How should we manage fatigue in on-call workers? A review of guidance materials and a systematic review of the evidence-base von Bumpstead, H., Kovac, K., Ferguson, S.A., Vincent, G.E., Bachmann, A., Signal, L., Aisbett, B., Thomas, M.J.W., Sprajcer, M.

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Genetic predisposition to hypertension is associated with preeclampsia in European and Central Asian women von Steinthorsdottir, Valgerdur, McGinnis, Ralph, Williams, Nicholas O., Stefansdottir, Lilja, Thorleifsson, Gudmar, Shooter, Scott, Fadista, João, Sigurdsson, Jon K., Auro, Kirsi M., Berezina, Galina, Borges, Maria-Carolina, Bumpstead, Suzannah, Bybjerg-Grauholm, Jonas, Colgiu, Irina, Dolby, Vivien A., Dudbridge, Frank, Engel, Stephanie M., Franklin, Christopher S., Frigge, Michael L., Frisbaek, Yr, Geirsson, Reynir T., Geller, Frank, Gretarsdottir, Solveig, Gudbjartsson, Daniel F., Harmon, Quaker, Hougaard, David Michael, Hegay, Tatyana, Helgadottir, Anna, Hjartardottir, Sigrun, Jääskeläinen, Tiina, Johannsdottir, Hrefna, Jonsdottir, Ingileif, Juliusdottir, Thorhildur, Kalsheker, Noor, Kasimov, Abdumadjit, Kemp, John P., Kivinen, Katja, Klungsøyr, Kari, Lee, Wai K., Melbye, Mads, Miedzybrodska, Zosia, Moffett, Ashley, Najmutdinova, Dilbar, Nishanova, Firuza, Olafsdottir, Thorunn, Perola, Markus, Pipkin, Fiona Broughton, Poston, Lucilla, Prescott, Gordon, Saevarsdottir, Saedis, Salimbayeva, Damilya, Scaife, Paula Juliet, Skotte, Line, Staines-Urias, Eleonora, Stefansson, Olafur A., Sørensen, Karina Meden, Thomsen, Liv Cecilie Vestrheim, Tragante, Vinicius, Trogstad, Lill, Simpson, Nigel A. B., Aripova, Tamara, Casas, Juan P., Dominiczak, Anna F., Walker, James J., Thorsteinsdottir, Unnur, Iversen, Ann-Charlotte, Feenstra, Bjarke, Lawlor, Deborah A., Boyd, Heather Allison, Magnus, Per, Laivuori, Hannele, Zakhidova, Nodira, Svyatova, Gulnara, Stefansson, Kari, Morgan, Linda

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Large-scale discovery of novel genetic causes of developmental disorders von van Kogelenberg, M, Goudie, D, Gray, E, Harrison, L, Hawkins, R, Henderson, A, Holder, S, Irving, M, Bayzetinova, T, Jones, D, Kini, U, Kinning, E, Kirby, G, Kirk, C, Kumar, D, Lachlan, K, Lees, M, Lim, D, Coomber, E L, Lowther, G, Lynch, S A, Maher, E, Mansour, S, Maye, U, McCann, E, McMullan, D J, McNerlan, S, Metcalfe, K, Mohammed, S, Jones, P, Moore, D, Morton, J, Mugalaasi, H, Newbury-Ecob, R, Ogilvie, C, Park, S, Parker, M J, Patel, C, Porteous, D, Mason, L E, Ragge, N, Rankin, J, Raymond, L, Rosser, E, Miller, R, Sarkar, A, Scott, C, Scott, R, Selby, A, Shannon, N, Simpkin, D, Singzon, R, Skitt, Z, Rajan, D, Splitt, M, Stewart, F, Swaminathan, G J, Tatton-Brown, K, Temple, I K, Torokwa, A, Turner, C, Turnpenny, P, Tysoe, C, Vandersteen, A, Walker, D, Ahmed, M, Widaa, S, Williams, N, Wragg, C, Yau, M, FitzPatrick, D R, Anjum, U, Balasubramanian, M, Banerjee, R, Baralle, D, Baty, D, Bennett, C, Berg, J, Bevan, A P, Bourdon, L, Brady, A, Burton, J, Chandler, K, Cooper, N, Cross, G, D'Alessandro, M, Dabir, T, Davidson, R, Davies, S, Dean, J, Deshpande, C, Donnelly, C, Douglas, A, Eason, J, Edkins, S, Foulds, N, Fryer, A, Gardiner, C, Pereira, S L Gomes, Goodship, J

