Resultados de búsqueda - Karin Egberts

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  1. 1
    Predictors of the resumption of menses in adolescent anorexia nervosa

    Predictors of the resumption of menses in adolescent anorexia nervosa por Astrid Dempfle, Beate Herpertz‐Dahlmann, Nina Timmesfeld, Reinhild Schwarte, Karin Egberts, E. F. Pfeiffer, Christian Fleischhaker, Christoph Wewetzer, Katharina Bühren

    Publicado 2013
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  2. 2
    AGNP Consensus Guidelines for Therapeutic Drug Monitoring in Psychiatry: Update 2011

    AGNP Consensus Guidelines for Therapeutic Drug Monitoring in Psychiatry: Update 2011 por Christoph Hiemke, Pierre Baumann, N. Bergemann, Andreas Conca, Otto Dietmaier, Karin Egberts, Mirijam Fric, M. Gerlach, C. Greiner, Gerhard Gründer, Ekkehard Haen, Ursula Havemann‐Reinecke, E Jaquenoud Sirot, Hartmut Kirchherr, Gerd Laux, Ulrich Lutz, Thomas Messer, Markus Müller, Bruno Pfuhlmann, B. Rambeck, Peter Riederer, Bernd Schoppek, Julia Stingl, Manfred Uhr, S. Ulrich, R. Waschgler, Gerald Zernig

    Publicado 2011
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  3. 3
    Premorbid body weight predicts weight loss in both anorexia nervosa and atypical anorexia nervosa: Further support for a single underlying disorder

    Premorbid body weight predicts weight loss in both anorexia nervosa and atypical anorexia nervosa: Further support for a single underlying disorder por Johannes Hebebrand, Jochen Seitz, Manuel Föcker, Hanna Preuss, Michael Huß, Katharina Bühren, Brigitte Dahmen, Katja Becker, Linda Weber, Christoph U. Correll, Charlotte Jaite, Karin Egberts, Marcel Romanos, Stefan Ehrlich, Maria Seidel, Veit Roessner, Christian Fleischhaker, Eva Möhler, Freia Hahn, Michael Kaess, Tanja Legenbauer, Daniela Hagmann, Tobias Renner, Ulrike Schulze, Ulf Thiemann, Ida Wessing, Gisela Antony, Beate Herpertz‐Dahlmann, Abigail Matthews, Triinu Peters

    Publicado 2024
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  4. 4
    Therapeutic drug monitoring of sertraline in children and adolescents: A naturalistic study with insights into the clinical response and treatment of obsessive-compulsive disorder

    Therapeutic drug monitoring of sertraline in children and adolescents: A naturalistic study with insights into the clinical response and treatment of obsessive-compulsive disorder por E. Tini, Lukasz Smigielski, Marcel Romanos, Christoph Wewetzer, Andreas Karwautz, Karl Reitzle, Christoph U. Correll, Paul L. Plener, Uwe Malzahn, Peter U. Heuschmann, Stefan Unterecker, Maike Scherf‐Clavel, Hans Rock, Gisela Antony, Wolfgang Briegel, Christian Fleischhaker, Tobias Banaschewski, Tobias Hellenschmidt, Hartmut Imgart, Michael Kaess, Michael Kölch, Tobias Renner, Su-Yin Reuter-Dang, Christian A. Rexroth, Gerd Schulte‐Körne, Frank Theisen, Stefanie Fekete, Regina Taurines, Manfred Gerlach, Karin Egberts, Susanne Walitza

    Publicado 2022
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  5. 5
    Consensus Guidelines for Therapeutic Drug Monitoring in Neuropsychopharmacology: Update 2017

    Consensus Guidelines for Therapeutic Drug Monitoring in Neuropsychopharmacology: Update 2017 por Christoph Hiemke, N. Bergemann, H.‐W. Clement, Andreas Conca, Jürgen Deckert, Katharina Domschke, Gabriel Eckermann, Karin Egberts, M. Gerlach, C. Greiner, Gerhard Gründer, Ekkehard Haen, Ursula Havemann‐Reinecke, Gudrun Hefner, Renate Helmer, G. Janßen, Eveline Jaquenoud, Gerd Laux, Thomas Messer, Rainald Mößner, Michael Müller, Michael Paulzen, Bruno Pfuhlmann, Peter Riederer, Alois Saria, Bernd Schoppek, Georgios Schoretsanitis, Markus Schwarz, Margarethe Silva Gracia, Benedikt Stegmann, Werner Steimer, Julia Stingl, Manfred Uhr, S. Ulrich, Stefan Unterecker, R. Waschgler, Gerald Zernig, Gabriela Zurek, Pierre Baumann

