Objects
Loth, Daan W., Artigas, María Soler, Lee, Mi Kyeong, Scott, Rodney J., Karrasch, Stefan, Grallert, Harald, Gaddis, Nathan C., Starr, John M., Wijmenga, Cisca, Minster, Ryan L., Lederer, David J., Pekkanen, Juha, Gyllensten, Ulf, Strachan, David P., Campbell, Harry, Morris, Andrew P., Gläeser, Sven, Hammond, Christopher J., Burkart, Kristin M., Beilby, John, Kritchevsky, Stephen B., Gucinason, Vilmundur, Hancock, Dana B., Williams, O. Dale, James, Alan L., Polasek, Ozren, Zemunik, Tatijana, Kolcic, Ivana, Petrini, Marcy F., Wjst, Matthias, Kim, Woo Jin, Porteous, David J., Scotland, Generation, Smith, Blair H., Viljanen, Anne, Huffman, Jennifer E., Heliovaara, Markku, Attia, John R., Sayers, Ian, Hampel, Regina, Gieger, Christian, Deary, Ian J., Boezen, H. Marike, Newman, Anne, Jarvelin, Marjo-Riitta, Wilson, James F., Vitart, Veronique, Lind, Lars, Stricker, Bruno H., Teumer, Alexander, Spector, Timothy D., Melén, Erik, Peters, Marjolein J., Lange, Leslie A., Barr, R. Graham, Bracke, Ken R., Verhamme, Fien M., Ramasamy, Adaikalavan, Sung, Joohon, Hiemstra, Pieter S., Cassano, Patricia A., Sood, Akshay, Hayward, Caroline, Dupuis, Josée, Hall, Ian P., Brusselle, Guy G., Tobin, Martin D., London, Stephanie J., Wareham, Nicholas J., Kaprio, Jaakko, Wang, Xin-Qun, Trochet, Holly, Gharib, Sina A., Kähönen, Mika, Flexeder, Claudia, Albrecht, Eva, Lopez, Lorna M., de Jong, Kim, Thyagarajan, Bharat, Alves, Alexessander Couto, Enroth, Stefan, Omenaas, Ernst, Joshi, Peter K., Wain, Louise V., Fall, Tove, Viñuela, Ana, Launer, Lenore J., Loehr, Laura R., Fornage, Myriam, Li, Guo, Wik, Jemma B., Tang, Wenbo, Manichaikul, Ani, Lahousse, Lies, Franceschini, Nora, Harris, Tamara B., North, Kari E., Rudnicka, Alicja R., Hui, Jennie, Gu, Xiangjun, Lumley, Thomas, Wright, Alan F., Hastie, Nicholas D., Campbell, Susan, Kumar, Rajesh, Koch, Beate, Pin, Isabelle, Scott, Robert A., Pietilainen, Kirsi H., Surakka, Ida, Liu, Yongmei, Holliday, Elizabeth G., Schulz, Holger, Heinrich, Joachim, Davies, Gail, Vonk, Judith M., Pottinger, Tess D., Wojczynski, Mary, Pouta, Anneli, Johansson, Åsa, Wild, Sarah H., Ingelsson, Erik, Rivadeneira, Fernando, Vöezke, Henry, Hysi, Pirro G., Eiriksdottir, Gudny, Morrison, Alanna C., Smith, Albert Vernon, Rotter, Jerome I., Gao, Wei, Postma, Dirkje S., White, Wendy B., Rich, Stephen S., Hofman, Albert, Aspelund, Thor, Couper, David, Smith, Lewis J., Psaty, Bruce M., Duan, Qing, Lohman, Kurt, Burchard, Esteban G., Uitterlinden, André G., Garcia, Melissa, Joubert, Bonnie R., McArdle, Wendy L., Musk, A. Bill, Hansel, Nadia, Heckbert, Susan R., Zgaga, Lina, Oldmeadow, Chris, van Meurs, Joyce B. J., Navarro, Pau, Rudan, Igor, Oh, Yeon-Mok, Redline, Susan, Jarvis, Deborah L., Zhao, Jing Hua, Rantanen, Taina, O'Connor, George T., Ripatti, Samuli. Nature Publishing Group; 2014. Genome-wide association analysis identifies six new loci associated with forced vital capacity.
