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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, Evelin, Eriksson, Joel, Ozel, Ayse Bilge, Zhang, Weihua, Nethander, Maria, Cheng, Yu-Ching, Aslibekyan, Stella, Ang, Wei, Gandin, Ilaria, Yengo, Loic, Portas, Laura, Kooperberg, Charles, Hofer, Edith, Rajan, Kumar B, Schurmann, Claudia, den Hollander, Wouter, Ahluwalia, Tarunveer S, Zhao, Jing, Draisma, Harmen HM, Ford, Ian, Timpson, Nicholas, Teumer, Alexander, Huang, Hongyan, Wahl, Simone, Liu, YongMei, Huang, Jie, Uh, Hae-Won, Geller, Frank, Joshi, Peter K, Yanek, Lisa R, Trabetti, Elisabetta, Lehne, Benjamin, Vozzi, Diego, Verbanck, Marie, Biino, Ginevra, Saba, Yasaman, Meulenbelt, Ingrid, O'Connell, Jeff R, Laakso, Markku, Giulianini, Franco, Magnusson, Patrik KE, Ballantyne, Christie M, Hottenga, Jouke Jan, Montgomery, GrantW, Rivadineira, Fernando, Rueedi, Rico, Steri, Maristella, Herzig, Karl-Heinz, Stott, David J, Menni, Cristina, Franberg, Mattias, St Pourcain, Beate, Felix, Stephan B, Pers, Tune H, Bakker, Stephan JL, Kraft, Peter, Peters, Annette, Vaidya, Dhananjay, Delgado, Graciela, Smit, Johannes H, Grossmann, Vera, Sinisalo, Juha, Seppala, Ilkka, Williams, Stephen R, Holliday, Elizabeth G, Moed, Matthijs, Langenberg, Claudia, Raikkonen, Katri, Ding, Jingzhong, Campbell, Harry, Sale, Michele M, Chen, Yii-Der I, James, Alan L, Ruggiero, Daniela, Soranzo, Nicole, Hartman, Catharina A, Smith, Erin N, Berenson, Gerald S, Fuchsberger, Christian, Hernandez, Dena, Tiesler, Carla MT, Giedraitis, Vilmantas, Liewald, David, Fischer, Krista, Mellstrom, Dan, Larsson, Anders, Wang, Yunmei, Scott, William R, Lorentzon, Matthias, Beilby, John, Ryan, Kathleen A, Pennell, Craig E, Vuckovic, Dragana, Balkau, Beverly, Concas, Maria Pina, Schmidt, Reinhold, de Leon, Carlos F Mendes, Bottinger, Erwin P, Kloppenburg, Margreet, Paternoster, Lavinia, Boehnke, Michael, Musk, AW, Willemsen, Gonneke, Evans, David M, Madden, Pamela AF, Kahonen, Mika, Kutalik, Zoltan, Zoledziewska, Magdalena, Karhunen, Ville, Kritchevsky, Stephen B, Sattar, Naveed, Lachance, Genevieve, Clarke, Robert, Harris, Tamara B, Raitakari, Olli T, Attia, John R, Van Heemst, Diana, Kajantie, Eero, Sorice, Rossella, Gambaro, Giovanni, Scott, Robert A, Hicks, Andrew A, Ferrucci, Luigi, Standl, Marie, Lindgren, Cecilia M, Starr, John M, Karlsson, Magnus, Lind, Lars, Li, Jun Z, Chambers, John C, Mori, Trevor A, de Geus, Eco JCN, Heath, Andrew C, Martin, Nicholas G, Auvinen, Juha, Buckley, Brendan M, de Craen, Anton JM, Waldenberger, Melanie, Strauch, Konstantin, Meitinger, Thomas, Scott, Rodney J, McEvoy, Mark, Beekman, Marian, Bombieri, Cristina, Ridker, Paul M, Mohlke, Karen L, Pedersen, Nancy L, Morrison, Alanna C, Boomsma, Dorret I, Whitfield, John B, Strachan, David P, Hofman, Albert, Vollenweider, Peter, Cucca, Francesco, Jarvelin, Marjo-Riitta, Jukema, J Wouter, Spector, Tim D, Hamsten, Anders, Zeller, Tanja, Uitterlinden, Andre G, Nauck, Matthias, Gudnason, Vilmundur, Qi, Lu, Grallert, Harald, Borecki, Ingrid B, Rotter, Jerome I, Maerz, Winfried, Wild, Philipp S, Lokki, Marja-Liisa, Boyle, Michael, Salomaa, Veikko, Melbye, Mads, Eriksson, Johan G, Wilson, James F, Penninx, Brenda WJH, Becker, Diane M, Worrall, Bradford B, Gibson, Greg, Krauss, Ronald M, Ciullo, Marina, Zaza, Gianluigi, Wareham, Nicholas J, Oldehinkel, Albertine J, Palmer, Lyle J, Murray, Sarah S, Pramstaller, Peter P, Bandinelli, Stefania, Heinrich, Joachim, Ingelsson, Erik, Deary, Ian J, Magi, Reedik, Vandenput, Liesbeth, van der Harst, Pim, Desch, Karl C, Kooner, Jaspal S, Ohlsson, Claes, Hayward, Caroline, Lehtimaki, Terho, Shuldiner, Alan R, Arnett, Donna K, Beilin, Lawrence J, Robino, Antonietta, Froguel, Philippe, Pirastu, Mario, Jess, Tine, Koenig, Wolfgang, Loos, Ruth JF, Evans, Denis A, Schmidt, Helena, Smith, George Davey, Slagboom, P Eline, Eiriksdottir, Gudny, Morris, Andrew P, Psaty, Bruce M, Tracy, Russell P, Nolte, Ilja M, Boerwinkle, Eric, Visvikis-Siest, Sophie, Reiner, Alex P, Gross, Myron, Bis, Joshua C, Franke, Lude, Franco, Oscar H, Benjamin, Emelia J, Chasman, Daniel I, Dupuis, Josee, Snieder, Harold, Dehghan, Abbas and Alizadeh, Behrooz Z (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). pp. 691-706.