    Publicado 2017
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  6. 6
    Consensus Guidelines for Therapeutic Drug Monitoring in Neuropsychopharmacology: Update 2017

    Consensus Guidelines for Therapeutic Drug Monitoring in Neuropsychopharmacology: Update 2017 por Christoph Hiemke, N. Bergemann, H.‐W. Clement, Andreas Conca, Jürgen Deckert, Katharina Domschke, Gabriel Eckermann, Karin Egberts, M. Gerlach, C. Greiner, G. Gründer, Ekkehard Haen, Ursula Havemann‐Reinecke, Gudrun Hefner, Renate Helmer, G. Janßen, Eveline Jaquenoud, Gerd Laux, Thomas Messer, Rainald Mößner, Matthias J. Müller, Michael Paulzen, Bruno Pfuhlmann, Peter Riederer, Alois Saria, Bernd Schoppek, Georgios Schoretsanitis, Markus Schwarz, Margarethe Silva Gracia, Benedikt Stegmann, Werner Steimer, Julia Stingl, M. Uhr, S. Ulrich, Stefan Unterecker, R. Waschgler, Gerald Zernig, G Zurek, Pierre Baumann

    Publicado 2018
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  7. 7
    Genome-wide association studies of binge-eating behaviour and anorexia nervosa yield insights into the unique and shared biology of eating disorder phenotypes

    Genome-wide association studies of binge-eating behaviour and anorexia nervosa yield insights into the unique and shared biology of eating disorder phenotypes por Jet D. Termorshuizen, Helena L. Davies, Sang Hyuck Lee, Jessica Dennis, Christopher Hübel, Jessica Johnson, Yi Lu, Melissa A. Munn‐Chernoff, Triinu Peters, Baiyu Qi, Katherine Schaumberg, Rebecca Signer, Karanvir Singh, Abigail ter Kuile, Laura M. Thornton, Jiayi Xu, Shuyang Yao, Zeynep Yılmaz, Ruyue Zhang, Johan Zvrskovec, Mohamed Abdulkadir, Ziada Ayorech, Elizabeth C. Corfield, Alexandra Havdahl, Kristi Krebs, Taralynn Mack, Maria Niarchou, Teemu Palviainen, Julia Sealock, Jessica H. Baker, Andrew W. Bergen, Andreas Birgegård, Vesna Boraska Perica, Katharina Bühren, Roland Burghardt, Matteo Cassina, Enrico Collantoni, James J. Crowley, Unna N. Danner, Franziska Degenhardt, Janiece DeSocio, Christian Dina, Monika Dmitrzak‐Węglarz, Laramie E. Duncan, Karin Egberts, Lenka Foretová, Ina Giegling, Fragiskos Gonidakis, Scott D. Gordon, Jakob Grove, Sébastien Guillaume, Jerry Guintivano, Annette M. Hartman, Konstantinos Hatzikotoulas, Stefan Herms, Hartmut Imgart, Susana Jiménez‐Múrcia, Antonio Julià, Gursharan Kalsi, Deborah Kaminská, Leila Karhunen, Kirsty Kiezebrink, Theresa Kolb, Janne Tidselbak Larsen, Dong Li, Lisa Lilenfeld, Mario Maj, Morten Mattingsdal, Paolo Meneguzzo, Allison L. Miller, Karen S. Mitchell, Alessio Maria Monteleone, Catherine M. Olsen, Leonid Padyukov, Jacques Pantel, Richard Parker, Dalila Pinto, Anu Raevuori, Samuli Ripatti, Marion Roberts, Paolo Santonastaso, Androula Savva, Ulrike Schmidt, Alexandra Schosser, Jochen Seitz, Lenka Šlachtová, Agnieszka Słopień, Sandro Sorbi, Péter Straub, Jin Szatkiewicz, Friederike I. Tam, Elena Tenconi, Alfonso Tortorella, Άρτεμις Τσίτσικα, Annemarie Elburg, Gudrun Wagner, Hunna J. Watson, Roger A.H. Adan, Lars Alfredsson, Ole A. Andreassen

    Publicado 2025
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  8. 8
    Genome-wide association study of obsessive-compulsive disorder

