Omar Gustafsson

Association of Copy Number Variation of the 15q11.2 BP1-BP2 Region With Cortical and Subcortical Morphology and Cognition.

Authors:

Dennis van der Meer Ida E Sønderby Tobias Kaufmann G Bragi Walters Abdel Abdellaoui David Ames Katrin Amunts Micael Andersson Nicola J Armstrong Manon Bernard Nicholas B Blackburn John Blangero Dorret I Boomsma Henry Brodaty Rachel M Brouwer Robin Bülow Wiepke Cahn Vince D Calhoun Svenja Caspers Gianpiero L Cavalleri Christopher R K Ching Sven Cichon Simone Ciufolini Aiden Corvin Benedicto Crespo-Facorro Joanne E Curran Shareefa Dalvie Paola Dazzan Eco J C de Geus Greig I de Zubicaray Sonja M C de Zwarte Norman Delanty Anouk den Braber Sylvane Desrivieres Marta Di Forti Joanne L Doherty Gary Donohoe Stefan Ehrlich Else Eising Thomas Espeseth Simon E Fisher Tormod Fladby Oleksandr Frei Vincent Frouin Masaki Fukunaga Thomas Gareau David C Glahn Hans J Grabe Nynke A Groenewold Ómar Gústafsson Jan Haavik Asta K Haberg Ryota Hashimoto Jayne Y Hehir-Kwa Derrek P Hibar Manon H J Hillegers Per Hoffmann Laurena Holleran Jouke-Jan Hottenga Hilleke E Hulshoff Pol Masashi Ikeda Sébastien Jacquemont Neda Jahanshad Christiane Jockwitz Stefan Johansson Erik G Jönsson Masataka Kikuchi Emma E M Knowles John B Kwok Stephanie Le Hellard David E J Linden Jingyu Liu Arvid Lundervold Astri J Lundervold Nicholas G Martin Karen A Mather Samuel R Mathias Katie L McMahon Allan F McRae Sarah E Medland Torgeir Moberget Clara Moreau Derek W Morris Thomas W Mühleisen Robin M Murray Jan E Nordvik Lars Nyberg Loes M Olde Loohuis Roel A Ophoff Michael J Owen Tomas Paus Zdenka Pausova Juan M Peralta Bruce Pike Carlos Prieto Erin Burke Quinlan Céline S Reinbold Tiago Reis Marques James J H Rucker Perminder S Sachdev Sigrid B Sando Peter R Schofield Andrew J Schork Gunter Schumann Jean Shin Elena Shumskaya Ana I Silva Sanjay M Sisodiya Vidar M Steen Dan J Stein Lachlan T Strike Christian K Tamnes Alexander Teumer Anbupalam Thalamuthu Diana Tordesillas-Gutiérrez Anne Uhlmann Magnús Ö Úlfarsson Dennis van 't Ent Marianne B M van den Bree Evangelos Vassos Wei Wen Katharina Wittfeld Margaret J Wright Tetyana Zayats Anders M Dale Srdjan Djurovic Ingrid Agartz Lars T Westlye Hreinn Stefánsson Kári Stefánsson Paul M Thompson Ole A Andreassen

JAMA Psychiatry 2020 Apr;77(4):420-430

Norwegian Centre for Mental Disorders Research, Division of Mental Health and Addiction, Oslo University Hospital and Institute of Clinical Medicine, University of Oslo, Oslo, Norway.

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April 2020

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

Transl Psychiatry 2019 10 17;9(1):258. Epub 2019 Oct 17.

deCODE genetics/Amgen, Reykjavík, Iceland.

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October 2019

Correction: Dose response of the 16p11.2 distal copy number variant on intracranial volume and basal ganglia.