Debette, Stéphanie, Ibrahim Verbaas, Carla A., Yang, Qiong, , , , , , , , , , , deStefano, Anita L., , , , , , , , , , , de Quervain, Dominique J. F., , , , , , Srikanth, Velandai, Lahti, Jari, Grabe, Hans J., Smith, Jennifer A., Priebe, Lutz, Yu, Lei, Karbalai, Nazanin, Bressler, Jan, Oldmeadow, Christopher, Holliday, Elizabeth G., Schofield, Peter, Attia, John, , , , , , , Schuur, Maaike, , , , , , , , , , , Smith, Albert, , , , , , , , , , , Bis, Joshua C., , , , , , , , , , , Davies, Gail, , , , , , , , , , , Wolf, Christiane, , , , , , , , , , , Gudnason, Vilmundur, , , , , , , , , , , Chibnik, Lori B., , , , , , , , , , . Elsevier; 2015. Genome-wide studies of verbal declarative memory in nondemented older people: the Cohorts for Heart and Aging Research in Genomic Epidemiology Consortium.
Traylor, Matthew, Farrall, Martin, Thorsteinsdottir, Unnur, Nalls, Mike A., Longstreth, W. T., Wiggins, Kerri L., Yadav, Sunaina, Parati, Eugenio A., Destefano, Anita L., Worrall, Bradford B., Kittner, Steven J., Khan, Muhammad Saleem, Holliday, Elizabeth G., Reiner, Alex P., Helgadottir, Anna, Achterberg, Sefanja, Fernandez-Cadenas, Israel, Abboud, Sherine, Schmidt, Reinhold, Walters, Matthew, Chen, Wei-Min, Ringelstein, E. Bernd, O'Donnell, Martin, Sudlow, Cathie, Ho, Weang Kee, Pera, Joanna, Lemmens, Robin, Norrving, Bo, Higgins, Peter, Benn, Marianne, Sale, Michele, Kuhlenbaumer, Gregor, Doney, Alexander S. F., Vicente, Astrid M., Hopewell, Jemma C., Delavaran, Hossein, Algra, Ale, Davies, Gail, Oliveira, Sophia A., Palmer, Colin N. A., Deary, Ian, Schmidt, Helena, Pandolfo, Massimo, Montaner, Joan, Carty, Cara, Cheng, Yu-Ching, De Bakker, Paul I. W., Kostulas, Konstantinos, Ferro, Jose M., Van Zuydam, Natalie R., Valdimarsson, Einar, Nordestgaard, Berge G., Lindgren, Anne, Thijs, Vincent, Slowik, Agnieszka, Saleheen, Danish, Fornage, Myriam, Paré, Guillaume, Berger, Klaus, Thorleifsson, Gudmar, Astc, W., Hofman, Albert, Mosley, Thomas H., Mitchell, Branxton D., Furie, Karen, Clarke, Robert, Levi, Christopher, Arfan Ikram, M,, Seshadri, Sudha, Gschwendtner, Andreas, Boncoraglio, Giorgio B., Sharma, Pankaj, Bis, Joshua C., Gretarsdottir, Solveig, Psaty, Bruce M., Rothwell, Peter M., Rosand, Jonathan, Meschia, James F., Malik, Rainer, Stefansson, Kari, Dichgans, Martin, Markus, Hugh S., Bevan, Steve. The Lancet Publishing Group; 2012. Genetic risk factors for ischaemic stroke and its subtypes (the METASTROKE Collaboration): a meta-analysis of genome-wide association studies.