    Genome-wide association study of obsessive-compulsive disorder por S. Evelyn Stewart, Dongmei Yu, Jeremiah M. Scharf, Benjamin M. Neale, Jesen Fagerness, Carol A. Mathews, Paul Arnold, Patrick Evans, Eric R. Gamazon, Lisa Osiecki, Lauren M. McGrath, Stephen A. Haddad, Jacquelyn Crane, Dianne M. Hezel, C Illman, C Mayerfeld, Anuar Konkashbaev, Chunyu Liu, Anna Pluzhnikov, А. А. Тихомиров, Christopher K. Edlund, Scott L. Rauch, R. Moessner, Peter Falkai, W. Maier, Stephan Ruhrmann, HJ Grabe, Leonhard Lennertz, Michael Wagner, Laura Bellodi, Maria Cristina Cavallini, Margaret A. Richter, Edwin H. Cook, James L. Kennedy, David Rosenberg, Dan J. Stein, Sian Hemmings, Christine Löchner, Amin Azzam, Denise A. Chavira, Eduardo Fournier, Helena Garrido, Brooke Sheppard, Paula Umaña, Dennis L. Murphy, Jens R. Wendland, Jeremy Veenstra‐VanderWeele, Damiaan Denys, Rianne M. Blom, Dieter Deforce, Filip Van Nieuwerburgh, H.G.M. Westenberg, Susanne Walitza, Karin Egberts, Tobias Renner, Eurípedes C. Miguel, Carolina Cappi, Ana Gabriela Hounie, Maria Conceição do Rosário, Aline S. Sampaio, Homero Vallada, Humberto Nicolini, Nuria Lanzagorta, Beatríz Camarena, Richard Delorme, Marion Leboyer, Carlos N. Pato, Michele T. Pato, Emanuel Voyiaziakis, Peter Heutink, Daniëlle C. Cath, Daniëlle Posthuma, Johannes H. Smit, Jack Samuels, O. Joseph Bienvenu, Bernadette Cullen, Abby J. Fyer, Marco A. Grados, Benjamin D. Greenberg, James T. McCracken, Mark A. Riddle, Ying Wang, Vladimir Coric, James F. Leckman, Michael H. Bloch, Christopher Pittenger, Valsamma Eapen, Donald W. Black, Roel A. Ophoff, E Strengman, Daniele Cusi, Maurizio Turiel, Francesca Frau, Fabìo Macciardi, J. Raphael Gibbs, Mark Cookson, Andrew Singleton, Sampath Arepalli, Mark Cookson, Allissa Dillman

    Publicado 2012
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  9. 9
    A genome-wide association study of anorexia nervosa

    A genome-wide association study of anorexia nervosa por Vesna Boraska Perica, Christopher S. Franklin, J A B Floyd, Laura M. Thornton, Laura M. Huckins, Lorraine Southam, Nigel W. Rayner, Ioanna Tachmazidou, Kelly L. Klump, Janet Treasure, Cathryn M. Lewis, Ulrike Schmidt, Federica Tozzi, Kirsty Kiezebrink, Johannes Hebebrand, Philip Gorwood, R A H Adan, Martien J. Kas, Angela Favaro, Paolo Santonastaso, Fernando Fernández‐Aranda, Mónica Gratacòs, Filip Rybakowski, Monika Dmitrzak‐Węglarz, Jaakko Kaprio, Anna Keski‐Rahkonen, Anu Raevuori, Eric F. van Furth, M Landt, James I. Hudson, Ted Reichborn‐Kjennerud, G P S Knudsen, Palmiero Monteleone, A S Kaplan, Andreas Karwautz, Hákon Hákonarson, Wade H. Berrettini, Yirin Guo, D Li, Nicholas J. Schork, Gen Komaki, Tetsuya Ando, Hidetoshi Inoko, Tõnu Esko, Krista Fischer, Katrin Männik, Andres Metspalu, Jessica H. Baker, Roger D. Cone, Jennifer Dackor, Janiece E. DeSocio, Christopher Hilliard, Julie K. O’Toole, Jacques Pantel, Jin P. Szatkiewicz, Chrysecolla Taico, Stephanie Zerwas, Sara E. Trace, Oliver S. P. Davis, Sietske G. Helder, Katharina Bühren, Roland Burghardt, Martina de Zwaan, Karin Egberts, Stefan Ehrlich, B Herpertz‐Dahlmann, Wolfgang Herzog, Hartmut Imgart, André Scherag, Susann Scherag, Stephan Zipfel, Claudette Boni, Nicolás Ramoz, Audrey Versini, Marek K. Brandys, Unna N. Danner, Carolien G. F. de Kovel, Judith Hendriks, Bobby P.C. Koeleman, Roel A. Ophoff, E Strengman, Annemarie Elburg, Alice Bruson, Massimo Clementi, Daniela Degortes, Monica Forzan, Elena Tenconi, Elisa Docampo, Geòrgia Escaramís, Susana Jiménez‐Múrcia, Jolanta Lissowska, Andrzej Rajewski, Neonila Szeszenia‐Dąbrowska, Agnieszka Slopien, Joanna Hauser, Leila Karhunen, Ingrid Meulenbelt, P. Eline Slagboom, Alfonso Tortorella, Mario Maj

