Výsledky vyhledávání - Philippe Goyette

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  1. 1
    Defining the Role of the MHC in Autoimmunity: A Review and Pooled Analysis

    Defining the Role of the MHC in Autoimmunity: A Review and Pooled Analysis Autor Michelle M. A. Fernando, Christine Stevens, Emily C. Walsh, Philip L. De Jager, Philippe Goyette, Robert M. Plenge, Timothy J. Vyse, John D. Rioux

    Vydáno 2008
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  2. 2
    A candidate genetic risk factor for vascular disease: a common mutation in methylenetetrahydrofolate reductase

    A candidate genetic risk factor for vascular disease: a common mutation in methylenetetrahydrofolate reductase Autor Phyllis Frosst, Henk J. Blom, Renate Milos, Philippe Goyette, Christal A. Sheppard, Rowena G. Matthews, GodfriedHJ Boers, Martin den Heijer, Leo A. J. Kluijtmans, L.P. van den Heuve, Rima Rozen

    Vydáno 1995
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  3. 3
    Epigenetic reader SP140 loss of function drives Crohn’s disease due to uncontrolled macrophage topoisomerases

    Epigenetic reader SP140 loss of function drives Crohn’s disease due to uncontrolled macrophage topoisomerases Autor Hajera Amatullah, Isabella Fraschilla, Sreehaas Digumarthi, Julie Y. Huang, Fatemeh Adiliaghdam, Gracia Bonilla, Lai Ping Wong, Marie-Ève Rivard, Claudine Beauchamp, Virginie Mercier, Philippe Goyette, Ruslan I. Sadreyev, Robert M. Anthony, John D. Rioux, Kate L. Jeffrey

    Vydáno 2022
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  4. 4
    Gene-centric association mapping of chromosome 3p implicates MST1 in IBD pathogenesis

    Gene-centric association mapping of chromosome 3p implicates MST1 in IBD pathogenesis Autor Philippe Goyette, Christine Lefebvre, Aylwin Ng, Steven R. Brant, J H Cho, Richard H. Duerr, Mark S. Silverberg, Kent D. Taylor, Anna Latiano, Guy Aumais, Colette Deslandres, Gilles Jobin, Vito Annese, Mark J. Daly, Ramnik J. Xavier, John D. Rioux

    Vydáno 2008
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  5. 5
    Deletion polymorphism upstream of IRGM associated with altered IRGM expression and Crohn's disease

    Deletion polymorphism upstream of IRGM associated with altered IRGM expression and Crohn's disease Autor Steven A. McCarroll, Alan Huett, Petric Kuballa, Shannon Chilewski, Aimee Landry, Philippe Goyette, Michael C. Zody, Jennifer L. Hall, Steven R. Brant, Judy H. Cho, Richard H. Duerr, Mark S. Silverberg, Kent D. Taylor, John D. Rioux, David Altshuler, Mark J. Daly, Ramnik J. Xavier

    Vydáno 2008
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  6. 6
    A Meta-Analysis of Genome-Wide Association Scans Identifies IL18RAP, PTPN2, TAGAP, and PUS10 As Shared Risk Loci for Crohn's Disease and Celiac Disease

    A Meta-Analysis of Genome-Wide Association Scans Identifies IL18RAP, PTPN2, TAGAP, and PUS10 As Shared Risk Loci for Crohn's Disease and Celiac Disease Autor Eleonora A. Festen, Philippe Goyette, Todd J. Green, Gabrielle Boucher, Claudine Beauchamp, Gosia Trynka, P Dubois, Caroline Lagacé, Pieter Stokkers, Daan W. Hommes, Donatella Barisani, Orazio Palmieri, Vito Annese, David A. van Heel, Rinse K. Weersma, Mark J. Daly, Cisca Wijmenga, John D. Rioux

    Vydáno 2011
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  7. 7
    A Major Histocompatibility Class I Locus Contributes to Multiple Sclerosis Susceptibility Independently from HLA-DRB1*15:01