Authors:

Ida E Sønderby Ómar Gústafsson Nhat Trung Doan Derrek P Hibar Sandra Martin-Brevet Abdel Abdellaoui David Ames Katrin Amunts Michael Andersson Nicola J Armstrong Manon Bernard Nicholas Blackburn John Blangero Dorret I Boomsma Janita Bralten Hans-Richard Brattbak Henry Brodaty Rachel M Brouwer Robin Bülow Vince Calhoun Svenja Caspers Gianpiero Cavalleri Chi-Hua Chen Sven Cichon Simone Ciufolini Aiden Corvin Benedicto Crespo-Facorro Joanne E Curran Anders M Dale Shareefa Dalvie Paola Dazzan Eco J C de Geus Greig I de Zubicaray Sonja M C de Zwarte Norman Delanty Anouk den Braber Sylvane Desrivières Gary Donohoe Bogdan Draganski Stefan Ehrlich Thomas Espeseth Simon E Fisher Barbara Franke Vincent Frouin Masaki Fukunaga Thomas Gareau David C Glahn Hans Grabe Nynke A Groenewold Jan Haavik Asta Håberg Ryota Hashimoto Jayne Y Hehir-Kwa Andreas Heinz Manon H J Hillegers Per Hoffmann Laurena Holleran Jouke-Jan Hottenga Hilleke E Hulshoff Masashi Ikeda Neda Jahanshad Terry Jernigan Christiane Jockwitz Stefan Johansson Gudrun A Jonsdottir Erik G Jönsson Rene Kahn Tobias Kaufmann Sinead Kelly Masataka Kikuchi Emma E M Knowles Knut K Kolskår John B Kwok Stephanie Le Hellard Costin Leu Jingyu Liu Astri J Lundervold Arvid Lundervold Nicholas G Martin Karen Mather Samuel R Mathias Mark McCormack Katie L McMahon Allan McRae Yuri Milaneschi Clara Moreau Derek Morris David Mothersill Thomas W Mühleisen Robin Murray Jan E Nordvik Lars Nyberg Loes M Olde Loohuis Roel Ophoff Tomas Paus Zdenka Pausova Brenda Penninx Juan M Peralta Bruce Pike Carlos Prieto Sara Pudas Erin Quinlan Daniel S Quintana Céline S Reinbold Tiago Reis Marques Alexandre Reymond Genevieve Richard Borja Rodriguez-Herreros Roberto Roiz-Santiañez Jarek Rokicki James Rucker Perminder Sachdev Anne-Marthe Sanders Sigrid B Sando Lianne Schmaal Peter R Schofield Andrew J Schork Gunter Schumann Jean Shin Elena Shumskaya Sanjay Sisodiya Vidar M Steen Dan J Stein Stacy Steinberg Lachlan Strike Alexander Teumer Anbu Thalamuthu Diana Tordesillas-Gutierrez Jessica Turner Torill Ueland Anne Uhlmann Magnus O Ulfarsson Dennis van 't Ent Dennis van der Meer Neeltje E M van Haren Anja Vaskinn Evangelos Vassos G Bragi Walters Yunpeng Wang Wei Wen Christopher D Whelan Katharina Wittfeld Margie Wright Hidenaga Yamamori Tetyana Zayats Ingrid Agartz Lars T Westlye Sébastien Jacquemont Srdjan Djurovic Hreinn Stefánsson Kári Stefánsson Paul Thompson Ole A Andreassen

Mol Psychiatry 2020 Mar;25(3):692-695

NORMENT, K.G. Jebsen Centre for Psychosis Research, Institute of Clinical Medicine, University of Oslo and Division of Mental Health and Addiction, Oslo University Hospital, Oslo, Norway.

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March 2020

Reciprocal White Matter Changes Associated With Copy Number Variation at 15q11.2 BP1-BP2: A Diffusion Tensor Imaging Study.

