Alexandre Reymond

1963–2025 年に発表

107
論文数
32,812
被引用数
76
h 指数
102
i10 指数

被引用数

Alexandre Reymond の年別被引用数1955 年: 被引用 1 件1964 年: 被引用 1 件1965 年: 被引用 1 件1968 年: 被引用 1 件1969 年: 被引用 1 件1970 年: 被引用 1 件1971 年: 被引用 1 件1972 年: 被引用 2 件1973 年: 被引用 1 件1974 年: 被引用 3 件1976 年: 被引用 1 件1977 年: 被引用 1 件1980 年: 被引用 1 件1981 年: 被引用 1 件1983 年: 被引用 1 件1984 年: 被引用 1 件1985 年: 被引用 2 件1986 年: 被引用 2 件1989 年: 被引用 1 件1990 年: 被引用 1 件1993 年: 被引用 2 件1994 年: 被引用 3 件1995 年: 被引用 5 件1996 年: 被引用 19 件1997 年: 被引用 25 件1998 年: 被引用 21 件1999 年: 被引用 25 件2000 年: 被引用 25 件2001 年: 被引用 29 件2002 年: 被引用 27 件2003 年: 被引用 35 件2004 年: 被引用 97 件2005 年: 被引用 123 件2006 年: 被引用 156 件2007 年: 被引用 205 件2008 年: 被引用 167 件2009 年: 被引用 175 件2010 年: 被引用 222 件2011 年: 被引用 238 件2012 年: 被引用 293 件2013 年: 被引用 451 件2014 年: 被引用 533 件2015 年: 被引用 569 件2016 年: 被引用 561 件2017 年: 被引用 548 件2018 年: 被引用 544 件2019 年: 被引用 1,277 件2020 年: 被引用 1,330 件2021 年: 被引用 1,300 件2022 年: 被引用 890 件2023 年: 被引用 684 件2024 年: 被引用 948 件2025 年: 被引用 367 件2026 年: 被引用 15 件1956〜1963 年は被引用が無いため表示していません1966〜1967 年は被引用が無いため表示していません1975 年は被引用が無いため表示していません1978〜1979 年は被引用が無いため表示していません1982 年は被引用が無いため表示していません1987〜1988 年は被引用が無いため表示していません1991〜1992 年は被引用が無いため表示していません

引用元

国・地域

この著者を引用した国・地域の世界地図アメリカ合衆国: 引用元論文 5,053 件、この内訳の 26%中国: 引用元論文 2,173 件、この内訳の 11.2%イギリス: 引用元論文 1,511 件、この内訳の 7.8%ドイツ: 引用元論文 1,118 件、この内訳の 5.8%カナダ: 引用元論文 699 件、この内訳の 3.6%イタリア: 引用元論文 695 件、この内訳の 3.6%フランス: 引用元論文 666 件、この内訳の 3.4%スペイン: 引用元論文 581 件、この内訳の 3%スイス: 引用元論文 574 件、この内訳の 2.9%オーストラリア: 引用元論文 543 件、この内訳の 2.8%オランダ: 引用元論文 497 件、この内訳の 2.6%日本: 引用元論文 477 件、この内訳の 2.5%
0%26%その他 24.8%

分野

  • Biochemistry, Genetics and Molecular Biology73.7%
  • Medicine12.9%
  • Immunology and Microbiology4.6%
  • Neuroscience3.1%
  • Agricultural and Biological Sciences3.1%
  • Computer Science0.5%
  • その他2.1%

トピック

  • 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%
  • その他67.4%

共著者

全論文

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  1. GENCODE reference annotation for the human and mouse genomes

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , 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 被引用: 3,502

  2. Landscape of transcription in human cells

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , 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 被引用: 5,413

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

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , 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 被引用: 5,035

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

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , 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 被引用: 371

  5. The tripartite motif family identifies cell compartments

    著者: , , , , , , , , , , , , , - The EMBO Journal 2001 被引用: 1,371

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

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , 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 ほか 207 名 - Science 2009 被引用: 1,349

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

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , 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 被引用: 688

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

    著者: , , , , , , , , , , , , , , - The American Journal of Human Genetics 2022 被引用: 92

  9. GENCODE: producing a reference annotation for ENCODE

    著者: , , , , , , , , , , , , , , - Genome biology 2006 被引用: 649

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

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , 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 ほか 81 名 - Nature 2011 被引用: 480

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

    著者: , , , , , , , , , , , , , , , , , , - Nature Communications 2021 被引用: 139

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

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , - European Journal of Human Genetics 2021 被引用: 90

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

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , 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 被引用: 560

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

    著者: , , , , , , , , , , , , - Nature 2012 被引用: 438

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

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , 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 被引用: 221

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

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , 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 ほか 5 名 - Human Brain Mapping 2021 被引用: 73

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

    著者: , , , - Human Genetics and Genomics Advances 2022 被引用: 65

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

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

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

    著者: , , , , , , , , , , , , , , , , , , , , , - Science 2019 被引用: 236

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

    著者: , , , , - Nature Reviews Genetics 2004 被引用: 714

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

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , 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 被引用: 296

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

    著者: , , , , , , , , , , , , , , , , , , , , - Cell 2015 被引用: 246

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

    著者: , , , , , , , , , , , , , , , , , , , - Molecular Psychiatry 2014 被引用: 227

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

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , - Nature 2016 被引用: 132