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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).
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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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Hypothesis-driven genome-wide association studies provide novel insights into genetics of reading disabilities.
TRANSLATIONAL PSYCHIATRY, 12 (1).
495-.
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Maternal and fetal genetic effects on birth weight and their relevance to cardio-metabolic risk factors.
NATURE GENETICS, 51 (5).
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Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity.
NATURE GENETICS, 50 (1).
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Protein-coding variants implicate novel genes related to lipid homeostasis contributing to body-fat distribution.
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Rare and low-frequency coding variants alter human adult height.
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Variation in the <i>SERPINA6/SERPINA1</i> locus alters morning plasma cortisol, hepatic corticosteroid binding globulin expression, gene expression in peripheral tissues, and risk of cardiovascular disease.
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