Torthaí cuardaigh - Engilbert Sigurðsson

Beachtaigh na torthaí
  1. 1
    Neutropenia and agranulocytosis during treatment of schizophrenia with clozapine versus other antipsychotics: an observational study in Iceland

    Neutropenia and agranulocytosis during treatment of schizophrenia with clozapine versus other antipsychotics: an observational study in Iceland de réir Oddur Ingimarsson, James H. MacCabe, Magnús Haraldsson, Halldóra Jónsdóttir, Engilbert Sigurðsson

    Foilsithe / Cruthaithe 2016
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  2. 2
    Polygenic risk scores for schizophrenia and bipolar disorder associate with addiction

    Polygenic risk scores for schizophrenia and bipolar disorder associate with addiction de réir Gunnar W. Reginsson, Andrés Ingason, Jack Euesden, Gyða Björnsdóttir, Sigurgeir Ólafsson, Engilbert Sigurðsson, Högni Óskarsson, Þórarinn Tyrfingsson, Valgerður Rúnarsdóttir, Ingunn Hansdóttir, Stacy Steinberg, Hreinn Stefánsson, Daníel F. Guðbjartsson, Thorgeir E. Thorgeirsson, Kāri Stefánsson

    Foilsithe / Cruthaithe 2017
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  3. 3
    A rare missense mutation in <i>MYH6</i> associates with non-syndromic coarctation of the aorta

    A rare missense mutation in <i>MYH6</i> associates with non-syndromic coarctation of the aorta de réir Þorsteinn Björnsson, Rósa B. Þórólfsdóttir, Garðar Sveinbjörnsson, Patrick Sulem, Gudmundur L. Norddahl, Anna Helgadóttir, Sólveig Grétarsdóttir, Audur Magnusdottir, Ragnar Daníelsen, Engilbert Sigurðsson, Berglind Aðalsteinsdóttir, Sverrir I. Gunnarsson, Ingileif Jónsdóttir, Davíð O. Arnar, Hróðmar Helgason, Tómas Guðbjartsson, Daníel F. Guðbjartsson, Unnur Þorsteinsdóttir, Hilma Hólm, Kāri Stefánsson

    Foilsithe / Cruthaithe 2018
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  4. 4
    Polygenic liability for antipsychotic dosage and polypharmacy - a real-world registry and biobank study

    Polygenic liability for antipsychotic dosage and polypharmacy - a real-world registry and biobank study de réir Elise Koch, Anders Kämpe, Maris Alver, Sindri Sigurðarson, Guðmundur Einarsson, Juulia Partanen, Robert L. Smith, Piotr Jahołkowski, Heidi Taipale, Markku Lähteenvuo, Nils Eiel Steen, Olav B. Smeland, Srdjan Djurovic, Espen Molden, Engilbert Sigurðsson, Hreinn Stefánsson, Kāri Stefánsson, Aarno Palotie, Lili Milani, Kevin S. O’Connell, Ole A. Andreassen

    Foilsithe / Cruthaithe 2024
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  5. 5
    Gene variants associated with schizophrenia in a Norwegian genome-wide study are replicated in a large European cohort

    Gene variants associated with schizophrenia in a Norwegian genome-wide study are replicated in a large European cohort de réir Lavinia Athanasiu, Morten Mattingsdal, Anna K. Kähler, Andrew Brown, Ómar Gústafsson, Ingrid Agartz, Ina Giegling, Pierandrea Muglia, Sven Cichon, Marcella Rietschel, Olli Pietiläinen, Leena Peltonen, Elvira Bramon, David Collier, David St Clair, Engilbert Sigurðsson, Hannes Pétursson, Dan Rujescu, Ingrid Melle, Vidar M. Steen, Srdjan Djurovic, Ole A. Andreassen

    Foilsithe / Cruthaithe 2010
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  6. 6
    Sequence variants with large effects on cardiac electrophysiology and disease

