Andrés Ingason

Active 2002–2026

60
Papers
19,261
Citations
45
h-index
58
i10-index

Citations

Citations per year for Andrés Ingason1965: 1 citations1996: 1 citations1999: 2 citations2002: 5 citations2003: 71 citations2004: 87 citations2005: 80 citations2006: 131 citations2007: 79 citations2008: 174 citations2009: 318 citations2010: 352 citations2011: 355 citations2012: 371 citations2013: 347 citations2014: 246 citations2015: 232 citations2016: 177 citations2017: 162 citations2018: 183 citations2019: 434 citations2020: 403 citations2021: 486 citations2022: 355 citations2023: 302 citations2024: 453 citations2025: 207 citations2026: 13 citations1966–1995: no citations, so these years are not shown1997–1998: no citations, so these years are not shown2000–2001: no citations, so these years are not shown

Citation sources

Countries

World map of the countries and regions citing this authorUnited States: 2,800 citing papers, 23.4% of this breakdownUnited Kingdom: 1,239 citing papers, 10.4% of this breakdownGermany: 701 citing papers, 5.9% of this breakdownChina: 581 citing papers, 4.8% of this breakdownAustralia: 504 citing papers, 4.2% of this breakdownNetherlands: 475 citing papers, 4% of this breakdownCanada: 459 citing papers, 3.8% of this breakdownDenmark: 370 citing papers, 3.1% of this breakdownSweden: 370 citing papers, 3.1% of this breakdownItaly: 355 citing papers, 3% of this breakdownFrance: 349 citing papers, 2.9% of this breakdownIceland: 248 citing papers, 2.1% of this breakdown
0%23.4%Other 29.3%

Fields

  • Biochemistry, Genetics and Molecular Biology52.9%
  • Medicine26.6%
  • Neuroscience14%
  • Psychology1.8%
  • Immunology and Microbiology1.1%
  • Agricultural and Biological Sciences0.8%
  • Other2.8%

Topics

  • Genetic Associations and Epidemiology8.8%
  • Genomic variations and chromosomal abnormalities4.9%
  • Genetics and Neurodevelopmental Disorders4%
  • Genomics and Rare Diseases3.4%
  • Tryptophan and brain disorders2.3%
  • Neuroscience and Neuropharmacology Research1.9%
  • Other74.7%

Coauthors

All papers

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  1. Genomic and drug target evaluation of 90 cardiovascular proteins in 30,931 individuals

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Sölve Elmståhl, Gunnar Engström, Eric B. Fauman, Céline Fernandez, Lude Franke, Paul W. Franks, Vilmantas Giedraitis, Chris Haley, Anders Hamsten, Andrés Ingason, Åsa Johansson, Peter K. Joshi, Lars Lind, Cecilia M. Lindgren, Steven A. Lubitz, Tom Palmer, Erin Macdonald-Dunlop, Martin Magnusson, Olle Melander, Karl Michaëlsson, Andrew P. Morris, Reedik Mägi, Michael W. Nagle, Peter M. Nilsson, Jan Nilsson, Marju Orho‐Melander, Ozren Polašek, Bram P. Prins, Erik Pålsson, Ting Qi, Marketa Sjögren, Johan Sundström, Praveen Surendran, Urmo Võsa, Thomas Werge, Rasmus Wernersson, Harm-Jan Westra, Jian Yang, Alexandra Zhernakova, Johan Ärnlöv, Jingyuan Fu, J. G. Smith, Tõnu Esko, Caroline Hayward, Ulf Gyllensten, Mikael Landén, Agneta Siegbahn, James F. Wilson, Lars Wallentin, Adam S. Butterworth, Michael V. Holmes, Erik Ingelsson, Anders Mälarstig - Nature Metabolism 2020 cited by 772

