檢索結果 - Annamari Tuulio‐Henriksson

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  1. 1
    Age at onset and cognitive functioning in schizophrenia

    Age at onset and cognitive functioning in schizophrenia 由 Annamari Tuulio‐Henriksson, Timo Partonen, Jaana Suvisaari, Jari Haukka, Jouko Lönnqvist

    出版 2004
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  2. 2
    Psychotic-like experiences of young adults in the general population predict mental disorders

    Psychotic-like experiences of young adults in the general population predict mental disorders 由 Maija Lindgren, Linda Numminen, Minna Torniainen‐Holm, Sebastian Therman, Annamari Tuulio‐Henriksson

    出版 2022
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  3. 3
    Long-term cognitive functioning is impaired in ICU-treated COVID-19 patients: a comprehensive controlled neuropsychological study

    Long-term cognitive functioning is impaired in ICU-treated COVID-19 patients: a comprehensive controlled neuropsychological study 由 Henriikka Ollila, Riikka Pihlaja, Sanna Koskinen, Annamari Tuulio‐Henriksson, Viljami Salmela, Marjaana Tiainen, Laura Hokkanen, Johanna Hästbacka

    出版 2022
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  4. 4
    Testing the reciprocal association between smoking and depressive symptoms from adolescence to adulthood: A longitudinal twin study

    Testing the reciprocal association between smoking and depressive symptoms from adolescence to adulthood: A longitudinal twin study 由 Anu Ranjit, Tellervo Korhonen, Jadwiga Buchwald, Kauko Heikkilä, Annamari Tuulio‐Henriksson, Richard J. Rose, Jaakko Kaprio, Antti Latvala

    出版 2019
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  5. 5
    Replication of Association Between Working Memory and Reelin, a Potential Modifier Gene in Schizophrenia

    Replication of Association Between Working Memory and Reelin, a Potential Modifier Gene in Schizophrenia 由 Juho Wedenoja, Annamari Tuulio‐Henriksson, Jaana Suvisaari, Anu Loukola, Tiina Paunio, Timo Partonen, Teppo Varilo, Jouko Lönnqvist, Leena Peltonen

    出版 2009
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  6. 6
    Associations of subjective and objective cognitive functioning after COVID-19: A six-month follow-up of ICU, ward, and home-isolated patients

    Associations of subjective and objective cognitive functioning after COVID-19: A six-month follow-up of ICU, ward, and home-isolated patients 由 Riikka Pihlaja, Lina-Lotta Kauhanen, Henriikka Ollila, Annamari Tuulio‐Henriksson, Sanna Koskinen, Marjaana Tiainen, Viljami Salmela, Johanna Hästbacka, Laura Hokkanen

    出版 2023
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  7. 7
    Association Between Genes of Disrupted in Schizophrenia 1 (DISC1) Interactors and Schizophrenia Supports the Role of the DISC1 Pathway in the Etiology of Major Mental Illnesses

    Association Between Genes of Disrupted in Schizophrenia 1 (DISC1) Interactors and Schizophrenia Supports the Role of the DISC1 Pathway in the Etiology of Major Mental Illnesses 由 Liisa Tomppo, William Hennah, Päivi Lahermo, Anu Loukola, Annamari Tuulio‐Henriksson, Jaana Suvisaari, Timo Partonen, Jesper Ekelund, Jouko Lönnqvist, Leena Peltonen

    出版 2009
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  8. 8
    Incidence of and Characteristics Associated With Long-term Benzodiazepine Use in Finland

    Incidence of and Characteristics Associated With Long-term Benzodiazepine Use in Finland 由 Heidi Taipale, Hanna Särkilä, Antti Tanskanen, Terhi Kurko, Tero Taiminen, Jari Tiihonen, Reijo Sund, Annamari Tuulio‐Henriksson, Leena Saastamoinen, Jarmo Hietala

    出版 2020
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  9. 9
    Alcohol-induced psychotic disorder and delirium in the general population

