Selket Delafontaine
8PUBLICATIONS
233CO-AUTHORS
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Publications (8)
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|Aug 27, 2025
Dominant negative ADA2 mutations cause ADA2 deficiency in heterozygous carriers.Marjon Wouters, Lisa Ehlers, Wout Van Eynde
|Dec 23, 2024
Dominant negative ADA2 mutations cause ADA2 deficiency in heterozygous carriers.Marjon Wouters, Lisa Ehlers, Wout Van Eynde
|Dec 06, 2024
A new severe congenital neutropenia syndrome associated with autosomal recessive COPZ1 mutations.Natalia Borbaran Bravo, Ekaterina Deordieva, Larissa Doll
|Nov 16, 2024
Autoinflammatory patients with Golgi-trapped CDC42 exhibit intracellular trafficking defects leading to STING hyperactivation and ER stress.Alberto Iannuzzo, Selket Delafontaine, Rana El Masri
|Dec 08, 2023
Inborn errors of immunity: A field without frontiers.Giorgia Bucciol, Selket Delafontaine, Isabelle Meyts
|Mar 08, 2023
Human germline heterozygous gain-of-function STAT6 variants cause severe allergic disease.Mehul Sharma, Daniel Leung, Mana Momenilandi
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Frequent Collaborators
7 joint publications
Isabelle Meyts
4 joint publications
Giorgia Bucciol
3 joint publications
Leen Moens
3 joint publications
Jean-Laurent Casanova
2 joint publications
Jérémie Le Pen
2 joint publications
Danyel Lee
2 joint publications
Filomeen Haerynck
2 joint publications
Gulsum Iclal Bayhan
2 joint publications
Marcela Moncada-Velez
2 joint publications
Lucy Bizien
