Supported Undecaphosphotungstate: An Ecofriendly and Efficient Solid Catalyst for Nonsolvent Liquid-Phase Aerobic Epoxidation of Alkenes von Shringarpure, Pragati A, Patel, Anjali

Volltext

An atlas of genetic influences on osteoporosis in humans and mice von Morris, John A., Kemp, John P., Youlten, Scott E., Laurent, Laetitia, Logan, John G., Chai, Ryan C., Vulpescu, Nicholas A., Forgetta, Vincenzo, Kleinman, Aaron, Mohanty, Sindhu T., Sergio, C. Marcelo, Quinn, Julian, Nguyen-Yamamoto, Loan, Luco, Aimee-Lee, Vijay, Jinchu, Simon, Marie-Michelle, Pramatarova, Albena, Medina-Gomez, Carolina, Trajanoska, Katerina, Ghirardello, Elena J., Butterfield, Natalie C., Curry, Katharine F., Leitch, Victoria D., Sparkes, Penny C., Adoum, Anne-Tounsia, Mannan, Naila S., Komla-Ebri, Davide S. K., Pollard, Andrea S., Dewhurst, Hannah F., Hassall, Thomas A. D., Beltejar, Michael-John G., Adams, Douglas J., Vaillancourt, Suzanne M., Kaptoge, Stephen, Baldock, Paul, Cooper, Cyrus, Reeve, Jonathan, Ntzani, Evangelia E., Evangelou, Evangelos, Ohlsson, Claes, Karasik, David, Rivadeneira, Fernando, Kiel, Douglas P., Tobias, Jonathan H., Gregson, Celia L., Harvey, Nicholas C., Grundberg, Elin, Goltzman, David, Adams, David J., Lelliott, Christopher J., Hinds, David A., Ackert-Bicknell, Cheryl L., Hsu, Yi-Hsiang, Maurano, Matthew T., Croucher, Peter I., Williams, Graham R., Bassett, J. H. Duncan, Evans, David M., Richards, J. Brent

Volltext

Genome-wide analysis of insomnia in 1,331,010 individuals identifies new risk loci and functional pathways von Jansen, Philip R., Watanabe, Kyoko, Stringer, Sven, Skene, Nathan, Bryois, Julien, Hammerschlag, Anke R., de Leeuw, Christiaan A., Benjamins, Jeroen S., Muñoz-Manchado, Ana B., Nagel, Mats, Savage, Jeanne E., Tiemeier, Henning, White, Tonya, Tung, Joyce Y., Hinds, David A., Vacic, Vladimir, Wang, Xin, Sullivan, Patrick F., van der Sluis, Sophie, Polderman, Tinca J. C., Smit, August B., Hjerling-Leffler, Jens, Van Someren, Eus J. W., Posthuma, Danielle

Volltext

Multi-trait analysis of genome-wide association summary statistics using MTAG von Turley, Patrick, Walters, Raymond K., Maghzian, Omeed, Okbay, Aysu, Lee, James J., Fontana, Mark Alan, Nguyen-Viet, Tuan Anh, Wedow, Robbee, Zacher, Meghan, Furlotte, Nicholas A., Magnusson, Patrik, Oskarsson, Sven, Johannesson, Magnus, Visscher, Peter M., Laibson, David, Cesarini, David, Neale, Benjamin M., Benjamin, Daniel J.

