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Activities

Funding (4)

Novel Muscular Dystrophy caused by SNUPN Mutations: From Innovative modeling to therapeutic insights

2024-10 to present | Grant
AFM-Téléthon (Paris, FR)
Source: Self-asserted source
Nathalie Escande-Beillard

Zebrafish modeling to decipher pathological basis of novel Mendelian Muscular Dystrophy

2023 to present | Award
Elife (Cambridge, GB)
Source: Self-asserted source
Nathalie Escande-Beillard

Unraveling and modeling a Novel Progeroid Lipodystrophy Syndrome

2022 to 2023 | Grant
Koc University (Istanbul, TR)
Source: Self-asserted source
Nathalie Escande-Beillard

From Mendelian diseases to functional genomics for therapeutic innovation

2020 to 2024 | Grant
Scientific and Technological Research Council of Turkey (Ankara, TR)
Source: Self-asserted source
Nathalie Escande-Beillard

Peer review (1 review for 1 publication/grant)

Review activity for Clinical genetics (1)