  2. 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

  3. 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

  4. Genome-wide mega-analysis identifies 16 loci and highlights diverse biological mechanisms in the common epilepsies

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Chantal Depondt, Orrin Devinsky, Dennis Dlugos, Colin P. Doherty, Christian E. Elger, Johan G. Eriksson, Thomas N. Ferraro, Martha Feucht, Ben Francis, André Franke, Jacqueline A. French, Saskia Freytag, Verena Gaus, Eric B. Geller, Christian Gieger, Tracy A. Glauser, Simon Glynn, David B. Goldstein, Hongsheng Gui, Youling Guo, Kevin F. Haas, Håkon Håkonarson, Kerstin Hallmann, Sheryl R. Haut, Erin L. Heinzen, Ingo Helbig, Christian Hengsbach, Helle Hjalgrim, Michele Iacomino, Andrés Ingason, Jennifer Jamnadas-Khoda, Michael R. Johnson, Reetta Kälviäinen, Anne-Mari Kantanen, Dalia Kasperavičiūtė, Dorothée Kasteleijn‐Nolst Trenité, Heidi E. Kirsch, Robert C. Knowlton, Bobby P.C. Koeleman, Roland Krause, Martin Krenn, Wolfram S. Kunz, Ruben Kuzniecky, Patrick Kwan, Dennis Lal, YL Lau, Anna‐Elina Lehesjoki, Holger Lerche, Costin Leu, Wolfgang Lieb, Dick Lindhout, Warren Lo, Íscia Lopes‐Cendes, Daniel H. Lowenstein, Alberto Malovini, Anthony G Marson, Thomas Mayer, Mark McCormack, James L. Mills, Nasir Mirza, Martina Moerzinger, Rikke S. Møller, Anne M. Molloy, Hiltrud Muhle, Mark R. Newton, Ping-Wing Ng, Markus M. Nöthen, Peter Nürnberg, Terence J. O’Brien, Karen Oliver and 58 more - Nature Communications 2018 cited by 513

  5. Population genomics of post-glacial western Eurasia

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Gabriel Renaud, Aaron J. Stern, Theis Zetner Trolle Jensen, Gabriele Scorrano, Hannes Schroeder, Per Lysdahl, Abigail Ramsøe, Andrey Skorobogatov, Andrew J. Schork, Anders Rosengren, Anthony Ruter, Alan K. Outram, Aleksey A. Timoshenko, Alexandra Buzhilova, Alfredo Coppa, А. В. Зубова, Ana María Silva, Anders J. Hansen, Andrey Gromov, Andrey Logvin, Anne Birgitte Gotfredsen, Bjarne Henning Nielsen, Borja González-Rabanal, Carles Lalueza‐Fox, Catriona J. McKenzie, Charleen Gaunitz, Concepción Blasco, Corina Liesau von Lettow‐Vorbeck, Cristina Martínez‐Labarga, Dmitri V. Pozdnyakov, David Cuenca-Solana, David Lordkipanidze, Dmitri En’shin, Domingo C. Salazar‐García, T. Douglas Price, Dušan Borić, Elena Kostyleva, Elizaveta Veselovskaya, Emma Usmanova, Enrico Cappellini, Erik Brinch Petersen, Esben Kannegaard, Francesca Radina, Fulya Eylem Yediay, Henri Duday, Igor Gutiérrez-Zugasti, I. Merts, Inna Potekhina, Irinа Shevnina, Isin Altinkaya, Jean Guilaine, Jesper Hansen, J. Emili Aura Tortosa, Joào Zilhão, Jorge R. Vega, Kristoffer Buck Pedersen, Krzysztof Tunia, Lei Zhao, Liudmila N. Mylnikova, Lars Larsson, Laure Metz, Levon Yepiskoposyan, Lisbeth Pedersen, Lucia Sarti, Ludovic Orlando, Ludovic Slimak, Lutz Klassen, Malou Blank, Manuel R. González Morales, Mara Silvestrini and 64 more - Nature 2024 cited by 206

  6. Population genomics of the Viking world

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Caroline Arcini, Ceri Falys, Charlotte Hedenstierna Jonson, Dariusz Błaszczyk, Denis V. Pezhemsky, Gordon Turner‐Walker, Hildur Gestsdóttir, Inge Lundstrøm, Ingrid Gustin, Ingrid Mainland, Inna Potekhina, Italo Maria Muntoni, Jade Yu Cheng, Jesper Stenderup, Jilong Ma, Julie Gibson, Jüri Peets, Jörgen Gustafsson, Katrine Iversen, Linzi Simpson, Lisa Strand, Louise Loe, Maeve Sikora, Marek Florek, Maria Vretemark, Mark Redknap, Monika Bajka, Tamara Pushkina, Morten Søvsø, Natalia Grigoreva, Tom Christensen, Ole Thirup Kastholm, Otto Uldum, Pasquale Favia, Per Holck, Sabine Sten, Símun V. Arge, Sturla Ellingvåg, Vayacheslav Moiseyev, Wiesław Bogdanowicz, Yvonne Magnusson, Ludovic Orlando, Peter Pentz, Mads Dengsø Jessen, Anne Pedersen, Mark Collard, Daniel G. Bradley, Marie Louise Schjellerup Jørkov, Jette Arneborg, Niels Lynnerup, Neil Price, M. Thomas P. Gilbert, Morten E. Allentoft, Jan Bill, Søren Michael Sindbæk, Lotte Hedeager, Kristian Kristiansen, Rasmus Nielsen, Thomas Werge, Eske Willerslev - Nature 2020 cited by 353

  7. The selection landscape and genetic legacy of ancient Eurasians

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Martin Sikora, Rasmus Nielsen, Fernando Racimo, Eske Willerslev - Nature 2024 cited by 139