    A Major Histocompatibility Class I Locus Contributes to Multiple Sclerosis Susceptibility Independently from HLA-DRB1*15:01 Autor Bruce Cree, John D. Rioux, Jacob L. McCauley, Pierre‐Antoine Gourraud, Philippe Goyette, Joseph P. McElroy, Philip L. De Jager, Adam Santaniello, Timothy J. Vyse, Peter K. Gregersen, Daniel B. Mirel, D Hafler, Jonathan L. Haines, Margaret A. Pericak‐Vance, Alastair Compston, Stephen Sawcer, Jorge R. Oksenberg, Stephen L. Hauser

    Vydáno 2010
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  8. 8
    Genetic variants in the region harbouring IL2/IL21 associated with ulcerative colitis

    Genetic variants in the region harbouring IL2/IL21 associated with ulcerative colitis Autor Eleonora A. Festen, Philippe Goyette, Rodney J. Scott, Vito Annese, Alexandra Zhernakova, Jingyao Lian, Christine Lefebvre, Steven R. Brant, J H Cho, Mark S. Silverberg, Kent D. Taylor, Dirk J. de Jong, P.C.F. Stokkers, Dermot McGovern, Orazio Palmieri, J-P Achkar, Ramnik J. Xavier, Mark Daly, Richard H. Duerr, Cisca Wijmenga, Rinse K. Weersma, John D. Rioux

    Vydáno 2009
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  9. 9
    High-density mapping of the MHC identifies a shared role for HLA-DRB1*01:03 in inflammatory bowel diseases and heterozygous advantage in ulcerative colitis

    High-density mapping of the MHC identifies a shared role for HLA-DRB1*01:03 in inflammatory bowel diseases and heterozygous advantage in ulcerative colitis Autor Philippe Goyette, Gabrielle Boucher, Dermot Mallon, Eva Ellinghaus, Luke Jostins, Hailiang Huang, Stephan Ripke, Elena S. Gusareva, Vito Annese, Stephen L. Hauser, Jorge R. Oksenberg, Ingo Thomsen, Stephen Leslie, Mark J. Daly, Kristel Van Steen, Richard H. Duerr, Jeffrey C. Barrett, Dermot McGovern, L. Philip Schumm, James A. Traherne, Mary Carrington, Vasilis Kosmoliaptsis, Tom H. Karlsen, André Franke, John D. Rioux

    Vydáno 2015
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  10. 10
    Genome-wide association study identifies new susceptibility loci for Crohn disease and implicates autophagy in disease pathogenesis

    Genome-wide association study identifies new susceptibility loci for Crohn disease and implicates autophagy in disease pathogenesis Autor John D. Rioux, Ramnik J. Xavier, Kent D. Taylor, Mark S. Silverberg, Philippe Goyette, Alan Huett, Todd J. Green, Petric Kuballa, M. Michael Barmada, Lisa W. Datta, Yin Yao Shugart, Anne M. Griffiths, Stephan R. Targan, Andrew Ippoliti, Edmond-Jean Bernard, Ling Mei, Dan L. Nicolae, Miguel Regueiro, L. Philip Schumm, A. Hillary Steinhart, Jerome I. Rotter, Richard H. Duerr, Judy H. Cho, Mark J. Daly, Steven R. Brant

    Vydáno 2007
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  11. 11
    <i><scp>TECRL</scp></i>, a new life‐threatening inherited arrhythmia gene associated with overlapping clinical features of both <scp>LQTS</scp> and <scp>CPVT</scp>

    <i><scp>TECRL</scp></i>, a new life‐threatening inherited arrhythmia gene associated with overlapping clinical features of both <scp>LQTS</scp> and <scp>CPVT</scp> Autor Harsha D. Devalla, Roselle Gélinas, Elhadi H. Aburawi, Abdelaziz Beqqali, Philippe Goyette, Christian Freund, Marie Chaix, Rafik Tadros, Hui Jiang, Antony Le Béchec, Jantine Monshouwer‐Kloots, Tom Zwetsloot, Georgios Kosmidis, Frédéric Latour, Azadeh Alikashani, Maaike Hoekstra, Jürg Schlaepfer, Christine L. Mummery, Brian J. Stevenson, Zoltán Kutalik, Antoine AF de Vries, Léna Rivard, Arthur AM Wilde, Mario Talajic, Arie O. Verkerk, Lihadh Al‐Gazali, John D. Rioux, Zahurul A. Bhuiyan, Robert Passier

