Nicholas G. Martin

Active 1975–2025

Also published as
Nicholas G Martin
666
Papers
121,355
Citations
184
h-index
629
i10-index

Citations

Citations per year for Nicholas G. Martin1939: 1 citations1944: 1 citations1974: 1 citations1975: 1 citations1976: 1 citations1977: 1 citations1978: 7 citations1979: 2 citations1980: 1 citations1981: 2 citations1982: 4 citations1983: 3 citations1984: 10 citations1985: 22 citations1986: 18 citations1987: 13 citations1988: 18 citations1989: 31 citations1990: 36 citations1991: 30 citations1992: 48 citations1993: 80 citations1994: 57 citations1995: 88 citations1996: 102 citations1997: 108 citations1998: 151 citations1999: 228 citations2000: 207 citations2001: 211 citations2002: 236 citations2003: 325 citations2004: 308 citations2005: 385 citations2006: 397 citations2007: 398 citations2008: 565 citations2009: 657 citations2010: 765 citations2011: 890 citations2012: 1,105 citations2013: 1,266 citations2014: 1,309 citations2015: 1,408 citations2016: 1,282 citations2017: 1,551 citations2018: 1,528 citations2019: 4,029 citations2020: 3,936 citations2021: 3,874 citations2022: 3,037 citations2023: 2,197 citations2024: 3,203 citations2025: 1,325 citations2026: 61 citations1940–1943: no citations, so these years are not shown1945–1973: no citations, so these years are not shown

Citation sources

Countries

World map of the countries and regions citing this authorUnited States: 13,078 citing papers, 22.4% of this breakdownUnited Kingdom: 6,024 citing papers, 10.3% of this breakdownChina: 3,581 citing papers, 6.1% of this breakdownAustralia: 3,265 citing papers, 5.6% of this breakdownGermany: 3,102 citing papers, 5.3% of this breakdownNetherlands: 2,821 citing papers, 4.8% of this breakdownCanada: 2,345 citing papers, 4% of this breakdownSweden: 1,882 citing papers, 3.2% of this breakdownItaly: 1,699 citing papers, 2.9% of this breakdownFrance: 1,573 citing papers, 2.7% of this breakdownSpain: 1,550 citing papers, 2.7% of this breakdownDenmark: 1,277 citing papers, 2.2% of this breakdown
0%22.4%Other 27.8%

Fields

  • Medicine38.7%
  • Biochemistry, Genetics and Molecular Biology34.8%
  • Neuroscience11.5%
  • Psychology7.8%
  • Immunology and Microbiology1.3%
  • Social Sciences1.1%
  • Other4.8%

Topics

  • Genetic Associations and Epidemiology7.1%
  • Epigenetics and DNA Methylation2.8%
  • Functional Brain Connectivity Studies2.3%
  • Genetic Mapping and Diversity in Plants and Animals2%
  • Genetic and phenotypic traits in livestock1.6%
  • Birth, Development, and Health1.3%
  • Other82.9%

Coauthors

All papers

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  1. Association studies of up to 1.2 million individuals yield new insights into the genetic etiology of tobacco and alcohol use

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Teemu Palviainen, Anita Pandit, Gunnar W. Reginsson, Anne Heidi Skogholt, Jennifer A. Smith, Amy E. Taylor, Constance Turman, Gonneke Willemsen, Hannah Young, Kendra A. Young, Gregory J. M. Zajac, Wei Zhao, Wei Zhou, Gyða Björnsdóttir, Jason D. Boardman, Michael Boehnke, Dorret I. Boomsma, Chu Chen, Francesco Cucca, Gareth E. Davies, Charles B. Eaton, Marissa A. Ehringer, Tõnu Esko, Edoardo Fiorillo, Nathan A. Gillespie, Daníel F. Guðbjartsson, Toomas Haller, Kathleen Mullan Harris, Andrew C. Heath, John K. Hewitt, Ian B. Hickie, John E. Hokanson, Christian J. Hopfer, David J. Hunter, William G. Iacono, Eric O. Johnson, Yoichiro Kamatani, Sharon L. R. Kardia, Matthew C. Keller, Manolis Kellis, Charles Kooperberg, Peter Kraft, Kenneth Krauter, Markku Laakso, Penelope A. Lind, Anu Loukola, Sharon M. Lutz, Pamela A. F. Madden, Nicholas G. Martin, Matt McGue, Matthew B. McQueen, Sarah E. Medland, Andres Metspalu, Karen L. Mohlke, Jonas B. Nielsen, Yukinori Okada, Ulrike Peters, Tinca J. C. Polderman, Daniëlle Posthuma, Alex P. Reiner, John P. Rice, Eric B. Rimm, Richard J. Rose, Valgerður Rúnarsdóttir, Michael C. Stallings, Alena Stančáková, Hreinn Stefánsson, Khanh K. Thai, Hilary A. Tindle, Þórarinn Tyrfingsson and 24 more - Nature Genetics 2019 cited by 2,142

