Alexandre Montpetit
2003–2025 年に発表
- 48
- 論文数
- 23,329
- 被引用数
- 47
- h 指数
- 47
- i10 指数
被引用数
引用元
国・地域
機関
- Harvard University1.2%
- Broad Institute0.7%
- Massachusetts General Hospital0.7%
- Inserm0.6%
- Heidelberg University0.6%
- University of Oxford0.6%
- その他95.6%
分野
- Biochemistry, Genetics and Molecular Biology51.8%
- Medicine35.4%
- Immunology and Microbiology3.8%
- Neuroscience2.9%
- Nursing2.4%
- Computer Science1%
- その他2.7%
トピック
- Genetic Associations and Epidemiology7.5%
- Glioma Diagnosis and Treatment4.4%
- Epigenetics and DNA Methylation4.1%
- Genomics and Rare Diseases2.3%
- RNA modifications and cancer2.1%
- Genomics and Chromatin Dynamics2%
- その他77.6%
共著者
- Thomas J. Hudson15
- Steffen Albrecht7
- László Bognár6
- Miklós Garami6
- Péter Hauser6
- Damien Faury5
- Dong-Anh Khuong-Quang5
- Jacek Majewski5
- Jeremy Schwartzentruber5
- Nada Jabado5
- A. Dessa Sadovnick4
- Adam M. Fontebasso4
- Constantin Polychronakos4
- Cynthia Hawkins4
- David A. Dyment4
- George C. Ebers4
- James C. Engert4
- Louis Létourneau4
- Pierre Lepage4
- Vincent Ferretti4
- Álmos Klekner4
- Alexandre Bélisle3
- Andrey Korshunov3
- Catherine Laprise3
全論文
- Driver mutations in histone H3.3 and chromatin remodelling genes in paediatric glioblastoma
著者: Jeremy Schwartzentruber, Andrey Korshunov, Xiao-Yang Liu, David Jones, Elke Pfaff, Karine Jacob, Dominik Sturm, Adam M. Fontebasso, Dong-Anh Khuong Quang, Martje Tönjes, Volker Hovestadt, Steffen Albrecht, Marcel Kool, André Nantel, Carolin Konermann, Anders M. Lindroth, Natalie Jäger, Tobias Rausch, Marina Ryzhova, Jan O. Korbel, Thomas Hielscher, Péter Hauser, Miklós Garami, Álmos Klekner, László Bognár, Martin Ebinger, Martin U. Schuhmann, Wolfram Scheurlen, Arnulf Pekrun, Michael C. Frühwald, Wolfgang Roggendorf, Christoph Kramm, Matthias Dürken, Jeffrey Atkinson, Pierre Lepage, Alexandre Montpetit, Magdalena Zakrzewska, Krzysztof Zakrzewski, Paweł P. Liberski, Zhifeng Dong, Peter M. Siegel, Andreas E. Kulozik, Marc Zapatka, Abhijit Guha, David Malkin, Jörg Felsberg, Guido Reifenberger, Andreas von Deimling, Koichi Ichimura, V. Peter Collins, Hendrik Witt, Till Milde, Olaf Witt, Cindy Zhang, Pedro Castelo‐Branco, Peter Lichter, Damien Faury, Uri Tabori, Christoph Plass, Jacek Majewski, Stefan M. Pfister, Nada Jabado - Nature 2012 被引用: 2,711
- The International HapMap Project
著者: Richard A. Gibbs, John W. Belmont, Paul Hardenbol, T. D. Willis, Fuli Yu, Huanming Yang, Lan-Yang Ch'ang, Wei Huang, Bin Liu, Yan Shen, Paul Kwong Hang Tam, Lap-Chee Tsui, Mary Miu Yee Waye, J. Tze‐Fei Wong, Changqing Zeng, Qingrun Zhang, Illumina, Mark S. Chee, Luana Galver, Semyon Kruglyak, Sarah S. Murray, Arnold Oliphant, Alexandre Montpetit, Thomas J. Hudson, Fanny Chagnon, Vincent Ferretti, Martin Leboeuf, Michael Phillips, Andrei Verner, Pui-Yan Kwok, Shenghui Duan, Denise L. Lind, Raymond D. Miller, John P. Rice, Nancy L. Saccone, Patricia Taillon‐Miller, Ming Xiao, Yusuke Nakamura, Akihiro Sekine, Koki Sorimachi, Toshihiro