Authors:

Ana I Silva Magnus O Ulfarsson Hreinn Stefansson Omar Gustafsson G Bragi Walters David E J Linden Lawrence S Wilkinson Mark Drakesmith Michael J Owen Jeremy Hall Kari Stefansson

Biol Psychiatry 2019 04 19;85(7):563-572. Epub 2018 Nov 19.

deCODE genetics/Amgen, Reykjavik, Iceland. Electronic address:

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April 2019

Dose response of the 16p11.2 distal copy number variant on intracranial volume and basal ganglia.

Authors:

Ida E Sønderby Ómar Gústafsson Nhat Trung Doan Derrek P Hibar Sandra Martin-Brevet Abdel Abdellaoui David Ames Katrin Amunts Michael Andersson Nicola J Armstrong Manon Bernard Nicholas Blackburn John Blangero Dorret I Boomsma Janita Bralten Hans-Richard Brattbak Henry Brodaty Rachel M Brouwer Robin Bülow Vince Calhoun Svenja Caspers Gianpiero Cavalleri Chi-Hua Chen Sven Cichon Simone Ciufolini Aiden Corvin Benedicto Crespo-Facorro Joanne E Curran Anders M Dale Shareefa Dalvie Paola Dazzan Eco J C de Geus Greig I de Zubicaray Sonja M C de Zwarte Norman Delanty Anouk den Braber Sylvane Desrivières Gary Donohoe Bogdan Draganski Stefan Ehrlich Thomas Espeseth Simon E Fisher Barbara Franke Vincent Frouin Masaki Fukunaga Thomas Gareau David C Glahn Hans Grabe Nynke A Groenewold Jan Haavik Asta Håberg Ryota Hashimoto Jayne Y Hehir-Kwa Andreas Heinz Manon H J Hillegers Per Hoffmann Laurena Holleran Jouke-Jan Hottenga Hilleke E Hulshoff Masashi Ikeda Neda Jahanshad Terry Jernigan Christiane Jockwitz Stefan Johansson Gudrun A Jonsdottir Erik G Jönsson Rene Kahn Tobias Kaufmann Sinead Kelly Masataka Kikuchi Emma E M Knowles Knut K Kolskår John B Kwok Stephanie Le Hellard Costin Leu Jingyu Liu Astri J Lundervold Arvid Lundervold Nicholas G Martin Karen Mather Samuel R Mathias Mark McCormack Katie L McMahon Allan McRae Yuri Milaneschi Clara Moreau Derek Morris David Mothersill Thomas W Mühleisen Robin Murray Jan E Nordvik Lars Nyberg Loes M Olde Loohuis Roel Ophoff Tomas Paus Zdenka Pausova Brenda Penninx Juan M Peralta Bruce Pike Carlos Prieto Sara Pudas Erin Quinlan Daniel S Quintana Céline S Reinbold Tiago Reis Marques Alexandre Reymond Genevieve Richard Borja Rodriguez-Herreros Roberto Roiz-Santiañez Jarek Rokicki James Rucker Perminder Sachdev Anne-Marthe Sanders Sigrid B Sando Lianne Schmaal Peter R Schofield Andrew J Schork Gunter Schumann Jean Shin Elena Shumskaya Sanjay Sisodiya Vidar M Steen Dan J Stein Stacy Steinberg Lachlan Strike Alexander Teumer Anbu Thalamuthu Diana Tordesillas-Gutierrez Jessica Turner Torill Ueland Anne Uhlmann Magnus O Ulfarsson Dennis van 't Ent Dennis van der Meer Neeltje E M van Haren Anja Vaskinn Evangelos Vassos G Bragi Walters Yunpeng Wang Wei Wen Christopher D Whelan Katharina Wittfeld Margie Wright Hidenaga Yamamori Tetyana Zayats Ingrid Agartz Lars T Westlye Sébastien Jacquemont Srdjan Djurovic Hreinn Stefánsson Kári Stefánsson Paul Thompson Ole A Andreassen

Mol Psychiatry 2020 03 3;25(3):584-602. Epub 2018 Oct 3.