  2. Discovery of the first genome-wide significant risk loci for attention deficit/hyperactivity disorder

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Duncan S. Palmer, Carsten Bøcker Pedersen, Marianne Giørtz Pedersen, Timothy Poterba, Jesper Buchhave Poulsen, Stephan Ripke, Elise Robinson, F. Kyle Satterstrom, Hreinn Stefánsson, Christine Stevens, Patrick Turley, G. Bragi Walters, Hyejung Won, Margaret J. Wright, Ole A. Andreassen, Philip Asherson, Christie L. Burton, Dorret I. Boomsma, Bru Cormand, Søren Dalsgaard, Barbara Franke, Joel Gelernter, Daniel H. Geschwind, Håkon Håkonarson, Jan Haavik, Henry R. Kranzler, Jonna Kuntsi, K. Langley, Klaus‐Peter Lesch, Christel M. Middeldorp, Andreas Reif, Luís Augusto Rohde, Panos Roussos, Russell Schachar, Pamela Sklar, Edmund Sonuga‐Barke, Patrick F. Sullivan, Anita Thapar, Joyce Y. Tung, Irwin D. Waldman, Sarah E. Medland, Kāri Stefánsson, Merete Nordentoft, David M. Hougaard, Thomas Werge, Ole Mors, Preben Bo Mortensen, Mark J. Daly, Stephen V. Faraone, Anders D. Børglum, Benjamin M. Neale - Nature Genetics 2018 cited by 2,320

  3. Conditional and joint multiple-SNP analysis of GWAS summary statistics identifies additional variants influencing complex traits

    Authors: , , , , , , , , , , , , , , - Nature Genetics 2012 cited by 1,942

  4. Common SNPs explain a large proportion of the heritability for human height

    Authors: , , , , , , , , , , , - Nature Genetics 2010 cited by 4,842

  5. Cortical abnormalities in adults and adolescents with major depression based on brain scans from 20 cohorts worldwide in the ENIGMA Major Depressive Disorder Working Group

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Miguel E. Rentería, Lachlan T. Strike, Margaret J. Wright, Natalie Mills, Greig I. de Zubicaray, Katie L. McMahon, Sarah E. Medland, Nicholas G. Martin, Nathan A. Gillespie, Roberto Goya‐Maldonado, Oliver Gruber, Bernd Krämer, Sean N. Hatton, Jim Lagopoulos, Ian B. Hickie, Thomas Frodl, Angela Carballedo, Eva-Maria Frey, Laura S. van Velzen, Brenda W.J.H. Penninx, M-J van Tol, Nic J. van der Wee, Christopher G. Davey, Ben J. Harrison, Benson Mwangi, Bo Cao, Jair C. Soares, Ilya M. Veer, Henrik Walter, Dieter Schoepf, Bartosz Zurowski, Carsten Konrad, Elisabeth Schramm, Claus Normann, Knut Schnell, Matthew D. Sacchet, Ian H. Gotlib, Glenda MacQueen, Beata R. Godlewska, Thomas E. Nickson, Andrew M. McIntosh, Martina Papmeyer, Heather C. Whalley, Jérémy Hall, J. E. Sussmann, Mingzhe Li, Martin Walter, Lyubomir I. Aftanas, Ivan Brack, Н. А. Бохан, Paul M. Thompson, Dick J. Veltman - Molecular Psychiatry 2016 cited by 1,338

  6. Common schizophrenia alleles are enriched in mutation-intolerant genes and in regions under strong background selection

