Author

Didier Samuel

Assistance Publique – Hôpitaux de ParisORCID 0000-0001-9481-3616Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Molecular Biology· 1

Signature Assays, Organisms & Methods

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Research Focus:differential expression· 1 Organism:human· 1 Assay:proteomics· 1 Approach:simulation· 1 Approach:statistical model· 1

Frequent Co-Authors

Afra Panahi· 1 shared Andrew G. Burwash· 1 shared Antoine DürrbachiD· 1 shared Antoine Pierre BréziniD· 1 shared Caroline Beugnet· 1 shared François ParafiD· 1 shared Isabel M MorgadoiD· 1 shared Jean Philippe RerolleiD· 1 shared

Activity by Year

2018-2018 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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1 shared paperMolecular Biology

Afra Panahi

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1 paper

Recent·Most cited

Molecular basis for a novel systemic form of human hereditary apoA-I amyloidosis with vision loss

Isabel M Morgado, Pierre-Raphaël Rothschild, Afra Panahi, Jean‐Claude Aldigier, Andrew G. Burwash, Madhurima Das, Magali Colombat, Thierry Frouget, Jean Philippe Rerolle, François Paraf, Nathalie C. Rioux-Leclercq, Jean‐Michel Goujon, Caroline Beugnet, Antoine Dürrbach, Didier Samuel, , Sophie Valleix

The paper identifies a novel form of hereditary apoA-I amyloidosis caused by Glu34Lys mutation, revealing structural changes that lead to amyloid formation and vision loss.

bioRxiv · Jun 22, 2018 · PreprintMolecular Biology