Publications | Page 5 | Cervo Brain Research Centre

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2022

“Association of Essential Tremor With Novel Risk Loci: A Genome-Wide Association Study and Meta-analysis.”, JAMA Neurol, vol. 79, no. 2, pp. 185-193, 2022.

2020

Z. Gan-Or, Rao, T., Leveille, E., Degroot, C., Chouinard, S., Cicchetti, F., Dagher, A., Das, S., Desautels, A., Drouin-Ouellet, J., Durcan, T., Gagnon, J. - F., Genge, A., Karamchandani, J., Lafontaine, A. - L., Sun, S. Lai Wing, Langlois, M., Lévesque, M., Melmed, C., Panisset, M., Parent, M., Poline, J. - B., Postuma, R. B., Pourcher, E., Rouleau, G. A., Sharp, M., Monchi, O., Dupré, N., and Fon, E. A., “The Quebec Parkinson Network: A Researcher-Patient Matching Platform and Multimodal Biorepository.”, J Parkinsons Dis, vol. 10, no. 1, pp. 301-313, 2020.

2016

Y. Ohta, Soucy, G., Phaneuf, D., Audet, J. - N., Gros-Louis, F., Rouleau, G. A., Blasco, H., Corcia, P., Andersen, P. M., Nordin, F., Yamashita, T., Abe, K., and J-P Julien, “Sex-dependent effects of chromogranin B P413L allelic variant as disease modifier in amyotrophic lateral sclerosis.”, Hum Mol Genet, 2016.

Y. Ohta, Soucy, G., Phaneuf, D., Audet, J. - N., Gros-Louis, F., Rouleau, G. A., Blasco, H., Corcia, P., Andersen, P. M., Nordin, F., Yamashita, T., Abe, K., and J-P Julien, “Sex-dependent effects of chromogranin B P413L allelic variant as disease modifier in amyotrophic lateral sclerosis.”, Hum Mol Genet, vol. 25, no. 21, pp. 4771-4786, 2016.

2013

S. Pickles, Destroismaisons, L., Peyrard, S. L., Cadot, S., Rouleau, G. A., Brown, R. H., J-P Julien, Arbour, N., and Velde, C. Vande, “Mitochondrial damage revealed by immunoselection for ALS-linked misfolded SOD1.”, Hum Mol Genet, vol. 22, no. 19, pp. 3947-59, 2013.

2011

V. Swarup, Phaneuf, D., Bareil, C., Robertson, J., Rouleau, G. A., Kriz, J., and J-P Julien, “Pathological hallmarks of amyotrophic lateral sclerosis/frontotemporal lobar degeneration in transgenic mice produced with TDP-43 genomic fragments.”, Brain, vol. 134, no. Pt 9, pp. 2610-26, 2011.

2009

F. Gros-Louis, Andersen, P. M., Dupré, N., Urushitani, M., Dion, P., Souchon, F., D'Amour, M., Camu, W., Meininger, V., Bouchard, J. - P., Rouleau, G. A., and J-P Julien, “Chromogranin B P413L variant as risk factor and modifier of disease onset for amyotrophic lateral sclerosis.”, Proc Natl Acad Sci U S A, vol. 106, no. 51, pp. 21777-82, 2009.

2008

F. Gros-Louis, Kriz, J., Kabashi, E., McDearmid, J., Millecamps, S., Urushitani, M., Lin, L., Dion, P., Zhu, Q., Drapeau, P., J-P Julien, and Rouleau, G. A., “Als2 mRNA splicing variants detected in KO mice rescue severe motor dysfunction phenotype in Als2 knock-down zebrafish.”, Hum Mol Genet, vol. 17, no. 17, pp. 2691-702, 2008.

2004

F. Gros-Louis, Larivière, R., Gowing, G., Laurent, S., Camu, W., Bouchard, J. - P., Meininger, V., Rouleau, G. A., and J-P Julien, “A frameshift deletion in peripherin gene associated with amyotrophic lateral sclerosis.”, J Biol Chem, vol. 279, no. 44, pp. 45951-6, 2004.

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