Richard Anney

2005–2025 年に発表

67
論文数
22,685
被引用数
53
h 指数
65
i10 指数

被引用数

Richard Anney の年別被引用数1992 年: 被引用 1 件1997 年: 被引用 1 件1999 年: 被引用 2 件2000 年: 被引用 1 件2005 年: 被引用 1 件2006 年: 被引用 4 件2007 年: 被引用 6 件2008 年: 被引用 23 件2009 年: 被引用 44 件2010 年: 被引用 106 件2011 年: 被引用 184 件2012 年: 被引用 191 件2013 年: 被引用 231 件2014 年: 被引用 309 件2015 年: 被引用 352 件2016 年: 被引用 254 件2017 年: 被引用 341 件2018 年: 被引用 311 件2019 年: 被引用 833 件2020 年: 被引用 991 件2021 年: 被引用 1,208 件2022 年: 被引用 864 件2023 年: 被引用 598 件2024 年: 被引用 821 件2025 年: 被引用 341 件2026 年: 被引用 15 件1993〜1996 年は被引用が無いため表示していません1998 年は被引用が無いため表示していません2001〜2004 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 3,281 件、この内訳の 23.3%イギリス: 引用元論文 1,420 件、この内訳の 10.1%ドイツ: 引用元論文 795 件、この内訳の 5.7%中国: 引用元論文 768 件、この内訳の 5.5%カナダ: 引用元論文 683 件、この内訳の 4.9%オランダ: 引用元論文 670 件、この内訳の 4.8%オーストラリア: 引用元論文 624 件、この内訳の 4.4%イタリア: 引用元論文 448 件、この内訳の 3.2%スウェーデン: 引用元論文 436 件、この内訳の 3.1%フランス: 引用元論文 395 件、この内訳の 2.8%スペイン: 引用元論文 353 件、この内訳の 2.5%デンマーク: 引用元論文 345 件、この内訳の 2.4%
0%23.3%その他 27.3%

分野

  • Biochemistry, Genetics and Molecular Biology44.5%
  • Neuroscience27.7%
  • Medicine19%
  • Psychology5.6%
  • Environmental Science0.7%
  • Immunology and Microbiology0.5%
  • その他2%

トピック

  • 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%
  • その他64.7%

共著者

全論文

検索で開く
  1. Identification of common genetic risk variants for autism spectrum disorder

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , 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 被引用: 2,632

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

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , 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 ほか 90 名 - Cell 2020 被引用: 2,501

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

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , 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 ほか 506 名 - Cell 2019 被引用: 1,516

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

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , 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 ほか 270 名 - Nature Genetics 2013 被引用: 2,353

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

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , 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 ほか 77 名 - Nature 2010 被引用: 2,066

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

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , 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

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

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , 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 ほか 275 名 - Nature Neuroscience 2015 被引用: 798

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

    著者: , , , , , , , , , , , , , , , , , , , , , , , - Nature Genetics 2017 被引用: 556

  9. Autism genetics: opportunities and challenges for clinical translation

    著者: , , , , , - Nature Reviews Genetics 2017 被引用: 500

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

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , 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 ほか 139 名 - Nature Communications 2015 被引用: 385

  11. Phenotypic effects of genetic variants associated with autism

    著者: , , , , , , , , , , , , , , , , , , , , , , , , - Nature Medicine 2023 被引用: 81

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

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , 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 ほか 11 名 - Nature Genetics 2022 被引用: 55

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

    著者: , , , , , , , , , , , , , , , , , , , , , - Journal of Child Psychology and Psychiatry 2010 被引用: 373

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

    著者: , , , , , , , , , , , , , , , , , , , , , - Translational Psychiatry 2017 被引用: 145

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

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , 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 ほか 66 名 - Human Molecular Genetics 2010 被引用: 588

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

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , 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 被引用: 66

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

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , 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 ほか 98 名 - Biological Psychiatry 2017 被引用: 201

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

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Marianne B. M. van den Bree - American Journal of Psychiatry 2021 被引用: 102

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

    著者: , , , , , , , , , - Biological Psychiatry 2019 被引用: 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

    著者: , , , , , , , - Molecular Psychiatry 2022 被引用: 50

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

    著者: , , , , , , - JAMA Psychiatry 2018 被引用: 168

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

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , 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 被引用: 405

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

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , - American Journal of Medical Genetics Part B Neuropsychiatric Genetics 2008 被引用: 390

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

    著者: - The Lancet Neurology 2014 被引用: 309