Volltext

Transancestral GWAS of alcohol dependence reveals common genetic underpinnings with psychiatric disorders von Walters, Raymond K., Polimanti, Renato, Adkins, Amy E., Aliev, Fazil, Bertelsen, Sarah, Biernacka, Joanna M., Bigdeli, Tim B., Chen, Li-Shiun, Degenhardt, Franziska, Docherty, Anna R., Foo, Jerome C., Frank, Josef, Gordon, Scott, Hartmann, Annette M., Hartz, Sarah M., Herms, Stefan, Hoffmann, Per, Jan Hottenga, Jouke, Konte, Bettina, Lahti, Jari, Lahti-Pulkkinen, Marius, Ligthart, Lannie, Loukola, Anu, Mbarek, Hamdi, McQueen, Matthew B., Milaneschi, Yuri, Palviainen, Teemu, Pearson, John F., Ripatti, Samuli, Salvatore, Jessica E., Schwandt, Melanie, Sherva, Richard, Webb, Bradley T., Wedow, Robbee, Wetherill, Leah, Wills, Amanda G., Chen, Danfeng, Choi, Doo-Sup, Copeland, William E., Dahmen, Norbert, Degenhardt, Louisa, Domingue, Benjamin W., Elson, Sarah L., Gäbel, Wolfgang, Ising, Marcus, Keyes, Margaret, Kiefer, Falk, Lucae, Susanne, Lynskey, Michael T., Maier, Wolfgang, Männistö, Satu, Nurnberger, John I., Palotie, Aarno, Preuss, Ulrich, Ridinger, Monika, Scherbaum, Norbert, Schuckit, Marc A., Soyka, Michael, Treutlein, Jens, Wodarz, Norbert, Adkins, Daniel E., Boden, Joseph M., Boomsma, Dorret I., Brown, Sandra A., Bucholz, Kathleen K., Cichon, Sven, Costello, E. Jane, Diazgranados, Nancy, Eriksson, Johan G., Foroud, Tatiana M., Gillespie, Nathan A., Hesselbrock, Victor, Hewitt, John K., Horwood, John, Johnson, Eric O., Kaprio, Jaakko A., Kendler, Kenneth S., Krauter, Kenneth, Lichtenstein, Paul, Lind, Penelope A., McGue, Matt, MacKillop, James, Madden, Pamela A. F., Martin, Nicholas G., Medland, Sarah E., Nöthen, Markus M., Palmer, Abraham A., Penninx, Brenda W. J. H., Porjesz, Bernice, Rice, John P., Rietschel, Marcella, Riley, Brien P., Rujescu, Dan, Shen, Pei-Hong, Silberg, Judy, Stallings, Michael C., Tarter, Ralph E., Vrieze, Scott, Wall, Tamara L., Whitfield, John B.

Volltext

Meta-analysis of genome-wide association studies for neuroticism in 449,484 individuals identifies novel genetic loci and pathways von Nagel, Mats, Jansen, Philip R., Stringer, Sven, Watanabe, Kyoko, de Leeuw, Christiaan A., Bryois, Julien, Savage, Jeanne E., Hammerschlag, Anke R., Skene, Nathan G., Muñoz-Manchado, Ana B., White, Tonya, Tiemeier, Henning, Linnarsson, Sten, Hjerling-Leffler, Jens, Polderman, Tinca J. C., Sullivan, Patrick F., van der Sluis, Sophie, Posthuma, Danielle

Volltext

Genome-wide association study of depression phenotypes in UK Biobank identifies variants in excitatory synaptic pathways von Howard, David M., Adams, Mark J., Shirali, Masoud, Clarke, Toni-Kim, Marioni, Riccardo E., Davies, Gail, Coleman, Jonathan R. I., Alloza, Clara, Shen, Xueyi, Barbu, Miruna C., Wigmore, Eleanor M., Gibson, Jude, Hagenaars, Saskia P., Lewis, Cathryn M., Ward, Joey, Smith, Daniel J., Sullivan, Patrick F., Haley, Chris S., Breen, Gerome, Deary, Ian J., McIntosh, Andrew M.

