Alexandre Reymond

Active 1963–2025

107
Papers
32,812
Citations
76
h-index
102
i10-index

Citations

Citations per year for Alexandre Reymond1955: 1 citations1964: 1 citations1965: 1 citations1968: 1 citations1969: 1 citations1970: 1 citations1971: 1 citations1972: 2 citations1973: 1 citations1974: 3 citations1976: 1 citations1977: 1 citations1980: 1 citations1981: 1 citations1983: 1 citations1984: 1 citations1985: 2 citations1986: 2 citations1989: 1 citations1990: 1 citations1993: 2 citations1994: 3 citations1995: 5 citations1996: 19 citations1997: 25 citations1998: 21 citations1999: 25 citations2000: 25 citations2001: 29 citations2002: 27 citations2003: 35 citations2004: 97 citations2005: 123 citations2006: 156 citations2007: 205 citations2008: 167 citations2009: 175 citations2010: 222 citations2011: 238 citations2012: 293 citations2013: 451 citations2014: 533 citations2015: 569 citations2016: 561 citations2017: 548 citations2018: 544 citations2019: 1,277 citations2020: 1,330 citations2021: 1,300 citations2022: 890 citations2023: 684 citations2024: 948 citations2025: 367 citations2026: 15 citations1956–1963: no citations, so these years are not shown1966–1967: no citations, so these years are not shown1975: no citations, so this year is not shown1978–1979: no citations, so these years are not shown1982: no citations, so this year is not shown1987–1988: no citations, so these years are not shown1991–1992: no citations, so these years are not shown

Citation sources

Countries

World map of the countries and regions citing this authorUnited States: 5,053 citing papers, 26% of this breakdownChina: 2,173 citing papers, 11.2% of this breakdownUnited Kingdom: 1,511 citing papers, 7.8% of this breakdownGermany: 1,118 citing papers, 5.8% of this breakdownCanada: 699 citing papers, 3.6% of this breakdownItaly: 695 citing papers, 3.6% of this breakdownFrance: 666 citing papers, 3.4% of this breakdownSpain: 581 citing papers, 3% of this breakdownSwitzerland: 574 citing papers, 2.9% of this breakdownAustralia: 543 citing papers, 2.8% of this breakdownNetherlands: 497 citing papers, 2.6% of this breakdownJapan: 477 citing papers, 2.5% of this breakdown
0%26%Other 24.8%

Fields

  • Biochemistry, Genetics and Molecular Biology73.7%
  • Medicine12.9%
  • Immunology and Microbiology4.6%
  • Neuroscience3.1%
  • Agricultural and Biological Sciences3.1%
  • Computer Science0.5%
  • Other2.1%

Topics

  • Cancer-related molecular mechanisms research7.9%
  • RNA modifications and cancer7.2%
  • RNA Research and Splicing6.4%
  • RNA and protein synthesis mechanisms4%
  • Genomics and Chromatin Dynamics3.6%
  • Genomics and Phylogenetic Studies3.5%
  • Other67.4%

Coauthors

All papers

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  1. GENCODE reference annotation for the human and mouse genomes

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Paul Muir, Fabio C. P. Navarro, Anne Parker, Baikang Pei, Fernando Pozo, Magali Ruffier, Bianca M. Schmitt, Eloise Stapleton, Marie-Marthe Suner, Irina Sycheva, Barbara Uszczynska-Ratajczak, Jinrui Xu, Andrew D. Yates, Daniel R. Zerbino, Yan Zhang, Bronwen L. Aken, Jyoti Choudhary, Mark Gerstein, Roderic Guigó, Tim J. P. Hubbard, Manolis Kellis, Benedict Paten, Alexandre Reymond, Michael L. Tress, Paul Flicek - Nucleic Acids Research, Nucleic Acids Res. 2018 cited by 3,502

  2. Landscape of transcription in human cells

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Thomas Derrien, Jörg Drenkow, Erica Dumais, Jacqueline Dumais, Radha Duttagupta, Emilie Falconnet, Meagan Fastuca, Kata Fejes-Toth, Pedro G. Ferreira, Sylvain Foissac, Melissa J. Fullwood, Hui Gao, David González, Assaf Gordon, Harsha P. Gunawardena, Cédric Howald, Sonali Jha, Rory Johnson, Philipp Kapranov, Brandon King, Colin Kingswood, Oscar Junhong Luo, Eddie Park, Kimberly Persaud, Jonathan Preall, Paolo Ribeca, Brian A. Risk, Daniel Robyr, Michael Sammeth, Lorian Schaffer, Lei-Hoon See, Atif Shahab, Jørgen Skancke, Ana Maria Suzuki, Hazuki Takahashi, Hagen Tilgner, Diane Trout, Nathalie Walters, Huaien Wang, John A. Wrobel, Yanbao Yu, Xiaoan Ruan, Yoshihide Hayashizaki, Jennifer Harrow, Mark Gerstein, Tim Hubbard, Alexandre Reymond, Stylianos E. Antonarakis, Gregory J. Hannon, Morgan C. Giddings, Yijun Ruan, B Wold, Piero Carninci, Roderic Guigó, T Gingeras - Nature 2012 cited by 5,413

