Estelle Escudier - Publications

UPMC Univ Paris 6, France 
, Nasal obstruction, Neurovegetative nasal dysfunction, Primary ciliary dyskinesia, Leber congenital amaurosis, Acoustic rhinometry, Nasal compliance

51 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2019 Blanchon S, Legendre M, Bottier M, Tamalet A, Montantin G, Collot N, Faucon C, Dastot F, Copin B, Clement A, Filoche M, Coste A, Amselem S, Escudier E, Papon JF, et al. Deep phenotyping, including quantitative ciliary beating parameters, and extensive genotyping in primary ciliary dyskinesia. Journal of Medical Genetics. PMID 31772028 DOI: 10.1136/jmedgenet-2019-106424  0.68
2019 Bequignon E, Dupuy L, Escabasse V, Zerah-Lancner F, Bassinet L, Honoré I, Legendre M, Devars du Mayne M, Crestani B, Escudier E, Coste A, Papon JF, Maître B. Follow-Up and Management of Chronic Rhinosinusitis in Adults with Primary Ciliary Dyskinesia: Review and Experience of Our Reference Centers. Journal of Clinical Medicine. 8. PMID 31546861 DOI: 10.3390/jcm8091495  0.68
2019 Mani R, Belkacem S, Soua Z, Chantot S, Montantin G, Tissier S, Copin B, Bouguila J, Le Gouard NR, Boughamoura L, Ben Ameur S, Hachicha M, Boussoffara R, Boussetta K, Hammouda S, ... ... Escudier E, et al. Primary ciliary dyskinesia gene contribution in Tunisia-identification of a major Mediterranean allele. Human Mutation. PMID 31469207 DOI: 10.1002/humu.23905  0.68
2019 Whitfield M, Thomas L, Bequignon E, Schmitt A, Stouvenel L, Montantin G, Tissier S, Duquesnoy P, Copin B, Chantot S, Dastot F, Faucon C, Barbotin AL, Loyens A, Siffroi JP, ... ... Escudier E, et al. Mutations in DNAH17, Encoding a Sperm-Specific Axonemal Outer Dynein Arm Heavy Chain, Cause Isolated Male Infertility Due to Asthenozoospermia. American Journal of Human Genetics. PMID 31178125 DOI: 10.1016/j.ajhg.2019.04.015  0.68
2019 Benjamin AT, Ganesh R, Gaspar BL, Lucas J, Jackson C, Legendre M, Mani R, Escudier E. A Novel Homozygous Nonsense HYDIN Gene Mutation p.(Arg951*) in Primary Ciliary Dyskinesia. Indian Journal of Pediatrics. PMID 31089940 DOI: 10.1007/s12098-019-02970-z  0.4
2019 Bequignon E, Dupuy L, Zerah-Lancner F, Bassinet L, Honoré I, Legendre M, Devars du Mayne M, Escabasse V, Crestani B, Maître B, Escudier E, Coste A, Papon JF. Critical Evaluation of Sinonasal Disease in 64 Adults with Primary Ciliary Dyskinesia. Journal of Clinical Medicine. 8. PMID 31067752 DOI: 10.3390/jcm8050619  0.68
2019 Bequignon E, Dhommée C, Angely C, Thomas L, Bottier M, Escudier E, Isabey D, Coste A, Louis B, Papon JF, Gouilleux-Gruart V. FcRn-Dependent Transcytosis of Monoclonal Antibody in Human Nasal Epithelial Cells In Vitro: A Prerequisite for a New Delivery Route for Therapy? International Journal of Molecular Sciences. 20. PMID 30893823 DOI: 10.3390/ijms20061379  0.68
2019 Bustamante-Marin XM, Yin WN, Sears PR, Werner ME, Brotslaw EJ, Mitchell BJ, Jania CM, Zeman KL, Rogers TD, Herring LE, Refabért L, Thomas L, Amselem S, Escudier E, Legendre M, et al. Lack of GAS2L2 Causes PCD by Impairing Cilia Orientation and Mucociliary Clearance. American Journal of Human Genetics. PMID 30665704 DOI: 10.1016/j.ajhg.2018.12.009  0.68