    Sequence variants with large effects on cardiac electrophysiology and disease de réir Kristján Norland, Garðar Sveinbjörnsson, Rósa B. Þórólfsdóttir, Olafur B. Davidsson, Vinicius Tragante, Sridharan Rajamani, Anna Helgadóttir, Sólveig Grétarsdóttir, Jessica van Setten, Folkert W. Asselbergs, Jon T. Sverrisson, Sigurdur S. Stephensen, Gylfi Óskarsson, Engilbert Sigurðsson, Karl Andersen, Ragnar Daníelsen, Guðmundur Þorgeirsson, Unnur Þorsteinsdóttir, Davíð O. Arnar, Patrick Sulem, Hilma Hólm, Daníel F. Guðbjartsson, Kāri Stefánsson

    Foilsithe / Cruthaithe 2019
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  7. 7
    A polygenic resilience score moderates the genetic risk for schizophrenia

    A polygenic resilience score moderates the genetic risk for schizophrenia de réir Jonathan Hess, Sang Lee, Manuel Mattheisen, Anders D. Børglum, Thomas D. Als, Jakob Grove, Thomas Werge, Preben Bo Mortensen, Ole Mors, Merete Nordentoft, David M. Hougaard, Jonas Byberg-Grauholm, Marie Bækvad‐Hansen, Tiffany A. Greenwood, Ming T. Tsuang, David Curtis, Stacy Steinberg, Engilbert Sigurðsson, Hreinn Stefánsson, Hreinn Stefánsson, Howard J. Edenberg, Peter Holmans, Stephen V. Faraone, Stephen J. Glatt

    Foilsithe / Cruthaithe 2019
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  8. 8
    Attention-deficit hyperactivity disorder shares copy number variant risk with schizophrenia and autism spectrum disorder

    Attention-deficit hyperactivity disorder shares copy number variant risk with schizophrenia and autism spectrum disorder de réir Ólafur Ó. Guðmundsson, G. Bragi Walters, Andrés Ingason, Stefan Johansson, Tetyana Zayats, Lavinia Athanasiu, Ida E. Sønderby, Ómar Gústafsson, Muhammad Sulaman Nawaz, Guðbjörn F. Jónsson, Lina Jönsson, Per-Morten Knappskog, Ester Ingvarsdottir, Katrín Davíðsdóttir, Srdjan Djurovic, Gun Peggy Knudsen, Ragna Bugge Askeland, Gyða S. Haraldsdóttir, Gísli Baldursson, Páll Magnússon, Engilbert Sigurðsson, Daníel F. Guðbjartsson, Hreinn Stefánsson, Ole A. Andreassen, Jan Haavik, Ted Reichborn‐Kjennerud, Kāri Stefánsson

    Foilsithe / Cruthaithe 2019
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  9. 9
    Rare loss-of-function variants in HECTD2 and AKAP11 confer risk of bipolar disorder

    Rare loss-of-function variants in HECTD2 and AKAP11 confer risk of bipolar disorder de réir Thorgeir E. Thorgeirsson, Vinicius Tragante, Garðar Sveinbjörnsson, Guðrún A. Jónsdóttir, G. Bragi Walters, Erna V. Ivarsdottir, Gudny A. Arnadottir, Árni Sturluson, Brynjar Ö. Jensson, Rún Friðriksdóttir, Ástrós Th. Skúladóttir, Gudmundur Einarsson, Gyða Björnsdóttir, Arni F. Gunnarsson, Rósa S. Gísladóttir, Ásgeir Sigurðsson, Ásmundur Oddsson, Hákon Jónsson, Ólafur Þ. Magnússon, Hannes Helgason, Gudmundur L. Norddahl, Guðmar Þorleifsson, Magnús Haraldsson, Engilbert Sigurðsson, Hilma Hólm, Gísli Másson, Daníel F. Guðbjartsson, Hreinn Stefánsson, Patrick Sulem, Kāri Stefánsson

    Foilsithe / Cruthaithe 2025
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  10. 10
    15q11.2 CNV affects cognitive, structural and functional correlates of dyslexia and dyscalculia

