Reinventing the role of the project manager in mobilising knowledge in construction von Kelly, Nicola, Edkins, Andrew John, Smyth, Hedley, Konstantinou, Efrosyni

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The UK10K project identifies rare variants in health and disease von Walter, Klaudia, Min, Josine L, Huang, Jie, Crooks, Lucy, Memari, Yasin, McCarthy, Shane, Perry, John R B, Xu, ChangJiang, Futema, Marta, Lawson, Daniel, Iotchkova, Valentina, Schiffels, Stephan, Hendricks, Audrey E, Danecek, Petr, Li, Rui, Floyd, James, Wain, Louise V, Barroso, Inês, Humphries, Steve E, Hurles, Matthew E, Zeggini, Eleftheria, Barrett, Jeffrey C, Plagnol, Vincent, Richards, J Brent, Greenwood, Celia M T, Timpson, Nicholas J, Durbin, Richard, Soranzo, Nicole

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An Expanded Genome-Wide Association Study of Type 2 Diabetes in Europeans von Scott, Robert A, Scott, Laura J, Mägi, Reedik, Marullo, Letizia, Gaulton, Kyle J, Kaakinen, Marika, Pervjakova, Natalia, Pers, Tune H, Johnson, Andrew D, Eicher, John D, Jackson, Anne U, Ferreira, Teresa, Lee, Yeji, Ma, Clement, Steinthorsdottir, Valgerdur, Thorleifsson, Gudmar, Qi, Lu, Van Zuydam, Natalie R, Mahajan, Anubha, Chen, Han, Almgren, Peter, Voight, Ben F, Grallert, Harald, Müller-Nurasyid, Martina, Ried, Janina S, Rayner, Nigel W, Robertson, Neil, Karssen, Lennart C, van Leeuwen, Elisabeth M, Willems, Sara M, Fuchsberger, Christian, Kwan, Phoenix, Teslovich, Tanya M, Chanda, Pritam, Li, Man, Lu, Yingchang, Dina, Christian, Thuillier, Dorothee, Yengo, Loic, Jiang, Longda, Sparso, Thomas, Kestler, Hans A, Chheda, Himanshu, Eisele, Lewin, Gustafsson, Stefan, Frånberg, Mattias, Strawbridge, Rona J, Benediktsson, Rafn, Hreidarsson, Astradur B, Kong, Augustine, Sigurðsson, Gunnar, Kerrison, Nicola D, Luan, Jian'an, Liang, Liming, Meitinger, Thomas, Roden, Michael, Thorand, Barbara, Esko, Tõnu, Mihailov, Evelin, Fox, Caroline, Liu, Ching-Ti, Rybin, Denis, Isomaa, Bo, Lyssenko, Valeriya, Tuomi, Tiinamaija, Couper, David J, Pankow, James S, Grarup, Niels, Have, Christian T, Jørgensen, Marit E, Jørgensen, Torben, Linneberg, Allan, Cornelis, Marilyn C, van Dam, Rob M, Hunter, David J, Kraft, Peter, Sun, Qi, Edkins, Sarah, Owen, Katharine R, Perry, John R B, Wood, Andrew R, Zeggini, Eleftheria, Tajes-Fernandes, Juan, Abecasis, Goncalo R, Bonnycastle, Lori L, Chines, Peter S, Stringham, Heather M, Koistinen, Heikki A, Kinnunen, Leena, Sennblad, Bengt, Mühleisen, Thomas W, Nöthen, Markus M, Pechlivanis, Sonali, Baldassarre, Damiano, Gertow, Karl, Humphries, Steve E, Tremoli, Elena, Klopp, Norman, Meyer, Julia, Steinbach, Gerald