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

  7. DNA methylation age of blood predicts all-cause mortality in later life

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Ian J. Deary - Genome Biology 2015 cited by 1,361

  8. Subcortical brain alterations in major depressive disorder: findings from the ENIGMA Major Depressive Disorder working group

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Greig I. de Zubicaray, Katie L. McMahon, Sarah E. Medland, Nicholas G. Martin, Nathan A. Gillespie, Margaret J. Wright, Geoffrey B. Hall, Glenda MacQueen, Eva-Maria Frey, Angela Carballedo, Laura S. van Velzen, Marie‐José van Tol, Nic J. van der Wee, Ilya M. Veer, Henrik Walter, Knut Schnell, Elisabeth Schramm, Claus Normann, Dieter Schoepf, Carsten Konrad, Bartosz Zurowski, Thomas E. Nickson, Andrew M. McIntosh, Martina Papmeyer, Heather C. Whalley, J. E. Sussmann, Beata R. Godlewska, Philip J. Cowen, Felix Fischer, Matthias Rose, Brenda W.J.H. Penninx, Paul M. Thompson, Derrek P. Hibar - Molecular Psychiatry 2015 cited by 1,189

  9. Genomic and phenotypic insights from an atlas of genetic effects on DNA methylation

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Alexia Cardona, Felix R. Day, Giovanni Cugliari, Clara Viberti, Simonetta Guarrera, Michael C. Lerro, Richa Gupta, Sailalitha Bollepalli, Pooja R. Mandaviya, Yanni Zeng, Toni‐Kim Clarke, Rosie M. Walker, Vanessa Schmoll, Darina Czamara, Carlos Ruiz-Arenas, Faisal I. Rezwan, Riccardo E. Marioni, Tian Lin, Yvonne Awaloff, Marine Germain, Dylan Aïssi, Ramona Zwamborn, Kristel van Eijk, Annelot M. Dekker, Jenny van Dongen, Jouke‐Jan Hottenga, Gonneke Willemsen, Cheng‐Jian Xu, Guillermo Barturen, Francesc Català‐Moll, Martin Kerick, Carol A. Wang, Phillip E. Melton, Hannah R. Elliott, Jean Shin, Manon Bernard, İdil Yet, Melissa Smart, T.J. Gorrie-Stone, Chris Shaw, Ammar Al‐Chalabi, Susan M. Ring, Göran Pershagen, Erik Melén, Jordi Jiménez‐Conde, Jaume Roquer, Debbie A. Lawlor, John Wright, Nicholas G. Martin, Grant W. Montgomery, Terrie E. Moffitt, Richie Poulton, Tõnu Esko, Lili Milani, Andres Metspalu, John R. B. Perry, Ken K. Ong, Nicholas J. Wareham, Giuseppe Matullo, Carlotta Sacerdote, Salvatore Panico, Avshalom Caspi, Louise Arseneault, France Gagnon, Miina Ollikainen, Jaakko Kaprio, Janine F. Felix, Fernando Rivadeneira, Henning Tiemeier, Marinus H. van IJzendoorn and 56 more - Nature Genetics 2021 cited by 539

  10. The genetic basis of endometriosis and comorbidity with other pain and inflammatory conditions

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , James P. Cook, Immaculata De Vivo, Amy D. DiVasta, O Dorien, Jacqueline F. Donoghue, Todd L. Edwards, Pierre Fontanillas, Jenny N. Fung, Reynir Tómas Geirsson, Jane E. Girling, Paivi Harkki, Holly R. Harris, Martin Healey, Oskari Heikinheimo, Sarah J. Holdsworth‐Carson, Isabel C. Hostettler, Henry Houlden, Sahar Houshdaran, Juan C. Irwin, Marjo‐Riitta Järvelin, Yoichiro Kamatani, Stephen Kennedy, Ewa Kępka, Johannes Kettunen, Michiaki Kubo, Bartosz Kulig, Venla Kurra, Hannele Laivuori, Marc R. Laufer, Cecilia M. Lindgren, Stuart MacGregor, Massimo Mangino, Nicholas G. Martin, Charoula Matalliotaki, Michail Matalliotakis, Alison D. Murray, Anne Ndungu, Camran Nezhat, Catherine M. Olsen, Jessica Opoku‐Anane, Sandosh Padmanabhan, Manish Paranjpe, Maire Peters, Grzegorz Polak, David J. Porteous, Joseph T. Rabban, Kathryn M. Rexrode, Hanna Romanowicz, Merli Saare, Liisu Saavalainen, Andrew J. Schork, Sushmita Sen, Amy L. Shafrir, Anna Siewierska-Górska, Marcin Słomka, Blair H. Smith, Beata Smolarz, Tomasz Szaflik, Krzysztof Szyłło, Atsushi Takahashi, Kathryn L. Terry, Carla Tomassetti, Susan A. Treloar, Arne Vanhie, Katy Vincent, Kim Chi Vo, David J. Werring, Eleftheria Zeggini, Maria I. Zervou, Kāri Stefánsson and 48 more - Nature Genetics 2023 cited by 287

