Sökresultat - Simon Girard

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  1. 1
    An anticlastogenic function for the Polycomb Group gene Bmi1

    An anticlastogenic function for the Polycomb Group gene Bmi1 av Jalila Chagraoui, Josée Hébert, Simon Girard, Guy Sauvageau

    Publicerad 2011
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  2. 2
    Human copy number variants are enriched in regions of low mappability

    Human copy number variants are enriched in regions of low mappability av Jean Monlong, Patrick Cossette, Caroline Meloche, Guy A. Rouleau, Simon Girard, Guillaume Bourque

    Publicerad 2018
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  3. 3
    RNA-seq analysis of 2 closely related leukemia clones that differ in their self-renewal capacity

    RNA-seq analysis of 2 closely related leukemia clones that differ in their self-renewal capacity av Brian T. Wilhelm, Mathieu Briau, Pamela Austin, Amélie Faubert, Geneviève Boucher, Pierre Chagnon, Kristin J. Hope, Simon Girard, Nadine Mayotte, Josette‐Renée Landry, Josée Hébert, Guy Sauvageau

    Publicerad 2010
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  4. 4
    Restless legs syndrome‐associated <i>MEIS1</i> risk variant influences iron homeostasis

    Restless legs syndrome‐associated <i>MEIS1</i> risk variant influences iron homeostasis av Hélène Catoire, Patrick A. Dion, Lan Xiong, Mourabit Amari, Rébecca Gaudet, Simon Girard, Anne Noreau, Cláudia Gaspar, Gustavo Turecki, Jacques Montplaisir, J. Alex Parker, Guy A. Rouleau

    Publicerad 2011
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  5. 5
    UM171 Preserves Epigenetic Marks that Are Reduced in Ex Vivo Culture of Human HSCs via Potentiation of the CLR3-KBTBD4 Complex

    UM171 Preserves Epigenetic Marks that Are Reduced in Ex Vivo Culture of Human HSCs via Potentiation of the CLR3-KBTBD4 Complex av Jalila Chagraoui, Simon Girard, Jean-François Spinella, Laura Simon, Éric Bonneil, Nadine Mayotte, Tara MacRae, Jasmin Coulombe‐Huntington, Thierry Bertomeu, Céline Moison, Elisa Tomellini, Pierre Thibault, Mike Tyers, Anne Marinier, Guy Sauvageau

    Publicerad 2021
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  6. 6
    De novo variants in sporadic cases of childhood onset schizophrenia

    De novo variants in sporadic cases of childhood onset schizophrenia av Amirthagowri Ambalavanan, Simon Girard, Kwangmi Ahn, Sirui Zhou, Alexandre Dionne‐Laporte, Dan Spiegelman, Cynthia V. Bourassa, Julie Gauthier, Fadi F. Hamdan, Lan Xiong, Patrick A. Dion, Ridha Joober, Judith L. Rapoport, Guy A. Rouleau

    Publicerad 2015
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  7. 7
    Paternal Age Explains a Major Portion of De Novo Germline Mutation Rate Variability in Healthy Individuals

    Paternal Age Explains a Major Portion of De Novo Germline Mutation Rate Variability in Healthy Individuals av Simon Girard, Cynthia V. Bourassa, Louis‐Philippe Lemieux Perreault, Marc‐André Legault, Amina Barhdadi, Amirthagowri Ambalavanan, Mara Brendgen, Frank Vitaro, Anne Noreau, Ginette Dionne, Richard E. Tremblay, Patrick A. Dion, Michel Boivin, Marie‐Pierre Dubé, Guy A. Rouleau

    Publicerad 2016
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  8. 8
    Global characterization of copy number variants in epilepsy patients from whole genome sequencing

    Global characterization of copy number variants in epilepsy patients from whole genome sequencing av Jean Monlong, Simon Girard, Caroline Meloche, Maxime Cadieux‐Dion, Danielle M. Andrade, Ron G. Lafrenière, Micheline Gravel, Dan Spiegelman, Alexandre Dionne‐Laporte, Cyrus Boelman, Fadi F. Hamdan, Jacques L. Michaud, Guy A. Rouleau, Berge A. Minassian, Guillaume Bourque, Patrick Cossette

    Publicerad 2018
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  9. 9
    MEIS1 intronic risk haplotype associated with restless legs syndrome affects its mRNA and protein expression levels

    MEIS1 intronic risk haplotype associated with restless legs syndrome affects its mRNA and protein expression levels av Lan Xiong, Hélène Catoire, Patrick A. Dion, Cláudia Gaspar, Ronald G. Lafrenière, Simon Girard, Аnastasia Levchenko, Jean‐Baptiste Rivière, Laura M. Fiori, Judith St‐Onge, Isabelle Bachand, Pascale Thibodeau, Richard P. Allen, Christopher J. Earley, Gustavo Turecki, Jacques Montplaisir, Guy A. Rouleau