    15q11.2 CNV affects cognitive, structural and functional correlates of dyslexia and dyscalculia de réir Magnús Ö. Úlfarsson, G. Bragi Walters, Ómar Gústafsson, Stacy Steinberg, Ana Isabel Silva, Orla Doyle, Michael Brammer, Daníel F. Guðbjartsson, Sunna Arnarsdóttir, Guðrún A. Jónsdóttir, Rósa S. Gísladóttir, Gyða Björnsdóttir, Hannes Helgason, Lotta M. Ellingsen, Jónas G. Halldórsson, Evald Sæmundsen, Berglind Stefánsdóttir, Lina Jönsson, Valgerdur Kristin Eiriksdottir, Guðný Eiríksdóttir, G H Johannesdottir, Unnur Unnsteinsdóttir, Birna Jónsdóttir, Brynja B. Magnúsdóttir, Patrick Sulem, U. Thorsteinsdottir, Engilbert Sigurðsson, Daniel Brandeis, Andreas Meyer‐Lindenberg, Hreinn Stefánsson, Hreinn Stefánsson

    Foilsithe / Cruthaithe 2017
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  11. 11
    Neuregulin 1 and Susceptibility to Schizophrenia

    Neuregulin 1 and Susceptibility to Schizophrenia de réir Hreinn Stefánsson, Hannes Pétursson, Engilbert Sigurðsson, Valgerður Steinthórsdóttir, Soley Bjornsdottir, Thordur Sigmundsson, Shyamali Ghosh, Jon Brynjolfsson, Steinunn Gunnarsdottir, Omar Ivarsson, Thomas T. Chou, Ómar Hjaltason, Birgitta Birgisdottir, Helgi Jónsson, Vala G Gudnadottir, Elsa Gudmundsdottir, Ásgeir Björnsson, Brynjolfur Ingvarsson, Andrés Ingason, Sigmundur Sigfússon, Hrönn Harðardóttir, Richard P. Harvey, Donna Lai, Mingdong Zhou, Daniela Brunner, Vincent Mutel, Acuna Gonzalo, Greg Lemke, Jesús Sainz, G Jóhannesson, Þorkell Andrésson, Daníel F. Guðbjartsson, Andrei Manolescu, Michael L. Frigge, Mark E. Gurney, Augustine Kong, Jeffrey R. Gulcher, Kāri Stefánsson

    Foilsithe / Cruthaithe 2002
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  12. 12
    Common variants on 8p12 and 1q24.2 confer risk of schizophrenia

    Common variants on 8p12 and 1q24.2 confer risk of schizophrenia de réir Yongyong Shi, Zhiqiang Li, Qi Xu, Ti Wang, Tao Li, Jiawei Shen, Fengyu Zhang, Jianhua Chen, Guoquan Zhou, Weidong Ji, Baojie Li, Yifeng Xu, Dengtang Liu, Peng Wang, Ping Yang, Benxiu Liu, Wensheng Sun, Chunling Wan, Shengying Qin, Guang He, Stacy Steinberg, Sven Cichon, Thomas Werge, Engilbert Sigurðsson, Sarah Tosato, Aarno Palotie, Markus M. Nöthen, Marcella Rietschel, Roel A. Ophoff, David Collier, Dan Rujescu, David St Clair, Hreinn Stefánsson, Hreinn Stefánsson, Jue Ji, Qingzhong Wang, Wenjin Li, Linqing Zheng, Hairong Zhang, Guoyin Feng, Lin He

    Foilsithe / Cruthaithe 2011
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  13. 13
    Convergent lines of evidence support CAMKK2 as a schizophrenia susceptibility gene

