Search Results - Christina C. Newton

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    GWAS meta-analysis of over 29,000 people with epilepsy identifies 26 risk loci and subtype-specific genetic architecture by Campbell, Ciarán, Chen, Siwei, Andrade, Danielle M, Annesi, Grazia, Auce, Pauls, Bebek, Nerses, Berkovic, Samuel F, Beydoun, Ahmad, Blatt, Ilan, Borggraefe, Ingo, Bradfield, Jonathan P, Brody, Lawrence C, Canafoglia, Laura, Castellotti, Barbara, Cerrato, Felecia, Cherny, Stacey S, Cheung, Ching-Lung, Cole, Andrew J, Cossette, Patrick, Daly, Mark J, Dlugos, Dennis J, Doherty, Colin P, Ellis, Colin A, Feucht, Martha, Franceschetti, Silvana, French, Jacqueline A, Gambardella, Antonio, Granata, Tiziana, Guerrini, Renzo, Haas, Kevin F, Howrigan, Daniel P, Jamnadas-Khoda, Jennifer, Jehi, Lara, Kanai, Masahiro, Kantanen, Anne-Mari, Kara, Bülent, Kasperavičiūte, Dalia, Kasteleijn-Nolst Trenite, Dorothee, Kegele, Josua, King, Chontelle, Klein, Karl M, Korczyn, Amos D, Koupparis, Andreas, Krey, Ilona, Kurki, Mitja I, Lauxmann, Stephen, Leech, Stephanie L, Lehesjoki, Anna-Elina, Lesca, Gaetan, Leu, Costin, Lewin, Naomi, Lopes-Cendes, Iscia, Magnusson, Sigurdur, Marson, Anthony G, May, Patrick, McGraw, Christopher M, Mei, Davide, Montomoli, Martino, Mostacci, Barbara, Muccioli, Lorenzo, Müller-Schlüter, Karen, Neubauer, Bernd, Nothnagel, Michael, Pendziwiat, Manuela, Pondrelli, Federica, Powell, Rob H. W, Privitera, Michael, Ragona, Francesca, Regan, Brigid M, Sadleir, Lynette G, Sander, Josemir W, Scala, Marcello, Sham, Pak, Sheidley, Beth R, Shih, Jerry J, Smith, Michael C, Sonsma, Anja C. M, Sperling, Michael R, Stephani, Ulrich, Stewart, William C, Stipa, Carlotta, Striano, Pasquale, Tan, K. Meng, Thomas, G. Neil, Timonen, Oskari, Todaro, Marian, Topaloğlu, Pınar, Tumiene, Birute, Utkus, Algirdas, van Baalen, Andreas, Visscher, Frank, Weber, Yvonne G, Weisenberg, Judith, Widdess-Walsh, Peter, Wolff, Markus, Wolking, Stefan, Yapıcı, Zuhal, Zagaglia, Sara, Zara, Federico, Zhou, Wei