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A Systematic Survey of Loss-of-Function Variants in Human Protein-Coding Genes von MacArthur, Daniel G., Balasubramanian, Suganthi, Frankish, Adam, Huang, Ni, Morris, James, Walter, Klaudia, Jostins, Luke, Habegger, Lukas, Pickrell, Joseph K., Montgomery, Stephen B., Albers, Cornelis A., Zhang, Zhengdong D., Conrad, Donald F., Lunter, Gerton, Zheng, Hancheng, Ayub, Qasim, DePristo, Mark A., Banks, Eric, Hu, Min, Handsaker, Robert E., Rosenfeld, Jeffrey A., Fromer, Menachem, Jin, Mike, Mu, Xinmeng Jasmine, Khurana, Ekta, Ye, Kai, Kay, Mike, Saunders, Gary Ian, Suner, Marie-Marthe, Hunt, Toby, Barnes, H. A., Amid, Clara, Carvalho-Silva, Denise R., Bignell, Alexandra H., Snow, Catherine, Yngvadottir, Bryndis, Bumpstead, Suzannah, Cooper, David N., Xue, Yali, Romero, Irene Gallego, Wang, Jun, Li, Yingrui, Gibbs, Richard A., McCarroll, Steven A., Dermitzakis, Emmanouil T., Pritchard, Jonathan K., Barrett, Jeffrey C., Harrow, Jennifer, Hurles, Matthew E., Gerstein, Mark B., Tyler-Smith, Chris

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Deep resequencing of GWAS loci identifies independent rare variants associated with inflammatory bowel disease von Rivas, Manuel A, Daly, Mark J, Beaudoin, Mélissa, Gardet, Agnes, Stevens, Christine, Sharma, Yashoda, Zhang, Clarence K, Boucher, Gabrielle, Ripke, Stephan, Ellinghaus, David, Burtt, Noel, Fennell, Tim, Kirby, Andrew, Latiano, Anna, Goyette, Philippe, Green, Todd, Halfvarson, Jonas, Haritunians, Talin, Korn, Joshua M, Kuruvilla, Finny, Lagacé, Caroline, Neale, Benjamin, Lo, Ken Sin, Schumm, Phil, Törkvist, Leif, Dubinsky, Marla C, Brant, Steven R, Silverberg, Mark S, Duerr, Richard H, Altshuler, David, Gabriel, Stacey, Lettre, Guillaume, Franke, Andre, D'Amato, Mauro, McGovern, Dermot P B, Cho, Judy H, Rioux, John D, Xavier, Ramnik J

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Identification of 15 new psoriasis susceptibility loci highlights the role of innate immunity von Tsoi, Lam C, Spain, Sarah L, Knight, Jo, Ellinghaus, Eva, Stuart, Philip E, Capon, Francesca, Ding, Jun, Li, Yanming, Tejasvi, Trilokraj, Gudjonsson, Johann E, Kang, Hyun M, Allen, Michael H, McManus, Ross, Novelli, Giuseppe, Samuelsson, Lena, Schalkwijk, Joost, Ståhle, Mona, Burden, A David, Smith, Catherine H, Cork, Michael J, Estivill, Xavier, Bowcock, Anne M, Krueger, Gerald G, Weger, Wolfgang, Worthington, Jane, Tazi-Ahnini, Rachid, Nestle, Frank O, Hayday, Adrian, Hoffmann, Per, Winkelmann, Juliane, Wijmenga, Cisca, Langford, Cordelia, Edkins, Sarah, Andrews, Robert, Blackburn, Hannah, Strange, Amy, Band, Gavin, Pearson, Richard D, Vukcevic, Damjan, Spencer, Chris C A, Deloukas, Panos, Mrowietz, Ulrich, Schreiber, Stefan, Weidinger, Stephan, Koks, Sulev, Kingo, Külli, Esko, Tonu, Metspalu, Andres, Lim, Henry W, Voorhees, John J, Weichenthal, Michael, Wichmann, H Erich, Chandran, Vinod, Rosen, Cheryl F, Rahman, Proton, Gladman, Dafna D, Griffiths, Christopher E M, Reis, Andre, Kere, Juha, Nair, Rajan P, Franke, Andre, Barker, Jonathan N W N, Abecasis, Goncalo R, Elder, James T, Trembath, Richard C