Volltext

Association studies of up to 1.2 million individuals yield new insights into the genetic etiology of tobacco and alcohol use von Liu, Mengzhen, Jiang, Yu, Wedow, Robbee, Li, Yue, Brazel, David M., Chen, Fang, Datta, Gargi, Davila-Velderrain, Jose, Tian, Chao, Zhan, Xiaowei, Choquet, Hélène, Docherty, Anna R., Faul, Jessica D., Foerster, Johanna R., Fritsche, Lars G., Gabrielsen, Maiken Elvestad, Gordon, Scott D., Haessler, Jeffrey, Hottenga, Jouke-Jan, Huang, Hongyan, Jang, Seon-Kyeong, Jansen, Philip R., Ling, Yueh, Matoba, Nana, McMahon, George, Orrù, Valeria, Palviainen, Teemu, Pandit, Anita, Reginsson, Gunnar W., Skogholt, Anne Heidi, Smith, Jennifer A., Taylor, Amy E., Turman, Constance, Willemsen, Gonneke, Young, Hannah, Young, Kendra A., Zhao, Wei, Zhou, Wei, Bjornsdottir, Gyda, Boehnke, Michael, Boomsma, Dorret I., Chen, Chu, Cucca, Francesco, Davies, Gareth E., Eaton, Charles B., Ehringer, Marissa A., Esko, Tõnu, Fiorillo, Edoardo, Gillespie, Nathan A., Heath, Andrew C., Hokanson, John E., Hopfer, Christian J., Iacono, William G., Kamatani, Yoichiro, Kardia, Sharon L. R., Keller, Matthew C., Kellis, Manolis, Kooperberg, Charles, Kraft, Peter, Krauter, Kenneth S., Laakso, Markku, Lind, Penelope A., Loukola, Anu, Lutz, Sharon M., Madden, Pamela A. F., Martin, Nicholas G., McQueen, Matthew B., Medland, Sarah E., Mohlke, Karen L., Nielsen, Jonas B., Okada, Yukinori, Peters, Ulrike, Polderman, Tinca J. C., Rimm, Eric, Rose, Richard J., Runarsdottir, Valgerdur, Stallings, Michael C., Stefansson, Hreinn, Thai, Khanh K., Tindle, Hilary A., Tyrfingsson, Thorarinn, Wall, Tamara L., Weir, David R., Weisner, Constance, Whitfield, John B., Yin, Jie, Zuccolo, Luisa, Bierut, Laura J., Hveem, Kristian, Lee, James J., Munafò, Marcus R., Saccone, Nancy L., David, Sean P., Jorgenson, Eric, Kaprio, Jaakko, Stefansson, Kari, Thorgeirsson, Thorgeir E., Abecasis, Gonçalo, Liu, Dajiang J., Vrieze, Scott

Volltext

A genome-wide association study with 1,126,563 individuals identifies new risk loci for Alzheimer’s disease von Wightman, Douglas P., Jansen, Iris E., Savage, Jeanne E., Shadrin, Alexey A., Bahrami, Shahram, Holland, Dominic, Rongve, Arvid, Børte, Sigrid, Winsvold, Bendik S., Drange, Ole Kristian, Martinsen, Amy E., Skogholt, Anne Heidi, Willer, Cristen, Bråthen, Geir, Bosnes, Ingunn, Nielsen, Jonas Bille, Fritsche, Lars G., Thomas, Laurent F., Pedersen, Linda M., Gabrielsen, Maiken E., Johnsen, Marianne Bakke, Meisingset, Tore Wergeland, Zhou, Wei, Proitsi, Petroula, Hodges, Angela, Dobson, Richard, Velayudhan, Latha, Heilbron, Karl, Auton, Adam, Sealock, Julia M., Davis, Lea K., Pedersen, Nancy L., Reynolds, Chandra A., Karlsson, Ida K., Magnusson, Sigurdur, Stefansson, Hreinn, Thordardottir, Steinunn, Jonsson, Palmi V., Snaedal, Jon, Zettergren, Anna, Skoog, Ingmar, Kern, Silke, Waern, Margda, Zetterberg, Henrik, Blennow, Kaj, Stordal, Eystein, Hveem, Kristian, Zwart, John-Anker, Athanasiu, Lavinia, Selnes, Per, Saltvedt, Ingvild, Sando, Sigrid B., Ulstein, Ingun, Djurovic, Srdjan, Fladby, Tormod, Aarsland, Dag, Selbæk, Geir, Ripke, Stephan, Stefansson, Kari, Andreassen, Ole A., Posthuma, Danielle