2018 Lorès P, Coutton C, Khouri EE, Stouvenel L, Givelet M, Thomas L, Rode B, Schmitt A, Louis B, Sakheli Z, Chaudhry M, Fernandez-Gonzales A, Mitsialis A, Dacheux D, Wolf JP, ... ... Escudier E, et al. Homozygous missense mutation L673P in adenylate kinase 7 (AK7) leads to primary male infertility and multiple morphological anomalies of the flagella but not to primary ciliary dyskinesia. Human Molecular Genetics. PMID 30517620 DOI: 10.1093/hmg/ddy368  0.68
2018 Fassad MR, Shoemark A, Legendre M, Hirst RA, Koll F, le Borgne P, Louis B, Daudvohra F, Patel MP, Thomas L, Dixon M, Burgoyne T, Hayes J, Nicholson AG, Cullup T, ... ... Escudier E, et al. Mutations in Outer Dynein Arm Heavy Chain DNAH9 Cause Motile Cilia Defects and Situs Inversus. American Journal of Human Genetics. PMID 30471717 DOI: 10.1016/j.ajhg.2018.10.016  0.68
2018 Fuger M, Aupiais C, Thouvenin G, Taytard J, Tamalet A, Escudier E, Boizeau P, Corvol H, Beydon N. Gas exchanges in children with cystic fibrosis or primary ciliary dyskinesia: A retrospective study. Respiratory Physiology & Neurobiology. PMID 29366817 DOI: 10.1016/j.resp.2018.01.010  0.32
2018 Lorès P, Coutton C, El Khouri E, Stouvenel L, Givelet M, Thomas L, Rode B, Schmitt A, Louis B, Sakheli Z, Chaudhry M, Fernandez-Gonzales A, Mitsialis A, Dacheux D, Wolf JP, ... ... Escudier E, et al. Homozygous missense mutation L673P in Adenylate Kinase 7 (AK7) leads to primary male infertility and Multiple Morphological Anomalies of the Flagella but not to Primary Ciliary Dyskinesia. Human Molecular Genetics. PMID 29365104 DOI: 10.1093/hmg/ddy034  0.68
2017 Vanaken GJ, Bassinet L, Boon M, Mani R, Honoré I, Papon JF, Cuppens H, Jaspers M, Laurent N, Coste A, Escudier E, Amselem S, Maitre B, Legendre M, Christin-Maitre S. Infertility in an adult cohort with primary ciliary dyskinesia: phenotype-gene association. The European Respiratory Journal. 50. PMID 29122913 DOI: 10.1183/13993003.00314-2017  0.68
2017 Ryan R, Failler M, Reilly ML, Garfa-Traore M, Delous M, Filhol E, Reboul T, Bole-Feysot C, Nitschké P, Baudouin V, Amselem S, Escudier E, Legendre M, Benmerah A, Saunier S. Functional characterization of tektin-1 in motile cilia and evidence for TEKT1 as a new candidate gene for motile ciliopathies. Human Molecular Genetics. PMID 29121203 DOI: 10.1093/hmg/ddx396  0.68
2017 Bottier M, Blanchon S, Pelle G, Bequignon E, Isabey D, Coste A, Escudier E, Grotberg JB, Papon JF, Filoche M, Louis B. A new index for characterizing micro-bead motion in a flow induced by ciliary beating: Part I, experimental analysis. Plos Computational Biology. 13: e1005605. PMID 28708889 DOI: 10.1371/journal.pcbi.1005605  0.68