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Genetic fine mapping and genomic annotation defines causal mechanisms at type 2 diabetes susceptibility loci von Reschen, Michael E, Mahajan, Anubha, William Rayner, N, Scott, Laura J, Yengo, Loic, Wahl, Simone, Kestler, Hans, Chheda, Himanshu, Eisele, Lewin, Steinthorsdottir, Valgerdur, Chen, Han, Fuchsberger, Christian, Kwan, Phoenix, Thomsen, Soren K, Rundle, Jana K, van de Bunt, Martijn, Voight, Benjamin F, Abecasis, Gonçalo R, Baldassarre, Damiano, Carey, Jason, Chines, Peter S, Crenshaw, Andrew T, Edkins, Sarah, Eury, Elodie, Fontanillas, Pierre, Franks, Paul W, Gertow, Karl, Groves, Christopher J, Hassinen, Maija, Herder, Christian, Hreidarsson, Astradur B, Jackson, Anne U, Jonsson, Anna, Jørgensen, Marit E, Jørgensen, Torben, Kao, Wen-Hong L, Kerrison, Nicola D, Kinnunen, Leena, Kravic, Jasmina, Langford, Cordelia, Lichtner, Peter, Lindholm, Eero, Lobbens, Stéphane, Luan, Jian'an, Meyer, Julia, Mihailov, Evelin, Mühleisen, Thomas W, Navarro, Carmen, Oskolkov, Nikolay N, Pechlivanis, Sonali, Platou, Carl G P, Rybin, Denis, van der Schouw, Yvonne T, Sennblad, Bengt, Steinbach, Gerald, Storm, Petter, Sun, Qi, Thorand, Barbara, Tikkanen, Emmi, Trakalo, Joseph, Tremoli, Elena, Wood, Andrew R, Zeggini, Eleftheria, Birney, Ewan, Pasquali, Lorenzo, Pankow, James S, van Duijn, Cornelia, Sijbrands, Eric, Hu, Frank B, Thorsteinsdottir, Unnur, Stefansson, Kari, Lakka, Timo A, Rauramaa, Rainer, Stumvoll, Michael, Korpi-Hyövälti, Eeva, Kuusisto, Johanna, Metspalu, Andres, Jöcke, Karl-Heinz, Moebus, Susanne, Bergman, Richard N, Collins, Francis S, Mohlke, Karen L, Koistinen, Heikki, Tuomilehto, Jaakko, Deloukas, Panagiotis, Donnelly, Peter J, Frayling, Timothy M, Sladek, Rob, Froguel, Philippe, Hansen, Torben, Kathiresan, Sekar, Barroso, Inês, Langenberg, Claudia, Wareham, Nicholas J, O'Callaghan, Christopher A, Gloyn, Anna L, Altshuler, David, Boehnke, Michael, Teslovich, Tanya M, Morris, Andrew P

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Improved imputation of low-frequency and rare variants using the UK10K haplotype reference panel von Huang, Jie, Howie, Bryan, McCarthy, Shane, Memari, Yasin, Walter, Klaudia, Min, Josine L., Danecek, Petr, Malerba, Giovanni, Trabetti, Elisabetta, Zheng, Hou-Feng, Gambaro, Giovanni, Richards, J. Brent, Durbin, Richard, Timpson, Nicholas J., Marchini, Jonathan, Soranzo, Nicole

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Gene filtering strategies for machine learning guided biomarker discovery using neonatal sepsis RNA-seq data von Parkinson, Edward, Liberatore, Federico, Watkins, W John, Andrews, Robert, Edkins, Sarah, Hibbert, Julie, Strunk, Tobias, Currie, Andrew, Ghazal, Peter

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Systematic sequencing of renal carcinoma reveals inactivation of histone modifying genes von Dalgliesh, Gillian L., Furge, Kyle, Greenman, Chris, Chen, Lina, Bignell, Graham, Butler, Adam, Davies, Helen, Edkins, Sarah, Hardy, Claire, Latimer, Calli, Teague, Jon, Andrews, Jenny, Barthorpe, Syd, Beare, Dave, Buck, Gemma, Campbell, Peter J., Forbes, Simon, Jia, Mingming, Jones, David, Knott, Henry, Kok, Chai Yin, Lau, King Wai, Leroy, Catherine, Lin, Meng-Lay, McBride, David J., Maddison, Mark, Maguire, Simon, McLay, Kirsten, Menzies, Andrew, Mironenko, Tatiana, Mulderrig, Lee, Mudie, Laura, O’Meara, Sarah, Pleasance, Erin, Rajasingham, Arjunan, Shepherd, Rebecca, Smith, Raffaella, Stebbings, Lucy, Stephens, Philip, Tang, Gurpreet, Tarpey, Patrick S., Turrell, Kelly, Dykema, Karl J., Khoo, Sok Kean, Petillo, David, Wondergem, Bill, Anema, John, Kahnoski, Richard J., Teh, Bin Tean, Stratton, Michael R., Futreal, P. Andrew

