Frank Dudbridge

Active 1990–2025

124
Papers
36,452
Citations
75
h-index
119
i10-index

Citations

Citations per year for Frank Dudbridge1973: 1 citations1974: 2 citations1991: 1 citations1992: 1 citations1993: 15 citations1994: 15 citations1995: 13 citations1996: 13 citations1997: 11 citations1998: 8 citations1999: 19 citations2000: 6 citations2001: 15 citations2002: 44 citations2003: 73 citations2004: 110 citations2005: 116 citations2006: 128 citations2007: 121 citations2008: 152 citations2009: 162 citations2010: 214 citations2011: 217 citations2012: 273 citations2013: 277 citations2014: 275 citations2015: 325 citations2016: 359 citations2017: 412 citations2018: 428 citations2019: 1,179 citations2020: 1,273 citations2021: 1,361 citations2022: 1,375 citations2023: 1,099 citations2024: 1,828 citations2025: 604 citations2026: 22 citations1975–1990: no citations, so these years are not shown

Citation sources

Countries

World map of the countries and regions citing this authorUnited States: 5,026 citing papers, 20.8% of this breakdownUnited Kingdom: 3,078 citing papers, 12.7% of this breakdownChina: 1,885 citing papers, 7.8% of this breakdownGermany: 1,227 citing papers, 5.1% of this breakdownAustralia: 1,106 citing papers, 4.6% of this breakdownNetherlands: 1,057 citing papers, 4.4% of this breakdownCanada: 957 citing papers, 3.9% of this breakdownSweden: 782 citing papers, 3.2% of this breakdownItaly: 663 citing papers, 2.7% of this breakdownFrance: 620 citing papers, 2.6% of this breakdownDenmark: 565 citing papers, 2.3% of this breakdownSpain: 539 citing papers, 2.2% of this breakdown
0%20.8%Other 27.7%

Fields

  • Biochemistry, Genetics and Molecular Biology50.3%
  • Medicine30.6%
  • Neuroscience8.5%
  • Psychology2.7%
  • Immunology and Microbiology2.1%
  • Mathematics1.2%
  • Other4.6%

Topics

  • Genetic Associations and Epidemiology13.2%
  • Genetic Mapping and Diversity in Plants and Animals2.3%
  • Bioinformatics and Genomic Networks2.3%
  • Genetics and Neurodevelopmental Disorders2.1%
  • Epigenetics and DNA Methylation2.1%
  • Tryptophan and brain disorders2%
  • Other76%

Coauthors

All papers

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  1. Mapping genomic loci implicates genes and synaptic biology in schizophrenia

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Mariam Al Eissa, Margot Albus, Madeline Alexander, Behrooz Z. Alizadeh, Köksal Alptekın, Thomas D. Als, Farooq Amin, Volker Arolt, Manuel Arrojo, Lavinia Athanasiu, M.H. Azevedo, Silviu‐Alin Bacanu, Nicholas Bass, Martin Begemann, Richard A. Belliveau, Judit Bene, Beben Benyamin, Sarah E. Bergen, Giuseppe Blasi, Julio Bobes, Stefano Bonassi, Alice Braun, Rodrigo A. Bressan, Evelyn J. Bromet, Richard Bruggeman, P.F. Buckley, Randy L. Buckner, Jonas Bybjerg‐Grauholm, Wiepke Cahn, Murray J. Cairns, Monica E. Calkins, Vaughan J. Carr, David Castle, Stanley V. Catts, Kimberley D. Chambert, Raymond Chan, Boris Chaumette, Wei Cheng, Eric F.C. Cheung, Siow Ann Chong, David Cohen, Angèle Consoli, Quirino Cordeiro, Javier Costas, Charles Curtis, Michael Davidson, Kenneth L. Davis, Lieuwe de Haan, Franziska Degenhardt, Lynn E. DeLisi, Ditte Demontis, Faith Dickerson, Dimitris Dikeos, Timothy G. Dinan, Srdjan Djurovic, Jubao Duan, Giuseppe Ducci, Frank Dudbridge, Johan G. Eriksson, Lourdes Fañanás, Stephen V. Faraone, Alessia Fiorentino, Andreas J. Forstner, Josef Frank, Nelson B. Freimer, Menachem Fromer, Alessandra Frustaci, Ary Gadelha, Giulio Genovese, Elliot S. Gershon and 513 more - Nature 2022 cited by 2,857

