N. Gaitch

Missense mutations in SLC26A8, encoding a sperm-specific activator of CFTR, are associated with human asthenozoospermia.

P. Tufféry, P. Ray, T. Dirami, 2013, American journal of human genetics.

p.Arg75Gln, a CFTR variant involved in the risk of CFTR-related disorders?

P. Burgel, E. Girodon, T. Bienvenu, 2014, Journal of Human Genetics.

CFTR and/or pancreatitis susceptibility genes mutations as risk factors of pancreatitis in cystic fibrosis patients?

P. Burgel, E. Girodon, T. Bienvenu, 2016, Pancreatology : official journal of the International Association of Pancreatology (IAP) ... [et al.].

Isolated Nonvisualization of the Fetal Gallbladder Should Be Considered for the Prenatal Diagnosis of Cystic Fibrosis

E. Girodon, T. Bienvenu, C. Raynal, 2018, Fetal Diagnosis and Therapy.

Two frequent loss‐of‐function mutations in Aurora Kinase C gene in Algerian infertile men with macrozoospermia

E. Girodon, T. Bienvenu, J. Wolf, 2020, Andrologia.

DCTN4 as a modifier of chronic Pseudomonas aeruginosa infection in cystic fibrosis

E. Génin, P. Burgel, E. Girodon, 2016, The clinical respiratory journal.

Combination of ENaC and CFTR mutations may predispose to cystic fibrosis-like disease

I. Fajac, T. Bienvenu, D. Hubert, 2009, European Respiratory Journal.

AQP5, a second gene at play with CFTR in aquagenic palmoplantar keratoderma

P. Burgel, I. Fajac, M. Audrézet, 2023, Journal of the European Academy of Dermatology and Venereology.