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Unbiased screen for interactors of leucine-rich repeat kinase 2 supports a common pathway for sporadic and familial Parkinson disease
Unbiased screen for interactors of leucine-rich repeat kinase 2 supports a common pathway for sporadic and familial Parkinson disease
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Unbiased screen for interactors of leucine-rich repeat kinase 2 supports a common pathway for sporadic and familial Parkinson disease

Beilina, Alexandria ; Rudenko, Iakov N. ; Kaganovich, Alice ; Civiero, Laura ; Chau, Hien ; Kalia, Suneil K. ; Kalia, Lorraine V. ; Lobbestael, Evy ; Chia, Ruth ; Ndukwe, Kelechi ; Ding, Jinhui ; Nalls, Mike A. ; Olszewski, Maciej ; Hauser, David N. ; Kumaran, Ravindran ; Lozano, Andres M. ; Baekelandt, Veerle ; Greene, Lois E. ; Taymans, Jean-Marc ; Greggio, Elisa ; Cookson, Mark R.

Proceedings of the National Academy of Sciences - PNAS, 2014-02, Vol.111 (7), p.2626-2631 [Periódico revisado por pares]

United States: National Academy of Sciences

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2
Correction: Dose response of the 16p11.2 distal copy number variant on intracranial volume and basal ganglia (Molecular Psychiatry, (2018), 10.1038/s41380-018-0118-1)
Correction: Dose response of the 16p11.2 distal copy number variant on intracranial volume and basal ganglia (Molecular Psychiatry, (2018), 10.1038/s41380-018-0118-1)
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Correction: Dose response of the 16p11.2 distal copy number variant on intracranial volume and basal ganglia (Molecular Psychiatry, (2018), 10.1038/s41380-018-0118-1)

Sønderby, Ida E ; Gústafsson, Ómar ; Doan, Nhat Trung ; Hibar, Derrek P ; Martin-Brevet, Sandra ; Abdellaoui, Abdel ; Ames, David ; Amunts, Katrin ; Andersson, Michael ; Armstrong, Nicola J ; Bernard, Manon ; Blackburn, Nicholas ; Blangero, John ; Boomsma, Dorret I ; Bralten, Janita ; Brattbak, Hans-Richard ; Brodaty, Henry ; Brouwer, Rachel M ; Bülow, Robin ; Calhoun, Vince ; Caspers, Svenja ; Cavalleri, Gianpiero ; Chen, Chi-Hua ; Cichon, Sven ; Ciufolini, Simone ; Corvin, Aiden ; Crespo-Facorro, Benedicto ; Curran, Joanne E ; Dale, Anders M ; Dalvie, Shareefa ; Dazzan, Paola ; de Geus, Eco J. C ; de Zubicaray, Greig I ; de Zwarte, Sonja M. C ; Delanty, Norman ; den Braber, Anouk ; Desrivières, Sylvane ; Donohoe, Gary ; Draganski, Bogdan ; Ehrlich, Stefan ; Espeseth, Thomas ; Fisher, Simon E ; Franke, Barbara ; Frouin, Vincent ; Fukunaga, Masaki ; Gareau, Thomas ; Glahn, David C ; Milaneschi, Yuri ; Penninx, Brenda ; Schmaal, Lianne ; Teumer, Alexander ; Whelan, Christopher D ; Wittfeld, Katharina ; Stefánsson, Hreinn ; Stefansson, Kari ; Thompson, Paul M ; Andreassen, Ole A

2019-01

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3
Rare chromosomal deletions and duplications in attention-deficit hyperactivity disorder: a genome-wide analysis
Rare chromosomal deletions and duplications in attention-deficit hyperactivity disorder: a genome-wide analysis
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Rare chromosomal deletions and duplications in attention-deficit hyperactivity disorder: a genome-wide analysis

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

The Lancet (British edition), 2010-10, Vol.376 (9750), p.1401-1408 [Periódico revisado por pares]