  2. Guidelines for performing Mendelian randomization investigations

    Authors: , , , , , , , , , , - Wellcome Open Research 2019 cited by 1,913

  3. Combining information on multiple instrumental variables in Mendelian randomization: comparison of allele score and summarized data methods

    Authors: , , - Statistics in Medicine 2015 cited by 1,258

  4. Re: “Multivariable Mendelian Randomization: The Use of Pleiotropic Genetic Variants to Estimate Causal Effects”

    Authors: , , - American Journal of Epidemiology 2015 cited by 1,009

  5. Guidelines for performing Mendelian randomization investigations: update for summer 2023

    Authors: , , , , , , , , , , , , , - Wellcome Open Research 2023 cited by 695

  6. Modeling Linkage Disequilibrium Increases Accuracy of Polygenic Risk Scores

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Peter M. Visscher, Peter Kraft, Nick Patterson, Alkes L. Price, Stephan Ripke, Benjamin M. Neale, Aiden Corvin, James Walters, Kai-How Farh, Peter Holmans, Phil Lee, Brendan Bulik‐Sullivan, David Collier, Hailiang Huang, Tune H. Pers, Ingrid Agartz, Esben Agerbo, Margot Albus, Madeline Alexander, Farooq Amin, Silviu‐Alin Bacanu, Martin Begemann, Richard A. Belliveau, Judit Bene, Sarah E. Bergen, Elizabeth Bevilacqua, Tim B. Bigdeli, Donald W. Black, Richard Bruggeman, Nancy G. Buccola, Randy L. Buckner, William Byerley, Wiepke Cahn, Guiqing Cai, Dominique Campion, Rita M. Cantor, Vaughan J. Carr, Noa Carrera, Stanley V. Catts, Kimberly D. Chambert, Raymond Chan, Ronald Y.L. Chen, Eric Chen, Wei Cheng, Eric F.C. Cheung, Siow Ann Chong, C. Robert Cloninger, David Cohen, Nadine Cohen, Paul Cormican, Nick Craddock, James J. Crowley, David Curtis, Michael Davidson, Kenneth L. Davis, Franziska Degenhardt, Jurgen Del‐Favero, Lynn E. DeLisi, Ditte Demontis, Dimitris Dikeos, Timothy G. Dinan, Srdjan Djurovic, Gary Donohoe, Elodie Drapeau, Jubao Duan, Frank Dudbridge, Naser Durmishi, Peter Eichhammer, Johan G. Eriksson, Valentina Escott‐Price and 302 more - The American Journal of Human Genetics 2015 cited by 1,489

  7. The interleukin-6 receptor as a target for prevention of coronary heart disease: a mendelian randomisation analysis

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Ian Tomlinson, Ioanna Tzoulaki, Jian'an Luan, Jolanda M A Boer, Nita G Forouhi, N Charlotte Onland-Moret, N. Charlotte Onland‐Moret, Renate B Schnabel, Jaroslav A Hubacek, Ruzena Kubinova, Migle Baceviciene, Abdonas Tamosiunas, Andrzej Pajak, Roman Topor-Madry, Sofia Malyutina, Damiano Baldassarre, Bengt Sennblad, Elena Tremoli, Ulf de Faire, Luigi Ferrucci, Stefania Bandenelli, Toshiko Tanaka, James F Meschia, Andrew Singleton, Gerjan Navis, Irene Mateo Leach, Stephan J L Bakker, Ron T Gansevoort, Ian Ford, Stephen E Epstein, Mary Susan Burnett, Joe M Devaney, J Wouter Jukema, J. Wouter Jukema, Gert Jan de Borst, Yolanda van der Graaf, Pim A de Jong, Anke-Hilse Mailand-van der Zee, Olaf H Klungel, Anthonius de Boer, Pieter A Doevendans, Jeffrey W Stephens, Charles B Eaton, Jennifer G Robinson, JoAnn E Manson, F Gerry Fowkes, Timonthy M Frayling, Jackie F Price, Peter H Whincup, Richard W Morris, Debbie A Lawlor, George Davey Smith, Yoav Ben-Shlomo, Susan Redline, Leslie A Lange, Meena Kumari, Nick J Wareham, W M Monique Verschuren, Emelia J Benjamin, John C Whittaker, Anders Hamsten, Frank Dudbridge, J A Chris Delaney, Andrew Wong, Diana Kuh, Rebecca Hardy, Berta Almoguera Castillo, John J Connolly, Pim van der Harst, Eric J Brunner and 16 more - The Lancet 2012 cited by 1,157