NORMENT, K.G. Jebsen Centre for Psychosis Research, Institute of Clinical Medicine, University of Oslo and Division of Mental Health and Addiction, Oslo University Hospital, Oslo, Norway.

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March 2020

MAP1B mutations cause intellectual disability and extensive white matter deficit.

Nat Commun 2018 08 27;9(1):3456. Epub 2018 Aug 27.

deCODE genetics/Amgen, Reykjavik, 101, Iceland.

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August 2018

Fourteen sequence variants that associate with multiple sclerosis discovered by meta-analysis informed by genetic correlations.

Authors:

Sigurgeir Olafsson Pernilla Stridh Steffan Daniël Bos Andres Ingason Jack Euesden Patrick Sulem Gudmar Thorleifsson Omar Gustafsson Ari Johannesson Arni J Geirsson Arni V Thorsson Bardur Sigurgeirsson Bjorn Runar Ludviksson Elias Olafsson Helga Kristjansdottir Jon G Jonasson Jon Hjaltalin Olafsson Kjartan B Orvar Rafn Benediktsson Ragnar Bjarnason Sjofn Kristjansdottir Thorarinn Gislason Trausti Valdimarsson Evgenia Mikaelsdottir Snaevar Sigurdsson Stefan Jonsson Thorunn Rafnar Dag Aarsland Srdjan Djurovic Tormod Fladby Gun Peggy Knudsen Elisabeth G Celius Kjell-Morten Myhr Gerdur Grondal Kristjan Steinsson Helgi Valdimarsson Sigurdur Bjornsson Unnur S Bjornsdottir Einar S Bjornsson Bjorn Nilsson Ole A Andreassen Lars Alfredsson Jan Hillert Ingrid Skelton Kockum Gisli Masson Unnur Thorsteinsdottir Daniel F Gudbjartsson Hreinn Stefansson Haukur Hjaltason Hanne F Harbo Tomas Olsson Ingileif Jonsdottir Kari Stefansson

NPJ Genom Med 2017 8;2:24. Epub 2017 Aug 8.

deCODE genetics/Amgen, Reykjavik, Iceland.

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August 2017

Reproductive fitness and genetic risk of psychiatric disorders in the general population.

Authors:

Niamh Mullins Andrés Ingason Heather Porter Jack Euesden Alexandra Gillett Sigurgeir Ólafsson Daniel F Gudbjartsson Cathryn M Lewis Engilbert Sigurdsson Evald Saemundsen Ólafur Ó Gudmundsson Michael L Frigge Augustine Kong Agnar Helgason G Bragi Walters Omar Gustafsson Hreinn Stefansson Kari Stefansson

Nat Commun 2017 06 13;8:15833. Epub 2017 Jun 13.

deCODE genetics, 101 Reykjavik, Iceland.

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June 2017

A sequence variant associating with educational attainment also affects childhood cognition.

Sci Rep 2016 11 4;6:36189. Epub 2016 Nov 4.

deCODE Genetics/Amgen, Inc., Reykjavik, Iceland.

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November 2016

Replication study and meta-analysis in European samples supports association of the 3p21.1 locus with bipolar disorder.

Biol Psychiatry 2012 Oct 5;72(8):645-50. Epub 2012 May 5.

MRC SGDP Centre, Institute of Psychiatry, King's College London, London, United Kingdom.

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October 2012

Association analysis of ANK3 gene variants in nordic bipolar disorder and schizophrenia case-control samples.

Authors:

Martin Tesli Pernille Koefoed Lavinia Athanasiu Morten Mattingsdal Omar Gustafsson Ingrid Agartz Lars M Rimol Andrew Brown Katrine V Wirgenes Lisa-Lena Smorr Anna K Kähler Thomas Werge Ole Mors Erling Mellerup Erik G Jönsson Ingrid Melle Gunnar Morken Srdjan Djurovic Ole A Andreassen

Am J Med Genet B Neuropsychiatr Genet 2011 Dec 3;156B(8):969-74. Epub 2011 Oct 3.

