Salachas, François
Centre National de la Recherche Scientifique · Inserm · Sorbonne Université · Laboratoire d’Imagerie Biomédicale · Pitié-Salpêtrière Hospital · Institut du Cerveau
7 papers on CoChat
Most cited papers
- Verified
Phase 1–2 Trial of Antisense Oligonucleotide Tofersen for SOD1 ALS
Miller, T., Cudkowicz, M., Shaw, P. J., Andersen, P. M., Atassi, N., Bucelli, R. C., Genge, A., Glass, J., Ladha, S., Ludolph, A. L., et al. (2020) · New England Journal of Medicine
Amyotrophic Lateral Sclerosis ResearchAlzheimer's disease research and treatments
Cited by 565
- Verified
Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology
van Rheenen, W., van der Spek, R. A. A., Bakker, M. K., van Vugt, J. J. F. A., Hop, P. J., Zwamborn, R. A. J., de Klein, N., Westra, H.-J., Bakker, O. B., Deelen, P., et al. (2021) · Nature Genetics
Amyotrophic Lateral Sclerosis ResearchGenetic Associations and Epidemiology
Cited by 542
- Verified
Mutations in SQSTM1 encoding p62 in amyotrophic lateral sclerosis: genetics and neuropathology
Teyssou, E., Takeda, T., Lebon, V., Boillée, S., Doukouré, B., Bataillon, G., Sazdovitch, V., Cazeneuve, C., Meininger, V., LeGuern, E., et al. (2013) · Acta Neuropathologica
Amyotrophic Lateral Sclerosis ResearchHereditary Neurological Disorders
Cited by 241
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Demographic, neurological and behavioural characteristics and brain perfusion SPECT in frontal variant of frontotemporal dementia
Ber, I. L., Guedj, E., Gabelle, A., Verpillat, P., Volteau, M., Thomas-Anterion, C., Decousus, M., Hannequin, D., Vera, P., Lacomblez, L., et al. (2006) · Brain
Dementia and Cognitive Impairment ResearchAlzheimer's disease research and treatments
Cited by 179
- Verified
Accumulation of TDP-43 and α-actin in an amyotrophic lateral sclerosis patient with the K17I ANG mutation
Seilhean, D., Cazeneuve, C., Thuriès, V., Russaouen, O., Millecamps, S., Salachas, F., Meininger, V., LeGuern, E., & Duyckaerts, C. (2009) · Acta Neuropathologica
Amyotrophic Lateral Sclerosis ResearchHereditary Neurological Disorders
Cited by 71
- Verified
Mutations in UBQLN2 are rare in French amyotrophic lateral sclerosis
Millecamps, S., Corcia, P., Cazeneuve, C., Boillée, S., Seilhean, D., Danel-Brunaud, V., Vandenberghe, N., Pradat, P.-F., Le Forestier, N., Lacomblez, L., et al. (2012) · Neurobiology of Aging
Amyotrophic Lateral Sclerosis ResearchHereditary Neurological Disorders
Cited by 40
- Verified
Environmental risk factors for amyotrophic lateral sclerosis: a case–control study in Canada and France
Beaudin, M., Salachas, F., Pradat, P.-F., & Dupré, N. (2022) · Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration
Amyotrophic Lateral Sclerosis ResearchPeripheral Neuropathies and Disorders
Cited by 12
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