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Complex landscapes of somatic rearrangement in human breast cancer genomes von Stephens, Philip J., McBride, David J., Lin, Meng-Lay, Varela, Ignacio, Pleasance, Erin D., Simpson, Jared T., Stebbings, Lucy A., Leroy, Catherine, Edkins, Sarah, Mudie, Laura J., Greenman, Chris D., Jia, Mingming, Latimer, Calli, Teague, Jon W., Lau, King Wai, Burton, John, Quail, Michael A., Swerdlow, Harold, Churcher, Carol, Natrajan, Rachael, Sieuwerts, Anieta M., Martens, John W. M., Silver, Daniel P., Langerød, Anita, Russnes, Hege E. G., Foekens, John A., Reis-Filho, Jorge S., van ’t Veer, Laura, Richardson, Andrea L., Børresen-Dale, Anne-Lise, Campbell, Peter J., Futreal, P. Andrew, Stratton, Michael R.

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Somatic mutations of the histone H3K27 demethylase gene UTX in human cancer von van Haaften, Gijs, Dalgliesh, Gillian L, Davies, Helen, Chen, Lina, Bignell, Graham, Greenman, Chris, Edkins, Sarah, Hardy, Claire, O'Meara, Sarah, Teague, Jon, Butler, Adam, Hinton, Jonathan, Latimer, Calli, Andrews, Jenny, Barthorpe, Syd, Beare, Dave, Buck, Gemma, Campbell, Peter J, Cole, Jennifer, Forbes, Simon, Jia, Mingming, Jones, David, Kok, Chai Yin, Leroy, Catherine, Lin, Meng-Lay, McBride, David J, Maddison, Mark, Maquire, Simon, McLay, Kirsten, Menzies, Andrew, Mironenko, Tatiana, Mulderrig, Lee, Mudie, Laura, Pleasance, Erin, Shepherd, Rebecca, Smith, Raffaella, Stebbings, Lucy, Stephens, Philip, Tang, Gurpreet, Tarpey, Patrick S, Turner, Rachel, Turrell, Kelly, Varian, Jennifer, West, Sofie, Widaa, Sara, Wray, Paul, Collins, V Peter, Ichimura, Koichi, Law, Simon, Wong, John, Yuen, Siu Tsan, Leung, Suet Yi, Tonon, Giovanni, DePinho, Ronald A, Tai, Yu-Tzu, Anderson, Kenneth C, Kahnoski, Richard J, Massie, Aaron, Khoo, Sok Kean, Teh, Bin Tean, Stratton, Michael R, Futreal, P Andrew

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Comparative performances of machine learning methods for classifying Crohn Disease patients using genome-wide genotyping data von Romagnoni, Alberto, Jégou, Simon, Van Steen, Kristel, Wainrib, Gilles, Hugot, Jean-Pierre

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Genetic diagnosis of developmental disorders in the DDD study: a scalable analysis of genome-wide research data von Wright, Caroline F, Dr, Fitzgerald, Tomas W, MS, Jones, Wendy D, MBBS, Clayton, Stephen, MRes, McRae, Jeremy F, PhD, van Kogelenberg, Margriet, PhD, King, Daniel A, MD, Ambridge, Kirsty, BSc, Barrett, Daniel M, BSc, Bayzetinova, Tanya, BSc, Bevan, A Paul, PhD, Bragin, Eugene, MSc, Chatzimichali, Eleni A, PhD, Gribble, Susan, PhD, Jones, Philip, MSc, Krishnappa, Netravathi, MSc, Mason, Laura E, BSc, Miller, Ray, PhD, Morley, Katherine I, PhD, Parthiban, Vijaya, PhD, Prigmore, Elena, PhD, Rajan, Diana, MSc, Sifrim, Alejandro, PhD, Swaminathan, G Jawahar, PhD, Tivey, Adrian R, MSc, Middleton, Anna, PhD, Parker, Michael, Prof, Carter, Nigel P, PhD, Barrett, Jeffrey C, PhD, Hurles, Matthew E, PhD, FitzPatrick, David R, Prof, Firth, Helen V, DM