Institute of Clinical Medicine, University of Oslo, Oslo, Norway.

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December 2011

Mirror extreme BMI phenotypes associated with gene dosage at the chromosome 16p11.2 locus.

Authors:

Sébastien Jacquemont Alexandre Reymond Flore Zufferey Louise Harewood Robin G Walters Zoltán Kutalik Danielle Martinet Yiping Shen Armand Valsesia Noam D Beckmann Gudmar Thorleifsson Marco Belfiore Sonia Bouquillon Dominique Campion Nicole de Leeuw Bert B A de Vries Tõnu Esko Bridget A Fernandez Fernando Fernández-Aranda José Manuel Fernández-Real Mònica Gratacòs Audrey Guilmatre Juliane Hoyer Marjo-Riitta Jarvelin R Frank Kooy Ants Kurg Cédric Le Caignec Katrin Männik Orah S Platt Damien Sanlaville Mieke M Van Haelst Sergi Villatoro Gomez Faida Walha Bai-Lin Wu Yongguo Yu Azzedine Aboura Marie-Claude Addor Yves Alembik Stylianos E Antonarakis Benoît Arveiler Magalie Barth Nathalie Bednarek Frédérique Béna Sven Bergmann Mylène Beri Laura Bernardini Bettina Blaumeiser Dominique Bonneau Armand Bottani Odile Boute Han G Brunner Dorothée Cailley Patrick Callier Jean Chiesa Jacqueline Chrast Lachlan Coin Charles Coutton Jean-Marie Cuisset Jean-Christophe Cuvellier Albert David Bénédicte de Freminville Bruno Delobel Marie-Ange Delrue Bénédicte Demeer Dominique Descamps Gérard Didelot Klaus Dieterich Vittoria Disciglio Martine Doco-Fenzy Séverine Drunat Bénédicte Duban-Bedu Christèle Dubourg Julia S El-Sayed Moustafa Paul Elliott Brigitte H W Faas Laurence Faivre Anne Faudet Florence Fellmann Alessandra Ferrarini Richard Fisher Elisabeth Flori Lukas Forer Dominique Gaillard Marion Gerard Christian Gieger Stefania Gimelli Giorgio Gimelli Hans J Grabe Agnès Guichet Olivier Guillin Anna-Liisa Hartikainen Délphine Heron Loyse Hippolyte Muriel Holder Georg Homuth Bertrand Isidor Sylvie Jaillard Zdenek Jaros Susana Jiménez-Murcia Géraldine Joly Helas Philippe Jonveaux Satu Kaksonen Boris Keren Anita Kloss-Brandstätter Nine V A M Knoers David A Koolen Peter M Kroisel Florian Kronenberg Audrey Labalme Emilie Landais Elisabetta Lapi Valérie Layet Solenn Legallic Bruno Leheup Barbara Leube Suzanne Lewis Josette Lucas Kay D MacDermot Pall Magnusson Christian Marshall Michèle Mathieu-Dramard Mark I McCarthy Thomas Meitinger Maria Antonietta Mencarelli Giuseppe Merla Alexandre Moerman Vincent Mooser Fanny Morice-Picard Mafalda Mucciolo Matthias Nauck Ndeye Coumba Ndiaye Ann Nordgren Laurent Pasquier Florence Petit Rolph Pfundt Ghislaine Plessis Evica Rajcan-Separovic Gian Paolo Ramelli Anita Rauch Roberto Ravazzolo Andre Reis Alessandra Renieri Cristobal Richart Janina S Ried Claudine Rieubland Wendy Roberts Katharina M Roetzer Caroline Rooryck Massimiliano Rossi Evald Saemundsen Véronique Satre Claudia Schurmann Engilbert Sigurdsson Dimitri J Stavropoulos Hreinn Stefansson Carola Tengström Unnur Thorsteinsdóttir Francisco J Tinahones Renaud Touraine Louis Vallée Ellen van Binsbergen Nathalie Van der Aa Catherine Vincent-Delorme Sophie Visvikis-Siest Peter Vollenweider Henry Völzke Anneke T Vulto-van Silfhout Gérard Waeber Carina Wallgren-Pettersson Robert M Witwicki Simon Zwolinksi Joris Andrieux Xavier Estivill James F Gusella Omar Gustafsson Andres Metspalu Stephen W Scherer Kari Stefansson Alexandra I F Blakemore Jacques S Beckmann Philippe Froguel