    Publicerad 2009
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  10. 10
    <i>SF3B1</i> mutations provide genetic vulnerability to copper ionophores in human acute myeloid leukemia

    <i>SF3B1</i> mutations provide genetic vulnerability to copper ionophores in human acute myeloid leukemia av Céline Moison, Deanne Gracias, Julie Schmitt, Simon Girard, Jean-François Spinella, Simon Fortier, Isabel Boivin, Rodrigo Mendoza‐Sanchez, Bounkham Thavonekham, Tara MacRae, Nadine Mayotte, Éric Bonneil, Mark D. Wittman, James Carmichael, Réjean Ruel, Pierre Thibault, Josée Hébert, Anne Marinier, Guy Sauvageau

    Publicerad 2024
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  11. 11
    Deleterious mutations in the essential mRNA metabolism factor, hGle1, in amyotrophic lateral sclerosis

    Deleterious mutations in the essential mRNA metabolism factor, hGle1, in amyotrophic lateral sclerosis av Hannah Kaneb, Andrew W. Folkmann, Véronique Belzil, Li-En Jao, Claire S. Leblond, Simon Girard, Hussein Daoud, Anne Noreau, Daniel Rochefort, Pascale Hince, Anna Szuto, Annie Levert, Sabrina Vidal, Catherine André-Guimont, William Camu, Jean-Pierre Bouchard, Nicolas Dupré, Guy A. Rouleau, Susan R. Wente, Patrick A. Dion

    Publicerad 2014
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  12. 12
    Whole-Exome Sequencing Reveals a Rapid Change in the Frequency of Rare Functional Variants in a Founding Population of Humans

    Whole-Exome Sequencing Reveals a Rapid Change in the Frequency of Rare Functional Variants in a Founding Population of Humans av Ferrán Casals, Alan Hodgkinson, Julie Hussin, Youssef Idaghdour, Vanessa Bruat, Thibault de Maillard, Jean‐Christophe Grenier, Elias Gbeha, Fadi F. Hamdan, Simon Girard, Jean-François Spinella, Mathieu Larivière, Virginie Saillour, Jasmine Healy, Isabel Fernández, Daniel Sinnett, Jacques L. Michaud, Guy A. Rouleau, Élie Haddad, Françoise Le Deist, Philip Awadalla

    Publicerad 2013
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  13. 13
    Exome Sequencing Identifies FUS Mutations as a Cause of Essential Tremor

    Exome Sequencing Identifies FUS Mutations as a Cause of Essential Tremor av Nancy D. Merner, Simon Girard, Hélène Catoire, Cynthia V. Bourassa, Véronique Belzil, Jean‐Baptiste Rivière, Pascale Hince, Annie Levert, Alexandre Dionne‐Laporte, Dan Spiegelman, Anne Noreau, Sabrina Diab, Anna Szuto, Hélène Fournier, John Raelson, Majid Belouchi, Michel Panisset, Patrick Cossette, Nicolas Dupré, Geneviève Bernard, Sylvain Chouinard, Patrick A. Dion, Guy A. Rouleau

    Publicerad 2012
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  14. 14
    Functional variants of POC5 identified in patients with idiopathic scoliosis

    Functional variants of POC5 identified in patients with idiopathic scoliosis av Scott B. Patten, Patricia Margaritte‐Jeannin, Jean‐Claude Bernard, Eudéline Alix, Audrey Labalme, Alicia Besson, Simon Girard, Khaled Fendri, Nicolas Fraisse, Bernard Biot, C. Poizat, Amandine Campan-Fournier, Kariman Abelin-Genevois, V. Cunin, Charlotte Zaouter, Meijiang Liao, Raphaelle Lamy, Gaëtan Lesca, Rita Menassa, Charles Marcaillou, Mélanie Letexier, Damien Sanlaville, J. Bérard, Guy A. Rouleau, Françoise Clerget‐Darpoux, Pierre Drapeau, Florina Moldovan, Patrick Edery

    Publicerad 2015
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  15. 15
    The role of common genetic variation in presumed monogenic epilepsies

    The role of common genetic variation in presumed monogenic epilepsies av Ciarán Campbell, Costin Leu, Yen‐Chen Anne Feng, Stefan Wolking, Claudia Moreau, Colin A. Ellis, Shiva Ganesan, Helena Martins, Karen Oliver, Isabelle Boothman, Katherine A. Benson, Anne M. Molloy, Lawrence C. Brody, Jacques L. Michaud, Fadi F. Hamdan, Berge A. Minassian, Holger Lerche, Ingrid E. Scheffer, Sanjay M. Sisodiya, Simon Girard, Patrick Cosette, Norman Delanty, Dennis Lal, Gianpiero L. Cavalleri