Tanaka, Yoïchi Tanaka, Tatsuhiko Tsunoda, Eiji Yoshino, David Bentley, Panos Deloukas, Sarah Hunt, Don Powell, David Altshuler, Stacey B. Gabriel, Houcan Zhang, Changqing Zeng, Ichiro Matsuda, Yoshimitsu Fukushima, Darryl Macer, Eiko Suda, Charles N. Rotimi, Clement Adebamowo, Toyin Aniagwu, Patricia A. Marshall, Olayemi Matthew, Chibuzor Nkwodimmah, Charmaine D. M. Royal, Mark Leppert, Missy Dixon, Lincoln D. Stein, Fiona Cunningham, Ardavan Kanani, Guðmundur Á. Þórisson, Aravinda Chakravarti, Peter E. Chen, David J. Cutler, Carl Kashuk, Peter Donnelly, Jonathan Marchini, Gil McVean, Simon Myers, Lon R. Cardon, Gonçalo R. Abecasis, Andrew P. Morris, Bruce S. Weir, James C. Mullikin, Stephen T. Sherry, Michael Feolo, David Altshuler, Mark Daly, Stephen F. Schaffner, Ren-Zong Qiu, Genetic Interest Group, Alastair Kent, Georgia M. Dunston, Kazuto Kato, Norio Niikawa, Bartha Maria Knoppers, Morris W. Foster, Ellen Wright Clayton, Vivian Ota Wang, Wellcome Trust, Jessica Watkin, Richard A. Gibbs ほか 83 名 - Nature 2003 被引用: 6,186
- K27M mutation in histone H3.3 defines clinically and biologically distinct subgroups of pediatric diffuse intrinsic pontine gliomas
著者: Dong-Anh Khuong-Quang, Pawel Buczkowicz, Patricia Rakopoulos, Xiao-Yang Liu, Adam M. Fontebasso, Éric Bouffet, Ute Bartels, Steffen Albrecht, Jeremy Schwartzentruber, Louis Létourneau, Mathieu Bourgey, Guillaume Bourque, Alexandre Montpetit, Geneviève Bourret, Pierre Lepage, Adam Fleming, Peter Lichter, Marcel Kool, Andreas von Deimling, Dominik Sturm, Andrey Korshunov, Damien Faury, David Jones, Jacek Majewski, Stefan M. Pfister, Nada Jabado, Cynthia Hawkins - Acta Neuropathologica 2012 被引用: 1,020
- H3K27M induces defective chromatin spread of PRC2-mediated repressive H3K27me2/me3 and is essential for glioma tumorigenesis
著者: Ashot S. Harutyunyan, Brian Krug, Haifeng Chen, Simon Papillon‐Cavanagh, Michele Zeinieh, Nicolas Jay, Shriya Deshmukh, Carol Chen, Jad I. Belle, Leonie G. Mikael, Dylan M. Marchione, Rui Li, Hamid Nikbakht, Bo Hu, Gaël Cagnone, Warren Cheung, Abdulshakour Mohammadnia, Denise Béchet, Damien Faury, Melissa K. McConechy, Manav Pathania, Siddhant U. Jain, Benjamin Ellezam, Alexander G. Weil, Alexandre Montpetit, Paolo Salomoni, Tomi Pastinen, Chao Lü, Peter W. Lewis, Benjamin A. García, Claudia L. Kleinman, Nada Jabado, Jacek Majewski - Nature Communications 2019 被引用: 392
- A genome-wide association study identifies novel risk loci for type 2 diabetes
著者: Robert Sladek, Ghislain Rocheleau, Johan Rung, Christian Dina, Li Shen, David Serre, Philippe Boutin, Daniel Vincent, Alexandre Bélisle, Samy Hadjadj, Beverley Balkau, Barbara Heude, G. Charpentier, Thomas J. Hudson, Alexandre Montpetit, Alexey V. Pshezhetsky, Marc Prentki, Barry I. Posner, David J. Balding, Stephen Eyre, Constantin Polychronakos, Philippe Froguel - Nature 2007 被引用: 3,015
- Genomic analysis of diffuse intrinsic pontine gliomas identifies three molecular subgroups and recurrent activating ACVR1 mutations
