Dominique Hubert

Most-cited papers

1. Genistein inhibits constitutive and inducible NFkappaB activation and decreases IL-8 production by human cystic fibrosis bronchial gland cells.

   O. Tabary, S. Escotte, Jean-Paul Couétil, Dominique Hubert +3 more

   1999American Journal of Pathology107 citations Open access

   Semantic Scholar

   Save

2. HLA class II polymorphism in cystic fibrosis. A possible modifier of pulmonary phenotype.

   Y. Aron, B. Polla, Thierry Bienvenu, Josette DALL'AVA +2 more

   1999American Journal of Respiratory and Critical Care Medicine83 citations

   Semantic Scholar

   Save

3. Malnutrition in adults with cystic fibrosis

   X. Dray, R. Kanaan, Thierry Bienvenu, N. Desmazes-Dufeu +3 more

   2005European Journal of Clinical Nutrition55 citations

   Semantic Scholar

   Save

4. Non‐classic cystic fibrosis associated with D1152H CFTR mutation

   P. Burgel, Isabelle Fajac, Dominique Hubert, Dominique Grenet +16 more

   2010Clinical Genetics44 citations Open access

   Semantic Scholar

   Save

5. HLA-DR polymorphism in allergic bronchopulmonary aspergillosis.

   Y. Aron, Thierry Bienvenu, Dominique Hubert, D. Dusser +2 more

   1999Journal of Allergy and Clinical Immunology25 citations

   Semantic Scholar

   Save

6. Cystic fibrosis patients with the 3272-26A>G splicing mutation have milder disease than F508del homozygotes: a large European study

   Margarida D. Amaral, Paula Pacheco, Sebastian Beck, C. M. Farinha +35 more

   2001Journal of Medical Genetics24 citations Open access

   Semantic Scholar

   Save

7. Improved activity of an actin-resistant DNase I variant on the cystic fibrosis airway secretions.

   J. Zahm, C. Debordeaux, C. Maurer, Dominique Hubert +4 more

   2001American Journal of Respiratory and Critical Care Medicine20 citations

   Semantic Scholar

   Save

8. Heat-shock proteins in host-pathogen interactions: implications for cystic fibrosis.

   B. S. Polla, Ewa Mariéthoz, Dominique Hubert, C. Barazzone

   1995Trends in Microbiology18 citations

   Semantic Scholar

   Save

9. Management of assisted reproductive technologies in women with cystic fibrosis.

   Sylvie Epelboin, Dominique Hubert, Catherine Patrat, F. Abi-Rached +2 more

   2001Fertility and Sterility17 citations Open access

   Semantic Scholar

   Save

10. [Management of acute and severe complications in adults with cystic fibrosis].

    J. Chapron, B. Zuber, R. Kanaan, Dominique Hubert +4 more

    2011Revue des maladies respiratoires5 citations

    Semantic Scholar

    Save

11. A new missense mutation (G27E) in exon 2 of the CFTR gene in a mildly affected cystic fibrosis patient.

    Thierry Bienvenu, Ceclle Cazeneuve, C. Beldjord, Daniel Dusser +2 more

    1994Human Molecular Genetics5 citations

    Semantic Scholar

    Save

12. [Specific aspects and care of lung involvement in adults with cystic fibrosis].

    I. Pin, D. Grenet, P. Scheid, P. Domblides +2 more

    2000Revue des maladies respiratoires4 citations

    Semantic Scholar

    Save

13. Severe cystic fibrosis phenotype in a delta F508/3272-26A-->G compound heterozygote.

    T. Bienvenu, Chérif Beldjord, J. Kaplan, Dominique Hubert +1 more

    1995Journal of Medical Genetics4 citations Open access

    Semantic Scholar

    Save

14. Mutations located in exon 24 of the CFTR gene are associated with a mild cystic fibrosis phenotype

    T. Bienvenu, M. Viel, C. Leroy, H. Van Esch +3 more

    2003Clinical Genetics1 citations

    Semantic Scholar

    Save

15. A novel missense mutation D513G in exon 10 of the cystic fibrosis transmembrane conductance regulator (CFTR) gene identified in a French CBAVD patient. Mutations in brief no. 175. Online.

    Thierry Bienvenu, S. Bousquet, D. Vidaud, Dominique Hubert +3 more

    1998Human Mutation1 citations

    Semantic Scholar

    Save

16. Genotype‐phenotype relationships in cystic fibrosis patients

    Dominique Hubert, T. Bienvenu, D. Dusser

    1997Pediatric pulmonology. Supplement1 citations

    Semantic Scholar

    Save

17. Identification of a novel missense mutation G239R in exon 6a of the CFTR gene.

    Thierry Bienvenu, Cécile Cazeneuve, Isabelle Fajac, Daniel Dusser +3 more

    1995Human Heredity1 citations

    Semantic Scholar

    Save

18. [How should chronic Pseudomonas aeruginosa bronchial infection be treated in the course of cystic fibrosis?].

    Dominique Hubert, N. Desmazes-Dufeu, D. Dusser

    2003Revue des maladies respiratoires0 citations

    Semantic Scholar

    Save

19. Mutation and Polymorphism Report

    Thierry Bienvenu, Dominique Hubert, Daniel Dusser, Chérif Beldjord +1 more

    19980 citations

    Semantic Scholar

    Save