Nature 2011 Aug 31;478(7367):97-102. Epub 2011 Aug 31.

Service of Medical Genetics, Centre Hospitalier Universitaire Vaudois, 1011 Lausanne, Switzerland.

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August 2011

Common variants at VRK2 and TCF4 conferring risk of schizophrenia.

Authors:

Stacy Steinberg Simone de Jong Ole A Andreassen Thomas Werge Anders D Børglum Ole Mors Preben B Mortensen Omar Gustafsson Javier Costas Olli P H Pietiläinen Ditte Demontis Sergi Papiol Johanna Huttenlocher Manuel Mattheisen René Breuer Evangelos Vassos Ina Giegling Gillian Fraser Nicholas Walker Annamari Tuulio-Henriksson Jaana Suvisaari Jouko Lönnqvist Tiina Paunio Ingrid Agartz Ingrid Melle Srdjan Djurovic Eric Strengman Gesche Jürgens Birte Glenthøj Lars Terenius David M Hougaard Torben Ørntoft Carsten Wiuf Michael Didriksen Mads V Hollegaard Merete Nordentoft Ruud van Winkel Gunter Kenis Lilia Abramova Vasily Kaleda Manuel Arrojo Julio Sanjuán Celso Arango Swetlana Sperling Moritz Rossner Michele Ribolsi Valentina Magni Alberto Siracusano Claus Christiansen Lambertus A Kiemeney Jan Veldink Leonard van den Berg Andres Ingason Pierandrea Muglia Robin Murray Markus M Nöthen Engilbert Sigurdsson Hannes Petursson Unnur Thorsteinsdottir Augustine Kong I Alex Rubino Marc De Hert János M Réthelyi István Bitter Erik G Jönsson Vera Golimbet Angel Carracedo Hannelore Ehrenreich Nick Craddock Michael J Owen Michael C O'Donovan Mirella Ruggeri Sarah Tosato Leena Peltonen Roel A Ophoff David A Collier David St Clair Marcella Rietschel Sven Cichon Hreinn Stefansson Dan Rujescu Kari Stefansson

Hum Mol Genet 2011 Oct 26;20(20):4076-81. Epub 2011 Jul 26.

deCODE Genetics, IS-101 Reykjavik, Iceland.

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October 2011

Common variants near FRK/COL10A1 and VEGFA are associated with advanced age-related macular degeneration.

Hum Mol Genet 2011 Sep 10;20(18):3699-709. Epub 2011 Jun 10.

Ophthalmic Epidemiology and Genetics Service, New England Eye Center, Tufts Medical Center, Tufts University School of Medicine, 800 WashingtonStreet, No. 450, Boston, MA 02111, USA.

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September 2011

Copy number variations in affective disorders and meta-analysis.

Authors:

Line Olsen Thomas Hansen Srdjan Djurovic Eva Haastrup Anders Albrecthsen Louise K E Hoeffding Anna Secher Omar Gustafsson Klaus D Jakobsen Finn C Nielsen Henrik Ullum Gunnar Morken Ingrid Agartz Ingrid Melle Ulrik Gether Ole A Andreassen Thomas Werge

Psychiatr Genet 2011 Dec;21(6):319-22

Institute for Biological Psychiatry, Mental Health Centre Sct. Hans, Roskilde, Norway.

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December 2011

At-risk variant in TCF7L2 for type II diabetes increases risk of schizophrenia.

