Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Karin Dellenvall"'
Autor:
Gun Karlsson, Christina M. Hultman, Lambertus Klei, Bernie Devlin, Jennifer Reichert, Sven Sandin, Dorothy E. Grice, Joseph D. Buxbaum, Aki Tuuliainen, Christina Gustavsson Mahjani, Silvia De Rubeis, Anna-Carin Säll Grahnat, Karin Dellenvall, Behrang Mahjani, Abraham Reichenberg
Publikováno v:
Social psychiatry and psychiatric epidemiology. 55(10)
The EGOS study (Epidemiology and Genetics of Obsessive–compulsive disorder and chronic tic disorders in Sweden) is a large-scale, epidemiological, prospective cohort that is used to identify genetic and environmental risk factors in the etiology of
Autor:
Julian Maller, Patrick Turley, Benjamin M. Neale, Terje Nærland, Bettella F, Elise B. Robinson, Manuel Mattheisen, A. Palotie, Evald Saemundsen, Jennifer L. Moran, Stacy Steinberg, Hong-Hee Won, E. Agerbo, Daniel P. Howrigan, Mark J. Daly, Srdjan Djurovic, St Pourcain B, Richard Anney, Jacqueline I. Goldstein, Marianne Giørtz Pedersen, Jennifer Reichert, A. Reichenberg, Kimberly Chambert, Bernie Devlin, Felecia Cerrato, Joanna Martin, Satterstrom Fk, Kathryn Roeder, Richard A. Belliveau, Stephan Ripke, De Rubeis S, Robin G. Walters, Hailiang Huang, Mette Nyegaard, Walters Gb, Jakob Grove, Ditte Demontis, Karola Rehnström, David M. Hougaard, Ole Mors, Sigrun Hope, Preben Bo Mortensen, Mads V. Hollegaard, Joseph D. Buxbaum, Sven Sandin, Cathy A. Stevens, Ole A. Andreassen, Duncan Palmer, Jesper Buchhave Poulsen, Carsten Bøcker Pedersen, Patrick F. Sullivan, Thomas Werge, Jane H. Christensen, Christine Søholm Hansen, Timothy Poterba, Jonatan Pallesen, Claire Churchhouse, Thomas Damm Als, Mads E. Hauberg, Anders D. Børglum, Jonas Bybjerg-Grauholm, Lambertus Klei, Kari Stefansson, Alicia R. Martin, Per Qvist, Ashley Dumont, Hreinn Stefansson, Panagiotis Roussos, Karin Dellenvall, George Davey Smith, Daniel H. Geschwind, Marie Bækved-Hansen, Merete Nordentoft, Christina M. Hultman, Xinyi Xu
Autism spectrum disorder (ASD) is a highly heritable and heterogeneous group of neurodevelopmental phenotypes diagnosed in more than 1% of children. Common genetic variants contribute substantially to ASD susceptibility, but to date no individual var
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9cd088a09a257b1d7781a34c29d98972
https://doi.org/10.1101/224774
https://doi.org/10.1101/224774