C
Claire Bardel
Researcher at University of Lyon
Publications - 61
Citations - 865
Claire Bardel is an academic researcher from University of Lyon. The author has contributed to research in topics: Medicine & Gene. The author has an hindex of 15, co-authored 54 publications receiving 658 citations. Previous affiliations of Claire Bardel include French Institute of Health and Medical Research & Claude Bernard University Lyon 1.
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Journal ArticleDOI
Solid lipid nanoparticles suspension versus commercial solutions for dermal delivery of minoxidil
Karine Padois,Céline Cantiéni,Valérie Bertholle,Claire Bardel,Fabrice Pirot,Françoise Falson +5 more
TL;DR: Solid lipid nanoparticles suspensions were shown as efficient as commercial solutions for skin penetration and were non-corrosive while commercial solutions presented a corrosive potential; and would constitute a promising formulation for hair loss treatment.
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The XmnI Gγ polymorphism influences hemoglobin F synthesis contrary to BCL11A and HBS1L-MYB SNPs in a cohort of 57 β-thalassemia intermedia patients
Thi Khanh Tien Nguyen,Philippe Joly,Philippe Joly,Claire Bardel,Mustapha Moulsma,Nathalie Bonello-Palot,Alain Francina +6 more
TL;DR: It is suggested that the BCL11A and HBS1L-MYB loci have a minor effect on HbF level compared to the XmnI QTL in beta-thalassemia intermedia patients.
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On the use of haplotype phylogeny to detect disease susceptibility loci
TL;DR: Under models where the susceptibility to the disease is caused by a single genetic variant, the cladistic test is neither really more powerful to detect an association nor really more efficient to localize the susceptibility site than an individual SNP testing, however, when two interacting sites are responsible for the disease, thecladistic analysis greatly improves the probability to find the two susceptibility sites.
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Whole genome paired-end sequencing elucidates functional and phenotypic consequences of balanced chromosomal rearrangement in patients with developmental disorders.
Caroline Schluth-Bolard,Flavie Diguet,Nicolas Chatron,Pierre-Antoine Rollat-Farnier,Claire Bardel,Alexandra Afenjar,Florence Amblard,Jeanne Amiel,Sophie Blesson,Patrick Callier,Yline Capri,Patrick Collignon,Marie-Pierre Cordier,Christine Coubes,Bénédicte Demeer,Annabelle Chaussenot,Florence Demurger,Françoise Devillard,Martine Doco-Fenzy,Céline Dupont,Jean-Michel Dupont,Sophie Dupuis-Girod,Laurence Faivre,Brigitte Gilbert-Dussardier,Anne-Marie Guerrot,Marine Houlier,Bertrand Isidor,Sylvie Jaillard,Géraldine Joly-Hélas,Valérie Kremer,Didier Lacombe,Cédric Le Caignec,Aziza Lebbar,Marine Lebrun,Gaetan Lesca,James Lespinasse,Jonathan Levy,Valérie Malan,Michèle Mathieu-Dramard,Julie Masson,Alice Masurel-Paulet,Cyril Mignot,Chantal Missirian,Fanny Morice-Picard,Sébastien Moutton,Gwenaël Nadeau,Céline Pebrel-Richard,Sylvie Odent,Véronique Paquis-Flucklinger,Laurent Pasquier,Nicole Philip,Morgane Plutino,Linda Pons,Marie-France Portnoï,Fabienne Prieur,Jacques Puechberty,Audrey Putoux,Marlène Rio,Caroline Rooryck-Thambo,Massimiliano Rossi,Catherine Sarret,Véronique Satre,Jean-Pierre Siffroi,Marianne Till,Renaud Touraine,Annick Toutain,Jérome Toutain,Stéphanie Valence,Alain Verloes,Sandra Whalen,Patrick Edery,Anne-Claude Tabet,Damien Sanlaville +72 more
TL;DR: Next-generation sequencing used to characterise breakpoints of balanced chromosomal rearrangements at the molecular level in patients with intellectual disability and/or congenital anomalies suggested that DNA breaks arose randomly and that there was no major influence of repeated elements.
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A genetic schizophrenia-susceptibility region located between the ANKK1 and DRD2 genes.
Caroline Dubertret,Claire Bardel,Claire Bardel,Nicolas Ramoz,Pierre-Marie Martin,Jean-Charles Deybach,Jean Adès,Philip Gorwood,Laurent Gouya +8 more
TL;DR: Intergenic rs2242592 appears to be involved in the genetic vulnerability to schizophrenia, whereas the ANKK1 rs1800497 appears to have a modifying rather than causative effect.