Volltext

Gene discovery and polygenic prediction from a genome-wide association study of educational attainment in 1.1 million individuals von Lee, James J., Wedow, Robbee, Okbay, Aysu, Kong, Edward, Maghzian, Omeed, Zacher, Meghan, Nguyen-Viet, Tuan Anh, Bowers, Peter, Sidorenko, Julia, Karlsson Linnér, Richard, Fontana, Mark Alan, Kundu, Tushar, Lee, Chanwook, Li, Hui, Li, Ruoxi, Royer, Rebecca, Timshel, Pascal N., Walters, Raymond K., Willoughby, Emily A., Yengo, Loïc, Alver, Maris, Bao, Yanchun, Clark, David W., Day, Felix R., Furlotte, Nicholas A., Joshi, Peter K., Kemper, Kathryn E., Kleinman, Aaron, Langenberg, Claudia, Mägi, Reedik, Trampush, Joey W., Verma, Shefali Setia, Wu, Yang, Lam, Max, Zhao, Jing Hua, Zheng, Zhili, Boardman, Jason D., Campbell, Harry, Freese, Jeremy, Harris, Kathleen Mullan, Hayward, Caroline, Herd, Pamela, Kumari, Meena, Lencz, Todd, Luan, Jian’an, Malhotra, Anil K., Metspalu, Andres, Milani, Lili, Ong, Ken K., Perry, John R. B., Porteous, David J., Ritchie, Marylyn D., Smart, Melissa C., Smith, Blair H., Tung, Joyce Y., Wareham, Nicholas J., Wilson, James F., Beauchamp, Jonathan P., Conley, Dalton C., Esko, Tõnu, Lehrer, Steven F., Magnusson, Patrik K. E., Oskarsson, Sven, Pers, Tune H., Robinson, Matthew R., Thom, Kevin, Watson, Chelsea, Chabris, Christopher F., Meyer, Michelle N., Laibson, David I., Yang, Jian, Johannesson, Magnus, Koellinger, Philipp D., Turley, Patrick, Visscher, Peter M., Benjamin, Daniel J., Cesarini, David

Volltext

Polygenic prediction of educational attainment within and between families from genome-wide association analyses in 3 million individuals von Okbay, Aysu, Wu, Yeda, Wang, Nancy, Jayashankar, Hariharan, Bennett, Michael, Nehzati, Seyed Moeen, Sidorenko, Julia, Kweon, Hyeokmoon, Goldman, Grant, Gjorgjieva, Tamara, Jiang, Yunxuan, Hicks, Barry, Tian, Chao, Hinds, David A., Ahlskog, Rafael, Magnusson, Patrik K. E., Oskarsson, Sven, Hayward, Caroline, Campbell, Archie, Porteous, David J., Freese, Jeremy, Herd, Pamela, Watson, Chelsea, Jala, Jonathan, Conley, Dalton, Koellinger, Philipp D., Johannesson, Magnus, Laibson, David, Meyer, Michelle N., Lee, James J., Kong, Augustine, Yengo, Loic, Cesarini, David, Turley, Patrick, Visscher, Peter M., Beauchamp, Jonathan P., Benjamin, Daniel J., Young, Alexander I.

Volltext

Incorporating functional priors improves polygenic prediction accuracy in UK Biobank and 23andMe data sets von Márquez-Luna, Carla, Gazal, Steven, Loh, Po-Ru, Kim, Samuel S., Furlotte, Nicholas, Auton, Adam, Price, Alkes L.