    Convergent lines of evidence support CAMKK2 as a schizophrenia susceptibility gene de réir X-j Luo, Mei LI, Liang Huang, Stacy Steinberg, Manuel Mattheisen, Guoqing Liang, Gary Donohoe, Yongyong Shi, Chuansheng Chen, Weihua Yue, Anna Alkelai, Bernard Lerer, Zhiqiang Li, Qizhong Yi, Marcella Rietschel, Sven Cichon, David Collier, Sarah Tosato, Jaana Suvisaari, Dan Rujescu, В. Е. Голимбет, Teimuraz Silagadze, Naser Durmishi, Miloš Milovančević, Hreinn Stefánsson, Thomas G. Schulze, Markus M. Nöthen, Chao Chen, Rachel Lyne, Derek W. Morris, Michael Gill, Aiden Corvin, D Zhang, Qian Dong, Robert K. Moyzis, Kāri Stefánsson, Engilbert Sigurðsson, Fang Hu, Bing Su, Lin Gan

    Foilsithe / Cruthaithe 2013
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  14. 14
    Maternally Derived Microduplications at 15q11-q13: Implication of Imprinted Genes in Psychotic Illness

    Maternally Derived Microduplications at 15q11-q13: Implication of Imprinted Genes in Psychotic Illness de réir Andrés Ingason, George Kirov, Ina Giegling, Thomas Hansen, Anthony R Isles, Klaus D. Jakobsen, Kári Kristinsson, Louise le Roux, Ómar Gústafsson, Nick Craddock, Hans‐Jürgen Möller, Andrew McQuillin, Pierandrea Muglia, Sven Cichon, Marcella Rietschel, Roel A. Ophoff, Srdjan Djurovic, Ole A. Andreassen, Olli Pietiläinen, Leena Peltonen, Emma Dempster, David Collier, David St Clair, Henrik B. Rasmussen, Birte Glenthøj, Lambertus A. Kiemeney, Barbara Franke, Sarah Tosato, Chiara Bonetto, Evald Sæmundsen, Stefán Hreiðarsson, Markus M. Nöthen, Hugh Gurling, Michael O’Donovan, Michael J. Owen, Engilbert Sigurðsson, Hannes Pétursson, Hreinn Stefánsson, Dan Rujescu, Hreinn Stefánsson, Thomas Werge

    Foilsithe / Cruthaithe 2011
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  15. 15
    Copy number variations of chromosome 16p13.1 region associated with schizophrenia

    Copy number variations of chromosome 16p13.1 region associated with schizophrenia de réir Andrés Ingason, Dan Rujescu, Sven Cichon, Engilbert Sigurðsson, Thordur Sigmundsson, Olli Pietiläinen, Jacobine E. Buizer‐Voskamp, E Strengman, Clyde Francks, Pierandrea Muglia, Arnaldur Gylfason, Ómar Gústafsson, Pall I. Olason, Stacy Steinberg, Thomas Hansen, Klaus D. Jakobsen, Henrik B. Rasmussen, Ina Giegling, HJ Möller, A. Hartmann, Caroline Crombie, G. T. Fraser, Nicholas Walker, Jouko Lönnqvist, Jaana Suvisaari, Annamari Tuulio‐Henriksson, Elvira Bramon, Lambertus A. Kiemeney, Barbara Franke, Robin Murray, Evangelos Vassos, Timothea Toulopoulou, Thomas W. Mühleisen, Sarah Tosato, Mirella Ruggeri, Srdjan Djurovic, Ole A. Andreassen, Z Zhang, Thomas Werge, Roel A. Ophoff, Marcella Rietschel, Markus M. Nöthen, Hannes Pétursson, Hreinn Stefánsson, L. Peltonen, David Collier, Hreinn Stefánsson, David M. St. Clair

    Foilsithe / Cruthaithe 2009
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  16. 16
    Genome-wide analysis yields new loci associating with aortic valve stenosis