    Alcohol-induced psychotic disorder and delirium in the general population 由 Jonna Perälä, Kimmo Kuoppasalmi, Sami Pirkola, Tommi Härkänen, Samuli I. Saarni, Annamari Tuulio‐Henriksson, Satu Viertiö, Antti Latvala, Seppo Koskinen, Jouko Lönnqvist, Jaana Suvisaari

    出版 2010
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  10. 10
    The Inheritance of Neuropsychological Dysfunction in Twins Discordant for Schizophrenia

    The Inheritance of Neuropsychological Dysfunction in Twins Discordant for Schizophrenia 由 Tyrone D. Cannon, Matti Huttunen, Jouko Lönnqvist, Annamari Tuulio‐Henriksson, Tiia Pirkola, David C. Glahn, Jennifer R. Judd Finkelstein, Marja Hietanen, Jaakko Kaprio, Markku Koskenvuo

    出版 2000
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  11. 11
    Association of DISC1/TRAX Haplotypes With Schizophrenia, Reduced Prefrontal Gray Matter, and Impaired Short- and Long-term Memory

    Association of DISC1/TRAX Haplotypes With Schizophrenia, Reduced Prefrontal Gray Matter, and Impaired Short- and Long-term Memory 由 Tyrone D. Cannon, William Hennah, Theo G.M. van Erp, Paul M. Thompson, Jouko Lönnqvist, Matti Huttunen, Timothy L. Gasperoni, Annamari Tuulio‐Henriksson, Tia Pirkola, Arthur W. Toga, Jaakko Kaprio, John C. Mazziotta, Leena Peltonen

    出版 2005
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  12. 12
    Deletion of TOP3β, a component of FMRP-containing mRNPs, contributes to neurodevelopmental disorders

    Deletion of TOP3β, a component of FMRP-containing mRNPs, contributes to neurodevelopmental disorders 由 Georg Stoll, Olli Pietiläinen, Bastian Linder, Jaana Suvisaari, Cornelia Brosi, William Hennah, Virpi Leppä, Minna Torniainen, Samuli Ripatti, Sirpa Ala‐Mello, Oliver Plöttner, Karola Rehnström, Annamari Tuulio‐Henriksson, Teppo Varilo, Jonna Tallila, Kati Kristiansson, Matti Isohanni, Jaakko Kaprio, Johan G. Eriksson, Olli T. Raitakari, Terho Lehtimäki, Marjo‐Riitta Järvelin, Veikko Salomaa, Matthew E. Hurles, Hreinn Stefánsson, Leena Peltonen, Patrick F. Sullivan, Tiina Paunio, Jouko Lönnqvist, Mark J. Daly, Utz Fischer, Nelson B. Freimer, Aarno Palotie

    出版 2013
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  13. 13
    A large replication study and meta-analysis in European samples provides further support for association of AHI1 markers with schizophrenia

    A large replication study and meta-analysis in European samples provides further support for association of AHI1 markers with schizophrenia 由 Andrés Ingason, Ina Giegling, Sven Cichon, Thomas Hansen, Henrik Berg Rasmussen, Jimmi Nielsen, Gesche Jürgens, Pierandrea Muglia, Annette M. Hartmann, Eric Strengman, Catalina Vasilescu, Thomas W. Mühleisen, Srdjan Djurovic, Ingrid Melle, Bernard Lerer, Hans‐Jürgen Möller, Clyde Francks, Olli Pietiläinen, Jouko Lönnqvist, Jaana Suvisaari, Annamari Tuulio‐Henriksson, Muriel Walshe, Evangelos Vassos, Marta Di Forti, Robin Murray, Chiara Bonetto, Sarah Tosato, Rita M. Cantor, Marcella Rietschel, Nick Craddock, Michael J. Owen, Leena Peltonen, Ole A. Andreassen, Markus M. Nöthen, David St Clair, Roel A. Ophoff, Michael O’Donovan, David Collier, Thomas Werge, Dan Rujescu

