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Anthony P. Monaco

1962–2022 年に発表

147
論文数
39,574
被引用数
106
h 指数
147
i10 指数

被引用数

Anthony P. Monaco の年別被引用数1962 年: 被引用 1 件1965 年: 被引用 3 件1966 年: 被引用 10 件1967 年: 被引用 19 件1968 年: 被引用 9 件1969 年: 被引用 4 件1970 年: 被引用 2 件1971 年: 被引用 3 件1973 年: 被引用 4 件1974 年: 被引用 1 件1975 年: 被引用 1 件1976 年: 被引用 9 件1977 年: 被引用 2 件1980 年: 被引用 1 件1981 年: 被引用 1 件1982 年: 被引用 1 件1984 年: 被引用 4 件1985 年: 被引用 8 件1986 年: 被引用 37 件1987 年: 被引用 116 件1988 年: 被引用 162 件1989 年: 被引用 172 件1990 年: 被引用 141 件1991 年: 被引用 135 件1992 年: 被引用 156 件1993 年: 被引用 163 件1994 年: 被引用 135 件1995 年: 被引用 170 件1996 年: 被引用 184 件1997 年: 被引用 162 件1998 年: 被引用 201 件1999 年: 被引用 242 件2000 年: 被引用 258 件2001 年: 被引用 264 件2002 年: 被引用 320 件2003 年: 被引用 336 件2004 年: 被引用 358 件2005 年: 被引用 363 件2006 年: 被引用 379 件2007 年: 被引用 255 件2008 年: 被引用 269 件2009 年: 被引用 294 件2010 年: 被引用 337 件2011 年: 被引用 307 件2012 年: 被引用 292 件2013 年: 被引用 308 件2014 年: 被引用 235 件2015 年: 被引用 293 件2016 年: 被引用 209 件2017 年: 被引用 194 件2018 年: 被引用 141 件2019 年: 被引用 530 件2020 年: 被引用 448 件2021 年: 被引用 525 件2022 年: 被引用 352 件2023 年: 被引用 203 件2024 年: 被引用 313 件2025 年: 被引用 112 件2026 年: 被引用 3 件1963〜1964 年は被引用が無いため表示していません1972 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1983 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 3,679 件、この内訳の 32.1%イギリス: 引用元論文 1,241 件、この内訳の 10.8%ドイツ: 引用元論文 707 件、この内訳の 6.2%カナダ: 引用元論文 618 件、この内訳の 5.4%フランス: 引用元論文 602 件、この内訳の 5.3%イタリア: 引用元論文 487 件、この内訳の 4.2%オランダ: 引用元論文 444 件、この内訳の 3.9%日本: 引用元論文 398 件、この内訳の 3.5%オーストラリア: 引用元論文 336 件、この内訳の 2.9%中国: 引用元論文 328 件、この内訳の 2.9%スイス: 引用元論文 225 件、この内訳の 2%ベルギー: 引用元論文 196 件、この内訳の 1.7%
0%32.1%その他 19.1%

機関

分野

  • Biochemistry, Genetics and Molecular Biology45.3%
  • Neuroscience19.9%
  • Medicine17.8%
  • Psychology5.5%
  • Immunology and Microbiology4.6%
  • Nursing3.5%
  • その他3.4%

トピック

  • Genetics and Neurodevelopmental Disorders5.4%
  • Muscle Physiology and Disorders4.9%
  • Autism Spectrum Disorder Research4.5%
  • Genomic variations and chromosomal abnormalities2.1%
  • Congenital heart defects research1.7%
  • Pancreatic function and diabetes1.3%
  • その他80.1%

共著者

全論文

検索で開く
  1. Meta-analysis of SHANK Mutations in Autism Spectrum Disorders: A Gradient of Severity in Cognitive Impairments