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Variants in the fetal genome near FLT1 are associated with risk of preeclampsia von McGinnis, Ralph, Steinthorsdottir, Valgerdur, Williams, Nicholas O, Thorleifsson, Gudmar, Shooter, Scott, Hjartardottir, Sigrun, Bumpstead, Suzannah, Stefansdottir, Lilja, Hildyard, Lucy, Sigurdsson, Jon K, Kemp, John P, Silva, Gabriela B, Thomsen, Liv Cecilie V, Jääskeläinen, Tiina, Kajantie, Eero, Chappell, Sally, Kalsheker, Noor, Moffett, Ashley, Hiby, Susan, Lee, Wai Kwong, Padmanabhan, Sandosh, Simpson, Nigel A B, Dolby, Vivien A, Staines-Urias, Eleonora, Engel, Stephanie M, Haugan, Anita, Trogstad, Lill, Svyatova, Gulnara, Zakhidova, Nodira, Najmutdinova, Dilbar, Dominiczak, Anna F, Gjessing, Håkon K, Casas, Juan P, Dudbridge, Frank, Walker, James J, Pipkin, Fiona Broughton, Thorsteinsdottir, Unnur, Geirsson, Reynir T, Lawlor, Debbie A, Iversen, Ann-Charlotte, Magnus, Per, Laivuori, Hannele, Stefansson, Kari, Morgan, Linda

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A genome-wide approach accounting for body mass index identifies genetic variants influencing fasting glycemic traits and insulin resistance von Hivert, Marie-France, Scott, Robert A, Grimsby, Jonna L, Chen, Han, Amin, Najaf, Barnes, Daniel, Cadby, Gemma, Hottenga, Jouke-Jan, Ingelsson, Erik, Kanoni, Stavroula, Ladenvall, Claes, Lagou, Vasiliki, Liu, Yongmei, Martinez-Larrad, Maria Teresa, Navarro, Pau, Strawbridge, Rona J, Tanaka, Toshiko, de Andrade, Mariza, Aulchenko, Yurii, Balkau, Beverley, Beilby, John P, Blangero, John, Boban, Mladen, Boomsma, Dorret I, Böttcher, Yvonne, Bouchard, Claude, Budimir, Danijela, Clarke, Robert, Corbatón-Anchuelo, Arturo, Couper, David, Dedoussis, George V, Erdos, Michael R, Eriksson, Johan G, Franzosi, Maria Grazia, Franks, Paul W, Galan, Pilar, de Geus, Eco, Hallmans, Göran, Hansson, Ola, Harris, Tamara B, Hayward, Caroline, Hingorani, Aroon, Johnson, Paul C D, Jukema, J Wouter, Jula, Antti, Kolcic, Ivana, Kumari, Meena, Lakka, Timo, Lannfelt, Lars, Lathrop, G Mark, Lind, Lars, Lobbens, Stéphane, Loos, Ruth J F, Lyssenko, Valeriya, Magnusson, Patrik K E, Marmot, Michael, Meneton, Pierre, Mooser, Vincent, Morken, Mario A, Ong, Ken K, Oostra, Ben A, Palmer, Lyle J, Palotie, Aarno, Peden, John F, Pedersen, Nancy L, Penninx, Brenda, Perola, Markus, Peyser, Patricia A, Räikkönen, Katri, Rehnberg, Emil, Rotter, Jerome I, Rudan, Igor, Ruokonen, Aimo, Saaristo, Timo, Sabater-Lleal, Maria, Salomaa, Veikko, Saxena, Richa, Sennblad, Bengt, Shuldiner, Alan R, Sijbrands, Eric J G, Small, Kerrin S, Smith, Nicholas L, Sun, Yan V, Tuomilehto, Jaakko, Uitterlinden, Andre G, Vikström, Max, Vitart, Veronique, Vohl, Marie-Claude, Voight, Benjamin F, Waeber, Gerard, Wheeler, Eleanor, Widen, Elisabeth, Willemsen, Gonneke, Wilson, James F, Witteman, Jacqueline C M, Yaghootkar, Hanieh, Barroso, Ines, Watanabe, Richard M, Florez, Jose C, Meigs, James B