    Publicerad 2022
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  16. 16
    Mubritinib Targets the Electron Transport Chain Complex I and Reveals the Landscape of OXPHOS Dependency in Acute Myeloid Leukemia

    Mubritinib Targets the Electron Transport Chain Complex I and Reveals the Landscape of OXPHOS Dependency in Acute Myeloid Leukemia av Irène Baccelli, Yves Gareau, Bernhard Lehnertz, Stéphane Gingras, Jean-François Spinella, Sophie Corneau, Nadine Mayotte, Simon Girard, Mélanie Fréchette, Valérie Blouin-Chagnon, Koryne Leveillé, Isabel Boivin, Tara MacRae, Jana Krošl, Clarisse Thiollier, Vincent‐Philippe Lavallée, Evgeny Kanshin, Thierry Bertomeu, Jasmin Coulombe‐Huntington, Corinne St‐Denis, Marie-Ève Bordeleau, Geneviève Boucher, Philippe P. Roux, Sébastien Lemieux, Mike Tyers, Pierre Thibault, Josée Hébert, Anne Marinier, Guy Sauvageau

    Publicerad 2019
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  17. 17
    Genome-wide association study in essential tremor identifies three new loci

    Genome-wide association study in essential tremor identifies three new loci av Stefanie H. Müller, Simon Girard, Franziska Hopfner, Nancy D. Merner, Cynthia V. Bourassa, Delia Lorenz, Lorraine N. Clark, Lukas Tittmann, Alexandra I. Soto‐Ortolaza, Stephan Klebe, Mark Hallett, Susanne A. Schneider, Colin A. Hodgkinson, Wolfgang Lieb, Zbigniew K. Wszołek, Manuela Pendziwiat, Oswaldo Lorenzo‐Betancor, Werner Poewe, Sara Ortega‐Cubero, Klaus Seppi, Alex Rajput, Anna Hussl, Ali H. Rajput, Daniela Berg, Patrick A. Dion, Isabel Wurster, Joshua Shulman, Karin Srulijes, Dietrich Haubenberger, Pau Pástor, Carles Vilariño‐Güell, Ronald B. Postuma, Geneviève Bernard, Karl‐Heinz Ladwig, Nicolas Dupré, Joseph Jankovic, Konstantin Strauch, Michel Panisset, Juliane Winkelmann, Claudia Testa, Eva Reischl, Kirsten E. Zeuner, Owen A. Ross, Thomas Arzberger, Sylvain Chouinard, Günther Deuschl, Elan D. Louis, Gregor Kuhlenbäumer, Guy A. Rouleau

    Publicerad 2016
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  18. 18
    Association of Essential Tremor With Novel Risk Loci

    Association of Essential Tremor With Novel Risk Loci av Calwing Liao, Charles-Etienne Castonguay, Karl Heilbron, Veikko Vuokila, Miranda Medeiros, Gabrielle Houle, Fulya Akçimen, Jay P. Ross, Hélène Catoire, Mónica Díez-Fairén, Jooeun Kang, Stefanie H. Mueller, Simon Girard, Franziska Hopfner, Delia Lorenz, Lorraine N. Clark, Alexandra I. Soto‐Beasley, Stephan Klebe, Mark Hallett, Zbigniew K. Wszołek, Manuela Pendziwiat, Oswaldo Lorenzo‐Betancor, Klaus Seppi, Daniela Berg, Carles Vilariño‐Güell, Ronald B. Postuma, Geneviève Bernard, Nicolas Dupré, Joseph Jankovic, Claudia M. Testa, Owen A. Ross, Thomas Arzberger, Sylvain Chouinard, Elan D. Louis, Paola Mandich, Carmine Vitale, Paolo Barone, Elena García‐Martín, Hortensia Alonso‐Navarro, José A. G. Agúndez, Félix Javier Jiménez‐Jiménez, Pau Pástor, Alex Rajput, Günther Deuschl, Gregor Kuhlenbäumer, Inge A. Meijer, Patrick A. Dion, Guy A. Rouleau

    Publicerad 2022
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  19. 19
    Rare coding variants in genes encoding GABAA receptors in genetic generalised epilepsies: an exome-based case-control study

