Suchergebnisse - Marianne Giørtz Pedersen

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  1. 1
    Epidemiology of autoimmune diseases in Denmark

    Epidemiology of autoimmune diseases in Denmark von William W. Eaton, Noel R. Rose, Amanda Kalaydjian, Marianne Giørtz Pedersen, Preben Bo Mortensen

    Veröffentlicht 2007
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  2. 2
    Birth Weight, Schizophrenia, and Adult Mental Disorder

    Birth Weight, Schizophrenia, and Adult Mental Disorder von Kathryn M. Abel, Susanne Wicks, Ezra Susser, Christina Dalman, Marianne Giørtz Pedersen, Preben Bo Mortensen, Roger T. Webb

    Veröffentlicht 2010
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  3. 3
    The impact of maternal celiac disease on birthweight and preterm birth: a Danish population-based cohort study

    The impact of maternal celiac disease on birthweight and preterm birth: a Danish population-based cohort study von Ali S. Khashan, Tine Brink Henriksen, Preben Bo Mortensen, Roseanne McNamee, Fergus P. McCarthy, Marianne Giørtz Pedersen, Louise C. Kenny

    Veröffentlicht 2009
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  4. 4
    CASPR2 autoantibodies are raised during pregnancy in mothers of children with mental retardation and disorders of psychological development but not autism

    CASPR2 autoantibodies are raised during pregnancy in mothers of children with mental retardation and disorders of psychological development but not autism von Estér Coutinho, Leslie Jacobson, Marianne Giørtz Pedersen, Michael E. Benros, Bent Nørgaard‐Pedersen, Preben Bo Mortensen, Paul J. Harrison, Angela Vincent

    Veröffentlicht 2017
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  5. 5
    The iPSYCH2015 Case-Cohort sample: updated directions for unravelling genetic and environmental architectures of severe mental disorders

    The iPSYCH2015 Case-Cohort sample: updated directions for unravelling genetic and environmental architectures of severe mental disorders von Jonas Bybjerg‐Grauholm, Carsten Bøcker Pedersen, Marie Bækvad‐Hansen, Marianne Giørtz Pedersen, Dea Adamsen, Christine Søholm Hansen, Esben Agerbo, Jakob Grove, Thomas D. Als, Andrew J. Schork, Alfonso Buil, Ole Mors, Merete Nordentoft, Thomas Werge, Anders D. Børglum, David M. Hougaard, Preben Bo Mortensen

    Veröffentlicht 2020
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  6. 6
    Genetic Variants Associated With Anxiety and Stress-Related Disorders

    Genetic Variants Associated With Anxiety and Stress-Related Disorders von Sandra Meier, Kalevi Trontti, Kirstin L. Purves, Thomas D. Als, Jakob Grove, Mikaela A. Laine, Marianne Giørtz Pedersen, Jonas Bybjerg‐Grauholm, Marie Bækved-Hansen, Ewa Sokołowska, Preben Bo Mortensen, David M. Hougaard, Thomas Werge, Merete Nordentoft, Gerome Breen, Anders D. Børglum, Thalia C. Eley, Iiris Hovatta, Manuel Mattheisen, Ole Mors

    Veröffentlicht 2019
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  7. 7
    The iPSYCH2012 case–cohort sample: new directions for unravelling genetic and environmental architectures of severe mental disorders

    The iPSYCH2012 case–cohort sample: new directions for unravelling genetic and environmental architectures of severe mental disorders von Carsten Bøcker Pedersen, Jonas Bybjerg‐Grauholm, Marianne Giørtz Pedersen, Jakob Grove, Esben Agerbo, Marie Bækvad‐Hansen, Jesper B. Poulsen, Christine Søholm Hansen, John J. McGrath, Thomas D. Als, J I Goldstein, Benjamin M. Neale, Mark J. Daly, David M. Hougaard, Ole Mors, Merete Nordentoft, Anders D. Børglum, Thomas Werge, Preben Bo Mortensen

    Veröffentlicht 2017
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  8. 8
    Variable DNA methylation in neonates mediates the association between prenatal smoking and birth weight

