Hypothesis-driven genome-wide association studies provide novel insights into genetics of reading disabilities

Kaitlyn M. Price, Karen G. Wigg, Else Eising, Yu Feng, Kirsten Blokland, Margaret Wilkinson, Elizabeth N. Kerr, Sharon L. Guger, Filippo Abbondanza, Andrea G. Allegrini, Till F.M. Andlauer, Timothy C. Bates, Manon Bernard, Milene Bonte, Dorret I. Boomsma, Thomas Bourgeron, Daniel Brandeis, Manuel Carreiras, Fabiola Ceroni, Valéria CsépePhilip S. Dale, John C. DeFries, Peter F. de Jong, Jean Francois Démonet, Eveline L. de Zeeuw, Marie Christine J. Franken, Clyde Francks, Margot Gerritse, Alessandro Gialluisi, Scott D. Gordon, Jeffrey R. Gruen, Marianna E. Hayiou-Thomas, Juan Hernández-Cabrera, Jouke Jan Hottenga, Charles Hulme, Philip R. Jansen, Juha Kere, Tanner Koomar, Karin Landerl, Gabriel T. Leonard, Zhijie Liao, Michelle Luciano, Heikki Lyytinen, Nicholas G. Martin, Angela Martinelli, Urs Maurer, Jacob J. Michaelson, Nazanin Mirza-Schreiber, Kristina Moll, Kaili Rimfeld

Research output: Contribution to journalArticlepeer-review

Original languageEnglish
Article number495
JournalTranslational Psychiatry
Volume12
Issue number1
Early online date29 Nov 2022
DOIs
Publication statusE-pub ahead of print - 29 Nov 2022

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