Biol Psychiatry 2011 Jul 16;70(1):59-63. Epub 2011 Mar 16.

Mental Health Centre Sct. Hans, Copenhagen University Hospital, Research Institute of Biological Psychiatry, Roskilde, Denmark; Copenhagen University, Center for Pharmacogenomics, Copenhagen, Denmark.

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July 2011

Genome-wide association study identifies genetic variation in neurocan as a susceptibility factor for bipolar disorder.

Authors:

Sven Cichon Thomas W Mühleisen Franziska A Degenhardt Manuel Mattheisen Xavier Miró Jana Strohmaier Michael Steffens Christian Meesters Stefan Herms Moritz Weingarten Lutz Priebe Britta Haenisch Michael Alexander Jennifer Vollmer René Breuer Christine Schmäl Peter Tessmann Susanne Moebus H-Erich Wichmann Stefan Schreiber Bertram Müller-Myhsok Susanne Lucae Stéphane Jamain Marion Leboyer Frank Bellivier Bruno Etain Chantal Henry Jean-Pierre Kahn Simon Heath Marian Hamshere Michael C O'Donovan Michael J Owen Nick Craddock Markus Schwarz Helmut Vedder Jutta Kammerer-Ciernioch Andreas Reif Johanna Sasse Michael Bauer Martin Hautzinger Adam Wright Philip B Mitchell Peter R Schofield Grant W Montgomery Sarah E Medland Scott D Gordon Nicholas G Martin Omar Gustafsson Ole Andreassen Srdjan Djurovic Engilbert Sigurdsson Stacy Steinberg Hreinn Stefansson Kari Stefansson Lejla Kapur-Pojskic Liliana Oruc Fabio Rivas Fermín Mayoral Alexander Chuchalin Gulja Babadjanova Alexander S Tiganov Galina Pantelejeva Lilia I Abramova Maria Grigoroiu-Serbanescu Carmen C Diaconu Piotr M Czerski Joanna Hauser Andreas Zimmer Mark Lathrop Thomas G Schulze Thomas F Wienker Johannes Schumacher Wolfgang Maier Peter Propping Marcella Rietschel Markus M Nöthen

Am J Hum Genet 2011 Mar 25;88(3):372-81. Epub 2011 Feb 25.

Institute of Neuroscience and Medicine (INM-1), Structural and Functional Organization of the Brain, Genomic Imaging, Research Center Juelich, Juelich, Germany.

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March 2011

Maternally derived microduplications at 15q11-q13: implication of imprinted genes in psychotic illness.

Am J Psychiatry 2011 Apr 15;168(4):408-17. Epub 2011 Feb 15.

Research Institute of Biological Psychiatry, Mental Health Center Sct. Hans, Copenhagen University Hospital, Roskilde, Denmark.

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April 2011

Candidate gene analysis of the human natural killer-1 carbohydrate pathway and perineuronal nets in schizophrenia: B3GAT2 is associated with disease risk and cortical surface area.

Biol Psychiatry 2011 Jan 15;69(1):90-6. Epub 2010 Oct 15.

Institute of Psychiatry, University of Oslo, Oslo University Hospital-Ulleval, Norway.

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January 2011

Rare chromosomal deletions and duplications in attention-deficit hyperactivity disorder: a genome-wide analysis.

Authors:

Nigel M Williams Irina Zaharieva Andrew Martin Kate Langley Kiran Mantripragada Ragnheidur Fossdal Hreinn Stefansson Kari Stefansson Pall Magnusson Olafur O Gudmundsson Omar Gustafsson Peter Holmans Michael J Owen Michael O'Donovan Anita Thapar

Lancet 2010 Oct 29;376(9750):1401-8. Epub 2010 Sep 29.

MRC Centre in Neuropsychiatric Genetics and Genomics and Department of Psychological Medicine and Neurology, Cardiff University School of Medicine, Cardiff, UK.

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October 2010