George Kirov
Active 1996–2025
- Also published as
- GEORGE KIROV
- 134
- Papers
- 53,904
- Citations
- 93
- h-index
- 128
- i10-index
Citations
Citation sources
Countries
Institutions
- Harvard University1.3%
- Broad Institute1%
- King's College London0.9%
- Massachusetts General Hospital0.8%
- Cardiff University0.6%
- Karolinska Institutet0.6%
- Other94.8%
Fields
- Biochemistry, Genetics and Molecular Biology51.9%
- Medicine22.9%
- Neuroscience16.1%
- Psychology3.2%
- Immunology and Microbiology2.4%
- Computer Science0.8%
- Other2.7%
Topics
- Genetic Associations and Epidemiology10.5%
- Genetics and Neurodevelopmental Disorders3.7%
- Genomic variations and chromosomal abnormalities3.6%
- Schizophrenia research and treatment3.1%
- Genomics and Rare Diseases3.1%
- Tryptophan and brain disorders2.6%
- Other73.4%
Coauthors
- Michael J. Owen71
- Michael O‘Donovan53
- Elliott Rees35
- James Walters28
- Peter Holmans27
- Nick Craddock25
- Ian Jones20
- David Collier16
- Jennifer L. Moran16
- Nadine Norton16
- Sophie E. Legge16
- Detelina Grozeva15
- Lisa Jones15
- Michael O’Donovan15
- Nigel Williams15
- Steven A. McCarroll15
- Valentina Escott‐Price15
- Ivan Nikolov14
- Marian L. Hamshere14
- Pamela Sklar14
- Valentina Moskvina14
- Antonio F. Pardiñas12
- Hywel Williams12
- Lyudmila Georgieva12
All papers
- Biological insights from 108 schizophrenia-associated genetic loci
Authors: Jacqueline I. Goldstein, Benjamin M. Neale, Stephan Ripke, Hailiang Huang, Kai-How Farh, Hailiang Huang, Menachem Fromer, Brendan Bulik‐Sullivan, Mark J. Daly, Kimberly D. Chambert, Giulio Genovese, Jordan W. Smoller, Phil Lee, Edward M. Scolnick, Stephan Ripke, Elizabeth Bevilacqua, Jennifer L. Moran, Aarno Palotie, Tracey L. Petryshen, Richard A. Belliveau, Steven A. McCarroll, Sarah E. Bergen, Joel N. Hirschhorn, Alkes Price, Eli A. Stahl, Tõnu Esko, Aiden Corvin, Paul Cormican, Jacqueline I. Goldstein, Derek W. Morris, Benjamin M. Neale, James T. R. Walters, Hailiang Huang, Noa Carrera, Alkes L. Price, Mark J. Daly, Lyudmila Georgieva, Marian L. Hamshere, Benjamin M. Neale, Jordan W. Smoller, Andrew J. Pocklington, Paul Cormican, Aiden Corvin, Michael Gill, Gary Donohoe, Michael J. Owen, Alexander Richards, David A. Collier, Michael J. Owen, Noa Carrera, Marian L. Hamshere, Nick Craddock, David Kavanagh, Morten Mattingsdal, Peter Holmans, George Kirov, Sophie E. Legge, Valentina Escott‐Price, Nigel Williams, Andrew Pocklington, Lyudmila Georgieva, James Walters, Nick Craddock, Henrik B. Rasmussen, Michael J. Owen, Peter Holmans, David Collier, Younes Mokrab, David Collier, Tune H. Pers, Farooq Amin, Silviu A. Bacanu, Tim B. Bigdeli, Erik Söderman, Brandon K. Wormley, Martin Begemann, Christian Hammer, Srdjan Djurovic, Morten Mattingsdal, Judit Bene, Ole A. Andreassen, Anna K. Kähler, Ingrid Melle, Esben Agerbo, Preben Bo Mortensen, Esben Agerbo, Preben Bo Mortensen, Preben Bo Mortensen, Randy L. Buckner, Henrik B. Rasmussen, Ditte Demontis, Esben Agerbo, Line Olsen, Eric Strengman, Roel A. Ophoff, Guiqing Cai, Thomas Folkmann Hansen, Margot Albus, Madeline Alexander, Claudine Laurent and 197 more - Nature 2014 cited by 8,166
- Rare coding variants in ten genes confer substantial risk for schizophrenia
