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Anthony P. Monaco

Active 1962–2022

147
Papers
39,574
Citations
106
h-index
147
i10-index

Citations

Citations per year for Anthony P. Monaco1962: 1 citations1965: 3 citations1966: 10 citations1967: 19 citations1968: 9 citations1969: 4 citations1970: 2 citations1971: 3 citations1973: 4 citations1974: 1 citations1975: 1 citations1976: 9 citations1977: 2 citations1980: 1 citations1981: 1 citations1982: 1 citations1984: 4 citations1985: 8 citations1986: 37 citations1987: 116 citations1988: 162 citations1989: 172 citations1990: 141 citations1991: 135 citations1992: 156 citations1993: 163 citations1994: 135 citations1995: 170 citations1996: 184 citations1997: 162 citations1998: 201 citations1999: 242 citations2000: 258 citations2001: 264 citations2002: 320 citations2003: 336 citations2004: 358 citations2005: 363 citations2006: 379 citations2007: 255 citations2008: 269 citations2009: 294 citations2010: 337 citations2011: 307 citations2012: 292 citations2013: 308 citations2014: 235 citations2015: 293 citations2016: 209 citations2017: 194 citations2018: 141 citations2019: 530 citations2020: 448 citations2021: 525 citations2022: 352 citations2023: 203 citations2024: 313 citations2025: 112 citations2026: 3 citations1963–1964: no citations, so these years are not shown1972: no citations, so this year is not shown1978–1979: no citations, so these years are not shown1983: no citations, so this year is not shown

Citation sources

Countries

World map of the countries and regions citing this authorUnited States: 3,679 citing papers, 32.1% of this breakdownUnited Kingdom: 1,241 citing papers, 10.8% of this breakdownGermany: 707 citing papers, 6.2% of this breakdownCanada: 618 citing papers, 5.4% of this breakdownFrance: 602 citing papers, 5.3% of this breakdownItaly: 487 citing papers, 4.2% of this breakdownNetherlands: 444 citing papers, 3.9% of this breakdownJapan: 398 citing papers, 3.5% of this breakdownAustralia: 336 citing papers, 2.9% of this breakdownChina: 328 citing papers, 2.9% of this breakdownSwitzerland: 225 citing papers, 2% of this breakdownBelgium: 196 citing papers, 1.7% of this breakdown
0%32.1%Other 19.1%

Institutions

Fields

  • Biochemistry, Genetics and Molecular Biology45.3%
  • Neuroscience19.9%
  • Medicine17.8%
  • Psychology5.5%
  • Immunology and Microbiology4.6%
  • Nursing3.5%
  • Other3.4%

Topics

  • 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%
  • Other80.1%

Coauthors

All papers

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

    Authors: 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 cited by 664

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

    Authors: 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 and 12 more - The American Journal of Human Genetics 2014 cited by 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

    Authors: M. Koenig, Eric P. Hoffman, Corlee J. Bertelson, Anthony P. Monaco, C. Feener, Louis M. Kunkel - Cell 1987 cited by 2,407

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

    Authors: Cecilia Lai, Simon E. Fisher, Jane A. Hurst, Faraneh Vargha‐Khadem, Anthony P. Monaco - Nature 2001 cited by 2,087

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

    Authors: 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 cited by 163

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

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

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

    Authors: 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 cited by 133

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

    Authors: 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 cited by 130

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

    Authors: Anthony P. Monaco, Corlee J. Bertelson, Sabina Liechti‐Gallati, Hans Moser, Louis M. Kunkel - Genomics 1988 cited by 1,192

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

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

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

    Authors: 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 cited by 734

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

    Authors: M. Koenig, Anthony P. Monaco, Louis M. Kunkel - Cell 1988 cited by 1,524

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

    Authors: 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 cited by 443

  14. Donation After Circulatory Death

    Authors: Paul Morrissey, Anthony P. Monaco - Transplantation 2013 cited by 239

  15. Analysis of the human VPS13 gene family

    Authors: Antonio Velayos‐Baeza, Andrea Vettori, Richard R. Copley, Carol Dobson‐Stone, Anthony P. Monaco - Genomics 2004 cited by 223

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

    Authors: 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 cited by 416

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

    Authors: 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 cited by 356

  18. A Functional Genetic Link between Distinct Developmental Language Disorders

    Authors: 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 cited by 691

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

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

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

    Authors: 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 cited by 449

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

    Authors: 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 cited by 360

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

    Authors: 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 cited by 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

    Authors: 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 cited by 144

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

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