    Variable DNA methylation in neonates mediates the association between prenatal smoking and birth weight von Eilís Hannon, Diana Schendel, Christine Ladd‐Acosta, Jakob Grove, Christine Søholm Hansen, David M. Hougaard, Michaeline Bresnahan, Ole Mors, Mads V. Hollegaard, Marie Bækvad‐Hansen, Mady Hornig, Preben Bo Mortensen, Anders D. Børglum, Thomas Werge, Marianne Giørtz Pedersen, Merete Nordentoft, Joseph D. Buxbaum, M. Daniele Fallin, Jonas Bybjerg‐Grauholm, Abraham Reichenberg, Jonathan Mill

    Veröffentlicht 2019
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  9. 9
    Elevated polygenic burden for autism is associated with differential DNA methylation at birth

    Elevated polygenic burden for autism is associated with differential DNA methylation at birth von Eilís Hannon, Diana Schendel, Christine Ladd‐Acosta, Jakob Grove, Christine Søholm Hansen, Shan V. Andrews, David M. Hougaard, Michaeline Bresnahan, Ole Mors, Mads V. Hollegaard, Marie Bækvad‐Hansen, Mady Hornig, Preben Bo Mortensen, Anders D. Børglum, Thomas Werge, Marianne Giørtz Pedersen, Merete Nordentoft, Joseph D. Buxbaum, M. Daniele Fallin, Jonas Bybjerg‐Grauholm, Abraham Reichenberg, Jonathan Mill

    Veröffentlicht 2018
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  10. 10
    Large-scale study of Toxoplasma and Cytomegalovirus shows an association between infection and serious psychiatric disorders

    Large-scale study of Toxoplasma and Cytomegalovirus shows an association between infection and serious psychiatric disorders von Kristoffer Sølvsten Burgdorf, Betina B. Trabjerg, Marianne Giørtz Pedersen, Janna Nissen, Karina Banasik, Ole Birger Pedersen, Erik Sørensen, Kaspar René Nielsen, Margit Hørup Larsen, Christian Erikstrup, Peter Bruun-Rasmussen, David Westergaard, Lise Wegner Thørner, Henrik Hjalgrim, Helene M. Paarup, Søren Brunak, Carsten Bøcker Pedersen, E. Fuller Torrey, Thomas Werge, Preben Bo Mortensen, Robert H. Yolken, Henrik Ullum

    Veröffentlicht 2019
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  11. 11
    A genome-wide association study of shared risk across psychiatric disorders implicates gene regulation during fetal neurodevelopment

    A genome-wide association study of shared risk across psychiatric disorders implicates gene regulation during fetal neurodevelopment von Andrew J. Schork, Hyejung Won, Vivek Appadurai, Ron Nudel, Michael J. Gandal, Olivier Delaneau, Malene Revsbech Christiansen, David M. Hougaard, Marie Bækved-Hansen, Jonas Bybjerg‐Grauholm, Marianne Giørtz Pedersen, Esben Agerbo, Carsten Bøcker Pedersen, Benjamin M. Neale, Mark J. Daly, Naomi R. Wray, Merete Nordentoft, Ole Mors, Anders D. Børglum, Preben Bo Mortensen, Alfonso Buil, Wesley K. Thompson, Daniel H. Geschwind, Thomas Werge

    Veröffentlicht 2019
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  12. 12
    Polygenic profiles define aspects of clinical heterogeneity in attention deficit hyperactivity disorder

    Polygenic profiles define aspects of clinical heterogeneity in attention deficit hyperactivity disorder von Sonja LaBianca, Isabell Brikell, Dorte Helenius, Robert Loughnan, Joel Mefford, Clare E. Palmer, Rebecca L. Walker, Jesper R. Gådin, Morten Dybdahl Krebs, Vivek Appadurai, Morteza Vaez, Esben Agerbo, Marianne Giørtz Pedersen, Anders D. Børglum, David M. Hougaard, Ole Mors, Merete Nordentoft, Preben Bo Mortensen, Kenneth S. Kendler, Terry L. Jernigan, Daniel H. Geschwind, Andrés Ingason, Andrew Dahl, Noah Zaitlen, Søren Dalsgaard, Thomas Werge, Andrew J. Schork

    Veröffentlicht 2023
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  13. 13
    Genome-wide association study of school grades identifies genetic overlap between language ability, psychopathology and creativity

