Dominique Campion

Universite Lyon 1, Villeurbanne, Auvergne-Rhône-Alpes, France 
"Dominique Campion"
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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
Husson T, Lecoquierre F, Cassinari K, et al. (2020) Rare genetic susceptibility variants assessment in autism spectrum disorder: detection rate and practical use. Translational Psychiatry. 10: 77
Miguel L, Frebourg T, Campion D, et al. (2020) Moderate Overexpression of Tau in Drosophila Exacerbates Amyloid-β-Induced Neuronal Phenotypes and Correlates with Tau Oligomerization. Journal of Alzheimer's Disease : Jad
Bis JC, Jian X, Kunkle BW, et al. (2019) Correction: Whole exome sequencing study identifies novel rare and common Alzheimer's-Associated variants involved in immune response and transcriptional regulation. Molecular Psychiatry
Miguel L, Rovelet-Lecrux A, Feyeux M, et al. (2019) Detection of all adult Tau isoforms in a 3D culture model of iPSC-derived neurons. Stem Cell Research. 40: 101541
Lacour M, Quenez O, Rovelet-Lecrux A, et al. (2019) Causative Mutations and Genetic Risk Factors in Sporadic Early Onset Alzheimer's Disease Before 51 Years. Journal of Alzheimer's Disease : Jad
Cassinari K, Quenez O, Joly-Hélas G, et al. (2019) A Simple, Universal, and Cost-Efficient Digital PCR Method for the Targeted Analysis of Copy Number Variations. Clinical Chemistry
Grangeon L, Wallon D, Charbonnier C, et al. (2019) Biallelic MYORG mutation carriers exhibit primary brain calcification with a distinct phenotype. Brain : a Journal of Neurology
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