High frequency of potentially pathogenic SORL1 mutations in autosomal dominant early-onset Alzheimer disease C Pottier, D Hannequin, S Coutant, A Rovelet-Lecrux, D Wallon, ... Molecular psychiatry 17 (9), 875-879, 2012 | 300 | 2012 |
FORRepeats: detects repeats on entire chromosomes and between genomes A Lefebvre, T Lecroq, H Dauchel, J Alexandre Bioinformatics 19 (3), 319-326, 2003 | 93 | 2003 |
Identification and isolation of a pectin methylesterase isoform that could be involved in flax cell wall stiffening S Al-Qsous, E Carpentier, D Klein-Eude, C Burel, A Mareck, H Dauchel, ... Planta 219, 369-378, 2004 | 84 | 2004 |
Expression of complement alternative pathway proteins by endothelial cells. Differential regulation by interleukin 1 and glucocorticoids H Dauchel, N Julen, C Lemercier, M Daveau, D Ozanne, M Fontaine, ... European journal of immunology 20 (8), 1669-1675, 1990 | 71 | 1990 |
Activation of the endothelium by IL-1α and glucocorticoids results in major increase of complement C3 and factor B production and generation of C3a M Coulpier, S Andreev, C Lemercier, H Dauchel, O Lees, M Fontaine, ... Clinical & Experimental Immunology 101 (1), 142-149, 1995 | 55 | 1995 |
In vitro biosynthesis of complement factor I by human endothelial cells N Julen, H Dauchel, C Lemercier, RB Sim, M Fontaine, J Ripoche European journal of immunology 22 (1), 213-217, 1992 | 49 | 1992 |
Differential modulation by glucocorticoids of alternative complement protein secretion in cells of the monocyte/macrophage lineage C Lemercier, N Julen, M Coulpier, H Dauchel, D Ozanne, M Fontaine, ... European journal of immunology 22 (4), 909-915, 1992 | 34 | 1992 |
Comparative in depth RNA sequencing of P. tricornutum’s morphotypes reveals specific features of the oval morphotype C Ovide, MC Kiefer-Meyer, C Bérard, N Vergne, T Lecroq, C Plasson, ... Scientific reports 8 (1), 14340, 2018 | 33 | 2018 |
Large‐scale comparative evaluation of user‐friendly tools for predicting variant‐induced alterations of splicing regulatory elements H Tubeuf, C Charbonnier, O Soukarieh, A Blavier, A Lefebvre, H Dauchel, ... Human Mutation 41 (10), 1811-1829, 2020 | 32 | 2020 |
Pectin methylesterase pattern in flax seedlings during their development. F Alexandre, O Morvan, J Gaffe, A Mareck, A Jauneau, H Dauchel, ... | 28 | 1997 |
EVA: Exome Variation Analyzer, an efficient and versatile tool for filtering strategies in medical genomics S Coutant, C Cabot, A Lefebvre, M Léonard, E Prieur-Gaston, D Campion, ... BMC bioinformatics 13, 1-12, 2012 | 24 | 2012 |
UMI-VarCal: a new UMI-based variant caller that efficiently improves low-frequency variant detection in paired-end sequencing NGS libraries V Sater, PJ Viailly, T Lecroq, É Prieur-Gaston, É Bohers, M Viennot, ... Bioinformatics 36 (9), 2718-2724, 2020 | 23 | 2020 |
Introduction à la bioinformatique C Gibas, P Jambeck O'Reilly France, 2002 | 23 | 2002 |
Isolation of a flax pectin methylesterase promoter and its expression in transgenic tobacco D Roger, J Lacoux, F Lamblin, D Gaillet, H Dauchel, D Klein, AP Balangé, ... Plant Science 160 (4), 713-721, 2001 | 23 | 2001 |
Local and systemic activation of the whole complement cascade in human leukocytoclastic cutaneous vasculitis; C3d,g and terminal complement complex as … H Dauchel, P Joly, A Delpech, E Thomine, E Sauger, XLE LOET, ... Clinical & Experimental Immunology 92 (2), 274-283, 1993 | 22 | 1993 |
Improving high-resolution copy number variation analysis from next generation sequencing using unique molecular identifiers PJ Viailly, V Sater, M Viennot, E Bohers, N Vergne, C Berard, H Dauchel, ... BMC bioinformatics 22, 1-15, 2021 | 13 | 2021 |
Poisson approximation for the number of repeats in a stationary Markov chain N Touyar, S Schbath, D Cellier, H Dauchel Journal of applied probability 45 (2), 440-455, 2008 | 7 | 2008 |
GenerateReports: an Ion Torrent plugin summarizing a whole NGS experiment for clinical interpretation PJ Viailly, S Mareschal, P Bertrand, S Dubois, E Bohers, C Maingonnat, ... 23rd Annual International Conference on Intelligent Systems for Molecular …, 2015 | 5 | 2015 |
PHRC GMAJ collaborators: High frequency of potentially causative SORL1 mutations in autosomal dominant early-onset alzheimer disease C Pottier, D Hannequin, S Coutant, A Rovelet-Lecrux, D Wallon, C Paquet, ... Mol. Psychiatry 17 (9), 875-879, 2012 | 4 | 2012 |
Findings from the Section on Bioinformatics and Translational Informatics H Dauchel, T Lecroq Yearbook of Medical Informatics 26 (01), 188-192, 2017 | 2 | 2017 |