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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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Ligthart, Symen, Vaez, Ahmad, Vosa, Urmo, Stathopoulou, Maria G, de Vries, Paul S, Prins, Bram P, Van der Most, Peter J, Tanaka, Toshiko, Naderi, Elnaz, Rose, Lynda M et al (show 276 more authors) , Wu, Ying, Karlsson, Robert, Barbalic, Maja, Lin, Honghuang, Pool, Rene, Zhu, Gu, Mace, Aurelien, Sidore, Carlo, Trompet, Stella, Mangino, Massimo, Sabater-Lleal, Maria, Kemp, John P, Abbasi, Ali, Kacprowski, Tim, Verweij, Niek, Smith, Albert V, Huang, Tao, Marzi, Carola, Feitosa, Mary F, Lohman, Kurt K, Kleber, Marcus E, Milaneschi, Yuri, Mueller, Christian, Huq, Mahmudul, Vlachopoulou, Efthymia, Lyytikainen, Leo-Pekka, Oldmeadow, Christopher, Deelen, Joris, Perola, Markus, Zhao, Jing Hua, Feenstra, Bjarke, Amini, Marzyeh, Lahti, Jari, Schraut, Katharina E, Fornage, Myriam, Suktitipat, Bhoom, Chen, Wei-Min, Li, Xiaohui, Nutile, Teresa, Malerba, Giovanni, Luan, Jian'an, Bak, Tom, Schork, Nicholas, Del Greco, Fabiola M, Thiering, Elisabeth, Mahajan, Anubha, Marioni, Riccardo E, Mihailov, 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(2018)
Genome Analyses of >200,000 Individuals Identify 58 Loci for Chronic Inflammation and Highlight Pathways that Link Inflammation and Complex Disorders.
AMERICAN JOURNAL OF HUMAN GENETICS, 103 (5).
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Bolton, Jennifer L, Hayward, Caroline, Direk, Nese, Lewis, John G, Hammond, Geoffrey L, Hill, Lesley A, Anderson, Anna, Huffman, Jennifer, Wilson, James F, Campbell, Harry et al (show 46 more authors) , Rudan, Igor, Wright, Alan, Hastie, Nicholas, Wild, Sarah H, Velders, Fleur P, Hofman, Albert, Uitterlinden, Andre G, Lahti, Jari, Räikkönen, Katri, Kajantie, Eero, Widen, Elisabeth, Palotie, Aarno, Eriksson, Johan G, Kaakinen, Marika, Järvelin, Marjo-Riitta, Timpson, Nicholas J, Davey Smith, George, Ring, Susan M, Evans, David M, St Pourcain, Beate, Tanaka, Toshiko, Milaneschi, Yuri, Bandinelli, Stefania, Ferrucci, Luigi, van der Harst, Pim, Rosmalen, Judith GM, Bakker, Stephen JL, Verweij, Niek, Dullaart, Robin PF, Mahajan, Anubha, Lindgren, Cecilia M, Morris, Andrew, Lind, Lars, Ingelsson, Erik, Anderson, Laura N, Pennell, Craig E, Lye, Stephen J, Matthews, Stephen G, Eriksson, Joel, Mellstrom, Dan, Ohlsson, Claes, Price, Jackie F, Strachan, Mark WJ, Reynolds, Rebecca M, Tiemeier, Henning and Walker, Brian R
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Genome wide association identifies common variants at the SERPINA6/SERPINA1 locus influencing plasma cortisol and corticosteroid binding globulin.
PLoS Genetics, 10 (7).
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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).
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Fan, Qiao, Pozarickij, Alfred, Tan, Nicholas YQ, Guo, Xiaobo, Verhoeven, Virginie JM ORCID: 0000-0001-7359-7862, Vitart, Veronique ORCID: 0000-0002-4991-3797, Guggenheim, Jeremy A ORCID: 0000-0001-5164-340X, Miyake, Masahiro, Tideman, J Willem L, Khawaja, Anthony P ORCID: 0000-0001-6802-8585 et al (show 50 more authors) , Zhang, Liang ORCID: 0000-0001-9264-170X, MacGregor, Stuart ORCID: 0000-0001-6731-8142, Höhn, René, Chen, Peng, Biino, Ginevra, Wedenoja, Juho ORCID: 0000-0002-6155-0378, Saffari, Seyed Ehsan ORCID: 0000-0002-6473-4375, Tedja, Milly S ORCID: 0000-0003-0356-9684, Xie, Jing, Lanca, Carla ORCID: 0000-0001-9918-787X, Wang, Ya Xing ORCID: 0000-0003-2749-7793, Sahebjada, Srujana, Mazur, Johanna, Mirshahi, Alireza, Martin, Nicholas G ORCID: 0000-0003-4069-8020, Yazar, Seyhan ORCID: 0000-0003-0994-6196, Pennell, Craig E, Yap, Maurice ORCID: 0000-0003-4687-4101, Haarman, Annechien EG, Enthoven, Clair A, Polling, JanRoelof, Consortium for Refractive Error and Myopia (CREAM), , UK Biobank Eye and Vision Consortium, , Hewitt, Alex W ORCID: 0000-0002-5123-5999, Jaddoe, Vincent WV ORCID: 0000-0003-2939-0041, van Duijn, Cornelia M ORCID: 0000-0002-2374-9204, Hayward, Caroline ORCID: 0000-0002-9405-9550, Polasek, Ozren ORCID: 0000-0002-5765-1862, Tai, E-Shyong ORCID: 0000-0003-2929-8966, Yoshikatsu, Hosoda, Hysi, Pirro G ORCID: 0000-0001-5752-2510, Young, Terri L ORCID: 0000-0001-6994-9941, Tsujikawa, Akitaka ORCID: 0000-0003-0779-7799, Wang, Jie Jing ORCID: 0000-0001-9491-4898, Mitchell, Paul, Pfeiffer, Norbert ORCID: 0000-0002-5766-2617, Pärssinen, Olavi, Foster, Paul J ORCID: 0000-0002-4755-177X, Fossarello, Maurizio, Yip, Shea Ping, Williams, Cathy, Hammond, Christopher J ORCID: 0000-0002-3227-2620, Jonas, Jost B ORCID: 0000-0003-2972-5227, He, Mingguang, Mackey, David A, Wong, Tien-Yin, Klaver, Caroline CW ORCID: 0000-0002-2355-5258, Saw, Seang-Mei, Baird, Paul N ORCID: 0000-0002-1305-3502 and Cheng, Ching-Yu
(2020)
Genome-wide association meta-analysis of corneal curvature identifies novel loci and shared genetic influences across axial length and refractive error.
Communications biology, 3 (1).
133-.
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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
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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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(2019)
Maternal and fetal genetic effects on birth weight and their relevance to cardio-metabolic risk factors.
NATURE GENETICS, 51 (5).
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