    Vydáno 2016
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  12. 12
    Mapping of multiple susceptibility variants within the MHC region for 7 immune-mediated diseases

    Mapping of multiple susceptibility variants within the MHC region for 7 immune-mediated diseases Autor John D. Rioux, Philippe Goyette, Timothy J. Vyse, Lennart Hammarström, Michelle M. A. Fernando, Todd J. Green, Philip L. De Jager, Sylvain Foisy, Joanne Wang, Paul I. W. de Bakker, Stephen J Leslie, Gil McVean, Leonid Padyukov, Lars Alfredsson, Vito Annese, David A. Hafler, Qiang Pan‐Hammarström, Ritva Matell, Stephen Sawcer, Alastair Compston, Bruce Cree, Daniel B. Mirel, Mark J. Daly, Tim Behrens, Lars Klareskog, Peter K. Gregersen, Jorge R. Oksenberg, Stephen L. Hauser

    Vydáno 2009
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  13. 13
    Deep Resequencing of GWAS Loci Identifies Rare Variants in CARD9, IL23R and RNF186 That Are Associated with Ulcerative Colitis

    Deep Resequencing of GWAS Loci Identifies Rare Variants in CARD9, IL23R and RNF186 That Are Associated with Ulcerative Colitis Autor Mélissa Beaudoin, Philippe Goyette, Gabrielle Boucher, Ken Sin Lo, Manuel A. Rivas, Christine Stevens, Azadeh Alikashani, Martin Ladouceur, David Ellinghaus, Leif Törkvist, Gautam Goel, Caroline Lagacé, Vito Annese, Alain Bitton, Jakob Begun, Steven R. Brant, Francesca Bresso, Judy H. Cho, Richard H. Duerr, Jonas Halfvarson, Dermot McGovern, Graham Radford‐Smith, Stefan Schreiber, L. Philip Schumm, Yashoda Sharma, Mark S. Silverberg, Rinse K. Weersma, Mauro D’Amato, Séverine Vermeire, André Franke, Guillaume Lettre, Ramnik J. Xavier, Mark J. Daly, John D. Rioux

    Vydáno 2013
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  14. 14
    Ulcerative colitis–risk loci on chromosomes 1p36 and 12q15 found by genome-wide association study

    Ulcerative colitis–risk loci on chromosomes 1p36 and 12q15 found by genome-wide association study Autor Mark S. Silverberg, Judy H. Cho, John D. Rioux, Dermot McGovern, Jing Qin Wu, Vito Annese, Jean Paul Achkar, Philippe Goyette, Regan Scott, Wei Xu, M. Michael Barmada, Lambertus Klei, Mark J. Daly, Clara Abraham, Theodore M. Bayless, Fabrizio Bossa, Anne M. Griffiths, Andrew Ippoliti, Raymond Lahaie, Anna Latiano, Pierre Paré, Deborah D. Proctor, Miguel Regueiro, A. Hillary Steinhart, Stephan R. Targan, L. Philip Schumm, Emily O. Kistner, Annette T. Lee, Peter K. Gregersen, Jerome I. Rotter, Steven R. Brant, Kent D. Taylor, Kathryn Roeder, Richard H. Duerr

    Vydáno 2009
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  15. 15
    Deep resequencing of GWAS loci identifies independent rare variants associated with inflammatory bowel disease

    Deep resequencing of GWAS loci identifies independent rare variants associated with inflammatory bowel disease Autor Manuel A. Rivas, Mélissa Beaudoin, Agnès Gardet, Christine Stevens, Yashoda Sharma, Hu Zhang, Gabrielle Boucher, Stephan Ripke, David Ellinghaus, Noël P. Burtt, Tim Fennell, Andrew Kirby, Anna Latiano, Philippe Goyette, Todd J. Green, Jonas Halfvarson, Talin Haritunians, Joshua M. Korn, Finny G. Kuruvilla, Caroline Lagacé, Benjamin M. Neale, Ken Sin Lo, L. Philip Schumm, Leif Törkvist, Marla C. Dubinsky, Steven R. Brant, Mark S. Silverberg, Richard H. Duerr, David Altshuler, Stacey Gabriel, Guillaume Lettre, André Franke, Mauro D’Amato, Dermot McGovern, Judy H. Cho, John D. Rioux, Ramnik J. Xavier, Mark J. Daly