Authors: Tarjinder Singh, Timothy Poterba, David Curtis, Huda Akil, Mariam Al Eissa, Jack D. Barchas, Nicholas Bass, Tim B. Bigdeli, Gerome Breen, Evelyn J. Bromet, P.F. Buckley, William E. Bunney, Jonas Bybjerg‐Grauholm, William Byerley, Sinéad B. Chapman, Wei J. Chen, Claire Churchhouse, Nicholas Craddock, Caroline Cusick, Lynn E. DeLisi, Sheila Dodge, Michael Escamilla, Saana Eskelinen, Ayman H. Fanous, Stephen V. Faraone, Alessia Fiorentino, Laurent C. Francioli, Stacey Gabriel, Diane Gage, Sarah A. Gagliano Taliun, Andrea Ganna, Giulio Genovese, David C. Glahn, Jakob Grove, Mei‐Hua Hall, Eija Hämäläinen, Henrike Heyne, Matti Holi, David M. Hougaard, Daniel P. Howrigan, Hailiang Huang, Hai‐Gwo Hwu, René S. Kahn, Hyun Min Kang, Konrad J. Karczewski, George Kirov, James A. Knowles, Francis S. Lee, Douglas S. Lehrer, Francesco Lescai, Dolores Malaspina, Stephen R. Marder, Steven A. McCarroll, Andrew M. McIntosh, Helena Medeiros, Lili Milani, Christopher P. Morley, Derek W. Morris, Preben Bo Mortensen, R Myers, Merete Nordentoft, Niamh L. O’Brien, Ana Maria Olivares, Döst Öngür, Willem H. Ouwehand, Duncan S. Palmer, Tiina Paunio, Digby Quested, Mark Hyman Rapaport, Elliott Rees, Brandi Rollins, F. Kyle Satterstrom, Alan F. Schatzberg, Edward M. Scolnick, Laura J. Scott, Sally I. Sharp, Pamela Sklar, Jordan W. Smoller, Janet L. Sobell, Matthew Solomonson, Eli A. Stahl, Christine Stevens, Jaana Suvisaari, Grace Tiao, Stanley J. Watson, Nicholas A. Watts, Douglas Blackwood, Anders D. Børglum, Bruce M. Cohen, Aiden Corvin, Tõnu Esko, Nelson B. Freimer, Stephen J. Glatt, Christina M. Hultman, Andrew McQuillin, Aarno Palotie, Carlos N. Pato, Michele T. Pato, Ann E. Pulver, David St Clair and 11 more - Nature 2022 cited by 916
- Genomic Relationships, Novel Loci, and Pleiotropic Mechanisms across Eight Psychiatric Disorders
Authors: Phil H. Lee, Verneri Anttila, Hyejung Won, Yen‐Chen Anne Feng, Jacob Rosenthal, Zhaozhong Zhu, Elliot M. Tucker–Drob, Michel G. Nivard, Andrew D. Grotzinger, Daniëlle Posthuma, Meg M.-J. Wang, Dongmei Yu, Eli A. Stahl, Raymond K. Walters, Richard Anney, Laramie E. Duncan, Tian Ge, Rolf Adolfsson, Tobias Banaschewski, Síntia Belangero, Edwin H. Cook, Giovanni Coppola, Eske M. Derks, Pieter J. Hoekstra, Jaakko Kaprio, Anna Keski‐Rahkonen, George Kirov, Henry R. Kranzler, Jurjen J. Luykx, Luís Augusto Rohde, 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
- Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls
Authors: Paul R. Burton, David G. Clayton, Lon R. Cardon, Nick Craddock, Panos Deloukas, Audrey Duncanson, Dominic Kwiatkowski, Mark I. McCarthy, Willem H. Ouwehand, Nilesh J. Samani, John A. Todd, Peter Donnelly, Jeffrey C. Barrett, Paul R. Burton, Dan Davison, Peter Donnelly, Doug Easton, David Evans, Hin-Tak Leung, Jonathan L. Marchini, Andrew P. Morris, Chris C. A. Spencer, Martin D. Tobin, Lon R. Cardon, David G. Clayton, Antony Attwood, James P. Boorman, Barbara Cant, Ursula Everson, Judith M. Hussey, Jennifer D. Jolley, Alexandra S. Knight, Kerstin Koch, Elizabeth Meech, Sarah Nutland, C V Prowse, Helen E. Stevens, Niall Taylor, Graham R. Walters, Neil M. Walker, Nicholas