Trottier, Yvon
Centre National de la Recherche Scientifique · Inserm · Institut de génétique et de biologie moléculaire et cellulaire · Université de Strasbourg
2 papers on CoChatORCID 0000-0001-7230-4810
Most cited papers
- Verified
Exon 1 of the HD gene with an expanded CAG repeat is sufficient to cause a progressive neurological phenotype in transgenic mice
Mangiarini, L., Sathasivam, K., Seller, M., Cozens, B., Harper, A., Hetherington, C., Lawton, M., Trottier, Y., Lehrach, H., Davies, S. W., et al. (1996) · Cell
Genetic Neurodegenerative DiseasesGenetics and Neurodevelopmental Disorders
Cited by 3,073
- Verified
A novel function of Huntingtin in the cilium and retinal ciliopathy in Huntington’s disease mice
Karam, A., Tebbe, L., Weber, C., Messaddeq, N., Morlé, L., Kessler, P., Wolfrum, U., & Trottier, Y. (2015) · Neurobiology of Disease
Genetic and Kidney Cyst DiseasesGenetic Neurodegenerative Diseases
Cited by 38
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