2017 Olcese C, Patel MP, Shoemark A, Kiviluoto S, Legendre M, Williams HJ, Vaughan CK, Hayward J, Goldenberg A, Emes RD, Munye MM, Dyer L, Cahill T, Bevillard J, Gehrig C, ... ... Escudier E, et al. X-linked primary ciliary dyskinesia due to mutations in the cytoplasmic axonemal dynein assembly factor PIH1D3. Nature Communications. 8: 14279. PMID 28176794 DOI: 10.1038/ncomms14279  0.68
2017 Frija-Masson J, Bassinet L, Honoré I, Dufeu N, Housset B, Coste A, Papon JF, Escudier E, Burgel PR, Maître B. Clinical characteristics, functional respiratory decline and follow-up in adult patients with primary ciliary dyskinesia. Thorax. 72: 154-160. PMID 27382041 DOI: 10.1136/thoraxjnl-2015-207891  0.68
2016 Lucas JS, Barbato A, Collins SA, Goutaki M, Behan L, Caudri D, Dell S, Eber E, Escudier E, Hirst RA, Hogg C, Jorissen M, Latzin P, Legendre M, Leigh MW, et al. European Respiratory Society guidelines for the diagnosis of primary ciliary dyskinesia. The European Respiratory Journal. PMID 27836958 DOI: 10.1183/13993003.01090-2016  0.68
2016 El Khouri E, Thomas L, Jeanson L, Bequignon E, Vallette B, Duquesnoy P, Montantin G, Copin B, Dastot-Le Moal F, Blanchon S, Papon JF, Lorès P, Yuan L, Collot N, Tissier S, ... ... Escudier E, et al. Mutations in DNAJB13, Encoding an HSP40 Family Member, Cause Primary Ciliary Dyskinesia and Male Infertility. American Journal of Human Genetics. 99: 489-500. PMID 27486783 DOI: 10.1016/j.ajhg.2016.06.022  0.68
2016 Jeanson L, Thomas L, Copin B, Coste A, Sermet-Gaudelus I, Moal FD, Duquesnoy P, Montantin G, Collot N, Tissier S, Papon JF, Clement A, Louis B, Escudier E, Amselem S, et al. Mutations in GAS8, A Gene Encoding A Nexin-Dynein Regulatory Complex Subunit, Cause Primary Ciliary Dyskinesia With Axonemal Disorganization. Human Mutation. PMID 27120127 DOI: 10.1002/humu.23005  0.52
2015 Jeanson L, Copin B, Papon JF, Dastot-Le Moal F, Duquesnoy P, Montantin G, Cadranel J, Corvol H, Coste A, Désir J, Souayah A, Kott E, Collot N, Tissier S, Louis B, ... ... Escudier E, et al. RSPH3 Mutations Cause Primary Ciliary Dyskinesia with Central-Complex Defects and a Near Absence of Radial Spokes. American Journal of Human Genetics. 97: 153-62. PMID 26073779 DOI: 10.1016/j.ajhg.2015.05.004  0.52
2015 Beydon N, Chambellan A, Alberti C, de Blic J, Clément A, Escudier E, Le Bourgeois M. Technical and practical issues for tidal breathing measurements of nasal nitric oxide in children. Pediatric Pulmonology. 50: 1374-82. PMID 25731630 DOI: 10.1002/ppul.23167  0.32
2015 Bourderioux M, Nguyen-Khoa T, Chhuon C, Jeanson L, Tondelier D, Walczak M, Ollero M, Bekri S, Knebelmann B, Escudier E, Escudier B, Edelman A, Guerrera IC. A new workflow for proteomic analysis of urinary exosomes and assessment in cystinuria patients. Journal of Proteome Research. 14: 567-77. PMID 25365230 DOI: 10.1021/pr501003q  0.44
2014 Jeanson L, Guerrera IC, Papon JF, Chhuon C, Zadigue P, Prulière-Escabasse V, Amselem S, Escudier E, Coste A, Edelman A. Proteomic analysis of nasal epithelial cells from cystic fibrosis patients. Plos One. 9: e108671. PMID 25268127 DOI: 10.1371/journal.pone.0108671  0.68
