检索结果 - Isabelle Cournu‐Rebeix

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  1. 1
    Hereditary Spastic Paraplegia SPG13 Is Associated with a Mutation in the Gene Encoding the Mitochondrial Chaperonin Hsp60

    Hereditary Spastic Paraplegia SPG13 Is Associated with a Mutation in the Gene Encoding the Mitochondrial Chaperonin Hsp60 由 Jens Jacob Hansen, Alexandra Dürr, Isabelle Cournu‐Rebeix, Costa Georgopoulos, Debbie Ang, Marit N. Nielsen, Claire‐Sophie Davoine, Alexis Brice, Bertrand Fontaine, Niels Gregersen, Peter Bross

    出版 2002
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  2. 2
    Adaptive human immunity drives remyelination in a mouse model of demyelination

    Adaptive human immunity drives remyelination in a mouse model of demyelination 由 Mohamed El Behi, Charles Sanson, Corinne Bachelin, Léna Guillot‐Noël, Jennifer Fransson, Bruno Stankoff, Élisabeth Maillart, Nadège Sarrazin, Vincent Guillemot, Hervé Abdi, Isabelle Cournu‐Rebeix, Bertrand Fontaine, Violetta Zujovic

    出版 2017
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  3. 3
    Tyrosine kinase 2 variant influences T lymphocyte polarization and multiple sclerosis susceptibility

    Tyrosine kinase 2 variant influences T lymphocyte polarization and multiple sclerosis susceptibility 由 Nicolas Couturier, Florence Bucciarelli, Ramil Nurtdinov, Marc Debouverie, Christine Lebrun‐Frénay, Gilles Defer, T. Moreau, Cyrille B. Confavreux, Sandra Vukusic, Isabelle Cournu‐Rebeix, Robert Goertsches, Uwe K. Zettl, Manuel Comabella, Xavier Montalbán, Peter Rieckmann, Frank Weber, Bertram Müller‐Myhsok, Gilles Edan, Bertrand Fontaine, Lennart T. Mars, Abdelhadi Saoudi, Jorge R. Oksenberg, M. Clanet, Roland Liblau, David Brassat

    出版 2011
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  4. 4
    MANBA, CXCR5, SOX8, RPS6KB1 and ZBTB46 are genetic risk loci for multiple sclerosis

    MANBA, CXCR5, SOX8, RPS6KB1 and ZBTB46 are genetic risk loci for multiple sclerosis 由 Christina M. Lill, Brit‐Maren M. Schjeide, Christiane Graetz, Maria Ban, Antonio Alcina, Miguel A. Ortiz, Jennifer Pérez‐Boza, Vincent Damotte, David R. Booth, Aitzkoa Lopez de Lapuente, Linda Broer, Marcel Schilling, Denis A. Akkad, Orhan Aktaş, Iraide Alloza, Alfredo Rodríguez Antigüedad, Rafa Arroyo, Paul Blaschke, Mathias Buttmann, Andrew Chan, Alastair Compston, Isabelle Cournu‐Rebeix, Thomas Dörner, Jörg T. Epplen, Óscar Fernández, Lisa-Ann Gerdes, Léna Guillot‐Noël, Hans-Peter Hartung, Sabine Hoffjan, Guillermo Izquierdo, Anu Kemppinen, Antje Kroner, Christian Kubisch, Tania Kümpfel, Shu Li, Ulman Lindenberger, Peter Lohse, Catherine Lubetzki, Felix Luessi, Sunny Malhotra, Julia Mescheriakova, Xavier Montalbán, Caroline Papeix, Lidia Fernández-Paredes, Peter Rieckmann, Elisabeth Steinhagen‐Thiessen, Alexander Winkelmann, Uwe K. Zettl, Rogier Hintzen, Koen Vandenbroeck, G. A. Stewart, Bertrand Fontaine, Manuel Comabella, Elena Urcelay, Fuencisla Matesanz, Stephen Sawcer, Lars Bertram, Frauke Zipp

    出版 2013
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  5. 5
    Genome-Wide Association Study Identifies Novel Restless Legs Syndrome Susceptibility Loci on 2p14 and 16q12.1