    Vydáno 2011
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  16. 16
    Inherited determinants of Crohn's disease and ulcerative colitis phenotypes: a genetic association study

    Inherited determinants of Crohn's disease and ulcerative colitis phenotypes: a genetic association study Autor Isabelle Cleynen, Gabrielle Boucher, Luke Jostins, L. Philip Schumm, Sebastian Zeißig, Tariq Ahmad, Vibeke Andersen, Jane M. Andrews, Vito Annese, Stephan Brand, Steven R. Brant, Judy H. Cho, Mark J. Daly, Marla C. Dubinsky, Richard H. Duerr, Lynnette R. Ferguson, André Franke, Richard B. Gearry, Philippe Goyette, Hákon Hákonarson, Jonas Halfvarson, Johannes R. Hov, H Huang, Nicholas A. Kennedy, Limas Kupčinskas, Ian C. Lawrance, James Lee, Jack Satsangi, S Schreiber, Emilie Théâtre, Andrea E. van der Meulen–de Jong, Rinse K. Weersma, David C. Wilson, Miles Parkes, Séverine Vermeire, John D. Rioux, John Mansfield, Mark S. Silverberg, Graham Radford‐Smith, Dermot McGovern, Jeffrey C. Barrett, Charlie W. Lees

    Vydáno 2015
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  17. 17
    Fine-mapping inflammatory bowel disease loci to single-variant resolution

    Fine-mapping inflammatory bowel disease loci to single-variant resolution Autor Hailiang Huang, Ming Fang, Luke Jostins, Maša Umićević Mirkov, Gabrielle Boucher, Carl A. Anderson, Vibeke Andersen, Isabelle Cleynen, Adrián Cortés, François Crins, Mauro D’Amato, Valérie Deffontaine, Julia Dmitrieva, Elisa Docampo, Mahmoud Elansary, Kyle Kai‐How Farh, André Franke, Ann-Stephan Gori, Philippe Goyette, Jonas Halfvarson, Talin Haritunians, Jo Knight, Ian C. Lawrance, Charlie W. Lees, Édouard Louis, Rob Mariman, T.H.E. Meuwissen, Myriam Mni, Yukihide Momozawa, Miles Parkes, Sarah L. Spain, Emilie Théâtre, Gosia Trynka, Jack Satsangi, Suzanne van Sommeren, Séverine Vermeire, Ramnik J. Xavier, Rinse K. Weersma, Richard H. Duerr, Christopher G. Mathew, John D. Rioux, Dermot McGovern, Judy H. Cho, Michel Georges, Mark J. Daly, Jeffrey C. Barrett

    Vydáno 2017
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  18. 18
    Genome-wide association identifies multiple ulcerative colitis susceptibility loci

    Genome-wide association identifies multiple ulcerative colitis susceptibility loci Autor Dermot McGovern, Agnès Gardet, Leif Törkvist, Philippe Goyette, Jonah Essers, Kent D. Taylor, Benjamin M. Neale, Rick Twee‐Hee Ong, Caroline Lagacé, Chun Li, Todd J. Green, Christine Stevens, Claudine Beauchamp, Phillip Fleshner, Marie Carlson, Mauro D’Amato, Jonas Halfvarson, Martin L. Hibberd, Mikael Lördal, Leonid Padyukov, Angelo Andriulli, Elisabetta Colombo, Anna Latiano, Orazio Palmieri, Edmond-Jean Bernard, Colette Deslandres, Daan W. Hommes, Dirk J. de Jong, Pieter Stokkers, Rinse K. Weersma, Yashoda Sharma, Mark S. Silverberg, Judy H. Cho, Jing Qin Wu, Kathryn Roeder, Steven R. Brant, L. Philip Schumm, Richard H. Duerr, Marla C. Dubinsky, Nicole L. Glazer, Talin Haritunians, Andy Ippoliti, Gil Melmed, David S. Siscovick, Eric A. Vasiliauskas, Stephan R. Targan, Vito Annese, Cisca Wijmenga, Sven Pettersson, Jerome I. Rotter, Ramnik J. Xavier, Mark J. Daly, John D. Rioux, Mark Seielstad

