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Doust, Catherine, Fontanillas, Pierre, Eising, Else, Gordon, Scott D, Wang, Zhengjun, Alagöz, Gökberk, Molz, Barbara, Aslibekyan, Stella, Auton, Adam, Babalola, Elizabeth et al (show 137 more authors) , Bell, Robert K, Bielenberg, Jessica, Bryc, Katarzyna, Bullis, Emily, Coker, Daniella, Partida, Gabriel Cuellar, Dhamija, Devika, Das, Sayantan, Elson, Sarah L, Filshtein, Teresa, Fletez-Brant, Kipper, Freyman, Will, Gandhi, Pooja M, Heilbron, Karl, Hicks, Barry, Hinds, David A, Jewett, Ethan M, Jiang, Yunxuan, Kukar, Katelyn, Lin, Keng-Han, Lowe, Maya, McCreight, Jey, McIntyre, Matthew H, Micheletti, Steven J, Moreno, Meghan E, Mountain, Joanna L, Nandakumar, Priyanka, Noblin, Elizabeth S, O’Connell, Jared, Petrakovitz, Aaron A, Poznik, G David, Schumacher, Morgan, Shastri, Anjali J, Shelton, Janie F, Shi, Jingchunzi, Shringarpure, Suyash, Tran, Vinh, Tung, Joyce Y, Wang, Xin, Wang, Wei, Weldon, Catherine H, Wilton, Peter, Hernandez, Alejandro, Wong, Corinna, Tchakouté, Christophe Toukam, Abbondanza, Filippo, Allegrini, Andrea G, Andlauer, Till FM, Barr, Cathy L, Bernard, Manon, Blokland, Kirsten, Bonte, Milene, Boomsma, Dorret I, Bourgeron, Thomas, Brandeis, Daniel, Carreiras, Manuel, Ceroni, Fabiola, Csépe, Valéria, Dale, Philip S, de Jong, Peter F, Démonet, Jean Francois, de Zeeuw, Eveline L, Feng, Yu, Franken, Marie-Christine J, Gerritse, Margot, Gialluisi, Alessandro, Guger, Sharon L, Hayiou-Thomas, Marianna E, Hernández-Cabrera, Juan, Hottenga, Jouke-Jan, Hulme, Charles, Jansen, Philip R, Kere, Juha, Kerr, Elizabeth N, Koomar, Tanner, Landerl, Karin, Leonard, Gabriel T, Liao, Zhijie, Lovett, Maureen W, Lyytinen, Heikki, Martinelli, Angela, Maurer, Urs, Michaelson, Jacob J, Mirza-Schreiber, Nazanin, Moll, Kristina, Morgan, Angela T, Müller-Myhsok, Bertram ORCID: 0000-0002-0719-101X, Newbury, Dianne F, Nöthen, Markus M, Paus, Tomas, Pausova, Zdenka, Pennell, Craig E, Plomin, Robert J, Price, Kaitlyn M, Ramus, Franck, Reilly, Sheena, Richer, Louis, Rimfeld, Kaili, Schulte-Körne, Gerd, Shapland, Chin Yang, Simpson, Nuala H, Snowling, Margaret J, Stein, John F, Strug, Lisa J, 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, Wigg, Karen G, Wilkinson, Margaret, Zhu, Gu, Pourcain, Beate St, Francks, Clyde, Marioni, Riccardo E, Zhao, Jingjing, Paracchini, Silvia, Talcott, Joel B, Monaco, Anthony P, Stein, John F, Gruen, Jeffrey R, Olson, Richard K, Willcutt, Erik G, DeFries, John C, Pennington, Bruce F, Smith, Shelley D, Wright, Margaret J, Martin, Nicholas G, Auton, Adam, Bates, Timothy C, Fisher, Simon E and Luciano, Michelle (2022) Discovery of 42 genome-wide significant loci associated with dyslexia. Nature Genetics, 54 (11). pp. 1621-1629.

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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-.