  8. Genomic Risk Prediction of Coronary Artery Disease in 480,000 Adults

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , - Journal of the American College of Cardiology 2018 cited by 834

  9. Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Nancy G. Buccola, Randy L. Buckner, Brendan Bulik‐Sullivan, William Byerley, Wiepke Cahn, Guiqing Cai, Murray J. Cairns, Dominique Campion, Rita M. Cantor, Vaughan J. Carr, Noa Carrera, Stanley V. Catts, Kimberley D. Chambert, Wei Cheng, C. Robert Cloninger, David Cohen, Paul Cormican, Nick Craddock, Benedicto Crespo‐Facorro, James J Crowley, David Curtis, Michael Davidson, Kenneth L. Davis, Franziska Degenhardt, Jurgen Del‐Favero, Lynn E. DeLisi, Dimitris Dikeos, Timothy G. Dinan, Srdjan Djurovic, Gary Donohoe, Elodie Drapeau, Jubao Duan, Frank Dudbridge, Peter Eichhammer, Johan G. Eriksson, Valentina Escott‐Price, Laurent Essioux, Ayman H. Fanous, Kai-How Farh, Martilias S. Farrell, Josef Frank, Lude Franke, Robert Freedman, Nelson B. Freimer, Joseph I. Friedman, Andreas J. Forstner, Menachem Fromer, Giulio Genovese, Lyudmila Georgieva, Elliot S. Gershon, Ina Giegling, Paola Giusti‐Rodríguez, Stephanie Godard, Jacqueline I. Goldstein, Jacob Gratten, Lieuwe de Haan, Marian L. Hamshere, Mark Hansen, Thomas Folkmann Hansen, Vahram Haroutunian, Annette M. Hartmann, Frans A. Henskens, Stefan Herms, Joel N. Hirschhorn, Per Hoffmann, Andrea Hofman, Hailiang Huang, Masashi Ikeda, Inge Joa, Anna K. Kähler and 163 more - Nature Genetics 2016 cited by 1,142

  10. Using genetic data to strengthen causal inference in observational research

    Authors: , , , , , - Nature Reviews Genetics 2018 cited by 492

  11. Power and Predictive Accuracy of Polygenic Risk Scores

    Authors: - PLoS Genetics 2013 cited by 1,639

  12. Mendelian randomization of blood lipids for coronary heart disease

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Sanjay R. Patel, Susan Redline, David S. Siscovick, Michael Y. Tsai, Konrad J. Karczewski, Marten H. Hofker, W. M. Monique Verschuren, Michiel L. Bots, Yvonne T. van der Schouw, Olle Melander, Anna F. Dominiczak, Richard Morris, Yoav Ben‐Shlomo, Jackie F. Price, Meena Kumari, Jens Baumert, Annette Peters, Barbara Thorand, Wolfgang Köenig, Tom R. Gaunt, Steve E. Humphries, Robert Clarke, Hugh Watkins, Martin Farrall, James G. Wilson, Stephen S. Rich, Paul I. W. de Bakker, Leslie A. Lange, George Davey Smith, Alex P. Reiner, Philippa J. Talmud, Mika Kivimäki, Debbie A. Lawlor, Frank Dudbridge, Nilesh J. Samani, Brendan J. Keating, Aroon D. Hingorani, Juan P. Casas - European Heart Journal 2014 cited by 792

  13. New genetic signals for lung function highlight pathways and chronic obstructive pulmonary disease associations across multiple ancestries