    出版 2010
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  14. 14
    Copy number variations of chromosome 16p13.1 region associated with schizophrenia

    Copy number variations of chromosome 16p13.1 region associated with schizophrenia 由 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

    出版 2009
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  15. 15
    Disruption of the neurexin 1 gene is associated with schizophrenia

    Disruption of the neurexin 1 gene is associated with schizophrenia 由 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

    出版 2008
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  16. 16
    Expanding the range of ZNF804A variants conferring risk of psychosis

    Expanding the range of ZNF804A variants conferring risk of psychosis 由 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

    出版 2010
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  17. 17
    The impact of rare protein coding genetic variation on adult cognitive function

    The impact of rare protein coding genetic variation on adult cognitive function 由 Chia‐Yen Chen, Ruoyu Tian, Tian Ge, Max Lam, Gabriela Sánchez-Andrade, Tarjinder Singh, Lea Urpa, Jimmy Z. Liu, Mark Sanderson, Christine Rowley, Holly Ironfield, Terry Fang, Aija Kyttälä, Amanda Elliott, Anders Kämpe, André Sourander, Annamari Tuulio‐Henriksson, Anssi Solismaa, Antti Tanskanen, Ari Ahola‐Olli, Arto Mustonen, Arttu Honkasalo, Asko Wegelius, Atiqul Haq Mazumder, Auli Toivola, Benjamin M. Neale, Elina Hietala, Elmo Saarentaus, Erik Cederlöf, Erkki Isometsä, Heidi Taipale, Imre Västrik, Jaana Suvisaari, Jari Tiihonen, Jarmo Hietala, Johan Ahti, Jonne Lintunen, Jouko Lönnqvist, Juha Veijola, Julia Moghadampour, Jussi Niemi-Pynttäri, Kaisla Lahdensuo, Katja Häkkinen, Katriina Hakakari, Kimmo Suokas, Marjo Taivalantti, Markku Lähteenvuo, Martta Kerkelä, Minna Torniainen‐Holm, Nina Lindberg, Noora Ristiluoma, Olli Kampman, Olli Pietiläinen, Risto Kajanne, Sari Lång-Tonteri, Solja Niemelä, Steven E. Hyman, Susanna Rask, Teemu Männynsalo, Tiina Paunio, Tuomas Jukuri, Tuomo Kiiskinen, Tuula Kieseppä, Ville Mäkipelto, Willehard Haaki, Zuzanna Misiewicz, Mitja Kurki, Jarmo Körkkö, Jukka S. Moilanen, Outi Kuismin, Mark J. Daly, Aarno Palotie, Ellen Tsai, Hailiang Huang, Matthew E. Hurles, Sebastian S. Gerety, Todd Lencz, Heiko Runz

    出版 2023
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  18. 18
    Common variants at VRK2 and TCF4 conferring risk of schizophrenia

    Common variants at VRK2 and TCF4 conferring risk of schizophrenia 由 Stacy Steinberg, Simone de Jong, Ole A. Andreassen, Thomas Werge, Anders D. Børglum, Ole Mors, Preben Bo Mortensen, Ómar Gústafsson, Javier Costas, Olli 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, Günter Kenis, Л. И. Абрамова, В. Г. Каледа, Manuel Arrojo, Julio Sanjuán, Celso Arango, Swetlana Sperling, Moritz J. Rossner, Michele Ribolsi, Valentina Magni, Alberto Siracusano, Claus Christiansen, Lambertus A. Kiemeney, Jan H. Veldink, Leonard van den Berg, Andrés Ingason, Pierandrea Muglia, Robin Murray, Markus M. Nöthen, Engilbert Sigurðsson, Hannes Pétursson, Unnur Þorsteinsdóttir, Augustine Kong, I. Alex Rubino, Marc D. Binder, János Réthelyi, István Bitter, Erik G. Jönsson, В. Е. Голимбет, Ángel Carracedo, Hannelore Ehrenreich, Nick Craddock, Michael J. Owen, Michael O’Donovan, Mirella Ruggeri, Sarah Tosato, Leena Peltonen, Roel A. Ophoff, David Collier, David St Clair, Marcella Rietschel, Sven Cichon, Hreinn Stefánsson, Dan Rujescu, Kāri Stefánsson

