Edwin H. Cook

Active 1975–2025

159
Papers
51,507
Citations
110
h-index
156
i10-index

Citations

Citations per year for Edwin H. Cook1965: 1 citations1975: 1 citations1976: 2 citations1977: 3 citations1978: 2 citations1979: 3 citations1980: 9 citations1981: 3 citations1983: 9 citations1984: 4 citations1985: 12 citations1986: 4 citations1987: 6 citations1988: 10 citations1989: 13 citations1990: 30 citations1991: 33 citations1992: 51 citations1993: 31 citations1994: 31 citations1995: 24 citations1996: 30 citations1997: 42 citations1998: 59 citations1999: 93 citations2000: 147 citations2001: 185 citations2002: 203 citations2003: 219 citations2004: 347 citations2005: 382 citations2006: 524 citations2007: 446 citations2008: 562 citations2009: 663 citations2010: 668 citations2011: 655 citations2012: 708 citations2013: 781 citations2014: 786 citations2015: 779 citations2016: 658 citations2017: 681 citations2018: 522 citations2019: 1,532 citations2020: 1,439 citations2021: 1,421 citations2022: 974 citations2023: 696 citations2024: 987 citations2025: 396 citations2026: 24 citations1966–1974: no citations, so these years are not shown1982: no citations, so this year is not shown

Citation sources

Countries

World map of the countries and regions citing this authorUnited States: 7,666 citing papers, 34.7% of this breakdownUnited Kingdom: 2,010 citing papers, 9.1% of this breakdownCanada: 1,256 citing papers, 5.7% of this breakdownGermany: 973 citing papers, 4.4% of this breakdownChina: 898 citing papers, 4.1% of this breakdownItaly: 794 citing papers, 3.6% of this breakdownNetherlands: 787 citing papers, 3.5% of this breakdownAustralia: 746 citing papers, 3.4% of this breakdownFrance: 665 citing papers, 3% of this breakdownJapan: 488 citing papers, 2.2% of this breakdownSweden: 442 citing papers, 2% of this breakdownSpain: 435 citing papers, 2% of this breakdown
0%34.7%Other 22.3%

Fields

  • Neuroscience46.2%
  • Biochemistry, Genetics and Molecular Biology28.1%
  • Medicine14.6%
  • Psychology8.2%
  • Agricultural and Biological Sciences0.4%
  • Environmental Science0.4%
  • Other2.1%

Topics

  • Autism Spectrum Disorder Research16.6%
  • Genetics and Neurodevelopmental Disorders8.9%
  • Genomic variations and chromosomal abnormalities3.2%
  • Family and Disability Support Research3.1%
  • Attention Deficit Hyperactivity Disorder2.8%
  • Child Nutrition and Feeding Issues2.6%
  • Other62.8%

Coauthors

All papers

Open in search
  1. The Autism Diagnostic Observation Schedule—Generic: A Standard Measure of Social and Communication Deficits Associated with the Spectrum of Autism

    Authors: , , , , , , , - Journal of Autism and Developmental Disorders 2000 cited by 7,557

  2. Rare coding variation provides insight into the genetic architecture and phenotypic context of autism

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Enrico Domenici, Giovanni Battista Ferrero, J. Jay Gargus, Gail E. Herman, Irva Hertz‐Picciotto, Patrı́cia Maciel, Dara S. Manoach, Maria Rita Passos‐Bueno, Antonio M. Persico, Alessandra Renieri, James S. Sutcliffe, Flora Tassone, Elisabetta Trabetti, Gabriele da Silva Campos, Simona Cardaropoli, Diana Carli, Marcus C.Y. Chan, Chiara Fallerini, Elisa Giorgio, Ana Cristina De Sanctis Girardi, Emily Hansen‐Kiss, So Lun Lee, Carla Lintas, Yunin Ludeña, Rachel Nguyen, Lisa Pavinato, Margaret A. Pericak‐Vance, Isaac N. Pessah, Rebecca J. Schmidt, Moyra Smith, Claudia Ismania Samogy Costa, Slavica Trajkova, Jaqueline Y. T. Wang, Mullin H.C. Yu, Branko Aleksić, Mykyta Artomov, Elisa Benetti, Monica Biscaldi-Schafer, Anders D. Børglum, Ángel Carracedo, Andreas G. Chiocchetti, Hilary Coon, Ryan N. Doan, Montse Fernández‐Prieto, Christine M. Freitag, Sherif Gerges, Stephen J. Guter, David M. Hougaard, Christina M. Hultman, Suma Jacob, Miia Kaartinen, A lexander Kolevzon, Itaru Kushima, Terho Lehtimäki, Caterina Lo Rizzo, Nell Maltman, Marianna Manara, Gal Meiri, Idan Menashe, Judith Miller, Nancy J. Minshew, Matthew W. Mosconi, Norio Ozaki, Aarno Palotie, Mara Parellada, Kaija Puura, Abraham Reichenberg, Sven Sandin, Stephen W. Scherer, Sabine Schlitt and 17 more - Nature Genetics 2022 cited by 617