著者: Pawel Buczkowicz, Christine M. Hoeman, Patricia Rakopoulos, Sanja Pajovic, Louis Létourneau, Misko Dzamba, Andrew Morrison, Peter W. Lewis, Éric Bouffet, Ute Bartels, Jennifer Zuccaro, Sameer Agnihotri, Scott Ryall, Mark Barszczyk, Yevgen Chornenkyy, Mathieu Bourgey, Guillaume Bourque, Alexandre Montpetit, Francisco J. Cordero, Pedro Castelo‐Branco, Joshua Mangerel, Uri Tabori, King Ching Ho, Annie Huang, Kathryn R. Taylor, Alan Mackay, Anne Bendel, Javad Nazarian, Jason Fangusaro, Matthias A. Karajannis, David Zagzag, Nicholas K. Foreman, Andrew M. Donson, Julia Hegert, Amy Smith, Jennifer A. Chan, Lucy Lafay-Cousin, Sandra E. Dunn, Juliette Hukin, Christopher Dunham, Katrin Scheinemann, Jean Michaud, Shayna Zelcer, David A. Ramsay, Jason E. Cain, Cameron Brennan, Mark M. Souweidane, Chris Jones, C. David Allis, Michael Brudno, Oren J. Becher, Cynthia Hawkins - Nature Genetics 2014 被引用: 654
- Integrated (epi)-Genomic Analyses Identify Subgroup-Specific Therapeutic Targets in CNS Rhabdoid Tumors
著者: Jonathon Torchia, Brian Golbourn, Shengrui Feng, King Ching Ho, Patrick Sin‐Chan, Alexandre Vasiljevic, Joseph Norman, Paul Guilhamon, Livia Garzia, Natalia R. Agamez, Mei Lu, Tiffany Sin Yu Chan, Daniel Picard, Pasqualino De Antonellis, Dong-Anh Khuong-Quang, Aline Cristiane Planello, Constanze Zeller, Dalia Baršytė-Lovejoy, Lucie Lafay‐Cousin, Louis Létourneau, Mathieu Bourgey, Man Yu, Deena M.A. Gendoo, Misko Dzamba, Mark Barszczyk, Tiago da Silva Medina, Alexandra N. Riemenschneider, A. Sorana Morrissy, Young‐Shin Ra, Vijay Ramaswamy, Marc Remke, Christopher Dunham, Stephen Yip, Ho‐Keung Ng, Jian‐Qiang Lu, Vivek Mehta, Steffen Albrecht, José Pimentel, Jennifer A. Chan, Gino R. Somers, Cláudia C. Faria, Lúcia Roque, Maryam Fouladi, Lindsey M. Hoffman, Andrew S. Moore, Yin Wang, Seung Ah Choi, Jordan R. Hansford, Daniel Catchpoole, Diane K. Birks, Nicholas K. Foreman, Doug Strother, Álmos Klekner, László Bognár, Miklós Garami, Péter Hauser, Tibor Hortobágyi, Beverly Wilson, Juliette Hukin, Anne‐Sophie Carret, Timothy Van Meter, Eugene Hwang, Amar Gajjar, Shih‐Hwa Chiou, Hideo Nakamura, Helen Toledano, Iris Fried, Daniel W. Fults, Takafumi Wataya, Chris Fryer, David D. Eisenstat, Katrin Scheinemann, Adam Fleming, Donna L. Johnston, Jean Michaud, Shayna Zelcer, Robert Hammond, Samina Afzal, David A. Ramsay, Nongnuch Sirachainan, Suradej Hongeng, Noppadol Larbcharoensub, Richard G. Grundy, Rishi Lulla, Jason Fangusaro, Harriet Druker, Ute Bartels, Ronald Grant, David Malkin, C. Jane McGlade, Theodore Nicolaides, Tarık Tihan, Joanna J. Phillips, Jacek Majewski, Alexandre Montpetit, Guillaume Bourque, Gary D. Bader, Alyssa Reddy, G. Yancey Gillespie, Monika Warmuth‐Metz ほか 18 名 - Cancer Cell 2016 被引用: 254
- Screening of dementia genes by whole-exome sequencing in early-onset Alzheimer disease: input and lessons
