Treffer 1 - 13 von 13 für Suche 'Uhlig, Manuel R', Suchdauer: 1,25s Treffer weiter einschränken
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    Large-scale sequencing identifies multiple genes and rare variants associated with Crohn’s disease susceptibility von Stevens, Christine R., Venkataraman, Guhan R., Avila, Brandon, Abreu, Maria T., Ahmad, Tariq, Allez, Matthieu, Ananthakrishnan, Ashwin N., Barrett, Jeffrey C., Barzilai, Nir, Beaugerie, Laurent, Beecham, Ashley, Bokemeyer, Bernd, Chan, Andrew, Cleynen, Isabelle, Cosnes, Jacques, Cutler, David J., Daly, Allan, Damas, Oriana M., Datta, Lisa W., Dawany, Noor, Devoto, Marcella, Dodge, Sheila, Ellinghaus, Eva, Farkkila, Martti, Faubion, William, Ferreira, Manuel, Gabriel, Stacey B., Ge, Tian, Georges, Michel, Gettler, Kyle, Giri, Mamta, Goyette, Philippe, Graham, Daniel, Hämäläinen, Eija, Haritunians, Talin, Heap, Graham A., Hiltunen, Mikko, Hoeppner, Marc, Horowitz, Julie E., Iyer, Vivek, Kelsen, Judith, Khalili, Hamed, Kirschner, Barbara S., Koskela, Jukka T., Kugathasan, Subra, Kupcinskas, Juozas, Laudes, Matthias, Levine, Adam P., Liefferinckx, Claire, Loescher, Britt-Sabina, Louis, Edouard, Mansfield, John, May, Sandra, McCauley, Jacob L., Mengesha, Emebet, Mni, Myriam, Moayyedi, Paul, Newberry, Rodney D., Okou, David T., Ostrer, Harry, Paquette, Jean, Pekow, Joel, Pierik, Marieke J., Ponsioen, Cyriel Y., Pontikos, Nikolas, Prescott, Natalie, Pulver, Ann E., Rahmouni, Souad, Sands, Bruce, Sartor, R. Balfour, Schiff, Elena R., Schreiber, Stefan, Schumm, L. Philip, Segal, Anthony W., Seksik, Philippe, Sheikh, Shehzad Z., Silverberg, Mark S., Simmons, Alison, Skeiceviciene, Jurgita, Sokol, Harry, Solomonson, Matthew, Somineni, Hari, Sun, Dylan, Targan, Stephan, Turner, Dan, van der Meulen, Andrea E., Vermeire, Séverine, Verstockt, Sare, Voskuil, Michiel D., Duerr, Richard H., Franke, Andre, Brant, Steven R., Cho, Judy, Parkes, Miles, Xavier, Ramnik J., Rivas, Manuel A., Rioux, John D., McGovern, Dermot P. B., Huang, Hailiang, Anderson, Carl A.

