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Alexandre Montpetit

Active 2003–2025

48
Papers
23,329
Citations
47
h-index
47
i10-index

Citations

Citations per year for Alexandre Montpetit1955: 1 citations1964: 1 citations1967: 1 citations1974: 1 citations1990: 2 citations1995: 1 citations1998: 1 citations2001: 1 citations2002: 1 citations2004: 78 citations2005: 155 citations2006: 133 citations2007: 229 citations2008: 378 citations2009: 384 citations2010: 417 citations2011: 335 citations2012: 359 citations2013: 348 citations2014: 375 citations2015: 326 citations2016: 267 citations2017: 262 citations2018: 195 citations2019: 637 citations2020: 610 citations2021: 530 citations2022: 407 citations2023: 263 citations2024: 347 citations2025: 146 citations2026: 4 citations1956–1963: no citations, so these years are not shown1965–1966: no citations, so these years are not shown1968–1973: no citations, so these years are not shown1975–1989: no citations, so these years are not shown1991–1994: no citations, so these years are not shown1996–1997: no citations, so these years are not shown1999–2000: no citations, so these years are not shown2003: no citations, so this year is not shown

Citation sources

Countries

World map of the countries and regions citing this authorUnited States: 3,381 citing papers, 26.1% of this breakdownUnited Kingdom: 1,173 citing papers, 9% of this breakdownCanada: 763 citing papers, 5.9% of this breakdownGermany: 759 citing papers, 5.9% of this breakdownChina: 651 citing papers, 5% of this breakdownFrance: 524 citing papers, 4% of this breakdownNetherlands: 438 citing papers, 3.4% of this breakdownItaly: 428 citing papers, 3.3% of this breakdownAustralia: 427 citing papers, 3.3% of this breakdownSpain: 329 citing papers, 2.5% of this breakdownSweden: 318 citing papers, 2.5% of this breakdownJapan: 311 citing papers, 2.4% of this breakdown
0%26.1%Other 26.7%

Institutions

Fields

  • Biochemistry, Genetics and Molecular Biology51.8%
  • Medicine35.4%
  • Immunology and Microbiology3.8%
  • Neuroscience2.9%
  • Nursing2.4%
  • Computer Science1%
  • Other2.7%

Topics

  • 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%
  • Other77.6%

Coauthors

All papers

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  1. Driver mutations in histone H3.3 and chromatin remodelling genes in paediatric glioblastoma

    Authors: 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 cited by 2,711

  2. The International HapMap Project

    Authors: 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 and 83 more - Nature 2003 cited by 6,186

  3. K27M mutation in histone H3.3 defines clinically and biologically distinct subgroups of pediatric diffuse intrinsic pontine gliomas

    Authors: 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 cited by 1,020

  4. H3K27M induces defective chromatin spread of PRC2-mediated repressive H3K27me2/me3 and is essential for glioma tumorigenesis

    Authors: 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 cited by 392

  5. A genome-wide association study identifies novel risk loci for type 2 diabetes

    Authors: 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 cited by 3,015

  6. Genomic analysis of diffuse intrinsic pontine gliomas identifies three molecular subgroups and recurrent activating ACVR1 mutations

    Authors: 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 cited by 654

  7. Integrated (epi)-Genomic Analyses Identify Subgroup-Specific Therapeutic Targets in CNS Rhabdoid Tumors

    Authors: 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 and 18 more - Cancer Cell 2016 cited by 254

  8. Screening of dementia genes by whole-exome sequencing in early-onset Alzheimer disease: input and lessons

    Authors: 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 cited by 97

  9. Mutations in SETD2 and genes affecting histone H3K36 methylation target hemispheric high-grade gliomas

    Authors: 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 cited by 292

  10. Genetic variant near IRS1 is associated with type 2 diabetes, insulin resistance and hyperinsulinemia

    Authors: 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 cited by 479

  11. Genome-wide association study for early-onset and morbid adult obesity identifies three new risk loci in European populations

    Authors: 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 cited by 654

  12. What can exome sequencing do for you?

    Authors: Jacek Majewski, Jeremy Schwartzentruber, Emilie Lalonde, Alexandre Montpetit, Nada Jabado - Journal of Medical Genetics 2011 cited by 382

  13. The Biobanque québécoise de la COVID-19 (BQC19)—A cohort to prospectively study the clinical and biological determinants of COVID-19 clinical trajectories

    Authors: 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 cited by 71

  14. Lung cancer susceptibility locus at 5p15.33

    Authors: 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 cited by 569

  15. Susceptibility to leprosy is associated with PARK2 and PACRG

    Authors: 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 cited by 478

  16. Rare variants in the CYP27B1 gene are associated with multiple sclerosis

    Authors: 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 cited by 228

  17. Disruption of AP1S1, Causing a Novel Neurocutaneous Syndrome, Perturbs Development of the Skin and Spinal Cord

    Authors: 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 cited by 172

  18. CAG Expansion in the Huntington Disease Gene Is Associated with a Specific and Targetable Predisposing Haplogroup

    Authors: 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 cited by 241

  19. NALP1 Influences Susceptibility to Human Congenital Toxoplasmosis, Proinflammatory Cytokine Response, and Fate ofToxoplasma gondii-Infected Monocytic Cells

    Authors: 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 cited by 193

  20. Buccals are likely to be a more informative surrogate tissue than blood for epigenome-wide association studies

    Authors: Robert Lowe, Carolina Gemma, Huriya Beyan, Mohammed I. Hawa, Alexandra Bazeos, Richard David Leslie, Alexandre Montpetit, Vardhman K. Rakyan, Sreeram V. Ramagopalan - Epigenetics 2013 cited by 165

  21. A PRDX1 mutant allele causes a MMACHC secondary epimutation in cblC patients

    Authors: 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 cited by 90

  22. A predominant role for the HLA class II region in the association of the MHC region with multiple sclerosis

    Authors: 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 cited by 333

  23. Genetic Variants of FTO Influence Adiposity, Insulin Sensitivity, Leptin Levels, and Resting Metabolic Rate in the Quebec Family Study

    Authors: Ron Do, Swneke D. Bailey, Katia Desbiens, Alexandre Bélisle, Alexandre Montpetit, Claude Bouchard, Louis Përusse, Marie‐Claude Vohl, James C. Engert - Diabetes 2008 cited by 235

  24. Fusion of TTYH1 with the C19MC microRNA cluster drives expression of a brain-specific DNMT3B isoform in the embryonal brain tumor ETMR

    Authors: 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 cited by 202