A. Watkins, Thilo Winzer, John A. Todd, Willem H. Ouwehand, 1958 Birth Cohort Controls, Richard W. Jones, Wendy L. McArdle, Susan M. Ring, David P. Strachan, Marcus Pembrey, Bipolar Disorder, Gerome Breen, David St Clair, Sian Caesar, Katherine Gordon‐Smith, Lisa Jones, Christine Fraser, Elaine Green, Detelina Grozeva, Marian L. Hamshere, Peter Holmans, Ian Jones, George Kirov, Valentina Moskvina, Ivan Nikolov, Michael O‘Donovan, Michael J. Owen, Nick Craddock, David Collier, Amanda Elkin, Anne Farmer, Richard Williamson, Peter McGuffin, Allan H. Young, I. Nicol Ferrier, Coronary Artery Disease, Stephen G. Ball, Anthony J. Balmforth, Jennifer H. Barrett, D. Timothy Bishop, Mark M. Iles, Azhar Maqbool, Nadira Yuldasheva, Alistair S. Hall, Peter S. Braund, Paul R. Burton, Richard J. Dixon, Massimo Mangino, Suzanne Stevens, Martin D. Tobin, J. Thompson, Nilesh J. Samani, Crohn’s Disease, Francesca Bredin, Mark Tremelling, Miles Parkes, Hazel E. Drummond, Charles W. Lees, Elaine R. Nimmo, Jack Satsangi and 176 more - Nature 2007 cited by 9,690
- Common polygenic variation contributes to risk of schizophrenia and bipolar disorder
Authors: Pamela Sklar, Jennifer L. Stone, Pamela Sklar, Shaun Purcell, Manuel A. R. Ferreira, Edward M. Scolnick, Andrew N. Kirby, Mark J. Daly, Kimberly Chambert, Finny Kuruvilla, Stacey B. Gabriel, Shaun Purcell, Jennifer L. Moran, Manuel A. R. Ferreira, Mark Daly, Stuart Macgregor, Michael C. O'Donovan, Peter A. Holmans, Michael C. O’Donovan, Nick J. Craddock, George K. Kirov, Michael J. Owen, Nigel M. Williams, Mark Daly, Ivan Nikolov, N. Norton, Edward M. Scolnick, Patrick F. Sullivan, Patrick Sullivan, Jennifer L. Moran, Hugh Gurling, Jennifer Stone, Kristin Ardlie, Jonathan Pimm, Stacey B. Gabriel, Robert Krasucki, Jacob Lawrence, Nicholas Bass, Derek W. Morris, Colm T. O’Dushlaine, Aiden Corvin, Finny G. Kuruvilla, Naomi R. Wray, Naomi R. Wray, Stuart MacGregor, Stuart MacGregor, Peter M. Visscher, Michael O‘Donovan, Michael O‘Donovan, Peter Holmans, Nadine Norton, Ivan Nikolov, Hywel Williams, George Kirov, Michael J. Owen, Lyudmila Georgieva, Michele T. Pato, Nick Craddock, Nigel Williams, Ayman Fanous, Patrick Sullivan, James A. Knowles, Patrick F. Sullivan, Jonathan Pimm, Jacob Lawrence, Hugh Gurling, Vinay Puri, Nicholas Bass, Andrew McQuillin, Khalid Choudhury, Robert Krasucki, Susmita Datta, Andrew McQuillin, Michael Gill, Elaine Kenny, Michael Gill - Nature 2009 cited by 5,069
- Common schizophrenia alleles are enriched in mutation-intolerant genes and in regions under strong background selection
Authors: Antonio F. Pardiñas, Peter Holmans, Andrew Pocklington, Valentina Escott‐Price, Stephan Ripke, Noa Carrera, Sophie E. Legge, Sophie Bishop, Darren Cameron, Marian L. Hamshere, Jun Han, Leon Hubbard, Amy Lynham, Kiran K. Mantripragada, Elliott Rees, James H. MacCabe, Steven A. McCarroll, Bernhard T. Baune, Gerome Breen, Enda M. Byrne, Udo Dannlowski, Thalia C. Eley, Caroline Hayward, Nicholas G. Martin, Andrew M. McIntosh, Robert Plomin, David J. Porteous, Naomi R. Wray, Armando Caballero, Daniel H. Geschwind, Laura M. Huckins, Douglas M. Ruderfer, Enrique Santiago, Pamela Sklar, Eli A. Stahl, Hyejung Won, Esben