    Genome-Wide Association Study Identifies Novel Restless Legs Syndrome Susceptibility Loci on 2p14 and 16q12.1 由 Juliane Winkelmann, Darina Czamara, Barbara Schormair, Felix Knauf, Eva C. Schulte, Claudia Trenkwalder, Yves Dauvilliers, Olli Polo, Birgit Högl, Kenneth I. Berger, Andrea Fuhs, Nadine Groß, Karin Stiasny‐Kolster, Wolfgang H. Oertel, Cornelius G. Bachmann, Walter Paulus, Lan Xiong, Jacques Montplaisir, Guy A. Rouleau, Ingo Fietze, Jana Vávrová, David Kemlink, Karel Šonka, Soňa Nevšímalová, Siong-Chi Lin, Zbigniew K. Wszołek, Carles Vilariño‐Güell, Matthew J. Farrer, Viola Gschliesser, Birgit Frauscher, Tina Falkenstetter, Werner Poewe, Richard P. Allen, Christopher J. Earley, William G. Ondo, Wei-Dong Le, Derek Spieler, Maria Kaffe, Alexander Zimprich, Johannes Kettunen, Markus Perola, Kaisa Silander, Isabelle Cournu‐Rebeix, Marcella Francavilla, Claire Fontenille, Bertrand Fontaine, Pavel Vodička, Holger Prokisch, Peter Lichtner, Paul E. Peppard, Juliette Faraco, Emmanuel Mignot, Christian Gieger, Thomas Illig, H.‐Erich Wichmann, Bertram Müller‐Myhsok, Thomas Meitinger

    出版 2011
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  6. 6
    Refining genetic associations in multiple sclerosis

    Refining genetic associations in multiple sclerosis 由 David R. Booth, Robert Heard, Graeme J. Stewart, An Goris, Rita Dobosi, Bénédicte Dubois, Annette Oturai, Helle Bach Søndergaard, Finn Sellebjerg, Janna Saarela, Virpi Leppä, Aarno Palotie, L. Peltonen, B. Fontaine, Isabelle Cournu‐Rebeix, Françoise Clerget‐Darpoux, Marie‐Claude Babron, Frank Weber, Herta Flor, Bertram Müller‐Myhsok, Peter Rieckmann, Antje Kroner, Colin A. Graham, Koen Vandenbroeck, Stanley Hawkins, Sandra D’Alfonso, Laura Bergamaschi, Paola Naldi, Franca Rosa Guerini, Marco Salvetti, Daniela Galimberti, Rogier Q. Hintzen, Cornelia M. van Duijn, Åslaug Rudjord Lorentzen, Elisabeth Gulowsen Celius, Hanne F. Harbo, Anne Spurkland, Francesco Cucca, Maria Giovanna Marrosu, Manuel Comabella, Xavier Montalbán, Pablo Villoslada, Tomas Olsson, Ingrid Kockum, Jan Hillert, Maria Ban, Andrew Walton, S. Sawcer, Alastair Compston, Clive Hawkins, Tania Mihalova, Neil P. Robertson, Gillian Ingram, Philip L. De Jager, David A. Hafler, John D. Rioux, Mark J. Daly, Lisa F. Barcellos, Adrian J. Ivinson, Margaret A. Pericak‐Vance, J. Hoksenberg, Stephen L. Hauser, Jacob L. McCauley, David Sexton, Jonathan L. Haines

    出版 2008
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  7. 7
    Network-Based Multiple Sclerosis Pathway Analysis with GWAS Data from 15,000 Cases and 30,000 Controls

    Network-Based Multiple Sclerosis Pathway Analysis with GWAS Data from 15,000 Cases and 30,000 Controls 由 Sergio E. Baranzini, Pouya Khankhanian, Nikolaos A. Patsopoulos, Michael Li, Jim Stankovich, Chris Cotsapas, Helle Bach Søndergaard, Maria Ban, Nadia Barizzone, Laura Bergamaschi, David R. Booth, Dorothea Buck, Paola Cavalla, Elisabeth Gulowsen Celius, Manuel Comabella, Gıancarlo Comı, Alastair Compston, Isabelle Cournu‐Rebeix, Sandra D’Alfonso, Vincent Damotte, Lennox Din, Bénédicte Dubois, Irina Elovaara, Federica Esposito, Bertrand Fontaine, André Franke, An Goris, Pierre‐Antoine Gourraud, Christiane Graetz, Franca Rosa Guerini, Léna Guillot‐Noël, D Hafler, Hákon Hákonarson, Per Hall, Anders Hamsten, Hanne F. Harbo, Bernhard Hemmer, Jan Hillert, Anu Kemppinen, Ingrid Kockum, Keijo Koivisto, Malin Larsson, Mark Lathrop, Maurizio Leone, Christina M. Lill, Fabìo Macciardi, Roland Martinꝉ, Vittorio Martinelli, Filippo Martinelli Boneschi, Jacob L. McCauley, Kjell‐Morten Myhr, Paola Naldi, Tomas Olsson, Annette Oturai, Margaret A. Pericak‐Vance, Franco Perla, Mauri Reunanen, Janna Saarela, Safa Saker-Delye, Marco Salvetti, Finn Sellebjerg, Per Soelberg Sørensen, Anne Spurkland, Graeme J. Stewart, Bruce Taylor, Pentti J. Tienari, Juliane Winkelmann, Frauke Zipp, Adrian J. Ivinson, Jonathan L. Haines, Stephen Sawcer, Philip L. DeJager, Stephen L. Hauser, Jorge R. Oksenberg