  3. Genomic Relationships, Novel Loci, and Pleiotropic Mechanisms across Eight Psychiatric Disorders

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Clement C. Zai, Esben Agerbo, María J. Arranz, Philip Asherson, Marie Bækvad‐Hansen, Gísli Baldursson, Mark A. Bellgrove, Richard A. Belliveau, Jan K. Buitelaar, Christie L. Burton, Jonas Bybjerg‐Grauholm, Miguel Casas, Felecia Cerrato, Kimberly Chambert, Claire Churchhouse, Bru Cormand, Jennifer Crosbie, Søren Dalsgaard, Ditte Demontis, Alysa E. Doyle, Ashley Dumont, Josephine Elia, Jakob Grove, Ólafur Ó. Guðmundsson, Jan Haavik, Håkon Håkonarson, Christine Søholm Hansen, Catharina A. Hartman, Ziarih Hawi, Amaia Hervás, David M. Hougaard, Daniel P. Howrigan, Hailiang Huang, Jonna Kuntsi, K. Langley, Klaus‐Peter Lesch, Patrick W. L. Leung, Sandra K. Loo, Joanna Martin, Alicia R. Martin, James J. McGough, Sarah E. Medland, Jennifer L. Moran, Ole Mors, Preben Bo Mortensen, Robert D. Oades, Duncan S. Palmer, Carsten Bøcker Pedersen, Marianne G. Pedersen, Triinu Peters, Timothy Poterba, Jesper Buchhave Poulsen, Josep Antoni Ramos‐Quiroga, Andreas Reif, Marta Ribasés, Aribert Rothenberger, Paula Rovira, Cristina Sánchez‐Mora, F. Kyle Satterstrom, Russell Schachar, María Soler Artigas, Stacy Steinberg, Hreinn Stefánsson, Patrick Turley, G. Bragi Walters, Thomas Werge, Tetyana Zayats, Dan E. Arking, Francesco Bettella, Joseph D. Buxbaum and 506 more - Cell 2019 cited by 1,516

  4. Synaptic, transcriptional and chromatin genes disrupted in autism

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Eftichia Duketis, Bridget A. Fernandez, Louise Gallagher, Evan Geller, Stephen J. Guter, R. Sean Hill, Iuliana Ionita‐Laza, Patricia González, Helena Kilpinen, Sabine M. Klauck, A lexander Kolevzon, Irene Lee, Jing Lei, Terho Lehtimäki, Chiao‐Feng Lin, Avi Ma’ayan, Christian R. Marshall, Alison McInnes, Benjamin M. Neale, Michael J. Owen, Norio Ozaki, Mara Parellada, Jeremy Parr, Shaun Purcell, Kaija Puura, Deepthi Rajagopalan, Karola Rehnström, Abraham Reichenberg, Aniko Sabo, Michael Sachse, Stephan Sanders, Chad Schafer, Martin Schulte‐Rüther, David Skuse, Christine Stevens, Péter Szatmári, Kristiina Tammimies, Otto Valladares, Annette Voran, Li‐San Wang, Lauren A. Weiss, A. Jeremy Willsey, Timothy W. Yu, Ryan K. C. Yuen, Edwin H. Cook, Christine M. Freitag, Michael Gill, Christina M. Hultman, Thomas Lehner, Aarno Palotie, Gerard D. Schellenberg, Pamela Sklar, Matthew W. State, James S. Sutcliffe, Christopher A. Walsh, Stephen W. Scherer, Michael E. Zwick, Jeffrey C. Barrett, David J. Cutler, Kathryn Roeder, Bernie Devlin, Mark J. Daly, Joseph D. Buxbaum - Nature 2014 cited by 2,974