    Publicado 2014
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  10. 10
    Cross-Disorder Genome-Wide Analyses Suggest a Complex Genetic Relationship Between Tourette’s Syndrome and OCD

    Cross-Disorder Genome-Wide Analyses Suggest a Complex Genetic Relationship Between Tourette’s Syndrome and OCD por Dongmei Yu, Carol A. Mathews, Jeremiah M. Scharf, Benjamin M. Neale, Lea K. Davis, Eric R. Gamazon, Eske M. Derks, Patrick Evans, Christopher K. Edlund, Jacquelyn Crane, Jesen Fagerness, Lisa Osiecki, Patience Gallagher, Gloria F. Gerber, Stephen A. Haddad, Cornelia Illmann, Lauren M. McGrath, C Mayerfeld, Sampath Arepalli, Cristina Barlassina, Cathy L. Barr, Laura Bellodi, Fortu Benarroch, Gabriel Bedoya Berrío, O. Joseph Bienvenu, Donald W. Black, Michael H. Bloch, Helena Brentani, Ruth D. Bruun, Cathy L. Budman, Beatríz Camarena, Desmond Campbell, Carolina Cappi, Julio César Cardona Silgado, Maria Cristina Cavallini, Denise A. Chavira, Sylvain Chouinard, Edwin H. Cook, Mark Cookson, Vladimir Coric, Bernadette Cullen, Daniele Cusi, Richard Delorme, Damiaan Denys, Yves Dion, Valsamma Eapen, Karin Egberts, Peter Falkai, Thomas Fernandez, Eduardo Fournier, Helena Garrido, Daniel Geller, Donald L. Gilbert, Simon Girard, Hans J. Grabe, Marco A. Grados, Benjamin D. Greenberg, Varda Gross‐Tsur, Edna Grünblatt, John Hardy, Gary A. Heiman, Sian Hemmings, Luis Diego Herrera, Dianne M. Hezel, Pieter J. Hoekstra, Joseph Jankovic, James L. Kennedy, Robert A. King, Anuar Konkashbaev, Bárbara Kremeyer, Roger Kurlan, Nuria Lanzagorta, Marion Leboyer, James F. Leckman, Leonhard Lennertz, Chunyu Liu, Christine Löchner, Thomas L. Lowe, Sara Lupoli, Fabìo Macciardi, Wolfgang Maier, Paolo Manunta, Maurizio Marconi, James T. McCracken, Sandra Catalina Mesa Restrepo, Rainald Moessner, Priya Moorjani, Jubel Morgan, Heike Müller, Dennis L. Murphy, Allan L. Naarden, Erika L. Nurmi, William Cornejo Ochoa, Roel A. Ophoff, A.J. Pakstis, Michele T. Pato, Carlos N. Pato, John Piacentini, Christopher Pittenger, Yehuda Pollak

    Publicado 2014
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  11. 11
    Evidence for three genetic loci involved in both anorexia nervosa risk and variation of body mass index

    Evidence for three genetic loci involved in both anorexia nervosa risk and variation of body mass index por Anke Hinney, Miriam Kesselmeier, Sigrid Jall, A-L Volckmar, Manuel Föcker, Jochen Antel, Vesna Boraska Perica, C. Franklin, James Floyd, Laura M. Thornton, Laura M. Huckins, Lorraine Southam, N. William Rayner, Ioanna Tachmazidou, Kelly L. Klump, Janet Treasure, Cathryn M. Lewis, Ulrike Schmidt, Federica Tozzi, Kirsty iezebrink, Johannes Hebebrand, Philip Gorwood, Roger A.H. Adan, Martien J. Kas, Angela Favaro, Paolo Santonastaso, Fernando Fernández‐Aranda, Mónica Gratacòs, Filip Rybakowski, Monika Dmitrzak‐Węglarz, Jaakko Kaprio, Anna Keski‐Rahkonen, Anu Raevuori, Eric F. van Furth, M Landt, James I. Hudson, Ted Reichborn‐Kjennerud, Gun Peggy Knudsen, Palmiero Monteleone, Allan S. Kaplan, Andreas Karwautz, Hákon Hákonarson, Wade H. Berrettini, Yiran Guo, Dong Li, Nicholas J. Schork, Gen Komaki, Tetsuya Ando, Hidetoshi Inoko, Tõnu Esko, Krista Fischer, Katrin Männik, Andres Metspalu, Jessica H. Baker, Roger D. Cone, Jennifer Dackor, Janiece E. DeSocio, Christopher Hilliard, Julie K. O’Toole, Jacques Pantel, Jin P. Szatkiewicz, Chrysecolla Taico, Stephanie Zerwas, Sara E. Trace, Oliver S. P. Davis, Sietske G. Helder, Katharina Bühren, Roland Burghardt, Martina de Zwaan, Karin Egberts, Stefan Ehrlich, Beate Herpertz‐Dahlmann, Wolfgang Herzog, Hartmut Imgart, André Scherag, Susann Scherag, Stephan Zipfel, Claudette Boni, Nicolás Ramoz, Audrey Versini, Marek K. Brandys, Unna N. Danner, Carolien de Kove, Judith Hendriks, Bobby P.C. Koeleman, Roel A. Ophoff, Eric Strengman, Annemarie Elburg, Alice Bruson, Maurizio Clementi, Daniela Degortes, Monica Forzan, Elena Tenconi, Elisa Docampo, Geòrgia Escaramí, Susana Jiménez‐Múrcia, Jolanta Lissowska, Andrzej Rajewski, Neonila Szeszenia‐Dąbrowska, Agnieszka Slopien