    著者: Claire S. Leblond, Caroline Nava, Anne Polge, Julie Gauthier, Guillaume Huguet, Serge Lumbroso, Fabienne Giuliano, Coline Stordeur, Christel Depienne, Kévin Mouzat, Dalila Pinto, Jennifer Howe, Nathalie Lemière, Christelle M. Durand, Jessica Guibert, Elodie Ey, Roberto Toro, Hugo Peyre, Alexandre Mathieu, Frédérique Amsellem, Maria Råstam, I. Carina Gillberg, Gudrun Rappold, Richard Holt, Anthony P. Monaco, Elena Maestrini, Pilar Galán, Delphine Héron, Aurélia Jacquette, Alexandra Afenjar, Agnès Rastetter, Alexis Brice, Françoise Devillard, Brigitte Assouline, Fanny Laffargue, James Lespinasse, Jean Chiésa, François Rivier, Dominique Bonneau, Béatrice Regnault, Diana Zélénika, Marc Délepine, Mark Lathrop, Damien Sanlaville, Caroline Schluth‐Bolard, Patrick Edery, Laurence Perrin, Anne Claude Tabet, Michael J. Schmeißer, Tobias M. Boeckers, Mary Coleman, Daisuke Sato, Péter Szatmári, Stephen W. Scherer, Guy A. Rouleau, Catalina Betancur, Marion Leboyer, Christopher Gillberg, Richard Delorme, Thomas Bourgeron - PLoS Genetics 2014 被引用: 664

  2. Convergence of Genes and Cellular Pathways Dysregulated in Autism Spectrum Disorders

    著者: Dalila Pinto, Elsa Delaby, Daniele Merico, Mafalda Barbosa, Alison Merikangas, Lambertus Klei, Bhooma Thiruvahindrapuram, Xiao Xu, Robert Ziman, Zhuozhi Wang, Jacob Vorstman, Ann Thompson, Regina Regan, Marion Pilorge, Giovanna Pellecchia, Alistair T. Pagnamenta, Bárbara Oliveira, Christian R. Marshall, Tiago R. Magalhães, Jennifer K. Lowe, Jennifer Howe, Anthony J. Griswold, John R. Gilbert, Eftichia Duketis, Beth A. Dombroski, Maretha Jonge, Michael L. Cuccaro, Emily L. Crawford, Catarina Correia, Judith Conroy, Inês C. Conceição, Andreas G. Chiocchetti, Jillian P. Casey, Guiqing Cai, Christelle Cabrol, Nadia Bolshakova, Elena Bacchelli, Richard Anney, Steven Gallinger, Michelle Cotterchio, Graham Casey, Lonnie Zwaigenbaum, Kerstin Wittemeyer, Kirsty Wing, Simon Wallace, Hermán van Engeland, Ana Tryfon, Susanne Thomson, Latha Soorya, Bernadette Rogé, Wendy Roberts, Fritz Poustka, Susana Mouga, Nancy J. Minshew, L. Alison McInnes, Susan G. McGrew, Catherine Lord, Marion Leboyer, Ann S. Couteur, A lexander Kolevzon, Patricia González, Suma Jacob, Richard Holt, Stephen J. Guter, Jonathan Green, Andrew Green, Christopher Gillberg, Bridget A. Fernandez, Frederico Duque, Richard Delorme, Géraldine Dawson, Pauline Chaste, Cátia Café, S. Brennan, Thomas Bourgeron, Patrick Bolton, Sven Bölte, Raphael Bernier, Gillian Baird, Anthony Bailey, Evdokia Anagnostou, Joana Almeida, Ellen M. Wijsman, Veronica J. Vieland, Astrid M. Vicente, Gerard D. Schellenberg, Margaret A. Pericak‐Vance, Andrew D. Paterson, Jeremy Parr, Guiomar Oliveira, John I. Nürnberger, Anthony P. Monaco, Elena Maestrini, Sabine M. Klauck, Håkon Håkonarson, Jonathan L. Haines, Daniel H. Geschwind, Christine M. Freitag, Susan E. Folstein, Sean Ennis ほか 12 名 - The American Journal of Human Genetics 2014 被引用: 1,028

  3. Complete cloning of the duchenne muscular dystrophy (DMD) cDNA and preliminary genomic organization of the DMD gene in normal and affected individuals

    著者: M. Koenig, Eric P. Hoffman, Corlee J. Bertelson, Anthony P. Monaco, C. Feener, Louis M. Kunkel - Cell 1987 被引用: 2,407

  4. A forkhead-domain gene is mutated in a severe speech and language disorder

    著者: Cecilia Lai, Simon E. Fisher, Jane A. Hurst, Faraneh Vargha‐Khadem, Anthony P. Monaco - Nature 2001 被引用: 2,087

  5. Human VPS13A is associated with multiple organelles and influences mitochondrial morphology and lipid droplet motility