    Genome-wide analysis yields new loci associating with aortic valve stenosis de réir Anna Helgadóttir, Guðmar Þorleifsson, Sólveig Grétarsdóttir, Ólafur Andri Stefánsson, Vinicius Tragante, Rósa B. Þórólfsdóttir, Ingileif Jónsdóttir, Þorsteinn Björnsson, Valgerður Steinthórsdóttir, Niek Verweij, Jonas B. Nielsen, Wei Zhou, Lasse Folkersen, Andreas Martinsson, Mahyar Heydarpour, Siddharth K. Prakash, Gylfi Óskarsson, Tómas Guðbjartsson, Arnar Geirsson, Ísleifur Ólafsson, Engilbert Sigurðsson, Peter Almgren, Olle Melander, Anders Franco‐Cereceda, Anders Hamsten, Lars G. Fritsche, Maoxuan Lin, Bo Yang, Whitney Hornsby, Dongchuan Guo, Chad M. Brummett, Gonçalo R. Abecasis, Michael R. Mathis, Dianna M. Milewicz, Simon C. Body, Per Eriksson, Cristen J. Willer, Kristian Hveem, Christopher Newton‐Cheh, J. G. Smith, Ragnar Daníelsen, Guðmundur Þorgeirsson, Unnur Þorsteinsdóttir, Daníel F. Guðbjartsson, Hilma Hólm, Kāri Stefánsson

    Foilsithe / Cruthaithe 2018
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  17. 17
    Multiomics study of nonalcoholic fatty liver disease

    Multiomics study of nonalcoholic fatty liver disease de réir Garðar Sveinbjörnsson, Magnús Ö. Úlfarsson, Rósa B. Þórólfsdóttir, Benedikt A. Jónsson, Eyþór Einarsson, Gylfi Gunnlaugsson, Sölvi Rögnvaldsson, Davíð O. Arnar, Magnús Baldvinsson, Ragnar Bjarnason, Thjodbjorg Eiriksdottir, Christian Erikstrup, Egil Ferkingstad, Gísli H. Halldórsson, Hannes Helgason, Anna Helgadóttir, Lotte Hindhede, Grimur Hjörleifsson, David A. Jones, Kirk U. Knowlton, Sigrún H. Lund, Páll Melsted, Kristján Norland, Ísleifur Ólafsson, Sigurður Ólafsson, Gudjon R. Oskarsson, Sisse Rye Ostrowski, Ole Birger Pedersen, Auðunn Skúta Snæbjarnarson, Engilbert Sigurðsson, Valgerður Steinthórsdóttir, Michael Schwinn, Guðmundur Þorgeirsson, Guðmar Þorleifsson, Ingileif Jónsdóttir, Henning Bundgaard, Lincoln Nadauld, Einar S. Björnsson, Ingrid C. Rulifson, Þórunn Rafnar, Gudmundur L. Norddahl, Unnur Þorsteinsdóttir, Patrick Sulem, Daníel F. Guðbjartsson, Hilma Hólm, Kāri Stefánsson

    Foilsithe / Cruthaithe 2022
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  18. 18
    Disruption of the neurexin 1 gene is associated with schizophrenia

    Disruption of the neurexin 1 gene is associated with schizophrenia de réir Dan Rujescu, Andrés Ingason, Sven Cichon, Olli Pietiläinen, Michael R. Barnes, Timothea Toulopoulou, Marco Picchioni, Evangelos Vassos, Ulrich Ettinger, Elvira Bramon, Robin Murray, Mirella Ruggeri, Sarah Tosato, Chiara Bonetto, Stacy Steinberg, Engilbert Sigurðsson, Thordur Sigmundsson, Hannes Pétursson, Arnaldur Gylfason, Pall I. Olason, Gudmundur Hardarsson, Guðrún A. Jónsdóttir, Ómar Gústafsson, Ragnheiður Fossdal, Ina Giegling, Hans‐Jürgen Möller, Annette M. Hartmann, Per Hoffmann, Caroline Crombie, Gillian Fraser, Nicholas Walker, Jouko Lönnqvist, Jaana Suvisaari, Annamari Tuulio‐Henriksson, Srdjan Djurovic, Ingrid Melle, Ole A. Andreassen, Thomas Hansen, Thomas Werge, Lambertus A. Kiemeney, Barbara Franke, Joris A. Veltman, Jacobine E. Buizer‐Voskamp, Chiara Sabatti, Roel A. Ophoff, Marcella Rietschel, Markus M. Nöthen, Kāri Stefánsson, Leena Peltonen, David St Clair, Hreinn Stefánsson, David Collier