    Publicado 2016
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  12. 12
    Significant Locus and Metabolic Genetic Correlations Revealed in Genome-Wide Association Study of Anorexia Nervosa

    Significant Locus and Metabolic Genetic Correlations Revealed in Genome-Wide Association Study of Anorexia Nervosa por Laramie Duncan, Zeynep Yılmaz, Helena Gaspar, Raymond K. Walters, Jackie Goldstein, Verneri Anttila, Brendan Bulik‐Sullivan, Stephan Ripke, Laura Thornton, Anke Hinney, Mark J. Daly, Patrick F. Sullivan, Eleftheria Zeggini, Gerome Breen, Cynthia M. Bulik, Laramie Duncan, Zeynep Yılmaz, Héléna A. Gaspar, Raymond K. Walters, Jackie Goldstein, Verneri Anttila, Brendan Bulik‐Sullivan, Stephan Ripke, Roger A.H. Adan, Lars Alfredsson, Tetsuya Ando, Ole A. Andreassen, H.N. Aschauer, Jessica H. Baker, Jeffrey C. Barrett, Vladimír Bencko, Andrew W. Bergen, Wade Berrettini, Andreas Birgegård, Claudette Boni, Vesna Boraska Perica, Harry Brandt, Roland Burghardt, Laura Carlberg, Matteo Cassina, Carolyn E. Cesta, Sven Cichon, Maurizio Clementi, Sarah Cohen‐Woods, Jonathan R. I. Coleman, Roger D. Cone, Philippe Courtet, Steven Crawford, Scott J. Crow, James L. Crowley, Unna N. Danner, Oliver S. P. Davis, Martina de Zwaan, George Dedoussis, Daniela Degortes, Janiece E. DeSocio, Danielle M. Dick, Dimitris Dikeos, Christian Dina, Bo Ding, Monika Dmitrzak‐Węglarz, Elisa Docampo, Karin Egberts, Stefan Ehrlich, Geòrgia Escaramís, Tõnu Esko, Thomas Espeseth, Xavier Estivill, Angela Favaro, Fernando Fernández‐Aranda, Manfred Fichter, Chris Finan, Krista Fischer, James Floyd, Manuel Föcker, Lenka Foretová, Monica Forzan, Caroline S. Fox, C. Franklin, Valérie Gaborieau, Steven Gallinger, Giovanni Gambaro, Ina Giegling, Fragiskos Gonidakis, Philip Gorwood, Mónica Gratacòs, Sébastien Guillaume, Yiran Guo, Hakon Hakonarson, Katherine A. Halmi, Rebecca Harrison, Konstantinos Hatzikotoulas, Joanna Hauser, Johannes Hebebrand, Sietske G. Helder, Judith Hendriks, Stefan Herms, Beate Herpertz‐Dahlmann, Wolfgang Herzog, Christopher Hilliard

    Publicado 2017
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  13. 13
    Associations Between Attention-Deficit/Hyperactivity Disorder and Various Eating Disorders: A Swedish Nationwide Population Study Using Multiple Genetically Informative Approaches