    Published in Nature genetics
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    Exome sequencing of 20,979 individuals with epilepsy reveals shared and distinct ultra-rare genetic risk across disorder subtypes by Chen, Siwei, Abou-Khalil, Bassel W., Afawi, Zaid, Ali, Quratulain Zulfiqar, Amadori, Elisabetta, Anderson, Alison, Anderson, Joe, Andrade, Danielle M., Annesi, Grazia, Arslan, Mutluay, Auce, Pauls, Bahlo, Melanie, Baker, Mark D., Balagura, Ganna, Balestrini, Simona, Banks, Eric, Barba, Carmen, Barboza, Karen, Bartolomei, Fabrice, Bass, Nick, Baum, Larry W., Baumgartner, Tobias H., Baykan, Betül, Bebek, Nerses, Becker, Felicitas, Bennett, Caitlin A., Beydoun, Ahmad, Bianchini, Claudia, Bisulli, Francesca, Blackwood, Douglas, Blatt, Ilan, Borggräfe, Ingo, Bosselmann, Christian, Braatz, Vera, Brand, Harrison, Brockmann, Knut, Buono, Russell J., Busch, Robyn M., Caglayan, S. Hande, Canafoglia, Laura, Canavati, Christina, Castellotti, Barbara, Cavalleri, Gianpiero L., Cerrato, Felecia, Chassoux, Francine, Cherian, Christina, Cherny, Stacey S., Cheung, Ching-Lung, Chou, I-Jun, Chung, Seo-Kyung, Churchhouse, Claire, Ciullo, Valentina, Clark, Peggy O., Cole, Andrew J., Cosico, Mahgenn, Cossette, Patrick, Cotsapas, Chris, Cusick, Caroline, Daly, Mark J., Davis, Lea K., Jonghe, Peter De, Delanty, Norman, Dennig, Dieter, Depondt, Chantal, Derambure, Philippe, Devinsky, Orrin, Vito, Lidia Di, Dickerson, Faith, Dlugos, Dennis J., Doccini, Viola, Doherty, Colin P., El-Naggar, Hany, Ellis, Colin A., Epstein, Leon, Evans, Meghan, Faucon, Annika, Feng, Yen-Chen Anne, Ferguson, Lisa, Ferraro, Thomas N., Silva, Izabela Ferreira Da, Ferri, Lorenzo, Feucht, Martha, Fields, Madeline C., Fitzgerald, Mark, Fonferko-Shadrach, Beata, Fortunato, Francesco, Franceschetti, Silvana, French, Jacqueline A., Freri, Elena, Fu, Jack M., Gabriel, Stacey, Gagliardi, Monica, Gambardella, Antonio, Gauthier, Laura, Giangregorio, Tania, Gili, Tommaso, Glauser, Tracy A., Goldberg, Ethan, Goldman, Alica, Goldstein, David B.

    Published in Nature neuroscience
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    Combining Asian and European genome-wide association studies of colorectal cancer improves risk prediction across racial and ethnic populations by Thomas, Minta, Su, Yu-Ru, Sakoda, Lori C., Schmit, Stephanie L., Timofeeva, Maria N., Chen, Zhishan, Fernandez-Rozadilla, Ceres, Law, Philip J., Murphy, Neil, Carreras-Torres, Robert, van Duijnhoven, Franzel J. B., Shin, Aesun, Wolk, Alicja, Phipps, Amanda I., Zauber, Ann G., Wu, Anna H., Um, Caroline Y., Tangen, Catherine M., Gignoux, Chris, Newton, Christina, Haiman, Christopher A., Qu, Conghui, Bishop, D. Timothy, Buchanan, Daniel D., Crosslin, David R., Kim, Dong-Hyun, Hauser, Elizabeth, White, Emily, Siegel, Erin, Rennert, Gad, Giles, Graham G., Hampel, Heather, Brenner, Hermann, Oze, Isao, Lee, Jeffrey K., Kim, Jeongseon, Huyghe, Jeroen R., Zheng, Jiayin, Hampe, Jochen, Greenson, Joel, Palmer, Julie R., Visvanathan, Kala, Matsuo, Keitaro, Jung, Keum Ji, Li, Li, Le Marchand, Loic, Vodickova, Ludmila, Bujanda, Luis, Matejcic, Marco, Jenkins, Mark A., Slattery, Martha L., D’Amato, Mauro, Hoffmeister, Michael, Woods, Michael O., Kim, Michelle, Song, Mingyang, Iwasaki, Motoki, Du, Mulong, Sawada, Norie, Vodicka, Pavel, Campbell, Peter T., Pearlman, Rachel, Pai, Rish K., Prentice, Ross L., Küry, Sébastien, Castellví-Bel, Sergi, Berndt, Sonja I., Lee, Soo Chin, Brezina, Stefanie, Weinstein, Stephanie J., Chanock, Stephen J., Jee, Sun Ha, Kweon, Sun-Seog, Vadaparampil, Susan, Harrison, Tabitha A., Yamaji, Taiki, Keku, Temitope O., Vymetalkova, Veronika, Arndt, Volker, Jia, Wei-Hua, Shu, Xiao-Ou, Lin, Yi, Ahn, Yoon-Ok, Stadler, Zsofia K., Van Guelpen, Bethany, Ulrich, Cornelia M., Li, Christopher I., Meester, Reinier, Moreno, Victor, Figueiredo, Jane C., Casey, Graham, Lansdorp Vogelaar, Iris, Dunlop, Malcolm G., Hayes, Richard B., Pharoah, Paul D. P., Houlston, Richard S., Jarvik, Gail P., Tomlinson, Ian P., Zheng, Wei, Corley, Douglas A.

    Published in Nature communications
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