Treffer 1 - 20 von 33 für Suche 'Langford, R. Alan', Suchdauer: 1,87s Treffer weiter einschränken
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    Recurrent emergence of SARS-CoV-2 spike deletion H69/V70 and its role in the Alpha variant B.1.1.7 von Curran, Martin D., Roy, Sunando, Shaaban, Sharif, de Cesare, Mariateresa, Stark, Richard, Palmer, Steve, Jeffries, Aaron R., da Silva Filipe, Ana, Davis, Thomas, Collins, Jennifer, Williams, Thomas, Haldenby, Sam T., Cook, Kate, Davies, Robert, Kay, Sally, Poplawski, Radoslaw, Reynolds, Nicola, Moll, Robin J., Thornton, Alicia, Gatica-Wilcox, Bree, Louka, Stavroula F., Kraemer, Moritz U.G., Freeman, Timothy M., Abudahab, Khalil, Menegazzo, Mirko, Mason, Jenifer, Holmes, Alison, Curran, Tanya, Mookerjee, Siddharth, Munn, Robert, Davies, Alisha, Smith, Nikki, Cormie, Claire, Lo, Stephanie, Auckland, Cressida, Mollett, Guy, Harper, Katherine L., Bonner, Stephen, Padgett, Debra, Burton-Fanning, Shirelle, Bedford, Luke, Coupland, Lindsay, Wright, Victoria, Ball, Jonathan, Boswell, Tim, Duckworth, Nichola, Williams, Rebecca, Cogger, Benjamin J., Farr, Ben W., Thurston, Scott A.J., Bronner, Iraad F., Aigrain, Louise, Gallagher, Michael D., Miah, Shahjahan, Ramsay, Mary, Schaefer, Ulf, Manesis, Nikos, Allara, Elias, Nichols, Jenna, Vamos, Edith E., Hughes, Margaret, Wilson, Harry D., Wilson, Rebekah E., Thompson, Thomas, O’Brien, Sarah, Rudder, Steven, McCluggage, Kathryn, Bonfield, James, Liddle, Jennifier, Rowe, Will, Bevan, Paul, Clark, Richard, Cutts, Tim, Densem, Aiden, Dodd, David, Griffiths, Coline, Kay, Keely, Lensing, Stefanie, Lewis-Wade, Amanah, Mamun, Irfan, Martin, Matt, McClintock, Jo, Nathwani, Claire, Nicholson, Jon, Patel, Gaurang, Petersen, Arabella, Reynolds, Joe, Rudd, Luke, Sadri, Ramin, Sizer, Dale, Soria, Carmen Diaz, Sousa, Catarina, Squares, Janet, Stickland, Tim, Still, Ian, Symons, Edward, Uphill, James, Van, Philip Jansen, Voak, Paul, Corti, Davide

    Veröffentlicht in Cell reports (Cambridge)

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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

    Veröffentlicht in Nature genetics

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    Common variants at the MHC locus and at chromosome 16q24.1 predispose to Barrett's esophagus von Gay, Laura J, Palles, Claire, Band, Gavin, Whiteman, David C, Lescai, Francesco, Langford, Cordelia, Nanji, Manoj, Edkins, Sarah, van der Winkel, Anouk, Sasieni, Peter, Howarth, Kimberley, Pirinen, Matti, Peppelenbosch, Maikel P, Kuipers, Ernst J, Peters, Wilbert H, Reynolds, John V, Kelleher, Dermot P, McManus, Ross, Grabsch, Heike, Prenen, Hans, Krishnadath, Kausila, Siersema, Peter D, van Baal, Jantine W P M, Middleton, Mark, Petty, Russell, Burch, Nicola, Bhandari, Pradeep, Edwards, Cathryn, Penman, Ian, Murray, Iain, Mullins, Paul, Wu, Anna H, Bird, Nigel C, Dallal, Helen, Shaheen, Nicholas J, Bernstein, Leslie, Corley, Douglas A, Reid, Brian J, Gammon, Marilie D, Smart, Howard, Dhar, Anjan, McMurtry, Hugh, Ali, Haythem, Liu, Geoffrey, Rutter, Matt, Tawil, Ashref, Morris, Danielle, Nwokolo, Chuka, Isaacs, Peter, Rodgers, Colin, Ragunath, Krish, MacDonald, Chris, Monk, David, Wajed, Saj, Johnston, David, Gibbons, Michael, Church, Nicholas, Langley, Ruth, Griffin, Michael, Alderson, Derek, Hunt, Sarah E, Gray, Emma, Dronov, Serge, Potter, Simon C, Tashakkori-Ghanbaria, Avazeh, Brooks, Claire, Bramon, Elvira, Brown, Matthew A, Casas, Juan P, Corvin, Aiden, Duncanson, Audrey, Markus, Hugh S, Mathew, Christopher G, Palmer, Colin N A, Plomin, Robert, Rautanen, Anna, Trembath, Richard C, Viswanathan, Ananth C, Wood, Nicholas, Trynka, Gosia, Wijmenga, Cisca, Cazier, Jean-Baptiste, Gellatly, Nichola L, Glancy, Deborah, Cooper, Sheldon C, Cunningham, David, Hapeshi, Julie, Ferry, David, Rathbone, Barrie, MacGregor, Stuart, Watson, Peter, Sanders, Scott, Ek, Weronica, Harrison, Rebecca F, de Caestecker, John, Barr, Hugh, Vaughan, Thomas L, Peltonen, Leena, Spencer, Chris C A, Jankowski, Janusz A Z

    Veröffentlicht in Nature genetics

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