Agerbo, Thomas D. Als, Ole A. Andreassen, Marie Bækvad‐Hansen, Preben Bo Mortensen, Carsten Bøcker Pedersen, Anders D. Børglum, Jonas Bybjerg‐Grauholm, Srdjan Djurovic, Naser Durmishi, Marianne Giørtz Pedersen, В. Е. Голимбет, Jakob Grove, David M. Hougaard, Manuel Mattheisen, Espen Molden, Ole Mors, Merete Nordentoft, Milica Pejović-Milovančević, Engilbert Sigurðsson, Teimuraz Silagadze, Christine Søholm Hansen, Kāri Stefánsson, Hreinn Stefánsson, Stacy Steinberg, Sarah Tosato, Thomas Werge, David Collier, Dan Rujescu, George Kirov, Michael J. Owen, Michael O‘Donovan, James Walters - Nature Genetics 2018 cited by 1,728
- De novo mutations in schizophrenia implicate synaptic networks
Authors: Menachem Fromer, Andrew Pocklington, David H. Kavanagh, Hywel Williams, Sarah Dwyer, Padhraig Gormley, Lyudmila Georgieva, Elliott Rees, Priit Palta, Douglas M. Ruderfer, Noa Carrera, Isla Humphreys, Jessica Johnson, Panos Roussos, Douglas Barker, Eric Banks, Vihra Milanova, Seth G. N. Grant, Eilís Hannon, Samuel A. Rose, Kimberly Chambert, Milind Mahajan, Edward M. Scolnick, Jennifer L. Moran, George Kirov, Aarno Palotie, Steven A. McCarroll, Peter Holmans, Pamela Sklar, Michael J. Owen, Shaun Purcell, Michael O‘Donovan - Nature 2014 cited by 1,722
- De novo CNV analysis implicates specific abnormalities of postsynaptic signalling complexes in the pathogenesis of schizophrenia
Authors: George Kirov, Andrew Pocklington, Peter Holmans, Dobril Ivanov, Masashi Ikeda, Douglas M. Ruderfer, Jennifer L. Moran, Kimberly Chambert, Драга Тончева, L. Georgieva, Detelina Grozeva, Marija Fjodorova, R Wollerton, Elliott Rees, Ivan Nikolov, Louie N. van de Lagemaat, Àlex Bayés, E Fernández, Pall I. Olason, Yvonne Böttcher, Noboru H. Komiyama, Mark O. Collins, Jyoti S. Choudhary, Kāri Stefánsson, Hreinn Stefánsson, Seth G. N. Grant, Shaun Purcell, Pamela Sklar, Michael O’Donovan, Michael J. Owen - Molecular Psychiatry 2011 cited by 877
- Discovery and Statistical Genotyping of Copy-Number Variation from Whole-Exome Sequencing Depth
Authors: Menachem Fromer, Jennifer L. Moran, Kimberly Chambert, Eric Banks, Sarah E. Bergen, Douglas M. Ruderfer, Robert E. Handsaker, Steven A. McCarroll, Michael O‘Donovan, Michael J. Owen, George Kirov, Patrick F. Sullivan, Christina M. Hultman, Pamela Sklar, Shaun Purcell - The American Journal of Human Genetics 2012 cited by 597
- Medical consequences of pathogenic CNVs in adults: analysis of the UK Biobank
Authors: Karen Crawford, Matthew Bracher‐Smith, David Owen, Kimberley Kendall, Elliott Rees, Antonio F. Pardiñas, Mark Einon, Valentina Escott‐Price, James Walters, Michael O‘Donovan, Michael J. Owen, George Kirov - Journal of Medical Genetics 2018 cited by 199
- Rare loss-of-function variants in SETD1A are associated with schizophrenia and developmental disorders