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A genome-wide association study in Europeans and South Asians identifies five new loci for coronary artery disease von Peden, John F., Hopewell, Jemma C., Saleheen, Danish, Chambers, John C., Hager, Jorg, Collins, Rory, Danesh, John, Elliott, Paul, Farrall, Martin, Stirrups, Kathy, Zhang, Weihua, Hamsten, Anders, Parish, Sarah, Lathrop, Mark, Watkins, Hugh, Clarke, Robert, Deloukas, Panos, Kooner, Jaspal S., Goel, Anuj, Ongen, Halit, Strawbridge, Rona J., Heath, Simon, Mälarstig, Anders, Helgadottir, Anna, Öhrvik, John, Murtaza, Muhammed, Potter, Simon, Hunt, Sarah E., Delepine, Marc, Jalilzadeh, Shapour, Axelsson, Tomas, Syvänen, Ann-Christine, Gwilliam, Rhian, Bumpstead, Suzannah, Gray, Emma, Edkins, Sarah, Folkersen, Lasse, Kyriakou, Theodosios, Franco-Cereceda, Anders, Gabrielsen, Anders, Seedorf, Udo, Eriksson, Per, Offer, Alison, Bowman, Louise, Sleight, Peter, Armitage, Jane, Peto, Richard, Abecasis, Goncalo, Ahmed, Nabeel, Caulfield, Mark, Donnelly, Peter, Froguel, Philippe, Kooner, Angad S., McCarthy, Mark I., Samani, Nilesh J., Scott, James, Sehmi, Joban, Silveira, Angela, Hellenius, Mai-Lis, van't Hooft, Ferdinand M., Olsson, Gunnar, Rust, Stephan, Assmann, Gerd, Barlera, Simona, Tognoni, Gianni, Franzosi, Maria Grazia, Linksted, Pamela, Green, Fiona R., Rasheed, Asif, Zaidi, Moazzam, Shah, Nabi, Samuel, Maria, Mallick, Nadeem H., Azhar, Muhammad, Zaman, Khan S., Samad, Abdus, Ishaq, Mohammad, Gardezi, Ali R., Frossard, Philippe M., Spector, Tim, Peltonen, Leena, Nieminen, Markku S., Sinisalo, Juha, Salomaa, Veikko, Ripatti, Samuli, Bennett, Derrick, Leander, Karin, Gigante, Bruna, de Faire, Ulf, Pietri, Silvia, Gori, Francesca, Marchioli, Roberto, Sivapalaratnam, Suthesh, Kastelein, John J. P., Trip, Mieke D., Theodoraki, Eirini V., Dedoussis, George V., Engert, Jamie C., Yusuf, Salim, Anand, Sonia S.

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The Lin28/let-7 Axis Regulates Glucose Metabolism von Zhu, Hao, Shyh-Chang, Ng, Segrè, Ayellet V., Shinoda, Gen, Shah, Samar P., Einhorn, William S., Takeuchi, Ayumu, Engreitz, Jesse M., Hagan, John P., Kharas, Michael G., Urbach, Achia, Thornton, James E., Triboulet, Robinson, Gregory, Richard I., Altshuler, David, Daley, George Q.

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Pharmacogenetic meta-analysis of genome-wide association studies of LDL cholesterol response to statins von Postmus, Iris, Trompet, Stella, Deshmukh, Harshal A., Barnes, Michael R., Li, Xiaohui, Warren, Helen R., Chasman, Daniel I., Zhou, Kaixin, Arsenault, Benoit J., Donnelly, Louise A., Wiggins, Kerri L., Avery, Christy L., Griffin, Paula, Feng, QiPing, Taylor, Kent D., Li, Guo, Evans, Daniel S., Smith, Albert V., de Keyser, Catherine E., Johnson, Andrew D., de Craen, Anton J. M., Buckley, Brendan M., Ford, Ian, Westendorp, Rudi G. J., Eline Slagboom, P., Sattar, Naveed, Munroe, Patricia B., Sever, Peter, Poulter, Neil, Stanton, Alice, Shields, Denis C., O’Brien, Eoin, Shaw-Hawkins, Sue, Ida Chen, Y.-D., Nickerson, Deborah A., Smith, Joshua D., Pierre Dubé, Marie, Matthijs Boekholdt, S., Kees Hovingh, G., Kastelein, John J. P., McKeigue, Paul M., Betteridge, John, Neil, Andrew, Durrington, Paul N., Doney, Alex, Carr, Fiona, Morris, Andrew, McCarthy, Mark I., Groop, Leif, Ahlqvist, Emma, Bis, Joshua C., Rice, Kenneth, Smith, Nicholas L., Lumley, Thomas, Whitsel, Eric A., Stürmer, Til, Boerwinkle, Eric, Ngwa, Julius S., O’Donnell, Christopher J., Wei, Wei-Qi, Wilke, Russell A., Liu, Ching-Ti, Sun, Fangui, Guo, Xiuqing, Heckbert, Susan R, Post, Wendy, Sotoodehnia, Nona, Arnold, Alice M., Stafford, Jeanette M., Ding, Jingzhong, Herrington, David M., Kritchevsky, Stephen B., Eiriksdottir, Gudny, Launer, Leonore J., Harris, Tamara B., Chu, Audrey Y., Giulianini, Franco, MacFadyen, Jean G., Barratt, Bryan J., Nyberg, Fredrik, Stricker, Bruno H., Uitterlinden, André G., Hofman, Albert, Rivadeneira, Fernando, Emilsson, Valur, Franco, Oscar H., Ridker, Paul M., Gudnason, Vilmundur, Liu, Yongmei, Denny, Joshua C., Ballantyne, Christie M., Adrienne Cupples, L., Psaty, Bruce M., Palmer, Colin N. A., Tardif, Jean-Claude, Colhoun, Helen M., Hitman, Graham, Krauss, Ronald M., Wouter Jukema, J, Caulfield, Mark J.