    Foilsithe / Cruthaithe 2008
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  19. 19
    Genome-wide association analysis identifies 13 new risk loci for schizophrenia

    Genome-wide association analysis identifies 13 new risk loci for schizophrenia de réir Stephan Ripke, Colm Ó'Dúshláine, Kimberly Chambert, Jennifer L. Moran, Anna K. Kähler, Susanne Akterin, Sarah E. Bergen, Ann L. Collins, James J. Crowley, Menachem Fromer, Yunjung Kim, Sang Lee, Patrik K. E. Magnusson, Nick Sanchez, Eli A. Stahl, Stephanie Williams, Naomi R. Wray, Kai Xia, Francesco Bettella, Anders D. Børglum, Brendan Bulik‐Sullivan, Paul Cormican, Nick Craddock, Christiaan de Leeuw, Naser Durmishi, Michael Gill, В. Е. Голимбет, Marian L. Hamshere, Peter Holmans, David M Hougaard, Kenneth S. Kendler, Kuang Lin, Derek W. Morris, Ole Mors, Preben Bo Mortensen, Benjamin M. Neale, F. Anthony O’Neill, Michael J. Owen, Miloš Milovančević, Daniëlle Posthuma, John Powell, Alexander Richards, Brien P. Riley, Douglas M. Ruderfer, Dan Rujescu, Engilbert Sigurðsson, Teimuraz Silagadze, August B. Smit, Hreinn Stefánsson, Stacy Steinberg, Jaana Suvisaari, Sarah Tosato, Matthijs Verhage, James Walters, Elvira Bramon, Aiden Corvin, Michael O’Donovan, Hreinn Stefánsson, Edward M. Scolnick, Shaun Purcell, Steven A. McCarroll, Pamela Sklar, Christina M. Hultman, Patrick F. Sullivan

    Foilsithe / Cruthaithe 2013
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  20. 20
    Expanding the range of ZNF804A variants conferring risk of psychosis

    Expanding the range of ZNF804A variants conferring risk of psychosis de réir Stacy Steinberg, Ole Mors, Anders D. Børglum, Ómar Gústafsson, Thomas Werge, Preben Bo Mortensen, Ole A. Andreassen, Engilbert Sigurðsson, Thorgeir E. Thorgeirsson, Yvonne Böttcher, Pall I. Olason, Roel A. Ophoff, Sven Cichon, Iris H Gudjonsdottir, Olli Pietiläinen, Mette Nyegaard, Annamari Tuulio‐Henriksson, Andrés Ingason, Thomas Hansen, Lavinia Athanasiu, Jaana Suvisaari, Jouko Lönnqvist, Tiina Paunio, Annette M. Hartmann, Gesche Jürgens, Merete Nordentoft, David M. Hougaard, B Nørgaard‐Pedersen, René Breuer, HJ Möller, Ina Giegling, Birte Glenthøj, Henrik Berg Rasmussen, Manuel Mattheisen, István Bitter, János Réthelyi, Thordur Sigmundsson, Ragnheiður Fossdal, Unnur Þorsteinsdóttir, Mirella Ruggeri, Sarah Tosato, E Strengman, Lambertus A. Kiemeney, Ingrid Melle, Srdjan Djurovic, Л. И. Абрамова, В. Г. Каледа, Muriel Walshe, Elvira Bramon, Evangelos Vassos, Tao Li, G. T. Fraser, Nicholas Walker, T. Toulopoulou, Joeng Lim Yoon, Nelson B. Freimer, Rita M. Cantor, Robin Murray, Augustine Kong, В. Е. Голимбет, Erik G. Jönsson, Lars Terenius, Ingrid Agartz, Hannes Pétursson, Markus M. Nöthen, Marcella Rietschel, Leena Peltonen, Dan Rujescu, David Collier, Hreinn Stefánsson, David St Clair, Kāri Stefánsson

    Foilsithe / Cruthaithe 2010
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