Kidlington: Elsevier Ltd

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4
1q21.1 distal copy number variants are associated with cerebral and cognitive alterations in humans
1q21.1 distal copy number variants are associated with cerebral and cognitive alterations in humans
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1q21.1 distal copy number variants are associated with cerebral and cognitive alterations in humans

van der Meer, Dennis ; Kaufmann, Tobias ; Abdellaoui, Abdel ; Ames, David ; Amunts, Katrin ; Andersson, Micael ; Armstrong, Nicola J ; Blackburn, Nicholas B ; Boomsma, Dorret I ; Brodaty, Henry ; Brouwer, Rachel M ; Bülow, Robin ; Bøen, Rune ; Cahn, Wiepke ; Caspers, Svenja ; Ching, Christopher R K ; Cichon, Sven ; Ciufolini, Simone ; Curran, Joanne E ; Dazzan, Paola ; de Zubicaray, Greig I ; de Zwarte, Sonja M C ; Doherty, Joanne L ; Draganski, Bogdan ; Eising, Else ; Espeseth, Thomas ; Fejgin, Kim ; Fladby, Tormod ; Frei, Oleksandr ; Frouin, Vincent ; Fukunaga, Masaki ; Gareau, Thomas ; Grabe, Hans J ; Groenewold, Nynke A ; Gústafsson, Ómar ; Haavik, Jan ; Haberg, Asta K ; Hall, Jeremy ; Hashimoto, Ryota ; Hibar, Derrek P ; Hillegers, Manon H J ; Hoffmann, Per ; Holleran, Laurena ; Holmes, Avram J ; Homuth, Georg ; Hottenga, Jouke-Jan ; Hulshoff Pol, Hilleke E ; Ikeda, Masashi ; Jockwitz, Christiane ; Jönsson, Erik G ; Jørgensen, Niklas R ; Kikuchi, Masataka ; Knowles, Emma E M ; Kumar, Kuldeep ; Leu, Costin ; Linden, David E J ; Lundervold, Arvid ; Lundervold, Astri Johansen ; Maillard, Anne M ; Mather, Karen A ; Mathias, Samuel R ; McMahon, Katie L ; McRae, Allan F ; Medland, Sarah E ; Meyer-Lindenberg, Andreas ; Moberget, Torgeir ; Modenato, Claudia ; Sánchez, Jennifer Monereo ; Mühleisen, Thomas W ; Nielsen, Jacob ; Nordvik, Jan E ; Nyberg, Lars ; Loohuis, Loes M Olde ; Ophoff, Roel A ; Paus, Tomas ; Peralta, Juan M ; Pike, G Bruce ; Quinlan, Erin B ; Marques, Tiago Reis ; Rucker, James J H ; Schumann, Gunter ; Shin, Jean ; Shumskaya, Elena ; Sisodiya, Sanjay M ; Steen, Vidar M ; Stein, Dan J ; Strike, Lachlan T ; Suzuki, Ikuo K ; Tamnes, Christian K ; Teumer, Alexander ; Ulfarsson, Magnus O ; van 't Ent, Dennis ; Vanderhaeghen, Pierre ; Wen, Wei ; Wright, Margaret J ; Agartz, Ingrid ; Westlye, Lars T ; Stefansson, Hreinn ; Stefansson, Kari ; Andreassen, Ole A

Translational psychiatry, 2021-03, Vol.11 (1), p.182-16, Article 182 [Periódico revisado por pares]

United States: Nature Publishing Group

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5
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
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
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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

Kähler, Anna K ; Djurovic, Srdjan ; Rimol, Lars M ; Brown, Andrew Anand ; Athanasiu, Lavinia ; Jönsson, Erik G ; Hansen, Thomas ; Gústafsson, Ómar ; Hall, Håkan ; Giegling, Ina ; Muglia, Pierandrea ; Cichon, Sven ; Rietschel, Marcella ; Pietiläinen, Olli P.H ; Peltonen, Leena ; Bramon, Elvira ; Collier, David ; Clair, David St ; Sigurdsson, Engilbert ; Petursson, Hannes ; Rujescu, Dan ; Melle, Ingrid ; Werge, Thomas ; Steen, Vidar M ; Dale, Anders M ; Matthews, Russell T ; Agartz, Ingrid ; Andreassen, Ole A

Biological psychiatry (1969), 2011, Vol.69 (1), p.90-96 [Periódico revisado por pares]

New York, NY: Elsevier Inc

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6
Assessing population differentiation and isolation from single-nucleotide polymorphism data
Assessing population differentiation and isolation from single-nucleotide polymorphism data
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Assessing population differentiation and isolation from single-nucleotide polymorphism data

Nicholson, George ; Smith, Albert V. ; Jónsson, Frosti ; Gústafsson, Ómar ; Stefánsson, Kári ; Donnelly, Peter

Journal of the Royal Statistical Society. Series B, Statistical methodology, 2002-01, Vol.64 (4), p.695-715 [Periódico revisado por pares]