  11. Integrative analysis of omics summary data reveals putative mechanisms underlying complex traits

    Authors: , , , , , , , , , , , , , , - Nature Communications 2018 cited by 689

  12. Meta-analysis of genome-wide association studies of anxiety disorders

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Peter J. van der Most, Ilja M. Nolte, Floor V. A. van Oort, Catharina A. Hartman, Albertine J. Oldehinkel, Martin Preisig, Hans J. Grabe, Christel M. Middeldorp, Brenda W.J.H. Penninx, Dorret I. Boomsma, Nicholas G. Martin, Grant W. Montgomery, Brion S. Maher, Edwin J. van den Oord, Naomi R. Wray, Henning Tiemeier, John M. Hettema - Molecular Psychiatry 2016 cited by 618

  13. Minimal phenotyping yields genome-wide association signals of low specificity for major depression

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Kenneth S. Kendler, Jonathan Flint - Nature Genetics 2020 cited by 375

  14. The transcriptional landscape of age in human peripheral blood

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Robert Walker, Ronald H. Zielke, Sampath Arepalli, Mina Ryten, Andrew Singleton, Y.F. Ramos, Harald H.H. Göring, Myriam Fornage, Ching‐Ti Liu, Sina A. Gharib, Barbara E. Stranger, Philip L. De Jager, Abraham Aviv, Daniel Levy, Joanne M. Murabito, Peter J. Munson, Tianxiao Huan, Albert Hofman, André G. Uitterlinden, Fernando Rivadeneira, Jeroen van Rooij, Lisette Stolk, Linda Broer, Michaël Verbiest, Mila Jhamai, Pascal Arp, Andres Metspalu, Liina Tserel, Lili Milani, Nilesh J. Samani, Pärt Peterson, Silva Kasela, Veryan Codd, Annette Peters, Cavin Ward‐Caviness, Christian Herder, Mélanie Waldenberger, Michael Roden, Paula Singmann, Sonja Zeilinger, Thomas Illig, Georg Homuth, Hans J. Grabe, Henry Völzke, Leif Steil, Thomas Kocher, Anna Murray, David Melzer, Hanieh Yaghootkar, Stefania Bandinelli, Eric K. Moses, Jack W. Kent, Joanne E. Curran, Matthew P. Johnson, Sarah Williams‐Blangero, Harm-Jan Westra, Allan F. McRae, Jennifer A. Smith, Sharon L. R. Kardia, Iiris Hovatta, Markus Perola, Samuli Ripatti, Veikko Salomaa, Anjali K. Henders, Nicholas G. Martin, Alicia K. Smith, Divya Mehta, Elisabeth B. Binder, K. Maria Nylocks, Elizabeth M. Kennedy and 37 more - Nature Communications 2015 cited by 760

  15. White matter disturbances in major depressive disorder: a coordinated analysis across 20 international cohorts in the ENIGMA MDD working group