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Genome-wide association study identifies loci influencing concentrations of liver enzymes in plasma von Chambers, John C, Elliott, Paul, Kooner, Jaspal S, Sehmi, Joban, Li, Xinzhong, Wass, Mark N, Van der Harst, Pim, Holm, Hilma, Kavousi, Maryam, Deng, Guohong, Gieger, Christian, Heard-Costa, Nancy L, Hottenga, Jouke-Jan, Kühnel, Brigitte, Kumar, Vinod, Lagou, Vasiliki, Liang, Liming, Luan, Jian'an, Vidal, Pedro Marques, Leach, Irene Mateo, O'Reilly, Paul F, Peden, John F, Rahmioglu, Nilufer, Speliotes, Elizabeth K, Yuan, Xin, Alizadeh, Behrooz Z, Atwood, Larry D, Borecki, Ingrid B, Charoen, Pimphen, Cucca, Francesco, de Geus, Eco J C, Dixon, Anna L, Döring, Angela, Ehret, Georg, Forouhi, Nita G, Goessling, Wolfram, Gudbjartsson, Daniel F, Harris, Tamara B, Hartikainen, Anna-Liisa, Hirschfield, Gideon M, Homuth, Georg, Hyppönen, Elina, Janssen, Harry L A, Kangas, Antti J, Kema, Ido P, Kühn, Jens P, Lai, Sandra, Lathrop, Mark, Lerch, Markus M, Li, Yun, Liang, T Jake, Loos, Ruth J F, Martin, Nicholas G, Moffatt, Miriam F, Montgomery, Grant W, Munroe, Patricia B, Musunuru, Kiran, O'Donnell, Christopher J, Prokopenko, Inga, Ruokonen, Aimo, Savolainen, Markku J, Schlessinger, David, Seedorf, Udo, Sen-Chowdhry, Srijita, Siminovitch, Katherine A, Smit, Johannes H, Spector, Timothy D, Tan, Wenting, Teslovich, Tanya M, Tukiainen, Taru, Wallace, Chris, Wallaschofski, Henri, Wichmann, H-Erich, Willemsen, Gonneke, Würtz, Peter, Xu, Chun, Yerges-Armstrong, Laura M, Boomsma, Dorret I, Froguel, Philippe, Matsuda, Koichi, McCarthy, Mark I, Meisinger, Christa, Pietiläinen, Kirsi H, Schumann, Gunter, Snieder, Harold, Sternberg, Michael J E, Stolk, Ronald P, Thomas, Howard C, Thorsteinsdottir, Unnur, Wareham, Nicholas J, Waterworth, Dawn M, Watkins, Hugh, Whitfield, John B, Witteman, Jacqueline C M, Wolffenbuttel, Bruce H R, Fox, Caroline S, Ala-Korpela, Mika, Stefansson, Kari, Völzke, Henry, Järvelin, Marjo-Riitta