    出版 2013
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  8. 8
    IL12A, MPHOSPH9/CDK2AP1 and RGS1 are novel multiple sclerosis susceptibility loci

    IL12A, MPHOSPH9/CDK2AP1 and RGS1 are novel multiple sclerosis susceptibility loci 由 Federica Esposito, Nikolaos A. Patsopoulos, Sabine Cepok, Ingrid Kockum, Virpi Leppä, David R. Booth, Robert Heard, Graeme J. Stewart, Mathew Cox, Rodney J. Scott, Jeannette Lechner‐Scott, An Goris, Rita Dobosi, Bénédicte Dubois, John D. Rioux, Annette Oturai, Helle Bach Søndergaard, Finn Sellebjerg, Per Soelberg Sørensen, Mauri Reunanen, Keijo Koivisto, Isabelle Cournu‐Rebeix, B. Fontaine, Juliane Winkelmann, Christian Gieger, Carmen Infante‐Duarte, Frauke Zipp, Laura Bergamaschi, Maurizio Leone, Roberto Bergamaschi, Paola Cavalla, Åslaug Rudjord Lorentzen, I.-L. Mero, Elisabeth Gulowsen Celius, Hanne F. Harbo, Anne Spurkland, Manuel Comabella, B. Bryneda, Lars Alfredsson, Luisa Bernardinelli, Neil P. Robertson, Clive Hawkins, Lisa F. Barcellos, Gary W. Beecham, William S. Bush, Bruce Cree, Mark J. Daly, Adrian J. Ivinson, Cristin Aubin, Alastair Compston, Sandra D’Alfonso, J.L. Haines, Stephen L. Hauser, Bernhard Hemmer, Jan Hillert, Jacob L. McCauley, J. Oksenberg, Tomas Olsson, Aarno Palotie, L. Peltonen, Margaret A. Pericak‐Vance, Janna Saarela, Stephen Sawcer, Barbara E. Stranger, Filippo Martinelli Boneschi, Giancarlo Comi, D A Hafler, Paul I. W. de Bakker, Philip L. De Jager

    出版 2010
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  9. 9
    Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis

    Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis 由 Stephen Sawcer, Garrett Hellenthal, Matti Pirinen, Chris C. A. Spencer, Nikolaos A. Patsopoulos, Loukas Moutsianas, Alexander Dilthey, Zhan Su, Colin Freeman, Sarah Hunt, Sarah Edkins, Emma Gray, David R. Booth, Simon Potter, An Goris, Gavin Band, Annette Oturai, Amy Strange, Janna Saarela, Céline Bellenguez, Bertrand Fontaine, Matthew Gillman, Bernhard Hemmer, Rhian Gwilliam, Frauke Zipp, Alagurevathi Jayakumar, Roland Martinꝉ, Stephen Leslie, Stanley Hawkins, Eleni Giannoulatou, Sandra D’Alfonso, Hannah Blackburn, Filippo Martinelli Boneschi, Jennifer Liddle, Hanne F. Harbo, M. L. Perez, Anne Spurkland, Matthew Waller, Marcin P. Mycko, Michelle Ricketts, Manuel Comabella, Naomi Hammond, Ingrid Kockum, Owen T McCann, Maria Ban, Pamela Whittaker, Anu Kemppinen, Paul A. Weston, Clive Hawkins, Sara Widaa, John Zajicek, Serge Dronov, Neil P. Robertson, Suzannah J. Bumpstead, Lisa F. Barcellos, Rathi Ravindrarajah, Roby Abraham, Lars Alfredsson, Kristin Ardlie, Cristin Aubin, Amie Baker, K. Baker, Sergio E. Baranzini, Laura Bergamaschi, Roberto Bergamaschi, Allan Bernstein, Achim Berthele, Mike Boggild, Jonathan P. Bradfield, David Brassat, Simon Broadley, Dorothea Buck, Helmut Butzkueven, Ruggero Capra, William M. Carroll, Paola Cavalla, Elisabeth Gulowsen Celius, Sabine Cepok, Rosetta Chiavacci, Françoise Clerget‐Darpoux, Katleen Clysters, Gıancarlo Comı, M. Cossburn, Isabelle Cournu‐Rebeix, Mathew Cox, Wendy Cozen, Bruce Cree, Anne H. Cross, Daniele Cusi, Mark J. Daly, Emma Davis, Paul I. W. de Bakker, Marc Debouverie, Marie D’hooghe, Katherine Dixon, Rita Dobosi, Bénédicte Dubois, David Ellinghaus, Irina Elovaara, Federica Esposito

