Eleonore Pairet
4PUBLICATIONS
12CO-AUTHORS
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Publications (4)
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|Dec 22, 2025
Likely Pathogenic/Pathogenic Variants in the Spliceosome Complex Genes SNRNP200, SF3B1, SF3B2, and SF3B4 Implicated in Nonsyndromic Orofacial Cleft.Peyman Ranji, Eleonore Pairet, Raphael Helaers
|Nov 06, 2024
Four putative pathogenic ARHGAP29 variants in patients with non-syndromic orofacial clefts (NsOFC).Peyman Ranji, Eleonore Pairet, Raphael Helaers
|Nov 06, 2023
Molecular investigation in individuals with orofacial clefts and microphthalmia-anophthalmia-coloboma spectrum.Milena Atique Tacla, Matheus de Mello Copelli, Eleonore Pairet
|Apr 28, 2023
SATB2-Associated Syndrome Due to a c.715C>T:p(Arg239*) Variant in Adulthood: Natural History and Literature Review.Matheus de Mello Copelli, Eleonore Pairet, Milena Atique-Tacla
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Frequent Collaborators
4 joint publications
Raphaël Helaers
4 joint publications
Miikka Vikkula
2 joint publications
Milena Atique-Tacla
2 joint publications
Társis Paiva Vieira
2 joint publications
Vera Lúcia Gil-da-Silva-Lopes
2 joint publications
Peyman Ranji
1 joint publications
Matheus de Mello Copelli
1 joint publications
Simone Appenzeller
1 joint publications
Pascal Brouillard
1 joint publications
Bénédicte Bayet