Authors: Swedish Schizophrenia Study, Tarjinder Singh, INTERVAL Study, DDD Study, Mitja Kurki, David Curtis, Shaun Purcell, Lucy Crooks, Jeremy F. McRae, Jaana Suvisaari, Himanshu Chheda, Douglas Blackwood, Gerome Breen, Olli Pietiläinen, Sebastian S. Gerety, Muhammad Ayub, Moira Blyth, Trevor Cole, David Collier, Eve L. Coomber, Nick Craddock, Mark J. Daly, John Danesh, Marta Di Forti, Alison Foster, Nelson B. Freimer, Daniel H. Geschwind, Mandy Johnstone, Shelagh Joss, George Kirov, Jarmo Körkkö, Outi Kuismin, Peter Holmans, Christina M. Hultman, Conrad Iyegbe, Jouko Lönnqvist, Minna Männikkö, Steve McCarroll, Peter McGuffin, Andrew M. McIntosh, Andrew McQuillin, Jukka S. Moilanen, Carmel Moore, Robin Murray, Ruth Newbury‐Ecob, Willem H. Ouwehand, Tiina Paunio, Elena Prigmore, Elliott Rees, David J. Roberts, Jennifer Sambrook, Pamela Sklar, David St Clair, Juha Veijola, James Walters, Hywel Williams, Patrick F. Sullivan, Matthew E. Hurles, Michael O‘Donovan, Aarno Palotie, Michael J. Owen, Jeffrey C. Barrett - Nature Neuroscience 2016 cited by 476
- Cognitive performance and functional outcomes of carriers of pathogenic copy number variants: analysis of the UK Biobank
Authors: Kimberley Kendall, Matthew Bracher‐Smith, H Fitzpatrick, Amy Lynham, Elliott Rees, Valentina Escott‐Price, Michael J. Owen, Michael O‘Donovan, James Walters, George Kirov - The British Journal of Psychiatry 2019 cited by 179
- Analysis of copy number variations at 15 schizophrenia-associated loci
Authors: Elliott Rees, James Walters, Lyudmila Georgieva, Anthony R Isles, Kimberly D. Chambert, Alexander Richards, Gerwyn Mahoney‐Davies, Sophie E. Legge, Jennifer L. Moran, Steven A. McCarroll, Michael O‘Donovan, Michael J. Owen, George Kirov - The British Journal of Psychiatry 2013 cited by 466
- Genome-wide association study of CNVs in 16,000 cases of eight common diseases and 3,000 shared controls
Authors: Elaine Green, Liz Forty, Ian Jones, Michael O‘Donovan, Michael J. Owen, Detelina Grozeva, George Kirov, Liz Forty, Nick Craddock, Ellie Russell, Matthew E. Hurles, Panos Deloukas, Richard Redon, Chris Tyler‐Smith, Kathy Stirrups, Hazel Arbury, C. Barnes, Armand Valsesia, Willem H. Ouwehand, Matthew E. Hurles, Eleanor Howard, Andrew Dunham, Anthony Attwood, Michael L. Mimmack, Dominic Kwiatkowski, Nigel P. Carter, Jan Aerts, Michael A. Quail, Sanjeev S. Bhaskar, Kevin Lewis, Naomi Hammond, Elilan Somaskantharajah, Donald F. Conrad, T. Daniel Andrews, Ifejinelo Onyiah, Chris M. Clee, Husam Hebaishi, Jeffrey C. Barrett, Cordelia F. Langford, John H. Burton, Samuel C. Robson, Sarah Hunt, Rhian Gwilliam, Emma Gray, Kirsten McLay, Carol Scott, Aarno Palotie, Kimmo Palin, Alison J. Coffey, Michael R. Stratton, Inês Barroso, Sarah Edkins, Tomas Fitzgerald, Christopher Yau, Zhan Su, Gil McVean, Niall J. Cardin, Christopher Holmes, Eleni Giannoulatou, Jonathan Marchini, Adam Auton, Simon Myers, Peter Donnelly, Julian Maller, Inga Prokopenko, Jake Byrnes, Richard D. Pearson, Andrew P. Morris, Mahim Jain, Adrian V. S. Hill, Dominic Kwiatkowski, Jake Byrnes, Neil Robertson, Damjan Vukcevic, Mark I. McCarthy, Vincent Plagnol, Oliver S. Burren, Mark I. McCarthy, Vincent Plagnol, Nigel Ovington, Meeta Maisuria-Armer, Joanna M. M. Howson, Jason D. Cooper, Oliver S. Burren, Debbie J. Smyth, Kate Downes, Matthew Woodburn, Neil Walker, John A. Todd, Helen E. Stevens, Chris Wallace, Matt Hardy, Helen Schuilenburg, J. Thompson, Louise V. Wain, Paul R. Burton, Martin D. Tobin, Tariq Ahmad, Nicholas A. Watkins, Jennifer D. Jolley and 117 more - Nature 2010 cited by 818