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Axel Krug, Jim Lagopoulos, Renick Lee, Tristram A. Lett, Meng Li, Frank P. MacMaster, Nicholas G. Martin, Andrew M. McIntosh, Quinn McLellan, Susanne Meinert, Igor Nenadić, Evgeny Osipov, Brenda W.J.H. Penninx, Marı́a J. Portella, Jonathan Repple, Annerine Roos, Matthew D. Sacchet, Philipp G. Sämann, Knut Schnell, Xueyi Shen, Kang Sim, Dan J. Stein, Marie‐José van Tol, A. S. Tomyshev, Leonardo Tozzi, Ilya M. Veer, Robert Vermeiren, Yolanda Vives‐Gilabert, Henrik Walter, Martin Walter, Nic J.A. van der Wee, Steven J.A. van der Werff, Mindy Westlund Schreiner, Heather C. Whalley, Margaret J. Wright, Tony T. Yang, Alyssa H. Zhu, Dick J. Veltman, Paul M. Thompson, Neda Jahanshad, Lianne Schmaal - Molecular Psychiatry 2019 cited by 373

  16. Shared genetic origin of asthma, hay fever and eczema elucidates allergic disease biology

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Melanie C. Matheson, Shyamali C. Dharmage, Lisa Bain, Lars G. Fritsche, Maiken E. Gabrielsen, Brunilda Balliu, Jonas B. Nielsen, Wei Zhou, Kristian Hveem, Arnulf Langhammer, Oddgeir L. Holmen, Mari Løset, Gonçalo R. Abecasis, Cristen J. Willer, Andreas Arnold, Georg Homuth, Carsten Oliver Schmidt, Philip J. Thompson, Nicholas G. Martin, David L Duffy, Natalija Novak, Holger Schulz, Stefan Karrasch, Christian Gieger, Konstantin Strauch, Ronald B. Melles, David A. Hinds, Norbert Hübner, Stephan Weidinger, Patrik K. E. Magnusson, Rick Jansen, Eric Jorgenson, Young‐Ae Lee, Dorret I. Boomsma, Catarina Almqvist, Robert Karlsson, Gerard H. Koppelman, Lavinia Paternoster - Nature Genetics 2017 cited by 570

  17. The ENIGMA Consortium: large-scale collaborative analyses of neuroimaging and genetic data

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , H. Jeremy Bockholt, Erlend Bøen, Catherine Bois, Dorret I. Boomsma, Tom Booth, Ian Bowman, Janita Bralten, Rachel M. Brouwer, Han G. Brunner, David G. Brohawn, Randy L. Buckner, Jan K. Buitelaar, Kazima Bulayeva, Juan Bustillo, Vince D. Calhoun, Dara M. Cannon, Rita M. Cantor, Melanie A. Carless, Xavier Caseras, Gianpiero L. Cavalleri, M. Mallar Chakravarty, Kiki Chang, Christopher R. K. Ching, Andrea Christoforou, Sven Cichon, Vincent P. Clark, Patricia Conrod, Giovanni Coppola, Benedicto Crespo‐Facorro, Joanne E. Curran, Michael Czisch, Ian J. Deary, Eco J. C. de Geus, Anouk den Braber, Giuseppe Delvecchio, Chantal Depondt, Lieuwe de Haan, Greig I. de Zubicaray, Danai Dima, Ralica Dimitrova, Srdjan Djurovic, Hong‐Wei Dong, Gary Donohoe, Ravindranath Duggirala, Thomas D. Dyer, Stefan Ehrlich, Carl Johan Ekman, Torbjørn Elvsåshagen, Louise Emsell, Susanne Erk, Thomas Espeseth, Jesen Fagerness, Scott C. Fears, Iryna O. Fedko, Guillén Fernández, Simon E. Fisher, Tatiana Foroud, Peter T. Fox, Clyde Francks, Sophia Frangou, Eva Frey, Thomas Frodl, Vincent Frouin, Hugh Garavan, Sudheer Giddaluru, David C. Glahn, Beata R. Godlewska, Rita Z. Goldstein, Randy L. Gollub, Hans J. Grabe and 189 more - Brain Imaging and Behavior 2014 cited by 876

  18. Multi-ancestry genome-wide association study of 21,000 cases and 95,000 controls identifies new risk loci for atopic dermatitis