    著者: Wondwossen M Yeshaw, Marianne van der Zwaag, Francesco Pinto, Liza L. Lahaye, Anita I. E. Faber, Rubén Gómez‐Sánchez, Amalia M. Dolga, Conor Poland, Anthony P. Monaco, Sven C. van IJzendoorn, Nicola A. Grzeschik, Antonio Velayos‐Baeza, Ody C.M. Sibon - eLife 2019 被引用: 163

  6. Molecular evolution of FOXP2, a gene involved in speech and language

    著者: Wolfgang Enard, Molly Przeworski, Simon E. Fisher, Cecilia Lai, Victor Wiebe, Takashi Kitano, Anthony P. Monaco, Svante Pääbo - Nature 2002 被引用: 1,618

  7. Genome-wide analyses of individual differences in quantitatively assessed reading- and language-related skills in up to 34,000 people

    著者: Else Eising, Nazanin Mirza‐Schreiber, Eveline L. de Zeeuw, Carol A. Wang, Dongnhu T. Truong, Andrea G. Allegrini, Chin Yang Shapland, Gu Zhu, Karen Wigg, Margot Gerritse, Barbara Molz, Gökberk Alagöz, Alessandro Gialluisi, Filippo Abbondanza, Kaili Rimfeld, Marjolein van Donkelaar, Zhijie Liao, Philip R. Jansen, Till F. M. Andlauer, Timothy C. Bates, Manon Bernard, Kirsten Blokland, Milene Bonte, Anders D. Børglum, Thomas Bourgeron, Daniel Brandeis, Fabiola Ceroni, Valéria Csépe, Philip S. Dale, Peter F. de Jong, John C. DeFries, Jean‐François Démonet, Ditte Demontis, Yu Feng, Scott D. Gordon, Sharon Guger, Marianna E. Hayiou‐Thomas, Juan Hernández, Jouke‐Jan Hottenga, Charles Hulme, Juha Kere, Elizabeth N. Kerr, Tanner Koomar, Karin Landerl, Gabriel Leonard, Maureen W. Lovett, Heikki Lyytinen, Nicholas G. Martin, Angela Martinelli, Urs Maurer, Jacob J. Michaelson, Kristina Moll, Anthony P. Monaco, Angela Morgan, Markus M. Nöthen, Zdenka Pausová, Craig E. Pennell, Bruce F. Pennington, Kaitlyn M. Price, Veera M. Rajagopal, Franck Ramus, Louis Richer, Nuala H. Simpson, Shelley D. Smith, Maggie Snowling, John Stein, Lisa J. Strug, Joel B. Talcott, Henning Tiemeier, Marc P. van der Schroeff, Ellen Verhoef, Kate E. Watkins, Margaret Wilkinson, Margaret J. Wright, Cathy L. Barr, Dorret I. Boomsma, Manuel Carreiras, Marie-Christine Franken, Jeffrey R. Gruen, Michelle Luciano, Bertram Müller‐Myhsok, Dianne F. Newbury, Richard K. Olson, Silvia Paracchini, Tomáš Paus, Robert Plomin, Sheena Reilly, Gerd Schulte‐Körne, J. Bruce Tomblin, Elsje van Bergen, Andrew Whitehouse, Erik G. Willcutt, Beaté St Pourcain, Clyde Francks, Simon E. Fisher - National Academy of Sciences, Proceedings of the National Academy of Sciences 2022 被引用: 133

  8. Genome-wide association study reveals new insights into the heritability and genetic correlates of developmental dyslexia

    著者: Alessandro Gialluisi, Till F. M. Andlauer, Nazanin Mirza‐Schreiber, Kristina Moll, Jessica Becker, Per Hoffmann, Kerstin U. Ludwig, Darina Czamara, Beaté St Pourcain, Ferenc Honbolygó, Dénes Tóth, Valéria Csépe, Guillaume Huguet, Yves Chaix, Stéphanie Iannuzzi, Jean‐François Démonet, Andrew P. Morris, Jacqueline Hulslander, Erik G. Willcutt, John C. DeFries, Richard K. Olson, Shelley D. Smith, Bruce F. Pennington, Anniek Vaessen, Urs Maurer, Heikki Lyytinen, Myriam Peyrard‐Janvid, Paavo H. T. Leppänen, Daniel Brandeis, Milene Bonte, John Stein, Joel B. Talcott, Fabien Fauchereau, Arndt Wilcke, Holger Kirsten, Bent Müller, Clyde Francks, Thomas Bourgeron, Anthony P. Monaco, Franck Ramus, Karin Landerl, Juha Kere, Thomas Scerri, Silvia Paracchini, Simon E. Fisher, Johannes Schumacher, Markus M. Nöthen, Bertram Müller‐Myhsok, Gerd Schulte‐Körne - Molecular Psychiatry 2020 被引用: 130