著者: Gaël Nicolas, David Wallon, Camille Charbonnier, Olivier Quenez, Stéphane Rousseau, Anne‐Claire Richard, Anne Rovelet‐Lecrux, Sophie Coutant, Kilan Le Guennec, Delphine Bacq, Jean-Guillaume Garnier, Robert Olaso, Anne Boland, Vincent Meyer, Jean‐François Deleuze, Hans Markus Münter, Guillaume Bourque, Daniel Auld, Alexandre Montpetit, Mark Lathrop, Lucie Guyant‐Maréchal, Olivier Martinaud, Jérémie Pariente, Adeline Rollin‐Sillaire, Florence Pasquier, Isabelle Le Ber, Marie Sarazin, Bernard Croisile, Claire Boutoleau‐Bretonnière, Catherine Thomas-Antérion, Claire Paquet, Mathilde Sauvée, Olivier Moreaud, Audrey Gabelle, François Sellal, Mathieu Ceccaldi, Ludivine Chamard, Frédéric Blanc, Thierry Frébourg, Dominique Campion, Didier Hannequin - European Journal of Human Genetics 2015 被引用: 97
- Mutations in SETD2 and genes affecting histone H3K36 methylation target hemispheric high-grade gliomas
著者: Adam M. Fontebasso, Jeremy Schwartzentruber, Dong-Anh Khuong-Quang, Xiao-Yang Liu, Dominik Sturm, Andrey Korshunov, David Jones, Hendrik Witt, Marcel Kool, Steffen Albrecht, Adam Fleming, Djihad Hadjadj, Stephan Busche, Pierre Lepage, Alexandre Montpetit, Alfredo Staffa, Noha Gerges, Magdalena Zakrzewska, Krzysztof Zakrzewski, Paweł P. Liberski, Péter Hauser, Miklós Garami, Álmos Klekner, László Bognár, Gelareh Zadeh, Damien Faury, Stefan M. Pfister, Nada Jabado, Jacek Majewski - Acta Neuropathologica 2013 被引用: 292
- Genetic variant near IRS1 is associated with type 2 diabetes, insulin resistance and hyperinsulinemia
著者: Johan Rung, Stéphane Cauchi, Anders Albrechtsen, Li Shen, Ghislain Rocheleau, Christine Cavalcanti-Proença, François Bacot, Beverley Balkau, Alexandre Bélisle, Knut Borch‐Johnsen, G. Charpentier, Christian Dina, Emmanuelle Durand, Paul Elliott, Samy Hadjadj, Marjo‐Riitta Järvelin, Jaana Laitinen, Torsten Lauritzen, Michel Marre, Alexander M. Mazur, Stephen Eyre, Alexandre Montpetit, Charlotta Pisinger, Barry I. Posner, Pernille Poulsen, Anneli Pouta, Marc Prentki, Rasmus Ribel‐Madsen, Aimo Ruokonen, Anelli Sandbæk, David Serre, Jean Tichet, Martine Vaxillaire, Jørgen F. P. Wojtaszewski, Allan Vaag, Torben Hansen, Constantin Polychronakos, Oluf Pedersen, Philippe Froguel, Robert Sladek - Nature Genetics 2009 被引用: 479
- Genome-wide association study for early-onset and morbid adult obesity identifies three new risk loci in European populations
著者: Stephen Eyre, Jérôme Delplanque, Jean-Claude Chèvre, Cécile Lecœur, Stéphane Lobbens, Sophie Gallina, Emmanuelle Durand, Vincent Vatin, Franck Degraeve, Christine Proença, Stefan Gaget, Antje Körner, Péter Kovács, Wieland Kieß, Jean Tichet, Michel Marre, Anna‐Liisa Hartikainen, Fritz Horber, Natascha Potoczna, Serge Herçberg, Claire Lévy‐Marchal, François Pattou, Barbara Heude, M. Tauber, Mark I. McCarthy, Alexandra I. F. Blakemore, Alexandre Montpetit, Constantin Polychronakos, Jacques Weill, Lachlan Coin, Julian E. Asher, Paul Elliott, Marjo‐Riitta Järvelin, Sophie Visvikis‐Siest, Beverley Balkau, Robert Sladek, David J. Balding, Andrew J. Walley, Christian Dina, Philippe Froguel - Nature Genetics 2009 被引用: 654
- What can exome sequencing do for you?