    Associations Between Attention-Deficit/Hyperactivity Disorder and Various Eating Disorders: A Swedish Nationwide Population Study Using Multiple Genetically Informative Approaches por Shuyang Yao, Ralf Kuja‐Halkola, Joanna Martin, Yi Lu, Paul Lichtenstein, Claes Norring, Andreas Birgegård, Zeynep Yılmaz, Christopher Hübel, Hunna J. Watson, Jessica Baker, Catarina Almqvist, Laura M. Thornton, Patrik K. E. Magnusson, Cynthia M. Bulik, Henrik Larsson, Roger A.H. Adan, Tetsuya Ando, Jessica Baker, Andrew W. Bergen, Wade Berrettini, Andreas Birgegård, Claudette Boni, Vesna Boraska Perica, Harry Brandt, Roland Burghardt, Matteo Cassina, Carolyn E. Cesta, Maurizio Clementi, Jonathan R. I. Coleman, Roger D. Cone, Philippe Courtet, Steven Crawford, Scott J. Crow, James Crowley, Unna N. Danner, Oliver S. P. Davis, Martina de Zwaan, George Dedoussis, Daniela Degortes, Janiece E. DeSocio, Danielle M. Dick, Dimitris Dikeos, Monika Dmitrzak‐Węglarz, Elisa Docampo, Karin Egberts, Stefan Ehrlich, Geòrgia Escaramís, Tõnu Esko, Xavier Estivill, Angela Favaro, Fernando Fernández‐Aranda, Manfred Fichter, Chris Finan, Krista Fischer, Manuel Föcker, Lenka Foretová, Monica Forzan, C. Franklin, Héléna A. Gaspar, Fragiskos Gonidakis, Philip Gorwood, Mónica Gratacòs, Sébastien Guillaume, Yiran Guo, Hakon Hakonarson, Katherine A. Halmi, Konstantinos Hatzikotoulas, Joanna Hauser, Johannes Hebebrand, Sietske G. Helder, Judith Hendriks, Beate Herpertz‐Dahlmann, Wolfgang Herzog, Christopher Hilliard, Anke Hinney, Laura M. Huckins, James I. Hudson, Julia Huemer, Hartmut Imgart, Hidetoshi Inoko, Susana Jiménez‐Múrcia, Craig Johnson, Jennifer Jordan, Anders Juréus, Gursharan Kalsi, Debora Kaminska, Allan S. Kaplan, Jaakko Kaprio, Leila Karhunen, Andreas Karwautz, Martien J. Kas, Walter H. Kaye, James L. Kennedy, Martin A. Kennedy, Anna Keski‐Rahkonen, Kirsty Kiezebrink, Youl‐Ri Kim, Kelly L. Klump, Gun Peggy Knudsen

    Publicado 2019
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  14. 14
    Genome-wide association study identifies eight risk loci and implicates metabo-psychiatric origins for anorexia nervosa

    Genome-wide association study identifies eight risk loci and implicates metabo-psychiatric origins for anorexia nervosa por Hunna J. Watson, Zeynep Yılmaz, Laura M. Thornton, Christopher Hübel, Jonathan R. I. Coleman, Héléna A. Gaspar, Julien Bryois, Anke Hinney, Virpi Leppä, Manuel Mattheisen, Sarah E. Medland, Stephan Ripke, Shuyang Yao, Paola Giusti‐Rodríguez, Ken B. Hanscombe, Kirstin L. Purves, Roger A.H. Adan, Lars Alfredsson, Tetsuya Ando, Ole A. Andreassen, Jessica H. Baker, Wade H. Berrettini, Ilka Boehm, Claudette Boni, Vesna Boraska Perica, Katharina Buehren, Roland Burghardt, Matteo Cassina, Sven Cichon, Maurizio Clementi, Roger D. Cone, Philippe Courtet, Scott J. Crow, James J. Crowley, Unna N. Danner, Oliver S. P. Davis, Martina de Zwaan, George Dedoussis, Daniela Degortes, Janiece E. DeSocio, Danielle M. Dick, Dimitris Dikeos, Christian Dina, Monika Dmitrzak‐Węglarz, Elisa Docampo, Laramie E. Duncan, Karin Egberts, Stefan Ehrlich, Geòrgia Escaramís, Tõnu Esko, Xavier Estivill, Anne Farmer, Angela Favaro, Fernando Fernández‐Aranda, Manfred M. Fichter, Krista Fischer, Manuel Föcker, Lenka Foretová, Andreas J. Forstner, Monica Forzan, Christopher S. Franklin, Steven Gallinger, Ina Giegling, Johanna Giuranna, Fragiskos Gonidakis, Philip Gorwood, Monica Gratacos Mayora, Sébastien Guillaume, Yiran Guo, Hákon Hákonarson, Konstantinos Hatzikotoulas, Joanna Hauser, Johannes Hebebrand, Sietske G. Helder, Stefan Herms, Beate Herpertz‐Dahlmann, Wolfgang Herzog, Laura M. Huckins, James I. Hudson, Hartmut Imgart, Hidetoshi Inoko, Vladimí­r Janout, Susana Jiménez‐Múrcia, Antonio Julià, Gursharan Kalsi, Deborah Kaminská, Jaakko Kaprio, Leila Karhunen, Andreas Karwautz, Martien J. Kas, James L. Kennedy, Anna Keski‐Rahkonen, Kirsty Kiezebrink, Youl‐Ri Kim, Lars Klareskog, Kelly L. Klump, Gun Peggy Knudsen, Maria C. La Via, Stéphanie Le Hellard, Robert D. Levitan