  3. GENCODE: The reference human genome annotation for The ENCODE Project

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , José Manuel Rodrı́guez, Iakes Ezkurdia, Jeltje van Baren, Michael R. Brent, David Haussler, Manolis Kellis, Alfonso Valencia, Alexandre Reymond, Mark Gerstein, Roderic Guigó, Tim Hubbard - Genome Research 2012 cited by 5,035

  4. A cross-disorder dosage sensitivity map of the human genome

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Matthew E. Hurles, Swaroop Aradhya, Erica E. Davis, Hilary K. Finucane, James F. Gusella, Aura Janze, Nicholas Katsanis, Ludmila Matyakhina, Benjamin M. Neale, D. B. Sanders, Stephanie Warren, Jennelle C. Hodge, Dennis Lal, Douglas M. Ruderfer, Jeanne Meck, Reedik Mägi, Tõnu Esko, Alexandre Reymond, Zoltán Kutalik, Håkon Håkonarson, Shamil Sunyaev, Harrison Brand, Michael E. Talkowski - Cell 2022 cited by 371

  5. The tripartite motif family identifies cell compartments

    Authors: , , , , , , , , , , , , , - The EMBO Journal 2001 cited by 1,371

  6. The Genome Sequence of Taurine Cattle: A Window to Ruminant Biology and Evolution

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Wratko Hlavina, Yuri Kapustin, Boris Kiryutin, Paul Kitts, Felix Kokocinski, Melissa Landrum, Donna Maglott, Kim D. Pruitt, Victor Sapojnikov, Stephen M. J. Searle, Victor Solovyev, Alexandre Souvorov, Catherine Ucla, Carine Wyss, Juan Manuel Anzola, Daniel Gerlach, Eran Elhaik, Dan Graur, Justin Reese, R. C. Edgar, John C. McEwan, Gemma M. Payne, Joy M Raison, Thomas Junier, Evgenia V. Kriventseva, Eduardo Eyras, Mireya Plass, Ravikiran Donthu, Denis M. Larkin, James M. Reecy, Mary Qu Yang, Lin Chen, Ze Cheng, Carol G. Chitko-McKown, George E. Liu, Lakshmi K. Matukumalli, Jiuzhou Song, Bin Zhu, Daniel G. Bradley, Fiona S. L. Brinkman, Lilian Pek Lian Lau, Matthew D. Whiteside, Angela M. Walker, Thomas T. Wheeler, Theresa Casey, J. Bruce German, Danielle G. Lemay, Nauman J. Maqbool, Adrian Molenaar, Seongwon Seo, Paul Stothard, Cynthia L. Baldwin, R. Baxter, Candice Brinkmeyer‐Langford, Wendy C. Brown, Christopher Childers, Timothy Connelley, Shirley A. Ellis, K. L. Fritz, Elizabeth Glass, Carolyn T.A. Herzig, Antti Iivanainen, Kevin K. Lahmers, Anna K. Bennett, C. Michael Dickens, James Gilbert, Darren E. Hagen, Hanni Salih, Jan Aerts, Alexandre Rodrigues Caetano and 207 more - Science 2009 cited by 1,349

  7. A High-Resolution Anatomical Atlas of the Transcriptome in the Mouse Embryo

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Frauke Grabbe, Cornelia Sieverding, Barbara Fischer, Kathrin Schrader, Maren Brockmeyer, Sarah Dettmer, Christin Helbig, Violaine Alunni, Marie-Annick Battaini, Carole Mura, Charlotte N. Henrichsen, Raquel García‐López, Diego Echevarrı́a, Eduardo Puelles, Elena Garcı́a-Calero, Stefan Kruse, M. Uhr, Christine Kauck, Guangjie Feng, Nestor Milyaev, Chuang Kee Ong, Lalit Kumar, MeiSze Lam, Colin A. Semple, Attila Gyenesei, Stefan Mundlos, Uwe Radelof, Hans Lehrach, Paolo Sarmientos, Alexandre Reymond, Duncan Davidson, Pascal Dollé, Stylianos E. Antonarakis, Marie‐Laure Yaspo, Salvador Martı́nez, Richard Baldock, Gregor Eichele, Andrea Ballabio - PLoS Biology 2011 cited by 688

  8. The individual and global impact of copy-number variants on complex human traits

    Authors: , , , , , , , , , , , , , , - The American Journal of Human Genetics 2022 cited by 92