著者: Jacek Majewski, Jeremy Schwartzentruber, Emilie Lalonde, Alexandre Montpetit, Nada Jabado - Journal of Medical Genetics 2011 被引用: 382
- The Biobanque québécoise de la COVID-19 (BQC19)—A cohort to prospectively study the clinical and biological determinants of COVID-19 clinical trajectories
著者: Karine Tremblay, Simon Rousseau, Ma’n H. Zawati, Daniel Auld, Michaël Chassé, Daniel Coderre, Emilia Liana Falcone, Nicolas Gauthier, Nathalie Grandvaux, François Gros‐Louis, Carole Jabet, Yann Joly, Daniel E. Kaufmann, Catherine Laprise, Catherine Larochelle, François Maltais, Anne‐Marie Mes‐Masson, Alexandre Montpetit, Alain Piché, J. Brent Richards, Sze Man Tse, Alexis F. Turgeon, Gustavo Turecki, Donald C. Vinh, Han Ting Wang, Vincent Mooser, on behalf of BQC19 - PLoS ONE 2021 被引用: 71
- Lung cancer susceptibility locus at 5p15.33
著者: EPIC Study, James McKay, Rayjean J Hung, Valérie Gaborieau, Paolo Boffetta, Amélie Chabrier, Graham Byrnes, Давид Заридзе, Anush Mukeria, Neonilia Szeszenia‐Dabrowska, Jolanta Lissowska, Péter Rudnai, Eleonóra Fabiánová, Dana Mateș, Vladimír Bencko, Lenka Foretová, Vladimír Janout, John McLaughlin, Frances A. Shepherd, Alexandre Montpetit, Steven A. Narod, Hans E. Krokan, Frank Skorpen, Maiken Bratt Elvestad, Lars J. Vatten, Inger Njølstad, Tomas Axelsson, Chu Chen, Gary E. Goodman, Matt J. Barnett, Melissa M. Loomis, Jan Lubiński, Joanna Matyjasik, Marcin Lener, Dorota Oszutowska–Mazurek, John K. Field, Triantafillos Liloglou, George Xinarianos, Adrian Cassidy, Diana Zélénika, Anne Boland, Marc Délepine, Mario Foglio, Doris Lechner, Fumihiko Matsuda, Hélène Blanché, Marta Gut, Simon Heath, Mark Lathrop, Paul Brennan - Nature Genetics 2008 被引用: 569
- Susceptibility to leprosy is associated with PARK2 and PACRG
著者: Marcelo Távora Mira, Alexandre Alcaïs, Nguyen Van Thuc, Milton Ozório Moraes, Celestino Di Flumeri, Vu Hong Thai, Mai Chi Phuong, Nguyễn Thu Hương, Nguyen Ngoc Ba, Pham Xuan Khoa, Euzenir Nunes Sarno, Andrea Alter, Alexandre Montpetit, M. E. Moraes, J. R. Moraes, Carole Doré, Caroline J. Gallant, Pierre Lepage, Andrei Verner, Esther van de Vosse, Thomas J. Hudson, Laurent Abel, Erwin Schurr - Nature 2004 被引用: 478
- Rare variants in the CYP27B1 gene are associated with multiple sclerosis
著者: Sreeram V. Ramagopalan, David A. Dyment, M. Zameel Cader, Katie Morrison, Giulio Disanto, Julia M. Morahan, Antonio J. Berlanga‐Taylor, Adam E. Handel, Gabriele C. DeLuca, A. Dessa Sadovnick, Pierre Lepage, Alexandre Montpetit, George C. Ebers - Annals of Neurology 2011 被引用: 228
- Disruption of AP1S1, Causing a Novel Neurocutaneous Syndrome, Perturbs Development of the Skin and Spinal Cord
著者: Alexandre Montpetit, Stéphanie Côté, Edna Brustein, Christian A. Drouin, Line Lapointe, Michèle Boudreau, Caroline Meloche, Régen Drouin, Thomas J. Hudson, Pierre Drapeau, Patrick Cossette - PLoS Genetics 2008 被引用: 172
- CAG Expansion in the Huntington Disease Gene Is Associated with a Specific and Targetable Predisposing Haplogroup