- Analysis of Intellectual Disability Copy Number Variants for Association With Schizophrenia
Authors: Elliott Rees, Kimberley Kendall, Antonio F. Pardiñas, Sophie E. Legge, Andrew Pocklington, Valentina Escott‐Price, James H. MacCabe, David Collier, Peter Holmans, Michael O’Donovan, Michael J. Owen, James Walters, George Kirov - JAMA Psychiatry 2016 cited by 169
- Schizophrenia, autism spectrum disorders and developmental disorders share specific disruptive coding mutations
Authors: Elliott Rees, Hugo Creeth, Hai‐Gwo Hwu, Wei J. Chen, Ming T. Tsuang, Stephen J. Glatt, Romain Rey, George Kirov, James Walters, Peter Holmans, Michael J. Owen, Michael O‘Donovan - Nature Communications 2021 cited by 99
- Rare chromosomal deletions and duplications increase risk of schizophrenia
Authors: Jennifer Stone, Douglas M. Ruderfer, Pamela Sklar, S M Purcell, Mark J. Daly, Edward M. Scolnick, Mark Daly, Kimberly Chambert, Joshua Korn, Steve McCarroll, Casey Gates, Stacey B. Gabriel, Scott Mahon, Kristen Ardlie, Michael C. O’Donovan, George Kirov, N Craddock, Michael J. Owen, Peter A. Holmans, Nia Williams, L. Georgieva, Ivan Nikolov, N. Norton, H. Williams, Hugh Gurling, Andrew McQuillin, Khalid Choudhury, Susmita Datta, Jonathan Pimm, Vinay Puri, Robert Krasucki, Jacob Lawrence, N J Bass, Douglas H. R. Blackwood, Walter J. Muir, Kevin A. McGhee, Ben Pickard, P. Malloy, AB MacLean, M. Van Beck, Aiden Corvin, M Gill, Derek W. Morris, Colm Ó'Dúshláine, Elaine Kenny, C M Hultman, Paul Lichtenstein, Emma F. Thelander, Carlos N. Pato, Michele T. Pato, Helena Medeiros, Celia Carvalho, A H Fanous, David Conti, James A. Knowles, David St Clair, Soh Leh Kwan, P F Sullivan, P F Sullivan, Stuart MacGregor, Peter M. Visscher, Draga Toncheva, Vihra Milanova, Waddington Jl, Srinivasa Thirumalai, Digby Quested, David Curtis, Caroline Crombie, Gillian Fraser, Nicholas Walker, Frank Middleton, Christopher Morley, Carlos Paz Ferreira, Antonio Macedo, M. Helena Azevedo - Nature 2008 cited by 1,512
- Microduplications of 16p11.2 are associated with schizophrenia
Authors: Shane McCarthy, Vladimir Makarov, George Kirov, Anjené Addington, Jon McClellan, Seungtai Yoon, Diana O. Perkins, Diane E. Dickel, Mary Kusenda, Olga Krastoshevsky, Verena Krause, Ravinesh A. Kumar, Detelina Grozeva, Dheeraj Malhotra, Tom Walsh, Elaine H. Zackai, Paige Kaplan, Jaya Ganesh, Ian D. Krantz, Nancy B. Spinner, Patricia Roccanova, Abhishek Bhandari, Kevin Pavon, B. Lakshmi, Anthony Leotta, Jude Kendall, Yoon-ha Lee, Vladimir Vacic, Sydney Gary, Lilia M. Iakoucheva, Timothy J. Crow, Susan L. Christian, Jeffrey A. Lieberman, T. Scott Stroup, Terho Lehtimäki, Kaija Puura, Chad Haldeman‐Englert, Justin Pearl, Meredith Goodell, Virginia L. Willour, Pamela DeRosse, Jo Steele, Layla Kassem, Jessica Wolff, Nisha Chitkara, Francis J. McMahon, Anil K. Malhotra, James B. Potash, Thomas G. Schulze, Markus M. Nöthen, Sven Cichon, Marcella Rietschel, Ellen Leibenluft, Vlad Kustanovich, Clara Lajonchere, James S. Sutcliffe, David Skuse, Michael Gill, Louise Gallagher, Nancy R. Mendell, Nick Craddock, Michael J. Owen, Michael O‘Donovan, Tamim H. Shaikh, Ezra Susser, Lynn E. DeLisi, Patrick F. Sullivan, Curtis K. Deutsch, Judith L. Rapoport, Deborah L. Levy, Mary‐Claire King, Jonathan Sebat - Nature Genetics 2009 cited by 736