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Terho Lehtimäki, Richard J. Allen, Per Bakke, Terri H. Beaty, Eugene R. Bleecker, Yohan Bossé, Corry‐Anke Brandsma, Zhengming Chen, James D. Crapo, John Danesh, Dawn L. DeMeo, Frank Dudbridge, Ralf Ewert, Christian Gieger, Amund Gulsvik, Anna Hansell, Ke Hao, Joshua Hoffman, John E. Hokanson, Georg Homuth, Peter K. Joshi, Philippe Joubert, Claudia Langenberg, Xuan Li, Liming Li, Kuang Lin, Lars Lind, Nicholas Locantore, Jian’an Luan, Anubha Mahajan, Joseph Maranville, Alison D. Murray, David C. Nickle, Richard Packer, Margaret M. Parker, Megan L. Paynton, David J. Porteous, Dmitry Prokopenko, Dandi Qiao, Rajesh Rawal, Heiko Runz, Ian Sayers, Don D. Sin, Blair H. Smith, María Soler Artigas, David Sparrow, Ruth Tal‐Singer, Paul R. H. J. Timmers, Maarten van den Berge, John C. Whittaker, Prescott G. Woodruff, Laura M. Yerges-Armstrong, Olga G. Troyanskaya, Olli Raitakari, Mika Kähönen, Ozren Polašek, Ulf Gyllensten, Igor Rudan, Ian J. Deary, Nicole Probst‐Hensch, Holger Schulz, Alan L James, James F. Wilson, Beate Stubbe, Eleftheria Zeggini, Marjo‐Riitta Järvelin, Nick Wareham, Edwin K. Silverman, Caroline Hayward, Andrew P. Morris and 10 more - Nature Genetics 2019 cited by 599

  14. Genome-wide association study identifies five new schizophrenia loci

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Stan Zammit, Michael C O'Donovan, Dan-Yu Lin, Roel A Ophoff, Eric Strengman, Rita M Cantor, Nelson B Freimer, Ole A Andreassen, Ingrid Agartz, Srdjan Djurovic, Morten Mattingsdal, Ingrid Melle, Edward Scolnick, Shaun Purcell, Benjamin M Neale, Sven Cichon, Manuel Mattheisen, Markus M Nöthen, David St. Clair, Aiden Corvin, Paul Cormican, Gary Donohoe, Michael Gill, Elaine Kenny, Derek W Morris, Colm T O'Dushlaine, Emma M Quinn, Hugh Gurling, Nicholas Bass, Khalid Choudhury, Susmita Datta, Robert Krasucki, Jacob Lawrence, Andrew McQuillin, Jonathan Pimm, Vinay Puri, Thomas Werge, Linh Duong, Thomas Hansen, Andrés Ingason, Klaus D Jakobsen, Line Olsen, Henrik B Rasmussen, Johan H Thygesen, Dan Rujescu, Marion Friedl, Ina Giegling, Annette M Hartmann, Heike Konnerth, Bettina Konte, Douglas H R Blackwood, Alan W Maclean, Pat Malloy, Kevin A McGhee, Andrew McIntosh, Carlos N Pato, Michele T Pato, Anil K Malhotra, Todd Lencz, Frank Dudbridge, Peter M Visscher, Danielle Posthuma, Richard L Amdur, Hreinn Stefansson, Stacy Steinberg, Kari Stefansson, Bryan J Mowry, John J McGrath, Deborah A Nertney, Vera Golimbet and 96 more - Nature Genetics 2011 cited by 1,954

  15. A Comparison of Ten Polygenic Score Methods for Psychiatric Disorders Applied Across Multiple Cohorts

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Judit Bene, Sarah E. Bergen, Elizabeth Bevilacqua, Tim B. Bigdeli, Donald W. Black, Richard Bruggeman, Nancy G. Buccola, Randy L. Buckner, William Byerley, Wiepke Cahn, Guiqing Cai, Dominique Campion, Rita M. Cantor, Vaughan J. Carr, Noa Carrera, Stanley V. Catts, Kimberley D. Chambert, Raymond C. K. Chan, Ronald Y.L. Chen, Eric Chen, Wei Cheng, Eric F.C. Cheung, Siow Ann Chong, C. Robert Cloninger, David Cohen, Nadine Cohen, Paul Cormican, Nick Craddock, James J. Crowley, Michael Davidson, Kenneth L. Davis, Franziska Degenhardt, Jurgen Del‐Favero, Ditte Demontis, Dimitris Dikeos, Timothy G. Dinan, Srdjan Djurovic, Gary Donohoe, Elodie Drapeau, Jubao Duan, Frank Dudbridge, Naser Durmishi, Peter Eichhammer, Johan G. Eriksson, Valentina Escott‐Price, Laurent Essioux, Ayman H. Fanous, Martilias S. Farrell, Josef Frank, Lude Franke, Robert Freedman, Nelson B. Freimer, Marion Friedl, Joseph I. Friedman, Menachem Fromer, Giulio Genovese, Lyudmila Georgieva, Ina Giegling, Paola Giusti‐Rodríguez, Stephanie Godard, Jacqueline I. Goldstein, В. Е. Голимбет, Srihari Gopal, Jacob Gratten, Lieuwe de Haan, Christian Hammer, Marian L. Hamshere, Mark Hansen, Thomas Folkmann Hansen, Vahram Haroutunian and 391 more - Biological Psychiatry 2021 cited by 207

