Dominique Campion
Affiliations: | Universite Lyon 1, Villeurbanne, Auvergne-Rhône-Alpes, France |
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Children
Sign in to add trainee| Grégory Raux | grad student | 2002 | University of Rouen |
| Hélène Jacquet-delmulle | grad student | 2004 | University of Rouen |
| Sébastien Feuillette | grad student | 2008 | University of Rouen |
| Anne Rovelet-lecrux | grad student | 2008 | University of Rouen |
| Caroline Demily | grad student | 2009 | Universite Lyon 1 |
| Laëtitia Miguel | grad student | 2012 | University of Rouen |
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Publications
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| Grangeon L, Charbonnier C, Zarea A, et al. (2023) Phenotype and imaging features associated with APP duplications. Alzheimer's Research & Therapy. 15: 93 |
| Holstege H, Hulsman M, Charbonnier C, et al. (2022) Exome sequencing identifies rare damaging variants in ATP8B4 and ABCA1 as risk factors for Alzheimer's disease. Nature Genetics |
| Miguel L, Rovelet-Lecrux A, Chambon P, et al. (2022) Generation of 17q21.31 duplication iPSC-derived neurons as a model for primary tauopathies. Stem Cell Research. 61: 102762 |
| Nicolas G, Sévigny M, Lecoquierre F, et al. (2022) A postzygotic de novo NCDN mutation identified in a sporadic FTLD patient results in neurochondrin haploinsufficiency and altered FUS granule dynamics. Acta Neuropathologica Communications. 10: 20 |
| Rovelet-Lecrux A, Feuillette S, Miguel L, et al. (2021) Impaired SorLA maturation and trafficking as a new mechanism for SORL1 missense variants in Alzheimer disease. Acta Neuropathologica Communications. 9: 196 |
| Grangeon L, Cassinari K, Rousseau S, et al. (2021) Early-Onset Cerebral Amyloid Angiopathy and Alzheimer Disease Related to an APP Locus Triplication. Neurology. Genetics. 7: e609 |
| Wallon D, Boluda S, Rovelet-Lecrux A, et al. (2021) Clinical and neuropathological diversity of tauopathy in MAPT duplication carriers. Acta Neuropathologica |
| Quenez O, Cassinari K, Coutant S, et al. (2020) Detection of copy-number variations from NGS data using read depth information: a diagnostic performance evaluation. European Journal of Human Genetics : Ejhg |
| Cassinari K, Rovelet-Lecrux A, Tury S, et al. (2020) Haploinsufficiency of the Primary Familial Brain Calcification Gene SLC20A2 Mediated by Disruption of a Regulatory Element. Movement Disorders : Official Journal of the Movement Disorder Society |
| Feuillette S, Charbonnier C, Frebourg T, et al. (2020) A Connected Network of Interacting Proteins Is Involved in Human-Tau Toxicity in . Frontiers in Neuroscience. 14: 68 |