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Large-scale meta-analysis of genome-wide association data identifies six new risk loci for Parkinson's disease von Nalls, Mike A, Pankratz, Nathan, Lill, Christina M, Do, Chuong B, Hernandez, Dena G, Saad, Mohamad, DeStefano, Anita L, Kara, Eleanna, Bras, Jose, Sharma, Manu, Schulte, Claudia, Keller, Margaux F, Arepalli, Sampath, Letson, Christopher, Edsall, Connor, Stefansson, Hreinn, Liu, Xinmin, Pliner, Hannah, Lee, Joseph H, Cheng, Rong, Ikram, M Arfan, Ioannidis, John P A, Hadjigeorgiou, Georgios M, Bis, Joshua C, Martinez, Maria, Perlmutter, Joel S, Goate, Alison, Marder, Karen, Fiske, Brian, Sutherland, Margaret, Xiromerisiou, Georgia, Myers, Richard H, Clark, Lorraine N, Stefansson, Kari, Hardy, John A, Heutink, Peter, Chen, Honglei, Wood, Nicholas W, Houlden, Henry, Payami, Haydeh, Brice, Alexis, Scott, William K, Gasser, Thomas, Bertram, Lars, Eriksson, Nicholas, Foroud, Tatiana, Singleton, Andrew B

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The genetics of blood pressure regulation and its target organs from association studies in 342,415 individuals von Chasman, Daniel I, Jackson, Anne U, Johnson, Toby, Thorleifsson, Gudmar, Luan, Jian'an, Pihur, Vasyl, Meirelles, Osorio, Bouatia-Naji, Nabila, Shah, Sonia, Nolte, Ilja M, Magnusson, Patrik K, Folkersen, Lasse, Kim, Young Jin, Zhao, Wei, Bochud, Murielle, Baldassarre, Damiano, Barroso, Inês, Chang, I-Shou, Chines, Peter S, Connell, John M, Döring, Angela, Dominiczak, Anna F, Doney, Alex S F, Erdmann, Jeanette, Eriksson, Per, Evangelou, Evangelos, Evans, Alun, Felix, Janine F, Gertow, Karl, Goodarzi, Mark O, Gorski, Mathias, Groves, Christopher J, Gyllensten, Ulf, Hallmans, Göran, Hercberg, Serge, Hicks, Andrew A, Hsiung, Chao A, Kang, Hyun Min, Kathiresan, Sekar, Khaw, Kay-Tee, Kim, Yun Kyoung, Klopp, Norman, Kolovou, Genovefa, Kooner, Jaspal S, Kosova, Gulum, Kutalik, Zoltan, Lee, I-Te, Lee, Wen-Jane, Lindström, Jaana, Lobbens, Stéphane, Männistö, Satu, Mach, François, Marouli, Eirini, McKenzie, Colin A, Menni, Cristina, Morris, Andrew D, Nagaraja, Ramaiah, Nikus, Kjell, O'Reilly, Paul F, Ong, Ken K, Parsa, Afshin, Penninx, Brenda W, Rossouw, Jacques, Saramies, Jouko, Shin, Young-Ah, Stanton, Alice V, Sundstrom, Johan, Syvänen, Ann-Christine, Tarasov, Kirill V, Thorsteinsdottir, Unnur, Uitterlinden, Andre G, Vaez, Ahmad, van Iperen, Erik P A, Vasan, Ramachandran S, Verwoert, Germaine C, Wain, Louise V, Watkins, Hugh, Westra, Harm-Jan, Wilks, Rainford, Wilsgaard, Tom, Yang, Tsun-Po, Yengo, Loic, Bovet, Pascal, Cooper, Richard S, Elliott, Paul, Willer, Cristen J, Lind, Lars, Assimes, Themistocles L, Snieder, Harold, Melander, Olle, Laakso, Markku, Rauramaa, Rainer, Ingelsson, Erik, Hveem, Kristian, Kumari, Meena, Rotter, Jerome I, Lakatta, Edward G, Palmer, Colin N A, Chakravarti, Aravinda, Deloukas, Panos