    Genome-wide association study of school grades identifies genetic overlap between language ability, psychopathology and creativity von Veera M. Rajagopal, Andrea Ganna, Jonathan R. I. Coleman, Andrea G. Allegrini, Georgios Voloudakis, Jakob Grove, Thomas D. Als, Henriette Thisted Horsdal, Liselotte Petersen, Vivek Appadurai, Andrew J. Schork, Alfonso Buil, Cynthia M. Bulik, Jonas Bybjerg‐Grauholm, Marie Bækvad‐Hansen, David M. Hougaard, Ole Mors, Merete Nordentoft, Thomas Werge, Rich Belliveau, Caitlin E. Carey, Felecia Cerrato, Kimberly Chambert, Tracy Air, Mark J. Daly, Ashley Dumont, Jacqueline I. Goldstein, Christine Søholm Hansen, Daniel P. Howrigan, Hailiang Huang, Julian Maller, Alicia R. Martin, Joanna Martin, Manuel Mattheisen, Jennifer L. Moran, Benjamin M. Neale, Jonatan Pallesen, Duncan S. Palmer, Carsten Bcker Pedersen, Marianne Giørtz Pedersen, Timothy Poterba, Stephan Ripke, F. Kyle Satterstrom, Wesley K. Thompson, Patrick Turley, Raymond K. Walters, Preben Bo Mortensen, Gerome Breen, Panos Roussos, Robert Plomin, Esben Agerbo, Anders D. Børglum, Ditte Demontis

    Veröffentlicht 2023
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  14. 14
    Discovery of the first genome-wide significant risk loci for ADHD

    Discovery of the first genome-wide significant risk loci for ADHD von Ditte Demontis, Raymond K. Walters, Joanna Martin, Manuel Mattheisen, Thomas D. Als, Esben Agerbo, Rich Belliveau, Jonas Bybjerg‐Grauholm, Marie Bækvad‐Hansen, Felecia Cerrato, Kimberly Chambert, Tracy Air, Ashley Dumont, Nicholas Eriksson, Michael J. Gandal, Jacqueline I. Goldstein, Jakob Grove, Christine Søholm Hansen, Mads E. Hauberg, Mads V. Hollegaard, Daniel P. Howrigan, Hailiang Huang, Julian Maller, Joanna Martin, Jennifer L. Moran, Jonatan Pallesen, Duncan S. Palmer, Carsten Bøcker Pedersen, Marianne Giørtz Pedersen, Timothy Poterba, Jesper Buchhave Poulsen, Stephan Ripke, Elise Robinson, Kyle F. Satterstrom, Christine Stevens, Patrick Turley, Hyejung Won, Ole A. Andreassen, Christie L. Burton, Dorret I. Boomsma, Bru Cormand, Søren Dalsgaard, Barbara Franke, Joel Gelernter, Daniel H. Geschwind, Hákon Hákonarson, Jan Haavik, Henry R. Kranzler, Jonna Kuntsi, K. Langley, Klaus‐Peter Lesch, Christel M. Middeldorp, Andreas Reif, Luís Augusto Rohde, Panos Roussos, Russell Schachar, Pamela Sklar, Edmund Sonuga‐Barke, Patrick F. Sullivan, Anita Thapar, Joyce Y. Tung, Irwin D. Waldman, Merete Nordentoft, David M. Hougaard, Thomas Werge, Ole Mors, Preben Bo Mortensen, Mark J. Daly, Stephen V. Faraone, Anders D. Børglum, Benjamin M. Neale

    Veröffentlicht 2017
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  15. 15
    Common risk variants identified in autism spectrum disorder