  5. Insights into Autism Spectrum Disorder Genomic Architecture and Biology from 71 Risk Loci

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Jennifer K. Lowe, Shrikant Mane, Donna M. Martin, Eric M. Morrow, Michael E. Talkowski, James S. Sutcliffe, Christopher A. Walsh, Timothy W. Yu, David H. Ledbetter, Christa Lese Martin, Edwin H. Cook, Joseph D. Buxbaum, Mark J. Daly, Bernie Devlin, Kathryn Roeder, Matthew W. State - Neuron 2015 cited by 1,547

  6. Whole genome sequencing resource identifies 18 new candidate genes for autism spectrum disorder

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Wilson W. L. Sung, Fiona J. Tsoi, John Wei, Lizhen Xu, Anne-Marie Tasse, Emily Kirby, William Van Etten, Simon Twigger, Wendy Roberts, Irene Drmic, Sanne Jilderda, Bonnie MacKinnon Modi, Barbara Kellam, Michael J. Szego, Cheryl Cytrynbaum, Rosanna Weksberg, Lonnie Zwaigenbaum, Marc Woodbury‐Smith, Jessica Brian, Lili Senman, Alana Iaboni, Krissy A.R. Doyle‐Thomas, Ann Thompson, Christina Chrysler, Jonathan Leef, Tal Savion‐Lemieux, Isabel M. Smith, Xudong Liu, Rob Nicolson, Vicki Seifer, Angie Fedele, Edwin H. Cook, Stephen R. Dager, Annette Estes, Louise Gallagher, Beth A. Malow, Jeremy Parr, Sarah Spence, Jacob Vorstman, Brendan J. Frey, James Robinson, Lisa J. Strug, Bridget A. Fernandez, Mayada Elsabbagh, Melissa T. Carter, Joachim Hallmayer, Bartha Maria Knoppers, Evdokia Anagnostou, Péter Szatmári, Robert H. Ring, David Glazer, Mathew T. Pletcher, Stephen W. Scherer - Nature Neuroscience 2017 cited by 936

  7. A framework for the interpretation of de novo mutation in human disease

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , - Nature Genetics 2014 cited by 1,123

  8. Autism genome-wide copy number variation reveals ubiquitin and neuronal genes

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Rachel M. Game, Danielle S. Rudd, Danielle Zurawiecki, Christopher J. McDougle, Lea K. Davis, Judith Miller, David J. Posey, Shana M. Michaels, A lexander Kolevzon, Jeremy M. Silverman, Raphael Bernier, Susan E. Levy, Robert T. Schultz, Géraldine Dawson, Thomas Owley, William M. McMahon, Thomas H. Wassink, John A. Sweeney, John I. Nürnberger, Hilary Coon, James S. Sutcliffe, Nancy J. Minshew, Struan F.A. Grant, Maja Bućan, Edwin H. Cook, Joseph D. Buxbaum, Bernie Devlin, Gerard D. Schellenberg, Håkon Håkonarson - Nature 2009 cited by 1,448

  9. Patterns and rates of exonic de novo mutations in autism spectrum disorders

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Lora Lewis, Yi Han, Benjamin F. Voight, Elaine T. Lim, Elizabeth J. Rossin, Andrew Kirby, Jason Flannick, Menachem Fromer, Khalid Shakir, Tim Fennell, Kiran Garimella, Eric Banks, Ryan Poplin, Stacey Gabriel, Mark A. DePristo, Jack R. Wimbish, Braden Boone, Shawn Levy, Catalina Betancur, Shamil Sunyaev, Eric Boerwinkle, Joseph D. Buxbaum, Edwin H. Cook, Bernie Devlin, Richard A. Gibbs, Kathryn Roeder, Gerard D. Schellenberg, James S. Sutcliffe, Mark J. Daly - Nature 2012 cited by 1,808

  10. Multiple Recurrent De Novo CNVs, Including Duplications of the 7q11.23 Williams Syndrome Region, Are Strongly Associated with Autism

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Anna D. McGrew, Kyle A. Meyer, William J. Moffat, John D. Murdoch, Brian J. O’Roak, G Ober, Rebecca S. Pottenger, Melanie J. Raubeson, Youeun Song, Qi Wang, Brian L. Yaspan, Timothy W. Yu, Ilana R. Yurkiewicz, Arthur L. Beaudet, Rita M. Cantor, Martin Curland, Dorothy E. Grice, Murat Günel, Richard P. Lifton, Shrikant Mane, Donna M. Martin, Chad A. Shaw, Michael Sheldon, Jay A. Tischfield, Christopher A. Walsh, Eric M. Morrow, David H. Ledbetter, Éric Fombonne, Catherine Lord, Christa Lese Martin, Andrew I. Brooks, James S. Sutcliffe, Edwin H. Cook, Daniel H. Geschwind, Kathryn Roeder, Bernie Devlin, Matthew W. State - Neuron 2011 cited by 1,292