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Whole-genome sequence-based analysis of thyroid function von Taylor, Peter N., Porcu, Eleonora, Chew, Shelby, Campbell, Purdey J., Traglia, Michela, Brown, Suzanne J., Mullin, Benjamin H., Shihab, Hashem A., Min, Josine, Walter, Klaudia, Memari, Yasin, Huang, Jie, Barnes, Michael R., Beilby, John P., Charoen, Pimphen, Danecek, Petr, Dudbridge, Frank, Forgetta, Vincenzo, Greenwood, Celia, Grundberg, Elin, Johnson, Andrew D., Hui, Jennie, Lim, Ee M., McCarthy, Shane, Muddyman, Dawn, Panicker, Vijay, Perry, John R.B., Bell, Jordana T., Yuan, Wei, Relton, Caroline, Gaunt, Tom, Schlessinger, David, Abecasis, Goncalo, Cucca, Francesco, Surdulescu, Gabriela L., Woltersdorf, Wolfram, Zeggini, Eleftheria, Zheng, Hou-Feng, Toniolo, Daniela, Dayan, Colin M., Naitza, Silvia, Walsh, John P., Spector, Tim, Davey Smith, George, Durbin, Richard, Brent Richards, J., Sanna, Serena, Soranzo, Nicole, Timpson, Nicholas J., Wilson, Scott G.

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Genetics of rheumatoid arthritis contributes to biology and drug discovery von Okada, Yukinori, Wu, Di, Trynka, Gosia, Raj, Towfique, Terao, Chikashi, Ikari, Katsunori, Kochi, Yuta, Ohmura, Koichiro, Suzuki, Akari, Yoshida, Shinji, Graham, Robert R., Manoharan, Arun, Ortmann, Ward, Bhangale, Tushar, Denny, Joshua C., Carroll, Robert J., Eyler, Anne E., Greenberg, Jeffrey D., Kremer, Joel M., Pappas, Dimitrios A., Jiang, Lei, Yin, Jian, Ye, Lingying, Su, Ding-Feng, Yang, Jian, Xie, Gang, Keystone, Ed, Westra, Harm-Jan, Esko, Tõnu, Metspalu, Andres, Zhou, Xuezhong, Gupta, Namrata, Mirel, Daniel, Stahl, Eli A., Diogo, Dorothée, Cui, Jing, Liao, Katherine, Guo, Michael H., Myouzen, Keiko, Kawaguchi, Takahisa, Coenen, Marieke J. H., van Riel, Piet L. C. M., van de Laar, Mart A. F. J., Guchelaar, Henk-Jan, Huizinga, Tom W. J., Dieudé, Philippe, Mariette, Xavier, Louis Bridges Jr, S., Zhernakova, Alexandra, Toes, Rene E. M., Tak, Paul P., Miceli-Richard, Corinne, Bang, So-Young, Lee, Hye-Soon, Martin, Javier, Gonzalez-Gay, Miguel A., Rodriguez-Rodriguez, Luis, Rantapää-Dahlqvist, Solbritt, Ärlestig, Lisbeth, Choi, Hyon K., Kamatani, Yoichiro, Galan, Pilar, Lathrop, Mark, Eyre, Steve, Bowes, John, Barton, Anne, de Vries, Niek, Moreland, Larry W., Criswell, Lindsey A., Karlson, Elizabeth W., Taniguchi, Atsuo, Yamada, Ryo, Kubo, Michiaki, Liu, Jun S., Bae, Sang-Cheol, Worthington, Jane, Padyukov, Leonid, Klareskog, Lars, Gregersen, Peter K., Raychaudhuri, Soumya, Stranger, Barbara E., De Jager, Philip L., Franke, Lude, Visscher, Peter M., Brown, Matthew A., Yamanaka, Hisashi, Mimori, Tsuneyo, Takahashi, Atsushi, Xu, Huji, Behrens, Timothy W., Siminovitch, Katherine A., Momohara, Shigeki, Matsuda, Fumihiko, Yamamoto, Kazuhiko, Plenge, Robert M.