  8. Loss-of-function variants in ABCA7 confer risk of Alzheimer's disease

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Pálmi V. Jónsson, Sigurbjörn Björnsson, Jón Snædal, Kari Stefansson - Nature Genetics 2015 cited by 332

  9. Detection of sharing by descent, long-range phasing and haplotype imputation

    Authors: , , , , , , , , , , , , , , , , - Nature Genetics 2008 cited by 481

  10. Common variants conferring risk of schizophrenia

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Ina Giegling, Henrik B. Rasmussen, Sally Timm, Manuel Mattheisen, István Bitter, János Réthelyi, Brynja B. Magnúsdóttir, Thordur Sigmundsson, Pall I. Olason, Gísli Másson, Jeffrey R. Gulcher, Magnús Haraldsson, Ragnheiður Fossdal, Thorgeir E. Thorgeirsson, Unnur Þorsteinsdóttir, Mirella Ruggeri, Sarah Tosato, Barbara Franke, Eric Strengman, Lambertus A. Kiemeney, Ingrid Melle, Srdjan Djurovic, Л. И. Абрамова, В. Г. Каледа, Julio Sanjuán, Rosa de Frutos, Elvira Bramon, Evangelos Vassos, Gillian Fraser, Ulrich Ettinger, Marco Picchioni, Nicholas Walker, Timi Toulopoulou, Anna C. Need, Dongliang Ge, Joeng Lim Yoon, Kevin V. Shianna, Nelson B. Freimer, Rita M. Cantor, Robin Murray, Augustine Kong, В. Е. Голимбет, Ángel Carracedo, Celso Arango, Javier Costas, Erik G. Jönsson, Lars Terenius, Ingrid Agartz, Hannes Pétursson, Markus M. Nöthen, Marcella Rietschel, Paul M. Matthews, Pierandrea Muglia, Leena Peltonen, David St Clair, David B. Goldstein, Kāri Stefánsson, David Collier - Nature 2009 cited by 1,720

  11. Multi-PGS enhances polygenic prediction by combining 937 polygenic scores

    Authors: , , , , , , , , , , , , , , , , , , - Nature Communications 2023 cited by 80

  12. A common inversion under selection in Europeans

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , - Nature Genetics 2005 cited by 872

  13. 100 ancient genomes show repeated population turnovers in Neolithic Denmark

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Gabriel Renaud, Aaron J. Stern, Niels Nørkjær Johannsen, Abigail Ramsøe, Andrew J. Schork, Anthony Ruter, Anne Birgitte Gotfredsen, Bjarne Henning Nielsen, Erik Brinch Petersen, Esben Kannegaard, Jesper Hansen, Kristoffer Buck Pedersen, Lisbeth Pedersen, Lutz Klassen, Morten Meldgaard, Morten Johansen, Otto Uldum, Per Lotz, Per Lysdahl, Pernille Bangsgaard, Peter Vang Petersen, Rikke Maring, Rune Iversen, Sidsel Wåhlin, Søren A. Sørensen, Søren H. Andersen, Thomas Martini Jørgensen, Niels Lynnerup, Daniel J. Lawson, Simon Rasmussen, Thorfinn Sand Korneliussen, Kurt H. Kjær, Richard Durbin, Rasmus Nielsen, Olivier Delaneau, Thomas Werge, Kristian Kristiansen, Eske Willerslev - Nature 2024 cited by 114

  14. A variant associated with nicotine dependence, lung cancer and peripheral arterial disease

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Peter F.A. Mulders, Dolores Isla, María Vidal, Laura Asín, Berta Sáez, Laura Murillo, Þorsteinn Blöndal, H. Kolbeinsson, Jón G. Stefánsson, Ingunn Hansdóttir, Valgerður Rúnarsdóttir, Roberto Pola, Bengt Lindblad, André M. van Rij, Benjamin Dieplinger, Meinhard Haltmayer, José Mayordomo, Lambertus A. Kiemeney, Stefán E. Matthíasson, Högni Óskarsson, Þórarinn Tyrfingsson, Daníel F. Guðbjartsson, Jeffrey R. Gulcher, Steinn Jónsson, Unnur Þorsteinsdóttir, Augustine Kong, Kāri Stefánsson - Nature 2008 cited by 1,529

  15. Attention-deficit hyperactivity disorder shares copy number variant risk with schizophrenia and autism spectrum disorder

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , - Translational Psychiatry 2019 cited by 134