    出版 2011
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  19. 19
    Common variants conferring risk of schizophrenia

    Common variants conferring risk of schizophrenia 由 Hreinn Stefánsson, Roel A. Ophoff, Stacy Steinberg, Ole A. Andreassen, Sven Cichon, Dan Rujescu, Thomas Werge, Olli Pietiläinen, Ole Mors, Preben Bo Mortensen, Engilbert Sigurðsson, Ómar Gústafsson, Mette Nyegaard, Annamari Tuulio‐Henriksson, Andrés Ingason, Thomas Hansen, Jaana Suvisaari, Jouko Lönnqvist, Tiina Paunio, Anders D. Børglum, Annette M. Hartmann, Anders Fink‐Jensen, Merete Nordentoft, David M. Hougaard, Bent Nørgaard‐Pedersen, Yvonne Böttcher, Jes Olesen, René Breuer, Hans‐Jürgen Möller, 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 Llanos, 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

    出版 2009
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  20. 20
    Association between genetic variation in a region on chromosome 11 and schizophrenia in large samples from Europe

    Association between genetic variation in a region on chromosome 11 and schizophrenia in large samples from Europe 由 M. Rietschel, Manuel Mattheisen, F. Degenhardt, René S. Kahn, Don Linszen, Jim van Os, Durk Wiersma, Richard Bruggeman, Wiepke Cahn, Lieuwe de Haan, Lydia Krabbendam, Inez Myin‐Germeys, Thomas W. Mühleisen, Peter Kirsch, Christine Esslinger, Stefan Herms, Ditte Demontis, Michael Steffens, J Strohmaier, Britta Haenisch, René Breuer, Piotr M. Czerski, I Giegling, E Strengman, C Schmael, Ole Mors, Preben Bo Mortensen, D M Hougaard, Torben Ørntoft, Paweł Kapelski, Lutz Priebe, F B Basmanav, Andreas J. Forstner, Per Hoffmann, S Meier, J A. Nikitopoulos, Susanne Moebus, Michael P. Alexander, R Mössner, H-E Wichmann, S. Schreiber, Fernando Rivandeneira, A. Hofman, André G. Uitterlinden, T. F. Wienker, J Schumacher, J Hauser, W. Maier, R. M. Cantor, Susanne Erk, Thomas G. Schulze, Hreinn Stefánsson, Stacy Steinberg, Ómar Gústafsson, Engilbert Sigurðsson, Hannes Pétursson, Augustine Kong, Kāri Stefánsson, Olli Pietiläinen, Annamari Tuulio‐Henriksson, Tiina Paunio, Jouko Lönnqvist, Jaana Suvisaari, Leena Peltonen, Mirella Ruggeri, Sarah Tosato, Muriel Walshe, Robin Murray, David Collier, David St Clair, Thomas Hansen, Andrés Ingason, Klaus D. Jakobsen, Linh Viet Duong, Thomas Werge, Ingrid Melle, Ole A. Andreassen, Srdjan Djurovic, István Bitter, János Réthelyi, Л. И. Абрамова, В. Г. Каледа, В. Е. Голимбет, Erik G. Jönsson, Lars Terenius, Ingrid Agartz, Ruud van Winkel, Günter Kenis, Marc D. Binder, Jan H. Veldink, Carsten Wiuf, Michael Didriksen, Nick Craddock, Michael J. Owen, Michael O’Donovan, Anders D. Børglum, Dan Rujescu, Henrik Walter, Andreas Meyer‐Lindenberg, Markus M. Nöthen

    出版 2011
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