    Veröffentlicht in Nature genetics

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    A protein-truncating R179X variant in RNF186 confers protection against ulcerative colitis von Rivas, Manuel A, Graham, Daniel, Stevens, Christine, Desch, A. Nicole, Goyette, Philippe, Gudbjartsson, Daniel, Jonsdottir, Ingileif, Thorsteinsdottir, Unnur, Degenhardt, Frauke, Kurki, Mitja I, Li, Dalin, Annese, Vito, Vermeire, Severine, Weersma, Rinse K, Halfvarson, Jonas, Paavola-Sakki, Paulina, Lappalainen, Maarit, Lek, Monkol, Cummings, Beryl, Tukiainen, Taru, Haritunians, Talin, Halme, Leena, Koskinen, Lotta L. E, Luo, Yang, Heap, Graham A, Barrett, J, de Lange, K, Edwards, C, Hart, A, Jostins, L, Kennedy, N, Lamb, C, Lees, C, Mansfield, J, Mowatt, C, Newman, W, Nimmo, E, Parkes, M, Pollard, M, Prescott, N, Rice, D, Satsangi, J, Simmons, A, Tremelling, M, Uhlig, H, Abraham, C, Achkar, J.P, Bitton, A, Glas, J, Limbergen, J.V, Schumm, P.L, Sharma, Y, Stempak, J.M, Targan, S.R, Neale, Benjamin M, Anderson, Carl A, Duerr, Richard H, Cho, Judy H, Saavalainen, Päivi, Kontula, Kimmo, McGovern, Dermot P. B, Franke, Andre, Stefansson, Kari, Rioux, John D, Xavier, Ramnik J, Daly, Mark J, Barrett, J, de Lane, K, Edwards, C, Hart, A, Hawkey, C, Jostins, L, Kennedy, N, Lamb, C, Lee, J, Lees, C, Mansfield, J, Mathew, C, Newman, B, Nimmo, E, Prescott, N, Randall, J, Rice, D, Satsangi, J, Simmons, A, Uhlig, H, Wilson, D, Abraham, C, Achkar, J. P, Bitton, A, Boucher, G, Croitoru, K, Limbergen, J. V, Milgrom, R, Proctor, D, Regueiro, M, Schumm, P. L, Sharma, Y, Targan, S. R, Wang, M. H


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    Large-scale sequencing identifies multiple genes and rare variants associated with Crohn's disease susceptibility von Sazonovs, Aleksejs, Stevens, Christine R, Venkataraman, Guhan R, Yuan, Kai, Abreu, Maria T, Ahmad, Tariq, Atzmon, Gil, Barzilai, Nir, Beecham, Ashley, Bernstein, Charles N, Bitton, Alain, Chan, Andrew, Chung, Daniel, Cosnes, Jacques, Cutler, David J, Daly, Allan, Damas, Oriana M, Datta, Lisa W, Dawany, Noor, Devoto, Marcella, Dodge, Sheila, Fachal, Laura, Farkkila, Martti, Ferreira, Manuel, Franchimont, Denis, Gabriel, Stacey B, Ge, Tian, Georges, Michel, Gettler, Kyle, Giri, Mamta, Glaser, Benjamin, Goerg, Siegfried, Goyette, Philippe, Graham, Daniel, Hiltunen, Mikko, Horowitz, Julie E, Irving, Peter, Iyer, Vivek, Jalas, Chaim, Kelsen, Judith, Khalili, Hamed, Kontula, Kimmo, Kugathasan, Subra, Laudes, Matthias, Levine, Adam P, Liefferinckx, Claire, Loescher, Britt-Sabina, Louis, Edouard, Mansfield, John, May, Sandra, Mengesha, Emebet, Mni, Myriam, Moayyedi, Paul, Moran, Christopher J, O'Charoen, Sirimon, Okou, David T, Oldenburg, Bas, Paquette, Jean, Pekow, Joel, Peter, Inga, Ponsioen, Cyriel Y, Prescott, Natalie, Rahmouni, Souad, Rice, Daniel L, Sartor, R Balfour, Schiff, Elena R, Schreiber, Stefan, Schumm, L Philip, Segal, Anthony W, Sheikh, Shehzad Z, Silverberg, Mark S, Simmons, Alison, Skeiceviciene, Jurgita, Sokol, Harry, Solomonson, Matthew, Somineni, Hari, Uhlig, Holm H, van der Meulen, Andrea E, Vermeire, Séverine, Winter, Harland S, Young, Justine, Belgium IBD Consortium, Cedars-Sinai IBD, International IBD Genetics Consortium, NIDDK IBD Genetics Consortium, NIHR IBD BioResource, Regeneron Genetics Center, SHARE Consortium, SPARC IBD Network, UK IBD Genetics Consortium, Duerr, Richard H, Franke, Andre, Brant, Steven R, Cho, Judy, Parkes, Miles, Rivas, Manuel A, Rioux, John D, McGovern, Dermot PB, Anderson, Carl A, Daly, Mark J

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