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Large-scale association analysis provides insights into the genetic architecture and pathophysiology of type 2 diabetes von MORRIS, Andrew P, VOIGHT, Benjamin F, PROKOPENKO, Inga, HYUN MIN KANG, DINA, Christian, ESKOE, Tonu, FRASER, Ross M, KANONI, Stavroula, KUMAR, Ashish, LAGOU, Vasiliki, LANGENBERG, Claudia, LUAN, Jian'an, TESLOVICH, Tanya M, LINDGREN, Cecilia M, MÜLLER-NURASYID, Martina, PECHLIVANIS, Sonali, RAYNER, N. William, SCOTT, Laura J, WILTSHIRE, Steven, YENGO, Loic, KINNUNEN, Leena, ROSSIN, Elizabeth J, RAYCHAUDHURI, Soumya, FERREIRA, Teresa, JOHNSON, Andrew D, DIMAS, Antigones, LOOS, Ruthj F, VEDANTAM, Sailaja, HAN CHEN, FLOREZ, Jose C, FOX, Caroline, LIU, Ching-Ti, RYBIN, Denis, COUPER, David J, SEGRE, Ayellet V, KAO, Wen Hong L, MAN LI, CORNELIS, Marilyn C, KRAFT, Peter, QI SUN, VAN DAM, Rob M, STRINGHAM, Heather M, CHINES, Peter S, FISCHER, Krista, FONTANILLAS, Pierre, STEINTHORSDOTTIR, Valgerdur, HOLMEN, Oddgeir L, HUNT, Sarah E, JACKSON, Anne U, KONG, Augustine, LAWRENCE, Robert, MEYER, Julia, PERRY, John R. B, PLATOU, Carl G. P, POTTER, Simon, REHNBERG, Emil, STRAWBRIDGE, Rona J, KHAN, Hassan, GRALLERT, Harald, MAHAJAN, Anubha

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Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibility von Below, Jennifer E, Horikoshi, Momoko, Johnson, Andrew D, Ng, Maggie C Y, Abecasis, Goncalo R, Been, Latonya F, Caulfield, Mark, Chang, Li-Ching, Chang, Tien-Jyun, Chang, Yi-Cheng, Chen, Chien-Hsiun, Chen, Han, Chidambaram, Manickam, Cho, Young Min, Collins, Francis S, Das, Debashish, Dedoussis, George, Dimas, Antigone S, Doney, Alex S F, Dorkhan, Mozhgan, Edkins, Sarah, Erbel, Raimund, Fontanillas, Pierre, Fox, Caroline, Froguel, Philippe, Gao, Yutang, Gieger, Christian, Gigante, Bruna, Grallert, Harald, Guiducci, Candace, Hamsten, Anders, Hattersley, Andrew T, Hayward, Caroline, Herder, Christian, Hofman, Albert, Holmen, Oddgeir L, Humphries, Steve E, Hydrie, Zafar I, Jackson, Anne U, Jia, Weiping, Kato, Norihiro, Kelly, Ann M, Khan, Hassan, Kim, Hyung-Lae, Kong, Augustine, Korpi-Hyövälti, Eeva, Kumar, Ashish, Laakso, Markku, Langenberg, Claudia, Li, Man, Li, Xinzhong, Li, Yun, Liang, Junbin, Liju, Samuel, Lind, Lars, Lindgren, Cecilia M, Lobbens, Stéphane, Lu, Wei, Luan, Jian'an, Lyssenko, Valeriya, Männistö, Satu, Meigs, James B, Meyer, Julia, Mohlke, Karen L, Musk, Bill, Nakamura, Jiro, Park, Kyong Soo, Rallidis, Loukianos, Rasheed, Asif, Rehnberg, Emil, Rudan, Igor, Rybin, Denis, Saaristo, Timo E, Sanghera, Dharambir K, Saramies, Jouko, Scott, Robert A, Shah, Nabi, Sim, Xueling, Sivapalaratnam, Suthesh, Stančáková, Alena, Steinthorsdottir, Valgerdur, Stirrups, Kathleen, Strawbridge, Rona J, Takeuchi, Fumihiko, Thorsteinsdottir, Unnur, Trip, Mieke D, Valladares-Salgado, Adan, Wang, Congrong, Wickremasinghe, Ananda R, Wu, Ying, Yamamoto, Ken, Yang, Mingyu, Young, Robin, Zhang, Fan, Zhang, Rong, Altshuler, David, Cho, Yoon Shin, Lee, Jong-Young, Teo, Yik Ying, Boehnke, Michael