    出版 2011
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  10. 10
    Analysis of immune-related loci identifies 48 new susceptibility variants for multiple sclerosis

    Analysis of immune-related loci identifies 48 new susceptibility variants for multiple sclerosis 由 Ashley Beecham, Nikolaos A. Patsopoulos, Dionysia K. Xifara, Mary F. Davis, Anu Kemppinen, Chris Cotsapas, Tejas Shah, Chris C. A. Spencer, David J. Booth, An Goris, Annette Oturai, Janna Saarela, Bertrand Fontaine, Bernhard Hemmer, Claes Martin, Frauke Zipp, Sandra D’Alfonso, Filippo Martinelli Boneschi, Bruce Taylor, Hanne F. Harbo, Ingrid Kockum, Jan Hillert, Tomas Olsson, Maria Ban, Jorge R. Oksenberg, Rogier Hintzen, Lisa F. Barcellos, Cristina Agliardi, Lars Alfredsson, Mehdi Alizadeh, Carl A. Anderson, Robert Andrews, Helle Bach Søndergaard, Amie Baker, Gavin Band, Sergio E. Baranzini, Nadia Barizzone, Jeffrey C. Barrett, Céline Bellenguez, Laura Bergamaschi, Luisa Bernardinelli, Achim Berthele, Viola Biberacher, Thomas M.C. Binder, Hannah Blackburn, Izaura Lima Bomfim, Paola Brambilla, Simon Broadley, Bruno Brochet, Lou Brundin, Dorothea Buck, Helmut Butzkueven, Stacy J. Caillier, William Camu, Wassila Carpentier, Paola Cavalla, Elisabeth Gulowsen Celius, Irène Coman, Gıancarlo Comı, Lucia Corrado, Leentje Cosemans, Isabelle Cournu‐Rebeix, Bruce Cree, Daniele Cusi, Vincent Damotte, Gilles Defer, Silvia Delgado, Panos Deloukas, Alessia Di Sapio, Alexander Dilthey, Peter Donnelly, Bénédicte Dubois, Martin Duddy, Sarah Edkins, Irina Elovaara, Federica Esposito, Nikos Evangelou, Barnaby Fiddes, Judith Field, André Franke, Colin Freeman, Irene Y. Frohlich, Daniela Galimberti, Christian Gieger, Pierre‐Antoine Gourraud, Christiane Graetz, Andrew Graham, Verena Grummel, Clara Guaschino, Athena Hadjixenofontos, Hákon Hákonarson, Christopher Halfpenny, Gillian Hall, Per Hall, Anders Hamsten, James Harley, Timothy Harrower, Clive Hawkins, Garrett Hellenthal, Charles Hillier

    出版 2013
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  11. 11
    Low-Frequency and Rare-Coding Variation Contributes to Multiple Sclerosis Risk