Oxford, UK: Blackwell Publishers

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7
Using genome-wide complex trait analysis to quantify 'missing heritability' in Parkinson's disease
Using genome-wide complex trait analysis to quantify 'missing heritability' in Parkinson's disease
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Using genome-wide complex trait analysis to quantify 'missing heritability' in Parkinson's disease

KELLER, Margaux F ; SAAD, Mohamad ; SCHULTE, Claudia ; MOSKVINA, Valentina ; DURR, Alexandra ; HOLMANS, Peter ; KILARSKI, Laura L ; GUERREIRO, Rita ; HERNANDEZ, Dena G ; BRICE, Alexis ; YLIKOTILA, Pauli ; STEFANSSON, Hreinn ; BRAS, Jose ; MAJAMAA, Kari ; MORRIS, Huw R ; WILLIAMS, Nigel ; GASSER, Thomas ; HEUTINK, Peter ; WOOD, Nicholas W ; HARDY, John ; MARTINEZ, Maria ; SINGLETON, Andrew B ; NALLS, Michael A ; BETTELLA, Francesco ; NICOLAOU, Nayia ; SIMON-SANCHEZ, Javier ; MITTAG, Florian ; BÜCHEL, Finja ; SHARMA, Manu ; RAPHAEL GIBBS, J

Human molecular genetics, 2012-11, Vol.21 (22), p.4996-5009 [Periódico revisado por pares]

Oxford: Oxford University Press

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8
A pathway-based analysis provides additional support for an immune-related genetic susceptibility to Parkinson's disease
A pathway-based analysis provides additional support for an immune-related genetic susceptibility to Parkinson's disease
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A pathway-based analysis provides additional support for an immune-related genetic susceptibility to Parkinson's disease

Holmans, Peter ; Moskvina, Valentina ; Jones, Lesley ; Sharma, Manu ; Vedernikov, Alexey ; Buchel, Finja ; Saad, Mohamad ; Sadd, Mohamad ; Bras, Jose M ; Bettella, Francesco ; Nicolaou, Nayia ; Simón-Sánchez, Javier ; Mittag, Florian ; Gibbs, J Raphael ; Schulte, Claudia ; Durr, Alexandra ; Guerreiro, Rita ; Hernandez, Dena ; Brice, Alexis ; Stefánsson, Hreinn ; Majamaa, Kari ; Gasser, Thomas ; Heutink, Peter ; Wood, Nicholas W ; Martinez, Maria ; Singleton, Andrew B ; Nalls, Michael A ; Hardy, John ; Morris, Huw R ; Williams, Nigel M

Human molecular genetics, 2013-03, Vol.22 (5), p.1039-1049 [Periódico revisado por pares]

England: Oxford University Press

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9
Reproductive fitness and genetic risk of psychiatric disorders in the general population
Reproductive fitness and genetic risk of psychiatric disorders in the general population
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Reproductive fitness and genetic risk of psychiatric disorders in the general population

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

Nature communications, 2017-06, Vol.8 (1), p.15833-15833, Article 15833 [Periódico revisado por pares]

England: Nature Publishing Group

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10
A sequence variant associating with educational attainment also affects childhood cognition
A sequence variant associating with educational attainment also affects childhood cognition
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A sequence variant associating with educational attainment also affects childhood cognition

Gunnarsson, Bjarni ; Jónsdóttir, Guðrún A ; Björnsdóttir, Gyða ; Konte, Bettina ; Sulem, Patrick ; Kristmundsdóttir, Snædís ; Kehr, Birte ; Gústafsson, Ómar ; Helgason, Hannes ; Iordache, Paul D ; Ólafsson, Sigurgeir ; Frigge, Michael L ; Þorleifsson, Guðmar ; Arnarsdóttir, Sunna ; Stefánsdóttir, Berglind ; Giegling, Ina ; Djurovic, Srdjan ; Sundet, Kjetil S ; Espeseth, Thomas ; Melle, Ingrid ; Hartmann, Annette M ; Thorsteinsdottir, Unnur ; Kong, Augustine ; Guðbjartsson, Daníel F ; Ettinger, Ulrich ; Andreassen, Ole A ; Dan Rujescu ; Halldórsson, Jónas G ; Stefánsson, Hreinn ; Halldórsson, Bjarni V ; Stefánsson, Kári

Scientific reports, 2016-11, Vol.6 (1), p.36189-36189, Article 36189 [Periódico revisado por pares]

England: Nature Publishing Group

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