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Mutations in UPF3B, a member of the nonsense-mediated mRNA decay complex, cause syndromic and nonsyndromic mental retardation von Tarpey, Patrick S, Lucy Raymond, F, Nguyen, Lam S, Rodriguez, Jayson, Hackett, Anna, Vandeleur, Lucianne, Smith, Raffaella, Shoubridge, Cheryl, Edkins, Sarah, Stevens, Claire, O'Meara, Sarah, Tofts, Calli, Barthorpe, Syd, Buck, Gemma, Cole, Jennifer, Halliday, Kelly, Hills, Katy, Jones, David, Mironenko, Tatiana, Perry, Janet, Varian, Jennifer, West, Sofie, Widaa, Sara, Teague, John, Dicks, Ed, Butler, Adam, Menzies, Andrew, Richardson, David, Jenkinson, Andrew, Shepherd, Rebecca, Raine, Keiran, Moon, Jenny, Luo, Yin, Parnau, Josep, Bhat, Shambhu S, Gardner, Alison, Corbett, Mark, Brooks, Doug, Thomas, Paul, Parkinson-Lawrence, Emma, Porteous, Mary E, Warner, John P, Sanderson, Tracy, Pearson, Pauline, Simensen, Richard J, Skinner, Cindy, Hoganson, George, Superneau, Duane, Wooster, Richard, Bobrow, Martin, Turner, Gillian, Stevenson, Roger E, Schwartz, Charles E, Andrew Futreal, P, Srivastava, Anand K, Stratton, Michael R, Gécz, Jozef

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Quality control and conduct of genome-wide association meta-analyses von Winkler, Thomas W, Day, Felix R, Croteau-Chonka, Damien C, Wood, Andrew R, Locke, Adam E, Mägi, Reedik, Ferreira, Teresa, Fall, Tove, Graff, Mariaelisa, Justice, Anne E, Luan, Jian'an, Gustafsson, Stefan, Randall, Joshua C, Vedantam, Sailaja, Workalemahu, Tsegaselassie, Kilpeläinen, Tuomas O, Scherag, André, Esko, Tonu, Kutalik, Zoltán, Heid, Iris M, Loos, Ruth J F

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Bayesian refinement of association signals for 14 loci in 3 common diseases von Maller, Julian B, McVean, Gilean, Byrnes, Jake, Vukcevic, Damjan, Palin, Kimmo, Su, Zhan, Howson, Joanna M M, Auton, Adam, Myers, Simon, Morris, Andrew, Pirinen, Matti, Brown, Matthew A, Burton, Paul R, Caulfield, Mark J, Compston, Alastair, Farrall, Martin, Hall, Alistair S, Hattersley, Andrew T, Hill, Adrian V S, Mathew, Christopher G, Pembrey, Marcus, Satsangi, Jack, Stratton, Michael R, Worthington, Jane, Craddock, Nick, Hurles, Matthew, Ouwehand, Willem, Parkes, Miles, Rahman, Nazneen, Duncanson, Audrey, Todd, John A, Kwiatkowski, Dominic P, Samani, Nilesh J, Gough, Stephen C L, McCarthy, Mark I, Deloukas, Panagiotis, Donnelly, Peter

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