  9. An explanation for the phenotypic differences between patients bearing partial deletions of the DMD locus

    著者: Anthony P. Monaco, Corlee J. Bertelson, Sabina Liechti‐Gallati, Hans Moser, Louis M. Kunkel - Genomics 1988 被引用: 1,192

  10. Isolation of candidate cDNAs for portions of the Duchenne muscular dystrophy gene

    著者: Anthony P. Monaco, Rachael L. Neve, Chris Colletti-Feener, Corlee J. Bertelson, David M. Kurnit, Louis M. Kunkel - Nature 1986 被引用: 1,056

  11. Mutations in ATP2A2, encoding a Ca2+ pump, cause Darier disease

    著者: Anavaj Sakuntabhai, Víctor L. Ruiz‐Pérez, Simon Carter, Nick Jacobsen, Susan Burge, Sarah Monk, Melanie Smith, Colin S. Munro, Michael O‘Donovan, Nick Craddock, Raju Kucherlapati, Jonathan L. Rees, Mike Owen, G.M. Lathrop, Anthony P. Monaco, Tom Strachan, Alain Hovnanian - Nature Genetics 1999 被引用: 734

  12. The complete sequence of dystrophin predicts a rod-shaped cytoskeletal protein

    著者: M. Koenig, Anthony P. Monaco, Louis M. Kunkel - Cell 1988 被引用: 1,524

  13. Genetic and Functional Analyses of SHANK2 Mutations Suggest a Multiple Hit Model of Autism Spectrum Disorders

    著者: Claire S. Leblond, Jutta Heinrich, Richard Delorme, Christian Proepper, Catalina Betancur, Guillaume Huguet, Marina Konyukh, Pauline Chaste, Elodie Ey, Maria Råstam, Henrik Anckarsäter, Gudrun Nygren, I. Carina Gillberg, Jonas Melke, Roberto Toro, Béatrice Regnault, Fabien Fauchereau, Oriane Mercati, Nathalie Lemière, David Skuse, Martin Poot, Richard Holt, Anthony P. Monaco, Irma Järvelä, Katri Kantojärvi, Raija Vanhala, Sarah Curran, David Collier, Patrick Bolton, Andreas G. Chiocchetti, Sabine M. Klauck, Fritz Poustka, Christine M. Freitag, Regina Waltes, Marnie Kopp, Eftichia Duketis, Elena Bacchelli, Fiorella Minopoli, Liliana Ruta, Agatino Battaglia, Luigi Mazzone, Elena Maestrini, Ana Filipa Sequeira, Bárbara Oliveira, Astrid M. Vicente, Guiomar Oliveira, Dalila Pinto, Stephen W. Scherer, Diana Zélénika, Marc Délepine, Mark Lathrop, Dominique Bonneau, Vincent Guinchat, Françoise Devillard, Brigitte Assouline, Marie–Christine Mouren, Marion Leboyer, Christopher Gillberg, Tobias M. Boeckers, Thomas Bourgeron - PLoS Genetics 2012 被引用: 443

  14. Donation After Circulatory Death

    著者: Paul Morrissey, Anthony P. Monaco - Transplantation 2013 被引用: 239

  15. Analysis of the human VPS13 gene family

    著者: Antonio Velayos‐Baeza, Andrea Vettori, Richard R. Copley, Carol Dobson‐Stone, Anthony P. Monaco - Genomics 2004 被引用: 223

  16. Identification of FOXP2 Truncation as a Novel Cause of Developmental Speech and Language Deficits

    著者: Kay MacDermot, Elena Bonora, Nuala Sykes, Anne-Marie Coupe, Cecilia Lai, Sonja C. Vernes, Faraneh Vargha‐Khadem, Fiona McKenzie, Robert L. Smith, Anthony P. Monaco, Simon E. Fisher - The American Journal of Human Genetics 2005 被引用: 416

  17. A conserved sorting-associated protein is mutant in chorea-acanthocytosis

    著者: Luca Rampoldi, Carol Dobson‐Stone, Justin P. Rubio, Adrian Danek, R. M. Chalmers, Nicholas Wood, Christine Verellen, Xavier Ferrer, Alessandro Malandrini, Gian Maria Fabrizi, Robert H. Brown, Jeffery M. Vance, Margaret A. Pericak‐Vance, Gabrielle Rudolf, Sophie Carré, Elisa Alonso, M. Manfredi, Andrea H. Németh, Anthony P. Monaco - Nature Genetics 2001 被引用: 356

