article :
Joly P, Gagnieu M C, Bardel C, Francina A, Pondarre C, Martin C (2012)
Genotypic screening of the main opiate-related polymorphisms in a cohort of 139 sickle cell disease patients, American Journal of Hematology, vol. 87 pp.534-536.
Joly P, Pondarré C, Bardel C, Francina A, Martin C (2012)
The alpha-globin genotype does not influence sickle cell disease severity in a retrospective cross-validation study of the pediatric severity score, European Journal of Haematology, vol. 88 pp.61-67.
Padois K, Cantiéni C, Bertholle V, Bardel C, Pirot F, Falson F (2011)
Solid lipid nanoparticles suspension versus commercial solutions for dermal delivery of minoxidil, International Journal of Pharmaceutics, vol. 416 pp.300-304.
Dubertret C, Bardel C, Ramoz N, Martin P-M, Deybach J-C, Adès J, Gorwood P, Gouya L (2010)
A genetic schizophrenia-susceptibility region located between the ANKK1 and DRD2 genes, Progress in Neuro-Psychopharmacology & Biological Psychiatry, vol. 34 pp.492-499.
Nguyen T K T, Joly P, Bardel C, Moulsma M, Bonello-Palot N, Francina A (2010)
The XmnI Gγ polymorphism influences hemoglobin F synthesis contrary to BCL11A and HBS1L-MYB SNPs in a cohort of 57β-thalassemia intermedia patients, Blood Cells Molecules and Diseases, vol. 45 pp.124-127, DOI.
Bardel C, Danjean V, Morange P, Génin E, Darlu P (2009)
On the Use of Phylogeny-Based Tests to Detect Association Between Quantitative Traits and Haplotypes, Genetic Epidemiology, vol. 33 pp.729-739.
Bardel C, Croiseau P, Génin E (2007)
Dealing with missing phase and missing data in phylogeny-based analysis, BMC Proceedings, vol. 1 pp.1-5.
Bickeböller H, Goddard A B, Igo Jr R P, Kraft P, Lozano J P, Pankratz N, Balavarca Y, Bardel C, Charoen P, Croiseau P, Guo C-Y, Joo J, Köhler K, Madsen A, Malzahn D, Monsees G, Sohns M, Ye Z (2007)
Issues in Association Mapping with High-Density SNP Data and Diverse Family Structures, Genetic Epidemiology, vol. 31 pp.S22-S33.
Croiseau P, Bardel C, Génin E (2007)
Efficiency of multiple imputation to test for association in the presence of missing data, BMC Proceedings, vol. 1 pp.1-5.
Ziegler A, DeStefano A L, König R, Bardel C, Brinza D, Bull S, Zhaohui C, Glaser B, Jiang W, Lee K E, Li C X, Li J, Li X, Majoram P, Meng Y, Nicodemus K K, Platt A, Schwarz D F, Shi W, Shugart Y Y, Stassen H H, Sun Y V, Won S, Wang W, Wahba G, Zagaar U A, Zhao Z (2007)
Data Mining Neural Nets Trees — Problems 2 and 3 of Genetic Analysis Workshop 15, Genetic Epidemiology, vol. 31 pp.S51-S60.
Bardel C, Danjean V, Génin E (2006)
ALTree: association detection and localization of susceptibility sites using haplotype phylogenetic trees, BIOINFORMATICS, vol. 22 pp.1402-1403.
Bardel C, Darlu P, Génin E (2006)
Cluster ing of haplotypes based on phylogeny: how good a strategy for association testing?, European Journal of Human Genetics, vol. 14 pp.202-206.
Bardel C, Danjean V, Hugot J-P, Darlu P, Génin E (2005)
On the use of haplotype phylogeny to detect disease susceptibility loci, BMC Genetics, vol. 6 pp.1-13.
phdthesis :
Bardel C (2005)
Mise en évidence de facteurs génétiques de risque en utilisant des phylogénies d’haplotypes .
