Elodie Fastré

Mutations in the VEGFR3 Signaling Pathway Explain 36% of Familial Lymphedema

Antonella Mendola, Matthieu J. Schlögel, Arash Ghalamkarpour et al. · Molecular Syndromology · 2013 · 105 citations · Full text

<i>RASA1</i> mosaic mutations in patients with capillary malformation-arteriovenous malformation

Nicole Revençu, Elodie Fastré, Marie Ravoet et al. · Journal of Medical Genetics · 2019 · 75 citations · Full text

Non-hotspot PIK3CA mutations are more frequent in CLOVES than in common or combined lymphatic malformations

Pascal Brouillard, Matthieu J. Schlögel, Nassim Homayun Sepehr et al. · Orphanet Journal of Rare Diseases · 2021 · 64 citations · Full text

Characterization of <i>ANGPT2</i> mutations associated with primary lymphedema

Veli‐Matti Leppänen, Pascal Brouillard, Emilia A. Korhonen et al. · Science Translational Medicine · 2020 · 44 citations · Full text

No evidence of locus heterogeneity in familial microcephaly with or without chorioretinopathy, lymphedema, or mental retardation syndrome

Matthieu J. Schlögel, Antonella Mendola, Elodie Fastré et al. · Orphanet Journal of Rare Diseases · 2015 · 32 citations · Full text