Richard Anney

Active 2005–2025

67
Papers
22,685
Citations
53
h-index
65
i10-index

Citations

Citations per year for Richard Anney1992: 1 citations1997: 1 citations1999: 2 citations2000: 1 citations2005: 1 citations2006: 4 citations2007: 6 citations2008: 23 citations2009: 44 citations2010: 106 citations2011: 184 citations2012: 191 citations2013: 231 citations2014: 309 citations2015: 352 citations2016: 254 citations2017: 341 citations2018: 311 citations2019: 833 citations2020: 991 citations2021: 1,208 citations2022: 864 citations2023: 598 citations2024: 821 citations2025: 341 citations2026: 15 citations1993–1996: no citations, so these years are not shown1998: no citations, so this year is not shown2001–2004: no citations, so these years are not shown

Citation sources

Countries

World map of the countries and regions citing this authorUnited States: 3,281 citing papers, 23.3% of this breakdownUnited Kingdom: 1,420 citing papers, 10.1% of this breakdownGermany: 795 citing papers, 5.7% of this breakdownChina: 768 citing papers, 5.5% of this breakdownCanada: 683 citing papers, 4.9% of this breakdownNetherlands: 670 citing papers, 4.8% of this breakdownAustralia: 624 citing papers, 4.4% of this breakdownItaly: 448 citing papers, 3.2% of this breakdownSweden: 436 citing papers, 3.1% of this breakdownFrance: 395 citing papers, 2.8% of this breakdownSpain: 353 citing papers, 2.5% of this breakdownDenmark: 345 citing papers, 2.4% of this breakdown
0%23.3%Other 27.3%

Fields

  • Biochemistry, Genetics and Molecular Biology44.5%
  • Neuroscience27.7%
  • Medicine19%
  • Psychology5.6%
  • Environmental Science0.7%
  • Immunology and Microbiology0.5%
  • Other2%

Topics

  • Autism Spectrum Disorder Research9.2%
  • Genetics and Neurodevelopmental Disorders8.7%
  • Genetic Associations and Epidemiology7%
  • Genomic variations and chromosomal abnormalities3.7%
  • Attention Deficit Hyperactivity Disorder3.5%
  • Genomics and Rare Diseases3.2%
  • Other64.7%

Coauthors

All papers

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  1. Identification of common genetic risk variants for autism spectrum disorder

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Mads V. Hollegaard, Sigrun Hope, Daniel P. Howrigan, Hailiang Huang, Christina M. Hultman, Lambertus Klei, Julian Maller, Joanna Martin, Alicia R. Martin, Jennifer L. Moran, Mette Nyegaard, Terje Nærland, Duncan S. Palmer, Aarno Palotie, Carsten Bøcker Pedersen, Marianne Giørtz Pedersen, Timothy dPoterba, Jesper Buchhave Poulsen, Beaté St Pourcain, Per Qvist, Karola Rehnström, Abraham Reichenberg, Jennifer Reichert, Elise Robinson, Kathryn Roeder, Panos Roussos, Evald Sæmundsen, Sven Sandin, F. Kyle Satterstrom, George Davey Smith, Hreinn Stefánsson, Stacy Steinberg, Christine Stevens, Patrick F. Sullivan, Patrick Turley, G. Bragi Walters, Xinyi Xu, Kāri Stefánsson, Daniel H. Geschwind, Merete Nordentoft, David M. Hougaard, Thomas Werge, Ole Mors, Preben Bo Mortensen, Benjamin M. Neale, Mark J. Daly, Anders D. Børglum - Nature Genetics 2019 cited by 2,632