  11. Autism Spectrum Disorders

    Authors: , , , - Neuron 2000 cited by 553

  12. A framework for an evidence-based gene list relevant to autism spectrum disorder

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , - Nature Reviews Genetics 2020 cited by 147

  13. Statistical and functional convergence of common and rare genetic influences on autism at chromosome 16p

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Celia van der Merwe, Bernie Devlin, Edwin H. Cook, Evan E. Eichler, Elisabeth Corfield, Gwen Dieleman, Gerard D. Schellenberg, Håkon Håkonarson, Hilary Coon, Isabel Dziobek, Jacob Vorstman, Jessica B. Girault, James S. Sutcliffe, Jinjie Duan, John I. Nürnberger, Joachim Hallmayer, Joseph D. Buxbaum, Joseph Piven, Lauren A. Weiss, Lea K. Davis, Magdalena Janecka, Manuel Mattheisen, Matthew W. State, Michael Gill, Mark J. Daly, Mohammed Uddin, Ole A. Andreassen, Péter Szatmári, Phil Hyoun Lee, Richard Anney, Stephan Ripke, Kyle Satterstrom, Susan L. Santangelo, Susan S. Kuo, Ludger Tebartz van Elst, Thomas Rolland, Thomas Bougeron, Tinca J. C. Polderman, Tychele N. Turner, Jack F. G. Underwood, Veera Manikandan, Vamsee Pillalamarri, Varun Warrier, Alexandra Philipsen, Andreas Reif, Anke Hinney, Bru Cormand, Claiton H.D. Bau, Diego Luiz Rovaris, Edmund Sonuga‐Barke, Elizabeth C. Corfield, Eugênio H. Grevet, Giovanni Abrahão Salum, Henrik Larsson, Jan Buitelaar, Jan Haavik, James J. McGough, Jonna Kuntsi, Josephine Elia, Klaus‐Peter Lesch, Marieke Klein, Mark A. Bellgrove, Martin Tesli, Patrick W. L. Leung, Pedro Mário Pan, Søren Dalsgaard, Sandra K. Loo, Sarah E. Medland, Stephen V. Faraone, Ted Reichborn‐Kjennerud and 11 more - Nature Genetics 2022 cited by 55

  14. Common genetic variants on 5p14.1 associate with autism spectrum disorders

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Thomas Owley, John A. Sweeney, Camille W. Brune, Rita M. Cantor, Raphael Bernier, John R. Gilbert, Michael L. Cuccaro, William M. McMahon, Judith Miller, Matthew W. State, Thomas H. Wassink, Hilary Coon, Susan E. Levy, Robert T. Schultz, John I. Nürnberger, Jonathan L. Haines, James S. Sutcliffe, Edwin H. Cook, Nancy J. Minshew, Joseph D. Buxbaum, Géraldine Dawson, Struan F.A. Grant, Daniel H. Geschwind, Margaret A. Pericak‐Vance, Gerard D. Schellenberg, Håkon Håkonarson - Nature 2009 cited by 975