  16. Partitioning Heritability of Regulatory and Cell-Type-Specific Variants across 11 Common Diseases

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Hailiang Huang, Tune H. Pers, Ingrid Agartz, Esben Agerbo, Margot Albus, Madeline Alexander, Farooq Amin, Silviu‐Alin Bacanu, Martin Begemann, Richard A. Belliveau, Judit Bene, Sarah E. Bergen, Elizabeth Bevilacqua, Tim B. Bigdeli, Donald W. Black, Anders D. Børglum, Richard Bruggeman, Nancy G. Buccola, Randy L. Buckner, William Byerley, Wiepke Cahn, Guiqing Cai, Dominique Campion, Rita M. Cantor, Vaughan J. Carr, Noa Carrera, Stanley V. Catts, Kimberly D. Chambert, Raymond Chan, Ronald Y.L. Chen, Eric Chen, Wei Cheng, Eric Cheung, Siow Ann Chong, C. Robert Cloninger, David Cohen, Nadine Cohen, Paul Cormican, Nick Craddock, James J. Crowley, David Curtis, Michael H. Davidson, Kenneth L. Davis, Franziska Degenhardt, Jurgen Del‐Favero, Lynn E. DeLisi, Ditte Demontis, Dimitris Dikeos, Timothy G. Dinan, Srdjan Djurovic, Gary Donohoe, Elodie Drapeau, Jubao Duan, Frank Dudbridge, Naser Durmishi, Peter Eichhammer, Johan G. Eriksson, Valentina Escott‐Price, Laurent Essioux, Ayman H. Fanous, Martilias S. Farrell, Josef Frank, Lude Franke, Robert Freedman, Nelson B. Freimer, Marion Friedl, Joseph I. Friedman, Menachem Fromer, Giulio Genovese, Lyudmila Georgieva and 245 more - The American Journal of Human Genetics 2014 cited by 654

  17. Genome-wide association meta-analysis identifies risk loci for abdominal aortic aneurysm and highlights PCSK9 as a therapeutic target

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Karina Banasik, Søren Brunak, Rikke Louise Jacobsen, Minerva T. Garcia-Barrio, Jifeng Zhang, Lars Melholt Rasmussen, Regent Lee, Ashok Handa, Anders Wanhainen, Kevin Mani, Jes S. Lindholt, Lasse M. Obel, Ewa Strauss, Grzegorz Oszkinis, Christopher P. Nelson, Katie Saxby, Joost A. van Herwaarden, Sander W. van der Laan, Jessica van Setten, Mercedes Camacho, Frank M. Davis, Rachael Wasikowski, Lam C. Tsoi, Jóhann E. Guðjónsson, Jonathan L. Eliason, Dawn M. Coleman, Peter K. Henke, Santhi K. Ganesh, Y. Eugene Chen, Weihua Guan, James S. Pankow, Nathan Pankratz, Ole Birger Pedersen, Christian Erikstrup, Weihong Tang, Kristian Hveem, Daníel F. Guðbjartsson, Sólveig Grétarsdóttir, Unnur Þorsteinsdóttir, Hilma Hólm, Kāri Stefánsson, Manuel A. R. Ferreira, Aris Baras, Iftikhar J. Kullo, Marylyn D. Ritchie, Alex Hørby Christensen, Kasper Iversen, Nikolaj Eldrup, Henrik Sillesen, Sisse Rye Ostrowski, Henning Bundgaard, Henrik Ullum, Stephen Burgess, Dipender Gill, Katherine Gallagher, Maria Sabater‐Lleal, DiscovEHR, UK Aneurysm Growth Study, Frank Dudbridge, Nilesh J. Samani, VA Million Veteran Program, Ida Surakka, Gregory T. Jones, Matthew J. Bown, Philip S. Tsao, Cristen J. Willer, Scott M. Damrauer - Nature Genetics 2023 cited by 94

