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Despina Sanoudou

Researcher at National and Kapodistrian University of Athens

Publications -  128
Citations -  5366

Despina Sanoudou is an academic researcher from National and Kapodistrian University of Athens. The author has contributed to research in topics: Phospholamban & Medicine. The author has an hindex of 37, co-authored 107 publications receiving 4558 citations. Previous affiliations of Despina Sanoudou include Ludwig Institute for Cancer Research & Academy of Athens.

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Interferon‐α/β–mediated innate immune mechanisms in dermatomyositis

TL;DR: An innate immune response characterized by plasmacytoid dendritic cell infiltration and interferon‐α/β inducible gene and protein expression may be an important part of the pathogenesis of dermatomyositis, as it appears to be in systemic lupus erythematosus.
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Gene expression comparison of biopsies from Duchenne muscular dystrophy (DMD) and normal skeletal muscle

TL;DR: To examine the pathogenic pathways and identify new or modifying factors involved in muscular dystrophy, expression microarrays were used to compare individual gene expression profiles of skeletal muscle biopsies from 12 DMD patients and 12 unaffected control patients and identified 105 genes that differ significantly in expression level between unaffected and DMD muscle.
Journal Article

A comparison of batch effect removal methods for enhancement of prediction performance using MAQC-II microarray gene expression data

TL;DR: Of the 120 cases studied using Support vector machines and K nearest neighbors as classifiers and Matthews correlation coefficient as performance metric, it is found that Ratio-G, Ratio-A, EJLR, mean-centering and standardization methods perform better or equivalent to no batch effect removal in 89, 85, 83, 79 and 75% of the cases, respectively, suggesting that the application of these methods is generally advisable and ratio-based methods are preferred.
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Molecular profiles of inflammatory myopathies

TL;DR: The molecular profiles of muscle tissue in patients with inflammatory myopathies are distinct and represent molecular signatures from which diagnostic insight may follow and as relevant to disease pathogenesis previously reported cytokines, major histocompatibility complex class I and II molecules, granzymes, and adhesion molecules, as well as newly identified members of these categories.