2013 Kott E, Legendre M, Copin B, Papon JF, Dastot-Le Moal F, Montantin G, Duquesnoy P, Piterboth W, Amram D, Bassinet L, Beucher J, Beydon N, Deneuville E, Houdouin V, Journel H, ... ... Escudier E, et al. Loss-of-function mutations in RSPH1 cause primary ciliary dyskinesia with central-complex and radial-spoke defects. American Journal of Human Genetics. 93: 561-70. PMID 23993197 DOI: 10.1016/j.ajhg.2013.07.013  0.52
2013 Vallet C, Escudier E, Roudot-Thoraval F, Blanchon S, Fauroux B, Beydon N, Boulé M, Vojtek AM, Amselem S, Clément A, Tamalet A. Primary ciliary dyskinesia presentation in 60 children according to ciliary ultrastructure. European Journal of Pediatrics. 172: 1053-60. PMID 23571820 DOI: 10.1007/s00431-013-1996-5  0.68
2013 Martin C, Coolen N, Wu Y, Thévenot G, Touqui L, Prulière-Escabasse V, Papon JF, Coste A, Escudier E, Dusser DJ, Fajac I, Burgel PR. CFTR dysfunction induces vascular endothelial growth factor synthesis in airway epithelium. The European Respiratory Journal. 42: 1553-62. PMID 23520314 DOI: 10.1183/09031936.00164212  0.68
2012 Kott E, Duquesnoy P, Copin B, Legendre M, Dastot-Le Moal F, Montantin G, Jeanson L, Tamalet A, Papon JF, Siffroi JP, Rives N, Mitchell V, de Blic J, Coste A, Clement A, ... ... Escudier E, et al. Loss-of-function mutations in LRRC6, a gene essential for proper axonemal assembly of inner and outer dynein arms, cause primary ciliary dyskinesia. American Journal of Human Genetics. 91: 958-64. PMID 23122589 DOI: 10.1016/j.ajhg.2012.10.003  0.68
2012 Papon JF, Bassinet L, Cariou-Patron G, Zerah-Lancner F, Vojtek AM, Blanchon S, Crestani B, Amselem S, Coste A, Housset B, Escudier E, Louis B. Quantitative analysis of ciliary beating in primary ciliary dyskinesia: a pilot study. Orphanet Journal of Rare Diseases. 7: 78. PMID 23057704 DOI: 10.1186/1750-1172-7-78  0.68
2012 Blanchon S, Legendre M, Copin B, Duquesnoy P, Montantin G, Kott E, Dastot F, Jeanson L, Cachanado M, Rousseau A, Papon JF, Beydon N, Brouard J, Crestani B, Deschildre A, ... ... Escudier E, et al. Delineation of CCDC39/CCDC40 mutation spectrum and associated phenotypes in primary ciliary dyskinesia. Journal of Medical Genetics. 49: 410-6. PMID 22693285 DOI: 10.1136/jmedgenet-2012-100867  0.68
2012 Magnin ML, Cros P, Beydon N, Mahloul M, Tamalet A, Escudier E, Clément A, Le Pointe HD, Blanchon S. Longitudinal lung function and structural changes in children with primary ciliary dyskinesia. Pediatric Pulmonology. 47: 816-25. PMID 22570319 DOI: 10.1002/ppul.22577  0.32
2011 Merveille AC, Davis EE, Becker-Heck A, Legendre M, Amirav I, Bataille G, Belmont J, Beydon N, Billen F, Clément A, Clercx C, Coste A, Crosbie R, de Blic J, Deleuze S, ... ... Escudier E, et al. CCDC39 is required for assembly of inner dynein arms and the dynein regulatory complex and for normal ciliary motility in humans and dogs. Nature Genetics. 43: 72-8. PMID 21131972 DOI: 10.1038/ng.726  0.52
