.61 (cluster 28)
Parents
Sign in to add mentor| Guy A. Rouleau | grad student | 2012 | Université de Montréal | |
| (Genetics of amyotrophic lateral sclerosis.) | ||||
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Publications
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| Li J, Jaiswal MK, Chien JF, et al. (2023) Divergent single cell transcriptome and epigenome alterations in ALS and FTD patients with C9orf72 mutation. Nature Communications. 14: 5714 |
| Ebbert MTW, Lank RJ, Belzil VV. (2018) An Epigenetic Spin to ALS and FTD. Advances in Neurobiology. 20: 1-29 |
| Ebbert MTW, Ross CA, Pregent LJ, et al. (2017) Conserved DNA methylation combined with differential frontal cortex and cerebellar expression distinguishes C9orf72-associated and sporadic ALS, and implicates SERPINA1 in disease. Acta Neuropathologica |
| Belzil VV, Katzman RB, Petrucelli L. (2016) ALS and FTD: an epigenetic perspective. Acta Neuropathologica |
| Esanov R, Belle KC, van Blitterswijk M, et al. (2015) C9orf72 promoter hypermethylation is reduced while hydroxymethylation is acquired during reprogramming of ALS patient cells. Experimental Neurology |
| Prudencio M, Belzil VV, Batra R, et al. (2015) Distinct brain transcriptome profiles in C9orf72-associated and sporadic ALS. Nature Neuroscience. 18: 1175-82 |
| Kaneb HM, Folkmann AW, Belzil VV, et al. (2015) Deleterious mutations in the essential mRNA metabolism factor, hGle1, in amyotrophic lateral sclerosis. Human Molecular Genetics. 24: 1363-73 |
| Belzil VV, Bauer PO, Gendron TF, et al. (2014) Characterization of DNA hypermethylation in the cerebellum of c9FTD/ALS patients. Brain Research. 1584: 15-21 |
| Gendron TF, Belzil VV, Zhang YJ, et al. (2014) Mechanisms of toxicity in C9FTLD/ALS. Acta Neuropathologica. 127: 359-76 |
| Belzil VV, Petrucelli L. (2014) Epigenetic modifications of the C9ORF72 gene: A potential biomarker of disease? Future Neurology. 9: 123-126 |