  18. A Functional Genetic Link between Distinct Developmental Language Disorders

    著者: Sonja C. Vernes, Dianne F. Newbury, Brett S. Abrahams, Laura Winchester, Jérôme Nicod, Matthias Groszer, Maricela Alarcón, Peter L. Oliver, Kay E. Davies, Daniel H. Geschwind, Anthony P. Monaco, Simon E. Fisher - New England Journal of Medicine 2008 被引用: 691

  19. Expression of four alternative dystrophin transcripts in brain regions regulated by different promoters

    著者: Dariusz C. Górecki, Anthony P. Monaco, Jonathan M.J. Derry, Ann P. Walker, Eric A. Barnard, Pene J. Barnard - Human Molecular Genetics 1992 被引用: 259

  20. Association Between X-Linked Mixed Deafness and Mutations in the POU Domain Gene POU3F4

    著者: Yvette J.M. de Kok, Silvère M. van der Maarel, Maria Bitner‐Glindzicz, Irene Huber, Anthony P. Monaco, S Malcolm, Marcus Pembrey, Hans‐Hilger Ropers, Frans P.M. Cremers - Science 1995 被引用: 449

  21. LRRTM1 on chromosome 2p12 is a maternally suppressed gene that is associated paternally with handedness and schizophrenia

    著者: Clyde Francks, Shinji Maegawa, Juha Laurén, Brett S. Abrahams, Antonio Velayos‐Baeza, Sarah E. Medland, Stefano Colella, Matthias Groszer, E Z McAuley, Tara M. Caffrey, Tõnis Timmusk, Priit Pruunsild, Indrek Koppel, Penelope A. Lind, N Matsumoto-Itaba, Jérôme Nicod, Lan Xiong, Ridha Joober, Wolfgang Enard, Benjamin H. Krinsky, Eiji Nanba, A.J. Richardson, Brien P. Riley, Nicholas G. Martin, Stephen M. Strittmatter, HJ Möller, Dan Rujescu, David St Clair, Pierandrea Muglia, Johannes L. Roos, Simon E. Fisher, Richard Wade‐Martins, Guy A. Rouleau, John Stein, Maria Karayiorgou, Dan Geschwind, Jiannis Ragoussis, Kenneth S. Kendler, Matti S. Airaksinen, Mitsuo Oshimura, Lynn E. DeLisi, Anthony P. Monaco - Molecular Psychiatry 2007 被引用: 360

  22. Common Variants in Left/Right Asymmetry Genes and Pathways Are Associated with Relative Hand Skill

    著者: William M. Brandler, Andrew P. Morris, David M. Evans, Thomas Scerri, John P. Kemp, Nicholas J. Timpson, Beaté St Pourcain, George Davey Smith, Susan M. Ring, John Stein, Anthony P. Monaco, Joel B. Talcott, Simon E. Fisher, Caleb Webber, Silvia Paracchini - PLoS Genetics 2013 被引用: 179

  23. High-density SNP association study and copy number variation analysis of the AUTS1 and AUTS5 loci implicate the IMMP2L–DOCK4 gene region in autism susceptibility

    著者: IMGSAC, Elena Maestrini, Alistair T. Pagnamenta, Janine A. Lamb, Elena Bacchelli, Nuala Sykes, Inês Sousa, Claudio Toma, Gabrielle Barnby, Helen Butler, Laura Winchester, Thomas Scerri, Fiorella Minopoli, Jennifer Reichert, Guiqing Cai, Joseph D. Buxbaum, Olena Korvatska, Gerry Schellenberg, Géraldine Dawson, Annelies de Bildt, Ruud B. Minderaa, E Mulder, Andrew P. Morris, Anthony Bailey, Anthony P. Monaco - Molecular Psychiatry 2009 被引用: 144

  24. Isolation of a candidate gene for Menkes disease that encodes a potential heavy metal binding protein

    著者: Jamel Chelly, Zeynep Tümer, T. Tønnesen, Anne Petterson, Yumiko Ishikawa-Brush, Niels Tommerup, Nina Horn, Anthony P. Monaco - Nature Genetics 1993 被引用: 728