  2. Large-Scale Exome Sequencing Study Implicates Both Developmental and Functional Changes in the Neurobiology of Autism

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Ángel Carracedo, Marcus C.Y. Chan, Andreas G. Chiocchetti, Brian Hon‐Yin Chung, Hilary Coon, Michael L. Cuccaro, Aurora Currò, Bernardo Dalla Bernardina, Ryan N. Doan, Enrico Domenici, Shan Dong, Chiara Fallerini, Montse Fernández‐Prieto, Giovanni Battista Ferrero, Christine M. Freitag, Menachem Fromer, J. Jay Gargus, Daniel H. Geschwind, Elisa Giorgio, Javier González‐Peñas, Stephen J. Guter, Danielle Halpern, Emily Hansen‐Kiss, Xin He, Gail E. Herman, Irva Hertz‐Picciotto, David M. Hougaard, Christina M. Hultman, Iuliana Ionita‐Laza, Suma Jacob, Jesslyn Jamison, Astanand Jugessur, Miia Kaartinen, Gun Peggy Knudsen, A lexander Kolevzon, Itaru Kushima, So Lun Lee, Terho Lehtimäki, Elaine T. Lim, Carla Lintas, W. Ian Lipkin, Diego Lopergolo, Fátima Lopes, Yunin Ludeña, Patrı́cia Maciel, Per Magnus, Behrang Mahjani, Nell Maltman, Dara S. Manoach, Gal Meiri, Idan Menashe, Judith Miller, Nancy J. Minshew, Eduarda Morgana Silva Montenegro, Danielle de Paula Moreira, Eric M. Morrow, Ole Mors, Preben Bo Mortensen, Matthew W. Mosconi, Pierandrea Muglia, Benjamin M. Neale, Merete Nordentoft, Norio Ozaki, Aarno Palotie, Mara Parellada, Maria Rita Passos‐Bueno, Margaret A. Pericak‐Vance, Antonio M. Persico, Isaac N. Pessah, Kaija Puura and 90 more - Cell 2020 cited by 2,501

  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. Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Peter A Holmans, Ian Jones, George K Kirov, Sarah E. Bergen, Ivan Nikolov, Michael J Owen, Peter Holmans, Stanley Zammit, Katherine Gordon‐Smith, Nicholas Craddock, Lyudmila Georgieva, John S Witte, Detelina Grozeva, Ian D. Jones, Marian L. Hamshere, Ole A Andreassen, Srdjan Djurovic, Morten Mattingsdal, Michael O‘Donovan, Michael J. Owen, Anita Thapar, Robert C Thompson, Stanley J Watson, Nicholas Craddock, Lyudmila Georgieva, Nicholas Bass, Ian D. Jones, Hugh Gurling, Radhika Kandaswamy, Michael O‘Donovan, Michael J. Owen, Anita Thapar, Michael E. Goddard, Michael E. Goddard, Richard Anney, Devin Absher, Richard M. Myers, Ingrid Agartz, Srdjan Djurovic, Morten Mattingsdal, Ole A. Andreassen, Ingrid Melle, Ingrid Agartz, Robert C. Thompson, Stanley J. Watson, Huda Akil, Fan Meng, Farooq Amin, Ole A. Andreassen, Ingrid Melle, Robert Krasucki, Adebayo Anjorin, Khalid Choudhury, Jacob Lawrence, Hugh Gurling, Jonathan Pimm, Nicholas Bass, Radhika Kandaswamy, Andrew McQuillin, Vinay Puri, Elaine Kenny, Aiden Corvin, Paul Cormican, Derek W. Morris, Richard Anney, Emma M. Quinn, Gary Donohoe, Michael Gill, Louise Gallagher, Dan E. Arking and 270 more - Nature Genetics 2013 cited by 2,353

  5. Functional impact of global rare copy number variation in autism spectrum disorders

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Emily L. Crawford, Andrew Crossett, Cheryl Cytrynbaum, Géraldine Dawson, Maretha Jonge, Richard Delorme, Irene Drmic, Eftichia Duketis, Frederico Duque, Annette Estes, Penny Farrar, Bridget A. Fernandez, Susan E. Folstein, Éric Fombonne, Christine M. Freitag, John R. Gilbert, Christopher Gillberg, Joseph Glessner, Jeremy Goldberg, Andrew Green, Jonathan Green, Stephen J. Guter, Håkon Håkonarson, Elizabeth A. Heron, Matthew Hill, Richard Holt, Jennifer Howe, Gillian Hughes, Vanessa Hus, Roberta Igliozzi, Cecilia Kim, Sabine M. Klauck, A lexander Kolevzon, Olena Korvatska, Vlad Kustanovich, Clara Lajonchere, Janine A. Lamb, Magdalena Laskawiec, Marion Leboyer, Ann Le Couteur, Bennett Leventhal, Anath C. Lionel, Xiao-Qing Liu, Catherine Lord, Linda Lotspeich, Sabata C. Lund, Elena Maestrini, William J. Mahoney, Carine Mantoulan, Christian R. Marshall, Helen McConachie, Christopher J. McDougle, Jane McGrath, William M. McMahon, Alison Merikangas, Ohsuke Migita, Nancy J. Minshew, Ghazala Mirza, Jeff Munson, Stanley F. Nelson, Carolyn Noakes, Abdul Noor, Gudrun Nygren, Guiomar Oliveira, Κaterina Papanikolaou, Jeremy Parr, Barbara Parrini, Tara Paton, Andrew Pickles, Marion Pilorge and 77 more - Nature 2010 cited by 2,066