  18. Genetic predisposition to hypertension is associated with preeclampsia in European and Central Asian women

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Hrefna Johannsdottir, Ingileif Jónsdóttir, Thorhildur Juliusdottir, Noor Kalsheker, A. K. Kasimov, John P. Kemp, Katja Kivinen, Kari Klungsøyr, Wai Lee, Mads Melbye, Zosia Miedzybrodska, Ashley Moffett, Dilbar Najmutdinova, Firuza Nishanova, Thorunn A. Olafsdottir, Markus Perola, Fiona Broughton Pipkin, Lucilla Poston, Gordon Prescott, Saedís Saevarsdóttir, Damilya Salimbayeva, Paula J. Scaife, Line Skotte, Eleonora Staines-Urias, Ólafur Andri Stefánsson, Karina Meden Sørensen, Liv Cecilie Vestrheim Thomsen, Vinicius Tragante, Lill Trogstad, Nigel Simpson, Hannele Laivuori, Seppo Heinonen, Eero Kajantie, Juha Kere, Katja Kivinen, Anneli Pouta, Linda Morgan, Fiona Broughton Pipkin, Noor Kalsheker, James J. Walker, Sheila Macphail, Mark D. Kilby, Marwan Habiba, Catherine Williamson, Kevin M. O’Shaughnessy, Shaughn O’Brien, Alan C. Cameron, Christopher W.G. Redman, Martin Farrall, Mark J. Caulfield, Anna F. Dominiczak, Tamara Aripova, Juan P. Casas, Anna F. Dominiczak, James J. Walker, Unnur Þorsteinsdóttir, Ann‐Charlotte Iversen, Bjarke Feenstra, Debbie A. Lawlor, Heather A. Boyd, Per Magnus, Hannele Laivuori, Nodira Zakhidova, Gulnara Svyatova, Kāri Stefánsson, Linda Morgan - Nature Communications 2020 cited by 193

  19. Interaction Testing and Polygenic Risk Scoring to Estimate the Association of Common Genetic Variants With Treatment Resistance in Schizophrenia

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Michael J. Owen, James H. MacCabe, Michael O‘Donovan, James Walters, Stephan Ripke, Benjamin M. Neale, Kai-How Farh, Phil Lee, Brendan Bulik‐Sullivan, David Collier, Hailiang Huang, Tune H. Pers, Ingrid Agartz, Esben Agerbo, Margot Albus, Madeline Alexander, Farooq Amin, Silviu‐Alin Bacanu, Martin Begemann, Richard A. Belliveau, Judit Bene, Sarah E. Bergen, Elizabeth Bevilacqua, Donald W. Black, Richard Bruggeman, Nancy G. Buccola, Randy L. Buckner, William Byerley, Wiepke Cahn, Guiqing Cai, Dominique Campion, Rita M. Cantor, Vaughan J. Carr, Noa Carrera, Stanley V. Catts, Kimberly D. Chambert, Raymond C. Chan, Ronald Y.L. Chen, Eric Chen, Wei Cheng, Eric F.C. Cheung, Siow Ann Chong, C. Robert Cloninger, David Cohen, Nadine Cohen, Paul Cormican, Nick Craddock, James J. Crowley, David Curtis, Michael Davidson, Kenneth L. Davis, Franziska Degenhardt, Jurgen Del‐Favero, Lynn E. DeLisi, Ditte Demontis, Dimitris Dikeos, Timothy G. Dinan, Srdjan Djurovic, Gary Donohoe, Elodie Drapeau, Jubao Duan, Frank Dudbridge, Naser Durmishi, Peter Eichhammer, Johan G. Eriksson, Valentina Escott‐Price, Laurent Essioux, Martilias S. Farrell, Lude Franke, Robert Freedman and 261 more - JAMA Psychiatry 2022 cited by 106

  20. Robust methods in Mendelian randomization via penalization of heterogeneous causal estimates

    Authors: , , , - PLoS ONE 2019 cited by 193

  21. Research Review: Polygenic methods and their application to psychiatric traits

    Authors: , , , , , - Journal of Child Psychology and Psychiatry 2014 cited by 710

  22. Mitochondrial dysfunction in schizophrenia: evidence for compromised brain metabolism and oxidative stress

    Authors: , , , , , , , , , , , , , , , , , - Molecular Psychiatry 2004 cited by 972

  23. Polygenic risk scores in cardiovascular risk prediction: A cohort study and modelling analyses

    Authors: , , , , , , , , , , , , , , , , , , , , - PLoS Medicine 2021 cited by 173

  24. Common variants on chromosome 6p22.1 are associated with schizophrenia

    Authors: , , , , , , , , , , , , , , , , , , , , , , - Nature 2009 cited by 1,194