著者: Simon C. Warby, Alexandre Montpetit, Anna Hayden, Jeffrey B. Carroll, Stefanie Butland, Henk Visscher, Jennifer A. Collins, Alicia Semaka, Thomas J. Hudson, Michael R. Hayden - The American Journal of Human Genetics 2009 被引用: 241
- NALP1 Influences Susceptibility to Human Congenital Toxoplasmosis, Proinflammatory Cytokine Response, and Fate ofToxoplasma gondii-Infected Monocytic Cells
著者: William H. Witola, Ernest Mui, Aubrey Hargrave, Susan Liu, Magali Hypolite, Alexandre Montpetit, Pierre Cavaillès, Cordelia Bisanz, Marie‐France Cesbron‐Delauw, Gilbert J. Fournié, Rima McLeod - Infection and Immunity 2010 被引用: 193
- Buccals are likely to be a more informative surrogate tissue than blood for epigenome-wide association studies
著者: Robert Lowe, Carolina Gemma, Huriya Beyan, Mohammed I. Hawa, Alexandra Bazeos, Richard David Leslie, Alexandre Montpetit, Vardhman K. Rakyan, Sreeram V. Ramagopalan - Epigenetics 2013 被引用: 165
- A PRDX1 mutant allele causes a MMACHC secondary epimutation in cblC patients
著者: Jean‐Louis Guéant, Céline Chéry, Abderrahim Oussalah, Javad Nadaf, David Coelho, Thomas Josse, Justine Flayac, Aurélie Robert, Isabelle Koscinski, Isabelle Gastin, Pierre Filhine-Trésarrieu, Mihaela Pupavac, Alison Brebner, David Watkins, Tomi Pastinen, Alexandre Montpetit, Fadi Hariri, David‐Alexandre Trégouët, Benjamin A. Raby, Wendy K. Chung, Pierre‐Emmanuel Morange, D. Sean Froese, Matthias R. Baumgartner, Jean‐François Benoist, Can Fıçıcıoğlu, Virginie Marchand, Yuri Motorin, C. Bonnemains, François Feillet, Jacek Majewski, David S. Rosenblatt - Nature Communications 2017 被引用: 90
- A predominant role for the HLA class II region in the association of the MHC region with multiple sclerosis
著者: Matthew R. Lincoln, Alexandre Montpetit, M. Zameel Cader, Janna Saarela, David A. Dyment, Milvi Tiislar, Vincent Ferretti, Pentti J. Tienari, A. Dessa Sadovnick, Leena Peltonen, George C. Ebers, Thomas J. Hudson - Nature Genetics 2005 被引用: 333
- Genetic Variants of FTO Influence Adiposity, Insulin Sensitivity, Leptin Levels, and Resting Metabolic Rate in the Quebec Family Study
著者: Ron Do, Swneke D. Bailey, Katia Desbiens, Alexandre Bélisle, Alexandre Montpetit, Claude Bouchard, Louis Përusse, Marie‐Claude Vohl, James C. Engert - Diabetes 2008 被引用: 235
- Fusion of TTYH1 with the C19MC microRNA cluster drives expression of a brain-specific DNMT3B isoform in the embryonal brain tumor ETMR
著者: Claudia L. Kleinman, Noha Gerges, Simon Papillon‐Cavanagh, Patrick Sin‐Chan, Albéna Pramatarova, Dong-Anh Khuong Quang, Véronique Adoue, Stephan Busche, Maxime Caron, Haig Djambazian, Amandine Bemmo, Adam M. Fontebasso, Tara Spence, Jeremy Schwartzentruber, Steffen Albrecht, Péter Hauser, Miklós Garami, Álmos Klekner, László Bognár, J.L. Martínez Montes, Alfredo Staffa, Alexandre Montpetit, Pierre Bérubé, Magdalena Zakrzewska, Krzysztof Zakrzewski, Paweł P. Liberski, Zhifeng Dong, Peter M. Siegel, Thomas F. Duchaîne, Christian Perotti, Adam Fleming, Damien Faury, Marc Remke, Marco Gallo, Peter B. Dirks, Michael D. Taylor, Robert Sladek, Tomi Pastinen, Jennifer A. Chan, Annie Huang, Jacek Majewski, Nada Jabado - Nature Genetics 2013 被引用: 202