    Publicado 2019
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  15. 15
    Genetic identification of cell types underlying brain complex traits yields insights into the etiology of Parkinson’s disease

    Genetic identification of cell types underlying brain complex traits yields insights into the etiology of Parkinson’s disease por Julien Bryois, Nathan Skene, Thomas Hansen, Lisette J. A. Kogelman, Hunna J. Watson, Zijing Liu, Roger A.H. Adan, Lars Alfredsson, Tetsuya Ando, Ole A. Andreassen, Jessica H. Baker, Andrew W. Bergen, Wade H. Berrettini, Andreas Birgegård, Joseph M. Boden, Ilka Boehm, Claudette Boni, Vesna Boraska Perica, Harry Brandt, Gerome Breen, Julien Bryois, Katharina Buehren, Cynthia M. Bulik, Roland Burghardt, Matteo Cassina, Sven Cichon, Maurizio Clementi, Jonathan R. I. Coleman, Roger D. Cone, Philippe Courtet, Steven Crawford, Scott J. Crow, James L. Crowley, Unna N. Danner, Oliver S. P. Davis, Martina de Zwaan, George Dedoussis, Daniela Degortes, Janiece E. DeSocio, Danielle M. Dick, Dimitris Dikeos, Christian Dina, Monika Dmitrzak‐Węglarz, Elisa Docampo Martínez, Laramie E. Duncan, Karin Egberts, Stefan Ehrlich, Geòrgia Escaramís, Tõnu Esko, Xavier Estivill, Anne Farmer, Angela Favaro, Fernando Fernández‐Aranda, Manfred Fichter, Krista Fischer, Manuel Föcker, Lenka Foretová, Andreas J. Forstner, Monica Forzan, C. Franklin, Steven Gallinger, Héléna A. Gaspar, Ina Giegling, Johanna Giuranna, Paola Giusti-Rodríquez, Fragiskos Gonidakis, Scott D. Gordon, Philip Gorwood, Monica Gratacos Mayora, Jakob Grove, Sébastien Guillaume, Yiran Guo, Hákon Hákonarson, Katherine A. Halmi, Ken B. Hanscombe, Konstantinos Hatzikotoulas, Joanna Hauser, Johannes Hebebrand, Sietske G. Helder, Anjali K. Henders, Stefan Herms, Beate Herpertz‐Dahlmann, Wolfgang Herzog, Anke Hinney, L. John Horwood, Christopher Hübel, Laura M. Huckins, James I. Hudson, Hartmut Imgart, Hidetoshi Inoko, Vladimí­r Janout, Susana Jiménez‐Múrcia, Craig Johnson, Jennifer Jordan, Antonio Julià, Anders Juréus, Gursharan Kalsi, Deborah Kaminská, Allan S. Kaplan, Jaakko Kaprio

    Publicado 2020
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  16. 16
    Partitioning the Heritability of Tourette Syndrome and Obsessive Compulsive Disorder Reveals Differences in Genetic Architecture