- Cognitive Performance Among Carriers of Pathogenic Copy Number Variants: Analysis of 152,000 UK Biobank Subjects
Authors: Kimberley Kendall, Elliott Rees, Valentina Escott‐Price, Mark Einon, Rhys H. Thomas, Jonathan Hewitt, Michael O’Donovan, Michael J. Owen, James Walters, George Kirov - Biological Psychiatry 2016 cited by 248
- Association of Genetic Liability to Psychotic Experiences With Neuropsychotic Disorders and Traits
Authors: Sophie E. Legge, Hannah Jones, Kimberley Kendall, Antonio F. Pardiñas, Georgina Menzies, Matthew Bracher‐Smith, Valentina Escott‐Price, Elliott Rees, Katrina A. S. Davis, Matthew Hotopf, Jeanne E. Savage, Daniëlle Posthuma, Peter Holmans, George Kirov, Michael J. Owen, Michael O’Donovan, Stanley Zammit, James Walters - JAMA Psychiatry 2019 cited by 163
- Association of Rare Copy Number Variants With Risk of Depression
Authors: Kimberley Kendall, Elliott Rees, Matthew Bracher‐Smith, Sophie E. Legge, Lucy Riglin, Stanley Zammit, Michael O’Donovan, Michael John Owen, Ian Jones, George Kirov, James Walters - JAMA Psychiatry 2019 cited by 161
- Characterisation of age and polarity at onset in bipolar disorder
Authors: János Kálmán, Loes M. Olde Loohuis, Annabel Vreeker, Andrew McQuillin, Eli A. Stahl, Douglas M. Ruderfer, Maria Grigoroiu‐Serbânescu, Georgia Panagiotaropoulou, Stephan Ripke, Tim B. Bigdeli, Frederike Stein, Tina Meller, Susanne Meinert, Helena Pelin, Fabian Streit, Sergi Papiol, Mark J. Adams, Rolf Adolfsson, Kristina Adorjan, Ingrid Agartz, Sofie R. Aminoff, Heike Anderson-Schmidt, Ole A. Andreassen, Raffaella Ardau, Jean‐Michel Aubry, Ceylan Balaban, Nicholas Bass, Bernhard T. Baune, Frank Bellivier, Antoni Benabarre, Susanne Bengesser, Wade H. Berrettini, Marco P. Boks, Evelyn J. Bromet, Katharina Brosch, Monika Budde, William Byerley, Pablo Cervantes, Catina Chillotti, Sven Cichon, Scott R. Clark, Ashley L. Comes, Aiden Corvin, William Coryell, Nick Craddock, David W. Craig, Paul E. Croarkin, Cristiana Cruceanu, Piotr M. Czerski, Nina Dalkner, Udo Dannlowski, Franziska Degenhardt, Maria Del Zompo, J. Raymond DePaulo, Srdjan Djurovic, Howard J. Edenberg, Mariam Al Eissa, Torbjørn Elvsåshagen, Bruno Étain, Ayman H. Fanous, Frederike T. Fellendorf, Alessia Fiorentino, Andreas J. Forstner, Mark A. Frye, Janice M. Fullerton, Katrin Gade, Julie Garnham, Elliot S. Gershon, Michael Gill, Fernando S. Goes, Katherine Gordon‐Smith, Paul Grof, José Guzmán‐Parra, Tim Hahn, Roland Hasler, Maria Heilbronner, Urs Heilbronner, Stéphane Jamain, Esther Jiménez, Ian Jones, Lisa Jones, Lina Jönsson, René S. Kahn, John R. Kelsoe, James L. Kennedy, Tilo Kircher, George Kirov, Sarah Kittel‐Schneider, Farah Klöhn‐Saghatolislam, James A. Knowles, Thorsten M. Kranz, Trine Vik Lagerberg, Mikael Landén, William Lawson, Marion Leboyer, Qingqin S. Li, Mario Maj, Dolores Malaspina, Mirko Manchia, Fermín Mayoral and 73 more - The British Journal of Psychiatry 2021 cited by 50
- Association scan of 14,500 nonsynonymous SNPs in four diseases identifies autoimmunity variants
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