  15. Recurrent 16p11.2 microdeletions in autism

    Authors: , , , , , , , , , , - Human Molecular Genetics 2007 cited by 744

  16. Copy-number variations associated with neuropsychiatric conditions

    Authors: , - Nature 2008 cited by 677

  17. Genome-wide association study of obsessive-compulsive disorder

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Maria Cristina Cavallini, Margaret A. Richter, Edwin H. Cook, James L. Kennedy, David Rosenberg, Dan J. Stein, Sian Hemmings, Christine Löchner, Amin Azzam, Denise A. Chavira, Eduardo Fournier, Helena Garrido, Brooke Sheppard, Paula Umaña, Dennis L. Murphy, Jens R. Wendland, Jeremy Veenstra‐VanderWeele, Damiaan Denys, Rianne M. Blom, Dieter Deforce, Filip Van Nieuwerburgh, H.G.M. Westenberg, Susanne Walitza, Karin Egberts, Tobias Renner, Eurı́pedes Constantino Miguel, Carolina Cappi, Ana Gabriela Hounie, Maria Conceição do Rosário, Aline S. Sampaio, Homero Vallada, Humberto Nicolini, Nuria Lanzagorta, Beatríz Camarena, Richard Delorme, Marion Leboyer, Carlos N. Pato, Michele T. Pato, Emanuel Voyiaziakis, Peter Heutink, Daniëlle C. Cath, Daniëlle Posthuma, Johannes H. Smit, Jack Samuels, O. Joseph Bienvenu, Bernadette Cullen, Abby J. Fyer, Marco A. Grados, Benjamin D. Greenberg, James T. McCracken, Mark A. Riddle, Ying Wang, Vladimir Coric, James F. Leckman, Michael H. Bloch, Christopher Pittenger, Valsamma Eapen, Donald W. Black, Roel A. Ophoff, E Strengman, Daniele Cusi, Maurizio Turiel, Francesca Frau, Fabìo Macciardi, J. Raphael Gibbs, M R Cookson, Andrew Singleton, Sampath Arepalli, M R Cookson, Allissa Dillman and 32 more - Molecular Psychiatry 2012 cited by 391

  18. Reduced behavioral flexibility in autism spectrum disorders.

    Authors: , , , , , - Neuropsychology 2013 cited by 283

  19. Combining Information From Multiple Sources in the Diagnosis of Autism Spectrum Disorders

    Authors: , , , , , , , , - Journal of the American Academy of Child & Adolescent Psychiatry 2006 cited by 572

  20. Autism as a disorder of neural information processing: directions for research and targets for therapy

    Authors: , , , , , , , , , , , , , - Molecular Psychiatry 2004 cited by 437

  21. A Bayesian framework that integrates multi-omics data and gene networks predicts risk genes from schizophrenia GWAS data

    Authors: , , , , , , , , , , , , , - Nature Neuroscience 2019 cited by 154

  22. Feedforward and Feedback Motor Control Abnormalities Implicate Cerebellar Dysfunctions in Autism Spectrum Disorder

    Authors: , , , , , - Journal of Neuroscience 2015 cited by 150

  23. Partitioning the Heritability of Tourette Syndrome and Obsessive Compulsive Disorder Reveals Differences in Genetic Architecture

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Bernadette Cullen, Dieter Deforce, Richard Delorme, Yves Dion, Christopher K. Edlund, Karin Egberts, Peter Falkai, Thomas Fernandez, Patience Gallagher, Helena Garrido, Daniel Geller, Simon Girard, Hans J. Grabe, Marco A. Grados, Benjamin D. Greenberg, Varda Gross‐Tsur, Stephen A. Haddad, Gary A. Heiman, Sian Hemmings, Ana Gabriela Hounie, Cornelia Illmann, Joseph Jankovic, Michael A. Jenike, James L. Kennedy, Robert A. King, Bárbara Kremeyer, Roger Kurlan, Nuria Lanzagorta, Marion Leboyer, James F. Leckman, Leonhard Lennertz, Chunyu Liu, Christine Löchner, Thomas L. Lowe, Fabìo Macciardi, James T. McCracken, Lauren M. McGrath, Sandra Catalina Mesa Restrepo, Rainald Moessner, Jubel Morgan, Heike Müller, Dennis L. Murphy, Allan L. Naarden, William Cornejo Ochoa, Roel A. Ophoff, Lisa Osiecki, A.J. Pakstis, Michele T. Pato, Carlos N. Pato, John Piacentini, Christopher Pittenger, Yehuda Pollak, Scott L. Rauch, Tobias Renner, Victor I. Reus, Margaret A. Richter, Mark A. Riddle, Mary M. Robertson, Roxana Romero, Maria Conceição do Rosário, David Rosenberg, Guy A. Rouleau, Stephan Ruhrmann, Andrés Ruiz‐Linares, Aline S. Sampaio, Jack Samuels, Paul Sandor, Brooke Sheppard, Harvey S. Singer, Jan Smit and 31 more - PLoS Genetics 2013 cited by 344

  24. A common X-linked inborn error of carnitine biosynthesis may be a risk factor for nondysmorphic autism

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Chad A. Shaw, Suzanne M. Leal, Edwin H. Cook, Robin P. Goin‐Kochel, Frédéric M. Vaz, Arthur L. Beaudet - National Academy of Sciences, Proceedings of the National Academy of Sciences 2012 cited by 142