2010 Prulière-Escabasse V, Coste A, Chauvin P, Fauroux B, Tamalet A, Garabedian EN, Escudier E, Roger G. Otologic features in children with primary ciliary dyskinesia. Archives of Otolaryngology--Head & Neck Surgery. 136: 1121-6. PMID 21079168 DOI: 10.1001/archoto.2010.183  0.56
2010 Prulière-Escabasse V, Clerici C, Vuagniaux G, Coste A, Escudier E, Planès C. Effect of neutrophil elastase and its inhibitor EPI-hNE4 on transepithelial sodium transport across normal and cystic fibrosis human nasal epithelial cells. Respiratory Research. 11: 141. PMID 20932306 DOI: 10.1186/1465-9921-11-141  0.56
2010 Prulière-Escabasse V, Gomez-Roca C, Escudier E, Coste A, Besse B, Massard C, Soria JC. Rhinitis in patients treated with a combination of an mTOR inhibitor and an EGFR inhibitor. Onkologie. 33: 401-2. PMID 20631489 DOI: 10.1159/000315757  0.56
2009 Duquesnoy P, Escudier E, Vincensini L, Freshour J, Bridoux AM, Coste A, Deschildre A, de Blic J, Legendre M, Montantin G, Tenreiro H, Vojtek AM, Loussert C, Clément A, Escalier D, et al. Loss-of-function mutations in the human ortholog of Chlamydomonas reinhardtii ODA7 disrupt dynein arm assembly and cause primary ciliary dyskinesia. American Journal of Human Genetics. 85: 890-6. PMID 19944405 DOI: 10.1016/j.ajhg.2009.11.008  0.68
2009 Mougou-Zerelli S, Thomas S, Szenker E, Audollent S, Elkhartoufi N, Babarit C, Romano S, Salomon R, Amiel J, Esculpavit C, Gonzales M, Escudier E, Leheup B, Loget P, Odent S, et al. CC2D2A mutations in Meckel and Joubert syndromes indicate a genotype-phenotype correlation. Human Mutation. 30: 1574-82. PMID 19777577 DOI: 10.1002/humu.21116  0.52
2009 Escudier E, Duquesnoy P, Papon JF, Amselem S. Ciliary defects and genetics of primary ciliary dyskinesia. Paediatric Respiratory Reviews. 10: 51-4. PMID 19410201 DOI: 10.1016/j.prrv.2009.02.001  0.68
2008 Botterel F, Gross K, Ibrahim-Granet O, Khoufache K, Escabasse V, Coste A, Cordonnier C, Escudier E, Bretagne S. Phagocytosis of Aspergillus fumigatus conidia by primary nasal epithelial cells in vitro. Bmc Microbiology. 8: 97. PMID 18564423 DOI: 10.1186/1471-2180-8-97  0.6
2007 Prulière-Escabasse V, Planès C, Escudier E, Fanen P, Coste A, Clerici C. Modulation of epithelial sodium channel trafficking and function by sodium 4-phenylbutyrate in human nasal epithelial cells. The Journal of Biological Chemistry. 282: 34048-57. PMID 17890229 DOI: 10.1074/jbc.M702384200  0.56
2007 Zhang Z, Zariwala MA, Mahadevan MM, Caballero-Campo P, Shen X, Escudier E, Duriez B, Bridoux AM, Leigh M, Gerton GL, Kennedy M, Amselem S, Knowles MR, Strauss JF. A heterozygous mutation disrupting the SPAG16 gene results in biochemical instability of central apparatus components of the human sperm axoneme Biology of Reproduction. 77: 864-871. PMID 17699735 DOI: 10.1095/biolreprod.107.063206  0.52
2007 Duriez B, Duquesnoy P, Escudier E, Bridoux AM, Escalier D, Rayet I, Marcos E, Vojtek AM, Bercher JF, Amselem S. A common variant in combination with a nonsense mutation in a member of the thioredoxin family causes primary ciliary dyskinesia. Proceedings of the National Academy of Sciences of the United States of America. 104: 3336-41. PMID 17360648 DOI: 10.1073/pnas.0611405104  0.68
