Delphine G. Bernard
5PUBLICATIONS
54CO-AUTHORS
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Publications (5)
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|Jan 23, 2026
De novo variants in the splicing factor gene SF3B1 are associated with neurodevelopmental disorders.Kevin Uguen, Tiffany Bergot, Marie-Pier Scott-Boyer
|Mar 01, 2023
Vitamin B5 and succinyl-CoA improve ineffective erythropoiesis in SF3B1-mutated myelodysplasia.Syed A Mian, Céline Philippe, Eleni Maniati
|Jul 27, 2022
Cytogenetic and Genetic Abnormalities with Diagnostic Value in Myelodysplastic Syndromes (MDS): Focus on the Pre-Messenger RNA Splicing Process.Nathalie Douet-Guilbert, Benoît Soubise, Delphine G Bernard
|Aug 14, 2020
Splicing Anomalies in Myeloproliferative Neoplasms: Paving the Way for New Therapeutic Venues.Marie Hautin, Clélia Mornet, Aurélie Chauveau
|Mar 15, 2020
Human Cancer-Associated Mutations of SF3B1 Lead to a Splicing Modification of Its Own RNA.Tiffany Bergot, Eric Lippert, Nathalie Douet-Guilbert
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Frequent Collaborators
2 joint publications
Eric Lippert
1 joint publications
Benoît Soubise
1 joint publications
Marie-Bérengère Troadec
1 joint publications
Syed A Mian
1 joint publications
Céline Philippe
1 joint publications
Eleni Maniati
1 joint publications
Tiffany Bergot
1 joint publications
Travis Nemkov
1 joint publications
Valle Morales
1 joint publications
Andrew J Finch