    Low-Frequency and Rare-Coding Variation Contributes to Multiple Sclerosis Risk 由 Mitja Mitrovič, Nikolaos A. Patsopoulos, Ashley Beecham, Theresa Dankowski, An Goris, Bénédicte Dubois, Marie D’hooghe, Robin Lemmens, Philip Van Damme, Helle Bach Søndergaard, Finn Sellebjerg, Per Soelberg Sorensen, Henrik Ullum, Lise Wegner Thørner, Thomas Werge, Janna Saarela, Isabelle Cournu‐Rebeix, Vincent Damotte, Bertrand Fontaine, Léna Guillot‐Noël, Mark Lathrop, Sandra Vukusik, Pierre‐Antoine Gourraud, Till F. M. Andlauer, Viola Pongratz, Dorothea Buck, Christiane Gasperi, Antonios Bayas, Christoph Heesen, Tania Kümpfel, Ralf A. Linker, Friedemann Paul, Martin Stangel, Björn Tackenberg, Florian Then Bergh, Clemens Warnke, Heinz Wiendl, Brigitte Wildemann, Uwe K. Zettl, Ulf Ziemann, Hayrettin Tumani, Ralf Gold, Verena Grummel, Bernhard Hemmer, Benjamin Knier, Christina M. Lill, Felix Luessi, Efthimios Dardiotis, Cristina Agliardi, Nadia Barizzone, Elisabetta Mascia, Luisa Bernardinelli, Giancarlo Comi, Daniele Cusi, Federica Esposito, Laura Ferrè, Cristoforo Comi, Daniela Galimberti, Maurizio Leone, Melissa Sorosina, Julia Mescheriakova, Rogier Hintzen, Cornelia M. van Duijn, Charlotte E. Teunissen, Steffan D. Bos, Kjell‐Morten Myhr, Elisabeth Gulowsen Celius, Benedicte A. Lie, Anne Spurkland, Manuel Comabella, Xavier Montalbán, Lars Alfredsson, Pernilla Stridh, Jan Hillert, Maja Jagodic, Fredrik Piehl, Ilijas Jelčić, Roland Martinꝉ, Mireia Sospedra, Maria Ban, Clive Hawkins, Pirro G. Hysi, Seema Kalra, Fredrik Karpe, Jyoti Khadake, Geneviève Lachance, Matthew Neville, Adam Santaniello, Stacy J. Caillier, Peter A. Calabresi, Bruce Cree, Anne H. Cross, Mary F. Davis, Jonathan L. Haines, Paul I. W. de Bakker, Silvia Delgado, Marieme Dembele, Keith R. Edwards, Kathryn C. Fitzgerald, Hákon Hákonarson

    出版 2018
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  12. 12
    Multiple sclerosis genomic map implicates peripheral immune cells and microglia in susceptibility

    Multiple sclerosis genomic map implicates peripheral immune cells and microglia in susceptibility 由 Nikolaos A. Patsopoulos, Sergio E. Baranzini, Adam Santaniello, Parisa Shoostari, Chris Cotsapas, Garrett Wong, Ashley Beecham, Tojo James, Joseph M. Replogle, Ioannis S. Vlachos, Cristin McCabe, Tune H. Pers, Aaron Brandes, Charles C. White, Brendan T Keenan, Maria Cimpean, Phoebe A. Winn, Ioannis-Pavlos Panteliadis, Allison Robbins, Till F. M. Andlauer, Onigiusz Zarzycki, Bénédicte Dubois, An Goris, Helle Bach Søndergaard, Finn Sellebjerg, Per Soelberg Sorensen, Henrik Ullum, Lise Wegner Thørner, Janna Saarela, Isabelle Cournu‐Rebeix, Vincent Damotte, Bertrand Fontaine, Léna Guillot‐Noël, Mark Lathrop, Sandra Vukusic, Achim Berthele, Viola Pongratz, Dorothea Buck, Christiane Gasperi, Christiane Graetz, Verena Grummel, Bernhard Hemmer, Muni Hoshi, Benjamin Knier, Thomas Korn, Christina M. Lill, Felix Luessi, Mark Mühlau, Frauke Zipp, Efthimios Dardiotis, Cristina Agliardi, Antonio Amoroso, Nadia Barizzone, Maria Donata Benedetti, Luisa Bernardinelli, Paola Cavalla, Ferdinando Clarelli, Gıancarlo Comı, Daniele Cusi, Federica Esposito, Laura Ferrè, Daniela Galimberti, Clara Guaschino, Maurizio Leone, Vittorio Martinelli, Lucia Moiola, Marco Salvetti, Melissa Sorosina, Domizia Vecchio, Andrea Zauli, Silvia Santoro, Nicasio Mancini, Miriam Zuccalà, Julia Mescheriakova, Cornelia M. van Duijn, Steffan D. Bos, Elisabeth Gulowsen Celius, Anne Spurkland, Manuel Comabella, Xavier Montalbán, Lars Alfredsson, Izaura Lima Bomfim, David Gómez-Cabrero, Jan Hillert, Maja Jagodic, Magdalena Lindén, Fredrik Piehl, Ilijas Jelčić, Roland Martinꝉ, Mirela Sospedra, Amie Baker, Maria Ban, Clive Hawkins, Pirro G. Hysi, Seema Kalra, Fredrik Karpe, Jyoti Khadake, Geneviève Lachance, Paul Molyneux, Matthew Neville

    出版 2019
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