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Eising, Else, Mirza-Schreiber, Nazanin, de Zeeuw, Eveline L, Wang, Carol A, Truong, Dongnhu T, Allegrini, Andrea G, Shapland, Chin Yang, Zhu, Gu, Wigg, Karen G, Gerritse, Margot L et al (show 85 more authors) , Molz, Barbara, Alagöz, Gökberk, Gialluisi, Alessandro, Abbondanza, Filippo, Rimfeld, Kaili, van Donkelaar, Marjolein, Liao, Zhijie, Jansen, Philip R, Andlauer, Till FM, Bates, Timothy C, Bernard, Manon, Blokland, Kirsten, Bonte, Milene, Børglum, Anders D, Bourgeron, Thomas, Brandeis, Daniel, Ceroni, Fabiola, Csépe, Valéria, Dale, Philip S, de Jong, Peter F, DeFries, John C, Démonet, Jean-François, Demontis, Ditte, Feng, Yu, Gordon, Scott D, Guger, Sharon L, Hayiou-Thomas, Marianna E, Hernández-Cabrera, Juan A, Hottenga, Jouke-Jan, Hulme, Charles, Kere, Juha, Kerr, Elizabeth N, Koomar, Tanner, Landerl, Karin, Leonard, Gabriel T, Lovett, Maureen W, Lyytinen, Heikki, Martin, Nicholas G, Martinelli, Angela, Maurer, Urs, Michaelson, Jacob J, Moll, Kristina, Monaco, Anthony P, Morgan, Angela T, Nöthen, Markus M, Pausova, Zdenka, Pennell, Craig E, Pennington, Bruce F, Price, Kaitlyn M, Rajagopal, Veera M, Ramus, Franck, Richer, Louis, Simpson, Nuala H, Smith, Shelley D, Snowling, Margaret J, Stein, John, Strug, Lisa J, Talcott, Joel B, Tiemeier, Henning, van der Schroeff, Marc P, Verhoef, Ellen, Watkins, Kate E, Wilkinson, Margaret, Wright, Margaret J, Barr, Cathy L, Boomsma, Dorret I, Carreiras, Manuel, Franken, Marie-Christine J, Gruen, Jeffrey R, Luciano, Michelle, Müller-Myhsok, Bertram ORCID: 0000-0002-0719-101X, Newbury, Dianne F, Olson, Richard K, Paracchini, Silvia, Paus, Tomáš, Plomin, Robert, Reilly, Sheena, Schulte-Körne, Gerd, Tomblin, J Bruce, van Bergen, Elsje, Whitehouse, Andrew JO, Willcutt, Erik G, St Pourcain, Beate, Francks, Clyde and Fisher, Simon E (2022) Genome-wide analyses of individual differences in quantitatively assessed reading- and language-related skills in up to 34,000 people. Proceedings of the National Academy of Sciences of the United States of America, 119 (35). e2202764119-e2202764119.

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Gialluisi, Alessandro, Andlauer, Till FM, Mirza-Schreiber, Nazanin, Moll, Kristina, Becker, Jessica, Hoffmann, Per, Ludwig, Kerstin U, Czamara, Darina, St Pourcain, Beate, Brandler, William et al (show 35 more authors) , Honbolygo, Ferenc, Toth, Denes, Csepe, Valeria, Huguet, Guillaume, Morris, Andrew P, Hulslander, Jacqueline, Willcutt, Erik G, DeFries, John C, Olson, Richard K, Smith, Shelley D, Pennington, Bruce F, Vaessen, Anniek, Maurer, Urs, Lyytinen, Heikki, Peyrard-Janvid, Myriam, Leppanen, Paavo HT, Brandeis, Daniel, Bonte, Milene, Stein, John F, Talcott, Joel B, Fauchereau, Fabien, Wilcke, Arndt, Francks, Clyde, Bourgeron, Thomas, Monaco, Anthony P, Ramus, Franck, Landerl, Karin, Kere, Juha, Scerri, Thomas S, Paracchini, Silvia, Fisher, Simon E, Schumacher, Johannes, Noethen, Markus M, Mueller-Myhsok, Bertram ORCID: 0000-0002-0719-101X and Schulte-Koerne, Gerd (2019) Genome-wide association scan identifies new variants associated with a cognitive predictor of dyslexia. TRANSLATIONAL PSYCHIATRY, 9 (1). 77-.