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Meta-analysis of genome-wide association studies identifies eight new loci for type 2 diabetes in east Asians von Cho, Yoon Shin, Chen, Chien-Hsiun, Hu, Cheng, Long, Jirong, Hee Ong, Rick Twee, Sim, Xueling, Takeuchi, Fumihiko, Wu, Ying, Go, Min Jin, Yamauchi, Toshimasa, Chang, Yi-Cheng, Kwak, Soo Heon, Ma, Ronald C W, Yamamoto, Ken, Adair, Linda S, Aung, Tin, Cai, Qiuyin, Chang, Li-Ching, Chen, Yuan-Tsong, Gao, Yutang, Hu, Frank B, Kim, Hyung-Lae, Kim, Sangsoo, Kim, Young Jin, Lee, Jeannette Jen-Mai, Lee, Nanette R, Li, Yun, Liu, Jian Jun, Lu, Wei, Nakamura, Jiro, Nakashima, Eitaro, Ng, Daniel Peng-Keat, Tay, Wan Ting, Tsai, Fuu-Jen, Wong, Tien Yin, Yokota, Mitsuhiro, Zheng, Wei, Zhang, Rong, Wang, Congrong, So, Wing Yee, Ohnaka, Keizo, Ikegami, Hiroshi, Hara, Kazuo, Cho, Young Min, Cho, Nam H, Chang, Tien-Jyun, Bao, Yuqian, Hedman, Åsa K, Morris, Andrew P, McCarthy, Mark I, Takayanagi, Ryoichi, Park, Kyong Soo, Jia, Weiping, Chuang, Lee-Ming, Chan, Juliana C N, Maeda, Shiro, Kadowaki, Takashi, Lee, Jong-Young, Wu, Jer-Yuarn, Teo, Yik Ying, Tai, E Shyong, Shu, Xiao Ou, Mohlke, Karen L, Kato, Norihiro, Han, Bok-Ghee, Seielstad, Mark

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A genome-wide association study identifies new psoriasis susceptibility loci and an interaction between HLA-C and ERAP1 von Strange, Amy, Capon, Francesca, Spencer, Chris C A, Knight, Jo, Weale, Michael E, Allen, Michael H, Barton, Anne, Band, Gavin, Bellenguez, Céline, Bergboer, Judith G M, Blackwell, Jenefer M, Bramon, Elvira, Bumpstead, Suzannah J, Casas, Juan P, Cork, Michael J, Corvin, Aiden, Deloukas, Panos, Dilthey, Alexander, Duncanson, Audrey, Edkins, Sarah, Estivill, Xavier, Fitzgerald, Oliver, Freeman, Colin, Giardina, Emiliano, Gray, Emma, Hofer, Angelika, Hüffmeier, Ulrike, Hunt, Sarah E, Irvine, Alan D, Jankowski, Janusz, Kirby, Brian, Langford, Cordelia, Lascorz, Jesús, Leman, Joyce, Leslie, Stephen, Mallbris, Lotus, Markus, Hugh S, Mathew, Christopher G, McLean, W H Irwin, McManus, Ross, Mössner, Rotraut, Moutsianas, Loukas, Naluai, Asa T, Nestle, Frank O, Novelli, Giuseppe, Onoufriadis, Alexandros, Palmer, Colin N A, Perricone, Carlo, Pirinen, Matti, Plomin, Robert, Potter, Simon C, Pujol, Ramon M, Rautanen, Anna, Riveira-Munoz, Eva, Ryan, Anthony W, Salmhofer, Wolfgang, Samuelsson, Lena, Sawcer, Stephen J, Schalkwijk, Joost, Smith, Catherine H, Ståhle, Mona, Su, Zhan, Tazi-Ahnini, Rachid, Traupe, Heiko, Viswanathan, Ananth C, Warren, Richard B, Weger, Wolfgang, Wolk, Katarina, Wood, Nicholas, Worthington, Jane, Young, Helen S, Zeeuwen, Patrick L J M, Hayday, Adrian, Burden, A David, Griffiths, Christopher E M, Kere, Juha, Reis, André, McVean, Gilean, Evans, David M, Brown, Matthew A, Barker, Jonathan N, Peltonen, Leena, Donnelly, Peter, Trembath, Richard C