    Common risk variants identified in autism spectrum disorder von Jakob Grove, Stephan Ripke, Thomas D. Als, Manuel Mattheisen, Raymond K. Walters, Hyejung Won, Jonatan Pallesen, Esben Agerbo, Ole A. Andreassen, Richard Anney, Rich Belliveau, Francesco Bettella, Joseph D. Buxbaum, Jonas Bybjerg‐Grauholm, Marie Bækved-Hansen, Felecia Cerrato, Kimberly Chambert, Jane Christensen, Tracy Air, Karin Dellenvall, Ditte Demontis, Silvia De Rubeis, Bernie Devlin, Srdjan Djurovic, Ashle Dumont, Jacqueline I. Goldstein, Christine Søholm Hansen, Mads E. Hauberg, Mads V. Hollegaard, Sigrun Hope, Daniel P. Howrigan, Hailiang Huang, Christina M. Hultman, Lambertus Klei, Julian Maller, Joanna Martin, Alicia R. Martin, Jennifer L. Moran, Mette Nyegaard, Terje Nærland, Duncan S. Palmer, Aarno Palotie, Carsten Bøcker Pedersen, Marianne Giørtz Pedersen, Timothy Poterba, Jesper Buchhave Poulsen, Beaté St Pourcain, Per Qvist, Karola Rehnström, Avi Reichenberg, Jennifer Reichert, Elise Robinson, Kathryn Roeder, Panos Roussos, Evald Sæmundsen, Sven Sandin, F. Kyle Satterstrom, George Davey Smith, Hreinn Stefánsson, Kāri Stefánsson, Stacy Steinberg, Christine Stevens, Patrick F. Sullivan, Patrick Turley, G. Bragi Walters, Xinyi Xu, Daniel H. Geschwind, Merete Nordentoft, David M. Hougaard, Thomas Werge, Ole Mors, Preben Bo Mortensen, Benjamin M. Neale, Mark J. Daly, Anders D. Børglum

    Veröffentlicht 2017
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  16. 16
    Common schizophrenia alleles are enriched in mutation-intolerant genes and in regions under strong background selection

    Common schizophrenia alleles are enriched in mutation-intolerant genes and in regions under strong background selection von Antonio F. Pardiñas, Peter Holmans, Andrew Pocklington, Valentina Escott‐Price, Stephan Ripke, Noa Carrera, Sophie E. Legge, Sophie Bishop, Darren Cameron, Marian L. Hamshere, Jun Han, Leon Hubbard, Amy Lynham, Kiran K. Mantripragada, Elliott Rees, James H. MacCabe, Steven A. McCarroll, Bernhard T. Baune, Gerome Breen, Enda M. Byrne, Udo Dannlowski, Thalia C. Eley, Caroline Hayward, Nicholas G. Martin, Andrew M. McIntosh, Robert Plomin, David J. Porteous, Naomi R. Wray, Armando Caballero, Daniel H. Geschwind, Laura M. Huckins, Douglas M. Ruderfer, Enrique Santiago, Pamela Sklar, Eli A. Stahl, Hyejung Won, Esben Agerbo, Thomas D. Als, Ole A. Andreassen, Marie Bækvad‐Hansen, Preben Bo Mortensen, Carsten Bøcker Pedersen, Anders D. Børglum, Jonas Bybjerg‐Grauholm, Srdjan Djurovic, Naser Durmishi, Marianne Giørtz Pedersen, В. Е. Голимбет, Jakob Grove, David M. Hougaard, Manuel Mattheisen, Espen Molden, Ole Mors, Merete Nordentoft, Milica Pejović-Milovančević, Engilbert Sigurðsson, Teimuraz Silagadze, Christine Søholm Hansen, Kāri Stefánsson, Hreinn Stefánsson, Stacy Steinberg, Sarah Tosato, Thomas Werge, David Collier, Dan Rujescu, George Kirov, Michael J. Owen, Michael O’Donovan, James Walters

    Veröffentlicht 2018
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  17. 17
    Identification of common genetic risk variants for autism spectrum disorder