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

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , 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

  7. Psychiatric genome-wide association study analyses implicate neuronal, immune and histone pathways

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , David Collier, Bryan J Mowry, Peter McGuffin, Anne Farmer, Jonna Kuntsi, Ian W. Craig, Stephen Newhouse, Stephen Newhouse, Katherine Gordon-Smith, Detelina Grozeva, Douglas M. Ruderfer, George K Kirov, Valentina Moskvina, Daniëlle Posthuma, Michael J Owen, Nigel Williams, Enda M. Byrne, Sang Lee, Nicholas Craddock, Naomi R. Wray, Pamela Sklar, Michael E Goddard, John S Witte, Tatiana Foroud, Daniel L Koller, Devin Absher, Richard M Myers, Anita Thapar, Ole A Andreassen, Ian Jones, Nigel Williams, Detelina Grozeva, Huda Akil, Peter Holmans, Michael J. Owen, Stanley J Watson, Farooq Amin, Adebayo Anjorin, Nicholas Bass, Khalid Choudhury, Hugh Gurling, Anita Thapar, Ian Jones, Nigel Williams, Pamela Sklar, Michael J. Owen, Vinay Puri, Richard Anney, Paul Cormican, Aiden Corvin, Gary J Donohoe, Louise Gallagher, John S. Witte, Daniel L. Koller, Tatiana Foroud, Richard M. Myers, Devin Absher, Srdjan Djurovic, Morten Mattingsdal, Maria H Azevedo, Ingrid Agartz, Lena Backlund, Ingrid Agartz, Huda Akil, Stanley J. Watson, Fan Meng, Robert C. Thompson, Farooq Amin, Tobias Banaschewski, Jack D Barchas and 275 more - Nature Neuroscience 2015 cited by 798

  8. Polygenic transmission disequilibrium confirms that common and rare variation act additively to create risk for autism spectrum disorders

    Authors: , , , , , , , , , , , , , , , , , , , , , , , - Nature Genetics 2017 cited by 556

  9. Autism genetics: opportunities and challenges for clinical translation

    Authors: , , , , , - Nature Reviews Genetics 2017 cited by 500

  10. Improved imputation of low-frequency and rare variants using the UK10K haplotype reference panel

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Chris Boustred, Gerome Breen, Mattia Calissano, Keren Carss, Juan P. Casas, John C. Chambers, Ruth Charlton, Krishna Chatterjee, Lu Chen, Antonio Ciampi, Sebahattin Çırak, Peter Clapham, Gail Clement, Guy Coates, Massimiliano Cocca, David Collier, Catherine Cosgrove, Tony Cox, Nick Craddock, Lucy Crooks, Sarah Curran, David Curtis, Allan Daly, Ian N.M. Day, Aaron Day-Williams, George Dedoussis, Thomas A. Down, Yuanping Du, Cornelia M. van Duijn, Ian Dunham, Sarah Edkins, Rosemary Ekong, Peter Ellis, David M. Evans, I. Sadaf Farooqi, David Fitzpatrick, Paul Flicek, James Floyd, A. Reghan Foley, Christopher S. Franklin, Marta Futema, Louise Gallagher, Paolo Gasparini, Tom R. Gaunt, Matthias Geihs, Daniel H. Geschwind, Celia M.T. Greenwood, Heather Griffin, Detelina Grozeva, Xiaosen Guo, Xueqin Guo, Hugh Gurling, Deborah Hart, Audrey E. Hendricks, Peter Holmans, Liren Huang, Tim Hubbard, Steve E. Humphries, Matthew E. Hurles, Pirro G. Hysi, Valentina Iotchkova, Aaron Isaacs, David K. Jackson, Yalda Jamshidi, Jon Johnson, Christopher Joyce, Konrad J. Karczewski, Jane Kaye, Thomas Keane, John P. Kemp and 139 more - Nature Communications 2015 cited by 385