  16. Large recurrent microdeletions associated with schizophrenia

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Annette M. Hartmann, Kevin V. Shianna, Dongliang Ge, Anna C. Need, Caroline Crombie, Gillian Fraser, Nicholas Walker, Jouko Lönnqvist, Jaana Suvisaari, Annamarie Tuulio-Henriksson, Tiina Paunio, Timi Toulopoulou, Elvira Bramon, Marta Di Forti, Robin Murray, Mirella Ruggeri, Evangelos Vassos, Sarah Tosato, Muriel Walshe, Tao Li, Catalina Vasilescu, Thomas W. Mühleisen, August G. Wang, Henrik Ullum, Srdjan Djurovic, Ingrid Melle, Jes Olesen, Lambertus A. Kiemeney, Barbara Franke, Chiara Sabatti, Nelson B. Freimer, Jeffrey R. Gulcher, Unnur Þorsteinsdóttir, Augustine Kong, Ole A. Andreassen, Roel A. Ophoff, Alexander Georgi, Marcella Rietschel, Thomas Werge, Hannes Pétursson, David B. Goldstein, Markus M. Nöthen, Leena Peltonen, David Collier, David St Clair, Kāri Stefánsson - Nature 2008 cited by 1,782

  17. Polygenic risk scores for schizophrenia and bipolar disorder predict creativity

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , - Nature Neuroscience 2015 cited by 504

  18. Variants associating with uterine leiomyoma highlight genetic background shared by various cancers and hormone-related traits

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Folkert W. Asselbergs, Jón G. Jónasson, Karl Olafsson, Unnur Þorsteinsdóttir, Bjarni V. Halldórsson, Guðmar Þorleifsson, Kāri Stefánsson - Nature Communications 2018 cited by 109

  19. A genome-wide cross-phenotype meta-analysis of the association of blood pressure with migraine

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Antti‐Pekka Sarin, Juho Wedenoja, David A. Hinds, Julie E. Buring, 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 and 37 more - Nature Communications 2020 cited by 76

  20. Common Variant Burden Contributes to the Familial Aggregation of Migraine in 1,589 Families

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Ville Artto, Markus Färkkilä, Michelle Agee, Babak Alipanahi, Adam Auton, Robert K. Bell, Katarzyna Bryc, Sarah L. Elson, Pierre Fontanillas, Nicholas A. Furlotte, Karen E. Huber, Aaron Kleinman, Nadia K. Litterman, Jennifer C. McCreight, 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, Verneri Anttila, Ville Artto, Andrea Carmine Belin, Dorret I. Boomsma, Sigrid Børte, Daniel I. Chasman, Lynn Cherkas, Anne Francke Christensen, Bru Cormand, Ester Cuenca-León, George Davey-Smith, Martin Dichgans, Cornelia M. van Duijn, Tõnu Esko, Ann-Louise Esserlind, Michel D. Ferrari, Rune R. Frants, Tobias Freilinger, Nick Furlotte, Padhraig Gormley, Lyn R. Griffiths, Eija Hämäläinen, Thomas Folkmann Hansen, Marjo Hiekkala, M. Arfan Ikram, Andrés Ingason, Marjo‐Riitta Järvelin, Risto Kajanne, Mikko Kallela, Jaakko Kaprio, Mari Kaunisto, Christian Kubisch, Mitja Kurki, Tobias Kurth, Lenore J. Launer, Terho Lehtimäki, Davor Lessel, Lannie Ligthart, Nadia K. Litterman, Arn van den Maagdenberg, Alfons Macaya, Rainer Malik, Massimo Mangino, George McMahon and 36 more - Neuron 2018 cited by 99

  21. Impute.me: An Open-Source, Non-profit Tool for Using Data From Direct-to-Consumer Genetic Testing to Calculate and Interpret Polygenic Risk Scores

    Authors: , , , , , - Frontiers in Genetics 2020 cited by 66

  22. Many sequence variants affecting diversity of adult human height

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Laufey Tryggvadóttír, Þórunn Rafnar, Jeffrey R. Gulcher, Lambertus A. Kiemeney, Augustine Kong, Unnur Þorsteinsdóttir, Kāri Stefánsson - Nature Genetics 2008 cited by 682

  23. Comparing Copy Number Variations in a Danish Case Cohort of Individuals With Psychiatric Disorders

    Authors: , , , , , , , , , , , , , , - JAMA Psychiatry 2021 cited by 56

  24. Disruption of the neurexin 1 gene is associated with schizophrenia

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Nicholas Walker, Jouko Lönnqvist, Jaana Suvisaari, Annamari Tuulio‐Henriksson, Srdjan Djurovic, Ingrid Melle, Ole A. Andreassen, Thomas Folkmann Hansen, Thomas Werge, Lambertus A. Kiemeney, Barbara Franke, Joris A. Veltman, Jacobine E. Buizer‐Voskamp, GROUP Investigators, Chiara Sabatti, Roel A. Ophoff, Marcella Rietschel, Markus M. Nöthen, Kāri Stefánsson, Leena Peltonen, David St Clair, Hreinn Stefánsson, David Collier - Human Molecular Genetics 2008 cited by 485