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Joyce Y. Tung, Chao Tian, David A. Hinds, Atsushi Takahashi, Anja Bauerfeind, Birgit Kalb, Norbert Hübner, Jorge Esparza-Gordillo, Franz Rüschendorf, Herman T den Dekker, Johan C de Jongste, Anja Bauerfeind, Liesbeth Duijts, Fernando Rivadeneira, Jorge Esparza-Gordillo, André G Uitterlinden, Alexessander Couto Alves, Jacob P. Thyssen, Nicholas G Martin, Vincent W. V. Jaddoe, Herman T. den Dekker, Johan C. de Jongste, Albert Hofman, Patrick M A Sleiman, Jin Li, Hakon Hakonarson, Feng Li Xiao, Xian Bo Zuo, Xiao Dong Zheng, Liesbeth Duijts, Niels J. Elbert, Fernando Rivadeneira, Juan R Gonzalez, Manuel A. R. Ferreira, Nicholas G. Martin, Jordi Sunyer, Susanne Lau, Maria Pino-Yanes, Christian Gieger, Annette Peters, Scott Huntsman, Janina S. Ried, Cheng-Jian Xu, Jin Li, Patrick Sleiman, Bjarke Feenstra, Patrick Sleiman, Mads Melbye, Xian Bo Zuo, Feng Li Xiao, Xian Yin, Xue Jun Zhang, Xiao Zheng, Liang Sun, Veronique Bataille, Tim Spector, Daniel Glass, Craig E Pennell, Jordi Sunyer, Sheila J Barton, Keith M Godfrey, Mariona Bustamante, Ivan Curjuric, Ashish Kumar, Juan R Gonzalez, Nicole M Probst-Hensch, Susanne Lau, Birgit Kalb, Scott Huntsman, Esteban G. Burchard and 50 more - Nature Genetics 2015 cited by 661

  19. Multitrait analysis of glaucoma identifies new risk loci and enables polygenic prediction of disease susceptibility and progression

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Andrea L. Vincent, Ivan Goldberg, Graham Radford‐Smith, Nicholas G. Martin, Grant W. Montgomery, Véronique Vitart, René Hoehn, Robert Wojciechowski, Jost B. Jonas, Tin Aung, Louis R. Pasquale, Angela J. Cree, Sobha Sivaprasad, Neeru A. Vallabh, Ananth C. Viswanathan, Francesca Pasutto, Jonathan L. Haines, Caroline C. W. Klaver, Cornelia M. van Duijn, Robert J. Casson, Paul J. Foster, Peng T. Khaw, Christopher J. Hammond, David A. Mackey, Paul Mitchell, Andrew Lotery, Janey L. Wiggs, Alex W. Hewitt, Stuart MacGregor - Nature Genetics 2020 cited by 360

  20. A large-scale genome-wide association study meta-analysis of cannabis use disorder

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Louis Fox, Alison Goate, Scott D. Gordon, Laura M. Hack, Dana B. Hancock, Sarah M. Hartz, Ian B. Hickie, David M. Hougaard, Kenneth Krauter, Penelope A. Lind, Jeanette N. McClintick, Matthew B. McQueen, Jacquelyn L. Meyers, Grant W. Montgomery, Ole Mors, Preben Bo Mortensen, Merete Nordentoft, John F. Pearson, Roseann E. Peterson, Maureen Reynolds, John P. Rice, Valgerður Rúnarsdóttir, Nancy L. Saccone, Richard Sherva, Judy L. Silberg, Ralph E. Tarter, Þórarinn Tyrfingsson, Tamara L. Wall, Bradley T. Webb, Thomas Werge, Leah Wetherill, Margaret J. Wright, Stephanie Zellers, Mark J. Adams, Laura J. Bierut, Jason D Boardman, William Copeland, Lindsay A. Farrer, Tatiana Foroud, Nathan A. Gillespie, Richard A. Grucza, Kathleen Mullan Harris, Andrew C. Heath, Victor Hesselbrock, John K. Hewitt, Christian J. Hopfer, John Horwood, William G. Iacono, Eric O. Johnson, Kenneth S. Kendler, Martin A. Kennedy, Henry R. Kranzler, Pamela A. F. Madden, Hermine H. Maes, Brion S. Maher, Nicholas G. Martin, Matthew McGue, Andrew M. McIntosh, Sarah E. Medland, Elliot C. Nelson, Bernice Porjesz, Brien P. Riley, Michael C. Stallings, Michael M. Vanyukov, Scott Vrieze, Raymond K. Walters, Renato Polimanti, Emma Johnson, Jeanette N. McClintick, Alexander S. Hatoum and 173 more - The Lancet Psychiatry 2020 cited by 379