  11. Phenotypic effects of genetic variants associated with autism

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , - Nature Medicine 2023 cited by 81

  12. 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

  13. Emotional lability in children and adolescents with attention deficit/hyperactivity disorder (ADHD): clinical correlates and familial prevalence

    Authors: , , , , , , , , , , , , , , , , , , , , , - Journal of Child Psychology and Psychiatry 2010 cited by 373

  14. Glutamatergic and GABAergic gene sets in attention-deficit/hyperactivity disorder: association to overlapping traits in ADHD and autism

    Authors: , , , , , , , , , , , , , , , , , , , , , - Translational Psychiatry 2017 cited by 145

  15. A genome-wide scan for common alleles affecting risk for autism

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Géraldine Dawson, Maretha Jonge, Richard Delorme, Irene Drmic, Eftichia Duketis, Frederico Duque, Annette Estes, Penny Farrar, Bridget A. Fernandez, Susan E. Folstein, Éric Fombonne, Christine M. Freitag, James Gilbert, C. Gillberg, Joseph Glessner, Joel O. Goldberg, Jonathan Green, Stephen J. Guter, Håkon Håkonarson, Elizabeth A. Heron, Matthew Hill, Richard Holt, Jennifer Howe, Gillian Hughes, Vanessa Hus, Roberta Igliozzi, C. Kim, Sabine M. Klauck, A lexander Kolevzon, Olena Korvatska, Vlad Kustanovich, Clara Lajonchere, Janine A. Lamb, Magdalena Laskawiec, Marion Leboyer, Ann Le Couteur, Bennett Leventhal, A. C. Lionel, Xiaoqing Liu, Catherine Lord, Linda Lotspeich, Sabata C. Lund, Elena Maestrini, William J. Mahoney, Carine Mantoulan, Christian R. Marshall, Helen McConachie, Christopher J. McDougle, Jane McGrath, William M. McMahon, Nadine Melhem, Alison Merikangas, Ohsuke Migita, Nancy J. Minshew, Ghazala Mirza, Jeff Munson, Stanley F. Nelson, C. Noakes, Abdul Noor, Gudrun Nygren, Guiomar Oliveira, Κaterina Papanikolaou, Jeremy Parr, Barbara Parrini, Tara Paton, Andrew Pickles, Joseph Piven, David J. Posey, Annemarie Poustka, Fritz Poustka and 66 more - Human Molecular Genetics 2010 cited by 588

  16. Meta-Analyses of Genome-Wide Association Studies for Postpartum Depression

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Mette Nyegaard, Antonio F. Pardiñas, Amy Perry, Nazmus Saquib, Aladdin H. Shadyab, Alexander Viktorin, Ole A. Andreassen, Tim B. Bigdeli, Lea K. Davis, Cindy‐Lee Dennis, Arianna Di Florio, Caroline Dubertret, Yen‐Chen Anne Feng, Benício N. Frey, Sophie Grigoriadis, Emilie Gloaguen, Ian Jones, James L. Kennedy, Holly Krohn, Theodora Kunovac Kallak, Yun Li, Nicholas G. Martin, Andrew M. McIntosh, Jeannette Milgrom, Trine Munk‐Olsen, Tim F. Oberlander, Catherine M. Olsen, Nicolás Ramoz, Ted Reichborn‐Kjennerud, Emma Robertson Blackmore, David Rubinow, Alkistis Skalkidou, Jordan W. Smoller, Dan J. Stein, Zachary N. Stowe, Valerie H. Taylor, Sarah Tebeka, Martin Tesli, Ryan J. Van Lieshout, Edwin J. C. G. van den Oord, Simone N. Vigod, Thomas Werge, Lars T. Westlye, David C. Whiteman, Heather J. Zar, Naomi R. Wray, Samantha Meltzer‐Brody, Patrick Sullivan - American Journal of Psychiatry 2023 cited by 66