    Partitioning the Heritability of Tourette Syndrome and Obsessive Compulsive Disorder Reveals Differences in Genetic Architecture por Lea K. Davis, Dongmei Yu, Clare L. Keenan, Eric R. Gamazon, Anuar Konkashbaev, Eske M. Derks, Benjamin M. Neale, Jian Yang, Sang Lee, Patrick Evans, Cathy L. Barr, Laura Bellodi, Fortu Benarroch, Gabriel Bedoya Berrío, O. Joseph Bienvenu, Michael H. Bloch, Rianne M. Blom, Ruth D. Bruun, Cathy L. Budman, Beatríz Camarena, Desmond Campbell, Carolina Cappi, Julio César Cardona Silgado, Daniëlle C. Cath, Maria Cristina Cavallini, Denise A. Chavira, Sylvain Chouinard, David V. Conti, Edwin H. Cook, Vladimir Coric, Bernadette Cullen, Dieter Deforce, Richard Delorme, Yves Dion, Christopher K. Edlund, Karin Egberts, Peter Falkai, Thomas Fernandez, Patience Gallagher, Helena Garrido, Daniel Geller, Simon Girard, Hans J. Grabe, Marco A. Grados, Benjamin D. Greenberg, Varda Gross‐Tsur, Stephen A. Haddad, Gary A. Heiman, Sian Hemmings, Ana Gabriela Hounie, Cornelia Illmann, Joseph Jankovic, Michael A. Jenike, James L. Kennedy, Robert A. King, Bárbara Kremeyer, Roger Kurlan, Nuria Lanzagorta, Marion Leboyer, James F. Leckman, Leonhard Lennertz, Chunyu Liu, Christine Löchner, Thomas L. Lowe, Fabìo Macciardi, James T. McCracken, Lauren M. McGrath, Sandra Catalina Mesa Restrepo, Rainald Moessner, Jubel Morgan, Heike Müller, Dennis L. Murphy, Allan L. Naarden, William Cornejo Ochoa, Roel A. Ophoff, Lisa Osiecki, A.J. Pakstis, Michele T. Pato, Carlos N. Pato, John Piacentini, Christopher Pittenger, Yehuda Pollak, Scott L. Rauch, Tobias Renner, Victor I. Reus, Margaret A. Richter, Mark A. Riddle, Mary M. Robertson, Roxana Romero, Maria Conceição do Rosário, David Rosenberg, Guy A. Rouleau, Stephan Ruhrmann, Andrés Ruiz‐Linares, Aline S. Sampaio, Jack Samuels, Paul Sandor, Brooke Sheppard, Harvey S. Singer, Jan Smit

    Publicado 2013
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  17. 17
    Shared genetic risk between eating disorder‐ and substance‐use‐related phenotypes: Evidence from genome‐wide association studies

    Shared genetic risk between eating disorder‐ and substance‐use‐related phenotypes: Evidence from genome‐wide association studies por Melissa A. Munn‐Chernoff, Emma C. Johnson, Yi‐Ling Chou, Jonathan R. I. Coleman, Laura M. Thornton, Raymond K. Walters, Zeynep Yılmaz, Jessica H. Baker, Christopher Hübel, Scott D. Gordon, Sarah E. Medland, Hunna J. Watson, Héléna A. Gaspar, Julien Bryois, Anke Hinney, Virpi Leppä, Manuel Mattheisen, Stephan Ripke, Shuyang Yao, Paola Giusti‐Rodríguez, Ken B. Hanscombe, Roger A.H. Adan, Lars Alfredsson, Tetsuya Ando, Ole A. Andreassen, Wade H. Berrettini, Ilka Boehm, Claudette Boni, Vesna Boraska Perica, Katharina Buehren, Roland Burghardt, Matteo Cassina, Sven Cichon, Maurizio Clementi, Roger D. Cone, Philippe Courtet, Scott J. Crow, James J. Crowley, Unna N. Danner, Oliver S. P. Davis, Martina de Zwaan, George Dedoussis, Daniela Degortes, Janiece E. DeSocio, Danielle M. Dick, Dimitris Dikeos, Christian Dina, Monika Dmitrzak‐Węglarz, Elisa Docampo, Laramie E. Duncan, Karin Egberts, Stefan Ehrlich, Geòrgia Escaramís, Tõnu Esko, Xavier Estivill, Anne Farmer, Angela Favaro, Fernando Fernández‐Aranda, Manfred M. Fichter, Krista Fischer, Manuel Föcker, Lenka Foretová, Andreas J. Forstner, Monica Forzan, Christopher S. Franklin, Steven Gallinger, Ina Giegling, Johanna Giuranna, Fragiskos Gonidakis, Philip Gorwood, Monica Gratacos Mayora, Sébastien Guillaume, Yiran Guo, Hákon Hákonarson, Konstantinos Hatzikotoulas, Joanna Hauser, Johannes Hebebrand, Sietske G. Helder, Stefan Herms, Beate Herpertz‐Dahlmann, Wolfgang Herzog, Laura M. Huckins, James I. Hudson, Hartmut Imgart, Hidetoshi Inoko, Vladimí­r Janout, Susana Jiménez‐Múrcia, Antonio Julià, Gursharan Kalsi, Deborah Kaminská, Leila Karhunen, Andreas Karwautz, Martien J. Kas, James L. Kennedy, Anna Keski‐Rahkonen, Kirsty Kiezebrink, Youl‐Ri Kim, Kelly L. Klump, Gun Peggy Knudsen, Maria C. La Via

    Publicado 2020
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