  21. Identification of 55,000 Replicated DNA Methylation QTL

    Authors: , , , , , , , , , , , , , , , , - Scientific Reports 2018 cited by 366

  22. Meta-analysis of 375,000 individuals identifies 38 susceptibility loci for migraine

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Markus Schürks, Paul M. Ridker, Maria Gudlaug Hrafnsdottir, Hreinn Stefánsson, Susan M. Ring, Jouke‐Jan Hottenga, Brenda W.J.H. Penninx, Markus Färkkilä, Ville Artto, Mari Kaunisto, Salli Vepsäläinen, Rainer Malik, Andrew C. Heath, Pamela A. F. Madden, Nicholas G. Martin, Grant W. Montgomery, Mitja Kurki, Mart Kals, Reedik Mägi, Kalle Pärn, Eija Hämäläinen, Hailiang Huang, Andrea Byrnes, Lude Franke, Jie Huang, Evie Stergiakouli, Phil H. Lee, Cynthia Sandor, Caleb Webber, M. Zameel Cader, Bertram Müller‐Myhsok, Stefan Schreiber, Thomas Meitinger, Johan G. Eriksson, Veikko Salomaa, Kauko Heikkilä, Elizabeth Loehrer, André G. Uitterlinden, Albert Hofman, Cornelia M. van Duijn, Lynn Cherkas, Linda M. Pedersen, Audun Stubhaug, Christopher Sivert Nielsen, Minna Männikkö, Evelin Mihailov, Lili Milani, Hartmut Göbel, Ann-Louise Esserlind, Anne Francke Christensen, Thomas Folkmann Hansen, Thomas Werge, Jaakko Kaprio, Arpo Aromaa, Olli T. Raitakari, M. Arfan Ikram, Tim D. Spector, Marjo‐Riitta Järvelin, Andres Metspalu, Christian Kubisch, David P. Strachan, Michel D. Ferrari, Andrea Carmine Belin, Martin Dichgans, Maija Wessman, Arn M. J. M. van den Maagdenberg, John‐Anker Zwart, Dorret I. Boomsma, George Davey Smith, Kāri Stefánsson and 7 more - Nature Genetics 2016 cited by 703

  23. Genome-wide association analyses identify 18 new loci associated with serum urate concentrations

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Xuan Liu, Giovanni Malerba, Lorna M. Lopez, Pim van der Harst, Man Li, Marcus E. Kleber, Andrew A. Hicks, Ilja M. Nolte, Åsa Johansson, Federico Murgia, Sarah H. Wild, Stephan J. L. Bakker, John F. Peden, Abbas Dehghan, Maristella Steri, Albert Tenesa, Vasiliki Lagou, Perttu Salo, Massimo Mangino, Lynda M. Rose, Terho Lehtimäki, Owen M. Woodward, Yukinori Okada, Adrienne Tin, Christian Müller, Christopher Oldmeadow, Margus Putku, Darina Czamara, Peter Kraft, Laura Frogheri, Gian Andri Thun, Anne Grotevendt, Gauti Kjartan Gíslason, Tamara B. Harris, Lenore J. Launer, Patrick F. McArdle, Alan R. Shuldiner, Eric Boerwinkle, Josef Coresh, Helena Schmidt, Michael Schallert, Nicholas G. Martin, Grant W. Montgomery, Michiaki Kubo, Yusuke Nakamura, Toshihiro Tanaka, Patricia B. Munroe, Nilesh J. Samani, David R. Jacobs, Kiang Liu, Pio D’Adamo, Sheila Ulivi, Jerome I. Rotter, Bruce M. Psaty, Péter Vollenweider, Gérard Waeber, Susan Campbell, Olivier Devuyst, Pau Navarro, Ivana Kolčić, Nicholas D. Hastie, Beverley Balkau, Philippe Froguel, Tõnu Esko, Andres Salumets, Kay‐Tee Khaw, Claudia Langenberg, Nicholas J. Wareham, Aaron Isaacs, Aldi T. Kraja and 126 more - Nature Genetics 2012 cited by 878

  24. Common genetic variants contribute to risk of rare severe neurodevelopmental disorders

    Authors: , , , , , , , , , , , , , , , , - Nature 2018 cited by 345