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Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease von Barrett, Jeffrey C, Hansoul, Sarah, Nicolae, Dan L, Cho, Judy H, Duerr, Richard H, Rioux, John D, Brant, Steven R, Silverberg, Mark S, Taylor, Kent D, Barmada, M Michael, Bitton, Alain, Dassopoulos, Themistocles, Datta, Lisa Wu, Green, Todd, Griffiths, Anne M, Kistner, Emily O, Murtha, Michael T, Regueiro, Miguel D, Rotter, Jerome I, Schumm, L Philip, Steinhart, A Hillary, Targan, Stephan R, Xavier, Ramnik J, Libioulle, Cécile, Sandor, Cynthia, Lathrop, Mark, Belaiche, Jacques, Dewit, Olivier, Gut, Ivo, Heath, Simon, Laukens, Debby, Mni, Myriam, Rutgeerts, Paul, Van Gossum, André, Zelenika, Diana, Franchimont, Denis, Hugot, Jean-Pierre, de Vos, Martine, Vermeire, Severine, Louis, Edouard, Cardon, Lon R, Anderson, Carl A, Drummond, Hazel, Nimmo, Elaine, Ahmad, Tariq, Prescott, Natalie J, Onnie, Clive M, Fisher, Sheila A, Marchini, Jonathan, Ghori, Jilur, Bumpstead, Suzannah, Gwilliam, Rhian, Tremelling, Mark, Deloukas, Panos, Mansfield, John, Jewell, Derek, Satsangi, Jack, Mathew, Christopher G, Parkes, Miles, Georges, Michel, Daly, Mark J

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Impact of Type 2 Diabetes Susceptibility Variants on Quantitative Glycemic Traits Reveals Mechanistic Heterogeneity von DIMAS, Antigone S, LAGOU, Vasiliki, CI SONG, FISCHER-ROSINSKY, Antje, BOESGAARD, Trine Welløv, GRARUP, Niels, ABBASI, Fahim A, ASSIMES, Themistocles L, KE HAO, XIA YANG, LECOEUR, Cécile, BARROSO, Inês, BARKER, Adam, BONNYCASTLE, Lori L, BÖTTCHER, Yvonne, BUMPSTEAD, Suzannah, CHINES, Peter S, ERDOS, Michael R, GRAESSLER, Jurgen, KOVACS, Peter, MORKEN, Mario A, NARISU, Narisu, PAYNE, Felicity, KNOWLES, Joshua W, STANCAKOVA, Alena, SWIFT, Amy J, TÖNJES, Anke, BORNSTEIN, Stefan R, CAUCHI, Stéphane, FROGUEL, Philippe, MEYRE, David, SCHWARZ, Peter E. H, HÄRING, Hans-Ulrich, SMITH, Ulf, MÄGI, Reedik, BOEHNKE, Michael, BERGMAN, Richard N, COLLINS, Francis S, MOHLKE, Karen L, TUOMILEHTO, Jaakko, QUERTEMOUS, Thomas, LIND, Lars, HANSEN, Torben, PEDERSEN, Oluf, WALKER, Mark, HIVERT, Marie-France, PFEIFFER, Andreas F. H, SPRANGER, Joachim, STUMVOLL, Michael, MEIGS, James B, WAREHAM, Nicholas J, KUUSISTO, Johanna, LAAKSO, Markku, LANGENBERG, Claudia, DUPUIS, Josée, BENAZZO, Andrea, RYBIN, Denis, JACKSON, Anne U, STRINGHAM, Heather M

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Deep resequencing of GWAS loci identifies rare variants in CARD9, IL23R and RNF186 that are associated with ulcerative colitis von Beaudoin, Mélissa, Goyette, Philippe, Boucher, Gabrielle, Lo, Ken Sin, Rivas, Manuel A, Stevens, Christine, Alikashani, Azadeh, Ladouceur, Martin, Ellinghaus, David, Törkvist, Leif, Goel, Gautam, Lagacé, Caroline, Annese, Vito, Bitton, Alain, Begun, Jakob, Brant, Steve R, Bresso, Francesca, Cho, Judy H, Duerr, Richard H, Halfvarson, Jonas, McGovern, Dermot P B, Radford-Smith, Graham, Schreiber, Stefan, Schumm, Philip L, Sharma, Yashoda, Silverberg, Mark S, Weersma, Rinse K, D'Amato, Mauro, Vermeire, Severine, Franke, Andre, Lettre, Guillaume, Xavier, Ramnik J, Daly, Mark J, Rioux, John D

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Pooled sequencing of 531 genes in inflammatory bowel disease identifies an associated rare variant in BTNL2 and implicates other immune related genes von Prescott, Natalie J, Lehne, Benjamin, Stone, Kristina, Lee, James C, Taylor, Kirstin, Knight, Jo, Papouli, Efterpi, Mirza, Muddassar M, Simpson, Michael A, Spain, Sarah L, Lu, Grace, Fraternali, Franca, Bumpstead, Suzannah J, Gray, Emma, Amar, Ariella, Bye, Hannah, Green, Peter, Chung-Faye, Guy, Hayee, Bu'Hussain, Pollok, Richard, Satsangi, Jack, Parkes, Miles, Barrett, Jeffrey C, Mansfield, John C, Sanderson, Jeremy, Lewis, Cathryn M, Weale, Michael E, Schlitt, Thomas, Mathew, Christopher G