Volltext

Genome-wide association analyses of risk tolerance and risky behaviors in over 1 million individuals identify hundreds of loci and shared genetic influences von Karlsson Linnér, Richard, Biroli, Pietro, Kong, Edward, Meddens, S. Fleur W., Wedow, Robbee, Fontana, Mark Alan, Lebreton, Maël, Tino, Stephen P., Abdellaoui, Abdel, Hammerschlag, Anke R., Nivard, Michel G., Okbay, Aysu, Rietveld, Cornelius A., Timshel, Pascal N., Trzaskowski, Maciej, Vlaming, Ronald de, Zünd, Christian L., Bao, Yanchun, Buzdugan, Laura, Caplin, Ann H., Chen, Chia-Yen, Eibich, Peter, Fontanillas, Pierre, Gonzalez, Juan R., Joshi, Peter K., Karhunen, Ville, Kleinman, Aaron, Levin, Remy Z., Lill, Christina M., Meddens, Gerardus A., Muntané, Gerard, Sanchez-Roige, Sandra, Rooij, Frank J. van, Taskesen, Erdogan, Wu, Yang, Zhang, Futao, Auton, Adam, Boardman, Jason D., Clark, David W., Conlin, Andrew, Dolan, Conor C., Fischbacher, Urs, Groenen, Patrick J. F., Harris, Kathleen Mullan, Hasler, Gregor, Hofman, Albert, Ikram, Mohammad A., Jain, Sonia, Karlsson, Robert, Kessler, Ronald C., Kooyman, Maarten, MacKillop, James, Männikkö, Minna, Morcillo-Suarez, Carlos, McQueen, Matthew B., Schmidt, Klaus M., Smart, Melissa C., Sutter, Matthias, Thurik, A. Roy, Uitterlinden, André G., White, Jon, Wit, Harriet de, Yang, Jian, Bertram, Lars, Boomsma, Dorret I., Esko, Tõnu, Fehr, Ernst, Hinds, David A., Johannesson, Magnus, Kumari, Meena, Laibson, David, Magnusson, Patrik K. E., Meyer, Michelle N., Navarro, Arcadi, Palmer, Abraham A., Pers, Tune H., Posthuma, Danielle, Schunk, Daniel, Stein, Murray B., Svento, Rauli, Tiemeier, Henning, Timmers, Paul R. H. J., Turley, Patrick, Ursano, Robert J., Wagner, Gert G., Wilson, James F., Gratten, Jacob, Lee, James J., Cesarini, David, Benjamin, Daniel J., Koellinger, Philipp D., Beauchamp, Jonathan P.

Volltext

Characterization of Prevalence and Health Consequences of Uniparental Disomy in Four Million Individuals from the General Population von Nakka, Priyanka, Pattillo Smith, Samuel, O’Donnell-Luria, Anne H., McManus, Kimberly F., Agee, Michelle, Auton, Adam, Bell, Robert K., Bryc, Katarzyna, Elson, Sarah L., Fontanillas, Pierre, Furlotte, Nicholas A., Hicks, Barry, Hinds, David A., Jewett, Ethan M., Jiang, Yunxuan, Lin, Keng-Han, McCreight, Jennifer C., Huber, Karen E., Kleinman, Aaron, Litterman, Nadia K., McIntyre, Matthew H., Noblin, Elizabeth S., Northover, Carrie A.M., Pitts, Steven J., Poznik, G. David, Shelton, Janie F., Shringarpure, Suyash, Tian, Chao, Tung, Joyce Y., Vacic, Vladimir, Wang, Xin, Mountain, Joanna L., Ramachandran, Sohini, Sathirapongsasuti, J. Fah

Volltext

Genetic Consequences of the Transatlantic Slave Trade in the Americas von Micheletti, Steven J., Bryc, Kasia, Ancona Esselmann, Samantha G., Freyman, William A., Moreno, Meghan E., Poznik, G. David, Shastri, Anjali J., Agee, M., Aslibekyan, S., Auton, A., Bell, R., Clark, S., Das, S., Elson, S., Fletez-Brant, K., Fontanillas, P., Gandhi, P., Heilbron, K., Hicks, B., Hinds, D., Huber, K., Jewett, E., Jiang, Y., Kleinman, A., Lin, K., Litterman, N., McCreight, J., McIntyre, M., McManus, K., Mozaffari, S., Nandakumar, P., Noblin, L., Northover, C., O’Connell, J., Petrakovitz, A., Pitts, S., Shelton, J., Shringarpure, S., Tian, C., Tung, J., Tunney, R., Vacic, V., Wang, X., Zare, A., Beleza, Sandra, Mountain, Joanna L.

Volltext

Disease risk scores for skin cancers von Fontanillas, Pierre, Alipanahi, Babak, Furlotte, Nicholas A., Johnson, Michaela, Wilson, Catherine H., Pitts, Steven J., Gentleman, Robert, Auton, Adam

Volltext

Genetic analyses identify widespread sex-differential participation bias von Pirastu, Nicola, Cordioli, Mattia, Nandakumar, Priyanka, Mignogna, Gianmarco, Abdellaoui, Abdel, Hollis, Benjamin, Kanai, Masahiro, Rajagopal, Veera M., Parolo, Pietro Della Briotta, Baya, Nikolas, Carey, Caitlin E., Karjalainen, Juha, Als, Thomas D., Van der Zee, Matthijs D., Day, Felix R., Ong, Ken K., Morisaki, Takayuki, de Geus, Eco, Bellocco, Rino, Okada, Yukinori, Børglum, Anders D., Joshi, Peter, Auton, Adam, Hinds, David, Neale, Benjamin M., Walters, Raymond K., Nivard, Michel G., Perry, John R. B., Ganna, Andrea