    Rare coding variants in genes encoding GABAA receptors in genetic generalised epilepsies: an exome-based case-control study av Patrick May, Simon Girard, Merle Harrer, Dheeraj Reddy Bobbili, Julian Schubert, Stefan Wolking, Felicitas Becker, Pamela Lachance‐Touchette, Caroline Meloche, Micheline Gravel, Cristina Elena Niturad, Julia Knaus, Carolien G. F. de Kovel, Mohamad Toliat, Anne Polvi, Michele Iacomino, Rosa Guerrero, Stéphanie Baulac, Carla Marini, Holger Thiele, Janine Altmüller, Kamel Jabbari, Ann‐Kathrin Ruppert, Wiktor Jurkowski, Dennis Lal, Raffaella Rusconi, Sandrine Cestèle, Benedetta Terragni, Ian D. Coombs, Christopher A. Reid, Pasquale Striano, Hande Çağlayan, Auli Sirén, Kate V. Everett, Rikke S. Møller, Helle Hjalgrim, Hiltrud Muhle, Ingo Helbig, Wolfram S. Kunz, Yvonne G. Weber, Sarah Weckhuysen, Peter De Jonghe, Sanjay M. Sisodiya, Rima Nabbout, Silvana Franceschetti, Antonietta Coppola, Maria Stella Vari, Dorothee Kasteleijn‐Nolst Trenité, Betül Baykan, Uğur Özbek, Nerses Bebek, Karl Martin Klein, Felix Rosenow, Dang Khoa Nguyen, François Dubeau, Lionel Carmant, Anne Lortie, Richard Desbiens, Jean-François Clément, Cécile Cieuta‐Walti, Graeme J. Sills, Pauls Auce, Ben Francis, Michael R. Johnson, Anthony G Marson, Bianca Berghuis, Josemir W. Sander, Andreja Avberšek, Mark McCormack, Gianpiero L. Cavalleri, Norman Delanty, Chantal Depondt, Martin Krenn, Fritz Zimprich, Sarah Peter, Marina Nikanorova, Robert Kraaij, Jeroen van Rooij, Rudi Balling, M. Arfan Ikram, André G. Uitterlinden, G. Avanzini, Stéphanie Schorge, Steven Petrou, Massimo Mantegazza, Thomas Sander, Eric LeGuern, José M. Serratosa, Bobby P.C. Koeleman, Aarno Palotie, Anna‐Elina Lehesjoki, Michael Nothnagel, Peter Nürnberg, Snezana Maljevic, Federico Zara, Patrick Cossette, Roland Krause, Holger Lerche, Patrick May, Simon Girard

    Publicerad 2018
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  20. 20
    Cross-Disorder Genome-Wide Analyses Suggest a Complex Genetic Relationship Between Tourette’s Syndrome and OCD

    Cross-Disorder Genome-Wide Analyses Suggest a Complex Genetic Relationship Between Tourette’s Syndrome and OCD av Dongmei Yu, Carol A. Mathews, Jeremiah M. Scharf, Benjamin M. Neale, Lea K. Davis, Eric R. Gamazon, Eske M. Derks, Patrick Evans, Christopher K. Edlund, Jacquelyn Crane, Jesen Fagerness, Lisa Osiecki, Patience Gallagher, Gloria F. Gerber, Stephen A. Haddad, Cornelia Illmann, Lauren M. McGrath, C Mayerfeld, Sampath Arepalli, Cristina Barlassina, Cathy L. Barr, Laura Bellodi, Fortu Benarroch, Gabriel Bedoya Berrío, O. Joseph Bienvenu, Donald W. Black, Michael H. Bloch, Helena Brentani, Ruth D. Bruun, Cathy L. Budman, Beatríz Camarena, Desmond Campbell, Carolina Cappi, Julio César Cardona Silgado, Maria Cristina Cavallini, Denise A. Chavira, Sylvain Chouinard, Edwin H. Cook, Mark Cookson, Vladimir Coric, Bernadette Cullen, Daniele Cusi, Richard Delorme, Damiaan Denys, Yves Dion, Valsamma Eapen, Karin Egberts, Peter Falkai, Thomas Fernandez, Eduardo Fournier, Helena Garrido, Daniel Geller, Donald L. Gilbert, Simon Girard, Hans J. Grabe, Marco A. Grados, Benjamin D. Greenberg, Varda Gross‐Tsur, Edna Grünblatt, John Hardy, Gary A. Heiman, Sian Hemmings, Luis Diego Herrera, Dianne M. Hezel, Pieter J. Hoekstra, Joseph Jankovic, James L. Kennedy, Robert A. King, Anuar Konkashbaev, Bárbara Kremeyer, Roger Kurlan, Nuria Lanzagorta, Marion Leboyer, James F. Leckman, Leonhard Lennertz, Chunyu Liu, Christine Löchner, Thomas L. Lowe, Sara Lupoli, Fabìo Macciardi, Wolfgang Maier, Paolo Manunta, Maurizio Marconi, James T. McCracken, Sandra Catalina Mesa Restrepo, Rainald Moessner, Priya Moorjani, Jubel Morgan, Heike Müller, Dennis L. Murphy, Allan L. Naarden, Erika L. Nurmi, William Cornejo Ochoa, Roel A. Ophoff, A.J. Pakstis, Michele T. Pato, Carlos N. Pato, John Piacentini, Christopher Pittenger, Yehuda Pollak

    Publicerad 2014
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