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Identification of new susceptibility loci for osteoarthritis (arcOGEN): a genome-wide association study von Zeggini, Eleftheria, Panoutsopoulou, Kalliope, Southam, Lorraine, Rayner, Nigel W, Day-Williams, Aaron G, Lopes, Margarida C, Boraska, Vesna, Esko, Tonu, Evangelou, Evangelos, Hoffman, Albert, Houwing-Duistermaat, Jeanine J, Ingvarsson, Thorvaldur, Jonsdottir, Ingileif, Jonnson, Helgi, Kerkhof, Hanneke J, Kloppenburg, Margreet, Bos, Steffan D, Mangino, Massimo, Metrustry, Sarah, Slagboom, P Eline, Thorleifsson, Gudmar, Raine, Emma V A, Ratnayake, Madhushika, Ricketts, Michelle, Beazley, Claude, Blackburn, Hannah, Bumpstead, Suzannah, Elliott, Katherine S, Hunt, Sarah E, Potter, Simon C, Shin, So-Youn, Yadav, Vijay K, Zhai, Guangju, Sherburn, Kate, Dixon, Kate, Arden, Elizabeth, Aslam, Nadim, Battley, Phillippa-kate, Carluke, Ian, Doherty, Sally, Gordon, Andrew, Joseph, John, Keen, Richard, Koller, Nicola C, Mitchell, Sheryl, O'Neill, Fiona, Paling, Ellen, Reed, Mike R, Rivadeneira, Fernando, Swift, Diane, Walker, Kirsten, Watkins, Bridget, Wheeler, Maggie, Birrell, Fraser, Ioannidis, John P A, Meulenbelt, Ingrid, Metspalu, Andres, Rai, Ashok, Salter, Donald, Stefansson, Kari, Stykarsdottir, Unnur, Uitterlinden, André G, van Meurs, Joyce B J, Chapman, Kay, Deloukas, Panos, Ollier, William E R, Wallis, Gillian A, Arden, Nigel, Carr, Andrew, Doherty, Michael, McCaskie, Andrew, Willkinson, J Mark, Ralston, Stuart H, Valdes, Ana M, Spector, Tim D, Loughlin, John

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Genome-Wide Association Identifies Nine Common Variants Associated With Fasting Proinsulin Levels and Provides New Insights Into the Pathophysiology of Type 2 Diabetes von STRAWBRIDGE, Rona J, DUPUIS, Josée, NICA, Alexandra, WHEELER, Eleanor, HAN CHEN, VOIGHT, Benjamin F, TANEERA, Jalal, KANONI, Stavroula, PEDEN, John F, TURRINI, Fabiola, GUSTAFSSON, Stefan, ZABENA, Carina, PROKOPENKO, Inga, ALMGREN, Peter, BARKER, David J. P, BARNES, Daniel, DENNISON, Elaine M, ERIKSSON, Johan G, ERIKSSON, Per, EURY, Elodie, FOLKERSEN, Lasse, FOX, Caroline S, FRAYLING, Timothy M, BARKER, Adam, GOEL, Anuj, GU, Harvest F, HORIKOSHI, Momoko, ISOMAA, Bo, JACKSON, Anne U, JAMESON, Karen A, KAJANTIE, Eero, KERR-CONTE, Julie, KUULASMAA, Teemu, KUUSISTO, Johanna, AHLQVIST, Emma, LOOS, Ruth J. F, JIAN'AN LUAN, MAKRILAKIS, Konstantinos, MANNING, Alisa K, MARTINEZ-LARRAD, Maria Teresa, NARISU, Narisu, MANNILA, Maria Nastase, OHRVIK, John, OSMOND, Clive, PASCOE, Laura, RYBIN, Denis, PAYNE, Felicity, SAYER, Avan A, SENNBLAD, Bengt, SILVEIRA, Angela, STANCAKOVA, Alena, STIRRUPS, Kathy, SWIFT, Amy J, SYVÄNEN, Ann-Christine, PETRIE, John R, TRAVERS, Mary E, BOUATIA-NAJI, Nabila, DIMAS, Antigone S

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