    Vydáno 2010
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  19. 19
    Identification of a Sudden Cardiac Death Susceptibility Locus at 2q24.2 through Genome-Wide Association in European Ancestry Individuals

    Identification of a Sudden Cardiac Death Susceptibility Locus at 2q24.2 through Genome-Wide Association in European Ancestry Individuals Autor Dan E. Arking, Juhani Junttila, Philippe Goyette, Adriana Huertas‐Vázquez, Mark Eijgelsheim, Marieke T. Blom, Christopher Newton‐Cheh, Kyndaron Reinier, Carmen Teodorescu, Audrey Uy‐Evanado, Naima Carter‐Monroe, Kari Kaikkonen, Marja‐Leena Kortelainen, Gabrielle Boucher, Caroline Lagacé, Anna Moes, Xiaoqing Zhao, Frank D. Kolodgie, Fernando Rivadeneira, Albert Hofman, Jacqueline C.M. Witteman, André G. Uitterlinden, Roos F. Marsman, Raha Pazoki, Abdennasser Bardai, Rudolph W. Koster, Abbas Dehghan, Shih‐Jen Hwang, Pallav Bhatnagar, Wendy S. Post, Gina M. Hilton, Ronald J. Prineas, Man Li, Anna Köttgen, Georg Ehret, Eric Boerwinkle, Josef Coresh, W.H. Linda Kao, Bruce M. Psaty, Gordon F. Tomaselli, Nona Sotoodehnia, David S. Siscovick, Greg Burke, Eduardo Marbán, Peter M. Spooner, L. Adrienne Cupples, Jonathan Jui, Karen Gunson, Y. Antero Kesäniemi, Arthur A.M. Wilde, Jean‐Claude Tardif, Christopher J. O’Donnell, Connie R. Bezzina, Renu Virmani, Bruno H. Stricker, Hanno L. Tan, Christine M. Albert, Aravinda Chakravarti, John D. Rioux, Heikki V. Huikuri, Sumeet S. Chugh

    Vydáno 2011
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  20. 20
    A comprehensive evaluation of the genetic architecture of sudden cardiac arrest

    A comprehensive evaluation of the genetic architecture of sudden cardiac arrest Autor Foram N. Ashar, Rebecca Mitchell, Christine M. Albert, Christopher Newton‐Cheh, Jennifer A. Brody, Martina Müller‐Nurasyid, Anna Moes, Thomas Meitinger, Angel C. Y. Mak, Heikki V. Huikuri, Juhani Junttila, Philippe Goyette, Sara L. Pulit, Raha Pazoki, Michael W.T. Tanck, Marieke T. Blom, Xiaoqing Zhao, Aki S. Havulinna, Reza Jabbari, Charlotte Glinge, Vinicius Tragante, Stefan Andersson Escher, Aravinda Chakravarti, Georg Ehret, Josef Coresh, Man Li, Ronald J. Prineas, Oscar H. Franco, Pui‐Yan Kwok, Thomas Lumley, Florence Dumas, Barbara McKnight, Jerome I. Rotter, Rozenn N. Lemaître, Susan R. Heckbert, Christopher J. O’Donnell, Shih‐Jen Hwang, Jean‐Claude Tardif, Martin VanDenburgh, André G. Uitterlinden, Albert Hofman, Bruno H. Stricker, Paul I. W. de Bakker, Paul W. Franks, Jan‐Håkan Jansson, Folkert W. Asselbergs, Marc K. Halushka, Joseph J. Maleszewski, Jacob Tfelt‐Hansen, Thomas Engstrøm, Veikko Salomaa, Renu Virmani, Frank D. Kolodgie, Arthur A.M. Wilde, Hanno L. Tan, Connie R. Bezzina, Mark Eijgelsheim, John D. Rioux, Xavier Jouven, Stefan Kääb, Bruce M. Psaty, David S. Siscovick, Dan E. Arking, Nona Sotoodehnia

    Vydáno 2018
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