  17. A Genetic Investigation of Sex Bias in the Prevalence of Attention-Deficit/Hyperactivity Disorder

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Sarah L. Elson, Pierre Fontanillas, Nicholas A. Furlotte, David A. Hinds, Bethann S. Hromatka, Karen E. Huber, Aaron Kleinman, Nadia K. Litterman, Matthew H. McIntyre, Joanna L. Mountain, Carrie A. M. Northover, Steven J. Pitts, J. Fah Sathirapongsasuti, Olga V. Sazonova, Janie F. Shelton, Suyash Shringarpure, Chao Tian, Joyce Y. Tung, Vladimir Vacic, Catherine H. Wilson, Özgür Albayrak, Richard Anney, Alejandro Arias Vásquez, María J. Arranz, Philip Asherson, Tobias Banaschewski, Tobias Banaschewski, Claiton H.D. Bau, Joseph Biederman, Preben Bo Mortensen, Anders D. Børglum, Jan K. Buitelaar, Miguel Casas, Alice Charach, Bru Cormand, Jennifer Crosbie, Soeren Dalsgaard, Mark J. Daly, Ditte Demontis, Astrid Dempfle, Alysa E. Doyle, Richard P. Ebstein, Josephine Elia, Stephen V. Faraone, Stephen V. Faraone, Manuel Föcker, Barbara Franke, Christine M. Freitag, Joel Gelernter, Michael Gill, Eugênio H. Grevet, Jan Haavik, Håkon Håkonarson, Ziarih Hawi, Johannes Hebebrand, Beate Herpertz‐Dahlmann, Amaia Hervás, Anke Hinney, Sarah Hohmann, Peter Holmans, Mara Helena Hutz, Abel Ickowitz, Stefan Johansson, Lindsey Kent, Sarah Kittel‐Schneider, Henry R. Kranzler, Jonna Kuntsi, Nanda Lambregts-Rommelse, K. Langley, Gerd Lehmkuhl and 98 more - Biological Psychiatry 2017 cited by 201

  18. A Genetics-First Approach to Dissecting the Heterogeneity of Autism: Phenotypic Comparison of Autism Risk Copy Number Variants

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Marianne B. M. van den Bree - American Journal of Psychiatry 2021 cited by 102

  19. Novel Insight Into the Etiology of Autism Spectrum Disorder Gained by Integrating Expression Data With Genome-wide Association Statistics

    Authors: , , , , , , , , , - Biological Psychiatry 2019 cited by 96

  20. Genetic common variants associated with cerebellar volume and their overlap with mental disorders: a study on 33,265 individuals from the UK-Biobank

    Authors: , , , , , , , - Molecular Psychiatry 2022 cited by 50

  21. Characterizing Developmental Trajectories and the Role of Neuropsychiatric Genetic Risk Variants in Early-Onset Depression

    Authors: , , , , , , - JAMA Psychiatry 2018 cited by 168

  22. Genome-wide copy number variation study associates metabotropic glutamate receptor gene networks with attention deficit hyperactivity disorder

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Herbert Roeyers, Jan K. Buitelaar, Klaus‐Peter Lesch, Tobias Banaschewski, Richard P. Ebstein, Fernando Mulas, Robert D. Oades, Joseph A. Sergeant, Edmund Sonuga‐Barke, Tobias Renner, Marcel Romanos, Jasmin Romanos, Andreas Warnke, Susanne Walitza, Jobst Meyer, Haukur Pálmason, Christiane Seitz, Sandra K. Loo, Susan L. Smalley, Joseph Biederman, Lindsey Kent, Philip Asherson, Richard Anney, J. William Gaynor, Philip Shaw, Marcella Devoto, Peter S. White, Struan F.A. Grant, Joseph D. Buxbaum, Judith L. Rapoport, Nigel M Williams, Stanley F. Nelson, Stephen V. Faraone, Håkon Håkonarson - Nature Genetics 2011 cited by 405

  23. Genome‐wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , - American Journal of Medical Genetics Part B Neuropsychiatric Genetics 2008 cited by 390

  24. Genetic determinants of common epilepsies: a meta-analysis of genome-wide association studies

    Authors: - The Lancet Neurology 2014 cited by 309