Rietveld, Cornelius A., Medland, Sarah E., Albrecht, Eva, Alizadeh, Behrooz Z., Amin, Najaf, Barnard, John, Baumeister, Sebastian E., Benke, Kelly S., Bielak, Lawrence F., Boatman, Jeffrey A., Boyle, Patricia A., Davies, Gail, Derringer, Jamie, Oldmeadow, Christopher J., Attia, John R., Holliday , Elizabeth G., Scott , Rodney J., Fischer, K, , , , , , Yang, Jian, , , , , , , , , , , Esko, Tõnu, , , , , , , , , , , Martin, Nicholas W., , , , , , , , , , , Westra, Harm-Jan, , , , , , , , , , , Shakhbazov, Konstantin, , , , , , , , , , , Abdellaoui, Abdel, , , , , , , , , , , Agrawal, Arpana, , , , , , , , , , . American Association for the Advancement of Science (AAAS); 2013. GWAS of 126,559 individuals identifies genetic variants associated with educational attainment.
Barban, Nicola, Jansen, Rick, de Vlaming, Ronald, Vaez, Ahmad, Mandemakers, Jornt J., Tropf, Felix C., Shen, Xia, Wilson, James F., Chasman, Daniel I., Nolte, Ilja M., Tragante, Vinicius, van der Laan, Sander W., Perry, John R. B., Kong, Augustine, BIOS Consortium, Ahluwalia, Tarunveer S., Albrecht, Eva, Yerges-Armstrong, Laura, Atzmon, Gil, Auro, Kirsi, Ayers, Kristin, Bakshi, Andrew, Ben-Avraham, Danny, Berger, Klaus, Bergman, Aviv, Bertram, Lars, Bielak, Lawrence F., Bjornsdottir, Gyda, Bonder, Marc Jan, Broer, Linda, Bui, Minh, Barbieri, Caterina, Cavadino, Alana, Chavarro, Jorge E., Turman, Constance, Concas, Maria Pina, Cordell, Heather J., Davies, Gail, Eibich, Peter, Eriksson, Nicholas, Esko, Tõnu, , Eriksson, Joel, Falahi, Fahimeh, Felix, Janine F., Fontana, Mark Alan, Franke, Lude, Gandin, Ilaria, Gaskins, Audrey J., Gieger, Christian, Gunderson, Erica P., Guo, Xiuqing, Hayward, Caroline, He, Chunyan, Hofer, Edith, Huang, Hongyang, Joshi, Peter K., Kanoni, Stavroula, Karlsson, Robert, Kiechl, Stefan, Kifley, Annette, Kluttig, Alexander, , Kraft, Peter, Lagou, Vasiliki, Lecoeur, Cecile, Lahti, Jari, Li-Gao, Ruifang, Lind, Penelope A., Liu, Tian, Makalic, Enes, Mamasoula, Crysovalanto, Matteson, Lindsay, , Mbarek, Hamdi, McArdle, Patrick F., Holliday, Elizabeth G.. Nature Publishing Group; 2016. Genome-wide analysis identifies 12 loci influencing human reproductive behavior.
Rannikmäe, Kristiina, Davies, Gail, Deka, Ranjan, Woo, Jessica G., Martin, Lisa J., Jimenez-Conde, Jordi, Selim, Magdy, Brown, Devin L., Silliman, Scott L., Kidwell, Chelsea S., Montaner, Joan, Langefeld, Carl D., Thomson, Pippa A., Holliday, Elizabeth G., Levi, Christopher R., Attia, John, Rothwell, Peter M., Poole, Deborah L., , , , , , Bevan, Steve, , , , , , , , , , , Devan, William J., , , , , , , , , , , Falcone, Guido J., , , Traylor, Matthew, Anderson, Christopher D., Battey, Thomas W. K., Radmanesh, Farid. Lippincott Williams & Wilkins; 2015. Common variation in COL4A1/COL4A2 is associated with sporadic cerebral small vessel disease.