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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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Rietschel, Liz, Streit, Fabian, Zhu, Gu, McAloney, Kerrie, Frank, Josef, Couvy-Duchesne, Baptiste ORCID: 0000-0002-0719-9302, Witt, Stephanie H ORCID: 0000-0002-1571-1468, Binz, Tina M ORCID: 0000-0001-6783-1202, CORtisolNETwork (CORNET) Consortium, , Major Depressive Disorder Working Group of the Psychiatric Genom, et al (show 16 more authors) , McGrath, John ORCID: 0000-0002-4792-6068, Hickie, Ian B ORCID: 0000-0001-8832-9895, Hansell, Narelle K ORCID: 0000-0002-8229-9741, Wright, Margaret J, Gillespie, Nathan A, Forstner, Andreas J, Schulze, Thomas G, Wüst, Stefan ORCID: 0000-0002-2315-8949, Nöthen, Markus M, Baumgartner, Markus R, Walker, Brian R, Crawford, Andrew A ORCID: 0000-0002-9260-0315, Colodro-Conde, Lucía ORCID: 0000-0002-9004-364X, Medland, Sarah E ORCID: 0000-0003-1382-380X, Martin, Nicholas G and Rietschel, Marcella (2017) Hair Cortisol in Twins: Heritability and Genetic Overlap with Psychological Variables and Stress-System Genes. Scientific reports, 7 (1). 15351-.

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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-.

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Morris, Andrew P, Le, Thu H, Wu, Haojia, Akbarov, Artur, van der Most, Peter J, Hemani, Gibran, Smith, George Davey, Mahajan, Anubha, Gaulton, Kyle J, Nadkarni, Girish N et al (show 62 more authors) , Valladares-Salgado, Adan, Wacher-Rodarte, Niels, Mychaleckyj, Josyf C, Dueker, Nicole D, Guo, Xiuqing, Hai, Yang, Haessler, Jeffrey, Kamatani, Yoichiro, Stilp, Adrienne M, Zhu, Gu, Cook, James P, Ärnlöv, Johan, Blanton, Susan H, de Borst, Martin H, Bottinger, Erwin P, Buchanan, Thomas A, Cechova, Sylvia, Charchar, Fadi J, Chu, Pei-Lun, Damman, Jeffrey, Eales, James, Gharavi, Ali G, Giedraitis, Vilmantas, Heath, Andrew C, Ipp, Eli, Kiryluk, Krzysztof, Kramer, Holly J, Kubo, Michiaki, Larsson, Anders, Lindgren, Cecilia M, Lu, Yingchang, Madden, Pamela AF, Montgomery, Grant W, Papanicolaou, George J, Raffel, Leslie J, Sacco, Ralph L, Sanchez, Elena, Stark, Holger, Sundstrom, Johan, Taylor, Kent D, Xiang, Anny H, Zivkovic, Aleksandra, Lind, Lars, Ingelsson, Erik, Martin, Nicholas G, Whitfield, John B, Cai, Jianwen, Laurie, Cathy C, Okada, Yukinori, Matsuda, Koichi, Kooperberg, Charles, Chen, Yii-Der Ida, Rundek, Tatjana, Rich, Stephen S, Loos, Ruth JF, Parra, Esteban J, Cruz, Miguel, Rotter, Jerome I, Snieder, Harold, Tomaszewski, Maciej, Humphreys, Benjamin D and Franceschini, Nora (2019) Trans-ethnic kidney function association study reveals putative causal genes and effects on kidney-specific disease aetiologies. Nature communications, 10 (1). p. 29.