    Identification of common genetic risk variants for autism spectrum disorder von Jakob Grove, Stephan Ripke, Thomas D. Als, Manuel Mattheisen, Raymond K. Walters, Hyejung Won, Jonatan Pallesen, Esben Agerbo, Ole A. Andreassen, Richard Anney, Swapnil Awashti, Rich Belliveau, Francesco Bettella, Joseph D. Buxbaum, Jonas Bybjerg‐Grauholm, Marie Bækvad‐Hansen, Felecia Cerrato, Kimberly Chambert, Jane Christensen, Tracy Air, Karin Dellenvall, Ditte Demontis, Silvia De Rubeis, Bernie Devlin, Srdjan Djurovic, Ashley Dumont, Jacqueline I. Goldstein, Christine Søholm Hansen, Mads E. Hauberg, Mads V. Hollegaard, Sigrun Hope, Daniel P. Howrigan, Hailiang Huang, Christina M. Hultman, Lambertus Klei, Julian Maller, Joanna Martin, Alicia R. Martin, Jennifer L. Moran, Mette Nyegaard, Terje Nærland, Duncan S. Palmer, Aarno Palotie, Carsten Bøcker Pedersen, Marianne Giørtz Pedersen, Timothy dPoterba, Jesper Buchhave Poulsen, Beaté St Pourcain, Per Qvist, Karola Rehnström, Abraham Reichenberg, Jennifer Reichert, Elise Robinson, Kathryn Roeder, Panos Roussos, Evald Sæmundsen, Sven Sandin, F. Kyle Satterstrom, George Davey Smith, Hreinn Stefánsson, Stacy Steinberg, Christine Stevens, Patrick F. Sullivan, Patrick Turley, G. Bragi Walters, Xinyi Xu, Kāri Stefánsson, Daniel H. Geschwind, Merete Nordentoft, David M. Hougaard, Thomas Werge, Ole Mors, Preben Bo Mortensen, Benjamin M. Neale, Mark J. Daly, Anders D. Børglum

    Veröffentlicht 2019
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  18. 18
    Discovery of the first genome-wide significant risk loci for attention deficit/hyperactivity disorder

    Discovery of the first genome-wide significant risk loci for attention deficit/hyperactivity disorder von Ditte Demontis, Raymond K. Walters, Joanna Martin, Manuel Mattheisen, Thomas D. Als, Esben Agerbo, Gísli Baldursson, Rich Belliveau, Jonas Bybjerg‐Grauholm, Marie Bækvad‐Hansen, Felecia Cerrato, Kimberly Chambert, Tracy Air, Ashley Dumont, Nicholas Eriksson, Michael J. Gandal, Jacqueline I. Goldstein, Katrina L. Grasby, Jakob Grove, Ólafur Ó. Guðmundsson, Christine Søholm Hansen, Mads E. Hauberg, Mads V. Hollegaard, Daniel P. Howrigan, Hailiang Huang, Julian Maller, Alicia R. Martin, Nicholas G. Martin, Jennifer L. Moran, Jonatan Pallesen, Duncan S. Palmer, Carsten Bøcker Pedersen, Marianne Giørtz Pedersen, Timothy Poterba, Jesper Buchhave Poulsen, Stephan Ripke, Elise Robinson, F. Kyle Satterstrom, Hreinn Stefánsson, Christine Stevens, Patrick Turley, G. Bragi Walters, Hyejung Won, Margaret J. Wright, Ole A. Andreassen, Philip Asherson, Christie L. Burton, Dorret I. Boomsma, Bru Cormand, Søren Dalsgaard, Barbara Franke, Joel Gelernter, Daniel H. Geschwind, Hákon Hákonarson, Jan Haavik, Henry R. Kranzler, Jonna Kuntsi, K. Langley, Klaus‐Peter Lesch, Christel M. Middeldorp, Andreas Reif, Luís Augusto Rohde, Panos Roussos, Russell Schachar, Pamela Sklar, Edmund Sonuga‐Barke, Patrick F. Sullivan, Anita Thapar, Joyce Y. Tung, Irwin D. Waldman, Sarah E. Medland, Kāri Stefánsson, Merete Nordentoft, David M. Hougaard, Thomas Werge, Ole Mors, Preben Bo Mortensen, Mark J. Daly, Stephen V. Faraone, Anders D. Børglum, Benjamin M. Neale

    Veröffentlicht 2018
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  19. 19
    Shared molecular neuropathology across major psychiatric disorders parallels polygenic overlap