  9. GENCODE: producing a reference annotation for ENCODE

    Authors: , , , , , , , , , , , , , , - Genome biology 2006 cited by 649

  10. Mirror extreme BMI phenotypes associated with gene dosage at the chromosome 16p11.2 locus

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Mieke M. van Haelst, Sergi Villatoro Gomez, Faida Walha, Bai-Lin Wu, Yongguo Yu, Azzedine Aboura, Marie‐Claude Addor, Yves Alembik, Stylianos E. Antonarakis, Benoı̂t Arveiler, Magalie Barth, Nathalie Bednarek, Frédérique Béna, Sven Bergmann, Mylène Béri, Laura Bernardini, Bettina Blaumeiser, Dominique Bonneau, Armand Bottani, Odile Boute, Han G. Brunner, Dorothée Cailley, Patrick Callier, Jean Chiésa, Jacqueline Chrast, Lachlan Coin, Charles Coutton, Jean‐Marie Cuisset, J. Cuvellier, Albert David, Bénédicte de Fréminville, Bruno Delobel, Marie‐Ange Delrue, Bénédicte Demeer, Dominique Descamps, Gérard Didelot, Klaus Dieterich, Vittoria Disciglio, Martine Doco‐Fenzy, Séverine Drunat, Bénédicte Duban‐Bedu, Christèle Dubourg, Julia S. El-Sayed Moustafa, Paul Elliott, Brigitte H. W. Faas, Laurence Faivre, Anne Faudet, Florence Fellmann, Alessandra Ferrarini, Richard Fisher, Elisabeth Flori, Lukas Forer, Dominique Gaillard, Marion Gérard, Christian Gieger, Stefania Gimelli, Giorgio Gimelli, Hans J. Grabe, Agnès Guichet, Olivier Guillin, Anna‐Liisa Hartikainen, Delphine Héron, Loyse Hippolyte, Muriel Holder, Georg Homuth, Bertrand Isidor, Sylvie Jaillard, Zdenek Jaros, Susana Jiménez‐Múrcia, Géraldine Joly Helas and 81 more - Nature 2011 cited by 480

  11. Differentially expressed genes reflect disease-induced rather than disease-causing changes in the transcriptome

    Authors: , , , , , , , , , , , , , , , , , , - Nature Communications 2021 cited by 139

  12. The use of polygenic risk scores in pre-implantation genetic testing: an unproven, unethical practice

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , - European Journal of Human Genetics 2021 cited by 90

  13. A new highly penetrant form of obesity due to deletions on chromosome 16p11.2

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Audrey Guilmatre, Anna Goldenberg, Nadège Calmels, Jean‐Louis Mandel, Cédric Le Caignec, A. David, Bertrand Isidor, Marie‐Pierre Cordier, Sophie Dupuis‐Girod, Audrey Labalme, Damien Sanlaville, Mylène Béri‐Dexheimer, Philippe Jonveaux, Bruno Leheup, Katrin Õunap, Elena G. Bochukova, Elana Henning, Julia M. Keogh, Richard J. Ellis, K D MacDermot, Mieke M. van Haelst, C. Vincent‐Delorme, Ghislaine Plessis, Renaud Touraine, Anne Philippe, Valérie Malan, M. Mathieu‐Dramard, Jean Chiésa, Bettina Blaumeiser, R. Frank Kooy, Robert Caïazzo, Marie Pigeyre, Beverley Balkau, Robert Sladek, Sven Bergmann, Vincent Mooser, Dawn Waterworth, Alexandre Reymond, Péter Vollenweider, Gérard Waeber, Ants Kurg, Priit Palta, Tõnu Esko, Andres Metspalu, Mari Nelis, Paul Elliott, Anna‐Liisa Hartikainen, Mark I. McCarthy, Laura‐Maria Peltonen, Lena Carlsson, Peter Jacobson, Lars Sjöström, Ni Huang, Matthew E. Hurles, Stephen O’Rahilly, I. Sadaf Farooqi, Katrin Männik, Marjo‐Riitta Järvelin, François Pattou, Stephen Eyre, Andrew J. Walley, Lachlan Coin, Alexandra I. F. Blakemore, Philippe Froguel, J. Beckmann - Nature 2010 cited by 560

  14. KCTD13 is a major driver of mirrored neuroanatomical phenotypes of the 16p11.2 copy number variant

    Authors: , , , , , , , , , , , , - Nature 2012 cited by 438

  15. Rare variants in the genetic background modulate cognitive and developmental phenotypes in individuals carrying disease-associated variants