Volltext

Genome-wide association and epidemiological analyses reveal common genetic origins between uterine leiomyomata and endometriosis von Gallagher, C. S., Mäkinen, N., Harris, H. R., Rahmioglu, N., Uimari, O., Cook, J. P., Shigesi, N., Ferreira, T., Velez-Edwards, D. R., Edwards, T. L., Mortlock, S., Ruhioglu, Z., Day, F., Becker, C. M., Karhunen, V., Martikainen, H., Järvelin, M.-R., Cantor, R. M., Ridker, P. M., Terry, K. L., Buring, J. E., Gordon, S. D., Medland, S. E., Montgomery, G. W., Nyholt, D. R., Hinds, D. A., Tung, J. Y., Perry, J. R. B., Lind, P. A., Painter, J. N., Martin, N. G., Morris, A. P., Chasman, D. I., Missmer, S. A., Zondervan, K. T., Morton, C. C.

Volltext

Multitrait genetic association analysis identifies 50 new risk loci for gastro-oesophageal reflux, seven new loci for Barrett’s oesophagus and provides insights into clinical heter... von Ong, Jue-Sheng, An, Jiyuan, Han, Xikun, Law, Matthew H, Nandakumar, Priyanka, Schumacher, Johannes, Gockel, Ines, Bohmer, Anne, Jankowski, Janusz, Palles, Claire, Olsen, Catherine M, Neale, Rachel E, Fitzgerald, Rebecca, Thrift, Aaron P, Vaughan, Thomas L, Buas, Matthew F, Hinds, David A, Gharahkhani, Puya, Kendall, Bradley J, MacGregor, Stuart, Fitzgerald, Rebecca, Buas, Matt, Gammon, Marilie D, Corley, Douglas A, Shaheen, Nicholas J, Hardie, Laura J, Bird, Nigel C, Reid, Brian J, Chow, Wong-Ho, Risch, Harvey A, Ye, Weimin, Liu, Geoffrey, Romero, Yvonne, Bernstein, Leslie, Wu, Anna H, Schumacher, Johannes, Gockel, Ines, Bohmer, Anne, Jankowski, Janusz, Palles, Claire, Whiteman, David C, Agee, Michelle, Aslibekyan, Stella, Auton, Adam, Bell, Robert K, Bryc, Katarzyna, Clark, Sarah K, Elson, Sarah L, Fletez-Brant, Kipper, Fontanillas, Pierre, Furlotte, Nicholas A, Gandhi, Pooja M, Heilbron, Karl, Hicks, Barry, Hinds, David A, Huber, Karen E, Jewett, Ethan M, Jiang, Yunxuan, Kleinman, Aaron, Lin, Keng-Han, Litterman, Nadia K, Luff, Marie K, McCreight, Jennifer C, McIntyre, Matthew H, McManus, Kimberly F, Mountain, Joanna L, Mozaffari, Sahar V, Nandakumar, Priyanka, Noblin, Elizabeth S, Northover, Carrie AM, O'Connell, Jared, Petrakovitz, Aaron A, Pitts, Steven J, David Poznik, G., Fah Sathirapongsasuti, J, Shastri, Anjali J, Shelton, Janie F, Shringarpure, Suyash, Tian, Chao, Tung, Joyce Y, Tunney, Robert J, Vacic, Vladimir, Wang, Xin, Zare, Amir S

Volltext

Genome-wide meta-analysis of insomnia prioritizes genes associated with metabolic and psychiatric pathways von Watanabe, Kyoko, Jansen, Philip R., Savage, Jeanne E., Nandakumar, Priyanka, Wang, Xin, Hinds, David A., Gelernter, Joel, Levey, Daniel F., Polimanti, Renato, Stein, Murray B., Van Someren, Eus J. W., Smit, August B., Posthuma, Danielle

Volltext