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Gialluisi, Alessandro, Andlauer, Till FM, Mirza-Schreiber, Nazanin, Moll, Kristina, Becker, Jessica, Hoffmann, Per, Ludwig, Kerstin U, Czamara, Darina, St Pourcain, Beate, Honbolygo, Ferenc et al (show 39 more authors) , Toth, Denes, Csepe, Valeria, Huguet, Guillaume, Chaix, Yves, Iannuzzi, Stephanie, Demonet, Jean-Francois, Morris, Andrew P, Hulslander, Jacqueline, Willcutt, Erik G, DeFries, John C, Olson, Richard K, Smith, Shelley D, Pennington, Bruce F, Vaessen, Anniek, Maurer, Urs, Lyytinen, Heikki, Peyrard-Janvid, Myriam, Leppanen, Paavo HT, Brandeis, Daniel, Bonte, Milene, Stein, John F, Talcott, Joel B, Fauchereau, Fabien, Wilcke, Arndt, Kirsten, Holger, Mueller, Bent, Francks, Clyde, Bourgeron, Thomas, Monaco, Anthony P, Ramus, Franck, Landerl, Karin, Kere, Juha, Scerri, Thomas S, Paracchini, Silvia, Fisher, Simon E, Schumacher, Johannes, Noethen, Markus M, Mueller-Myhsok, Bertram ORCID: 0000-0002-0719-101X and Schulte-Koerne, Gerd (2021) Genome-wide association study reveals new insights into the heritability and genetic correlates of developmental dyslexia. MOLECULAR PSYCHIATRY, 26 (7). pp. 3004-3017.

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Price, Kaitlyn M, Wigg, Karen G, Eising, Else, Feng, Yu, Blokland, Kirsten, Wilkinson, Margaret, Kerr, Elizabeth N, Guger, Sharon L, Abbondanza, Filippo, Allegrini, Andrea G et al (show 80 more authors) , Andlauer, Till FM, Bates, Timothy C, Bernard, Manon, Bonte, Milene, Boomsma, Dorret I, Bourgeron, Thomas, Brandeis, Daniel, Carreiras, Manuel, Ceroni, Fabiola, Csepe, Valeria, Dale, Philip S, DeFries, John C, de Jong, Peter F, Demonet, Jean Francois, de Zeeuw, Eveline L, Franken, Marie-Christine J, Francks, Clyde, Gerritse, Margot, Gialluisi, Alessandro, Gordon, Scott D, Gruen, Jeffrey R, Hayiou-Thomas, Marianna E, Hernandez-Cabrera, Juan, Hottenga, Jouke-Jan, Hulme, Charles, Jansen, Philip R, Kere, Juha, Koomar, Tanner, Landerl, Karin, Leonard, Gabriel T, Liao, Zhijie, Luciano, Michelle, Lyytinen, Heikki, Martin, Nicholas G, Martinelli, Angela, Maurer, Urs, Michaelson, Jacob J, Mirza-Schreiber, Nazanin, Moll, Kristina, Monaco, Anthony P, Morgan, Angela T, Mueller-Myhsok, Bertram ORCID: 0000-0002-0719-101X, Newbury, Dianne F, Noethen, Markus M, Olson, Richard K, Paracchini, Silvia, Paus, Tomas, Pausova, Zdenka, Pennell, Craig E, Pennington, Bruce F, Plomin, Robert J, Ramus, Franck, Reilly, Sheena, Richer, Louis, Rimfeld, Kaili, Schulte-Korne, Gerd, Shapland, Chin Yang, Simpson, Nuala H, Smith, Shelley D, Snowling, Margaret J, St Pourcain, Beate, Stein, John F, Talcott, Joel B, Tiemeier, Henning, Tomblin, J Bruce, Truong, Dongnhu T, van Bergen, Elsje, van der Schroeff, Marc P, Van Donkelaar, Marjolein, Verhoef, Ellen, Wang, Carol A, Watkins, Kate E, Whitehouse, Andrew JO, Willcutt, Erik G, Wright, Margaret J, Zhu, Gu, Fisher, Simon E, Lovett, Maureen W, Strug, Lisa J and Barr, Cathy L (2022) Hypothesis-driven genome-wide association studies provide novel insights into genetics of reading disabilities. TRANSLATIONAL PSYCHIATRY, 12 (1). 495-.