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Claire Bénéteau, Sophie Blesson, Dominique Martin‐Coignard, Anne-Laure Mosca-Boidron, Jean-Hubert Caberg, Maja Bućan, Susan Zeesman, Małgorzata J.M. Nowaczyk, Mathilde Lefebvre, Laurence Faivre, Patrick Callier, Cindy Skinner, Boris Keren, Perrine Charles, Paolo Prontera, Nathalie Marle, Alessandra Renieri, Alexandre Reymond, R. Frank Kooy, Bertrand Isidor, Charles E. Schwartz, Corrado Romano, Erik A. Sistermans, David J. Amor, Joris Andrieux, Santhosh Girirajan - Genetics in Medicine 2018 cited by 221

  16. Effects of copy number variations on brain structure and risk for psychiatric illness: Large‐scale studies from theENIGMAworking groups onCNVs

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Bogdan Draganski, Courtney A. Durdle, Stefan Ehrlich, Beverly S. Emanuel, Thomas Espeseth, Simon E. Fisher, Tian Ge, David C. Glahn, Hans J. Grabe, Raquel E. Gur, Boris A. Gutman, Jan Haavik, Asta K. Håberg, Laura A. Hansen, Ryota Hashimoto, Derrek P. Hibar, Avram J. Holmes, Jouke‐Jan Hottenga, Hilleke E. Hulshoff Pol, Maria Jalbrzikowski, Emma E. M. Knowles, Leila Kushan, David E.J. Linden, Jingyu Liu, Astri J. Lundervold, Sandra Martin‐Brevet, Kenia Martínez, Karen A. Mather, Samuel R. Mathias, Donna M. McDonald‐McGinn, Allan F. McRae, Sarah E. Medland, Torgeir Moberget, Claudia Modenato, Jennifer Monereo Sánchez, Clara Moreau, Thomas W. Mühleisen, Tomáš Paus, Zdenka Pausová, Carlos Alberto Vanegas Prieto, Anjanibhargavi Ragothaman, Céline S. Reinbold, Tiago Reis Marques, Gabriela M. Repetto, Alexandre Reymond, David R. Roalf, Borja Rodríguez‐Herreros, James Rucker, Perminder S. Sachdev, James E. Schmitt, Peter R. Schofield, Ana Isabel Silva, Hreinn Stefánsson, Dan J. Stein, Christian K. Tamnes, Diana Tordesillas‐Gutiérrez, Magnús Ö. Úlfarsson, Ariana Vajdi, Dennis van ‘t Ent, Marianne B. M. van den Bree, Evangelos Vassos, Javier Vázquez-Bourgón, Fidel Vila‐Rodriguez, G. Bragi Walters, Wei Wen, Lars T. Westlye, Katharina Wittfeld, Elaine H. Zackai, Kári Stefánsson, Sébastien Jacquemont and 5 more - Human Brain Mapping 2021 cited by 73

  17. From pharmacogenetics to pharmaco-omics: Milestones and future directions

    Authors: , , , - Human Genetics and Genomics Advances 2022 cited by 65

  18. A 600 kb deletion syndrome at 16p11.2 leads to energy imbalance and neuropsychiatric disorders

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Jennifer Tjernagel, John E. Spiro, Alexandre Reymond, J. Beckmann, Wendy K. Chung, Sébastien Jacquemont - Journal of Medical Genetics 2012 cited by 357

  19. Chromatin three-dimensional interactions mediate genetic effects on gene expression

    Authors: , , , , , , , , , , , , , , , , , , , , , - Science 2019 cited by 236

  20. Chromosome 21 and Down syndrome: from genomics to pathophysiology

    Authors: , , , , - Nature Reviews Genetics 2004 cited by 714

  21. Defining the Effect of the 16p11.2 Duplication on Cognition, Behavior, and Medical Comorbidities

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Cédric Le Caignec, Christa Lese Martin, Katrin Männik, Andres Metspalu, Cyril Mignot, Pratik Mukherjee, Michael J. Owen, Marzia Passeggeri, Caroline Rooryck, Jill A. Rosenfeld, Sarah Spence, Kyle J. Steinman, Jennifer Tjernagel, Mieke M. van Haelst, Yiping Shen, Bogdan Draganski, Elliott H. Sherr, David H. Ledbetter, Marianne B. M. van den Bree, J. Beckmann, John E. Spiro, Alexandre Reymond, Sébastien Jacquemont, Wendy K. Chung - JAMA Psychiatry 2015 cited by 296

  22. Population Variation and Genetic Control of Modular Chromatin Architecture in Humans

    Authors: , , , , , , , , , , , , , , , , , , , , - Cell 2015 cited by 246

  23. The 16p11.2 locus modulates brain structures common to autism, schizophrenia and obesity

    Authors: , , , , , , , , , , , , , , , , , , , - Molecular Psychiatry 2014 cited by 227

  24. Emergence of a Homo sapiens-specific gene family and chromosome 16p11.2 CNV susceptibility

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , - Nature 2016 cited by 132