2007 Lazard DS, Prulière-Escabasse V, Papon JF, Escudier E, Coste A. [Injury and epithelial wound healing: a pathophysiologic hypothesis for nasal and sinus polyposis]. Presse Medicale (Paris, France : 1983). 36: 1104-8. PMID 17306500 DOI: 10.1016/j.lpm.2007.01.021  0.68
2007 Khoufache K, Puel O, Loiseau N, Delaforge M, Rivollet D, Coste A, Cordonnier C, Escudier E, Botterel F, Bretagne S. Verruculogen associated with Aspergillus fumigatus hyphae and conidia modifies the electrophysiological properties of human nasal epithelial cells. Bmc Microbiology. 7: 5. PMID 17244350 DOI: 10.1186/1471-2180-7-5  0.56
2006 Zariwala MA, Leigh MW, Ceppa F, Kennedy MP, Noone PG, Carson JL, Hazucha MJ, Lori A, Horvath J, Olbrich H, Loges NT, Bridoux AM, Pennarun G, Duriez B, Escudier E, et al. Mutations of DNAI1 in primary ciliary dyskinesia: evidence of founder effect in a common mutation. American Journal of Respiratory and Critical Care Medicine. 174: 858-66. PMID 16858015 DOI: 10.1164/rccm.200603-370OC  0.52
2006 Mitchell V, Rives N, Albert M, Peers MC, Selva J, Clavier B, Escudier E, Escalier D. Outcome of ICSI with ejaculated spermatozoa in a series of men with distinct ultrastructural flagellar abnormalities. Human Reproduction (Oxford, England). 21: 2065-74. PMID 16644911 DOI: 10.1093/humrep/del130  0.44
2006 Mahut B, Escudier E, de Blic J, Zerah-Lancner F, Coste A, Harf A, Delclaux C. Impairment of nitric oxide output of conducting airways in primary ciliary dyskinesia. Pediatric Pulmonology. 41: 158-63. PMID 16353174 DOI: 10.1002/ppul.20329  0.6
2005 Prulière-Escabasse V, Fanen P, Dazy AC, Lechapt-Zalcman E, Rideau D, Edelman A, Escudier E, Coste A. TGF-beta 1 downregulates CFTR expression and function in nasal polyps of non-CF patients. American Journal of Physiology. Lung Cellular and Molecular Physiology. 288: L77-83. PMID 15361357 DOI: 10.1152/ajplung.00048.2004  0.56
2002 Papon JF, Coste A, Gendron MC, Cordonnier C, Wingerstmann L, Peynègre R, Escudier E. HLA-DR and ICAM-1 expression and modulation in epithelial cells from nasal polyps. The Laryngoscope. 112: 2067-75. PMID 12439183 DOI: 10.1097/00005537-200211000-00030  0.68
2002 Escudier E, Couprie M, Duriez B, Roudot-Thoraval F, Millepied MC, Prulière-Escabasse V, Labatte L, Coste A. Computer-assisted analysis helps detect inner dynein arm abnormalities. American Journal of Respiratory and Critical Care Medicine. 166: 1257-62. PMID 12403696 DOI: 10.1164/rccm.2111070  0.56
2002 Pennarun G, Bridoux AM, Escudier E, Dastot-Le Moal F, Cacheux V, Amselem S, Duriez B. Isolation and expression of the human hPF20 gene orthologous to Chlamydomonas PF20: evaluation as a candidate for axonemal defects of respiratory cilia and sperm flagella. American Journal of Respiratory Cell and Molecular Biology. 26: 362-70. PMID 11867345 DOI: 10.1165/ajrcmb.26.3.4738  0.68
Show low-probability matches.