    Shared molecular neuropathology across major psychiatric disorders parallels polygenic overlap von Michael J. Gandal, Jillian R. Haney, Neelroop Parikshak, Virpi Leppä, Gokul Ramaswami, Christopher Hartl, Andrew J. Schork, Vivek Appadurai, Alfonso Buil, Thomas Werge, Chunyu Liu, Kevin P. White, Steve Horvath, Daniel H. Geschwind, Nenad Šestan, Flora M. Vaccarino, Mark Gerstein, Sherman M. Weissman, Sirisha Pochareddy, Matthew W. State, James A. Knowles, Peggy Farnham, Schahram Akbarian, Dalila Pinto, Harm Van Baekl, Stella Dracheva, Andrew E. Jaffe, Thomas M. Hyde, Peter P. Zandi, Gregory E. Crawford, Pat Sullivan, Wesley K. Thompson, Preben Bo Mortensen, Esben Agerbo, Marianne Giørtz Pedersen, Carsten Bøcker Pedersen, Ole Mors, Anders D. Børglum, Merete Nordentoft, David M. Hougaard, Jonas Bybjerg‐Grauholm, Marie Bækvad‐Hansen, Alicia R. Martin, Ashley Dumont, Christine Stevens, Tracy Air, Daniel P. Howrigan, Duncan S. Palmer, Elise Robinson, Kyle F. Satterstrom, Felecia Cerrato, Hailiang Huang, Jacqueline I. Goldstein, Jennifer L. Moran, Joanna Martin Julian, M. Alonge Kimberly, C. Seed Patrick, Patrick Turley, Raymond K. Walters, Rich Belliveau, Stephan Ripke, Timothy Poterba, Mark J. Daly, Benjamin M. Neale, Menachem Fromer, Panos Roussos, Jessica Johnson, Hardik Shah, Milind Mahajan, Eric E. Schadt, Vahram Haroutunian, Douglas M. Ruderfer, Joseph D. Buxbaum, Solveig K. Sieberts, Kristen K. Dang, Ben Logsdon, Lara M. Mangravite, Mette A. Peters, Raquel E. Gur, Chang-Gyu Hahn, Bernie Devlin, Lambertus Klei, David A. Lewis, Barbara K. Lipska, Keisuke Hirai, Hiroyoshi Toyoshiba, Enrico Domenici

    Veröffentlicht 2018
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  20. 20
    A Genetic Investigation of Sex Bias in the Prevalence of Attention-Deficit/Hyperactivity Disorder

    A Genetic Investigation of Sex Bias in the Prevalence of Attention-Deficit/Hyperactivity Disorder von Joanna Martin, Raymond K. Walters, Ditte Demontis, Manuel Mattheisen, Sang Lee, Elise Robinson, Isabell Brikell, Laura Ghirardi, Henrik Larsson, Paul Lichtenstein, Nicholas Eriksson, Thomas Werge, Preben Bo Mortensen, Marianne Giørtz Pedersen, Ole Mors, Merete Nordentoft, David M. Hougaard, Jonas Bybjerg‐Grauholm, Naomi R. Wray, Barbara Franke, Stephen V. Faraone, Michael O’Donovan, Anita Thapar, Anders D. Børglum, Benjamin M. Neale, Michelle Agee, Babak Alipanahi, Adam Auton, Robert K. Bell, Katarzyna Bryc, Sarah L. Elson, Pierre Fontanillas, Nicholas A. Furlotte, David A. Hinds, Bethann S. Hromatka, Karen E. Huber, Aaron Kleinman, Nadia K. Litterman, 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, Özgür Albayrak, Richard Anney, Alejandro Arias Vásquez, María J. Arranz, Philip Asherson, Tobias Banaschewski, Tobias Banaschewski, Claiton Henrique Dotto Bau, Joseph Biederman, Preben Bo Mortensen, Anders D. Børglum, Jan K. Buitelaar, Miguel Casas, Alice Charach, Bru Cormand, Jennifer Crosbie, Søren Dalsgaard, Mark J. Daly, Ditte Demontis, Astrid Dempfle, Alysa E. Doyle, Richard P. Ebstein, Josephine Elia, Stephen V. Faraone, Stephen V. Faraone, Manuel Föcker, Barbara Franke, Christine M. Freitag, Joel Gelernter, Michael Gill, Eugênio H. Grevet, Jan Haavik, Hákon Hákonarson, Ziarih Hawi, Johannes Hebebrand, Beate Herpertz‐Dahlmann, Amaia Hervás, Anke Hinney, Sarah Hohmann, Peter Holmans, Mara Helena Hutz, Abel Ickowitz, Stefan Johansson, Lindsey Kent, Sarah Kittel‐Schneider, Henry R. Kranzler, Jonna Kuntsi, Nanda Lambregts-Rommelse, K. Langley, Gerd Lehmkuhl

    Veröffentlicht 2017
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